https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdk9-antibody-a00794-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00794-cdk9-primary-antibodies-wb-testing-3_1.jpgAnti-Cyclin-dependent kinase 9 Cdk9 AntibodyWestern Blot Results of Anti-cdk9 (PITALRE) Antibody.
Lane 1: Opal Prestined Molecular Weight Marker .
Lane 2: Human Kidney Lysate [5µg] [+].
Lane 3: PC3 Lysate [20µg] [+].
Lane 4: Null [-].
Primary Antibody: Anti-cdk9 at 1:1000 overnight at 2-8°C.
Secondary Antibody: Goat Anti-Rabbit HRP mx10 at 1:70,000 for 30 mins RT.
Blocking: 5% BLOTTO, 3%BSA in 1XTBST for 1 hr at RT.
Expected MW: ~42-55kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00794-cdk9-primary-antibodies-if-testing-1_1.jpgAnti-Cyclin-dependent kinase 9 Cdk9 AntibodyImmunocytochemical staining of mouse tissue using anti-cdk9 (PITALRE) antiserum. The staining shows the location of mcdk9/PITALRE protein in developing mouse tissue. Arrows indicate areas of high expression. Panel A: Peroxidase-DAB immunostaining of mcdk9/PITALRE protein in the developing mouse brain in the differentiated region of the medulla oblongata just below the fourth ventricle. Similar staining is shown in Panel B in the dorsal root ganglia. Panel C: Fluorescein immunofluorescence of mcdk9IPITALRE in skeletal muscle. Similar staining is shown in Panel D in cardiac muscle. Other detection systems should yield similar results. Sections from each specimen were cut at 5-7 µm, mounted on glass and dried overnight at 37°C. All sections then were deparaffinized in xylene, rehydrated through a graded alcohol series and washed in phosphate-buffered saline (PBS). PBS was used for all subsequent washes and for antiserum dilution. Tissue sections were quenched sequentially in 0.5% hydrogen peroxide and blocked with diluted 10% normal goat anti-rabbit serum. Slides were incubated at 20° C for 1 h with rabbit anti-cdk9 (1:500) dilution, washed, and then reacted with diluted goat anti-rabbit biotinylated antibody for 30 min. All the slides were then reacted with streptavidin-peroxidase conjugate for 30 min at 20° C. Diaminobenzidine was used as the final chromogen and hematoxylin was used as the nuclear counterstain. Negative controls for each tissue section were prepared by substituting the primary antiserum with pre-immune serum.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00794-cdk9-primary-antibodies-wb-testing-2_1.jpgAnti-Cyclin-dependent kinase 9 Cdk9 AntibodyBoster anti cdk9 antibody (100-401-167 1:1500 ) was used for Western blot analysis of 1) PC3 and 2) DU145 prostate cancer cells (50ug per lane). Bands at the expected MW of 55 and 42 Kda were detected. Personal communication Flavio Rizzolio, Temple University
https://www.bosterbio.com/products/primary-antibodies/anti-cd31-antibody-a01513-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-pecam1-primary-antibodies-wb-testing-2_1.jpgAnti-CD31 PECAM1 AntibodyWestern Blot of Rabbit Anti-CD31 Antibody. Lane 1: 3T3 Whole cell lysate . Lane 2: Jurkat Whole cell lysate . Lane 3: HT-29 Whole cell lysate . Load: 10µg/lane. Primary Antibody Anti-CD-31 used 1:500 with 0.75% TBS with Casein overnight. Secondary Antibody Goat anti-rabbit HRP used 1:40,000 for 30 min at room temp. Expect MW: 80kda.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-pecam1-primary-antibodies-ihc-testing-1_1.jpgAnti-CD31 PECAM1 AntibodyImmunohistochemistry with anti-CD31 antibody showing CD31 staining of vascular endothelium in human colon at 20x and 40x (B & C). Formalin fixed/paraffin embedded sections were subjected to heat induced epitope retrieval (HIER) at pH 6.2 and then incubated with rabbit anti-human CD31 antibody at 4.0 µg/ml for 60 minutes. The reaction was developed using MACH 1 universal HRP polymer detection system and visualized with 3’3-diamino-benzidine substrate (DAB).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-41598_2015_article_bfsrep08888_fig3_html.jpgAnti-CD31 PECAM1 AntibodySH inhibits angiogenesis and promotes vessel normalization. (A) Staining for CD31 (red) showing the vessel area (CD31 + area, %) and vessel diameters in tumors. (B) Staining for FITC-conjugated lectin (green) and CD31 (red) indicating perfused lectin + CD31 + vessels (% of CD31 + vessels) in tumors. (C) The tumor oxygen supply was determined by HIF-1α staining (HIF-1α + /total cells). (D) HE staining showing necrosis (necrotic area is marked with red lines) in tumors. (E) Double staining for CD31 (red) and α-SMA (green) showing pericyte-covered tumor vessels within tumors which is further emphasized by confocal microscopy analysis of double staining of thick tumor sections followed by 3D projection of z-slice images (F). (G) Tumor volumes in mice injected intravenously with a suboptimal dose of doxorubicin (Doxo) or saline combined with SH administration. Bars: 100 μm. Statistical significance: P < 0.05 (*), P < 0.01 (**) or P < 0.001 (***), N = 6–8. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fsrep08888'>25749075</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-mlf1-antibody-a07180-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07180-cenpu-primary-antibodies-wb-testing-3.jpgAnti-MLF1 CENPU AntibodyWestern blot using Boster's affinity purified anti-MLF1IP / PBIP1 antibody shows detection of endogenous MLF1IP protein (a tier of four modified protein bands indicated by the arrowheads) in lysates of Hela cells (- lane). Cells treated with MLF1IP / PBIP1 shRNA (+ lane) show no staining. The identities of the higher and lower molecular weight bands are unknown. Primary antibody was used at 1:1,000. Personal Communication, K.S. Lee, NCI, Bethesda, MD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07180-cenpu-primary-antibodies-ihc-testing-1.jpgAnti-MLF1 CENPU AntibodyImmunohistochemistry of rabbit anti-MLF1 antibody. Tissue: brain, cerebellum. Fixation: formalin fixed paraffin embedded. Antigen retrieval: not required. Primary antibody: Anti-MLF1 at 5 µg/mL for 1 h at RT. Secondary antibody: Peroxidase rabbit secondary antibody at 1:10,000 for 45 min at RT. Staining: MLF1 as precipitated red signal with hematoxylin purple nuclear counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07180-cenpu-primary-antibodies-ihc-testing-2.jpgAnti-MLF1 CENPU AntibodyImmunohistochemistry of rabbit anti-MLF1 antibody. Tissue: heart. Fixation: formalin fixed paraffin embedded. Antigen retrieval: not required. Primary antibody: Anti-MLF1 at 5 µg/mL for 1 h at RT. Secondary antibody: Peroxidase rabbit secondary antibody at 1:10,000 for 45 min at RT. Staining: MLF1 as precipitated red signal with hematoxylin purple nuclear counterstain.
https://www.bosterbio.com/products/primary-antibodies/anti-alg6-antibody-a07747-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07747-alg6-primary-antibodies-ihc-testing-1.jpgAnti-ALG6 AntibodyImmunohistochemistry with anti-ALG6 antibody showing ALG6 staining in the squamous epithelium of the uterine cervix as well as in inflammatory elements diffused in the stroma of human cervical cancer tissue at 20x and 40x (B & C). Formalin fixed/paraffin embedded sections were subjected to heat induced epitope retrieval (HIER) at pH 6.2 and then incubated with rabbit anti-human ALG6 antibody at 4.0 µg/ml for 60 minutes. The reaction was developed using MACH 1 universal HRP polymer detection system and visualized with 3’3-diamino-benzidine substrate (DAB).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07747-alg6-primary-antibodies-wb-testing-2.jpgAnti-ALG6 AntibodyWestern Blot of Rabbit anti-ALG6 antibody. Lane 1: HeLa Whole Cell lysate . Lane 2: MOLT4 Whole Cell lysate . Lane 3: K-562 Whole Cell lysate . Load: 10 µg per lane. Primary antibody: ALG6 antibody at 1:500 for overnight at 4°C. Secondary antibody: Peroxidase rabbit secondary antibody at 1:40,000 for 30 min at RT. Block: TBS-Casein overnight at 4°C. Predicted/Observed size: 58 kDa ALG-6.
https://www.bosterbio.com/products/primary-antibodies/anti-ldb2-antibody-a09871-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09871-ldb2-primary-antibodies-ihc-testing-1.jpgAnti-LIM domain-binding protein 2 LDB2 AntibodyBoster's Affinity Purified anti-LDB2 (Clim1) antibody was used at a 5 µg/ml to detect LDB2 in human brain cortex tissue. The image shows the localization of antibody as the precipitated red signal, with a hematoxylin purple nuclear counter stain. Tissue was formalin-fixed and paraffin embedded.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09871-ldb2-primary-antibodies-wb-testing-2.jpgAnti-LIM domain-binding protein 2 LDB2 AntibodyWestern blot using Boster's Affinity Purified anti-LDB2 antibody shows detection of a 43-kDa band corresponding to LDB2 in a lysates prepared from human kidney (lane 1) and mouse spleen (lane 2) tissues. Approximately 18 µg of lysate was run on a SDS-PAGE and transferred onto nitrocellulose followed by reaction with a 1:500 dilution of anti-LDB2 antibody. Detection occurred using a 1:5,000 dilution of HRP-labeled Goat anti-Rabbit IgG for 1 hour at room temperature. A chemiluminescence system was used for signal detection (Roche) using a 1 min exposure time.
https://www.bosterbio.com/products/primary-antibodies/anti-sumo-antibody-a19764-boster.html2026-03-24T05:06:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19764-sumo1-primary-antibodies-pathway-testing-2.jpgAnti-SUMO SUMO1P1 AntibodyMost modifiers mature by proteolytic processing from inactive precursors (a; amino acid). Arrowheads point to the cleavage sites. Ubiquitin is expressed either as polyubiquitin or as a fusion with ribosomal proteins. Conjugation requires activating (E1) and conjugating (E2) enzymes that form thiolesters (S) with the modifiers. Modification of cullins by RUB involves SCF(SKP1/cullin-1/F-box protein) /CBC(cullin-2/elongin B/elonginC) -like E3 enzymes that are also involved in ubiquitination. In contrast to ubiquitin, the UBLs do not seem to form multi-UBL chains. UCRP(ISG15) resembles two ubiquitin moieties linked head-to-tail. Whether HUB1 functions as a modifier is currently unclear. APG12 and URM1 are distinct from the other modifiers because they are unrelated in sequence to ubiquitin. Data contributed by S.Jentsch.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19764-sumo1-primary-antibodies-wb-testing-1.jpgAnti-SUMO SUMO1P1 AntibodyWestern blot of hSUMO fusion protein. Anti-SUMO antibody, generated by immunization with recombinant human SUMO, was tested by western blot against a SUMO-GFP fusion protein after cleavage by proteases. Dilution of the antibody between 1:1,000 and 1:5,000 showed strong reactivity specifically with the SUMO portion of the fusion protein ~11.5kDa (arrowhead). In this blot the antibody was used at a 1:2000 dilution incubated overnight at 4° C in 5% BLOTTO in TTBS. Detection occurred using a 1:2000 dilution of HRP-labeled Donkey anti-Rabbit IgG for 1 hour at room temperature. A chemiluminescence system was used for signal detection (Roche). Other detection systems will yield similar results. Data contributed by M. Malakhov, www.lifesensors.com, personal communication.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pax6-antibody-m00273-boster.html2026-03-24T05:06:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-pax6-primary-antibodies-if-testing-1.jpgAnti-PAX6 Monoclonal AntibodyImmunofluorescence Microscopy of Mouse anti-PAX6 antibody. Tissue: Hela Cell,20X. Fixation: 4% PFA room temp for 10 min. Antigen retrieval: not required. Primary antibody: PAX6 antibody at 1:100 for 1 h at RT. Secondary antibody: goat anti-mouse secondary antibody at 1:1,000 for 45 min at RT. Localization: PAX6 is nuclear. Staining: PAX6 as red fluorescent signal with DAPI (blue) nuclear counterstain. Images courtesy of Yang Xiang with Boston Children's Hospital.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bin1-antibody-m01551-boster.html2026-03-24T05:06:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01551-bin1-primary-antibodies-wb-testing-1.jpgAnti-BIN1/Amphiphysin Ii Monoclonal AntibodyWestern Blot of Anti-BIN1 Antibody. Lane 1: Keratinocyte derived from Bin1 wild type mice. Lane 2: Keratinocyte derived from Bin1 null mice. Load: 35 µg per lane. Primary antibody: BIN1 monoclonal Antibody. Secondary antibody: IRDye800™ mouse secondary antibody at 1:10,000 for 45 min at RT. Block: 1xPBS, 0.4% Tween-20. Other band(s): non-specific.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01551-bin1-primary-antibodies-fcm-testing-3.jpgAnti-BIN1/Amphiphysin Ii Monoclonal AntibodyFlow Cytometry of Mouse Anti-BIN1 Antibody. Cells: C2C12 cells. Stimulation: none. Primary antibody: Anti-IgD (control), Anti-BIN-1 Antibody (99D clone). Secondary antibody: Biotin mouse secondary antibody at 1:10,000 for 45 min at RT and streptavidin PE at 1:5,000 for 30 min at RT.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ido1-antibody-m01705-boster.html2026-03-24T05:06:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-if-testing-1.jpgAnti-IDO1/Ido Monoclonal AntibodyImmunofluorescence Microscopy of Mouse Anti-IDO1 Antibody. Cells: HEK293 cells. Fixation: 0.5% PFA. Expressing: mouse IDO-1 (left) and mouse IDO-2 (right). Primary antibody: IDO1 (2E2) monoclonal antibody. Antigen retrieval: not required. Secondary antibody: mouse secondary antibody at 1:10,000 for 45 min at RT. Localization: IDO-1 is located in the cytosol. Staining: IDO1 as red fluorescent signal with bis-benzimide nuclear counterstain (blue).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-ihc-testing-2.jpgAnti-IDO1/Ido Monoclonal AntibodyImmunohistochemistry of Mouse anti-IDO1 antibody. Tissue: epididymis from wild-type (left) or IDO1 null mice (right). Fixation: paraffin-embedded. Primary antibody: IDO1 (2E2) monoclonal antibody. Secondary antibody: Peroxidase mouse secondary antibody at 1:10,000 for 45 min at RT. Localization: IDO-1 is located in the cytosol. Staining: IDO 1 as precipitated brown signal.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-ihc-testing-3.jpgAnti-IDO1/Ido Monoclonal AntibodyImmunohistochemistry of Mouse Anti-IDO1 Antibody. Tissue: epididymis from wild-type (left) or IDO1 null mice (right). Fixation: frozen sections. Antigen retrieval: not required. Primary antibody: IDO1 (2E2) monoclonal antibody. Secondary antibody: Peroxidase mouse secondary antibody at 1:10,000 for 45 min at RT. Localization: IDO-1 is located in the cytosol. Staining: IDO 1 as precipitated brown signal.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-wb-testing-4.jpgAnti-IDO1/Ido Monoclonal AntibodyWestern Blot of Mouse Anti-IDO1 Antibody. Extracts from 293HEK Cells expressing: Lane 1: Control Vector. Lane 2: His-tagged mouse IDO1. Lane 3: mouse IDO1. Lane 4: His-tagged mouse IDO2. Lane 5: mouse IDO2. Lane 6: Epididymis from IDO null. Lane 7: wild type mice. Primary antibody: IDO-1(2E2) monoclonal antibody. Secondary antibody: IRDye800™ mouse secondary antibody at 1:10,000 for 45 min at RT. Block: 1xPBST overnight at 4°C. Predicted/Observed size: 41-42 kDa/41-42 kDa for IDO-1. Other band(s): none.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-fcm-testing-5.jpgAnti-IDO1/Ido Monoclonal AntibodyFlow Cytometry of Mouse Anti-IDO1 antibody. Cells: HEK293 cells. Expresing: mouse IDO-1(blue) and mouse IDO-2 (red). Primary antibody: IDO1 (2E2) monoclonal antibody. Secondary antibody: Biotin mouse secondary antibody at 1:10,000 for 45 min at RT and streptavidin PE at 1:5,000 for 30 min at RT.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-ido1-primary-antibodies-wb-testing-6.jpgAnti-IDO1/Ido Monoclonal AntibodyWestern Blot of mouse anti-IDO1 antibody. Lane 1: HEK293 control vector. Lane 2: HEK293 expressing mouse IDO1. Lane 3: HEK293 expressing mouse IDO2. Load: 35 µg per lane. Primary antibody: IDO 1 antibody at 1:400 for overnight at 4°C. Secondary antibody: IRDye800™ mouse secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO overnight at 4°C. Predicted/Observed size: 45.6 kDa, ~44 kDa for IDO1. Other band(s): non-specifics.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ido1-antibody-m01705-1-boster.html2026-03-24T05:06:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01705-1-ido1-primary-antibodies-wb-testing-1.jpgAnti-IDO1/Ido Monoclonal AntibodyWestern Blot of Mouse Anti-IDO1 Antibody. Lane 1: untreated HeLa cells . Lane 2: IFN-r treated HeLa cells. Load: 35 µg per lane. Primary antibody: IDO 1 Antibody at 1:1000 for overnight at 4°C. Secondary antibody: IRDye800™ mouse secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO overnight at 4°C. Predicted/Observed size: 41-42 kDa, 41-42 kDa for IDO-1. Other band(s): none.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nte-antibody-a04071-boster.html2026-03-24T05:06:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04071-pnpla6-primary-antibodies-wb-testing-2.jpgAnti-NTE PNPLA6 AntibodyWestern Blot analysis of AD293 cells using NTE Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04071-pnpla6-primary-antibodies-wb-testing-3.jpgAnti-NTE PNPLA6 AntibodyWestern blot analysis of lysate from AD293 cells, using PNPLA6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04071-pnpla6-primary-antibodies-ihc-testing-4.jpgAnti-NTE PNPLA6 AntibodyImmunohistochemical analysis of paraffin-embedded rat-testis, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04071-pnpla6-primary-antibodies-ihc-testing-1.jpgAnti-NTE PNPLA6 AntibodyImmunohistochemical analysis of paraffin-embedded rat-testis, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cytokeratin-13-antibody-a04299-boster.html2026-03-24T05:06:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04299-krt13-primary-antibodies-wb-testing-2.jpgAnti-Cytokeratin 13 KRT13 AntibodyWestern Blot analysis of various cells using Cytokeratin 13 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04299-krt13-primary-antibodies-wb-testing-3.jpgAnti-Cytokeratin 13 KRT13 AntibodyWestern Blot analysis of HepG2 cells using Cytokeratin 13 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04299-krt13-primary-antibodies-wb-testing-4.jpgAnti-Cytokeratin 13 KRT13 AntibodyWestern blot analysis of lysate from HepG2 cells, using Cytokeratin 13 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04299-krt13-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 13 KRT13 AntibodyImmunohistochemistry analysis of Cytokeratin 13 antibody in paraffin-embedded human heart tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbl1x-antibody-a07014-boster.html2026-03-24T05:06:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07014-tbl1x-primary-antibodies-wb-testing-1.jpgAnti-TBL1X Monoclonal AntibodyWestern Blot analysis using TBL1X Monoclonal Antibody against HEK293 (1) cell lysate.
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-lipocalin-2-ngal-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0853-boster.html2026-03-24T05:06:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0853-2-ELISA-human-lipocalin-2-ngal-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman Lipocalin-2/NGAL ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human Lipocalin-2/NGAL EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/primary-antibodies/anti-acsl3-picoband-trade-antibody-a05945-boster.html2026-03-24T05:06:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05945-1-WB-anti-acsl3-picoband-antibody.jpgAnti-ACSL3 Antibody Picoband® Western blot analysis of ACSL3 using anti-ACSL3 antibody (A05945).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACSL3 antigen affinity purified polyclonal antibody (Catalog # A05945) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACSL3 at approximately 80KD. The expected band size for ACSL3 is at 80KD.
https://www.bosterbio.com/products/primary-antibodies/anti-aff4-picoband-trade-antibody-a03824-boster.html2026-03-24T05:06:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03824-aff4-primary-antibodies-wb-testing-1.jpgAnti-AFF4 Antibody Picoband® Western blot analysis of AFF4 using anti-AFF4 antibody (A03824). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human 293T whole cell lysates, <br>
Lane 4: human U87 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AFF4 antigen affinity purified polyclonal antibody (Catalog # A03824) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AFF4 at approximately 150 kDa. The expected band size for AFF4 is at 127 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03824-aff4-primary-antibodies-ip-testing-1.jpgAnti-AFF4 Antibody Picoband®Immunoprecipitating (IP) AFF4 in 293T whole cell lysate.<br>
Western blot analysis of AFF4 using anti-AFF4 antibody (A03824); <br>
Lane 1: 293T whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-AFF4 antibody in 293T whole cell lysate;<br>
Lane 3: anti-AFF4 antibody (2μg) + 293T whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AFF4 antigen affinity purified polyclonal antibody (A03824) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for AFF4 at approximately 150 kDa. The expected band size for AFF4 is at 127 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03824-2.pngAnti-AFF4 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-AFF4 antibody (A03824). <br> Overlay histogram showing SiHa cells stained with A03824 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-AFF4 Antibody (A03824,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03824-aff4-primary-antibodies-ihc-testing-3.jpgAnti-AFF4 Antibody Picoband® IHC analysis of AFF4 using anti-AFF4 antibody (A03824). <br>
AFF4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AFF4 Antibody (A03824) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-alpp-picoband-trade-antibody-a01718-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-alpp-primary-antibodies-wb-testing-1.jpgAnti-Placental alkaline phosphatase (PLAP)/ALPP Antibody Picoband® Western blot analysis of ALPP using anti-ALPP antibody (A01718). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates, <br>
Lane 2: human placenta tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALPP antigen affinity purified polyclonal antibody (Catalog # A01718) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ALPP at approximately 70 kDa. The expected band size for ALPP is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-alpp-primary-antibodies-if-testing-4.jpgAnti-Placental alkaline phosphatase (PLAP)/ALPP Antibody Picoband® IF analysis of ALPP using anti-ALPP antibody (A01718). <br>
ALPP was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ALPP Antibody (A01718) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-alpp-primary-antibodies-fcm-testing-5.jpgAnti-Placental alkaline phosphatase (PLAP)/ALPP Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-ALPP antibody (A01718). <br>Overlay histogram showing SiHa cells stained with A01718 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ALPP Antibody (A01718, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-alpp-primary-antibodies-ihc-testing-2.jpgAnti-Placental alkaline phosphatase (PLAP)/ALPP Antibody Picoband® IHC analysis of ALPP using anti-ALPP antibody (A01718). <br>
ALPP was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ALPP Antibody (A01718) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-alpp-primary-antibodies-if-testing-3_1.jpgAnti-Placental alkaline phosphatase (PLAP)/ALPP Antibody Picoband® IF analysis of ALPP using anti- ALPP antibody (A01718). <br>
ALPP was detected in immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti- ALPP Antibody (A01718) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-angiogenin-ang-picoband-trade-antibody-a00146-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-12964_2024_1584_fig3_html.pngAnti-Angiogenin/ANG Antibody Picoband®Significant up- or downregulated exosomal proteins by SAL and Enz. A Bar chart shows up and downregulated proteins ( n = 4). B-C Volcano plots show the differentially expressed exosomal proteins. Proteins that were not classified as up- or downregulated are represented in black color (B: SAL vs. DMSO; C: Enz vs. DMSO; p < 0.05; n = 4). Red vertical lines define fold change ≥0.2 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01584-z'>38589887</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-wb-testing-1.jpgAnti-Angiogenin/ANG Antibody Picoband® Western blot analysis of Angiogenin/ANG using anti-Angiogenin/ANG antibody (A00146). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Angiogenin/ANG antigen affinity purified polyclonal antibody (Catalog # A00146) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Angiogenin/ANG at approximately 17 kDa. The expected band size for Angiogenin/ANG is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-ihc-testing-2.jpgAnti-Angiogenin/ANG Antibody Picoband® IHC analysis of Angiogenin/ANG using anti-Angiogenin/ANG antibody (A00146). <br>
Angiogenin/ANG was detected in a paraffin-embedded section of human hepatocellular carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Angiogenin/ANG Antibody (A00146) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-ihc-testing-3.jpgAnti-Angiogenin/ANG Antibody Picoband® IHC analysis of Angiogenin/ANG using anti-Angiogenin/ANG antibody (A00146). <br>
Angiogenin/ANG was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Angiogenin/ANG Antibody (A00146) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-if-testing-4.jpgAnti-Angiogenin/ANG Antibody Picoband® IF analysis of Angiogenin/ANG using anti-Angiogenin/ANG antibody (A00146) and anti-Beta Tubulin antibody (M01857-3).<br>
Angiogenin/ANG was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Angiogenin/ANG Antibody (A00146) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-fcm-testing-5.jpgAnti-Angiogenin/ANG Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Angiogenin/ANG antibody (A00146). <br>
Overlay histogram showing HepG2 cells stained with A00146 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Angiogenin/ANG Antibody (A00146, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00146-ang-primary-antibodies-elisa-testing-6.jpgAnti-Angiogenin/ANG Antibody Picoband® Sandwich ELISA - Recombinant human ANG protein standard curve.<br>
Use in combination with reagents from Human ANG ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0305).
https://www.bosterbio.com/products/primary-antibodies/anti-ap2b1-picoband-trade-antibody-a06544-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06544-ap2b1-primary-antibodies-wb-testing-1.jpgAnti-AP2B1 Antibody Picoband® Western blot analysis of AP2B1 using anti-AP2B1 antibody (A06544). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AP2B1 antigen affinity purified polyclonal antibody (Catalog # A06544) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AP2B1 at approximately 105 kDa. The expected band size for AP2B1 is at 105 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ap2m1-picoband-trade-antibody-a06179-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06179-ap2m1-primary-antibodies-wb-testing-1.jpgAnti-AP2M1 Antibody Picoband® Western blot analysis of AP2M1 using anti-AP2M1 antibody (A06179). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human U2OS whole cell lysates, <br> Lane 2: human MCF-7 whole cell lysates, <br> Lane 3: rat kidney tissue lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AP2M1 antigen affinity purified polyclonal antibody (Catalog # A06179) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AP2M1 at approximately 50KD. The expected band size for AP2M1 is at 50KD.
https://www.bosterbio.com/products/primary-antibodies/anti-arfgap1-antibody-a04959-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-ihc-testing-4.jpgAnti-ARFGAP1 Antibody Picoband®IHC analysis of ARFGAP1 using anti-ARFGAP1 antibody (A04959). <br>ARFGAP1 was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARFGAP1 Antibody (A04959) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-wb-testing-1.jpgAnti-ARFGAP1 Antibody Picoband® Western blot analysis of ARFGAP1 using anti-ARFGAP1 antibody (A04959). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MOLT-4 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARFGAP1 antigen affinity purified polyclonal antibody (Catalog # A04959) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARFGAP1 at approximately 45 kDa. The expected band size for ARFGAP1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-ihc-testing-2.jpgAnti-ARFGAP1 Antibody Picoband® IHC analysis of ARFGAP1 using anti-ARFGAP1 antibody (A04959). <br>
ARFGAP1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARFGAP1 Antibody (A04959) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-ihc-testing-3.jpgAnti-ARFGAP1 Antibody Picoband® IHC analysis of ARFGAP1 using anti-ARFGAP1 antibody (A04959). <br>
ARFGAP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARFGAP1 Antibody (A04959) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-if-testing-4.jpgAnti-ARFGAP1 Antibody Picoband® IF analysis of ARFGAP1 using anti-ARFGAP1 antibody (A04959). <br>
ARFGAP1 was detected in an immunocytochemical section of CACO-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ARFGAP1 Antibody (A04959) overnight at 4°C. DyLight594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04959-arfgap1-primary-antibodies-fcm-testing-5.jpgAnti-ARFGAP1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ARFGAP1 antibody (A04959). <br>Overlay histogram showing HepG2 cells stained with A04959 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARFGAP1 Antibody (A04959, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-atf4-picoband-trade-antibody-a00371-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00371-atf4-primary-antibodies-wb-testing-1_1.jpgAnti-ATF4 Antibody Picoband® Western blot analysis of ATF4 using anti-ATF4 antibody (A00371). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF4 antigen affinity purified polyclonal antibody (Catalog # A00371) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF4 at approximately 50 kDa. The expected band size for ATF4 is at 39 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-calpastatin-picoband-trade-antibody-a00337-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00337-calpastatin-primary-antibodies-wb-testing-1.jpgAnti-Calpastatin/CAST Antibody Picoband® Western blot analysis of Calpastatin using anti-Calpastatin antibody (A00337). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human Hacat whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calpastatin antigen affinity purified polyclonal antibody (Catalog # A00337) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calpastatin at approximately 120 kDa. The expected band size for Calpastatin is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00337-2-IHC-anti-calpastatin-picoband-antibody.jpgAnti-Calpastatin/CAST Antibody Picoband® IHC analysis of Calpastatin using anti-Calpastatin antibody (A00337).<br> Calpastatin was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Calpastatin Antibody (A00337) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00337-3-IHC-anti-calpastatin-picoband-antibody.jpgAnti-Calpastatin/CAST Antibody Picoband® IHC analysis of Calpastatin using anti-Calpastatin antibody (A00337).<br> Calpastatin was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Calpastatin Antibody (A00337) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00337-calpastatin-primary-antibodies-fc-testing-4.jpgAnti-Calpastatin/CAST Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-Calpastatin antibody (A00337). <br>Overlay histogram showing A549 cells stained with A00337 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpastatin Antibody (A00337,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00337-calpastatin-primary-antibodies-fc-testing-5.jpgAnti-Calpastatin/CAST Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-Calpastatin antibody (A00337). <br>Overlay histogram showing A431 cells stained with A00337 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpastatin Antibody (A00337,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00337-calpastatin-primary-antibodies-fc-testing-6.jpgAnti-Calpastatin/CAST Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Calpastatin antibody (A00337). <br>Overlay histogram showing U20S cells stained with A00337 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpastatin Antibody (A00337,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00337-calpastatin-primary-antibodies-if-testing-7.jpgAnti-Calpastatin/CAST Antibody Picoband® IF analysis of Calpastatin using anti-Calpastatin antibody (A00337). <br>
Calpastatin was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Calpastatin Antibody (A00337) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-pd-l1-b7-h1-picoband-trade-antibody-a00109-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00109-1-WB-anti-pd-l1-b7-h1-picoband-antibody.jpgAnti-PD-L1/B7-H1/CD274 Antibody Picoband® Western blot analysis of PD-L1/B7-H1 using anti-PD-L1/B7-H1 antibody (A00109). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HELA whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PD-L1/B7-H1 antigen affinity purified polyclonal antibody (Catalog # A00109) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PD-L1/B7-H1 at approximately 62KD. The expected band size for PD-L1/B7-H1 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cnpase-picoband-trade-antibody-a01017-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01017-1-WB-anti-cnpase-picoband-antibody.jpgAnti-CNPase Antibody Picoband® Western blot analysis of CNPase using anti-CNPase antibody (A01017).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysates,<br>
lane 2: mouse brain tissue lysates,<br>
lane 3: HELA whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CNPase antigen affinity purified polyclonal antibody (Catalog # A01017) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CNPase at approximately 47KD. The expected band size for CNPase is at 47KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cpm-picoband-trade-antibody-a01650-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01650-cpm-primary-antibodies-wb-testing-1.jpgAnti-Carboxypeptidase M/CPM Antibody Picoband® Western blot analysis of CPM using anti-CPM antibody (A01650). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human U20S whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CPM antigen affinity purified polyclonal antibody (Catalog # A01650) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CPM at approximately 65 kDa. The expected band size for CPM is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01650-cpm-primary-antibodies-fcm-testing-2.pngAnti-Carboxypeptidase M/CPM Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-CPM antibody (A01650). <br>
Overlay histogram showing Hela cells stained with A01650 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CPM Antibody (A01650, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cyp17a1-picoband-trade-antibody-a00615-1-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00615-1-cyp17a1-primary-antibodies-wb-testing-1.jpgAnti-Cytochrome P450 17A1/CYP17A1 Antibody Picoband® Western blot analysis of CYP17A1 using anti-CYP17A1 antibody (A00615-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP17A1 antigen affinity purified polyclonal antibody (Catalog # A00615-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYP17A1 at approximately 57 kDa. The expected band size for CYP17A1 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00615-1-2-IHC-anti-cyp17a1-cytochrome-p450-17a1-picoband-antibody.jpgAnti-Cytochrome P450 17A1/CYP17A1 Antibody Picoband® IHC analysis of CYP17A1 using anti-CYP17A1 antibody (A00615-1).<br>
CYP17A1 was detected in paraffin-embedded section of human testis tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CYP17A1 Antibody (A00615-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00615-1-3.pngAnti-Cytochrome P450 17A1/CYP17A1 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-CYP17A1 antibody (A00615-1). <br> Overlay histogram showing U87 cells stained with A00615-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CYP17A1 Antibody (A00615-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-doublecortin-picoband-trade-antibody-a01053-1-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01053-1-1-WB-anti-doublecortin-picoband-antibody.jpgAnti-Doublecortin/DCX Antibody Picoband® Western blot analysis of Doublecortin using anti-Doublecortin antibody (A01053-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysates,<br>
lane 2: mouse brain tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Doublecortin antigen affinity purified polyclonal antibody (Catalog # A01053-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Doublecortin at approximately 40KD. The expected band size for Doublecortin is at 40KD.
https://www.bosterbio.com/products/primary-antibodies/anti-e2f3-picoband-trade-antibody-a03068-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03068-1_1-WB-anti-e2f3-picoband-antibody.jpgAnti-E2F3 Antibody Picoband® Western blot analysis of E2F3 using anti-E2F3 antibody (A03068).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat liver tissue lysate,<br>
lane 2: mouse cardiac muscle tissue lysate,<br>
lane 3: U2OS whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-E2F3 antigen affinity purified polyclonal antibody (Catalog # A03068) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for E2F3 at approximately 49KD. The expected band size for E2F3 is at 49KD.
https://www.bosterbio.com/products/primary-antibodies/anti-emerin-picoband-trade-antibody-a00714-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-emerin-primary-antibodies-wb-testing-1.jpgAnti-Emerin/EMD Antibody Picoband® Western blot analysis of Emerin using anti-Emerin antibody (A00714). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: rat NRK whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Emerin antigen affinity purified polyclonal antibody (Catalog # A00714) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Emerin at approximately 34 kDa. The expected band size for Emerin is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-2_1.jpgAnti-Emerin/EMD Antibody Picoband® IHC analysis of Emerin using anti-Emerin antibody (A00714). <br> Emerin was detected in paraffin-embedded section of human endometrial carcinoma tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Emerin Antibody (A00714) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-3_1.jpgAnti-Emerin/EMD Antibody Picoband® IHC analysis of Emerin using anti-Emerin antibody (A00714). <br> Emerin was detected in paraffin-embedded section of human colon cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Emerin Antibody (A00714) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-4.jpgAnti-Emerin/EMD Antibody Picoband® IHC analysis of Emerin using anti-Emerin antibody (A00714). <br> Emerin was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Emerin Antibody (A00714) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-5.jpgAnti-Emerin/EMD Antibody Picoband® IF analysis of Emerin using anti-Emerin antibody (A00714) <br> Emerin was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-Emerin Antibody (A00714) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-6.jpgAnti-Emerin/EMD Antibody Picoband® IF analysis of Emerin using anti-Emerin antibody (A00714) <br> Emerin was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-Emerin Antibody (A00714) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-7_1.jpgAnti-Emerin/EMD Antibody Picoband® IF analysis of Emerin using anti-Emerin antibody (A00714). <br> Emerin was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Emerin Antibody (A00714) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-8.pngAnti-Emerin/EMD Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Emerin antibody (A00714). <br> Overlay histogram showing U20S cells stained with A00714 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Emerin Antibody (A00714,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00714-9.jpgAnti-Emerin/EMD Antibody Picoband® IF analysis of Emerin using anti-Emerin antibody (A00714). <br>
Emerin was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-Emerin Antibody (A00714) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using DyLight®488 Conjugated Avidin (BA1128). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-ephx2-picoband-trade-antibody-a01999-1-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01999-1-ephx2-primary-antibodies-wb-testing-1.jpgAnti-EPHX2 Antibody Picoband® Western blot analysis of EPHX2 using anti-EPHX2 antibody (A01999-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: rat liver tissue lysates, <br>
Lane 3: rat kidney tissue lysates, <br>
Lane 4: mouse liver tissue lysates, <br>
Lane 5: mouse kidney tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EPHX2 antigen affinity purified polyclonal antibody (Catalog # A01999-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EPHX2 at approximately 63 kDa. The expected band size for EPHX2 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01999-1-2_.pngAnti-EPHX2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-EPHX2 antibody (A01999-1). <br> Overlay histogram showing PC-3 cells stained with A01999-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EPHX2 Antibody (A01999-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-fgb-picoband-trade-antibody-a01204-1-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01204-1-fgb-primary-antibodies-ihc-testing-1.jpgAnti-Fibrinogen beta chain/FGB Antibody Picoband®IHC analysis of Fibrinogen Beta Chain/FGB using anti-Fibrinogen Beta Chain/FGB antibody (A01204-1). <br>Fibrinogen Beta Chain/FGB was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Fibrinogen Beta Chain/FGB Antibody (A01204-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01204-1-fgb-primary-antibodies-wb-testing-1.jpgAnti-Fibrinogen beta chain/FGB Antibody Picoband® Western blot analysis of Fibrinogen beta chain/FGB using anti-Fibrinogen beta chain/FGB antibody (A01204-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: rat kidney tissue lysates,<br>
Lane 3: rat liver tissue lysates,<br>
Lane 4: mouse kidney tissue lysates,<br>
Lane 5: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Fibrinogen beta chain/FGB antigen affinity purified polyclonal antibody (Catalog # A01204-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Fibrinogen beta chain/FGB at approximately 56 kDa. The expected band size for Fibrinogen beta chain/FGB is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01204-1-fgb-primary-antibodies-fcm-testing-3.jpgAnti-Fibrinogen beta chain/FGB Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Fibrinogen beta chain/FGB antibody (A01204-1). <br>Overlay histogram showing HepG2 cells stained with A01204-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Fibrinogen beta chain/FGB Antibody (A01204-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01204-1-fgb-primary-antibodies-if-testing-2.jpgAnti-Fibrinogen beta chain/FGB Antibody Picoband® IF analysis of Fibrinogen beta chain/FGB using anti-Fibrinogen beta chain/FGB antibody (A01204-1). <br>
Fibrinogen beta chain/FGB was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Fibrinogen beta chain/FGB Antibody (A01204-1) overnight at 4°C. DyLight594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-fgfr1-picoband-trade-antibody-a00098-boster.html2026-03-24T05:06:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00098-1-WB-anti-fgfr1-picoband-antibody.jpgAnti-FGFR1 Antibody Picoband® Western blot analysis of FGFR1 using anti-FGFR1 antibody (A00098).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HEPG2 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGFR1 antigen affinity purified polyclonal antibody (Catalog # A00098) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGFR1 at approximately 100KD. The expected band size for FGFR1 is at 91KD.
https://www.bosterbio.com/products/primary-antibodies/anti-fgg-picoband-trade-antibody-a00790-1-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00790-1-FGG-primary-antibodies-WB-testing-1.jpgAnti-Fibrinogen gamma chain/FGG Antibody Picoband® Western blot analysis of FGG using anti-FGG antibody (A00790-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human hepatocellular carcinoma tumor tissue (HCCT) lysates,<br>
Lane 3: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGG antigen affinity purified polyclonal antibody (Catalog # A00790-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGG at approximately 52 kDa. The expected band size for FGG is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00790-2-IHC-anti-fgg-picoband-antibody.jpgAnti-Fibrinogen gamma chain/FGG Antibody Picoband® IHC analysis of FGG using anti-FGG antibody (A00790-1).<br>
FGG was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FGG Antibody (A00790-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00790-1-3.pngAnti-Fibrinogen gamma chain/FGG Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-FGG antibody (A00790-1). <br> Overlay histogram showing SiHa cells stained with A00790-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FGG Antibody (A00790-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00790-1-4.pngAnti-Fibrinogen gamma chain/FGG Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-FGG antibody (A00790-1). <br> Overlay histogram showing A549 cells stained with A00790-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FGG Antibody (A00790-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-gab1-picoband-trade-antibody-a01989-1-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01989-1-1-WB-anti-gab1-picoband-antibody.jpgAnti-GAB1 Antibody Picoband® Western blot analysis of GAB1 using anti-GAB1 antibody (A01989-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat testis tissue lysates,<br>
lane 2: K562 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAB1 antigen affinity purified polyclonal antibody (Catalog # A01989-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAB1 at approximately 77KD. The expected band size for GAB1 is at 77KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hdgf-picoband-trade-antibody-a01057-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01057-hdgf-primary-antibodies-wb-testing-1.jpgAnti-HDGF Antibody Picoband® Western blot analysis of HDGF using anti-HDGF antibody (A01057). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDGF antigen affinity purified polyclonal antibody (Catalog # A01057) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDGF at approximately 38 kDa. The expected band size for HDGF is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01057-2_1-IHC-anti-hdgf-picoband-antibody.jpgAnti-HDGF Antibody Picoband® IHC analysis of HDGF using anti-HDGF antibody (A01057).<br>
HDGF was detected in paraffin-embedded section of mouse liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HDGF Antibody (A01057) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01057-3_1-IHC-anti-hdgf-picoband-antibody.jpgAnti-HDGF Antibody Picoband® IHC analysis of HDGF using anti-HDGF antibody (A01057).<br>
HDGF was detected in paraffin-embedded section of rat liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HDGF Antibody (A01057) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01057-4-IHC-anti-hdgf-picoband-antibody.jpgAnti-HDGF Antibody Picoband® IHC analysis of HDGF using anti-HDGF antibody (A01057).<br>
HDGF was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HDGF Antibody (A01057) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01057-5-IHC-anti-hdgf-picoband-antibody.jpgAnti-HDGF Antibody Picoband® IHC analysis of HDGF using anti-HDGF antibody (A01057).<br>
HDGF was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HDGF Antibody (A01057) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01057-6.jpgAnti-HDGF Antibody Picoband® IF analysis of HDGF using anti-HDGF antibody (A01057). <br>
HDGF was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HDGF Antibody (A01057) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01057-7.jpgAnti-HDGF Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-HDGF antibody (A01057).<br>Overlay histogram showing A431 cells stained with A01057 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDGF Antibody (A01057,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-hexokinase-ii-picoband-trade-antibody-a01389-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-12935_2020_1454_fig2_html.pngAnti-Hexokinase II/HK2 Antibody Picoband®The influences of circPOSTN silencing on proliferation, apoptosis and aerobic glycolysis of glioma cells. a – l LN229 and U251 cells were transfected with si-circPOSTN or si-NC. a The interference efficiency of si-circPOSTN was analyzed with RT-qPCR assay in LN229 and U251 cells. b , c Effect of circPOSTN silencing on the cell viability of LN229 and U251 cells was assessed with MTT assay. d The apoptosis rate was computed with flow cytometry assay in transfected LN229 and U251 cells. e The western blot assay showed the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The caspase-3 activity was measured with a caspase-3 assay kit. g – i The concentration of glucose and lactate in the culture medium, as well as ATP production level were measured with a series of kits, respectively. j The protein expression levels of HK2 and LDHA were determined with western blot assay in transfected LN229 and U251 cells. k – l LDHA enzyme activity and ROS accumulation were evaluated in LN229 and U251 cells post-transfection with lactate dehydrogenase activity detection kit and reactive oxygen species assay kit, respectively. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-12935_2020_1454_fig5_html.pngAnti-Hexokinase II/HK2 Antibody Picoband®CircPOSTN silencing inhibited aerobic glycolysis of glioma cells via regulating miR-361-5p. a – l LN229 and U251 cells were transfected with si-NC, si-circPOSTN, si-circPOSTN + anti-miR-NC, or si-circPOSTN + anti-miR-361-5p. a – f The concentration of glucose and lactate, as well as cellular ATP level were detected with different kits. g , h The protein expression levels of HK2 and LDHA in LN229 and U251 cells were measured with western blot assay. i – l The enzyme activity of LDHA and ROS level were measured in transfected LN229 and U251 cells. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-12935_2020_1454_fig7_html.pngAnti-Hexokinase II/HK2 Antibody Picoband®TPX2 regulated proliferation, apoptosis, and aerobic glycolysis in glioma cells. a – l LN229 and U251 cells were introduced with si-NC or si-TPX2. a The transfection efficiency of si-TPX2 was checked with RT-qPCR assay in LN229 and U251 cells. b , c The cell viability of LN229 and U251 cells was determined with MTT assay. d The apoptosis rate of transfected LN229 and U251 cells was represented by flow cytometry assay. e The western blot assay was used to assay the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The activity of caspase-3 was detected with a caspase-3 assay kit. g – i The glucose, lactate, and ATP production levels were shown. j The protein expression levels of HK2 and LDHA were estimated by western blot assay in LN229 and U251 cells. k , l LDHA enzyme activity and ROS content were evaluated in LN229 and U251 cells post-transfection. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-hk2-primary-antibodies-wb-testing-1_1.jpgAnti-Hexokinase II/HK2 Antibody Picoband®Western blot analysis of Hexokinase II using anti-Hexokinase II antibody (A01389). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human HepG2 whole cell lysates, <br>
Lane 4: rat skeletal muscle tissue lysates, <br>
Lane 5: rat heart tissue lysates, <br>
Lane 6: mouse skeletal muscle tissue lysates, <br>
Lane 7: mouse heart tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hexokinase II antigen affinity purified polyclonal antibody (A01389) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Hexokinase II at approximately 102 kDa. The expected band size for Hexokinase II is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-hk2-primary-antibodies-ihc-testing-1.jpgAnti-Hexokinase II/HK2 Antibody Picoband®IHC analysis of Hexokinase II using anti-Hexokinase II antibody (A01389). <br>
Hexokinase II was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hexokinase II Antibody (A01389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-hk2-primary-antibodies-ihc-testing-2.jpgAnti-Hexokinase II/HK2 Antibody Picoband®IHC analysis of Hexokinase II using anti-Hexokinase II antibody (A01389). <br>
Hexokinase II was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hexokinase II Antibody (A01389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-hk2-primary-antibodies-ihc-testing-3.jpgAnti-Hexokinase II/HK2 Antibody Picoband®IHC analysis of Hexokinase II using anti-Hexokinase II antibody (A01389). <br>
Hexokinase II was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hexokinase II Antibody (A01389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01389-hk2-primary-antibodies-fcm-testing-1.jpgAnti-Hexokinase II/HK2 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-Hexokinase II antibody (A01389). <br>
Overlay histogram showing HepG2 cells stained with A01389 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Hexokinase II Antibody (A01389, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-hla-dpb1-picoband-trade-antibody-a00487-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00487-hla-dpb1-primary-antibodies-wb-testing-1_1.jpgAnti-HLA-DPB1 Antibody Picoband® Western blot analysis of HLA-DPB1 using anti-HLA-DPB1 antibody (A00487). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates, <br>
Lane 2: human Raji whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HLA-DPB1 antigen affinity purified polyclonal antibody (Catalog # A00487) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HLA-DPB1 at approximately 29 kDa. The expected band size for HLA-DPB1 is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00487-hla-dpb1-primary-antibodies-ihc-testing-2.jpgAnti-HLA-DPB1 Antibody Picoband® IHC analysis of HLA-DPB1 using anti-HLA-DPB1 antibody (A00487). <br>
HLA-DPB1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HLA-DPB1 Antibody (A00487) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-a1-picoband-trade-antibody-a01476-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-hnrnp-a1-primary-antibodies-wb-testing-1.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® Western blot analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human Daudi whole cell lysates, <br>
Lane 3: human MOLT-4 whole cell lysates, <br>
Lane 4: human HL-60 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HnRNP A1 antigen affinity purified polyclonal antibody (Catalog # A01476) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HnRNP A1 at approximately 36 kDa. The expected band size for HnRNP A1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01476-2-IHC-anti-hnrnp-a1-picoband-antibody.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IHC analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476).<br>
HnRNP A1 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01476-3-IHC-anti-hnrnp-a1-picoband-antibody.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IHC analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476).<br>
HnRNP A1 was detected in paraffin-embedded section of mouse kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01476-4-IHC-anti-hnrnp-a1-picoband-antibody.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IHC analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476).<br>
HnRNP A1 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01476-5-IHC-anti-hnrnp-a1-picoband-antibody.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IHC analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476).<br>
HnRNP A1 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01476-6-IHC-anti-hnrnp-a1-picoband-antibody.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IHC analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476).<br>
HnRNP A1 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-7.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IF analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
HnRNP A1 was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-hnrnpa1-primary-antibodies-if-testing-8.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IF analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
HnRNP A1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-hnrnpa1-primary-antibodies-if-testing-9.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IF analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
HnRNP A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-12.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-HnRNP A1 antibody (A01476).<br>Overlay histogram showing K562 cells stained with A01476 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HnRNP A1 Antibody (A01476,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-10_1.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IF analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
HnRNP A1 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01476-11.jpgAnti-HnRNP A1/HNRNPA1 Antibody Picoband® IF analysis of HnRNP A1 using anti-HnRNP A1 antibody (A01476). <br>
HnRNP A1 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HnRNP A1 Antibody (A01476) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-f-picoband-trade-antibody-a05806-boster.html2026-03-29T05:00:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-hnrnpf-primary-antibodies-wb-testing-1.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® Western blot analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SKOV3 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human PANC-1 whole cell lysates,<br>
Lane 5: human RT4 whole cell lysates,<br>
Lane 6: human K562 whole cell lysates,<br>
Lane 7: human U20S whole cell lysates,<br>
Lane 8: human PC-3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HnRNPF antigen affinity purified polyclonal antibody (Catalog # A05806) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HnRNPF at approximately 46 kDa. The expected band size for HnRNPF is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-hnrnpf-primary-antibodies-wb-testing-2.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® Western blot analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat RH35 whole cell lysates,<br>
Lane 3: rat C6 whole cell lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse SP2/0 whole cell lysates,<br>
Lane 6: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HnRNPF antigen affinity purified polyclonal antibody (Catalog # A05806) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HnRNPF at approximately 46 kDa. The expected band size for HnRNPF is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05806-3-IHC-anti-hnrnp-f-picoband-antibody.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® IHC analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br> HnRNPF was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNPF Antibody (A05806) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-4-ihc-anti-hnrnp-f-picoband-antibody.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® IHC analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br> HnRNPF was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNPF Antibody (A05806) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-5.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® IHC analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br> HnRNPF was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNPF Antibody (A05806) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-6.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® IHC analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br> HnRNPF was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HnRNPF Antibody (A05806) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-8.pngAnti-HnRNP F/HNRNPF Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-HnRNPF antibody (A05806). <br> Overlay histogram showing U87 cells stained with A05806 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HnRNPF Antibody (A05806, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05806-7.jpgAnti-HnRNP F/HNRNPF Antibody Picoband® IF analysis of HnRNPF using anti-HnRNPF antibody (A05806). <br> HnRNPF was detected in immunocytochemical section of SKOV-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HnRNPF Antibody (A05806) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-h-picoband-trade-antibody-a07691-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-wb-testing-1.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® Western blot analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human LNCAP whole cell lysates,<br>
Lane 6: human U2OS whole cell lysates,<br>
Lane 7: human RT4 whole cell lysates,<br>
Lane 8: rat C6 whole cell lysates,<br>
Lane 9: rat PC-12 whole cell lysates,<br>
Lane 10: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HnRNP H/HNRNPH1 antigen affinity purified polyclonal antibody (Catalog # A07691) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HnRNP H/HNRNPH1 at approximately 49 kDa. The expected band size for HnRNP H/HNRNPH1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-2.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-3.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-4.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-5.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-6.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-7.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-8.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-9.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-10.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-11.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-ihc-testing-12.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IHC analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of rat brain hippocampus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-if-testing-13.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IF analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-if-testing-14.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IF analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/mL rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-if-testing-15.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® IF analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
HnRNP H/HNRNPH1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/mL rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-fcm-testing-16_1.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
Overlay histogram showing 293T cells stained with A07691 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-fcm-testing-17.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® Flow Cytometry analysis of Neuro2a cells using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
Overlay histogram showing Neuro2a cells stained with A07691 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-hnrnph1-primary-antibodies-fcm-testing-18.jpgAnti-HnRNP H/HNRNPH1 Antibody Picoband® Flow Cytometry analysis of C6 cells using anti-HnRNP H/HNRNPH1 antibody (A07691). <br>
Overlay histogram showing C6 cells stained with A07691 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HnRNP H/HNRNPH1 Antibody (A07691, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-il12rb1-picoband-trade-antibody-a03401-1-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03401-1-1-WB-anti-il12rb1-il-12-r-beta-1-picoband-antibody.jpgAnti-IL12RB1 Antibody Picoband® Western blot analysis of IL12RB1 using anti-IL12RB1 antibody (A03401-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL12RB1 antigen affinity purified polyclonal antibody (Catalog # A03401-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL12RB1 at approximately 70KD. The expected band size for IL12RB1 is at 73KD.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnq1-picoband-trade-antibody-a00310-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-wb-testing-1_1.jpgAnti-KCNQ1 Antibody Picoband® Western blot analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates, <br>
Lane 2: rat stomach tissue lysates, <br>
Lane 3: rat lung tissue lysates, <br>
Lane 4: rat PC-12 whole cell lysates, <br>
Lane 5: mouse stomach tissue lysates, <br>
Lane 6: mouse lung tissue lysates, <br>
Lane 7: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KCNQ1 antigen affinity purified polyclonal antibody (Catalog # A00310-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KCNQ1 at approximately 75 kDa. The expected band size for KCNQ1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-ihc-testing-2.jpgAnti-KCNQ1 Antibody Picoband® IHC analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
KCNQ1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KCNQ1 Antibody (A00310-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-ihc-testing-3.jpgAnti-KCNQ1 Antibody Picoband® IHC analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
KCNQ1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KCNQ1 Antibody (A00310-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-ihc-testing-4.jpgAnti-KCNQ1 Antibody Picoband® IHC analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
KCNQ1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KCNQ1 Antibody (A00310-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-ihc-testing-5.jpgAnti-KCNQ1 Antibody Picoband® IHC analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
KCNQ1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KCNQ1 Antibody (A00310-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-if-testing-6.jpgAnti-KCNQ1 Antibody Picoband® IF analysis of KCNQ1 using anti-KCNQ1 antibody (A00310-1). <br>
KCNQ1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-KCNQ1 Antibody (A00310-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00310-1-kcnq1-primary-antibodies-fcm-testing-7_1.pngAnti-KCNQ1 Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-KCNQ1 antibody (A00310-1). <br>Overlay histogram showing U937 cells stained with A00310-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-KCNQ1 Antibody (A00310-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd11b-picoband-trade-antibody-a00144-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00144-1_1.jpgAnti-CD11b/ITGAM Antibody Picoband® Western blot analysis of CD11b using anti-CD11b antibody (A00144). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: mouse brain tissue lysates,<br>
Lane 2: HEPA whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD11b antigen affinity purified polyclonal antibody (Catalog # A00144) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD11b at approximately 128KD. The expected band size for CD11b is at 127KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cytokeratin-5-picoband-trade-antibody-a00398-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00398-krt5-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 5/KRT5 Antibody Picoband® Western blot analysis of Cytokeratin 5 using anti-Cytokeratin 5 antibody (A00398). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample unde<br>r reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 5 antigen affinity purified polyclonal antibody (Catalog # A00398) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytokeratin 5 at approximately 62 kDa. The expected band size for Cytokeratin 5 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00398-2-IHC-anti-cytokeratin-5-picoband-antibody.jpgAnti-Cytokeratin 5/KRT5 Antibody Picoband® IHC analysis of Cytokeratin 5 using anti-Cytokeratin 5 antibody (A00398).<br>
Cytokeratin 5 was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 5 Antibody (A00398) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00398-3-IHC-anti-cytokeratin-5-picoband-antibody.jpgAnti-Cytokeratin 5/KRT5 Antibody Picoband® IHC analysis of Cytokeratin 5 using anti-Cytokeratin 5 antibody (A00398).<br>
Cytokeratin 5 was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 5 Antibody (A00398) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cytokeratin-14-picoband-trade-antibody-a01432-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01432-1-WB-anti-cytokeratin-14-picoband-antibody.jpgAnti-Cytokeratin 14/KRT14 Antibody Picoband® Western blot analysis of Cytokeratin 14 using anti-Cytokeratin 14 antibody (A01432).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysates,<br>
lane 2: NIH3T3 whole cell lysates,<br>
lane 3: HEPG2 whole cell lysates <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 14 antigen affinity purified polyclonal antibody (Catalog # A01432) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytokeratin 14 at approximately 60KD. The expected band size for Cytokeratin 14 is at 51KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01432-2-IHC-anti-cytokeratin-14-picoband-antibody.jpgAnti-Cytokeratin 14/KRT14 Antibody Picoband® IHC analysis of Cytokeratin 14 using anti-Cytokeratin 14 antibody (A01432).<br>
Cytokeratin 14 was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 14 Antibody (A01432) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01432-fbioe-08-00388-g005.jpgAnti-Cytokeratin 14/KRT14 Antibody Picoband®Immunofluorescence staining of filaggrin, CK10, CK14, Ki67, vimentin, perilipin A, and DAPI of native skin and skin models. Cell nuclei (stained with DAPI) are illustrated in white, characteristic proteins (stained with respective specific antibody) in green. White dashed line shows epidermal-dermal border. Scale bar: 50 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/bioengineering-and-biotechnology/articles/10.3389/fbioe.2020.00388/full'>32457884</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01432-3-IHC-anti-cytokeratin-14-picoband-antibody.jpgAnti-Cytokeratin 14/KRT14 Antibody Picoband® IHC analysis of Cytokeratin 14 using anti-Cytokeratin 14 antibody (A01432).<br>
Cytokeratin 14 was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 14 Antibody (A01432) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01432-4-IHC-anti-cytokeratin-14-picoband-antibody.jpgAnti-Cytokeratin 14/KRT14 Antibody Picoband® IHC analysis of Cytokeratin 14 using anti-Cytokeratin 14 antibody (A01432).<br>
Cytokeratin 14 was detected in paraffin-embedded section of human oesophagus squama cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 14 Antibody (A01432) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01432-5_1.pngAnti-Cytokeratin 14/KRT14 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Cytokeratin 14 antibody (A01432). <br> Overlay histogram showing SiHa cells stained with A01432 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cytokeratin 14 Antibody (A01432,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-mpi-picoband-trade-antibody-a00175-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00175-mpi-primary-antibodies-wb-testing-1_1.jpgAnti-Mannose Phosphate Isomerase/MPI Antibody Picoband® Western blot analysis of MPI using anti-MPI antibody (A00175). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human HEK293 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPI antigen affinity purified polyclonal antibody (Catalog # A00175) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPI at approximately 47 kDa. The expected band size for MPI is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00175-1-mpi-primary-antibodies-ihc-testing-2.jpgAnti-Mannose Phosphate Isomerase/MPI Antibody Picoband® IHC analysis of MPI using anti-MPI antibody (A00175).<br> MPI was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MPI Antibody (A00175) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00175-1-mpi-primary-antibodies-ihc-testing-3.jpgAnti-Mannose Phosphate Isomerase/MPI Antibody Picoband® IHC analysis of MPI using anti-MPI antibody (A00175).<br> MPI was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MPI Antibody (A00175) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00175-mpi-primary-antibodies-ihc-testing-4.jpgAnti-Mannose Phosphate Isomerase/MPI Antibody Picoband® IHC analysis of MPI using anti-MPI antibody (A00175). <br> MPI was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MPI Antibody (A00175) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00175-mpi-primary-antibodies-fc-testing-5.pngAnti-Mannose Phosphate Isomerase/MPI Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-MPI antibody (A00175). <br> Overlay histogram showing A549 cells stained with A00175 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPI Antibody (A00175, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-nedd8-picoband-trade-antibody-a00547-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00547-nedd8-primary-antibodies-wb-testing-1.jpgAnti-NEDD8 Antibody Picoband® Western blot analysis of NEDD8 using anti-NEDD8 antibody (A00547). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NEDD8 antigen affinity purified polyclonal antibody (Catalog # A00547) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NEDD8 at approximately 10-12 kDa. The expected band size for NEDD8 is at 9 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00547-2-IHC-anti-nedd8-picoband-antibody.jpgAnti-NEDD8 Antibody Picoband® IHC analysis of NEDD8 using anti-NEDD8 antibody (A00547).<br> NEDD8 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NEDD8 Antibody (A00547) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00547-3.pngAnti-NEDD8 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-NEDD8 antibody (A00547). <br> Overlay histogram showing A431 cells stained with A00547 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NEDD8 Antibody (A00547,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00547-4.jpgAnti-NEDD8 Antibody Picoband® IF analysis of NEDD8 using anti-NEDD8 antibody (A00547). <br>
NEDD8 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-NEDD8 Antibody (A00547) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-ebp1-picoband-trade-antibody-a02791-boster.html2026-03-24T05:06:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02791-1-WB-anti-ebp1-picoband-antibody.jpgAnti-EBP1/PA2G4 Antibody Picoband® Western blot analysis of EBP1 using anti-EBP1 antibody (A02791). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat liver tissue lysates,<br>
lane 2: NIH3T3 whole cell lysates,<br>
lane 3: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EBP1 antigen affinity purified polyclonal antibody (Catalog # A02791) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EBP1 at approximately 43KD. The expected band size for EBP1 is at 43KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02791-2-IHC-anti-ebp1-picoband-antibody.jpgAnti-EBP1/PA2G4 Antibody Picoband® IHC analysis of EBP1 using anti-EBP1 antibody (A02791).<br>
EBP1 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EBP1 Antibody (A02791) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02791-pa2g4-primary-antibodies-ihc-testing-5.jpgAnti-EBP1/PA2G4 Antibody Picoband®IHC analysis of PA2G4 using anti-PA2G4 antibody (A02791). <br>PA2G4 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PA2G4 Antibody (A02791) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02791-3-IHC-anti-ebp1-picoband-antibody.jpgAnti-EBP1/PA2G4 Antibody Picoband® IHC analysis of EBP1 using anti-EBP1 antibody (A02791).<br>
EBP1 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EBP1 Antibody (A02791) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02791-4-IHC-anti-ebp1-picoband-antibody.jpgAnti-EBP1/PA2G4 Antibody Picoband® IHC analysis of EBP1 using anti-EBP1 antibody (A02791).<br>
EBP1 was detected in paraffin-embedded section of mouse brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EBP1 Antibody (A02791) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-slc18a3-picoband-trade-antibody-a04891-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04891-1-WB-anti-slc18a3-vacht-picoband-antibody.jpgAnti-Vesicular Acetylcholine Transporter/SLC18A3 Antibody Picoband® Western blot analysis of SLC18A3 using anti-SLC18A3 antibody (A04891). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: HELA whole cell lysates,<br>
lane 2: HEPA whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC18A3 antigen affinity purified polyclonal antibody (Catalog # A04891) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC18A3 at approximately 55KD. The expected band size for SLC18A3 is at 57KD.
https://www.bosterbio.com/products/primary-antibodies/anti-st7-picoband-trade-antibody-a07235-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07235-st7-primary-antibodies-wb-testing-1.jpgAnti-ST7 Antibody Picoband® Western blot analysis of ST7 using anti-ST7 antibody (A07235). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ST7 antigen affinity purified polyclonal antibody (Catalog # A07235) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ST7 at approximately 67 kDa. The expected band size for ST7 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07235-st7-primary-antibodies-if-testing-2.jpgAnti-ST7 Antibody Picoband® IF analysis of ST7 using anti-ST7 antibody (A07235) and anti-Beta Tubulin antibody (M01857-3).<br>
ST7 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ST7 Antibody (A07235) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07235-st7-primary-antibodies-fcm-testing-3.jpgAnti-ST7 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-ST7 antibody (A07235). <br>
Overlay histogram showing 293T cells stained with A07235 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ST7 Antibody (A07235, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-tacc1-picoband-trade-antibody-a04196-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04196-1-WB-anti-tacc1-picoband-antibody.jpgAnti-TACC1 Antibody Picoband® Western blot analysis of TACC1 using anti-TACC1 antibody (A04196). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: mouse testis tissue lysate,<br>
lane 2: U87 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TACC1 antigen affinity purified polyclonal antibody (Catalog # A04196) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TACC1 at approximately 100KD. The expected band size for TACC1 is at 88KD.
https://www.bosterbio.com/products/primary-antibodies/anti-atty-picoband-trade-antibody-a00622-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00622-1-WB-anti-atty-picoband-antibody.jpgAnti-ATTY/TAT Antibody Picoband® Western blot analysis of ATTY using anti-ATTY antibody (A00622). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat spleen tissue lysates,<br>
Lane 2: mouse liver tissue lysates,<br>
Lane 3: A549 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATTY antigen affinity purified polyclonal antibody (Catalog # A00622) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATTY at approximately 42KD. The expected band size for ATTY is at 50KD.
https://www.bosterbio.com/products/primary-antibodies/anti-dr4-picoband-trade-antibody-a02152-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02152-1-WB-anti-dr4-picoband-antibody.jpgAnti-DR4/TNFRSF10A Antibody Picoband® Western blot analysis of DR4 using anti-DR4 antibody (A02152). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> lane 1: rat spleen tissue lysates,<br> lane 2: mouse spleen tissue lysates,<br> lane 3: MCF-7 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DR4 antigen affinity purified polyclonal antibody (Catalog # A02152) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DR4 at approximately 50KD. The expected band size for DR4 is at 50KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02152-atg14l-primary-antibodies-if-testing-2.jpgAnti-DR4/TNFRSF10A Antibody Picoband® IF analysis of ATG14L using anti-ATG14L antibody (A02152). <br>
ATG14L was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ATG14L Antibody (A02152) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02152-oncotarget-05-4959-g001.jpgAnti-DR4/TNFRSF10A Antibody Picoband®The cytotoxic effect of TRAIL on human HCC and GC cell lines. (A) Detection of DNA fragmentation by DNA ladder assay. LH86, Huh7, HLCZ01 and HLCZ02 cells were exposed to TRAIL for 4 hours. 2 μg of cellular DNA was separated on 1% agarose gel at 50V for one hour. The data are one representative of three independent experiments. (B) Detection of apoptosis by flow cytometry and western blot. LH86, Huh7, HLCZ01, HLCZ02, HGC-27 and BGC-823 cells were exposed to TRAIL for 4 hours. Samples were analyzed on a FACS Caliber Cytometer. A minimum of 30000 events per samples were acquired, and subsequently analyzed with CellQuest software. The results are the average of at least three independent experiments. (C) Cleaved PARP was detected by western blot. β–actin was used as control. The data are one representative of three independent experiments. (D) Detection of DR4 and DR5 in HCC and GC cell lines by real-time PCR and western blot analysis. DR4 or DR5 mRNA were detected by real-time RT-PCR and normalized with GAPDH respectively. The results are the average of three independent experiments performed in triplicate. DR4 and DR5 protein was detected by western blot. The data are one representative of three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4148114/&orig_host=www.ncbi.nlm.nih.gov'>24970806</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-beta-tubulin-picoband-trade-antibody-a01857-1-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g010.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of licochalcone A on LPS-induced activation of AKT/NF-κB and MAPK signaling pathways in mMECs. (A–E) Total protein in mMECs was collected after 4 h of LPS stimulation. Licochalcone A was added 1 h before LPS stimulation. Protein levels of p-AKT, p-JNK1/2, p-ERK1/2, and p-P38 were detected via western blot and quantitatively assessed via densitometry using β-tubulin as an internal control. Protein levels were measured using ImageJ software ( ) and normalized to that of β-tubulin. (F–I) MMECs were divided into LPS (1 μg/mL) or LPS + licochalcone A (2.4 μg/mL) groups. After adding LPS to serum-free medium for 1 h, licochalcone A was added. Protein was collected after 0, 15, 30, 45, and 60 min. (F) Western blot analysis of p-IκBα, IκBα, p-P65, and P65 in mMECs were treated with LPS + licochalcone A. (G) Western blot analysis of p-IκBα, IκBα, p-P65, and P65 in mMECs were treated with LPS only. (H–I) The phosphorylation of P65 and IκBα at different time-points under LPS and LPS + licochalcone A treatment were detected via western blot. Values are presented as means ± SD ( n = 3) (** p < 0.01 vs. LPS, **** p < 0.0001 vs. LPS).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g011.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of licochalcone A on the protein levels of ZO-1, Occludin, and claudin3 in mMECs. mMECs were serum-starved for 3 h before treatment with Licochalcone A (1.8, 2.4 μg/mL) for 24 h (A) . The protein levels of ZO-1 (B) , claudin3 (C) , and Occludin (D) were determined by western blot, and the relative protein levels were quantified by scanning densitometry and normalized to β-tubulin. Values are presented as means ± SD ( n = 3) (** p < 0.01, *** p < 0.001 and **** p < 0.0001 vs. Control group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g009.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of Licochalcone A on LPS-induced inflammatory response in mouse mammary epithelial cells (mMECs). Cells were cultured with different concentrations of licochalcone A (1.2, 1.8, 2.4, and 3 μg/mL) for 4 h and viability determined with the CCK8 assay. (A) The effect of licochalcone A and licochalcone A + LPS were determined by CCK8 assay. mMECs were pretreated with Licochalcone A (1.2, 1.8, 2.4, and 3 μg/mL) for 1 h and then stimulated with LPS for 4 h, protein and mRNA levels were determined by qRT-PCR and western blot. The mRNA levels of IL-6 (B) , IL-1 β (C) , and TNF- α (D) , and the relative mRNA level was normalized to β -actin mRNA. The protein levels of COX-2 (E,G) and iNOS (E,F) , and the relative protein levels were quantified by scanning densitometry and normalized to β-tubulin. Values are presented as means ± SD ( n = 3) (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001 vs. LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g007.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Protein levels change in claudin-3, occluding, and ZO-1 after LPS or LPS + licochalcone A injection. Protein levels was measured using ImageJ software ( ) and normalized to that of β-tubulin. (A–D) Results of western blot analysis of claudin-3, occludin, ZO-1, and β-tubulin in mammary glands after LPS and LPS + licochalcone A injection. (B–D) Protein levels of claudin-3, occludin and ZO-1 normalized to that of β-tubulin. (E) Immunostaining images of ZO-1 (green) and nuclear staining with DAPI (blue) in mammary glands treated with LPS and licochalcone A. Values are presented as means ± SD ( n = 10 in each group) (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001 vs. LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g005.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of licochalcone A on AKT/NF-κB signaling pathway in LPS-induced mice mastitis. Mammary gland tissues from different experimental groups were obtained 24 h after LPS administration and total protein. The tissue lysates were prepared and subjected to western blot by using p-AKT (A,B) , p-IκBα (A,C) , and p-P65 (A,D) antibodies, respectively. Each immunoreactive band was digitized and expressed as a ratio of the β-tubulin level. Values are presented as means ± SD (* p < 0.05, *** p < 0.001, and **** p < 0.0001 vs. LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g004.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of licochalcone A on mitogen-activated protein kinase (MAPK) signaling pathway in LPS-induced mice mastitis. Mammary gland tissues from different experimental groups were obtained 24 h after LPS administration. The tissue lysates were prepared and subjected to western blot by using p-ERK1/2 (A,B) , p-JNK1/2 (A,C) , p-P38 (A,D) antibodies, respectively. Each immunoreactive band was digitized and expressed as a ratio of the β-tubulin level. Values are presented as means ± SD (**** p < 0.0001 vs. LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-fimmu-10-00287-g003.jpgAnti-Beta Tubulin/TUBB Antibody Picoband®Effects of Licochalcone A on inflammatory response in LPS-induced mice mastitis. Mammary gland tissues from each experimental group ( n = 10) were obtained at 24 h after LPS administration. (A) Myeloperoxidase (MPO) activity assay. The protein levels of IL-1β (B) , TNF-α (C) , and IL-6 (D) were detected using ELISA. Western blot assay of inducible nitric oxide synthase (iNOS) (E,F) and cyclooxygenase-2 (COX-2) (E,G) , and the relative protein levels were quantified by scanning densitometry and normalized to β-tubulin. Values are presented as means ± SD (* p < 0.05, ** p < 0.01, and **** p < 0.0001 vs. LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2019.00287/full'>30858849</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-wb-testing-1_1.jpgAnti-Beta Tubulin/TUBB Antibody Picoband® Western blot analysis of Beta Tubulin using anti-Beta Tubulin antibody (A01857-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human HepG2 whole cell lysates, <br>
Lane 4: monkey COS-7 whole cell lysates, <br>
Lane 5: chicken heart tissue lysates, <br>
Lane 6: rat brain tissue lysates, <br>
Lane 7: rat PC-12 whole cell lysates, <br>
Lane 8: mouse brain tissue lysates, <br>
Lane 9: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Beta Tubulin antigen affinity purified polyclonal antibody (Catalog # A01857-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Beta Tubulin at approximately 50 kDa. The expected band size for Beta Tubulin is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-wb-testing-2_1.pngAnti-Beta Tubulin/TUBB Antibody Picoband®Western blot analysis of TUBB using anti-TUBB antibody (A01857-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 2-3: human OCI-LY1-SRPK1 KO whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBB antigen affinity purified polyclonal antibody (A04887-1) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a HRP-conjugated Anti-Rabbit IgG Secondary Antibodyat for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TUBB at approximately 55 kDa. The expected band size for TUBB is at 50 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-ihc-testing-2_1.jpgAnti-Beta Tubulin/TUBB Antibody Picoband® IHC analysis of Beta Tubulin using anti-Beta Tubulin antibody (A01857-1). <br>
Beta Tubulin was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Beta Tubulin Antibody (A01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-ihc-testing-3_1.jpgAnti-Beta Tubulin/TUBB Antibody Picoband® IHC analysis of Beta Tubulin using anti-Beta Tubulin antibody (A01857-1). <br>
Beta Tubulin was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Beta Tubulin Antibody (A01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-if-testing-4_1.jpgAnti-Beta Tubulin/TUBB Antibody Picoband® IF analysis of Beta Tubulin using anti-Beta Tubulin antibody (A01857-1). <br>
Beta Tubulin was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Beta Tubulin Antibody (A01857-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01857-1-tubb-primary-antibodies-fcm-testing-5_1.jpgAnti-Beta Tubulin/TUBB Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Beta Tubulin antibody (A01857-1). <br>
Overlay histogram showing SiHa cells stained with A01857-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Beta Tubulin Antibody (A01857-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-vasp-picoband-trade-antibody-a00303-1-boster.html2026-03-24T05:06:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00303-1-vasp-primary-antibodies-wb-testing-1.jpgAnti-VASP Antibody Picoband® Western blot analysis of VASP using anti-VASP antibody (A00303-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates, <br>
Lane 2: human RT4 whole cell lysates, <br>
Lane 3: human SiHa whole cell lysates, <br>
Lane 4: human K562 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VASP antigen affinity purified polyclonal antibody (A00303-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VASP at approximately 40 kDa. The expected band size for VASP is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00303-1-vasp-primary-antibodies-ihc-testing-2.jpgAnti-VASP Antibody Picoband® IHC analysis of VASP using anti-VASP antibody (A00303-1). <br>VASP was detected in a paraffin-embedded section of rat intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VASP Antibody (A00303-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/picokine-elisa-kits/human-a1bg-alpha-1b-glycoprotein-picokine-trade-elisa-kit-ek1488-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1488_1.pngHuman A1BG/alpha 1B-Glycoprotein ELISA Kit PicoKine®Human A1BG/alpha 1B-Glycoprotein PicoKine ELISA Kit standard curve
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https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-cxcl9-mig-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0732-boster.html2026-03-24T05:07:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0732-2-ELISA-human-cxcl9-mig-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman CXCL9/Mig ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human CXCL9 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-cxcl16-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0741-boster.html2026-03-24T05:07:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0741-2-ELISA-human-cxcl16-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman CXCL16 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human CXCL16 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-galectin-1-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0762-boster.html2026-03-24T05:07:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0762_.pngHuman Galectin-1 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human Galectin-1 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-lox-1-olr1-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0824-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0824-2-ELISA-human-lox-1-olr1-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman LOX-1/OLR1 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human LOX-1/OLR1 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/mouse-rank-cd265-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0830-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0830-2-ELISA-mouse-rank-ez-set-elisa-kit-diy-antibody-pairs.jpgMouse RANK/CD265 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse RANK EZ Set ELISA Kit standard curvehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0830.pngMouse RANK/CD265 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse RANK/CD265 EZ-Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-bmp-7-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0884-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0884-2-ELISA-human-bmp-7-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman BMP-7 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human BMP-7 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-tryptase-tpsab1-b2-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0898-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0898_1.pngHuman Tryptase/TPSAB1,B2 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human Tryptase/TPSAB1,B2 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-adamts13-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0927-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0927_1.pngHuman ADAMTS13 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human ADAMTS13 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-tissue-factor-f3-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0928-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0928-2-ELISA-human-tissue-factor-f3-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman Tissue Factor/F3 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human Tissue factor/F3 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-fgf21-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0994-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez0994-2-ELISA-human-fgf21-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman FGF21 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human FGF21 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-elafin-pi3-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1117-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez1117-2-ELISA-human-elafin-pi3-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman Elafin/PI3 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human Elafin/PI3 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-fgf19-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1160-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez1160-2-ELISA-human-fgf19-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman FGF19 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human FGF19 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-sp-d-surfactant-protein-d-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1171-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez1171-ELISA-human-sp-d-ez-set-elisa-kit-diy-antibody-pairs.jpgHuman SP-D/Surfactant protein D EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human SP-D EZ Set ELISA Kit standard curvehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1171.pngHuman SP-D/Surfactant protein D EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human SP-D/Surfactant protein D EZ-Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/rat-mip-1alpha-ccl3-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1219-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez1219-2-ELISA-rat-mip-1alpha-ccl3-ez-set-elisa-kit-diy-antibody-pairs.jpgRat MIP-1Alpha/CCL3 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Rat MIP-1alpha/CCL3 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-tnfrsf14-hvem-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1226-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1226.pngHuman TNFRSF14/HVEM ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human TNFRSF14/HVEM EZ Set standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/rat-mmp-8-neutrophil-collagenase-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1248-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1248.pngRat MMP-8/Neutrophil collagenase EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat MMP-8 EZ Set ELISA Kit standard curvehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1248_1.pngRat MMP-8/Neutrophil collagenase EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat MMP-8/Neutrophil collagenase EZ-Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/mouse-cxcl3-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1364-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1364_1.pngMouse CXCL3 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Mouse CXCL3 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/mouse-mmp-8-neutrophil-collagenase-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1423-boster.html2026-03-24T05:07:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1423.pngMouse MMP-8/Neutrophil collagenase EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse MMP-8 EZ Set ELISA Kit standard curvehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1423_1.pngMouse MMP-8/Neutrophil collagenase EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse MMP-8/Neutrophil collagenase EZ-Set ELISA Kit standard curve
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-tafi-cpb2-elisa-kit-ez-set-trade-diy-antibody-pairs-ez1502-boster.html2026-03-24T05:07:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/ez1502-ELISA-human-tafi-cpb2-ez-set-elisa-kit-diy-antibody-pairs.pngHuman TAFI/CPB2 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human TAFI/CPB2 EZ Set ELISA Kit standard curve
https://www.bosterbio.com/products/primary-antibodies/anti-hdac-1-near-c-terminus-antibody-a00256-2-boster.html2026-03-24T05:07:09+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-presenilin-1-antibody-a00138-1-boster.html2026-03-24T05:07:09+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-cad-antibody-a05374-boster.html2026-03-24T05:07:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05374-dffb-primary-antibodies-ihc-testing-1.jpgAnti-CAD Dffb AntibodyImmunohistochemical analysis of paraffin-embedded human brain tumor. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05374-dffb-primary-antibodies-wb-testing-3.jpgAnti-CAD Dffb AntibodyWestern blot analysis of lysates from KB cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05374-dffb-primary-antibodies-wb-testing-2.jpgAnti-CAD Dffb AntibodyWestern blot analysis of lysates from DU145 cells, primary antibody was diluted at 1:1000, 4°over night
https://www.bosterbio.com/products/primary-antibodies/anti-olfml2b-antibody-a07745-boster.html2026-03-24T05:07:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07745-olfm1-primary-antibodies-ihc-testing-1.jpgAnti-OLFML2B Olfm1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07745-olfm1-primary-antibodies-wb-testing-2.jpgAnti-OLFML2B Olfm1 AntibodyWestern Blot analysis of various cells using Photomedin-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07745-olfm1-primary-antibodies-wb-testing-3.jpgAnti-OLFML2B Olfm1 AntibodyWestern blot analysis of lysates from HUVEC cells, using OLFML2B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mcd25-antibody-monoclonal-pc61-m00214-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00214-Flow-Cytometry-Analysis-1.jpgAnti-mCD25 Antibody (Monoclonal, PC61)Cell Surface flow staining of mCD25 on Con-A treated mouse splenocytes using 0.5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-apip-antibody-monoclonal-abm19c7-m09029-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M09029-Flow-Cytometry-Analysis-2.jpgAnti-APIP Antibody (Monoclonal, ABM19C7)Intracellular flow cytometric analysis of APIP in HeLa cells using 0.5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M09029-Western-Blotting-Analysis-1.jpgAnti-APIP Antibody (Monoclonal, ABM19C7)Western blot analysis of APIP. Anti-APIP antibody (Clone: ABM19C7) was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bi-1-antibody-monoclonal-abm20e4-m05462-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05462-Western-Blotting-Analysis-1.jpgAnti-Bi-1 TMBIM6 Antibody (Monoclonal, ABM20E4)Expression analysis of Bi-1. Anti-Bi-1 antibody (Clone: ABM20E4) was tested at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dectin-2-antibody-monoclonal-abm2h28-m11863-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M11863-Flow-Cytometry-Analysis-3.jpgAnti-Dectin-2 CLEC6A Antibody (Monoclonal, ABM2H28)Intracellular flow analysis of Dectin-2 in human PBMC (Lymphocytes) using 0.5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M11863-Immunostaining-Analysis-2.jpgAnti-Dectin-2 CLEC6A Antibody (Monoclonal, ABM2H28)Immunohistochemical analysis of Dectin-2 in Renal Cell Carcinoma using Dectin-2 antibody (Clone: ABM2H28) at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M11863-Western-Blotting-Analysis-1.jpgAnti-Dectin-2 CLEC6A Antibody (Monoclonal, ABM2H28)Western blot analysis of Dectin 2 Anti-Dectin 2 antibody (Clone: ABM2H28) was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ebi3-mouse-antibody-monoclonal-abm2c40-m07190-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M07190-Western-Blotting-Analysis-1.jpgAnti-EBI3 Mouse Antibody (Monoclonal, ABM2C40)Western blot analysis of mEBI3. Anti-mEBI3 antibody (Clone: ABM2C40) was tested at 2 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M07190-Western-Blotting-Analysis-1_1.jpgAnti-EBI3 Mouse Antibody (Monoclonal, ABM2C40)Westernblot analysis of hEBI3. Anti-hEBI3 antibody (Clone: ABM40H9) was tested at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-siglec-h-antibody-monoclonal-abm2b55-m30285-boster.html2026-03-24T05:07:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30285-Western-Blotting-Analysis-1.jpgAnti-Siglec-H Antibody (Monoclonal, ABM2B55)Western blot analysis of Siglec-H. Anti-Siglec-H antibody (Clone: ABM2B55) was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-17re-antibody-monoclonal-abm2g70-m11492-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M11492-Western-Blotting-Analysis-1.jpgAnti-IL-17RE Antibody (Monoclonal, ABM2G70)Western blot analysis of IL-17RE. Anti-IL-17RE antibody (Clone: ABM2G70) was tested at 2 μg/ml on (1) Jurkat, (2) PC3 and (3) NIH3T3 lysates.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ddx3-antibody-monoclonal-abm27h2-m00751-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00751-Western-Blotting-Analysis-1.jpgAnti-DDX3 DDX3X Antibody (Monoclonal, ABM27H2)Western blot analysis of DDX3. Anti-DDX3 antibody (Clone: ABM27H2) was used at 2 μg/ml on (1) MCF-7,(2) NIH3T3 (3) HEK293 and (4) EL-4 lysates.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tslp-receptor-antibody-monoclonal-abm28b6-m04167-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M04167-Western-Blotting-Analysis-1.jpgAnti-TSLP Receptor Antibody (Monoclonal, ABM28B6)Western blot analysis of TSLP Receptor. Anti-TSLP Receptor antibody (Clone: ABM28B6) was tested at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd4-rabbit-monoclonal-antibody-m00344-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-wb7.jpgAnti-CD4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-41467_2024_54685_fig6_html.pngAnti-CD4 Rabbit Monoclonal AntibodyInteraction between GZMK + CD8 + T cells and fibroblasts contributes to neutrophilic inflammation in nasal polyps. a Representative immunofluorescence staining of collagen I (COL1A1, green), CD8 (red), and GZMK (yellow) in NPs. The right image shows a greater magnification of the outlined area. b Spatial distribution analysis of GZMK + CD8 + T and COL1A1 + cells in the same tissue field demonstrated in ( a ) using HALO software. c–d The number of COL1A1 + fibroblasts within a radius of 25 μm from the nuclear center of GZMK + CD8 + T, GZMB + CD8 + T, CD4 + T, or CD19 + B cells in CIT group (left, n = 10 samples) and NP group (right, n = 10 samples) ( c ). Average distance from the indicated cell types to the closest COL1A1 + fibroblasts in CIT group (left, n = 10 samples) and NP group (right, n = 10 samples) ( d ). e DEGs between NP-derived primary fibroblasts (NPDF) treated with and without recombinant human GZMK ( n = 4). Two-sided Wald test (default for DESeq2 r-package) was used for differential expression analysis utilizing standard cutoffs of https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-41467_2024_54685_fig3_html.pngAnti-CD4 Rabbit Monoclonal AntibodyGZMK + CD8 + T cells are the primary cellular source of GZMK in nasal polyps. a The UMAP depicting the expression pattern of GZMK in CD45 + lymphocytes in 25 samples (5 CBL, 8 NP-BL, 4 CIT, and 8 NP samples) of our dataset. b The doughnut chart showing the composition of GZMK expressing cells in our dataset. c The UMAP depicting the expression pattern of GZMK in all CD8 + T cells from our dataset. d Violin plot showing the expression levels of GZMK in the indicated cell types. e The doughnut chart showing the composition of GZMK expressing CD8 + T cells in different sample groups in our dataset. Representative flow cytometry plots ( f ) and cumulative data ( g ) showing GZMK and GZMB expression among CD8 + T cells from indicated groups (22 CBL, 27 NP-BL, 14 CIT, and 30 NP samples). Data are presented as median with interquartile ranges; Two-sided Kruskal-Wallis with Dunn’s multiple comparisons test. h Dot plot displaying the expression of selected cell surface markers and transcription factors in GZMK + CD8 + T and GZMB + CD8 + T cells from NPs. i , j Flow cytometry showing mean fluorescence intensity (MFI) of CXCR4, PD-1, EOMES, and T-bet protein levels in GZMK + CD8 + T and GZMB + CD8 + T cells from NPs ( n = 17 samples). Two-sided paired t test. k , l Representative immunofluorescence staining of GZMK (green) and CD8 (red) colocalization in control inferior turbinate tissues (CIT, left) and NP samples (NP, right) ( k ). Quantified results of GZMK and CD8 double-positive cells in the indicated group (17 CIT and 57 NP samples) ( l ). Scale bar: 40 μm. HPF high power field. Data are presented as median with interquartile ranges; Two-sided unpaired Wilcoxon test. m , n Representative immunofluorescence staining of GZMB (green) and CD8 (red) colocalization in CIT (left) and NP samples (right) ( m ). Quantified results of GZMB and CD8 double-positive cells in the indicated group (10 CIT and 10 NP samples) ( n ). Scale bar: 40 μm. HPF high power field. Data are presented as median with interquartile ranges; Two-sided unpaired Wilcoxon test. CBL control blood sample, CD8 + Tpex, CD8 + progenitor exhausted cells, CIT control inferior turbinate sample, MAIT mucosal associated invariant T cell, NP nasal polyp, NP-BL blood sample from CRSwNP patient, Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54685-1'>39614076</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-41467_2024_54685_fig5_html.pngAnti-CD4 Rabbit Monoclonal AntibodySpatial proximity between GZMK + CD8 + T cells and fibroblasts revealed by Visium HD. a HE staining of the nasal polyp specimen from a representative CRSwNP patient (HD_NP4) in Visium HD (left). Cellular annotation of each 16 × 16 µm bin in the tissue specimen by deconvolution using the public ScRNA-seq dataset (right). b Spatial distribution of CD8T_GZMK (left) and GZMK expression (right) in the HD_NP4 sample. c Spatial distribution of CD8T_GZMB (left) and GZMB expression (right) in the HD_NP4 sample. d Spatial distribution of epithelial cells (left) and KRT19 expression (right) in the HD_NP4 sample. e Spatial distribution of fibroblasts (left) and FBLN1 expression (right) in the HD_NP4 sample. f Bar plots showing the cell type composition in each sample from control participants and patients with CRSwNP. g Bar plots showing the total counts of each cell type in CIT (left, n = 4 samples) and NP (right, n = 6 samples) groups. h , i , j Proportions of CD8T_GZMK and CD8T_GZMB in CD8 + T cells in nasal tissue samples in the indicated group (4 CIT and 6 NP samples) ( h ). Proportions of the major immune cells (B cells and CD4T cells) detected in the indicated group (4 CIT and 6 NP samples) ( i ). Proportions of the major structural cells (fibroblasts, epithelial cells, and SMCs) detected in the indicated group (4 CIT and 6 NP samples) ( j ). In ( h – j ), Box plots show median, quantiles, minimum and maximum. Two-sided unpaired Wilcoxon test. k Neighborhood enrichment analysis between cell types in spatial coordinates. The “CD8T_GZMK” and “fibroblasts” show a positive enrichment score. l Dot plots showing interactions between chemokine ligands (in structural cells) and receptors (in CD8 + T subsets). P values are computed from one-sided permutation test (default for CellChat r-package). Dot size represents P value. The color represents the communication possibility between CD8 + T subsets and structural cells. CIT control inferior turbinate sample, ECs endothelial cells, ILC innate lymphoid cell, NK natural killer cell, NP nasal polyp, pDCs plasmacytoid dendritic cells, SMCs smooth muscle cells. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54685-1'>39614076</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-wb8.jpgAnti-CD4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-wb.jpgAnti-CD4 Rabbit Monoclonal AntibodyWestern blot analysis of CD4 expression in THP-1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-2.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-3.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-4.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-5.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-6.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-7.jpgAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-cd4-primary-antibodies-ihc-testing-8.pngAnti-CD4 Rabbit Monoclonal Antibody IHC analysis of CD4 using anti-CD4 antibody (M00344). <br>
CD4 was detected in a paraffin-embedded section of human cervical cance tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CD4 Antibody (M00344) overnight at 4°C. Two-step IHC detection kit was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd73-antibody-monoclonal-abm40e2-m02120-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02120-Immunostaining-Analysis-WB1.jpgAnti-CD73 Antibody (Monoclonal, ABM40E2)Western blot analysis of CD73. Anti-CD73 antibody (Clone: ABM40E2) was tested at 2 µg/ml on human liver lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02120-Immunostaining-Analysis-human-spleen.jpgAnti-CD73 Antibody (Monoclonal, ABM40E2)Immunohistochemical analysis of CD73 in human Spleen using CD73 antibody (Clone: ABM40E2) at 5 µg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02120-Immunostaining-Analysis-1.jpgAnti-CD73 Antibody (Monoclonal, ABM40E2)Immunohistochemical analysis of CD73 in endomatrium carcinoma using CD73 antibody (Clone: ABM40E2) at 5 µg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02120-Immunostaining-Analysis-human-liver-_2_.jpgAnti-CD73 Antibody (Monoclonal, ABM40E2)Immunohistochemical analysis of CD73 in human Liver using CD73 antibody (Clone: ABM40E2) at 5 µg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02120-Immunostaining-Analysis-IHC.jpgAnti-CD73 Antibody (Monoclonal, ABM40E2)Immunohistochemical analysis of CD73 in renal cell carcinoma using CD73 antibody (Clone: ABM40E2) at 5 µg/ml.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hcd39-antibody-monoclonal-abm41e2-m03196-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M03196-Western-Blotting-Analysis-1.jpgAnti-hCD39 Antibody (Monoclonal, ABM41E2)Western blot analysis of hCD39. Anti-hCD39 antibody (Clone: ABM41E2) was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clec4e-antibody-monoclonal-abm42e6-m06084-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M06084-Western-Blotting-Analysis-1.jpgAnti-CLEC4E Antibody (Monoclonal, ABM42E6)Western blot analysis of CLEC4E. Anti-CLEC4E antibody (Clone: ABM42C6) was tested at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd3-zeta-rabbit-monoclonal-antibody-m02421-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02421-wb7.jpgAnti-CD3 zeta CD247 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02421-cd3z-primary-antibodies-ihc-testing-1.jpgAnti-CD3 zeta CD247 Rabbit Monoclonal AntibodyIHC analysis of CD3Z using anti-CD3Z antibody (M02421). <br>CD3Z was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3Z Antibody (M02421) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02421-cd3z-primary-antibodies-ihc-testing-2.jpgAnti-CD3 zeta CD247 Rabbit Monoclonal AntibodyIHC analysis of CD3Z using anti-CD3Z antibody (M02421). <br>CD3Z was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3Z Antibody (M02421) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02421-cd3z-primary-antibodies-ihc-testing-3.jpgAnti-CD3 zeta CD247 Rabbit Monoclonal AntibodyIHC analysis of CD3Z using anti-CD3Z antibody (M02421). <br>CD3Z was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3Z Antibody (M02421) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02421-cd3z-primary-antibodies-ihc-testing-4.jpgAnti-CD3 zeta CD247 Rabbit Monoclonal AntibodyIHC analysis of CD3Z using anti-CD3Z antibody (M02421). <br>CD3Z was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3Z Antibody (M02421) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hcd6-antibody-monoclonal-spv14-m03913-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M03913-Flow-Cytometry-Analysis-1.jpgAnti-hCD6 Antibody (Monoclonal, SPV14)Cell Surface flow analysis of hCD6 in PBMC (Lymphocyte gated) using 0.5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hmhcii-hla-dq-antibody-monoclonal-spvl3-m00232-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00232-Flow-Cytometry-Analysis-1.jpgAnti-hMHCII/HLA DQ Antibody (Monoclonal, SPVL3)Cell Surface flow analysis of MHCII-DLADQ in PBMC (Lymphocyte gated) using 0.5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hcd50-antibody-monoclonal-101-1d2-m03651-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M03651-Flow-Cytometry-Analysis-1.jpgAnti-hCD50 Antibody (Monoclonal, 101-1D2)Cell Surface flow analysis of hCD50 in PBMC (Lymphocyte gated) using 1 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hcd45r-antibody-monoclonal-bra-11g-m30397-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30397-Flow-Cytometry-Analysis-1.jpgAnti-hCD45R Antibody (Monoclonal, BRA-11G)Cell Surface flow analysis of hCD45R in PBMC (Lymphocyte gated) using 0.5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-36r-antibody-monoclonal-abm47a2-m09203-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M09203-Western-Blotting-Analysis-1.jpgAnti-IL-36R IL1RL2 Antibody (Monoclonal, ABM47A2)Western blot analysis of IL-36R. Anti-IL-36R antibody (Clone: ABM47A2) was tested at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mbd2-mbd3-antibody-monoclonal-abm14a8-m02571-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in Squamous cell carcinoma of Lungs using MBD3 antibody (Clone: ABM14A8) at 5 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-squamous-cell-carcinoma-of-lungs.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in Squamous cell carcinoma of Lungs using MBD3 antibody (Clone: ABM14A8) at 5 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-human-colon.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human Colon tissue using MBD3 antibody (Clone: ABM14A8) at 5 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-human-spleen.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human Spleen tissue using MBD3 antibody (Clone: ABM14A8) at 5 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-Jurkat.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human Testis tissue using MBD3 antibody (Clone: ABM14A8) at 10 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-10-7006-Kidney-882244.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human Kidney tissue using MBD3 antibody (Clone: ABM14A8) at 10 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-10-7006-Testis-882246.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human Testis tissue using MBD3 antibody (Clone: ABM14A8) at 10 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Immunostaining-Analysis-2.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Immunohistochemical analysis of MBD3 in human breast tissue using MBD3 antibody (Clone: ABM14A8) at 5 μg/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02571-Western-Blotting-Analysis-1.jpgAnti-MBD2/MBD3 Antibody (Monoclonal, ABM14A8)Western blot analysis of MBD3 (and MBD2). Anti-MBD3 (and MBD2) antibody (Clone: ABM14A8) was used at 2 μg/ml on A431, K562, A375 and HEK293 lysates.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-galectin-13-antibody-monoclonal-abm4e42-m08143-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M08143-Immunostaining-Analysis-2.jpgAnti-Galectin 13 LGALS13 Antibody (Monoclonal, ABM4E42)Immunohistochemical analysis of Galectin 13 in human placenta tissue using Galectin 13 antibody (Clone: ABM4E42) at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M08143-Western-Blotting-Analysis-1.jpgAnti-Galectin 13 LGALS13 Antibody (Monoclonal, ABM4E42)Western blot analysis of Galectin 13. Anti-Galectin 13 antibody (Clone: ABM4E42) was tested at 0.5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-napsin-antibody-monoclonal-abm4h60-m05685-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05685-Immunostaining-Analysis-2.jpgAnti-Napsin NAPSA Antibody (Monoclonal, ABM4H60)Immunohistochemical analysis of Napsin in Lung Adenocarcinoma tissue using Napsin antibody (Clone: ABM4H60) at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05685-Western-Blotting-Analysis-1.jpgAnti-Napsin NAPSA Antibody (Monoclonal, ABM4H60)Western blot analysis of Napsin. Anti-Napsin antibody (Clone: ABM4H60) was tested at 0.5 μg/ml on K562, Liver and Hek 293 lysates.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-papp-a-antibody-monoclonal-abm4c62-m06838-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M06838-Immunostaining-Analysis-1.jpgAnti-PAPP-A Antibody (Monoclonal, ABM4C62)Immunohistochemical analysis of PAPP-A in human Placenta tissue using PAPP-A antibody (Clone: ABM4C62) at 5 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-krt76-antibody-monoclonal-abm51a8-m12092-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M12092-Western-Blotting-Analysis-1.jpgAnti-KRT76 Antibody (Monoclonal, ABM51A8)Expression analysis of KRT76. Anti-KRT76 antibody (Clone: ABM51A8) was tested at 0.5 μg/ml on Hela, MCF7 and A431 lysates.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-krt77-antibody-monoclonal-abm5g22-m14209-boster.html2026-03-24T05:07:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M14209-Western-Blotting-Analysis-1.jpgAnti-KRT77 Antibody (Monoclonal, ABM5G22)Expression analysis of KRT77. Anti-KRT77 antibody (Clone: ABM5G22) was tested at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mitf-antibody-monoclonal-abm1h91-m00269-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00269-Immunostaining-Analysis-10-8004-Skin-882284.jpgAnti-MITF Antibody (Monoclonal, ABM1H91)2 Immunohistochemical analysis of MITF in human Skin tissue using MITF antibody (Clone: ABM1H91) at 10 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00269-Western-Blotting-Analysis-1.jpgAnti-MITF Antibody (Monoclonal, ABM1H91)Western blot analysis of MITF. Anti-MITF antibody (Clone: ABM1H91) was tested at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-asc2-asc-2-pop-antibody-a11388-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A11388-Immunostaining-Analysis-3.jpgAnti-ASC2 (ASC-2/POP) PYDC1 AntibodyImmunhistochemical analysis of ASC2/POP1 expression in mouse spleen using primary antibody dilution ratio of 1:2000. A and A1, spleen at low and high magnification, respectively. ASC2/POP1 staining is seen in the granulocytes, whereas the lymph and megakaryocytes are negative.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A11388-Immunostaining-Analysis-2.jpgAnti-ASC2 (ASC-2/POP) PYDC1 AntibodyImmunhistochemical analysis of ASC2/POP1 expression in mouse using primary antibody dilution ratio of 1:2000. A, prostate tissue from a male mouse prostatitis. B, kidney from a mouse with pyelonephritis. A1 and B1, high magnification of A and B, respectively. ASC2/POP1 staining is seen in the granulocytes.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A11388-Western-Blotting-Analysis-1.jpgAnti-ASC2 (ASC-2/POP) PYDC1 AntibodyWestern blot analysis of ASC2/POP1 using primary antibody dilution ratio of 1:2000. HEK-293 cells were transiently transfected with plasmids encoding ASC2, POP1 or a negative control plasmid. ASC2 and POP1 were detected at the expected 12 kDa molecular weight.
https://www.bosterbio.com/products/primary-antibodies/anti-bag-1-antibody-a02423-1-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02423-1-Immunostaining-Analysis-2.jpgAnti-Bag-1 AntibodyFormalin-fixed, paraffin-embedded section of human colon stained for Bag-1 using primary antibody dilution ratio of 1:2000. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02423-1-Immunostaining-Analysis-1.jpgAnti-Bag-1 AntibodyFormalin-fixed, paraffin-embedded sections of human colorectal cancer stained for Bag-1 using primary antibody dilution ratio of 1:2000. Hematoxylin-eosin counterstain. Samples from two patients (A and B) are shown. A1 and B1 are higher magnifications from A and B, respectively.
https://www.bosterbio.com/products/primary-antibodies/anti-bfar-bar-antibody-a10479-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10479-Western-Blotting-Analysis-1.jpgAnti-BFAR (BAR) AntibodyFig:1 Western blot analysis of BAR in normal prostate and prostate carcinoma tissue lysates. 25 ug protein was loaded per lane. Tissue lysates from 15 different prostate carcinoma patients show variable expression of BAR with respect to banding patterns and amount of BAR expression. Major BAR bands typically migrate as a single band or as a doublet. These bands are typically observed at ~50-54 kDa. This is higher than the predicted molecular weight from the 450 amino acid BAR sequence, and may represent phosphorylation or other post-translational modifications. N = tissue lysate from normal prostate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10479-Immunostaining-Analysis-2.jpgAnti-BFAR (BAR) AntibodyFig:2 Formalin-fixed, paraffin-embedded human prostate carcinoma tissue array stained for BAR expression using A10479 at 1:2000. Hematoxylin-eosin counterstain. Variable BAR expression is seen between patient sampleshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10479-Immunostaining-Analysis-3.jpgAnti-BFAR (BAR) AntibodyFig:3 Formalin-fixed, paraffin-embedded tissue sections stained for BAR expression using A10479 at 1:2000. A. Two cores from a human gliobastoma tissue microarray: 1 = fibrillary astrocytoma (grade I), and 2 = anaplastic glioma (grade III). B. Higher magnification from the fibrillary astrocytoma (shown in A). C. Higher magnification from the anaplastic glioma (shown in A). D. Normal human brain striatum with positive medium spiny neurons, the major neuronal cell type of the striatum. Hematoxylin-eosin counterstain.
https://www.bosterbio.com/products/primary-antibodies/anti-caspase-7-active-cleaved-antibody-a01044-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01044-Western-Blotting-Analysis-1.jpgAnti-Caspase-7 (active/cleaved) AntibodyWestern blot analysis of Caspase-7. Recombinant catalytically active Caspase-7 was Western blotted with anti-Active/Cleaved Caspase-7. The antisera detected both the large and small subunits of active/cleaved Caspase-7.
https://www.bosterbio.com/products/primary-antibodies/anti-dedd2-ded4-antibody-a11263-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A11263-Western-Blotting-Analysis-20-1061.jpgAnti-DEDD2 (DED4) AntibodyWestern blot analysis of DEDD2 (DED4). Anti-DEDD2 (DED4) antibody was used with 1:1000 dilution on h Heart lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-ptpn13-ptpl1-fap1-antibody-a02481-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02481-Immunostaining-Analysis-2.jpgAnti-PTPN13/PTPL1 (FAP1) AntibodyImmunohistochemisty of FAP-1 in formalin-fixed, paraffin embedded ovarian carcinoma cores from a tissue microarray using primary antibody dilution ratio of 1:2000. A-D, samples are from four different patients. A1-D1 are high magnification images from A-D, respectively. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02481-Immunostaining-Analysis-3.jpgAnti-PTPN13/PTPL1 (FAP1) AntibodyImmunocytochemical analysis of FAP-1 in cell lines using primary antibody dilution ratio of 1:2000. In ovarian carcinoma cell lines FAP-1 expression was detected in SK-OV-3 and OVCAR-3, but not in BG-1 or HEY. Human 293 kidney and Jurkat T cell lines were used as positive and negative controls, respectively. The staining data correlates with the western blot data (to the left).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02481-Western-Blotting-Analysis-1.jpgAnti-PTPN13/PTPL1 (FAP1) AntibodyWestern blot analysis of FAP-1 using primary antibody dilution ratio of 1:2000. In ovarian carcinoma cell lines FAP-1 expression was detected in SK-OV-3 and OVCAR-3, but not in BG-1 or HEY. Human Jurkat T and 293 kidney cell lines were used as negative and positive controls, respectively.
https://www.bosterbio.com/products/primary-antibodies/anti-itraf-antibody-a00445-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00445-Immunostaining-Analysis-1.jpgAnti-ITRAF TANK AntibodyImmunohistochemical analysis of TANK/I-TRAF1 expression in formalin-fixed, paraffin-embedded normal human colon using primary antibody dilution ratio of 1:2000. A-A3, low and high magnification images. Hematoxylin-eosin counterstain.
https://www.bosterbio.com/products/primary-antibodies/anti-nidd-zdhhc23-antibody-a13972-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A13972-Western-Blotting-Analysis-20-1073.jpgAnti-NIDD/ZDHHC23 AntibodyWestern blot analysis of NIDD. Anti-NIDD antibody was used with 1:4000 dilution on h Spleen lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-survivin-antibody-a30032-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/3/A30032-Immunostaining-Analysis-3.jpgAnti-Survivin birc5.1-a AntibodyImmunohistochemical analysis of Survivin in a formalin-fixed, paraffin-embedded human brain tissue microarray using primary antibody dilution ratio of 1:2000. A. Differential expression of Survivin in brain tumors from six different patients. A1-A3, high magnification from A. A1, gemistocytic astrocytoma. A2, medulloblastoma. A3, choroid plexus papilloma. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/3/A30032-Immunostaining-Analysis-2.jpgAnti-Survivin birc5.1-a AntibodyImmunohistochemical analysis of Survivin in formalin-fixed, paraffin-embedded human prostate and breast cancer using primary antibody dilution ratio of 1:2000. A and A1, prostate cancer at low and high magnification, respectively. B and B1, breast cancer. B1 is a high magnification of an area of metastasis. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/3/A30032-Western-Blotting-Analysis-1.jpgAnti-Survivin birc5.1-a AntibodyWestern blot analysis of Survivin using primary antibody dilution ratio of 1:2000. Survivin was detected in the two tumor cell lines, Jurkat (T cell lymphoma) and RS11846 (non-Hodgkin's lymphoma), but not in lysates from normal tissues. Survivin RP, full-length recombiant human survivin protein was used as a positive control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30032-41598_2017_12713_fig3_html.jpgAnti-Survivin birc5.1-a AntibodyAgarose gel of some apoptosis-related genes in S. frugiperda PCR amplified with the specific primers shown in Supplement Table . Lanes: M, Marker 2000, Lane 1–15, Sf-Caspase-1 , Sf-Caspase-2 , Sf-AIF , Sf-BI , Sf-IBM1 , Sf-Grim-19 , Sf-Survivin , Sf-IAP , Sf-Ras , Sf-Cyt C , Sf-Traf 6 , Sf-Pcdp 5 , Sf-Rptor , Sf-Pkar 1 , and Sf-Buffy . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41598-017-12713-9'>29038528</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-traf-5-antibody-a03076-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03076-Immunostaining-Analysis-3.jpgAnti-TRAF-5 AntibodyFormalin-fixed, paraffin-embedded mouse tissue stained for TRAF5 expression using primary antibody dilution ratio of 1:2000. Hematoxylin-eosin counterstain. A, thymus. B, bone marrow.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03076-Immunostaining-Analysis-2.jpgAnti-TRAF-5 AntibodyFormalin-fixed, paraffin-embedded mouse spleen stained for TRAF5 expression using primary antibody dilution ratio of 1:2000. Hematoxylin-eosin counterstain. A1 is a higher magnification of A.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03076-Western-Blotting-Analysis-1.jpgAnti-TRAF-5 AntibodyWestern blot analysis of TRAF5 in normal human tissues using primary antibody dilution ratio of 1:2000. TRAF5 is observed at ~64 kDa. Additional bands of lower molecular weight were seen in some cases, and may represent TRAF5 degradation fragments.
https://www.bosterbio.com/products/primary-antibodies/anti-card8-tucan-antibody-a03404-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03404-Immunostaining-Analysis-3.jpgAnti-CARD8 (Tucan) AntibodyFormalin-fixed, paraffin-embedded tumor/normal adjacent tissue cores from a human colon tissue microarray stained for TUCAN/CARD8 expression at 1:2000. A and B are tumor tissue cores. A1 and B1 are the matched normal adjacent cores from A and B, respectively. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03404-Immunostaining-Analysis-2.jpgAnti-CARD8 (Tucan) AntibodyFormalin-fixed, paraffin-embedded tissue human colon microarray stained for TUCAN/CARD8 expression at 1:2000. A-A2, sucessively higher magnifications of the microarray. A, low magnification overview. A1, differential TUCAN/CARD8 staining between tissue cores is observed. A2, Areas of intense TUCAN/CARD8 staining in a colon carcinoma tissue core. Hematoxylin eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03404-Western-Blotting-Analysis-1.jpgAnti-CARD8 (Tucan) AntibodyWestern blot analysis of TUCAN/CARD8 in tumor cell lines using primary antibody dilution ratio of 1:2000. Cell lysates were normalized for total protein content.
https://www.bosterbio.com/products/primary-antibodies/anti-ciap-1-hiap-2-antibody-a01700-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01700-Immunostaining-Analysis-2.jpgAnti-cIAP-1/HIAP-2 BIRC2 AntibodyImmunohistochemical analysis of cIAP1 in formalin-fixed, paraffin-embedded human prostate using primary antibody dilution ratio of 1:2000. A, normal prostate. B, prostate intraepithelial neoplasia (PIN). PIN is a premalignant proliferation arising within the prostate. C, prostate cancer. Hematoxylin-eosin counterstain. Increased cIAP1 expression is PIN and in prostate cancer compared to normal prostate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01700-Western-Blotting-Analysis-1.jpgAnti-cIAP-1/HIAP-2 BIRC2 AntibodyWestern blot analysis of cIAP1 in human prostate using primary antibody dilution ratio of 1:1000. PBH (benign prostate hyperplasia), PIN (prostate intraepithelial neoplasia). Elevated levels of cIAP1 were seen in certain cases of BPH/PIN and prostate cancer compared to normal prostate.
https://www.bosterbio.com/products/primary-antibodies/anti-nod2-card15-antibody-a00087-boster.html2026-03-24T05:07:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00087-Immunostaining-Analysis-2.jpgAnti-NOD2 (Card15) AntibodyFormalin-fixed, paraffin-embedded normal human colon stained for NOD2 expression using primary antibody dilution ratio of 1:2000. A, tissue core from a colon tissue microarray. A1, high magnification of A. Hematoxylin-eosin counterstain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00087-Western-Blotting-Analysis-1.jpgAnti-NOD2 (Card15) AntibodyWestern blot analysis of NOD2 using primary antibody dilution ratio of 1:2000. 30 ug total protein was loaded per lane. Samples from human tumor cell lines: PPC-1 (prostate carcinoma), NCI-H226 and NCI-H332M (lung carcinoma), SF-268 (glioblastoma), UO-31 and A498 (renal/kidney carcinoma), SK-MEL-5 and SK-MEL-28 (melanoma), and MCF-7 (breast carcinoma). Lymphoma is from a cell line generated from a tumor growing in nude mice following injection of primary human lymphoma cells.
https://www.bosterbio.com/products/primary-antibodies/anti-dapper-homolog-1-antibody-a04683-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04683-Western-Blotting-Analysis-1.jpgAnti-Dapper homolog 1 DACT1 AntibodyWestern blot analysis of Dapper homolog 1. Anti-Dapper homolog 1 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-vang-like-1-antibody-a07587-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07587-Western-Blotting-Analysis-1.jpgAnti-Vang like-1 VANGL1 AntibodyWestern blot analysis of Vang like-1. Anti-Vang like-1 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-brachyury-antibody-a02161-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02161-Western-Blotting-Analysis-1.jpgAnti-Brachyury AntibodyWestern blot analysis of Brachyury. Anti-Brachyury antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-twistnb-antibody-a12525-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12525-Western-Blotting-Analysis-1.jpgAnti-Twistnb AntibodyExpression analysis of Twistnb. Anti-Twistnb antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-gnpda1-antibody-a10820-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10820-Western-Blotting-Analysis-1.jpgAnti-GNPDA1 AntibodyExpression analysis of GNPDA1. Anti-GNPDA1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-them2-antibody-a07288-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07288-Western-Blotting-Analysis-1.jpgAnti-THEM2 ACOT13 AntibodyExpression analysis of THEM2. Anti-THEM2 antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-mrf2-antibody-a02880-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02880-Western-Blotting-Analysis-1.jpgAnti-MRF2 ARID5B AntibodyExpression analysis of MRF2. Anti-MRF2 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-spz1-tsp1-antibody-a09034-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09034-Western-Blotting-Analysis-1.jpgAnti-SPZ1/TSP1 AntibodyExpression analysis of SPZ1/TSP1. Anti-SPZ1/TSP1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-dppa4-antibody-a10283-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10283-Western-Blotting-Analysis-1.jpgAnti-DPPA4 AntibodyExpression analysis DPPA4. Anti-DPPA4 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-trbp-antibody-a01680-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01680-Western-Blotting-Analysis-1.jpgAnti-TRBP TARBP2 AntibodyWestern blot analysis of TRBP. Anti-TRBP antibody was used at 6 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-tril-antibody-a09398-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09398-Western-Blotting-Analysis-1.jpgAnti-TRIL AntibodyWestern blot analysis of TRIL. Anti-TRIL antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-cactin-antibody-a09699-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09699-Western-Blotting-Analysis-1.jpgAnti-Cactin AntibodyWestern blot analysis of Cactin. Anti-Cactin antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-embigin-emb-antibody-a02826-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02826-Western-Blotting-Analysis-1.jpgAnti-Embigin, EMB AntibodyWestern blot analysis of Embigin, EMB. Anti-Embigin, EMB antibody was used at 2 μg/ml on (1) PC3 and (2) Jurkat lysates.
https://www.bosterbio.com/products/primary-antibodies/anti-tis7-antibody-a07201-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07201-Western-Blotting-Analysis-1.jpgAnti-Tis7 IFRD1 AntibodyWestern blot analysis of Tis7. Anti-Tis7 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-il-37-antibody-a03607-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03607-Western-Blotting-Analysis-1.jpgAnti-IL-37 AntibodyWestern blot analysis of IL-37. Anti-IL-37 antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-samhd1-antibody-a00592-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00592-Western-Blotting-Analysis-1.jpgAnti-SAMHD1 AntibodyWestern blot analysis of SAMHD1. Anti-SAMHD1 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-ifit2-antibody-a04428-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04428-Western-Blotting-Analysis-1.jpgAnti-IFIT2 AntibodyWestern blot analysis of IFIT2. Anti-IFIT2 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-reg3a-antibody-a05686-boster.html2026-03-24T05:07:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05686-Western-Blotting-Analysis-1.jpgAnti-REG3A AntibodyWestren blot analysis of REG3A. Anti-REG3A antibody was used at 0.1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-tox-antibody-a08441-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A08441-Immunostaining-Analysis-11-4065-Testis-882298.jpgAnti-TOX AntibodyImmunohistochemical analysis of TOX. Anti-TOX antibody in human Testis tissue at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A08441-Western-Blotting-Analysis-1.jpgAnti-TOX AntibodyWestern blot analysis of TOX. Anti-TOX antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-tab3-antibody-a05084-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05084-Western-Blotting-Analysis-1.jpgAnti-TAB3/Map3K7Ip3 AntibodyWestern blot analysis of TAB3. Anti-TAB3 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-nfkbil1-antibody-a05691-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05691-Western-Blotting-Analysis-1.jpgAnti-NFKBIL1 AntibodyWestern blot analysis of NFKBIL1. Anti-NFKBIL1 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-brd4-hunk1-antibody-a00123-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00123-Western-Blotting-Analysis-1.jpgAnti-BRD4, HUNK1 AntibodyWestern blot analysis of BRD4, HUNK1. Anti-BRD4, HUNK1 antibody was used at 2 μg/ml on SKM lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-cela3b-antibody-a09940-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09940-Western-Blotting-Analysis-1.jpgAnti-CELA3B AntibodyExpression analysis of CELA3B. Anti-CELA3B antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-mum1-antibody-a02544-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02544-Western-Blotting-Analysis-1.jpgAnti-MUM1 AntibodyExpression analysis of MUM1. Anti-MUM1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-mtap-antibody-a05448-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05448-Western-Blotting-Analysis-1.jpgAnti-MTAP AntibodyWestern blot analysis of MTAP. Anti-MTAP antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-cd141-antibody-a01325-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01325-Western-Blotting-Analysis-1.jpgAnti-CD141 THBD AntibodyWestern blot analysis of CD141. Anti-CD141 antibody was used at 2 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-pacs-1-antibody-a06811-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06811-Western-Blotting-Analysis-1.jpgAnti-PACS-1 AntibodyWestern blot analysis of PACS-1. Anti-PACS-1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-importin-9-antibody-a10216-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10216-Immunostaining-Analysis-11-8012-Lung_-Respiratory-Epithelium-882671.jpgAnti-Importin-9 IPO9 AntibodyImmunohistochemical analysis of Importin-9. Anti-Importin-9 antibody (Respiratory Epithelium tissue at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10216-Immunostaining-Analysis-11-8012-Colon-882669.jpgAnti-Importin-9 IPO9 AntibodyImmunohistochemical analysis of Importin-9. Anti-Importin-9 antibody in human Colon tissue at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10216-Western-Blotting-Analysis-1.jpgAnti-Importin-9 IPO9 AntibodyWestern blot analysis of Importin-9. Anti-Importin-9 antibody was used at 0.25 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-exportin-4-antibody-a08052-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A08052-Western-Blotting-Analysis-1.jpgAnti-Exportin-4 XPO4 AntibodyWestern blot analysis of Exportin-4. Anti-Exportin-4 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-lst8-gbl-antibody-a05357-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05357-Western-Blotting-Analysis-1.jpgAnti-LST8/GBL MLST8 AntibodyWestern blot analysis of LST8/GBL. Anti-LST8/GBL was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-trh-r-antibody-a06451-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06451-Western-Blotting-Analysis-1.jpgAnti-TRH-R AntibodyWestern blot analysis of TRH-R. Anti-TRH-R antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-sapk-interacting-protein-1-mip1-antibody-a04068-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04068-Western-Blotting-Analysis-1.jpgAnti-SAPK interacting protein 1/Mip1 MAPKAP1 AntibodyWestern blot analysis of SAPK interacting protein 1/Mip1. Anti-SAPK interacting protein 1/Mip1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-dusp13-skrp4-antibody-a11187-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A11187-Western-Blotting-Analysis-1.jpgAnti-DUSP13, SKRP4 AntibodyWestern blot analysis of DUSP13,SKRP4. Anti-DUSP13,SKRP4 antibody was used at 1 ug/ml on THP-1 lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-trk-fused-gene-antibody-a02870-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02870-Immunostaining-Analysis-11-8031-Small-Intestine-886701.jpgAnti-TRK Fused gene TFG AntibodyImmunohistochemical analysis of TRK Fused gene. Anti-TRK Fused gene antibody in human Small Intestine tissue at 20 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02870-Immunostaining-Analysis-11-8031-Kidney-886703.jpgAnti-TRK Fused gene TFG AntibodyImmunohistochemical analysis of TRK Fused gene. Anti-TRK Fused gene antibody in human Kidney tissue at 20 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02870-Western-Blotting-Analysis-1.jpgAnti-TRK Fused gene TFG AntibodyWestern blot analysis of TRK Fused gene. Anti-TRK Fused gene antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-gpr35-antibody-a06269-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06269-Western-Blotting-Analysis-1.jpgAnti-GPR35 AntibodyWestern blot analysis of GPR35. Anti-GPR35 antibody was used at 2 μg/ml on HCT-116 lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/r/a/rawlysate.jpgAnti-GPR35 AntibodyWestern blot analysis of GPR35. Anti-GPR35 antibody was used at 1
https://www.bosterbio.com/products/primary-antibodies/anti-ucp3-antibody-a01769-boster.html2026-03-24T05:07:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01769-Western-Blotting-Analysis-1.jpgAnti-UCP3 AntibodyWestern blot analysis of UCP3. Anti-UCP3 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-spi-b-antibody-a02805-boster.html2026-03-24T05:07:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02805-Immunostaining-Analysis-11-8052-Colon-882681.jpgAnti-Spi-B AntibodyImmunohistochemical analysis of Spi-B. Anti-Spi-B antibody in human Colon tissue at 5 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02805-Western-Blotting-Analysis-1.jpgAnti-Spi-B AntibodyWestern blot analysis of Spi-B. Anti-Spi-B antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-asap2-antibody-a09026-boster.html2026-03-24T05:07:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09026-Western-Blotting-Analysis-1.jpgAnti-ASAP2/Pag3 AntibodyWestern blot analysis of ASAP2. Anti-ASAP2 antibody was used at 4 &mu
https://www.bosterbio.com/products/primary-antibodies/anti-ruvb-like-1-antibody-a02049-boster.html2026-03-24T05:07:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02049-Immunostaining-Analysis-11-8077-Testis-882683.jpgAnti-RuvB-like 1 RUVBL1 AntibodyImmunohistochemical analysis of RuvB-like 1. Anti-RuvB-like 1 antibody in human Testis tissue at 10 &muhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02049-Western-Blotting-Analysis-1.jpgAnti-RuvB-like 1 RUVBL1 Antibodyblot analysis of RuvB-like 1. Anti-RuvB-like 1 antibody was used at 1 &mu
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-glur1-s845-rabbit-monoclonal-antibody-p02677-boster.html2026-03-24T05:07:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02677-wb.jpgAnti-Phospho-GluR1 (S845) GRIA1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-GluR1 (S845) expression in (1) Human brain lysate treated with Lambda phosphatase lysate; (2) Human brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-synapsin-i-s9-rabbit-monoclonal-antibody-p03794-boster.html2026-03-24T05:07:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03794-wb.jpgAnti-Phospho-Synapsin I (S9) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Synapsin I (S9) expression in (1) Human brain lysate; (2) Human brain lysate treated with AP.
https://www.bosterbio.com/products/primary-antibodies/anti-hepatitis-b-virus-picoband-trade-antibody-a30379-boster.html2026-03-24T05:07:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a30379-2-IHC-anti-hepatitis-b-virus-picoband-antibody.jpgAnti-Hepatitis B Virus Antibody Picoband® IHC analysis of Hepatitis B Virus using anti-Hepatitis B Virus antibody (A30379).
Hepatitis B Virus was detected in paraffin-embedded section of human hepatitis B tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hepatitis B Virus Antibody (A30379) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a30379-1-IHC-anti-hepatitis-b-virus-picoband-antibody.jpgAnti-Hepatitis B Virus Antibody Picoband® IHC analysis of Hepatitis B Virus using anti-Hepatitis B Virus antibody (A30379).
Hepatitis B Virus was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hepatitis B Virus Antibody (A30379) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-12985_2020_1304_fig1_html.pngAnti-Hepatitis B Virus Antibody Picoband®Over-expression of USP18 and its catalytic activity. HepAD38 cells were transfected with WT-USP18 plasmid, USP18-C64S plasmid or empty vector (MOCK) or left untreated. a : Twenty-four hours after transfection, USP18 mRNA was determined by real-time PCR (normalized by GAPDH). b : Forty-eight hours after transfection, USP18 protein expressions were analyzed by western blot (left). The relative expression levels of USP18 (normalized by GAPDH) were calculated by densitometry analysis (right). c : Cleavage of ISG15-GST fusion in vitro. USP18, ISG15/GST and WT-USP18 (or USP18-C64S) were co-transfected into Hela cells. Total intracellular protein was collected to perform Western blot. WT-USP18, wide type USP18; MOCK, empty plasmid. Results are presented as means ± SD ( n ≥ 3). ** p ≤ 0.01; *** p ≤ 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://virologyj.biomedcentral.com/articles/10.1186/s12985-020-01304-2'>32248821</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-12985_2020_1304_fig2_html.pngAnti-Hepatitis B Virus Antibody Picoband®Over-expression of USP18 in HepAD38 cells promoted HBV production independent of its protease activity. HepAD38 cells were transfected with USP18 plasmids as indicated. Real-time PCR was performed to quantify HBV production. Total supernatant HBV DNA ( a ), total intracellular HBV DNA ( b ), HBV cccDNA ( c ) and HBV pgRNA ( d ) 48 h post transfection with 4 μg WT-USP18 plasmid. Supernatant HBV total DNA 48 h post transfection with 4 μg WT-USP18 or 4 μg USP18-C64S plasmid, respectively ( e ). WT-USP18, wide type USP18; MOCK, empty plasmid. Results are presented as means ± SD (n ≥ 3). * p ≤ 0.05; ** p ≤ 0.01; ***p ≤ 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://virologyj.biomedcentral.com/articles/10.1186/s12985-020-01304-2'>32248821</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-12985_2020_1304_fig3_html.pngAnti-Hepatitis B Virus Antibody Picoband®Over-expression of USP18 in HepAD38 cells did not affect expression of HBV proteins. HepAD38 cells were transfected with the 4 μg WT-USP18, 4 μg USP18-C64S or 4 μg MOCK, respectively. Forty-eight hours later, culture medium was collected to quantify HBsAg ( a ) and HBeAg ( b ) expression level by ELISA assay. Intracellular HBcAgwas detected by western blot ( c, left ) and ( c, right ) analyzed by densitometry analysis. WT-USP18, wide type USP18; MOCK, empty plasmid. Results are presented as means ± SD (n ≥ 3) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://virologyj.biomedcentral.com/articles/10.1186/s12985-020-01304-2'>32248821</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-12985_2020_1304_fig4_html.pngAnti-Hepatitis B Virus Antibody Picoband®Silencing USP18 in HepAD38 suppressed HBV production. HepAD38 cells were seeded at 3 × 10 5 /ml, 2 ml per well in 6-well plates. 24 h later, the cells were left untreated or transfected with 20 nM siUSP18 or 20 nM NC. 48 h post transfection, knockdown efficiency was evaluated by detecting USP18 mRNA expression ( a, left ), which was further confirmed by western blot ( a, right ). Intracellular total RNA and DNA, as well as supernatant DNA, were collected respectively. Real-time PCR was performed to detect supernatant HBV total DNA ( b ), intracellular HBV total DNA ( c ), HBV cccDNA ( d ) and pgRNA ( e ). siUSP18, USP18 small inhibitory RNA; NC, the negative control siRNA. Results are presented as means ± SD (n ≥ 3). *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://virologyj.biomedcentral.com/articles/10.1186/s12985-020-01304-2'>32248821</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-12985_2020_1304_fig5_html.pngAnti-Hepatitis B Virus Antibody Picoband®USP18 upregulation inhibited IFN-induced Jak/STAT signaling pathway. HepAD38 cells and HepG2 cells were seeded in 6-well plate without any treatment, respectively. Forty-eight hours later, supernatant IFNα ( a, left ) and IFNβ ( a, right ) and intracellular mRNA expression of ISGs ( b ) were analyzed by ELISA assay and real-time PCR, respectively. To investigate the effects of USP18 on STAT phosphorylation, HepAD38 cells were transfected with WT-USP18, USP18-C64S or MOCK for 48 h and treated with 500 IU/ml IFNα for 30 min before harvested. Western blot was used to analyze the expression of STAT1 and p-STAT1 ( c, left ). The interferon stimulated response element (ISRE) activity was quantified by dual luciferase reporter gene assay. Briefly, HepAD38 cells were co-transfected with WT-USP18, USP18-C64S or MOCK and ISRE-luc reporter plasmid /pRL-TK reporter plasmid for 24 h, and then left untreated or treated with 100 IU/ml or 1000 IU/ml IFNα for 24 h before the cells were lysed ( c, middle ). HepAD38 cells were transfected with WT-USP18, USP18-C64S or MOCK for 48 h and treated with 500 IU/ml IFNα for additional 24 h. Expression of ISGs mRNA including MxA and OAS2 were detected by real-time PCR ( c, right ). WT-USP18, wide type USP18; MOCK, empty plasmid. Results are presented as means ± SD (n ≥ 3). *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://virologyj.biomedcentral.com/articles/10.1186/s12985-020-01304-2'>32248821</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig1_html.jpgAnti-Hepatitis B Virus Antibody Picoband®Expression of TMEM2 in liver tissues and HepG2 and HepG2.2.15 cells. ( a ) Expression of TMEM2 in liver tissues based on IHC. (Left) Grainy staining of TMEM2 was observed in the cytoplasm in normal liver tissues. (Middle) Reduced TMEM2 expression in the liver tissues from a patient with chronic HBV infection. (Right) HE staining of normal liver tissues (scale bar, 50 μ m). ( b ) Western blot results showed reduced expression of TMEM2 in the liver tissues from a patient with chronic HBV infection compared with normal liver tissues (above) (healthy livers compared with HBV livers: * P <0.05, ** P <0.01). Western blot results showed reduced expression of TMEM2 in HepG2.2.15 cells compared with HepG2 cells (below) (HepG2 versus HepG2215: ** P <0.01). ( c ) RT-qPCR results showed reduced TMEM2 mRNA levels in the liver tissues from a patient with chronic HBV infection compared with that in normal liver tissues (left) (healthy livers versus HBV livers: * P <0.05). RT-qPCR results showed reduced TMEM2 mRNA levels in HepG2.2.15 cells compared with HepG2 cells (right) (HepG2 versus HepG2215: ** P <0.01). Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig2_html.jpgAnti-Hepatitis B Virus Antibody Picoband®Expression of TMEM2 in stable cell lines. ( a ) HepG2 GFP cells (the control HepG2 cells), HepG2 shTMEM2 cells with TMEM2 silenced, HepG2 TMEM2 cells with TMEM2 overexpression, HepG2.2.15 GFP cells (normal HepG2.2.15 cells), and HepG2.2.15 TMEM2 cells with TMEM2 overexpression. ( b ) Western blot results showed reduced expression of TMEM2 in HepG2 shTMEM2 cells (GFP versus HepG2 shTMEM2: * P <0.05; GFP versus HepG2 TMEM2: * P <0.05) and increased expression of TMEM2 in HepG2 TMEM2 and HepG2.2.15 TMEM2 cells (GFP versus HepG2215 TMEM2: ** P <0.01). ( c ) RT-qPCR results showed reduced levels of TMEM2 mRNA in HepG2 shTMEM2 cells (GFP versus HepG2 shTMEM2: * P <0.05; GFP versus HepG2 TMEM2: ** P <0.01) and increased mRNA levels of TMEM2 in HepG2 TMEM2 and HepG2.2.15 TMEM2 cells (GFP versus HepG2215 TMEM2: ** P <0.01)). ( d ) Effect of TMEM2 silencing or overexpression on the kinetics of cell growth/cell death. Overexpression of TMEM2 slightly promoted the proliferation of HepG2 and HepG2.2.15 ( P >0.05), and TMEM2 silencing slightly repressed the proliferation of HepG2 cells ( P >0.05). Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig6_html.jpgAnti-Hepatitis B Virus Antibody Picoband®INF promoted the inhibitory effects of TMEM2 on HBV infection. ( a ) IFN pre-treatment increased the levels of p-JAK1 and p-STAT1 in HepG2 GFP and HepG2 shTMEM2 cells (Control versus IFN: * P <0.05). ( b ) IFN pre-treatment significantly increased the expression of MxA and OAS1 in HepG2 GFP and HepG2 shTMEM2 cells ( ## P <0.01). The expression of MxA and OAS1 in HepG2 shTMEM2 cells was significantly lower than that in HepG2 GFP cells (** P <0.01). ( c ) IFN pre-treatment reduced the levels of HBsAg and HBcAg in HepG2 shTMEM2 cells infected with HBV; the relative HBcAg and HBsAg levels are represented in the column graph on the right of . ( d ) IFN pre-treatment significantly reduced the mRNA levels of HBV DNA and HBV cccDNA in HepG2 GFP and HepG2 shTMEM2 cells infected with HBV ( ## P <0.01). Ctr, Control (HepG2 GFP). Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig7_html.jpgAnti-Hepatitis B Virus Antibody Picoband®JAK1 inhibitor repressed the inhibitory effects of TMEM2 on HBV infection. ( a ) JAK1 inhibitor significantly reduced the levels of p-JAK1 and p-STAT1 in HepG2.2.15 GFP and HepG2.2.15 TMEM2 cells. However, the expression of JAK1 and STAT1 in HepG2.2.15 GFP and HepG2.2.15 TMEM2 cells was not significantly affected by JAK1 inhibitor; quantitation of p-JAK1 and p-STAT1 is shown in the column graph on the right of . ( b ) JAK1 inhibitor significantly reduced the expression of OAS1 in HepG2.2.15 GFP and HepG2.2.15 TMEM2 cells ( # P <0.05, ## P <0.01). Prior to JAK1 inhibitor pre-treatment, the expression of OAS1 in HepG2.2.15 TMEM2 cells was significantly higher than that in HepG2.2.15 GFP cells (** P <0.01). ( c ) JAK1 inhibitor increased the levels of HBsAg and HBcAg in HepG2.2.15 TMEM2 cells infected with HBV. ( d ) JAK1 inhibitor significantly increased the levels of HBV DNA and HBV cccDNA in HepG2.2.15 GFP and HepG2.2.15 TMEM2 cells infected with HBV ( ## P <0.01). Ctr, Control (HepG2.2.15 GFP). Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig3_html.jpgAnti-Hepatitis B Virus Antibody Picoband®Levels of HBsAg, HBcAg, HBV DNA, and HBV cccDNA in HBV-infected HepG2 and HepG2.2.15 with TMEM2 overexpression or silencing. ( a ) IHC results showed higher levels of HBsAg and HBcAg in HepG2 shTMEM2 cells than in HepG2 GFP cells. The levels of HBsAg and HBcAg were lower in HepG2 TMEM2 cells than in HepG2 GFP cells. In addition, the levels of HBsAg and HBcAg were lower in HepG2.2.15 TMEM2 cells than in HepG2.2.15 GFP cells. HBc: HBcAg; HBs: HBsAg. ( b ) Quantitative analysis of HBV DNA in HBV-infected HepG2 and HepG2.2.15 with TMEM2 overexpression or silencing. After HBV infection, the HBV DNA level increased in all cells. After HBV infection, the level of HBV DNA in HepG2 shTMEM2 cells was higher than that in HepG2 GFP and HepG2 TMEM2 cells (left, ** P <0.01; ## P <0.01). After HBV infection, the level of HBV DNA in HepG2.2.15 GFP cells was significantly increased (right, ## P <0.01). After HBV infection, the level of HBV DNA in HepG2.2.15 TMEM2 cells was lower than that in HepG2.2.15 GFP cells (right, ** P <0.01). ( c ) Quantitative analysis of HBV cccDNA in HBV-infected HepG2 and HepG2.2.15 with TMEM2 overexpression or silencing. After HBV infection, HBV cccDNA levels were increased in HepG2 GFP and HepG2 shTMEM2 cells (left, ## P <0.01). After HBV infection, HBV cccDNA levels were increased in HepG2 shTMEM2 cells compared with HepG2 GFP and HepG2 TMEM2 cells (left, ** P <0.01). After HBV infection, HBV cccDNA were significantly increased in HepG2.2.15 GFP cells (right, # P <0.05). After HBV infection, HBV cccDNA levels were lower in HepG2.2.15 TMEM2 cells compared with HepG2.2.15 GFP cells (right, * P <0.05). Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig4_html.jpgAnti-Hepatitis B Virus Antibody Picoband®TMEM2 regulated JAK–STAT signaling pathway. ( a ) The expression levels of a number of key components of the JAK–STAT signaling pathway were evaluated by western blotting. The levels of p-Tyk2, p-JAK1, p-STAT1, and p-STAT2 were significantly reduced after HBV infection (Control versus HBV: * P <0.05, ** P <0.01). However, the levels of Tyk2, JAK1, STAT1, and STAT2 were not significantly affected by HBV infection. The levels of p-Tyk2, p-JAK1, p-STAT1, and p-STAT2 were significantly reduced in HepG2 shTMEM2 cells than compared with HepG2 GFP cells (HepG2 GFP versus HepG2 shTMEM2: # P <0.05, ## P <0.01). The levels of p-Tyk2, p-JAK1, p-STAT1, and p-STAT2 were significantly elevated in HepG2 TMEM2 cells compared with HepG2 GFP cells (HepG2 GFP versus HepG2 TMEM2: & P <0.05). The levels of p-Tyk2, p-JAK1, p-STAT1, and p-STAT2 were significantly elevated in HepG2.2.15 TMEM2 cells compared with HepG2.2.15 GFP cells (HepG2.2.15 GFP versus HepG2.2.15 TMEM2: $ P <0.05, $$ P <0.05). No significant changes in cellular levels of total IRF9 were observed by HBV infection in any groups based on western blot analysis. HBsAg was significantly induced after HBV infection (Control versus HBV: * P <0.05, ** P <0.01). ( b ) qPCR detection of the expression of MxA and OAS1 in HepG2 GFP and HepG2.2.15 cells. (* P< 0.05 compared with HepG2 GFP cells without HBV infection; $ P< 0.05 compared with HepG2.2.15 GFP cells without HBV infection; ^ P< 0.05 compared with HepG2.2.15 GFP cells infected with HBV.) Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30379-41419_2016_article_bfcddis2016146_fig5_html.jpgAnti-Hepatitis B Virus Antibody Picoband®Effects of TMEM2 on the translocation of IRF9 into nuclei and the expression of MxA and OAS1. ( a ) IRF9 localization was analyzed by IFA. The level of IRF9 in the nuclei of HepG2 shTMEM2 cells did not change significantly in response to HBV infection compared with that in HepG2 GFP cells. In contrast, the level of IRF9 in the nuclei of non-HBV-infected HepG2 TMEM2 cells was remarkably higher than that in non-HBV-infected HepG2 GFP and HepG2 shTMEM2 cells. HBV infection reduced the level of IRF9 in the nuclei in HepG2 TMEM2 cells. Similar results were observed in HepG2.2.15 cells, which overexpressed TMEM2; nuclear translocation is represented by column shown on the right side of . ( b ) Using a plasmid that expresses a reporter gene (firefly luciferase) under the control of a promoter containing ISRE motifs, we showed that transfection of this plasmid into HepG2 TMEM2 cells, either with HBV infection or without, significantly increased luciferase activity compared with HepG2 GFP and HepG2 shTMEM2 cells (* P <0.05 compared with HepG2 GFP cells without HBV infection; # P <0.05 compared with HepG2 GFP cells with HBV infection). Similar results were observed in TMEM2-overexpressing HepG2.2.15 cells ( $ P <0.05 compared with HepG2.2.15 GFP cells without HBV infection, ^ P <0.05 compared with HepG2.2.15 GFP cells with HBV infection). When TMEM2 was silenced in HepG2 cells, the luciferase activity was markedly reduced. Error bars are presented as S.D. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/cddis2016146'>27253403</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-abca4-picoband-trade-antibody-a01048-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01048-abca4-primary-antibodies-wb-testing-1.jpgAnti-ABCA4 Antibody Picoband® Western blot analysis of ABCA4 using anti-ABCA4 antibody (A01048). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: rat eye tissue lysates,<br>
Lane 3: mouse eye tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCA4 antigen affinity purified polyclonal antibody (Catalog # A01048) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABCA4 at approximately 256-300 kDa. The expected band size for ABCA4 is at 256 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp4-picoband-trade-antibody-a01596-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01596-mrp4-primary-antibodies-wb-testing-1.jpgAnti-MRP4/ABCC4 Antibody Picoband® Western blot analysis of MRP4 using anti-MRP4 antibody (A01596). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SW620 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MRP4 antigen affinity purified polyclonal antibody (Catalog # A01596) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MRP4 at approximately 200-250 kDa. The expected band size for MRP4 is at 150 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-abcg8-picoband-trade-antibody-a01482-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01482-1-abcg8-primary-antibodies-wb-testing-1.jpgAnti-ABCG8 Antibody Picoband® Western blot analysis of ABCG8 using anti-ABCG8 antibody (A01482-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates, <br>
Lane 2: human K562 whole cell lysates, <br>
Lane 3: human HepG2 whole cell lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: rat PC-12 whole cell lysates, <br>
Lane 6: mouse liver tissue lysates, <br>
Lane 7: mouse HEPA1-6 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCG8 antigen affinity purified polyclonal antibody (Catalog # A01482-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABCG8 at approximately 76 kDa. The expected band size for ABCG8 is at 76 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01482-1-abcg8-primary-antibodies-if-testing-2.jpgAnti-ABCG8 Antibody Picoband® IF analysis of ABCG8 using anti-ABCG8 antibody (A01482-1). <br>
ABCG8 was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ABCG8 Antibody (A01482-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-acsl5-picoband-trade-antibody-a05087-2-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-2-acsl5-primary-antibodies-wb-testing-1.jpgAnti-ACSL5 Antibody Picoband® Western blot analysis of ACSL5 using anti-ACSL5 antibody (A05087-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACSL5 antigen affinity purified polyclonal antibody (Catalog # A05087-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACSL5 at approximately 76 kDa. The expected band size for ACSL5 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-2-acsl5-primary-antibodies-fcm-testing-2.jpgAnti-ACSL5 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ACSL5 antibody (A05087-2). <br>
Overlay histogram showing HepG2 cells stained with A05087-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ACSL5 Antibody (A05087-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-adam2-picoband-trade-antibody-a08379-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08379-1-1-WB-anti-adam2-picoband-antibody.jpgAnti-ADAM2 Antibody Picoband® Western blot analysis of ADAM2 using anti-ADAM2 antibody (A08379-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat testis tissue lysate,<br>
lane 2: mouse testis tissue lysate,<br>
lane 3: MCF-7 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM2 antigen affinity purified polyclonal antibody (Catalog # A08379-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM2 at approximately 100KD. The expected band size for ADAM2 is at 82KD.
https://www.bosterbio.com/products/primary-antibodies/anti-adam28-picoband-trade-antibody-a06873-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a06873-1-1-WB-anti-adam28-picoband-antibody.jpgAnti-ADAM28 Antibody Picoband®<b> Western blot analysis of ADAM28 using anti-ADAM28 antibody (A06873-1). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>lane 1: HELA whole cell lysates,<br>lane 2: K562 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM28 antigen affinity purified polyclonal antibody (Catalog # A06873-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM28 at approximately 87/61KD. The expected band size for ADAM28 is at 87KD.
https://www.bosterbio.com/products/primary-antibodies/anti-adamts4-picoband-trade-antibody-a02899-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02899-1-WB-anti-adamts4-picoband-antibody.jpgAnti-ADAMTS4/ADAMTS4 Antibody Picoband®<b> Western blot analysis of ADAMTS4 using anti-ADAMTS4 antibody (A02899). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>
Lane 1: Recombinant Human ADAMTS4 Protein 0.5ng <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAMTS4 antigen affinity purified polyclonal antibody (Catalog # A02899) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAMTS4 at approximately 58KD. The expected band size for ADAMTS4 is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-anterior-gradient-2-picoband-trade-antibody-a02922-2-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-wb-testing-1.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband® Western blot analysis of AGR2 using anti-AGR2 antibody (A02922-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human T47D whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: rat stomach tissue lysates,<br>
Lane 4: rat small intestine tissue lysates,<br>
Lane 5: mouse stomach tissue lysates,<br>
Lane 6: mouse small intestine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AGR2 antigen affinity purified polyclonal antibody (Catalog # A02922-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AGR2 at approximately 17 kDa. The expected band size for AGR2 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-ihc-testing-2.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband® IHC analysis of AGR2 using anti-AGR2 antibody (A02922-2). <br>
AGR2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AGR2 Antibody (A02922-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-ihc-testing-3.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband® IHC analysis of AGR2 using anti-AGR2 antibody (A02922-2). <br>
AGR2 was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AGR2 Antibody (A02922-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-ihc-testing-4.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband® IHC analysis of AGR2 using anti-AGR2 antibody (A02922-2). <br>
AGR2 was detected in a paraffin-embedded section of human bladder infiltrating urothelial carcinoma with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AGR2 Antibody (A02922-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-if-testing-1.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband®IF analysis of AGR2 using anti-AGR2 antibody (A02922-2). <br>
AGR2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AGR2 Antibody (A02922-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-ip-testing-1.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband®Immunoprecipitating (IP) AGR2 in A549 whole cell lysate.<br>
Western blot analysis of AGR2 using anti-AGR2 antibody (A02922-2); <br>
Lane 1: A549 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-AGR2 antibody in A549 whole cell lysate;<br>
Lane 3: anti-AGR2 antibody (2μg) + A549 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AGR2 antigen affinity purified polyclonal antibody (A02922-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for AGR2 at approximately 17 kDa. The expected band size for AGR2 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02922-2-agr2-primary-antibodies-fcm-testing-5.jpgAnti-Anterior Gradient 2/AGR2 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-AGR2 antibody (A02922-2). <br>
Overlay histogram showing CACO-2 cells stained with A02922-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-AGR2 Antibody (A02922-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-angiotensinogen-picoband-trade-antibody-a02103-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02103-1-agt-primary-antibodies-wb-testing-1.jpgAnti-Angiotensinogen/AGT Antibody Picoband® Western blot analysis of Angiotensinogen using anti-Angiotensinogen antibody (A02103-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Angiotensinogen antigen affinity purified polyclonal antibody (Catalog # A02103-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Angiotensinogen at approximately 53-55 kDa. The expected band size for Angiotensinogen is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02103-1-2_1-IHC-anti-angiotensinogen-picoband-antibody.jpgAnti-Angiotensinogen/AGT Antibody Picoband® IHC analysis of Angiotensinogen using anti-Angiotensinogen antibody (A02103-1).<br>
Angiotensinogen was detected in paraffin-embedded section of mouse kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti--Angiotensinogen Antibody (A02103-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-iba1-picoband-trade-antibody-a01394-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-wb-testing-1.jpgAnti-Iba1/AIF1 Antibody Picoband® Western blot analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Iba1/AIF1 antigen affinity purified polyclonal antibody (Catalog # A01394) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Iba1/AIF1 at approximately 17 kDa. The expected band size for Iba1/AIF1 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-2.jpgAnti-Iba1/AIF1 Antibody Picoband® IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-3.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-4.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-5.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-6.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-7.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01394-aif1-primary-antibodies-ihc-testing-8.jpgAnti-Iba1/AIF1 Antibody Picoband®IHC analysis of Iba1/AIF1 using anti-Iba1/AIF1 antibody (A01394). <br>
Iba1/AIF1 was detected in a paraffin-embedded section of pig brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Iba1/AIF1 Antibody (A01394) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-akap2-picoband-trade-antibody-a09279-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09279-akap2-primary-antibodies-wb-testing-1.jpgAnti-AKAP2 Antibody Picoband® Western blot analysis of AKAP2 using anti-AKAP2 antibody (A09279). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AKAP2 antigen affinity purified polyclonal antibody (Catalog # A09279) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AKAP2 at approximately 150-170 kDa. The expected band size for AKAP2 is at 95 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-12-lipoxygenase-picoband-trade-antibody-a02275-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02275-1-alox12-primary-antibodies-wb-testing-1.jpgAnti-12 Lipoxygenase/ALOX12 Antibody Picoband®Western blot analysis of ALOX12 using anti-ALOX12 antibody (A02275-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat spleen tissue lysates,<br>
Lane 2: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALOX12 antigen affinity purified polyclonal antibody (A02275-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALOX12 at approximately 76 kDa. The expected band size for ALOX12 is at 76 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-angiopoietin-1-picoband-trade-antibody-a00853-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00853-1-western-blotting.jpgAnti-Angiopoietin-1/ANGPT1 Antibody Picoband®<b> Western blot analysis of Angiopoietin-1 using anti-Angiopoietin-1 antibody (A00853). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>
lane 1: recombinant human ANGPT1 protein 1ng <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Angiopoietin-1 antigen affinity purified polyclonal antibody (Catalog # A00853) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Angiopoietin-1 at approximately 70KD. The expected band size for Angiopoietin-1 is at 57KD.
https://www.bosterbio.com/products/primary-antibodies/anti-angiopoietin-2-picoband-trade-antibody-a00370-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00370-1-IHC-anti-angiopoietin-2-picoband-antibody.jpgAnti-Angiopoietin-2/ANGPT2 Antibody Picoband® IHC analysis of Angiopoietin-2 using anti-Angiopoietin-2 antibody (A00370).<br>
Angiopoietin-2 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Angiopoietin-2 Antibody (A00370) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00370-2-IHC-anti-angiopoietin-2-picoband-antibody.jpgAnti-Angiopoietin-2/ANGPT2 Antibody Picoband® IHC analysis of Angiopoietin-2 using anti-Angiopoietin-2 antibody (A00370).<br>
Angiopoietin-2 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Angiopoietin-2 Antibody (A00370) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00370-angpt2-primary-antibodies-wb-testing-3.jpgAnti-Angiopoietin-2/ANGPT2 Antibody Picoband® Western blot analysis of ANGPT2 using anti-ANGPT2 antibody (A00370). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANGPT2 antigen affinity purified polyclonal antibody (Catalog # A00370) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANGPT2 at approximately 70KD. The expected band size for ANGPT2 is at 57KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00370-angpt2-primary-antibodies-elisa-testing-4.jpgAnti-Angiopoietin-2/ANGPT2 Antibody Picoband® Sandwich ELISA - Recombinant human Angiopoietin-2 protein standard curve.<br>
Use in combination with reagents from Human Angiopoietin-2 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0657).
https://www.bosterbio.com/products/primary-antibodies/anti-angptl2-picoband-trade-antibody-a05747-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05747-1-angptl2-primary-antibodies-wb-testing-1.jpgAnti-ANGPTL2 Antibody Picoband®Western blot analysis of ANGPTL2 using anti-ANGPTL2 antibody (A05747-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HUVEC whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: rat heart tissue lysates,<br>
Lane 4: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANGPTL2 antigen affinity purified polyclonal antibody (A05747-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ANGPTL2 at approximately 60-65 kDa. The expected band size for ANGPTL2 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05747-1-angptl2-primary-antibodies-ihc-testing-1.jpgAnti-ANGPTL2 Antibody Picoband®IHC analysis of ANGPTL2 using anti-ANGPTL2 antibody (A05747-1). <br>ANGPTL2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANGPTL2 Antibody (A05747-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05747-1-angptl2-primary-antibodies-ihc-testing-2.jpgAnti-ANGPTL2 Antibody Picoband®IHC analysis of ANGPTL2 using anti-ANGPTL2 antibody (A05747-1). <br>ANGPTL2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANGPTL2 Antibody (A05747-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-angptl4-picoband-trade-antibody-a01147-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01147-angptl4-primary-antibodies-wb-testing-1.jpgAnti-Angiopoietin-like 4/ANGPTL4 Antibody Picoband® Western blot analysis of ANGPTL4 using anti-ANGPTL4 antibody (A01147). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: human hepatocellular carcinoma tumor tissue (HCCT) lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANGPTL4 antigen affinity purified polyclonal antibody (Catalog # A01147) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANGPTL4 at approximately 65 kDa. The expected band size for ANGPTL4 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01147-angptl4-primary-antibodies-ihc-testing-2.jpgAnti-Angiopoietin-like 4/ANGPTL4 Antibody Picoband® IHC analysis of ANGPTL4 using anti-ANGPTL4 antibody (A01147). <br>
ANGPTL4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANGPTL4 Antibody (A01147) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01147-angptl4-primary-antibodies-ihc-testing-3.jpgAnti-Angiopoietin-like 4/ANGPTL4 Antibody Picoband® IHC analysis of ANGPTL4 using anti-ANGPTL4 antibody (A01147). <br>
ANGPTL4 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANGPTL4 Antibody (A01147) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-annexin-viii-picoband-trade-antibody-a08645-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08645-annexin-viii-primary-antibodies-wb-testing-1.jpgAnti-Annexin VIII/ANXA8 Antibody Picoband® Western blot analysis of Annexin VIII using anti-Annexin VIII antibody (A08645). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human placenta tissue lysates, <br>
Lane 3: human A549 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin VIII antigen affinity purified polyclonal antibody (Catalog # A08645) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Annexin VIII at approximately 37 kDa. The expected band size for Annexin VIII is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08645-2.pngAnti-Annexin VIII/ANXA8 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Annexin VIII antibody (A08645). <br> Overlay histogram showing U20S cells stained with A08645 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Annexin VIII Antibody (A08645,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-apex2-picoband-trade-antibody-a07203-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07203-1_1.jpgAnti-APEX2 Antibody Picoband® Western blot analysis of APEX2 using anti-APEX2 antibody (A07203).
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>
lane 1: rat brain tissue lysate,
<br>
lane 2: mouse brain tissue lysate, <br>
lane 3: HEK293 whole cell lysate, <br>
lane 4: COS-7 whole cell lysate. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APEX2 antigen affinity purified polyclonal antibody (Catalog # A07203) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APEX2 at approximately 57KD. The expected band size for APEX2 is at 57KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07203-2.jpgAnti-APEX2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-CYP7A1 antibody (A07203). <br>Overlay histogram showing A549 cells stained with A07203 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CYP7A1 Antibody (A07203, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-atp4b-picoband-trade-antibody-a08719-1-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08719-1-1-WB-anti-atp4b-picoband-antibody.jpgAnti-Hydrogen Potassium ATPase Beta/ATP4B Antibody Picoband® Western blot analysis of ATP4B using anti-ATP4B antibody (A08719-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat stomach tissue lysate,<br>
lane 2: mouse stomach tissue lysate,<br>
lane 3: SGC7901 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP4B antigen affinity purified polyclonal antibody (Catalog # A08719-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP4B at approximately 60KD. The expected band size for ATP4B is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-bax-picoband-trade-antibody-a00183-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-medscimonit-25-5482-g005.jpgAnti-Bax Antibody Picoband®The contribution of rL-RVG, α7-nAChR antagonist MLA, agonist ACB, or siRNA downregulation to the expression of α7-nAChR, p-AKT, PI3K, and apoptosis-associated proteins in HGC cells after infection. ( A ) For α7-nAChR antagonist. ( B ) For α7-nAChR agonist. ( C ) For α7-nAChR siRNA. When the groups were pretreated with α7-nAChR antagonist MLA, the expression of Bax/Bcl-2 and cleaved caspase 3 proteins increased in HGC cells compared to cells without MLA or α7-nAChR siRNA treatment (** P<0.01), except for the rL-RVG +MLA group and the rL-RVG group. The expression of the Bax/Bcl-2 and cleaved caspase 3 proteins decreased significantly (** P<0.01) in cells with α7-nAChR agonist ACB treatment compared with cells without pretreatment. The expression of α7-nAChR proteins decreased in MLA-pretreated groups (** P<0.01), but increased in ACB-pretreated groups (** P<0.01). The expression of p-AKT and PI3K proteins decreased in MLA and α7-nAChR siRNA-pretreated groups (** P<0.01), except for the rL-RVG group and the pretreated groups, but increased in the ACB-pretreated groups (** P<0.01). * P<0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6671559/&orig_host=www.ncbi.nlm.nih.gov'>31337746</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-nrr-12-96-g005.jpgAnti-Bax Antibody Picoband®Nicotiflorin effect on Bcl-2 and Bax immunreactivity in the ischemic cerebral cortex of I/R rats (immunohistochemical staining). (A) High-magnification images of Bcl-2 and Bax immunohistochemical staining (arrows show immunoreactive cells). Scale bar: 25 μm. (B) For each antibody staining, immunoreactive cells in a 1 mm width were counted under optical microscopy. The average count number was used for quantitation and comparison between groups. Respective numbers of Bcl-2- and Bax-positive cells show that nicotiflorin decreases Bax immunoreactivity and increases Bcl-2 immunoreactivity. * P < 0.05, ** P < 0.01, vs . I/R group (mean ± SEM, n = 3, one-way analysis of variance followed by post hoc Tukey test). I/R: Ischemia/reperfusion.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5319249/&orig_host=www.ncbi.nlm.nih.gov'>28250754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183_12645_2025_336_fig9_html.pngAnti-Bax Antibody Picoband®a Western blotting was used to examine mitochondrial apoptotic pathway-related proteins after treatment with control (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Key proteins involved in apoptosis such as Bax, Bcl-2, cytochrome c, and cleaved caspase-3 were examined to better understand how each treatment affects cell death at the mitochondrial level. b To further investigate the underlying molecular mechanisms, western blotting was used to investigate the PI3K/AKT/mTOR pathway (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Expression levels of PI3K, AKT (total and phosphorylated), and mTOR were evaluated to assess whether this survival pathway was activated or suppressed. Protein levels were quantified and compared to the control group to determine statistical significance. * p < 0.05, ** p < 0.01, *** p < 0.001 in comparison to the respective control <br><b>Index in Springer Nature under a CC BY license. DOI: <a href='https://link.springer.com/article/10.1186/s12645-025-00336-z'>10.1186/s12645-025-00336-z</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-medscimonit-22-3951-g006.jpgAnti-Bax Antibody Picoband®( A, B ) Protein expression levels of p21, p53, Bax, and Bcl-2 were detected by Western blot assays and compared by quantitative analysis of the gray value. * p <0.05 and ** p <0.01 vs. siR-NC group. siR-NC – control siRNA; siR-HMGB3 – HMGB3 siRNA; HMGB3 – high mobility group-box 3.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5081235/&orig_host=www.ncbi.nlm.nih.gov'>27774979</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-oncotarget-09-4475-g005.jpgAnti-Bax Antibody Picoband®( A ) Expression of Bcl-2 (A1–A3), ( B ) Bax (B1–B3), ( C ) Caspase-3 (C1–C3) in ovaries of HEV inoculation rabbits. A1, B1 and C1 are control group. A2, B2, C2 are HEV RNA positive ovaries in 28 dpi. A3, B3, C3 are HEV RNA positive ovaries in 49 dpi. (Original magnification:40×).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5796988/&orig_host=www.ncbi.nlm.nih.gov'>29435117</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-fphar-08-00044-g007.jpgAnti-Bax Antibody Picoband®Celastrol attenuates ganglion cells apoptosis in the retina of EAE rats. Treatment of celastrol decreased the number of TUNEL-positive cells (A) , upregulated expression of Bcl-2 (B) and downregulated expression of Bax, cleaved-caspase 3 and cleaved-PARP. Scale bar: 100 μm. Data were shown as mean ± SD, n = 5. ∗∗ P < 0.01 versus control group, ## P < 0.01 versus EAE group, †† P < 0.01 versus low dosage of celastrol group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00044/full'>28239352</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2018_34156_fig4_html.pngAnti-Bax Antibody Picoband®Effects of maltol on the levels of inflammation cytokines in cisplatin-induced renal toxicity. ( A ) Effects of maltol on the positive expressions of Bax, Bcl-2, iNOS and COX-2 in renal tissues were examined by IHC in renal tissues (magnification × 200), And the column chart shows stained area, semiquantitative analysis of Bax, Bcl-2, iNOS and COX-2 expression in kidneys to IHC. ( B ) Inflammation cytokines level of TNF-α, IL-1β, iNOS and NF-κB in serum of mice were measured by ELISA kits. All values were expressed as mean ± S.D. * p < 0.05, ** p < 0.01 vs . normal group; # p < 0.05, ## p < 0.01 vs . cisplatin group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-34156-6'>30374107</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-13567_2018_599_fig2_html.pngAnti-Bax Antibody Picoband®V protein overexpression in DF-1 cells inhibited apoptosis through the Bcl-2\Bax-Caspase-3 pathway. A V and control (pCAGEN-flag) plasmids were transfected into DF-1 cells for 48 h before the cells were harvested. The RNA was extracted according to the previously described method. The mRNA levels of some apoptosis-related genes (proapoptosis genes Caspase-3, Caspase-9, and FasLG, and the antiapoptosis gene Bcl-2) were detected using Q-PCR. B DF-1 cells were transfected with V and control (pCAGEN-flag) plasmids for 48 h. Whole-cell extracts were prepared for Western blot analysis that was specific for the indicated proteins. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13567-018-0599-6'>30290847</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12967_2022_3500_fig5_html.pngAnti-Bax Antibody Picoband®Anti-SEMA4D antibody can inhibit the survival of AML cell lines in vivo and in vitro. A CCK-8 analysis of U937 and Molm-13 cells treated with VX15/2503 or not. B Cell apoptosis rate of U937 and Molm-13 cells treated with VX15/2503 or not was detected by flow cytometry using Annexin V-APC/PI staining. C Western blotting analysis was used to determine the expression of apoptosis-related proteins (Bcl-2, Bax, and cleaved-caspase3) in U937 and Molm-13 cells treated with VX15/2503 or not. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. D Western blotting analysis was used to determine the expression of p-PI3K, PI3K, p-Akt, Akt in U937 and Molm-13 cells treated with VX15/2503 or not. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. E Schematic outline of the mouse model delineating this experiment. F Nude mice were subcutaneously inoculated with U937 cells to establish AML xenograft tumors and treated with VX15/2503. Volumes of tumors were monitored by direct measurement. G Tumor size of xenograft mice in two groups. H Weights of tumors of xenograft mice in two groups. I Immunohistochemistry stain was used to measure the expression of Bcl-2, Bax, cleaved-caspase3, p-PI3K, p-Akt in xenograft tumors. J Western blotting analysis was used to determine the expression of Bcl-2, Bax, cleaved-caspase3, p-PI3K, PI3K, p-Akt, Akt in xenograft tumors. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. Data with statistical significance are as indicated, *P < 0.05, **P < 0.01, ***P < 0.001, ns not significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-022-03500-w'>35794581</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-fonc-12-865067-g005.jpgAnti-Bax Antibody Picoband®(A) Proliferation ability of MDA-MB-231 and MCF-7 induced by TGF-β1 by plate cloning experiment. The effect of TGF-β1 on the proliferation of MDA-MB-231 cells (B) and MCF-7 (C) cells were analyzed by CCK-8 (*p < 0.05, **p < 0.01). Analysis of the effect of TGF-β1 on the apoptosis of MDA-MB-231 cells (D) and MCF-7 (E) cells by Annexin V-FITC/PI stain flow cytometry (*p < 0.05, **p < 0.01). The expression level of the apoptosis and TP63 proteins in MDR-MB-231 cells (F) and MCF-7 (G) cells with TGF-β1 induced. GAPDH was used as an internal control. Quantitative analysis of TP63, Bcl-2 and Bax are expressed as the mean ± SD. *, **p < 0.01 vs. control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9035888/&orig_host=www.ncbi.nlm.nih.gov'>35480110</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12967_2022_3500_fig2_html.pngAnti-Bax Antibody Picoband®SEMA4D promotes proliferation and inhibits apoptosis of AML cells. A Western blot was used to detect SEMA4D protein level when U937 and Molm-13 cells were transfected with stably knocking down or overexpressing SEMA4D lentivirus. B CCK-8 analysis of U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D or control. C Colony formation assay of U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D or control. D Cell apoptosis rate of U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D or control was detected by flow cytometry using Annexin V-APC/PI staining. E Western blotting analysis was used to determine the expression of apoptosis-related proteins (Bcl-2, Bax, and cleaved-caspase3) in U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D or control. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. Data with statistical significance are as indicated, *P < 0.05, **P < 0.01, ***P < 0.001, ns not significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-022-03500-w'>35794581</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12967_2022_3500_fig4_html.pngAnti-Bax Antibody Picoband®SEMA4D functions through its receptor PlexinB1. A Western blot was used to detect PlexinB1 protein level when U937 and Molm-13 cells were transfected with siRNA-PlexinB1 or siRNA-control. B CCK-8 analysis of U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D when PlexinB1 was knocked down or not. C Western blotting analysis was used to determine the expression of apoptosis-related proteins (Bcl-2, Bax, and cleaved-caspase3) in U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D when PlexinB1 was knocked down or not. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. D Cell apoptosis rate of U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D when PlexinB1 was knocked down or not was detected by flow cytometry using Annexin V-APC/PI staining. E Western blotting analysis was used to determine the expression of p-PI3K, PI3K, p-Akt, Akt in U937 and Molm-13 cells transfected with lentivirus targeting SEMA4D when PlexinB1 was knocked down or not. Results of densitometry analysis of relative expression levels after normalization to loading control β-actin are presented. Data with statistical significance are as indicated, *P < 0.05, **P < 0.01, ***P < 0.001, ns not significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-022-03500-w'>35794581</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2023_50720_fig10_html.pngAnti-Bax Antibody Picoband®Key proteins of apoptosis are upregulated in ACLF rats. ( A ) Western blot analysis for the BAX, CASP3, C-CASP3, CASP7, C-CASP7, CASP8, C-CASP8, and GAPDH proteins. Normal group: Lanes 1 to 3, ACLF group: Lanes 4 to 6. Relative expression level of ( B ) CASP3/GAPDH ( C ) C-CASP3/GAPDH ( D ) CASP7/GAPDH ( E ) C-CASP7/GAPDH ( F ) BAX/GAPDH ( G ) CASP8/GAPDH ( H ) C-CASP8/GAPDH. * P < 0.05 and ** P < 0.01. n = 3 per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-023-50720-1'>38172209</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2024_69356_fig6_html.pngAnti-Bax Antibody Picoband®FGF21 release from DEX-treated brown adipocytes attenuated H/R-induced injury in HL-1 cells through regulating the Keap1/Nrf2 complex. ( A ) Representative photographs of flow cytometry apoptosis assay. ( B ) Statistics of Cell apoptosis rate. ( C ) CCK-8 cell viability assay. ( D ) Lactate dehydrogenase (LDH) release assay. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group. ( F ) Representative photographs of DHE staining. Scale bar = 100 μm. ( G ) The protein expression of Keap1 were determined by western blot. ( H ) The interaction of Keap1 with Nrf2 was determined by Co-IP. ( I ) The protein expression of Nrf2 in nucleus and cytoplasm were determined by western blot. ( J ) Relative mRNA levels of antioxidant genes in cardiomyocytes after CM-DEX treatment. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2024_69356_fig5_html.pngAnti-Bax Antibody Picoband®DEX had minimal effect on the H/R-induced injury in HL-1 cells. ( A ) Representative photographs of flow cytometry apoptosis assay. ( B ) Statistics of Cell apoptosis rate. ( C ) CCK-8 cell viability assay. ( D ) lactate dehydrogenase (LDH) release assay.( E ) Representative photographs of PI staining. Scale bar = 100 μm. ( F ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group.* means P < 0.05 vs Control, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-medscimonit-25-5482-g006.jpgAnti-Bax Antibody Picoband®AKT antagonist and AKT agonist contributed to upregulating p-AKT, PI3K, and apoptosis-associated proteins expression in HGC cells after infection. ( A ) For AKT inhibitor. ( B ) For AKT agonist. When the groups were pretreated with AKT antagonist MK-2206, the expression of the Bax/Bcl-2 and cleaved caspase 3 proteins increased in HGC cells compared with cells without AKT antagonist (** P<0.01). The expression of the Bax/Bcl-2 and cleaved caspase 3 proteins decreased significantly (** P<0.01) in cells with AKT agonist IGF-1 treatment compared with cells without pretreatment. On the other hand, the expression of PI3K and p-AKT proteins decreased in AKT antagonist-pretreated groups (** P<0.01), but increased in AKT agonist-pretreated groups (** P<0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6671559/&orig_host=www.ncbi.nlm.nih.gov'>31337746</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41420_2021_448_fig2_html.pngAnti-Bax Antibody Picoband®CircHIPK3 promotes H/R-induced cardiomyocyte apoptosis. A The intracellular ROS level was detected by flow cytometry. n = 3. B Annexin V-FITC/PI flow cytometry was used to evaluate the effect of circHIPK3 on cardiomyocyte apoptosis. n = 3. C Apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2, were detected by western blotting. n = 3. * P < 0.05 compared with the normal group. # P < 0.05 compared with the H/R group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2024_69356_fig3_html.pngAnti-Bax Antibody Picoband®Exogenous administration of FGF21 neutralizing antibody significantly inhibited the cardioprotective effect of DEX. ( A ) Representative echocardiographic M-mode images were obtained 24 h after myocardial ischemia/reperfusion (MI/R), n = 6/group. ( B ) Left ventricular ejection fraction (LVEF) and fractional shortening (LVFS), n = 6/group. ( C ) Representative images of TTC staining 24 h after MI/R. Myocardial infarction area was calculated as a percentage of the myocardial area at risk, n = 6/group. ( D ) The levels of serum CK-MB, n = 6/group. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group. ( F ) Representative photographs of cardiomyocyte apoptosis examined by TUNEL assay. Bar graphs present the quantification analysis of cell apoptosis, n = 6/group. scale bar = 200 μm. ( G ) Morphological changes in myocardium was determined by HE staining. scale bar = 100 μm.* means P < 0.05 vs Control,† means P < 0.05 vs I/R group,‡ means P < 0.05 vs. I/R + DEX group, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41420_2021_448_fig4_html.pngAnti-Bax Antibody Picoband®MiR-20b-5p inhibits autophagy and apoptosis of cardiomyocytes under H/R conditions. A Transfection efficacy of miR-20b-5p mimics and miR-20b-5p inhibitors in cardiomyocytes. B Western blot showed the effect of transfection of miR-20b-5p mimics and miR-20b-5p inhibitors on the expression of LC3II and P62 in normal cardiomyocytes. n = 3. C Western blot showed the effect of transfection of miR-20b-5p mimics and miR-20b-5p inhibitors on the expression of apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2 in normal cardiomyocytes. n = 3. D Western blot showed the effects of miR-20b-5p mimics and miR-20b-5p inhibitor transfection on the expression of LC3II and P62 in cardiomyocytes under H/R conditions. n = 3. E Annexin V-FITC/PI flow cytometry was used to evaluate the effect of miR-20b-5p mimics and miR-20b-5p inhibitors on cardiomyocyte apoptosis under H/R conditions. n = 3. F Western blot analyzed the expression of apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2 in cardiomyocytes under H/R conditions by miR-20b-5p mimics and miR-20b-5p inhibitors transfection. n = 3. * P < 0.05 compared with the mimics-NC (MNC) group. # P < 0.05 compared with the inhibitors-NC (INC) group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2018_34156_fig5_html.pngAnti-Bax Antibody Picoband®Protective effects of maltol on cisplatin-induced injury in HEK293 cells. ( A ) The cytotoxic effects of cisplatin on HEK293 cells. ( B ) Effect of maltol on the activity of normal cells. ( C ) The viability of HEK293 cells incubated with maltol after cisplatin exposure. Effects of maltol on the protein expression levels of Bcl-2, Bax and caspase 3, 8, 9 as well as GAPDH protein was used as a loading control. ( D ) Cells were used for western blot analysis of indicated proteins (upper panel). Column chart represents relative protein levels compared with the control group after normalization to GAPDH levels (lower panel) Values are expressed as mean ± S.D. n = 8. ** p < 0.01 vs . normal group; # p < 0.05, ## p < 0.01 vs . cisplatin group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-34156-6'>30374107</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41420_2021_448_fig5_html.pngAnti-Bax Antibody Picoband®CircHIPK3 regulates autophagy and apoptosis via the CircHIPK3/miR-20b-5p/ATG7 axis. A Luciferase reporter assay showed that miR-20b-5p mimics directly binds to the 3′-UTR of ATG7 and inhibits luciferase activity. * P < 0.05 compared with the NC-mimics group. B ATG7 protein expression was detected by western blotting. n = 3. * P < 0.05 compared with the MNC group. # P < 0.05 compared with the INC group. C The protein expression levels of LC3-II, P62, and ATG7 were measured by western blotting. n = 3. D The intracellular ROS level was detected by flow cytometry. n = 3. E Annexin V-FITC/PI flow cytometry was used to evaluate apoptosis under different treatment conditions. n = 3. F Apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2, were detected by western blotting. n = 3. * P < 0.05 compared with the H/R group. # P < 0.05 compared with the H/R + sicircHIPK3 group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-13567_2018_599_fig4_html.pngAnti-Bax Antibody Picoband®TXNL1 induces apoptosis in DF-1 cells through the Bcl-2\Bax-Caspase-3 pathway. A Dot plot showing the flow cytometric analysis of phosphatidylserine (PS) translocation after staining with annexin V and PI in mock, control (pCMV-HA), and TXNL1-transfected DF-1 cells at 48 h. A representative of three independent experiments is shown. The lower right quadrant represents the early apoptotic cells (annexin v-positive), while the upper right quadrant shows the late apoptotic and necrotic cell populations (annexin v and PI-positive). B Dot plot showing the flow cytometric analysis of PS translocation after staining with annexin V and PI in mock, NC, and si290-transfected DF-1 cells at 36 h. C pCMV-HA-TXNL1 and control plasmids were transfected into DF-1 cells for 48 h before the cells were harvested. The RNA was extracted according to the previously described method. The mRNA level of some apoptosis-related genes (proapoptosis genes Caspase-3, Caspase-9, and FasLG and the antiapoptosis gene Bcl-2) were detected using Q-PCR. D DF-1 cells were transfected with pCMV-HA-TXNL1 and control plasmids for 48 h. Whole-cell extracts were prepared for Western blot analysis that was specific for the proteins indicated. E TXNL1 and control were transfected into DF-1 cells for 48 h before the cells were harvested. The mRNA levels of some interferon-related genes (IFN-α, IFN-β, IFN-γ, IRF1, IRF3) were detected using Q-PCR. F Si290 and NC were transfected into DF-1 cells for 36 h before the cells were harvested. The mRNA level of some apoptosis-related genes were detected using Q-PCR. G DF-1 cells were transfected with si290 and NC for 36 h. Whole-cell extracts were prepared for Western blot analysis that was specific for the indicated proteins. H si290 and NC were transfected into DF-1 cells for 36 h before the cells were harvested. The mRNA levels of some interferon-related genes were detected using Q-PCR. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13567-018-0599-6'>30290847</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12935_2020_1454_fig2_html.pngAnti-Bax Antibody Picoband®The influences of circPOSTN silencing on proliferation, apoptosis and aerobic glycolysis of glioma cells. a – l LN229 and U251 cells were transfected with si-circPOSTN or si-NC. a The interference efficiency of si-circPOSTN was analyzed with RT-qPCR assay in LN229 and U251 cells. b , c Effect of circPOSTN silencing on the cell viability of LN229 and U251 cells was assessed with MTT assay. d The apoptosis rate was computed with flow cytometry assay in transfected LN229 and U251 cells. e The western blot assay showed the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The caspase-3 activity was measured with a caspase-3 assay kit. g – i The concentration of glucose and lactate in the culture medium, as well as ATP production level were measured with a series of kits, respectively. j The protein expression levels of HK2 and LDHA were determined with western blot assay in transfected LN229 and U251 cells. k – l LDHA enzyme activity and ROS accumulation were evaluated in LN229 and U251 cells post-transfection with lactate dehydrogenase activity detection kit and reactive oxygen species assay kit, respectively. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-oncotarget-09-4475-g006.jpgAnti-Bax Antibody Picoband®Expression level of protein of Bcl-2, Bax and Caspase-3 in ovary tissue of different groups at 28 dpi and 49 dpi. ( A ) intensity of expression of Bcl-2 ( B ) Bax, ( C ) Caspase-3 in ovaries of HEV inoculation rabbits. ( D ) Western blot analysis of Bcl-2, Bax and Caspase-3 in ovaries in different groups.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5796988/&orig_host=www.ncbi.nlm.nih.gov'>29435117</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12935_2020_1454_fig4_html.pngAnti-Bax Antibody Picoband®Knockdown of circPOSTN mediated-effects on proliferation and apoptosis of glioma cells could be eliminated by silencing miR-361-5p. a – j LN229 and U251 cells were transfected with si-NC, si-circPOSTN, si-circPOSTN + anti-miR-NC, or si-circPOSTN + anti-miR-361-5p. a , b The relativity expression level of miR-361-5p was analyzed with RT-qPCR assay in LN229 and U251 cells. c , d MTT assay was administrated to assess cell viability of LN229 and U251 cells after transfection. e , f The apoptosis of transfected LN229 and U251 cells was monitored by flow cytometry. g , h The western blot assay was employed to show the expression levels of Bcl-2 and Bax in LN229 and U251 cells. i , j The caspase-3 activity was examined by caspase-3 assay kit. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-oncotarget-08-29785-g002.jpgAnti-Bax Antibody Picoband®TGF-β1 suppresses the HCC cells proliferative capacity but does not promote apoptosis. SMMC-7721 and BEL-7402 cells were treated with 0, 5ng/mL and 10ng/mL TGF-β1 for 48 hours. A . apoptosis B . western blotting examined the expression levels of Bcl-2 and Bax. Data are expressed as the mean ± SEM of three independent experiments, #P>0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5444703/&orig_host=www.ncbi.nlm.nih.gov'>28076850</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-12935_2020_1454_fig7_html.pngAnti-Bax Antibody Picoband®TPX2 regulated proliferation, apoptosis, and aerobic glycolysis in glioma cells. a – l LN229 and U251 cells were introduced with si-NC or si-TPX2. a The transfection efficiency of si-TPX2 was checked with RT-qPCR assay in LN229 and U251 cells. b , c The cell viability of LN229 and U251 cells was determined with MTT assay. d The apoptosis rate of transfected LN229 and U251 cells was represented by flow cytometry assay. e The western blot assay was used to assay the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The activity of caspase-3 was detected with a caspase-3 assay kit. g – i The glucose, lactate, and ATP production levels were shown. j The protein expression levels of HK2 and LDHA were estimated by western blot assay in LN229 and U251 cells. k , l LDHA enzyme activity and ROS content were evaluated in LN229 and U251 cells post-transfection. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-nrr-12-96-g006.jpgAnti-Bax Antibody Picoband®Nicotiflorin effect on Bcl-2, Bax, and caspase-3 expression in the ischemic cerebral cortex of I/R rats (western blot assay). (A, C, E) Western blot images of Bax, Bcl-2, and caspases-3 protein; (B, D, F) Western blot assay shows up-regulation of caspase-3 and Bax expreesssion and down-regulation of Bcl-2 expression in the I/R group (* P < 0.05, ** P < 0.01, vs . I/R group). Both Bax and caspase-3 expression were decreased and Bcl-2 expreesssion increased in the nicotiflorin group. Data are expressed as the mean ± SEM, n = 3, one-way analysis of variance followed by post hoc Tukey test. I/R: Ischemia/reperfusion.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5319249/&orig_host=www.ncbi.nlm.nih.gov'>28250754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-fphar-10-00285-g005.jpgAnti-Bax Antibody Picoband®The effect of the combination of alteronol and ADM on protein levels of apoptosis-related molecules in 4T1 cells. (A) The protein levels of Bax and Bcl-2 were measured by western blot. (B) Quantitative analysis of Bax and Bcl-2 protein levels in 4T1 cells after treatment with alteronol and/or ADM. (C) The protein levels of cleaved PARP, cleaved caspase-9, and cleaved caspase-3 were examined by western blot. (D) Quantitative analysis of cleaved PARP, cleaved caspase-9, and cleaved caspase-3 protein levels after the indicated treatments. ∗ P < 0.05, ∗∗ P < 0.01 vs. control group. # P < 0.05, ## P < 0.01 vs. alteronol group. & P < 0.05, && P < 0.01 vs. ADM group. All data are expressed as mean ± SD of three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00285/full'>31001113</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-41598_2024_69356_fig2_html.pngAnti-Bax Antibody Picoband®Suidical iBAT ablation significantly inhibited the cardioprotective effect of DEX. ( A ) Representative echocardiographic M-mode images were obtained 24 h after myocardial ischemia/reperfusion (MI/R), n = 6/group. ( B ) Left ventricular ejection fraction (LVEF) and fractional shortening (LVFS), n = 6/group. ( C ) Representative images of TTC staining 24 h after MI/R. Myocardial infarction area was calculated as a percentage of the myocardial area at risk, n = 6/group. ( D ) The levels of serum CK-MB, n = 6/group. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3 expression, n = 3/group. ( F ) Representative photographs of cardiomyocyte apoptosis examined by TUNEL assay. Bar graphs present the quantification analysis of cell apoptosis, n = 6/group. Scale bar = 200 μm. ( G ) Morphological changes in myocardium was determined by HE staining. Scale bar = 100 μm. ( H ) The levels of serum FGF21 in Mice, n = 6/group.* means P < 0.05 vs Control, † means P < 0.05 vs I/R group, ‡ means P < 0.05 vs. I/R + DEX group, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-wb-testing-1.jpgAnti-Bax Antibody Picoband® Western blot analysis of Bax using anti-Bax antibody (A00183). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bax antigen affinity purified polyclonal antibody (A00183) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Bax at approximately 21 kDa. The expected band size for Bax is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-ihc-testing-2.jpgAnti-Bax Antibody Picoband® IHC analysis of Bax using anti-Bax antibody (A00183). <br>
Bax was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bax Antibody (A00183) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-ihc-testing-3.jpgAnti-Bax Antibody Picoband® IHC analysis of Bax using anti-Bax antibody (A00183). <br>
Bax was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bax Antibody (A00183) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-ihc-testing-4.jpgAnti-Bax Antibody Picoband® IHC analysis of Bax using anti-Bax antibody (A00183). <br>
Bax was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bax Antibody (A00183) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-if-testing-5.jpgAnti-Bax Antibody Picoband® IF analysis of Bax using anti-Bax antibody (A00183). <br>
Bax was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Bax Antibody (A00183) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-if-testing-1.jpgAnti-Bax Antibody Picoband®IF analysis of BAX using anti-BAX antibody (A00183).<br>
BAX was detected in a paraffin-embedded section of FFPE mouse uterus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with rabbit anti-BAX Antibody (A00183) at 10 μg/ml overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00183-bax-primary-antibodies-fcm-testing-6.jpgAnti-Bax Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-Bax antibody (A00183). <br>
Overlay histogram showing THP-1 cells stained with A00183 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Bax Antibody (A00183, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-bcl-xl-picoband-trade-antibody-a00181-boster.html2026-03-24T05:07:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00181-bcl-xl-primary-antibodies-wb-testing-1.jpgAnti-Bcl-XL/BCL2L1 Antibody Picoband® Western blot analysis of Bcl-XL using anti-Bcl-XL antibody (A00181). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human Raji whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bcl-XL antigen affinity purified polyclonal antibody (Catalog # A00181) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bcl-XL at approximately 26-30 kDa. The expected band size for Bcl-XL is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00181-bcl-xl-primary-antibodies-ihc-testing-1.jpgAnti-Bcl-XL/BCL2L1 Antibody Picoband®IHC analysis of Bcl-XL using anti-Bcl-XL antibody (A00181). <br>
Bcl-XL was detected in a paraffin-embedded section of human pancrease cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bcl-XL Antibody (A00181) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00181-bcl-xl-primary-antibodies-if-testing-1.jpgAnti-Bcl-XL/BCL2L1 Antibody Picoband®IF analysis of Bcl-XL using anti-Bcl-XL antibody (A00181). <br>
Bcl-XL was detected in an immunocytochemical section of TPC-1 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Bcl-XL Antibody (A00181) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00181-bcl-xl-primary-antibodies-ip-testing-1.jpgAnti-Bcl-XL/BCL2L1 Antibody Picoband®Immunoprecipitating (IP) Bcl-XL in A549 whole cell lysate.<br>
Western blot analysis of Bcl-XL using anti-Bcl-XL antibody (A00181); <br>
Lane 1: A549 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-Bcl-XL antibody in A549 whole cell lysate;<br>
Lane 3: anti-Bcl-XL antibody (2μg) + A549 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Bcl-XL antigen affinity purified polyclonal antibody (A00181) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for Bcl-XL at approximately 26-30 kDa. The expected band size for Bcl-XL is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00181-bcl-xl-primary-antibodies-fcm-testing-2.jpgAnti-Bcl-XL/BCL2L1 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-Bcl-XL antibody (A00181). <br>
Overlay histogram showing Jurkat cells stained with A00181 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Bcl-XL Antibody (A00181, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-brca1-picoband-trade-antibody-a00005-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00005-brca1-primary-antibodies-wb-testing-1.jpgAnti-BRCA1 Antibody Picoband® Western blot analysis of BRCA1 using anti-BRCA1 antibody (A00005). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human T47D whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BRCA1 antigen affinity purified polyclonal antibody (Catalog # A00005) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BRCA1 at approximately 290 kDa. The expected band size for BRCA1 is at 208 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00005-brca1-primary-antibodies-if-testing-2.jpgAnti-BRCA1 Antibody Picoband® IF analysis of BRCA1 using anti-BRCA1 antibody (A00005) and anti-Beta Tubulin antibody (M01857-3).<br>
BRCA1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BRCA1 Antibody (A00005) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Donkey Anti-Rabbit IgG (BA1144) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-cd147-emmprin-picoband-trade-antibody-a00248-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-bsg-primary-antibodies-wb-testing-1.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® Western blot analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD147/Emmprin antigen affinity purified polyclonal antibody (Catalog # A00248-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD147/Emmprin at approximately 38-55 kDa. The expected band size for CD147/Emmprin is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00248-1-2-IHC-anti-cd147-emmprin-picoband-antibody.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IHC analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1).<br>
CD147/Emmprin was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00248-1-3-IHC-anti-cd147-emmprin-picoband-antibody.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IHC analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1).<br>
CD147/Emmprin was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00248-1-4-IHC-anti-cd147-emmprin-picoband-antibody.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IHC analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1).<br>
CD147/Emmprin was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-fc-testing-5.pngAnti-CD147/Emmprin/BSG Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-CD147/Emmprin antibody (A00248-1).<br>
Overlay histogram showing A549 cells stained with A00248-1 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD147/Emmprin Antibody (A00248-1,1μg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-fc-testing-6.pngAnti-CD147/Emmprin/BSG Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-CD147/Emmprin antibody (A00248-1).<br>
Overlay histogram showing Hela cells stained with A00248-1 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD147/Emmprin Antibody (A00248-1,1μg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-icc-testing-7.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IF analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1) <br> CD147/Emmprin was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-icc-testing-8.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IF analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1) <br> CD147/Emmprin was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-icc-testing-9.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IF analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1) <br> CD147/Emmprin was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-cd147-primary-antibodies-if-testing-10.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® IF analysis of CD147/Emmprin using anti-CD147/Emmprin antibody (A00248-1) <br> CD147/Emmprin was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-CD147/Emmprin Antibody (A00248-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00248-1-emmprin-primary-antibodies-elisa-testing-11.jpgAnti-CD147/Emmprin/BSG Antibody Picoband® Sandwich ELISA - Recombinant human Emmprin protein standard curve.<br>
Use in combination with reagents from Human Emmprin ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0751).
https://www.bosterbio.com/products/primary-antibodies/anti-ccs-picoband-trade-antibody-a00314-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00314-1-1-WB-anti-ccs-picoband-antibody.jpgAnti-Superoxide Dismutase 4/CCS Antibody Picoband® Western blot analysis of CCS using anti-CCS antibody (A00314-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysate,<br>
Lane 2: rat spleen tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse spleen tissue lysates,<br>
Lane 5: 293T whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCS antigen affinity purified polyclonal antibody (Catalog # A00314-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCS at approximately 34KD. The expected band size for CCS is at 29KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00314-1-2-IHC-anti-ccs-picoband-antibody.jpgAnti-Superoxide Dismutase 4/CCS Antibody Picoband® IHC analysis of CCS using anti-CCS antibody (A00314-1).<br>
CCS was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CCS Antibody (A00314-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd48-picoband-trade-antibody-a03281-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03281-1-cd48-primary-antibodies-wb-testing-1.jpgAnti-CD48 Antibody Picoband®Western blot analysis of CD48 using anti-CD48 antibody (A03281-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human Hacat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD48 antigen affinity purified polyclonal antibody (A03281-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD48 at approximately 43-50 kDa. The expected band size for CD48 is at 28 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-cdr2-picoband-trade-antibody-a02973-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02973-1-1-WB-anti-cdr2-picoband-antibody.jpgAnti-CDR2 Antibody Picoband® Western blot analysis of CDR2 using anti-CDR2 antibody (A02973-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: mouse kidney tissue lysate,<br>
lane 2: MCF-7 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDR2 antigen affinity purified polyclonal antibody (Catalog # A02973-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDR2 at approximately 52KD. The expected band size for CDR2 is at 52KD.
https://www.bosterbio.com/products/primary-antibodies/anti-chrm2-picoband-trade-antibody-a02733-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02733-1-WB-anti-chrm2-machr-m2-picoband-antibody.jpgAnti-Muscarinic Acetylcholine Receptor 2/CHRM2 Antibody Picoband® Western blot analysis of CHRM2 using anti-CHRM2 antibody (A02733). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysates,<br>
lane 2: mouse brain tissue lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHRM2 antigen affinity purified polyclonal antibody (Catalog # A02733) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHRM2 at approximately 52KD. The expected band size for CHRM2 is at 52KD.
https://www.bosterbio.com/products/primary-antibodies/anti-chrna5-picoband-trade-antibody-a02359-2-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-1-WB-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® Western blot analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> lane 1: rat skeletal muscle tissue lysates,<br> lane 2: HEPG2 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHRNA5 antigen affinity purified polyclonal antibody (Catalog # A02359-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHRNA5 at approximately 53KD. The expected band size for CHRNA5 is at 53KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-2-IHC-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® IHC analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> CHRNA5 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FBXL4 Antibody (A02359-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-3-IHC-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® IHC analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> CHRNA5 was detected in paraffin-embedded section of mouse cardiac muscle tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHRNA5 Antibody (A02359-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-4-IHC-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® IHC analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> CHRNA5 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHRNA5 Antibody (A02359-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-5-IHC-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® IHC analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> CHRNA5 was detected in paraffin-embedded section of rat cardiac muscle tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FBXL4 Antibody (A02359-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02359-2-6-IHC-anti-chrna5-picoband-antibody.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® IHC analysis of CHRNA5 using anti-CHRNA5 antibody (A02359-2). <br> CHRNA5 was detected in paraffin-embedded section of human prostatic cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHRNA5 Antibody (A02359-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02359-2-chrna5-primary-antibodies-fc-testing-7.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-CHRNA5 antibody (A02359-2). <br>Overlay histogram showing U251 cells stained with A02359-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHRNA5 Antibody (A02359-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02359-2-chrna5-primary-antibodies-fc-testing-8.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-CHRNA5 antibody (A02359-2). <br>Overlay histogram showing A549 cells stained with A02359-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHRNA5 Antibody (A02359-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02359-2-chrna5-primary-antibodies-fc-testing-9.jpgAnti-Nicotinic Acetylcholine Receptor alpha 5/CHRNA5 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-CHRNA5 antibody (A02359-2). <br>Overlay histogram showing MCF-7 cells stained with A02359-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHRNA5 Antibody (A02359-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ckap4-picoband-trade-antibody-a02154-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02154-1-1-WB-anti-ckap4-p63-picoband-antibody.jpgAnti-CKAP4 Antibody Picoband® Western blot analysis of CKAP4 using anti-CKAP4 antibody (A02154-1).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: mouse brain tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CKAP4 antigen affinity purified polyclonal antibody (Catalog # A02154-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CKAP4 at approximately 66KD. The expected band size for CKAP4 is at 66KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cytoglobin-picoband-trade-antibody-a01197-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01197-2_1-IHC-anti-cytoglobin-picoband-antibody.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> IHC analysis of Cytoglobin using anti-Cytoglobin antibody (A01197).</b><br>
Cytoglobin was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytoglobin Antibody (A01197) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01197-3_1-IHC-anti-cytoglobin-picoband-antibody.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> IHC analysis of Cytoglobin using anti-Cytoglobin antibody (A01197).</b><br>
Cytoglobin was detected in paraffin-embedded section of mouse cardiac muscle tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytoglobin Antibody (A01197) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01197-4_1-IHC-anti-cytoglobin-picoband-antibody.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> IHC analysis of Cytoglobin using anti-Cytoglobin antibody (A01197).</b><br>
Cytoglobin was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytoglobin Antibody (A01197) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01197-5_1-IHC-anti-cytoglobin-picoband-antibody.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> IHC analysis of Cytoglobin using anti-Cytoglobin antibody (A01197).</b><br>
Cytoglobin was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytoglobin Antibody (A01197) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01197-6-IHC-anti-cytoglobin-picoband-antibody.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> IHC analysis of Cytoglobin using anti-Cytoglobin antibody (A01197).</b><br>
Cytoglobin was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytoglobin Antibody (A01197) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01197-1.jpgAnti-Cytoglobin/CYGB Antibody Picoband®<b> Western blot analysis of Cytoglobin using anti-Cytoglobin antibody (A01197). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat small intestine tissue lysates,<br> Lane 2: mouse small intestine tissue lysates, <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytoglobin antigen affinity purified polyclonal antibody (Catalog # A01197) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytoglobin at approximately 21KD. The expected band size for Cytoglobin is at 21KD.
https://www.bosterbio.com/products/primary-antibodies/anti-alpha-defensin-1-picoband-trade-antibody-a10546-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10546-1-WB-anti-alpha-defensin-1-picoband-antibody.jpgAnti-Alpha Defensin 1/DEFA1 Antibody Picoband® Western blot analysis of Alpha Defensin 1 using anti-Alpha Defensin 1 antibody (A10546). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat testis tissue lysate,<br>
lane 2: HELA whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha Defensin 1 antigen affinity purified polyclonal antibody (Catalog # A10546) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha Defensin 1 at approximately 19KD. The expected band size for Alpha Defensin 1 is at 10KD.
https://www.bosterbio.com/products/primary-antibodies/anti-gad65-picoband-trade-antibody-a03142-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03142-gad65-primary-antibodies-wb-testing-1.jpgAnti-GAD65/GAD2 Antibody Picoband® Western blot analysis of GAD65 using anti-GAD65 antibody (A03142). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAD65 antigen affinity purified polyclonal antibody (Catalog # A03142) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAD65 at approximately 65 kDa. The expected band size for GAD65 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03142-2-IHC-anti-gad65-picoband-antibody.jpgAnti-GAD65/GAD2 Antibody Picoband® IHC analysis of GAD65 using anti-GAD65 antibody (A03142).<br>
GAD65 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAD65 Antibody (A03142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03142-3-IHC-anti-gad65-picoband-antibody.jpgAnti-GAD65/GAD2 Antibody Picoband® IHC analysis of GAD65 using anti-GAD65 antibody (A03142).<br>
GAD65 was detected in paraffin-embedded section of human intetsinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAD65 Antibody (A03142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03142-4-IHC-anti-gad65-picoband-antibody.jpgAnti-GAD65/GAD2 Antibody Picoband® IHC analysis of GAD65 using anti-GAD65 antibody (A03142).<br>
GAD65 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAD65 Antibody (A03142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/loading-control-antibodies/anti-gapdh-picoband-trade-antibody-a00227-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-13287_2018_955_fig4_html.pngAnti-GAPDH Antibody Picoband®Continuous effects of EMF on BMSC chondrogenic differentiation capacity. a SOX9, CoL2, and Aggrecan mRNA levels of two groups determined by RT-PCR. GAPDH used as internal control for quantification ( n = 3). b Expression of Col2 and Sox9 proteins of both groups detected by western blot analysis. Relative densitometer values quantified by ImageJ software, GAPDH served as loading control ( n = 3). c Presentation of Alcian Blue staining of both groups. Scale bar = 100 μm. d Semi-quantitative analysis of Alcian Blue staining among both groups ( n = 6). Data shown as mean ± SD. * P < 0.05, ** P < 0.01. EMF electromagnetic field <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-018-0955-5'>30092831</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-40752108-figure-6.jpgAnti-GAPDH Antibody Picoband®(L and M) (L) The apoptosis of LX-2 cells determined using flow cytometry and (M) percentages of apoptotic cells (early and late apoptotic cells). NC, LV-control-shRNA; KD, LV-4EBP1-shRNA. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-40752108-figure-5.jpgAnti-GAPDH Antibody Picoband®(M and N) (M) The apoptosis of vehicle or TGF-β1-stimulated LX-2 cells transducted with LV-empty or LV-4EBP1-4A-3xflag determined using flow cytometry and (N) percentages of apoptotic cells (early and late apoptotic cells). EV, LV-empty; OE, LV-4EBP1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-40752108-figure-3.jpgAnti-GAPDH Antibody Picoband®(H) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; BDL, bile duct ligation; DAPI, 4′,6-diamidino-2-phenylindole; DBIL, direct bilirubin; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin-eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, Interleukin 6; TBIL, total bilirubin; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gsta1-5-primary-antibodies-wb-testing-1.jpgAnti-GAPDH Antibody Picoband® Western blot analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: human CCRF-CEM whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody (Catalog # A00227-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-40752108-figure-2.jpgAnti-GAPDH Antibody Picoband®(J) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin and eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, interleukin 6; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-ihc-testing-2.jpgAnti-GAPDH Antibody Picoband® IHC analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
GAPDH was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAPDH Antibody (A00227-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-40752108-figure-1.jpgAnti-GAPDH Antibody Picoband®(E and F) Immunofluorescence double staining of α-SMA and p-4EBP1 in TGF-β1-stimulated LX-2 cells for 0, 6, 12, 24, and 48 h (×400 magnification). Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001. α-SMA, alpha-smooth muscle actin; BDL, bile duct ligation; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin and eosin; TGF-β1, transforming growth factor β1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-ihc-testing-3.jpgAnti-GAPDH Antibody Picoband® IHC analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
GAPDH was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAPDH Antibody (A00227-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-rsob.230427.f008.pngAnti-GAPDH Antibody Picoband®Effects of EGCG on the MYH7 R453C mutation H9C2 cells. (a) Effects of EGCG on the MYH7 R453C mutation H9C2 cell survival rate. (b) Protective effects of EGCG in MYH7 R453C mutation on ROS production. (c) Effect of EGCG on Bax and Bcl-2 activities of the MYH7 R453C mutation H9C2 cells. (d) Bcl-2 expression were quantified by densitometry and normalized to GAPDH levels. (e) Bax expression was quantified by densitometry and normalized to GAPDH levels. (f) Quantitative analysis of the ratio of Bcl-2 to Bax in protein expression was evaluated. Data are expressed as the mean ± s.d. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. n = 3 biologically independent samples. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://royalsocietypublishing.org/doi/abs/10.1098/rsob.230427'>38862020</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-ihc-testing-4.jpgAnti-GAPDH Antibody Picoband® IHC analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
GAPDH was detected in a paraffin-embedded section of human ovarian serous cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAPDH Antibody (A00227-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1_12672_2025_3032_fig3_html.jpgAnti-GAPDH Antibody Picoband®(a) The representative cell apoptosis photos using flow cytometry, (i) The blank control group; (ii) The miR-NC transfection group; (iii) The miR-145 mimics transfection group. (b) The apoptosis rate of the miR-145 mimics transfection group increased significantly, ** p < 0.01. (c) The representative protein expression (Caspase-9: 46 kD, Caspase-3: 32 kD, GAPDH: 36 kD) photos using western blot. (d) The expression of Caspase-9 and Caspase-3 in three groups, ** p < 0.01<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12214196/'>40591050</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-41598_2018_23568_fig3_html.jpgAnti-GAPDH Antibody Picoband®Alcohol interferes with Hcy metabolism leading to hyperhomocysteinemia (HHcy). ( a,b ) Scatter dot plots represent data for the CBS enzyme activity and total homocysteine (tHcy) levels in the different mice groups. ( c–f ) Representative western blot analysis for the vital enzymes (CBS, CSE, MTHFR, SAHH and Hcy) involved in homocysteine metabolism in different mice groups. Bar graphs showing quantitative estimation of key proteins after normalization with GAPDH. ( g,h ) q-PCR analysis showing the data for real‐time transcript levels of CBS, CSE, MTHFR and SAHH mRNAs in the different groups of mice. All the data are represented as mean values ± standard error (SE) in 5 independent experiments. * ,# p < 0.05 considered significant. *p < 0.05 vs. CT and # p < 0.05 vs. AL group.Uncropped blots for c and e are presented in Supplementary Figs and . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-23568-z'>29581524</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-09-01286-g005.jpgAnti-GAPDH Antibody Picoband®Taxifolin suppresses expression of osteoclast specific genes and proteins. RAW264.7 cells were treated with RANKL and with or without different concentrations of taxifolin for 3 days, (A) expression of Trap, Mmp-9, Cathepsin K, C-Fos, Nfatc1 , and Rank was determined by qRT-PCR and calculated in relation to the internal control GAPDH mRNA by the comparative Ct method; (B) immunoblots with MMP-9, TRAP, Cathepsin K, RANK, NFATc1 and C-Fos antibodies demonstrating that taxifolin repressed osteoclast-specific protein expression. GAPDH antibody was used as loading controls. (C) RAW264.7 cells were cultured with taxifolin for 36 h, then stimulated with RANKL (50 ng/ml) for 30 min, and RAW264.7 cells without RANKL or taxifolin was considered as “100% control,” our results showed taxifolin decreased the release of intracellular ROS. Data are presented as mean ± SD. n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.01286/full'>30483128</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-09-01016-g005.jpgAnti-GAPDH Antibody Picoband®Ulinastatin reduces the expression of uPAR, NFATc1 and osteoclast marker genes induced by RANKL. C represents control group, R represents RANKL group, R + ulinastatin represents RANKL + 800 units/mL ulinastatin group. (A) Ulinastatin reduces RANKL-induced mRNA expression of cathepsin K, Trap, Rank, NFATc1, and uPAR. BMMs were cultured with M-CSF (30 ng/mL) and RANKL (100 ng/mL), and treated with or without ulinastatin (800 units/mL) for 4 days. mRNA expression was detected by qRT-PCR. The qRT-PCR experiments have been repeated with different RNA preparations for 3 times independently. Data are represented as mean ± SD . ∗ P < 0.05 and ∗∗ P < 0.01. (B,C,D) Ulinastatin reduces RANKL-induced protein expression of uPAR, cathepsin K and Trap. BMMs were cultured with M-CSF (30 ng/mL) and RANKL (100 ng/mL), and treated with or without ulinastatin (800 units/mL) for 2 or 4 days. Protein expression levels of uPAR, cathepsin K and Trap were examined by western blotting at the indicated times. The amount of loaded protein was 25 μg. The experiment was performed three times independently and GAPDH was used as a loading control. ∗ P < 0.05, ∗∗ P < 0.01 versus RANKL group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.01016/full'>30245631</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00041-g002.jpgAnti-GAPDH Antibody Picoband®Effects of Schisandrin A on IL-1β-induced production of NO, PGE2, iNOS, and COX2 in rat chondrocytes. Cells were treated with Schisandrin A (25, 50 μM) in the presence or absence of IL-1β (10 ng/ml) for 24 h. Cell culture supernatants were collected. (A) Griess reaction was used to measure the NO concentration ( n = 3). (B) PGE2 level was accessed by ELISA ( n = 3). (C) Expression of iNOS and COX2 were detected by Western blot. (D) Relative protein expression was qualified by ImageJ software, GAPDH was served as the loading control ( n = 3). # P < 0.05 vs. control group; ∗ P < 0.05 vs. IL-1β group; ∗∗ P < 0.01 vs. IL-1β group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00041/full'>30761007</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00041-g004.jpgAnti-GAPDH Antibody Picoband®Effects of Schisandrin A on IL-1β-induced cartilage degradation. (A) Cells were treated with Schisandrin A (25, 50 μM) in the presence or absence of IL-1β (10 ng/ml) for 24 h. Protein levels of Collagen II, Aggrecan and Sox9 were determined by Western Blot. (B) Relative protein expression was qualified by Image-J software, GAPDH was used as the loading control ( n = 3). (C) Aggrecan and (D) Collagen II were observed by Immunofluorescence after cells were treated with IL-1β (10 ng/ml) with or without Schisandrin A (50 μM) for 24 h. # P < 0.05 vs. control group; ∗ P < 0.05 vs. IL-1β group; ∗∗ P < 0.01 vs. IL-1β group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00041/full'>30761007</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-nrr-16-916-g005.jpgAnti-GAPDH Antibody Picoband®Effects of acupuncture treatment on cytosine methylation in the promoter region of the GSK-3β gene and GSK-3β mRNA levels in the dorsal raphe nucleus in the rat model of D-galactose-induced aging. (A) The methylation level in the promoter region of GSK-3β was detected using bisulfite sequencing-polymerase chain reaction. (B) Quantitation of GSK-3β mRNA levels, detected using real-time polymerase chain reaction. (C) Quantitation of methylation levels in CpG islands of the GSK-3β gene promoter. The data are expressed as the mean ± SD ( n = 3). ** P < 0.01, vs . control group; ▲ P < 0.05, ▲▲ P < 0.01, vs . model group; ## P < 0.01, vs . PEA group (one-way analysis of variance followed by the least significant difference test). Control: Normal; Model: D-galactose-induced aging; PEA + inhibitor: D-galactose-induced aging + preventive electroacupuncture + 5-aza-2′-deoxycytidine; Inhibitor: D-galactose-induced aging + 5-aza-2′-deoxycytidine; PMA: D-galactose-induced aging + preventive manual acupuncture; PEA: D-galactose-induced aging + preventive electroacupuncture. GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GSK-3β: glycogen synthase kinase-3β.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8178792/&orig_host=www.ncbi.nlm.nih.gov'>33229729</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00618-g004.jpgAnti-GAPDH Antibody Picoband®Effects of a SIRT1-specific inhibitor (EX 527) on the enhanced expression of an osteoblast-specific gene of bone marrow mesenchymal stem cells by Bergenin. (A and B) The expression of RUNX2 and SIRT1 in blank, control + EX 527, Bergenin (10 μM), and Bergenin (10 μM) + EX 527 groups was determined by Western blot analysis. EX 527 (10 μM) was applied for 1 h, followed by culture in osteogenic induction medium with Bergenin for 3 days. Protein expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase. Data are expressed as the mean ± standard deviation (SD) of three independent experiments, and one of three independent experiments is shown. Data are expressed as the mean ± SD. * P < 0.05 vs. group with osteogenic induction medium alone. (C) Alizarin red staining and quantification of mineralization at day 12 of osteogenic differentiation. (D) The mRNA expression of RUNX2, ALP, and COL1A1 in blank, control + EX 527, Bergenin (10 μM), and Bergenin (10 μM) + EX 527 groups was determined by quantitative reverse transcription polymerase chain reaction. EX 527 (10 μM) was applied for 1 h, followed by culture in osteogenic induction medium with Bergenin for 3 days. mRNA expression levels were normalized to GAPDH. * P < 0.05 vs. BMSCs treated with osteogenic induction medium alone.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00618/full'>31258473</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-nrr-16-916-g003.jpgAnti-GAPDH Antibody Picoband®Effects of acupuncture treatment on the expression of phosphorylated tau in the dorsal raphe nucleus in the rat model of D-galactose-induced aging. (A) The protein expression levels of tau-5, PHF-1 and tau-pS262 in the dorsal raphe nucleus were detected using western blot assay. GAPDH was used as a loading control. (B–D) Quantitative results for tau-5 (B), PHF-1 (C) and tau-pS262 (D) expression (optical density ratio to GAPDH). The data are expressed as the mean ± SD ( n = 6). ** P < 0.01, vs . control group; ▲▲ P < 0.01, vs . model group; # P < 0.05, ## P < 0.01, vs . PEA group (one-way analysis of variance followed by the least significant difference test). Control: Normal; Model: D-galactose-induced aging; PEA + inhibitor: D-galactose-induced aging + preventive electroacupuncture + 5-aza-2′-deoxycytidine (an inhibitor of DNA methyltransferase); Inhibitor: D-galactose-induced aging + 5-aza-2′-deoxycytidine; PMA: D-galactose-induced aging + preventive manual acupuncture; PEA: D-galactose-induced aging + preventive electroacupuncture. GAPDH: glyceraldehyde-3-phosphate dehydrogenase; PHF-1: paired helical filament 1.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8178792/&orig_host=www.ncbi.nlm.nih.gov'>33229729</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-nrr-16-916-g004.jpgAnti-GAPDH Antibody Picoband®Effects of acupuncture treatment on the expression of GSK-3β in the dorsal raphe nucleus in the rat model of D-galactose-induced aging. (A) The protein levels of total GSK-3β, GSK-3β-pTyr216 and GSK-3β-pSer9 in the dorsal raphe nucleus were detected by western blot assay. GAPDH was used as a loading control. (B–D) Quantitative results for GSK-3β (B), GSK-3β-pTyr216 (C) and GSK-3β-pSer9 (D) levels. The data are expressed as the mean ± SD ( n = 6). ** P < 0.01, vs . control group; ▲▲ P < 0.01, vs . model group; # P < 0.05, ## P < 0.01, vs . PEA group (one-way analysis of variance followed by the least significant difference test). Control: Normal; Model: D-galactose-induced aging; PEA + inhibitor: D-galactose-induced aging + preventive electroacupuncture + 5-aza-2′-deoxycytidine (an inhibitor of DNA methyltransferase); Inhibitor: D-galactose-induced aging + 5-aza-2′-deoxycytidine; PMA: D-galactose-induced aging + preventive manual acupuncture; PEA: D-galactose-induced aging + preventive electroacupuncture. GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GSK-3β: glycogen synthase kinase-3β.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8178792/&orig_host=www.ncbi.nlm.nih.gov'>33229729</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fgene-16-1529797-g001.jpgAnti-GAPDH Antibody Picoband®H19 and PPARγ are upregulated in the femoral head and BMSCs of patients with SONFH. (A, B) X-ray photo and pathological structure of the femoral head from an ARCO stage V SONFH patient. The images show alterations in the morphology of the femoral head, characterized by collapse and flattening, as well as radiographic signs indicative of hip osteoarthritis. (C) Morphology of BMSCs from a patient with SONFH. (D, E) Expression levels of H19 and PPARγ in the femoral head and BMSCs from a patient with SONFH. All experimental procedures were performed in triplicate with internal normalization to GAPDH expression levels. The relative expression levels of each gene were analyzed using the 2 −△△Ct method (n = 8, all data are shown as the mean ± SD of three independent experiments, *p < 0.05, **p < 0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1529797/full'>40259926</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-jgo-16-02-679-f8.jpgAnti-GAPDH Antibody Picoband®The inhibitory effect of CPT2 on CCA cells may be related to inhibition of the TNFα/NF-κB signaling pathway. (A-C) Expression of related proteins of the TNFα/NF-κB signaling pathway in CCA cells with CPT2 (A,B) overexpression, or (C) knockdown. (D) The specific process of CPT2 regulating the TNFα/NF-κB signaling pathway (created with BioRender.com). The differences were analyzed with two-tailed Student t -tests. The data are presented as the mean ± SD. *, P<0.05; **, P<0.01; ***, P<0.001. Experiments were repeated three times. CCA, cholangiocarcinoma; CPT2, carnitine palmitoyltransferase II; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12078819/'>40386589</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-jgo-16-02-679-f7.jpgAnti-GAPDH Antibody Picoband®CPT2 knockdown could promote the proliferation, migration, and invasion of CCA cells. (A,B) CPT2 knockdown efficiency of HCCC9810 was evaluated by (A) qRT-PCR and (B) Western blotting. (C) Cell viabilities of the CPT2 knockdown group and Scramble group were analyzed by CCK-8. The (D) cell cycle and (E) apoptosis of HCCC9810 cells with CPT2 knockdown were analyzed by flow cytometry. (F,G) The expressions of (F) CDK4, CDK6, (G) Bcl2, Bax, caspase 3, and cleaved-caspase 3 in HCCC9810 cells with CPT2 knockdown were analyzed by Western blotting. (H) The migration and invasion of HCCC9810 cells with CPT2 knockdown were analyzed by transwell assay and visualized by crystal violet staining. Scale bars: 100 μm. (I) The expressions of EMT-related proteins in HCCC9810 cells with CPT2 knockdown were analyzed by Western blotting. The differences were analyzed with two-tailed Student t -tests. The data are presented as the mean ± SD. *, P<0.05; **, P<0.01; ***, P<0.001; ****, P<0.0001. Experiments were repeated three times. G1, G1 phase of the cell cycle; G2, G2 phase of the cell cycle; S, S phase of the cell cycle; CCA, cholangiocarcinoma; CPT2, carnitine palmitoyltransferase II; CCK8, Cell Counting Kit-8; EMT, epithelial-mesenchymal transition; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; qRT-PCR, quantitative real-time polymerase chain reaction; SD, standard deviation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12078819/'>40386589</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-41598_2018_23568_fig5_html.jpgAnti-GAPDH Antibody Picoband®Effect of exercise on alcohol induced DNA methyltransferase (DNMT) activity and transcriptional regulation through ATF6-Herp signaling. ( a–c ) Representative western blot analysis showing the levels of DNMT1 and DNMT3a in brain tissue extract from the different mice groups. Bar graphs showing the quantitative estimation of DNMT1 and DNMT3a proteins after normalization with GAPDH. Scatter dot plot representing the DNMT activity in brain tissue of different mice groups. ( d–f ) ChIP assay to examine the ER activated ATF6 binding to the endogenous Herp promoter in vivo . After cross linking and immunoprecipitation with ATF6 antibody from isolated brain tissue extract, PCR was performed to identify the presence of Herp promoter DNA using primers flanking the CpG islands in the Herp promoter sites. Scatter dot plot representing the percent of input DNA in different experimental mice groups. ( g,h ) Representative western blot analysis showing the levels of Herp protein expression in brain tissue extract from the different mice groups. Scatter dot plot showing the quantitative estimation of Herp proteins after normalization with GAPDH. All the data are represented as mean values ± standard error (SE) in 5 independent experiments. * ,# p < 0.05 considered significant. *p < 0.05 vs. CT and # p < 0.05 vs. AL group. Uncropped blots for a,e,g are presented in Supplementary Figs and . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-23568-z'>29581524</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-nrr-16-916-g006.jpgAnti-GAPDH Antibody Picoband®Effects of acupuncture treatment on the expression of DNMT1 in the dorsal raphe nucleus in the rat model of D-galactose-induced aging. The expression level of DNMT1 in the dorsal raphe nucleus (DRN) in the model group and inhibitor group were significantly decreased. PEA, PMA and PEA + inhibitor treatments all increased the expression levels of DNMT1, and PEA treatment was more effective than PMA or PEA + inhibitor treatment. (A) The immuoreactivity of DNMT1 in the DRN was detected using immunofluorescence staining. Arrows indicate DNMT1-positive cells. (B) The protein levels of DNMT1 in the DRN detected by western blot assay. GAPDH was used as a loading control. (C) Quantitation of DNMT1-positive cells. (D) Quantitation of protein expression of DNMT1. The data are expressed as the mean ± SD ( n = 3 for immunofluorescence staining, n = 6 for western blot assay). * P < 0.05, ** P < 0.01, vs . control group; ▲ P < 0.05, ▲▲ P < 0.01, vs . model group; # P < 0.05, ## P < 0.01, vs . PEA group (one-way analysis of variance followed by the least significant difference test). Control: Normal; Model: D-galactose-induced aging; PEA + inhibitor: D-galactose-induced aging + preventive electroacupuncture + 5-aza-2′-deoxycytidine; Inhibitor: D-galactose-induced aging + 5-aza-2′-deoxycytidine; PMA: D-galactose-induced aging + preventive manual acupuncture; PEA: D-galactose-induced aging + preventive electroacupuncture. GSK-3β: Glycogen synthase kinase-3β; DNMT1: DNA methyltransferase 1; GAPDH: glyceraldehyde-3-phosphate dehydrogenase.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8178792/&orig_host=www.ncbi.nlm.nih.gov'>33229729</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-41598_2018_23568_fig7_html.jpgAnti-GAPDH Antibody Picoband®Effect of exercise on alcohol induced neuronal damage. ( a,b ) Representative western blot analysis showing the levels of neuronal proteins (NeuN and NSC) in different mice groups ( a ). Histogram showing the quantitative estimation of nNOS and NSE proteins after normalization with GAPDH (b). ( c,d ) Representative images showing coronal slices of mice brains stained with cresyl violet (40× magnification) ( c ). Scatter dot plot showing the number of cresyl violet positive cells in different groups of mice ( d ). ( e,f ) Representative images showing Fluoro-Jade C (FJC) staining in brain sections of the different groups of mice (10× magnification). A marked decrease of FJC-stained degenerating neurons (arrows) were observed in CT, EX and AL+EX groups, indicating a lesser degree of neuronal cell death. Brain sections of AL treated mice showing a greater number of FJC-positive neurons (arrows), reflecting increased neuronal cell death ( e ). Scatter dot plot showing the numbers of degenerating neurons in different experimental mice groups ( f ). All the data are represented as mean values ± standard error (SE) in 5 independent experiments. * ,# p < 0.05 considered significant. *p < 0.05 vs. CT and # p < 0.05 vs. AL group. Uncropped blots for a are presented in Supplementary Fig. . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-23568-z'>29581524</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-bmj-37-208-g2.jpgAnti-GAPDH Antibody Picoband®Expression of sirtuin 1 (SIRT1), P53, and KAI1 in PC-14/B and BEAS-2B cells. (A) The mRNA level of SIRT1, P53, and KAI1 in PC-14/B and BEAS-2B cells by quantitative polymerase chain reaction. (B) The protein levels of SIRT1, P53, and KAI1 in the two cells by Western blotting. Upper: representative blots. Lower: the fold change of the optical density of the target bands. Data are expressed as the mean ± standard deviation of at least three independent experiments. **P<0.01 vs controls GAPDH: glyceraldehyde 3-phosphate dehydrogenase<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7285661/&orig_host=www.ncbi.nlm.nih.gov'>32267139</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-dddt-13-623fig5.jpgAnti-GAPDH Antibody Picoband®D206008 activates β-catenin signaling pathway via the phosphorylation of GSK-3β and Akt. Notes: ( A ) Cells were treated with different concentrations (0–100 µM) of D206008 for 48 hours, and the levels of p-Akt, p-GSK-3β, p-β-catenin, and β-catenin proteins were analyzed relative to β-actin expression. ( B ) B16 cells treated with either vehicle (0.1% DMSO) or D206008 (100 µM) for 48 hours were analyzed for the levels of nuclear and cytoplasmic β-catenin. Cytoplasmic protein levels were normalized against GAPDH and nuclear protein against nup98. The band densities of proteins were measured by the Quantity One program. The data are shown as mean ± SD and analyzed by one-way ANOVA followed by Tukey’s test. ** P <0.01, compared to control group. All experiments were performed three times. Abbreviations: D206008, 5-(morpholinomethyl)-3-phenyl-7 H -furo[3,2- g ]chromen-7-one; GSK-3β, glycogen synthase kinase-3β.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6387609/&orig_host=www.ncbi.nlm.nih.gov'>30858693</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-bmj-37-208-g6.jpgAnti-GAPDH Antibody Picoband®Expression of the pathway-related proteins. The fold change of (A) sirtuin 1 (SIRT1), (B) P53, (C) KAI1, (D) MMP-9, (E) E-cadherin, and (F) β-catenin protein in transfected cells. *P<0.05. **P<0.01 vs controls, GAPDH: glyceraldehyde 3-phosphate dehydrogenase Lv: lentivirus<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7285661/&orig_host=www.ncbi.nlm.nih.gov'>32267139</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-jgo-16-02-679-f4.jpgAnti-GAPDH Antibody Picoband®Overexpression of CPT2 inhibited the proliferation of CCA. (A) mRNA and protein levels of CPT2 in CCA cell lines and HIBEpiC were analyzed by qRT-PCR and Western blotting. (B) The fluorescence expression of RBE cells was detected using a fluorescence microscope. Scale bars: 100 μm. (C,D) The overexpression efficiency of RBE and HCCC9810 cells was evaluated by qRT-PCR and Western blotting. (E) Cell viabilities of RBE and HCCC9810 cells with CPT2 overexpression were analyzed by CCK-8. The differences were analyzed with two-tailed Student t- tests. The data are presented as the mean ± SD. *, P<0.05; **, P<0.01; ***, P<0.001; ****, P<0.0001. Experiments were repeated three times. CCA, cholangiocarcinoma; CCK8, Cell Counting Kit-8; CPT2, carnitine palmitoyltransferase II; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIBEpiC, human normal bile duct epithelial cell; mRNA, messenger RNA; qRT-PCR, quantitative real-time polymerase chain reaction; SD, standard deviation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12078819/'>40386589</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-01459-g006.jpgAnti-GAPDH Antibody Picoband®Effects of magnolol on mice alcohol-induced liver damage in the AKT/PI3K signaling pathway. Liver tissues were extracted for protein analysis by western blotting. AKT and PI3K, proteins expression were detected. The levels of AKT and PI3K were compared with GAPDH. The data were demonstrated as means ± SD. (*P < 0.05, **P < 0.01, ***P < 0.001).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01459/full'>31920652</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00041-g006.jpgAnti-GAPDH Antibody Picoband®Effects of Schisandrin A on NF-κB signaling pathway. Cells were exposed to Schisandrin A (25, 50 μM) with or without IL-1β (10 ng/ml) for 30 min. (A) Protein levels of p-IκBα, IκBα, p-p65, p65 were detected by Western blot. (B) Relative protein expression was qualified by ImageJ software, GAPDH and p65 were used as the loading control, respectively ( n = 3). (C) p65 translocation was observed by Immunofluorescence. (D) Quantitative analysis of p65 nuclear location/total ratio of three groups. # P < 0.05 vs. control group; ∗ P < 0.05 vs. IL-1β group; ∗∗ P < 0.01 vs. IL-1β group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00041/full'>30761007</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-01459-g007.jpgAnti-GAPDH Antibody Picoband®Effects of magnolol on mice alcohol-induced liver damage in the Nrf2/HO-1 signaling pathway. After the completion of modeling and samples were collected, the liver of mice was lysed to detect the proteins by western blotting analysis. The levels of Nrf2 and HO-1 were compared with GAPDH. The data were demonstrated as means ± SD. (*P < 0.05, ***P < 0.001 and "ns" means not significant).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01459/full'>31920652</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-09-01286-g006.jpgAnti-GAPDH Antibody Picoband®Taxifolin represses multiple pathways of osteoclastogenesis in RAW264.7 cells. (A) RAW264.7 cells were pre-treated with 100 μM taxifolin for 2 h, then stimulated with RANKL (50 ng/ml) for the indicated time, protein was extracted for immunoblotting, the same GAPDH was used as loading control. (B) RAW264.7 cells were pre-treated with taxifolin in indicating concentrations for 2 h, then stimulated with RANKL (50 ng/ml) for 15 min, protein was extracted for immunoblotting, the same GAPDH was used as loading control. (C) Electrophoretic mobility shift assay for DNA binding activity of NF-κB and AP-1. After treatment with 100 μM taxifolin for 2 h, RAW264.7 cells were stimulated with RANKL (50 ng/ml) for 30 min, then nuclear extracts were prepared and analyzed for DNA binding activity. Data are of three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.01286/full'>30483128</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-01459-g008.jpgAnti-GAPDH Antibody Picoband®Effects of magnolol on mice alcohol-induced liver damage in PPARγ expression. The collected samples were analyzed for the expression of PPARγ using western blotting analysis. The expression of PPARγ was compared with GAPDH. The data were demonstrated as means ± SD. (*P < 0.05, **P < 0.01, ***P < 0.001 and "ns" means not significant).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01459/full'>31920652</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-13287_2018_955_fig3_html.pngAnti-GAPDH Antibody Picoband®BMSCs pretreated with EMF exhibited stronger osteogenic differentiation potential. a RUNX2, ALP, OPN, and OCN mRNA levels of two groups analyzed by RT-PCR. GAPDH used as loading control for quantification ( n = 3). b Expression of OPN and RUNX2 proteins of both groups determined by western blot analysis. Relative densitometer values quantified by ImageJ software, GAPDH used as internal control ( n = 3). c Images of Alizarin Red S staining exhibited plaques of calcified extracellular matrix of both groups. Scale bar = 100 μm. d Semi-quantitative analysis of Alizarin Red S staining among both groups ( n = 6). Data shown as mean ± SD. * P < 0.05, ** P < 0.01. EMF electromagnetic field <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-018-0955-5'>30092831</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-01459-g010.jpgAnti-GAPDH Antibody Picoband®Effects of magnolol on NLRP3 inflammasome, caspase-1 and caspase-3 signaling pathway in ALD mice. Magnolol was given to mice for three times, and then alcohol was gavaged. The level of NLRP3 inflammasome, caspase-1 and caspase-3 was detected by western blotting analysis with the compared with the internal control (GAPDH). The data is presented as mean ± SD. (*P < 0.05, **P < 0.01, ***P < 0.001).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01459/full'>31920652</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-13287_2018_955_fig5_html.pngAnti-GAPDH Antibody Picoband®EMF treatment had lasting impact on BMSC adipogenic differentiation potential. a PPARγ2, AP2, and ADIPOQ mRNA levels of two groups detected by RT-PCR. GAPDH served as loading control for quantification ( n = 3). b Expression of ADIPOQ and PPARγ2 proteins of both groups determined by western blot analysis. Relative densitometer values quantified by ImageJ software, GAPDH used as internal control ( n = 3). c Images of Oil Red O staining showed lipid droplets of both groups. Scale bar = 25 μm. d Semiquantitative analysis of Oil Red O staining among both groups ( n = 6). Data shown as mean ± SD. * P < 0.05, ** P < 0.01. EMF electromagnetic field <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-018-0955-5'>30092831</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-12885_2019_6379_fig1_html.pngAnti-GAPDH Antibody Picoband®Different PPARα ligands exhibited different abilities to inhibit tumour sizes and metastasis. a Serum triglyceride levels in TC-1 tumour-bearing mice ( n = 6–11). * P < 0.05, vs control. b Relative mRNA levels of Ptgs1 ( Cox1 ), Ptgs2 ( Cox2 ), Cyp2c44 , Cyp2c39 , Cyp2c38 , Cyp2c29 , Alox5, Alox12, Acot1 ( n = 6). * P < 0.05, vs control. c1 and c2 Images of the primary xenograft tumours and their growth curves in mice treated with three different PPARα ligands, AVE8134 (AVE), Wy-14,643 (Wy), and Bezafibrate (Beza; n = 8–11). * P < 0.05, AVE vs control; # P < 0.05, Wy vs control. d The weight of lungs in TC-1 tumour-bearing mice ( n = 8–11). * P < 0.05, vs control. e1 and e2 Hematoxylin and eosin (HE) staining and the number of lung metastatic tumours (red arrowhead; n = 8–11). * P < 0.05, vs control. f The ratio of liver weight to body weight ( n = 8–11). * P < 0.05, vs control; # P < 0.05, vs AVE. g The levels of serum ALT ( n = 6). * P < 0.05, vs control. h1 and h2 Tumour vascularization was quantified by CD31 antibodies in the paraffin sections of primary xenograft tumours. * P < 0.05, vs control; # P < 0.05 vs AVE; & P < 0.05 vs Wy. (I1 and I2) Representative bands of Cyp2c44 and GAPDH in tumours were evaluated by western blot. * P < 0.05, vs control ( n ≥ 3) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-6379-5'>31791289</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-41598_2018_23568_fig4_html.jpgAnti-GAPDH Antibody Picoband®Effect of exercise on alcohol induced oxidative and endoplasmic reticular (ER) stress. ( a,b ) Representative western blot analysis showing the levels of antioxidant marker CAT and oxidative stress marker NOX4 in the different mice groups. Bar graphs showing the quantitative estimation of CAT and NOX4 proteins after normalization with GAPDH. ( c–e ) Scatter dot plots representing the levels of malondialdehyde (MDA), glutathione peroxidase (GPx) and production of H 2 S in brain tissue in different mice groups. ( f,g ) Representative western blot analysis showing the levels of GRP78 and ATF6 (hallmarks of ER stress) in the different groups of mice. Bar graphs showing the quantitative estimation of GRP78 and ATF6 proteins after normalization with GAPDH. ( h ) Scatter dot plot represents data for the cellular calcium ion (Ca +2 ) level in brain tissue extract of different mice groups. All the data are represented as mean values ± standard error (SE) in 5 independent experiments. * ,# p < 0.05 considered significant. *p < 0.05 vs. CT and # p < 0.05 vs. AL group. Uncropped blots for a and f are presented in Supplementary Fig. . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-23568-z'>29581524</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00618-g002.jpgAnti-GAPDH Antibody Picoband®Effects of Bergenin on osteogenesis of bone marrow mesenchymal stem cells (BMSCs). (A) The effects of Bergenin on alkaline phosphatase activity at days 3 and 5 during the osteogenic differentiation of BMSCs. (B – E) mRNA expression of RUNX2, ALP, and COL1A1 was determined by quantitative reverse transcription polymerase chain reaction at day 3 and day 5 during osteogenic differentiation. mRNA expression levels were normalized to GAPDH. (F – K) The expression of RUNX2 and SIRT1 protein was determined by Western blot analysis after osteogenic differentiation at days 3 and 5. Protein expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase. Data are expressed as the mean ± standard deviation (SD) of three independent experiments, and one of three independent experiments is shown. Data are expressed as the mean ± SD, n = 3. * P < 0.05 vs. BMSCs treated with osteogenic induction medium alone. (L) Alizarin red staining at days 12 and 14 of osteogenic differentiation. Magnification ×40. (M) Immunofluorescence staining showing that the protein levels of RUNX2, COL1A1, and SIRT1 are upregulated by the addition of Bergenin (10 or 100 μM) at day 3 of osteogenic differentiation. COL1A1 is stained green. RUNX2 and SIRT1 are stained red. Nuclei are stained with 4′,6-diamidino-2-phenylindole (blue). Magnification ×200.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00618/full'>31258473</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-41598_2018_23568_fig6_html.jpgAnti-GAPDH Antibody Picoband®( a , b ) Effect of exercise on alcohol induced vascular permeability and BBB dysfunction. Representative western blot analysis showing the levels of tight junction (TJ) proteins (ZO-1 and Claudin-5) in the different mice groups ( a ). Histogram showing the quantitative estimation of ZO-1 and Claudin-5 proteins after normalization with GAPDH (b). ( c,d ) Representative images showing fluorescent protein (FITC-BSA) leakage from pial vessels into brain parenchyma – indicating alteration in microvascular permeability in the different groups of mice ( c ). Scatter dot plot showing quantitative estimation of fluorescent intensity units (FIU) in the different mice groups after FITC-BSA injection ( d ). ( e , f ) Representative images of cerebral angiogram with barium sulfate contrast in experimental mice groups ( e ). Scatter dot plot showing the pattern of vascular density in the form of percentage of vascular area in the different mice groups ( f ). ( g , h ) Representative images for the in vitro model showing microvascular permeability in brain endothelial cells (bEnd.3 cells) by FITC-BSA diffusion assay. Fluorescence intensity of bovine serum albumin conjugated with FITC (BSA-488) in lower chambers of Transwells was measured by fluorimetry and presented as FIU ( g ). Histogram showing quantitative estimation of FIU in different experimental conditions after FITC-BSA treatment in Transwell chambers ( h ). ( i , j ) Representative western blot analysis showing the levels of junctional proteins (VE-Cadherin, Claudin-5 and ZO-2) in different experimental conditions of mouse brain endothelial cells (i). Histograms showing the quantitative estimation of ZO-2, Claudin-5 and VE-Cadherin proteins after normalization with GAPDH (j). All the data are represented as mean values ± standard error (SE) in 5 independent experiments. * ,# p < 0.05 considered significant.*p < 0.05 vs. CT and # p < 0.05 vs. AL group. Uncropped blots for Fig. are presented in Supplementary Fig. and . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-23568-z'>29581524</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-fphar-10-00041-g003.jpgAnti-GAPDH Antibody Picoband®Effects of Schisandrin A on IL-1β-induced MMPs and ADAMTS5 protein expression. Chondrocytes were exposed to Schisandrin A (25, 50 μM) with or without IL-1β (10 ng/ml) for 24 h. (A) Western blot was employed to determine the expression of MMP1, MMP3, MMP13, and ADAMTS5. (B) Relative protein expression was qualified by Image-J software, GAPDH was used as the internal control ( n = 3). # P < 0.05 vs. control group; ∗ P < 0.05 vs. IL-1β group; ∗∗ P < 0.01 vs. IL-1β group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00041/full'>30761007</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-jgo-16-02-679-f1.jpgAnti-GAPDH Antibody Picoband®CPT2 expression was down-regulated in CCA and other cancers. (A,B) The expression of CPT2 was significantly lower in CCA cancer tissues than in adjacent normal tissues in (A) GEO, and (B) TCGA datasets. (C) Pan-cancer analysis of CPT2. (D,E) The mRNA level of CPT2 was measured by qRT-PCR in (D), CCA peripheral blood and (E), 11 pairs of CCA tissues. (F) Protein expression of CPT2 was measured by Western blotting in 9 pairs of CCA tissues. The differences were analyzed with two-tailed Student t -tests or paired t -tests. The data are presented as the mean ± SD. *, P<0.05; **, P<0.01; ***, P<0.001; ****, P<0.0001. Experiments were repeated three times. CCA, cholangiocarcinoma; CPT2, carnitine palmitoyltransferase II; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GEO, Gene Expression Omnibus; mRNA, messenger RNA; qRT-PCR, quantitative real-time polymerase chain reaction; SD, standard deviation; TCGA, The Cancer Genome Atlas; TPM, transcripts per million.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12078819/'>40386589</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-wb-testing-2.jpg.jpgAnti-GAPDH Antibody Picoband®Western blot analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: human SK-HEP1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody (A00227-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-wb-testing-3.pngAnti-GAPDH Antibody Picoband® Western blot analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-6: mouse intestinal tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody (Catalog # A00227-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti rabbit secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for GAPDH at approximately 37 kDa. The expected band size for GAPDH is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gsta1-5-primary-antibodies-wb-testing-4.pngAnti-GAPDH Antibody Picoband® Western blot analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-2: human OCI-LY1whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody (Catalog # A00227-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for GAPDH at approximately 35 kDa. The expected band size for GAPDH is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-if-testing-5.jpgAnti-GAPDH Antibody Picoband® IF analysis of GAPDH using anti-GAPDH antibody (A00227-1). <br>
GAPDH was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GAPDH Antibody (A00227-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00227-1-gapdh-primary-antibodies-fcm-testing-6.jpgAnti-GAPDH Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-GAPDH antibody (A00227-1). <br>
Overlay histogram showing Hela cells stained with A00227-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GAPDH Antibody (A00227-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-hmgb1-picoband-trade-antibody-a00066-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-wb-testing-1.jpgAnti-HMGB1 Antibody Picoband® Western blot analysis of HMGB1 using anti-HMGB1 antibody (A00066-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HMGB1 antigen affinity purified polyclonal antibody (Catalog # A00066-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HMGB1 at approximately 25 kDa. The expected band size for HMGB1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig2_html.pngAnti-HMGB1 Antibody Picoband®HMGB1 expression in the mPFC was increased temporally in parallel to comorbid anxiety in neuropathic pain. a Schedule of experimental procedures. b Representative photomicrographs of HMGB1 immunostaining in the mPFC, BLA, vHPC and PBN. Scale bar, 200 μm. c Quantification of HMGB1 fluorescence intensity in the mPFC, BLA, vHPC and PBN on D9 PO. d, e Representative images of protein bands in western blotting (left) and quantification of HMGB1 expression (right) in the mPFC ( d ) and BLA ( e ) on D9 and D30 PO. *, ** and *** indicate P < 0.05, 0.01 and 0.001, respectively, compared with the indicated groups, ordinary one-way ANOVA with Tukey post hoc or Kruskal–Wallis test with Dunn’s post hoc in ( c ) and ordinary one-way ANOVA with Dunnett post hoc in ( d ) and ( e ). n = 4/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f02.jpgAnti-HMGB1 Antibody Picoband®Glycyrrhizin, RAP, A box and EP exert efficient neutralizing effects on extracellular HMGB1 without altering tumor cell proliferation and apoptosis/necrosis. (A) Schematic representation of different modes of inhibition for extracellular HMGB1. Mouse RAW 264.7 cells were stimulated with recombinant HMGB1 (B) or conditioned media from 4T1 basal-like breast cancer cells (C) in the absence or presence of glycyrrhizin, RAP or a box (several concentrations were tested). Note the significant decrease of HMGB1-induced TNFα secretion when HMGB1 inhibitors were added in the cell cultures, indicating their efficient neutralizing effect. (D) EP was directly added in the culture medium of 4 different mouse basal-like breast cancer cell lines (4T1, 67NR, EpRas and EpH4). Forty-eight hours later, HMGB1 concentrations were determined by ELISA and the ability of EP to inhibit HMGB1 release in a dose-dependent manner was highlighted. (E) Oxygen consumption rate (OCR) and (F) extracellular acidification rate (ECAR) in 4T1 cells in the absence or presence of glycyrrhizin (1 nM), RAP (10 µM) and a box (0.5 µg/mL) were determined using Seahorse extracellular flux analyzer. No modification of OCR/ECAR was detected with these three HMGB1 inhibitors. (G) OCR and (H) ECAR in 4T1 cells following EP addition (concentration range: 0.1–10 mM). Histograms representing OCR (I) and ECAR (J) before (baseline) and after (stressed) oligomycin and FCCP addition in the absence or presence of EP. Both OCR and ECAR were strongly decreased with 5 and 10 mM EP. No significant change was detected with lower concentrations (0.1–1 mM). (K) Cell proliferation and (L) apoptosis of mouse 4T1 cells cultured without or with HMGB1 inhibitors (glycyrrhizin (1 nM), RAP (10 µM), a box (0.5 µg/mL) and EP (1 mM)) were determined using IncuCyte live cell analyzing system and annexin V-propidium iodide staining assay, respectively. No significant change was reported. The means±SEM (plus each individual data point) for at least three independent experiments are represented. Asterisks indicate statistically significant differences (*p<0.05; **p<0.01; ***p<0.001). P values were determined using one-way ANOVA, followed by Dunnett’s multiple comparison post-test (B, C, D, I, J, K, L). ANOVA, analysis of variance; ECAR, extracellular acidification rate; EP, ethyl pyruvate; HMGB1, high-mobility group box 1; RAGE, receptor for advanced glycation endproducts; RAP, RAGE antagonist peptide; TNFα, tumor necrosis factor-α.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00066-1-3-IHC-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of mouse liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f01.jpgAnti-HMGB1 Antibody Picoband®HMGB1 is highly secreted by basal-like breast cancer cells and its tumor-specific cytoplasmic expression is associated with immune tolerance and poor outcome. (A) The METABRIC dataset was used for analyzing HMGB1 expression level in breast cancers according to molecular subtypes, histologic grades, nodal and metastatic statuses. (B) Representative pictures of normal mammary glands and breast cancers stained for HMGB1. Note the two distinct HMGB1 staining patterns detected in tumor specimens: nuclear versus cytoplasmic. (C) Semiquantitative evaluation of cytoplasmic HMGB1 immunoreactivity (negative, 0%–10% or >10% positive cells) in both normal mammary glands (n=120) and neoplasms (LumA, n=35; LumB, n=31; HER2+, n=37; basal-like, n=172). (D) Disease-free survival of patients treated for basal-like breast cancer according to cytoplasmic HMGB1 expression (negative, n=72; 0%–10%, n=61; >10%, n=39). This latter parameter was clearly found to be an independent prognostic factor. (E) Illustration of the different steps for DAB-positive cell quantification using computerized image analysis (QuPath). (F) CD3 + , Foxp3 + , CD68 + and CD206 + cell infiltrations in microenvironment of basal-like breast tumors. Whereas the global number (CD68 + ) did not significantly change, an increased density of CD206 + M2 macrophages was detected in cytoplasmic HMGB1-positive cancers. A similar increase was also reported with Foxp3 + Treg lymphocytes. the number of positive cells was reported to tumor area (mm 2 ). (G) Representative examples of normal (HMEC and MCF10A) and malignant cells (LumA: T-47D and MCF7; basal-like: MDA-MB-468 and Hs578T) stained for HMGB1. Note the exclusive nuclear immunoreactivity displayed by normal mammary cells. Secretion/release of HMGB1 analyzed by ELISA in (H) human and (I) mouse cell culture supernatants. High concentrations were especially detected in cell cultures derived from triple negative/basal-like tumors. The means±SEM (plus each individual data point) for at least three independent experiments are represented. The scale bar represents 100 µm. Asterisks indicate statistically significant differences (*p<0.05; **p<0.01; ***p<0.001). P values were determined using one-way ANOVA followed by Bonferroni post-test (A), unpaired t-test (A), χ 2 test (C), log-rank (Mantel-Cox) test (D) and one-way ANOVA followed by Dunnett’s multiple comparison post-test (F, H, I). ANOVA, analysis of variance; HMGB1, high-mobility group box 1; METABRIC, Molecular Taxonomy of Breast Cancer International Consortium.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00066-1-4-IHC-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-ijbsv18p2146g008.jpgAnti-HMGB1 Antibody Picoband®UA alleviates APAP-induced oxidative stress through Nrf2 signaling pathway. The mice were pretreated with AAV8-sh-Nrf2 (5 × 10 10 vg/mL) or Scramble shRNA via tail vein injection. One week after AAV infection, the mice were challenged with APAP injection with or without UA treatment (50 mg/kg). The liver tissue and serum were harvested at 12 h after APAP challenge. n = 6 mice per group. (A) Serum ALT levels from different groups. (B) Representative images of hematoxylin and eosin-stained liver sections, scale bar: 100 μm. (C) The quantification of necrosis area of the liver tissue. (D) Representative immunoblots and analysis of NQO1 expression in mice were treated with or without Nrf2 shRNA. (E) The L02 cells were transfected with the siNrf2 RNA or Scramble siRNA for 48 h and then treated with or without UA (5 μM) in the presence or absence of APAP (10 mM) for 24 h. Cell viability was determined by CCK8 assay. (F) HMGB1 immunofluorescence of L02 cells. scale bar: 50 μm. (G) Quantification of colocalization of HMGB1 and nuclei. (H) Representative immunoblots and analysis of NQO1 expression in L02 cells. (I) Representative images of DHE staining of L02 cells, scale bar, 100 μm. (J) The quantification of the DHE positive intensity. Data are expressed as mean ± SEM. The in vitro experiment was repeated at least 3 times. *** P < 0.001 vs. CTL; ## P < 0.01, ### P < 0.001 vs. APAP; & P < 0.05, &&& P < 0.001 vs. siNC-APAP + UA or sh-NC-APAP + UA.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8935220/&orig_host=www.ncbi.nlm.nih.gov'>35342347</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00066-1-5-IHC-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of rat liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-13659_2022_325_fig3_html.pngAnti-HMGB1 Antibody Picoband®Anti-inflammation of naringin in vitro and in vivo. A – D Effect of naringin on LPS-induced mRNA expression of COX-2, iNOS, IL-1β, and IL-6 in RAW 264.7 macrophages. The concentration of LPS is 1 μg/mL. A COX-2 mRNA relative expression level; B IL-1β mRNA relative expression level; C iNOS mRNA relative expression level; D IL-6 mRNA relative expression level. Different letters show significant differences ( p < 0.05). E – G Anti-inflammation effect of naringin on myocardial ischemia/reperfusion injury in rats. E Representative images of the Western blot results. F HMGB1 protein Expression level; G p-P38 protein expression levels. * p < 0.05 vs. the Sham group; # p < 0.05 vs. the I/R group. COX-2, cyclooxygenase-2; HMGB1, high mobility group box 1 protein; IL-1β, interleukin-1β; IL-6, interleukin 6; iNOS, inducible nitric oxide synthase; I/R, ischemia/reperfusion; LPS, lipopolysaccharide; Nar, naringin <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1007/s13659-022-00325-4'>35157175</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00066-1-6-IHC-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-ijbsv18p2146g003.jpgAnti-HMGB1 Antibody Picoband®UA Protected against Acetaminophen-induced Cytotoxicity in vitro . (A) L02 hepatocytes were subjected to UA at different concentrations with or without APAP (10 mM) for 24 h. Cell viability was determined by CCK8 assay. (B) HMGB1 (green) staining of L02 cells. Representative images with amplification indicating example cells with cytoplasmic HMGB1 staining and hollow nuclei (scale bars: 50 μm for upper and 10 μm for bottom), and quantification of colocalization of HMGB1 and nuclei by Image J software in at least 20 randomly selected individual cells. (C) Quantification of LDH released into the culture medium of L02 cells. Data were represented as the means ± SEM, the experiment was repeated at least 3 times, *** P < 0.001 vs. CTL; # P < 0.05, ### P < 0.001 vs. APAP.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8935220/&orig_host=www.ncbi.nlm.nih.gov'>35342347</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00066-1-7-IHC-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f06.jpgAnti-HMGB1 Antibody Picoband®A significant fraction of HMGB1 contained in tumor-extruded fluids is in its oxidized form and displays RAGE-dependent tolerogenic properties. (A, B) The ROS accumulation in both breast (4T1, 67NR, EpRas) and lung (TC-1) cancer cells used in the present study was assessed by flow cytometry. N-acetylcysteine (5 mM) and tert-butyl hydroperoxide (100 µM) were used as negative and positive controls, respectively. Results represent the means±SEM of four independent experiments (each individual data point is shown). (C) The redox state of extracellular HMGB1 contained in tumor-extruded fluids was analyzed by Western blot. All samples were directly alkylated in order to ‘freeze’ the redox state of HMGB1 molecules. Recombinant HMGB1 (0.5 µg) incubated with either H 2 O 2 or DTT (and then alkylated) were used as controls. (D) Oxidized/reduced-disulfide HMGB1 ratio (%) was calculated from the Western blot bands using ImageJ software. (E) DCs were incubated with terminally oxidized, fully reduced or disulfide HMGB1 for 24 hours before being stimulated with LPS for 24 hours. The expression of cell-surface molecules (CD80, CD83, CD86, HLA-DR, HLA-ABC and CCR7) was then measured by flow cytometry. All data were normalized to LPS-stimulated DC. Data represent the relative mean fluorescent intensity (MFI)±SEM of at least five independent experiments (each individual data point is shown). (F) DCs were incubated with terminally oxidized HMGB1 for 24 hours before being stimulated with LPS for 24 hours. When indicated, an inhibitor of RAGE (10 µM RAP) or TLR4 (2 µM LPS-RS) was added in the cell culture. The expression of DC activation markers was determined by flow cytometry. All data were normalized to LPS-stimulated DC. The relative MFI±SEM of 7 independent experiments are shown. Asterisks indicate statistically significant differences (*p<0.05, **p<0.01, ***p<0.001). P values were determined using one-way ANOVA, followed by Dunnett’s multiple comparison post-test (A, B, E, F). ANOVA, analysis of variance; DC, dendritic cell; HMGB1, high-mobility group box 1.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig8_html.pngAnti-HMGB1 Antibody Picoband®Systemic anti-HMGB1 mAb simultaneously alleviated pain sensitization and anxiety after p-IONX. a Schedule of experimental procedures. b Paw withdrawal thresholds to mechanical stimulation and noxious heat stimulation at the left hind paw and head withdrawal threshold to noxious heat stimulation at the left vibrissal pad before and after p-IONX. ## and ### indicate P < 0.01 and 0.001, respectively, compared with the saline-treated group at the same time points, two-way ANOVA with Bonferroni post hoc . c Anxiety-like behaviors measured by EPM, LDB and OFT on D15/16 after p-IONX. * and *** indicate P < 0.05 and 0.001, respectively, compared with the saline-treated group, ordinary one-way ANOVA with Dunnett post hoc . n = 8/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-if-testing-9.jpgAnti-HMGB1 Antibody Picoband® IF analysis of HMGB1 using anti-HMGB1 antibody (A00066-1). <br>
HMGB1 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig7_html.pngAnti-HMGB1 Antibody Picoband®Systemic anti-HMGB1 mAb reversed the hyperexcitability of pyramidal neurons in mPFC layer 2/3 after p-IONX. a Schedule of experimental procedures. Anti-HMGB1 mAb was administered intraperitoneally. b Example image of whole cell patch-clamp recordings on mPFC layer 2/3 pyramidal neurons. Scale bar, 150 μm. c Example traces of sEPSCs and sIPSCs in sham + saline, p-IONX + saline and p-IONX + anti-HMGB1 mAb groups. d, e Amplitude, frequency and charge transfer of sEPSCs ( d ) and sIPSCs ( e ). f Quantification of E/I ratio ( ∣ CsEPSC ∣ /CsIPSC). g, h Resting potential ( g ) and rheobase (the lowest current that evoked action potential firing, h ). i, j Representative traces of firing ( i ) and number of spikes ( j ) of action potentials evoked by injecting current at two-fold of rheobase. k Firing rate of action potentials evoked by step-current injection. l Autocorrelation and waveform (inset) of a representative glutamatergic neuron in in vivo single-unit recordings. m Mean frequency of spontaneous firing. *, ** and *** indicate P < 0.05, 0.01 and 0.001, respectively, compared with the indicated groups, unpaired t test or Mann–Whitney test. n = 9–10 neurons from 4 mice/group in ( d - k ) and n = 20 neurons from 8 mice/group in ( m ) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig6_html.pngAnti-HMGB1 Antibody Picoband®HMGB1 in the mPFC was sufficient to induce anxiety-like behaviors and aversion but not pain sensitization in naïve mice. a Schedule of experimental procedures. b Paw withdrawal thresholds to mechanical stimulation and noxious heat stimulation at the left hind paw and head withdrawal threshold to noxious heat stimulation at the left vibrissal pad. c, d Anxiety-like behaviors measured by EPM, LDB and OFT on D8/9 ( c ) and D15/16 ( d ) after administration. e Representative heat maps in the CPP test. f Time spend by mice in the saline- and ds-HMGB1-paired boxes. *, ** and *** indicate P < 0.05, 0.01 and 0.001, respectively, compared with the saline-treated group in ( c ) and pre-conditioning in ( f ), unpaired t test. n = 8/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig4_html.pngAnti-HMGB1 Antibody Picoband®Local neutralization of HMGB1 in the mPFC reduced anxiety-like behaviors and aversion but not pain sensitization after p-IONX. a Schedule of procedures of mPFC drug delivery experiments in the early phase after p-IONX. b Schematic (upper) and representative photomicrograph (lower) of the cannula implantation in bilateral mPFC for local infusion of agents. Dashed lines indicate the trace of implanted canula. Scale bar, 100 μm. c Paw withdrawal thresholds to mechanical stimulation and noxious heat stimulation at the left hind paw and head withdrawal threshold to noxious heat stimulation at the left vibrissal pad before and after p-IONX. *, ** and *** indicate P < 0.05, 0.01 and 0.001, respectively, compared with the baseline (BL), Kruskal–Wallis test with repeated measures and Dunn’s post hoc . #, ## and ### indicate P < 0.05, 0.01 and 0.001, respectively, compared with the sham + mAb group at the same time points, two-way ANOVA with Bonferroni post hoc . d, e Anxiety-like behaviors measured by EPM, LDB and OFT on D8/9 ( d ) and D15/16 ( e ) after p-IONX, respectively. * indicates P < 0.05, compared with the indicated groups, ordinary one-way ANOVA with Tukey post hoc . f Schedule (left) and schematic (right) of the experiment procedures for the CPP test. g Representative heat maps in the CPP test. h-j Time spend by the mice in the control IgG- and anti-HMGB1 mAb-paired boxes ( h ), preference ( i ) and shift preference ( j ) for the anti-HMGB1 mAb-paired box in pre- (Pre) and post-conditioning (Post) phases. *, ** and *** indicate P < 0.05, 0.01 and 0.001, respectively, compared with the indicated groups, unpaired t test. ## indicates P < 0.01, compared with the sham group in ( i ), two-way ANOVA with Bonferroni post hoc . n = 8/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig5_html.pngAnti-HMGB1 Antibody Picoband®HMGB1 upregulation in the mPFC maintained comorbid anxiety in neuropathic pain. a Schedule of procedures of mPFC drug delivery experiments in the late phase after p-IONX. b , c Anxiety-like behaviors measured by EPM, LDB and OFT on D29/30 and D36/37 after p-IONX and PSL, respectively. * indicates P < 0.05, compared with the IgG-treated groups, unpaired t test. n = 8/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-10194_2022_1475_fig3_html.pngAnti-HMGB1 Antibody Picoband®Cellular and subcellular distribution of HMGB1 in the mPFC after p-IONX in MRL/MPJ mice . a-c Representative photomicrographs indicating the cellular distribution of HMGB1 in neurons (NeuN + , a ), microglia (Iba1 + , b ) and astrocytes (S100b + , c ) in the mPFC on D9 PO. DAPI was used to label nuclei. Scale bar, 50 μm. d Percentage of HMGB1-positive cells in neurons (NeuN + ), microglia (Iba1 + ) and astrocytes (S100b + ) on D9 PO in the mPFC. e Percentage of cells with HMGB1 cytoplasmic translocation in neurons (NeuN + ), astrocytes (S100b + ) and microglia (Iba1 + ) on D9 PO in the mPFC. f Quantification of Iba1 and S100b fluorescence intensity in the mPFC. g-h Representative images of western blot bands ( g ) and quantification of HMGB1 ( h ) in nuclear and cytoplasmic fractions from the mPFC on D9 PO. * and ** indicate P < 0.05 and 0.01, respectively, compared with the indicated groups, unpaired t test. n = 4/group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10194-022-01475-z'>35974316</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f04.jpgAnti-HMGB1 Antibody Picoband®Extracellular HMGB1 blockade enhances anti-PD-1-induced inhibition of tumor growth in vivo. (A) PD-1 mRNA expression ( PDCD1 gene) in the four major molecular subtypes of breast cancer was determined using the METABRIC public dataset. (B) Representative example of breast cancer stained for PD-1. Positive cells were observed in the epithelial component of the tumor as well as in the stroma surrounding cancer cells. (C) PD-1 + cell infiltration within tumor microenvironment was determined by computerized counting. Each point represents the number of positive cells/mm 2 for one independent tumor specimen. (D) Mouse breast cancer cells (4T1 and 67NR) were orthotopically injected into the mammary fat pad of immunocompetent BALB/c mice. Anti-PD-1 antibody was tested alone (i.p. injection of 200 µg at days 4, 7 and 11) and in combination with HMGB1 inhibitors (RAP (10 µM/kg) and EP (1 mM/kg), treatment at 3 day intervals). In parallel, the anticancer efficacy of these combination regimens was also compared with that displayed by each individual HMGB1 inhibitor used in monotherapy. The mean tumor volumes±SEM are represented. (E) The apoptotic cancer cells (cleaved caspase 3 + ) were detected by immunohistochemistry and quantified using QuPath software. The number of positive cells was reported to tumor area (mm 2 ). (F) The total number of (CD45 + ) immune cells per milligram of tumor was determined in the different treatment groups. (G) Scatter dot plots illustrating the percentage of each individual immune cell population (DC, PDC, CD4 + and CD8 + T cells, monocytic and granulocytic MDSC, neutrophils, M1 and M2 macrophages) among CD45 + cells in both control and treated groups. Reduced densities of granulocytic MDSC as well as an increase of M1 macrophages were especially observed in case of combination therapy. The intratumoral immune cells were analyzed in five mice per condition. (H) Scatter dot plots showing the percentage of tumor-infiltrating Treg (Foxp3 + ) CD4 + and CD8 + cells among total CD4 + and CD8 + populations in the different treatment groups. the activation status of DC (I) and pDC (J) was determined by flow cytometry. the expression of several surface markers (CD80, CD86, I-A/I-E, ILT3 and ICOSL) was analyzed. Data represent the mean fluorescent intensity (MFI)±SEM of 5 independent experiments in each group (each individual data point is shown). The scale bar represents 100 µm. Asterisks indicate statistically significant differences (*p<0.05; **p<0.01; ***p<0.001; ****p<0.0001). P values were determined using one-way ANOVA followed by Bonferroni post-test (A, C, E) or Dunnett’s multiple comparison post-test (D, F, G, H, I, J). ANOVA, analysis of variance; DC, dendritic cell; HMGB1, high-mobility group box 1; METABRIC, Molecular Taxonomy of Breast Cancer International Consortium; MDSC, myeloid-derived suppressor cells; pDC, plasmacytoid DC; RAP, RAGE antagonist peptide.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f05.jpgAnti-HMGB1 Antibody Picoband®Combination of anti-PD-L1 with HMGB1 inhibitors strongly inhibits tumor growth in syngeneic mouse models of basal-like breast cancer. (A) mRNA level of PD-L1 ( CD274 gene) in the four major molecular subtypes of breast cancer was determined using the METABRIC public dataset. (B) Representative example of breast cancer stained for PD-L1. Positive signals were detected on cancer cells and/or on inflammatory cells within tumor microenvironment. Semiquantitative evaluation of PD-L1 immunoreactivity (negative or >1% membrane staining) displayed by cancer cells (C) or inflammatory cells infiltrating the tumor microenvironment (D). The analyzed cancer specimens were categorized into the four molecular subtypes of breast cancer (LumA, LumB, HER2 + and basal-like). (E) The percentage of PD-L1 + cells in both epithelial/cancer (CD45 - ) and inflammatory (CD45 + ) components of untreated harvested 4T1/67NR tumors was determined by flow cytometry. Note the distinct profile displayed by these two cell lines. (F) Mouse breast cancer cells (4T1 and 67NR) were orthotopically injected into the mammary fat pad of immunocompetent BALB/c mice. Anti-PD-L1 antibody was tested alone (i.p. injection of 100 µg at days 4, 7 and 11) and in combination with HMGB1 inhibitors (RAP (10 µM/kg) and EP (1 mM/kg), treatment at 3-day intervals). The mean tumor volumes±SEM are represented. (G) The total number of (CD45 + ) immune cells per milligram of tumor was determined in the different treatment groups by flow cytometry. (H) Scatter dot plots illustrating the percentage of each individual immune cell population (DC, PDC, CD4 + and CD8 + T cells, monocytic and granulocytic MDSC, neutrophils, M1 and M2 macrophages) among CD45 + cells in both control and treated groups. The intratumoral immune cell infiltration was analyzed in five mice per condition. (I) scatter dot plots showing the percentage of tumor-infiltrating Treg (Foxp3 + ) CD4 + and CD8 + cells among total CD4 + and CD8 + populations in the different treatment groups. The activation status of DC (J) and pDC (K) was determined by flow cytometry. the expression of several surface markers (CD80, CD86, I-A/I-E, ILT3 and ICOSL) was assessed. Data represent the mean fluorescent intensity (MFI)±SEM of five independent experiments in each group (each individual data point is shown). (L) The apoptotic cancer cells (cleaved caspase 3 + ) were detected by immunohistochemistry and quantified using QuPath software. The number of positive cells was reported to tumor area (mm 2 ). The scale bar represents 100 µm. Asterisks indicate statistically significant differences (*p<0.05; **p<0.01; ***p<0.001; ****p<0.0001). P values were determined using one-way ANOVA, followed by Bonferroni post-test (A, L), Fisher’s exact test (C, D) and one-way ANOVA followed by Dunnett’s multiple comparison post-test (F, G, H, I, J, K). ANOVA, analysis of variance; DC, dendritic cell; EP, ethyl pyruvate; HMGB1, high-mobility group box 1; i.p, intraperitoneal; METABRIC, Molecular Taxonomy of Breast Cancer International Consortium; pDC, plasmacytoid DC; RAP, RAGE antagonist peptide.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-ijbsv18p2146g002.jpgAnti-HMGB1 Antibody Picoband®UA Protected against Acetaminophen-induced liver injury in vivo . (A) Serum ALT and (B) AST activities in mice with various concentrations of Urolithin A in the presence or absence of APAP administration (500 mg/kg), n = 6. (C) The representative image of liver tissue (scale bar: 500 mm) and representative image of H&E-stained liver sections at 100 × magnification, scale bar: 200 μm. APAP-induced centrilobular necrosis was indicated by the dotted line. (D) The quantification of necrosis area of the liver tissue, n = 6. (E) HMGB1 staining of liver sections (scale bar: 50 μm). (F) Quantification of colocalization of HMGB1 and nuclei by Image J (NIH, Bethesda, MD) software, n = 6. (G) The survival rate in the APAP challenged (750 mg/kg) mice with or without UA treatment (15 mice per group). Data were represented as the means ± SEM. *** P < 0.001 vs. CTL; # P < 0.05, ### P < 0.001 vs. APAP.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8935220/&orig_host=www.ncbi.nlm.nih.gov'>35342347</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-jitc-2020-001966f03.jpgAnti-HMGB1 Antibody Picoband®Extracellular HMGB1 blockade inhibits the growth of pre-established solid tumors in immunocompetent mice through activating anticancer immune responses. (A) Mouse basal-like breast cancer cells (4T1, 67NR and EpRas) were orthotopically injected into the mammary fat pad of immunocompetent BALB/c mice. Tumor-bearing mice were then treated at 3-day intervals with PBS (control) or HMGB1 inhibitors (glycyrrhizin (1 nM/kg), RAP (10 µM/kg), a box (500 µg/kg) and EP (1 mM/kg)). The mean tumor volumes±SEM are represented. (B) HMGB1 inhibitors were tested in nude mice implanted with 67NR cells. Note the absence of beneficial effect in these latter immunocompromised mice, indicating the dependence on the adaptive immune responses. (C) At day 17, 19 or 20 (depending on the analyzed cell line), tumors were harvested, CD45 + immune cells were isolated and analyzed by flow cytometry. The proportions of each analyzed immune cell population in both control and treated groups (pooled results) are shown. Note the drastic reduction of MDSC following extracellular HMGB1 blockade. (D) Total number of (CD45 + ) immune cells per milligram of tumor in both control and treated groups. (E) Scatter dot plots showing the percentage of each individual immune cell population (DC, PDC, CD4 + and CD8 + T cells, monocytic and granulocytic MDSC, neutrophils, M1 and M2 macrophages) among CD45 + cells in the different treatment groups. an increased M1/M2 ratio of macrophages was observed in most HMGB1 inhibitor-treated tumors. The intratumoral immune cells were analyzed in five mice per condition. (F) Scatter dot plots illustrating the percentage of tumor-infiltrating Treg (Foxp3 + ) CD4 + and CD8 + cells among total CD4 + and CD8 + populations in the different treatment groups. (G) Scatter dot plots illustrating the percentage of tumor-infiltrating PD-1 + CD4 + and PD-1 + CD8 + cells among total CD4 + and CD8 + populations in the treatment groups. The activation status of both DC (H) and PDC (I) in the different treatment groups was also determined by analyzing the expression of several cell surface markers (CD80, CD86, I-A/I-E, ILT3 and ICOSL). Data represent the mean fluorescent intensity (MFI)±SEM of 5 independent experiments in each group (each individual data point is shown). The number of apoptotic cancer cells (cleaved caspase 3 + ) (J) as well as the density of blood vessels within tumor microenvironment (CD31 + ) (K) were determined by computerized counting (using QuPath software). The number of cleaved caspase 3 + cells and the percentage of CD31 + pixels were reported to tumor area. The scale bar represents 100 µm. Asterisks indicate statistically significant differences (*p<0.05; **p<0.01; ***p<0.001). P values were determined using one-way ANOVA followed by Dunnett’s multiple comparison post-test (A, B, D, E, F, G, H, I) and (Welch-corrected) unpaired t-test (J, K). ANOVA, analysis of variance; DC, dendritic cell; EP, ethyl pyruvate; HMGB1, high-mobility group box 1; i.p, intraperitoneal; MDSC, myeloid-derived suppressor cells; pDC, plasmacytoid DC; RAP, RAGE antagonist peptide.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7959241/&orig_host=www.ncbi.nlm.nih.gov'>33712445</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-wb-testing-2_1.jpgAnti-HMGB1 Antibody Picoband® Western blot analysis of HMGB1 using anti-HMGB1 antibody (A00066-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse RAW264.7- WT whole cell lysates,<br>
Lane 2: mouse RAW264.7-Hmgb1 KO whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. Then the membrane was incubated with rabbit anti-HMGB1 antigen affinity purified polyclonal antibody (A00066-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HMGB1 at approximately 25 kDa. The expected band size for HMGB1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-8-ihc-anti-hmgb1-hmg-1-picoband-antibody.jpgAnti-HMGB1 Antibody Picoband® IHC analysis of HMGB1 using anti-HMGB1 antibody (A00066-1).<br>
HMGB1 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-if-testing-10.jpgAnti-HMGB1 Antibody Picoband® IF analysis of HMGB1 using anti- HMGB1 antibody (A00066-1). <br>
HMGB1 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti- HMGB1 Antibody (A00066-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-if-testing-10.pngAnti-HMGB1 Antibody Picoband®IF analysis of HMGB1 using anti-HMGB1 antibody (A00066-1). <br>
HMGB1 was detected in an immunocytochemical section of Mouse 4T1 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HMGB1 Antibody (A00066-1) overnight at 4°C. DyLight 550-conjugated Goat Anti-Mouse was used as secondary antibody incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a laser confocal microscope with filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00066-1-hmgb1-primary-antibodies-fcm-testing-11.pngAnti-HMGB1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-HMGB1 antibody (A00066-1). <br>
Overlay histogram showing THP-1 cells stained with A00066-1 (Blue line).To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HMGB1 Antibody (A00066-1, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-gtpase-hras-picoband-trade-antibody-a00114-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00114-hras-primary-antibodies-wb-testing-1.jpgAnti-GTPase HRAS Antibody Picoband® Western blot analysis of GTPase HRAS using anti-GTPase HRAS antibody (A00114). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: rat brain tissue lysates, <br>
Lane 3: rat PC-12 whole cell lysates, <br>
Lane 4: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GTPase HRAS antigen affinity purified polyclonal antibody (Catalog # A00114) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GTPase HRAS at approximately 21 kDa. The expected band size for GTPase HRAS is at 21 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ifnar1-picoband-trade-antibody-a00306-2-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00306-2-ifnar1-primary-antibodies-wb-testing-1.jpgAnti-IFNAR1 Antibody Picoband® Western blot analysis of IFNAR1 using anti-IFNAR1 antibody (A00306-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFNAR1 antigen affinity purified polyclonal antibody (Catalog # A00306-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFNAR1 at approximately 130 kDa. The expected band size for IFNAR1 is at 64 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ifngr1-picoband-trade-antibody-a01716-1-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01716-1-1-WB-anti-ifngr1-cd119-picoband-antibody.jpgAnti-IFNGR1 Antibody Picoband® Western blot analysis of IFNGR1 using anti-IFNGR1 antibody (A01716-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: HEPG2 whole cell lysates,<br>
lane 2: SKOV3 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFNGR1 antigen affinity purified polyclonal antibody (Catalog # A01716-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFNGR1 at approximately 95KD. The expected band size for IFNGR1 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01716-1-ifngr1-primary-antibodies-fc-testing-2.pngAnti-IFNGR1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-IFNGR1 antibody (A01716-1).<br>
Overlay histogram showing A549 cells stained with A01716-1 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFNGR1 Antibody (A01716-1,1μg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-il13-picoband-trade-antibody-a00077-boster.html2026-03-24T05:07:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00077-1.jpgAnti-IL13 Antibody Picoband® Western blot analysis of IL13 using anti-IL13 antibody (A00077). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: K562 whole cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL13 antigen affinity purified polyclonal antibody (Catalog # A00077) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL13 at approximately 20KD. The expected band size for IL13 is at 16KD.<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00077-2-IHC-anti-il13-picoband-antibody.jpgAnti-IL13 Antibody Picoband®<b> IHC analysis of IL13 using anti-IL13 antibody (A00077).</b><br>
IL13 was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL13 Antibody (A00077) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-islet-1-picoband-trade-antibody-a02969-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02969-1-1-WB-anti-islet-1-picoband-antibody.jpgAnti-Islet 1/ISL1 Antibody Picoband® Western blot analysis of Islet 1 using anti-Islet 1 antibody (A02969-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>
lane 1: PC12 whole cell lysates,<br>
lane 2: MCF-7 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Islet 1 antigen affinity purified polyclonal antibody (Catalog # A02969-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Islet 1 at approximately 39KD. The expected band size for Islet 1 is at 39KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02969-1-2-IHC-anti-islet-1-picoband-antibody.jpgAnti-Islet 1/ISL1 Antibody Picoband® IHC analysis of Islet 1 using anti-Islet 1 antibody (A02969-1).<br>
Islet 1 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Islet 1 Antibody (A02969-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd11a-picoband-trade-antibody-a04466-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04466-1-1-WB-anti-cd11a-picoband-antibody.jpgAnti-CD11a/ITGAL Antibody Picoband® Western blot analysis of CD11a using anti-CD11a antibody (A04466-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: JURKAT cell lysates,<br>
lane 2: CEM whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD11a antigen affinity purified polyclonal antibody (Catalog # A04466-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD11a at approximately 150KD. The expected band size for CD11a is at 129KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04466-1-cd11a-primary-antibodies-fc-testing-2.pngAnti-CD11a/ITGAL Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-CD11a antibody (A04466-1).<br>
Overlay histogram showing U937 cells stained with A04466-1 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD11a Antibody (A04466-1,1μg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
"
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04466-1-cd11a-primary-antibodies-ihc-testing-3.jpgAnti-CD11a/ITGAL Antibody Picoband® IHC analysis of CD11a using anti-CD11a antibody (A04466-1).<br> CD11a was detected in immunocytochemical section of U937 Cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1μg/ml rabbit anti-CD11a Antibody (A04466-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-jak1-picoband-trade-antibody-a00330-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00330-1-WB-anti-jak1-picoband-antibody.jpgAnti-JAK1 Antibody Picoband® Western blot analysis of JAK1 using anti-JAK1 antibody (A00330). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>
Lane 1: rat kidney tissue lysates,<br>
Lane 2: mouse kidney tissue lysates,<br>
Lane 3: HELA whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JAK1 antigen affinity purified polyclonal antibody (Catalog # A00330) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for JAK1 at approximately 133KD. The expected band size for JAK1 is at 133KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cytokeratin-18-picoband-trade-antibody-a01357-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-13287_2021_2280_fig1_html.pngAnti-Cytokeratin 18/KRT18 Antibody Picoband®Characterization of hAECs, detection of the survival hAECs encapsulated in SA-BG, and schematic illustration of the surgical procedure. a The morphology of cultured hAECs was observed under a microscope. Scale bar 100 μm. b Flow cytometry analysis of cell surface markers on hAECs. The isotypes (ISO) of SSEA4 and CD324 were used as negative controls. c Immunostaining images showed the high expression of epithelial marker (CK18) and stem cell marker (TRA-1-60). Scale bar 100 μm. d The fabrication method of SA-BG-loaded hAECs and CM. e Representative live/dead images of hAECs encapsulated in SA-BG at days 1, 7, 10, and 14, respectively. hAECs encapsulated in SA-BG treated with 70% alcohol were positive for PI. Live cells were shown green color and dead cells were red color. Scale bar 100 μm. f Bright field image of hAECs capsulated in SA-BG at day 1 ( a ) and 14 ( b ). Scale bar 100 μm. g The percentage of live cells to total cells. h Schematic of the experimental procedure for the transplantation of SA-BG-loaded hAECs/CM into mice with chemotherapy-induced POF <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-021-02280-2'>33794993</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-13287_2021_2280_fig6_html.pngAnti-Cytokeratin 18/KRT18 Antibody Picoband®The effect of SA-BG extracts on the biological characterization and paracrine capacity of hAECs. a The viability of hAECs cultured with SA-BG extracts was detected by CCK-8 assay. b – d Expression of stemness (Oct-4 and Nanog) and epithelial (CK18) genes of hAECs cultured with SA-BG extracts at different time points. e , f The results of cytokine array of CM from hAECs and SA-BG extract-treated hAECs, respectively. g Column displayed the higher expression of cytokines in the SA-BG extract-treated hAECs than in the control hAECs. h , i The results of quantification of angiogenic factors released from SA-BG extract-treated hAECs and control hAECs by ELISA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-021-02280-2'>33794993</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-13287_2021_2260_fig1_html.pngAnti-Cytokeratin 18/KRT18 Antibody Picoband®hAECs express specific surface markers and have stem cell characteristics with low immunogenicity. a hAECs presented an epithelial morphology under bright-field microscopy. Scale bar = 100 μm. b hAECs were labeled with CFSE to track implanted cells. The expression rate of green fluorescence staining was nearly 100%. Scale bar = 100 μm. c-f By flow cytometry, hAECs were positive for stem cell marker SSEA-4 ( c ) and epithelial marker CD324 ( d ) and were negative for mesenchymal markers CD146 ( e ) and HLA-DR ( f ). g Immunofluorescence staining for CK18 (an epithelial marker) expression and vimentin (a mesenchymal marker) in hAECs. Scale bar = 200 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-021-02260-6'>33762002</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-wb-testing-1_1.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®Western blot analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: human CACO2 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT18 antigen affinity purified polyclonal antibody (A01357-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT18 at approximately 48 kDa. The expected band size for KRT18 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-5.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-ihc-testing-6.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IHC analysis of KRT18 using anti-KRT18 antibody (A01357-1). <br>KRT18 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-if-testing-1.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IF analysis of KRT18 using anti-KRT18 antibody (A01357-1) <br> KRT18 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Cy3 Conjugated Avidin (BA1037). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-if-testing-2.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IF analysis of KRT18 using anti-KRT18 antibody (A01357-1) <br> KRT18 was detected in paraffin-embedded section of human gastric cancer tissues. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Cy3 Conjugated Avidin (BA1037). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-if-testing-3.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IF analysis of KRT18 using anti-KRT18 antibody (A01357-1) <br> KRT18 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Cy3 Conjugated Avidin (BA1037). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-if-testing-4.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IF analysis of KRT18 using anti-KRT18 antibody (A01357-1) <br> KRT18 was detected in paraffin-embedded section of human prostatic cancer tissues. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Cy3 Conjugated Avidin (BA1037). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-if-testing-5.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®IF analysis of KRT18 using anti-KRT18 antibody (A01357-1) <br> KRT18 was detected in paraffin-embedded section of human ovarian cancer tissues. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-KRT18 Antibody (A01357-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Cy3 Conjugated Avidin (BA1037). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01357-1-krt18-primary-antibodies-fcm-testing-1.jpgAnti-Cytokeratin 18/KRT18 Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-KRT18 antibody (A01357-1). <br>
Overlay histogram showing A431 cells stained with A01357-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-KRT18 Antibody (A01357-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-lbp-picoband-trade-antibody-a00809-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00809-1-1-WB-anti-lbp-picoband-antibody.jpgAnti-LBP Antibody Picoband® Western blot analysis of LBP using anti-LBP antibody (A00809-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat thymus tissue lysates,<br>
Lane 2: mouse thymus tissue lysates,<br>
Lane 3: HELA whole cell lysates,<br>
Lane 4: K562 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LBP antigen affinity purified polyclonal antibody (Catalog # A00809-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LBP at approximately 65KD. The expected band size for LBP is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-leptin-receptor-antibody-a00350-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00350-lepr-primary-antibodies-ihc-testing-1.jpgAnti-Leptin Receptor/LEPR Antibody IHC analysis of Leptin Receptor/LEPR using anti-Leptin Receptor/LEPR antibody (A00350). <br>
Leptin Receptor/LEPR was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Leptin Receptor/LEPR Antibody (A00350) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00350-lepr-primary-antibodies-ihc-testing-3.jpgAnti-Leptin Receptor/LEPR AntibodyIHC analysis of LEPR using anti-LEPR antibody (A00350). <br>LEPR was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEPR Antibody (A00350) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00350-fendo-09-00476-g006.jpgAnti-Leptin Receptor/LEPR AntibodyEffects of long-term L -serine administration on the leptin signaling pathway in aging mice. (A–E) LepRb expression as determined by immunohistochemistry; (F) leptin content in the hypothalamus; (G) relative LepRb mRNA expression; (H,I) relative pSTAT3 protein expression. Aged, untreated control mice; Low-ser, mice fed with 0.1% (wt/vol) L -serine dissolved in the drinking water; Middle-ser, mice fed with 0.2% (wt/vol) L -serine dissolved in the drinking water; High-ser, mice fed with 0.5% (wt/vol) L -serine dissolved in the drinking water. Young, adult male mice at the age of 18 months. Arrow (yellow), expression of LepRb protein; LepRb, leptin receptor. Values are expressed as mean ± SEM, n = 3 for the statistical analysis of western blotting data and n = 8 for the statistical analysis of other data; a, b Means of the bars with different letters were significantly different among groups ( p < 0.05).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2018.00476/full'>30190704</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00350-lepr-primary-antibodies-ihc-testing-2.jpgAnti-Leptin Receptor/LEPR Antibody IHC analysis of Leptin Receptor/LEPR using anti-Leptin Receptor/LEPR antibody (A00350). <br>
Leptin Receptor/LEPR was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Leptin Receptor/LEPR Antibody (A00350) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-lmo1-picoband-trade-antibody-a06093-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a06093-1-1-WB-anti-lmo1-picoband-antibody.jpgAnti-LMO1 Antibody Picoband® Western blot analysis of LMO1 using anti-LMO1 antibody (A06093-1).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysate,<br>
lane 2: NIH3T3 whole cell lysates,<br>
lane 3: HELA whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMO1 antigen affinity purified polyclonal antibody (Catalog # A06093-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMO1 at approximately 18KD. The expected band size for LMO1 is at 18KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mc1-receptor-picoband-trade-antibody-a00855-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00855-1-1-WB-anti-mc1-receptor-picoband-antibody.jpgAnti-MC1 Receptor/MC1R Antibody Picoband® Western blot analysis of MC1 using anti-MC1 antibody (A00855-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: PC12 whole cell lysates,<br>
Lane 2: HEPA1-6 whole cell lysates,<br>
Lane 3: HELA whole cell lysates,<br>
Lane 4: A375 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MC1 antigen affinity purified polyclonal antibody (Catalog # A00855-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MC1 at approximately 35KD. The expected band size for MC1 is at 35KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mc2-receptor-picoband-trade-antibody-a02306-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02306-1-mc2r-primary-antibodies-wb-testing-1.jpgAnti-MC2 receptor/MC2R Antibody Picoband®Western blot analysis of MC2R using anti-MC2R antibody (A02306-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MC2R antigen affinity purified polyclonal antibody (A02306-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MC2R at approximately 34 kDa. The expected band size for MC2R is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02306-1-mc2r-primary-antibodies-fcm-testing-1.jpgAnti-MC2 receptor/MC2R Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-MC2R antibody (A02306-1). <br>
Overlay histogram showing U251 cells stained with A02306-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MC2R Antibody (A02306-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp2-picoband-trade-antibody-a00286-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00286-fig-1-1x.jpgAnti-MMP2 Antibody Picoband®Regulation of FLT on xenograft EMS. (A) Ectopic volume was detected by vernier caliper in xenograft EMS model. GTN was performed as positive control. (B) Weight of nude mice was measured every 7 days during 28 days’ treatment. * P < 0.05 to pretreatment. Columns, mean ( n = 6). (C–E) Ectopic endometrium of EMS and FLT groups were collected for RNA isolation. Eutopic endometrium of C3H mice without transplantation were supplied as the control group. mRNA levels of MMP-2, MMP-9, and TIMP-1 were detected by qPCR in different groups. (F–I) Protein levels of MMP-2, MMP-9, and TIMP-1 were measured by western blotting, and the ratio of MMP-2, MMP-9, and TIMP-1 with β-actin were shown. # P < 0.05 to control, ## P < 0.01 to control, * P < 0.05 to EMS, ** P < 0.01 to EMS. Columns, mean ( n = 3). Bars, SD. EMS, endometriosis; FLT, ferulic acid, ligustrazine and tetrahydropalmatine; GTN, gestrinone. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/11664/'>34249506</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00286-fig-5-1x.jpgAnti-MMP2 Antibody Picoband®Gene expression of MMP/TIMP signaling adjusted by FLT for 24h. The mRNA levels of MMP-2, MMP-9, and TIMP-1 were detected by qPCR in hEM15A (A–C) and HEC1-B (D–F) cells. * P < 0.05 to control group, ** P < 0.01 to control group. Columns, mean ( n = 3). Bars, SD. FLT, ferulic acid, ligustrazine and tetrahydropalmatine. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/11664/'>34249506</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00286-fig-6-1x.jpgAnti-MMP2 Antibody Picoband®Modification of MMP/TIMP signaling protein treating with FLT for 24h. Protein levels of MMP-2, MMP-9, and TIMP-1 were detected by western blot in hEM15A (A–D) and HEC1-B (E–H) cells. The ratio of MMP-2, MMP-9, and TIMP-1 with β-actin were shown. * P < 0.05 to control group, ** P < 0.01 to control group. Columns, mean ( n = 3). Bars, SD. FLT, ferulic acid, ligustrazine and tetrahydropalmatine. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/11664/'>34249506</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00286-fphar-09-00811-g006.jpgAnti-MMP2 Antibody Picoband®Effect of JFS on invasion and metastasis. (A–C) The mRNA levels of MMP-2, MMP-9, and TIMP-1 were detected by qPCR in different groups. (D–G) The protein levels of MMP-2, MMP-9, and TIMP-1 were detected by western blotting, and the ratio of MMP-2, MMP-9, and TIMP-1 with β-actin were shown. # P < 0.05 to control, ## P < 0.01 to control, ∗ P < 0.05 to EMS, ∗∗ P < 0.01 to EMS. Columns, mean ( n = 3). Bars, SD. EMS, endometriosis; JFS, Jiawei Foshou San .<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00811/full'>30093862</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00286-mmp2-primary-antibodies-wb-testing-1.jpgAnti-MMP2 Antibody Picoband® Western blot analysis of MMP2 using anti-MMP2 antibody (A00286). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U87 whole cell lysates, <br>
Lane 2: rat H9C2 whole cell lysates, <br>
Lane 3: mouse 3T3-L1 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP2 antigen affinity purified polyclonal antibody (A00286) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MMP2 at approximately 72 kDa. The expected band size for MMP2 is at 74 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-mc3-receptor-picoband-trade-antibody-a02841-2-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02841-2-mc3r-primary-antibodies-wb-testing-1.jpgAnti-MC3 Receptor/MC3R Antibody Picoband®Western blot analysis of MC3R using anti-MC3R antibody (A02841-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MC3R antigen affinity purified polyclonal antibody (A02841-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MC3R at approximately 42 kDa. The expected band size for MC3R is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02841-2-mc3r-primary-antibodies-ihc-testing-1.jpgAnti-MC3 Receptor/MC3R Antibody Picoband®IHC analysis of MC3R using anti-MC3R antibody (A02841-2). <br>MC3R was detected in a paraffin-embedded section of human hippocampus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MC3R Antibody (A02841-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02841-2-mc3r-primary-antibodies-ihc-testing-2.jpgAnti-MC3 Receptor/MC3R Antibody Picoband®IHC analysis of MC3R using anti-MC3R antibody (A02841-2). <br>MC3R was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MC3R Antibody (A02841-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02841-2-mc3r-primary-antibodies-ihc-testing-3.jpgAnti-MC3 Receptor/MC3R Antibody Picoband®IHC analysis of MC3R using anti-MC3R antibody (A02841-2). <br>MC3R was detected in a paraffin-embedded section of rat hippocampus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MC3R Antibody (A02841-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02841-2-mc3r-primary-antibodies-ihc-testing-4.jpgAnti-MC3 Receptor/MC3R Antibody Picoband®IHC analysis of MC3R using anti-MC3R antibody (A02841-2). <br>MC3R was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MC3R Antibody (A02841-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp11-picoband-trade-antibody-a04490-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04490-1-1-WB-anti-mmp11-picoband-antibody.jpgAnti-MMP11 Antibody Picoband® Western blot analysis of MMP11 using anti-MMP11 antibody (A04490-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat spleen tissue lysate,<br>
lane 2: MM231 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP11 antigen affinity purified polyclonal antibody (Catalog # A04490-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP11 at approximately 55KD. The expected band size for MMP11 is at 55KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04490-1-2-IHC-anti-mmp11-picoband-antibody.jpgAnti-MMP11 Antibody Picoband® IHC analysis of MMP11 using anti-MMP11 antibody (A04490-1).<br>
MMP11 was detected in paraffin-embedded section of mouse spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP11 Antibody (A04490-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04490-1-3-IHC-anti-mmp11-picoband-antibody.jpgAnti-MMP11 Antibody Picoband® IHC analysis of MMP11 using anti-MMP11 antibody (A04490-1).<br>
MMP11 was detected in paraffin-embedded section of rat spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP11 Antibody (A04490-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04490-1-4-IHC-anti-mmp11-picoband-antibody.jpgAnti-MMP11 Antibody Picoband® IHC analysis of MMP11 using anti-MMP11 antibody (A04490-1).<br>
MMP11 was detected in paraffin-embedded section of human appendicitis tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP11 Antibody (A04490-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-narg1-picoband-trade-antibody-a05636-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05636-1-naa15-primary-antibodies-wb-testing-1.jpgAnti-NARG1/NAA15 Antibody Picoband®Western blot analysis of NARG1/NAA15 using anti-NARG1/NAA15 antibody (A05636-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: mouse brain tissue lysates,<br>
Lane 5: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NARG1/NAA15 antigen affinity purified polyclonal antibody (A05636-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NARG1/NAA15 at approximately 101 kDa. The expected band size for NARG1/NAA15 is at 101 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05636-1-naa15-primary-antibodies-ihc-testing-1.jpgAnti-NARG1/NAA15 Antibody Picoband®IHC analysis of NARG1/NAA15 using anti-NARG1/NAA15 antibody (A05636-1). <br>NARG1/NAA15 was detected in a paraffin-embedded section of human gastric cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NARG1/NAA15 Antibody (A05636-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-nanog-picoband-trade-antibody-a00153-3-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00153-3-1-WB-anti-nanog-picoband-antibody.jpgAnti-Nanog Antibody Picoband® Western blot analysis of Nanog using anti-Nanog antibody (A00153-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat ovary tissue lysates,<br>
Lane 2: mouse ovary tissue lysates,<br>
Lane 3: MCF-7 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Nanog antigen affinity purified polyclonal antibody (Catalog # A00153-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Nanog at approximately 48KD. The expected band size for Nanog is at 34KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00153-3-2.pngAnti-Nanog Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-Nanog antibody (A00153-3). <br> Overlay histogram showing A549 cells stained with A00153-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Nanog Antibody (A00153-3,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00153-3-3.pngAnti-Nanog Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-Nanog antibody (A00153-3). <br> Overlay histogram showing PC-3 cells stained with A00153-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Nanog Antibody (A00153-3,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-nat1-picoband-trade-antibody-a01386-1-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01386-1-1-WB-anti-nat1-picoband-antibody.jpgAnti-NAT1 Antibody Picoband® Western blot analysis of NAT1 using anti-NAT1 antibody (A01386-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: A431 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAT1 antigen affinity purified polyclonal antibody (Catalog # A01386-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAT1 at approximately 34KD. The expected band size for NAT1 is at 34KD.
https://www.bosterbio.com/products/primary-antibodies/anti-nnos-neuronal-picoband-trade-antibody-a01070-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01070-1-WB-anti-nnos-neuronal-picoband-antibody.jpgAnti-nNOS (neuronal)/NOS1 Antibody Picoband® Western blot analysis of nNOS using anti-nNOS antibody (A01070). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
lane 1: rat brain tissue lysates,<br>
lane 2: mouse brain tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-nNOS antigen affinity purified polyclonal antibody (Catalog # A01070) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for nNOS at approximately 160KD. The expected band size for nNOS is at 160KD.
https://www.bosterbio.com/products/primary-antibodies/anti-inos-picoband-trade-antibody-a00368-boster.html2026-03-24T05:07:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00368-nos2-primary-antibodies-wb-testing-1.jpgAnti-iNOS/NOS2 Antibody Picoband® Western blot analysis of NOS2 using anti-NOS2 antibody (A00368). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOS2 antigen affinity purified polyclonal antibody (Catalog # A00368) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOS2 at approximately 131 kDa. The expected band size for NOS2 is at 131 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00368-nos2-primary-antibodies-ihc-testing-1.jpgAnti-iNOS/NOS2 Antibody Picoband®IHC analysis of iNOS/NOS2 using anti-iNOS/NOS2 antibody (A00368). <br>iNOS/NOS2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-iNOS/NOS2 Antibody (A00368) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00368-fphar-08-00044-g006.jpgAnti-iNOS/NOS2 Antibody Picoband®Celastrol inhibited inducible nitric oxide synthase (iNOS) expression and activation of NF-κB in optic nerve in EAE rats. (A) IHC staining of iNOS in optic nerve. (B) Quantification of iNOS-positive areas. (C) Quantitative real-time PCR analysis of iNOS expression. (D) Western blot analysis of iNOS expression. (E–G) Western blot analysis of IκBα, p65 and p-p65 expression, respectively. Treatment of celastrol reduced expression of iNOS and inhibited the activation of NF-κB in optic nerve in EAE rats. Scale bar: 100 μm. Data were shown as mean ± SD, n = 5. ∗∗ P < 0.01 versus control group, ## P < 0.01 versus EAE group, †† P < 0.01 versus low dosage of celastrol group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00044/full'>28239352</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-nephrin-picoband-trade-antibody-a01991-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01991-fphar-15-1447249-g006.jpgAnti-Nephrin/NPHS1 Antibody Picoband®Shensu IV regulates the PI3K/AKT signaling pathway through H2S. (A) The effects of Shensu IV and NaHS on the mRNA expression of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, and AKT in renal tissue of PAN rats were analyzed by RT-qPCR. (B) Western blot analysis of the effects of Shensu IV and NaHS on the protein levels of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, p-PI3K,AKT,p-AKT in renal tissue of PAN rats. * P < 0.05, ** P < 0.01, *** P < 0.001. Abbreviations: CD2AP, CD2-associated protein; CBS, Cystathionine β-synthase; CSE, Cystathionine γ-lyase; PI3K, Phosphoinositide 3-Kinase; AKT, Protein Kinase B.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1447249/full'>39720588</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01991-fphar-15-1447249-g008.jpgAnti-Nephrin/NPHS1 Antibody Picoband®Shensu IV regulates the PI3K/AKT signaling pathway through H2S in podocytes. (A) The effects of Shensu IV and NaHS on the mRNA expression of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, and AKT in podocytes were analyzed by RT-qPCR. (B) Western blot analysis of the effects of Shensu IV and NaHS on the protein levels of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, p-PI3K,AKT,p-AKT in PAN-induced podocyocytes. * P < 0.05, ** P < 0.01, *** P < 0.001. Abbreviations: CD2AP, CD2-associated protein; CBS, Cystathionine β-synthase; CSE, Cystathionine γ-lyase; PI3K, Phosphoinositide 3-Kinase; AKT, Protein Kinase B.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1447249/full'>39720588</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01991-nephrin-primary-antibodies-wb-testing-1.jpgAnti-Nephrin/NPHS1 Antibody Picoband® Western blot analysis of Nephrin using anti-Nephrin antibody (A01991). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat kidney tissue lysates, <br>
Lane 2: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Nephrin antigen affinity purified polyclonal antibody (Catalog # A01991) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Nephrin at approximately 185 kDa. The expected band size for Nephrin is at 135 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01991-nephrin-primary-antibodies-ihc-testing-2.jpgAnti-Nephrin/NPHS1 Antibody Picoband® IHC analysis of Nephrin using anti-Nephrin antibody (A01991). <br>
Nephrin was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Nephrin Antibody (A01991) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01991-nephrin-primary-antibodies-ihc-testing-3.jpgAnti-Nephrin/NPHS1 Antibody Picoband® IHC analysis of Nephrin using anti-Nephrin antibody (A01991). <br>
Nephrin was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Nephrin Antibody (A01991) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0003) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-pde5a-picoband-trade-antibody-a02490-2-boster.html2026-04-01T05:01:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02490-2-pde5a-primary-antibodies-wb-testing-1.jpgAnti-PDE5A Antibody Picoband®Western blot analysis of PDE5A using anti-PDE5A antibody (A02490-2). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat lung tissue lysates, <br>
Lane 2: mouse lung tissue lysates. <br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDE5A antigen affinity purified polyclonal antibody (A02490-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDE5A at approximately 100 kDa. The expected band size for PDE5A is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02490-2-pde5a-primary-antibodies-ihc-testing-1.jpgAnti-PDE5A Antibody Picoband®IHC analysis of PDE5A using anti-PDE5A antibody (A02490-2). <br>PDE5A was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDE5A Antibody (A02490-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-periplakin-picoband-trade-antibody-a02098-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-fcm-testing-6.jpgAnti-Periplakin/PPL Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Periplakin antibody (A02098-1).<br>Overlay histogram showing U20S cells stained with A02098-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Periplakin Antibody (A02098-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-wb-testing-1.jpgAnti-Periplakin/PPL Antibody Picoband® Western blot analysis of Periplakin using anti-Periplakin antibody (A02098-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human A549 whole cell lysates, <br>
Lane 3: human SW620 whole cell lysates, <br>
Lane 4: human HepG2 whole cell lysates, <br>
Lane 5: human SK-OV-3 whole cell lysates,<br>
Lane 6: human PANC-1 whole cell lysates, <br>
Lane 7: human SGC-7801 whole cell lysates, <br>
Lane 8: rat lung tissue lysates, <br>
Lane 9: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Periplakin antigen affinity purified polyclonal antibody (Catalog # A02098-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Periplakin at approximately 202 kDa. The expected band size for Periplakin is at 205 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-ihc-testing-2.jpgAnti-Periplakin/PPL Antibody Picoband® IHC analysis of Periplakin using anti-Periplakin antibody (A02098-1). <br>
Periplakin was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Periplakin Antibody (A02098-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-ihc-testing-3.jpgAnti-Periplakin/PPL Antibody Picoband® IHC analysis of Periplakin using anti-Periplakin antibody (A02098-1). <br>
Periplakin was detected in a paraffin-embedded section of human oesophagus squama cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Periplakin Antibody (A02098-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-ihc-testing-4.jpgAnti-Periplakin/PPL Antibody Picoband® IHC analysis of Periplakin using anti-Periplakin antibody (A02098-1). <br>
Periplakin was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Periplakin Antibody (A02098-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1023) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02098-1-periplakin-primary-antibodies-if-testing-5.jpgAnti-Periplakin/PPL Antibody Picoband® IF analysis of Periplakin using anti-Periplakin antibody (A02098-1). <br>
Periplakin was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-Periplakin Antibody (A02098-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-prkar1a-picoband-trade-antibody-a00699-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00699-1-1-WB-anti-prkar1a-picoband-antibody.jpgAnti-Protein Kinase A regulatory subunit I alpha/PRKAR1A Antibody Picoband® Western blot analysis of PRKAR1A using anti-PRKAR1A antibody (A00699-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat thymus tissue lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKAR1A antigen affinity purified polyclonal antibody (Catalog # A00699-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRKAR1A at approximately 48 kDa. The expected band size for PRKAR1A is at 43KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00699-1-2-IHC-anti-prkar1a-picoband-antibody.jpgAnti-Protein Kinase A regulatory subunit I alpha/PRKAR1A Antibody Picoband® IHC analysis of PRKAR1A using anti-PRKAR1A antibody (A00699-1). <br>
PRKAR1A was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-PRKAR1A Antibody (A00699-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00699-1-3-IHC-anti-prkar1a-picoband-antibody.jpgAnti-Protein Kinase A regulatory subunit I alpha/PRKAR1A Antibody Picoband® IHC analysis of PRKAR1A using anti-PRKAR1A antibody (A00699-1). <br>
PRKAR1A was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-PRKAR1A Antibody (A00699-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00699-1-4-IHC-anti-prkar1a-picoband-antibody.jpgAnti-Protein Kinase A regulatory subunit I alpha/PRKAR1A Antibody Picoband® IHC analysis of PRKAR1A using anti-PRKAR1A antibody (A00699-1). <br>
PRKAR1A was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-PRKAR1A Antibody (A00699-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-serpina5-picoband-trade-antibody-a01916-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01916-1-1-WB-anti-serpina5-protein-c-inhibitor-picoband-antibody.jpgAnti-Protein C inhibitor/SERPINA5 Antibody Picoband® Western blot analysis of SERPINA5 using anti-SERPINA5 antibody (A01916-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: human SKOV3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPINA5 antigen affinity purified polyclonal antibody (Catalog # A01916-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SERPINA5 at approximately 46 kDa. The expected band size for SERPINA5 is at 46KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01916-1-2-IHC-anti-serpina5-protein-c-inhibitor-picoband-antibody.jpgAnti-Protein C inhibitor/SERPINA5 Antibody Picoband® IHC analysis of SERPINA5 using anti-SERPINA5 antibody (A01916-1). <br>
SERPINA5 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-SERPINA5 Antibody (A01916-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01916-1-3-IHC-anti-serpina5-protein-c-inhibitor-picoband-antibody.jpgAnti-Protein C inhibitor/SERPINA5 Antibody Picoband® IHC analysis of SERPINA5 using anti-SERPINA5 antibody (A01916-1). <br>
SERPINA5 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-SERPINA5 Antibody (A01916-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tecta-picoband-trade-antibody-a02840-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02840-1-WB-anti-tecta-tectorin-alpha-picoband-antibody.jpgAnti-TECTA Antibody Picoband® Western blot analysis of TECTA using anti-TECTA antibody (A02840). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat testis tissue lysates,<br>
Lane 2: mouse HEPA1-6 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TECTA antigen affinity purified polyclonal antibody (Catalog # A02840) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TECTA at approximately 239 kDa. The expected band size for TECTA is at 239KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02840-2-IHC-anti-tecta-tectorin-alpha-picoband-antibody.jpgAnti-TECTA Antibody Picoband® IHC analysis of TECTA using anti-TECTA antibody (A02840). <br>
TECTA was detected in a paraffin-embedded section of human intetsinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-TECTA Antibody (A02840) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02840-3-IHC-anti-tecta-tectorin-alpha-picoband-antibody.jpgAnti-TECTA Antibody Picoband® IHC analysis of TECTA using anti-TECTA antibody (A02840). <br>
TECTA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-TECTA Antibody (A02840) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02840-4-IHC-anti-tecta-tectorin-alpha-picoband-antibody.jpgAnti-TECTA Antibody Picoband® IHC analysis of TECTA using anti-TECTA antibody (A02840). <br>
TECTA was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-TECTA Antibody (A02840) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-trf2-picoband-trade-antibody-a00650-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00650-1-1-WB-anti-trf2-picoband-antibody.jpgAnti-TRF2/TERF2 Antibody Picoband® Western blot analysis of TRF2 using anti-TRF2 antibody (A00650-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat thymus tissue lysates,<br>
Lane 2: human COLO320 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRF2 antigen affinity purified polyclonal antibody (Catalog # A00650-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRF2 at approximately 75 kDa. The expected band size for TRF2 is at 59KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00650-1-2-IHC-anti-trf2-picoband-antibody.jpgAnti-TRF2/TERF2 Antibody Picoband® IHC analysis of TRF2 using anti-TRF2 antibody (A00650-1). <br>
TRF2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-TRF2 Antibody (A00650-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00650-1-3-IHC-anti-trf2-picoband-antibody.jpgAnti-TRF2/TERF2 Antibody Picoband® IHC analysis of TRF2 using anti-TRF2 antibody (A00650-1). <br>
TRF2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-TRF2 Antibody (A00650-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tnf-alpha-picoband-trade-antibody-a00002-2-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00002-2-1-WB-anti-tnf-alpha-picoband-antibody.jpgAnti-TNF alpha Antibody Picoband®<b> Western blot analysis of TNF alpha using anti-TNF alpha antibody (A00002-2). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: mouse thymus tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNF alpha antigen affinity purified polyclonal antibody (Catalog # A00002-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNF alpha at approximately 25KD. The expected band size for TNF alpha is at 25KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00002-2-12276_2021_702_fig4_html.pngAnti-TNF alpha Antibody Picoband®Inflammation response were reduced by NLRC4 siRNA after ICH. a – g , j Western blot assay to detect NLRC4, pNLRC4, Pro-IL-1β, IL-1β, Pro-caspase-1, caspase-1, Pro-IL-18, IL-18, TNF-α, and IL-6, ( k , l ) ELISA for IL–18 and IL–1β ( h , i ) Immunostaining for MPO-positive cells (×400 and ×200) at peri-hematoma area in sham, ICH, negative control siRNA, and NLRC4 siRNA groups at 72 h after ICH (six rats for each group). * P < 0.05, compared with ICH. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs12276-021-00702-y'>34848837</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-tsg6-antibody-a03433-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03433-1-1-WB-anti-tsg6-antibody.jpgAnti-TSG6/TNFAIP6 Antibody Picoband® Western blot analysis of TSG6 using anti-TSG6 antibody (A03433-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: human Hela whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSG6 antigen affinity purified polyclonal antibody (Catalog # A03433-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSG6 at approximately 31 kDa. A specific band was detected for TSG6 at approximately 31 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-dr5-picoband-trade-antibody-a00410-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-dr5-primary-antibodies-wb-testing-1.jpgAnti-DR5/TNFRSF10B Antibody Picoband®Western blot analysis of DR5 using anti-DR5 antibody (A00410). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DR5 antigen affinity purified polyclonal antibody (A00410) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DR5 at approximately 38, 48 kDa. The expected band size for DR5 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00410-2-IHC-anti-dr5-picoband-antibody.jpgAnti-DR5/TNFRSF10B Antibody Picoband® IHC analysis of DR5 using anti-DR5 antibody (A00410). <br>
DR5 was detected in a paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-DR5 Antibody (A00410) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-oncotarget-05-4959-g001.jpgAnti-DR5/TNFRSF10B Antibody Picoband®The cytotoxic effect of TRAIL on human HCC and GC cell lines. (A) Detection of DNA fragmentation by DNA ladder assay. LH86, Huh7, HLCZ01 and HLCZ02 cells were exposed to TRAIL for 4 hours. 2 μg of cellular DNA was separated on 1% agarose gel at 50V for one hour. The data are one representative of three independent experiments. (B) Detection of apoptosis by flow cytometry and western blot. LH86, Huh7, HLCZ01, HLCZ02, HGC-27 and BGC-823 cells were exposed to TRAIL for 4 hours. Samples were analyzed on a FACS Caliber Cytometer. A minimum of 30000 events per samples were acquired, and subsequently analyzed with CellQuest software. The results are the average of at least three independent experiments. (C) Cleaved PARP was detected by western blot. β–actin was used as control. The data are one representative of three independent experiments. (D) Detection of DR4 and DR5 in HCC and GC cell lines by real-time PCR and western blot analysis. DR4 or DR5 mRNA were detected by real-time RT-PCR and normalized with GAPDH respectively. The results are the average of three independent experiments performed in triplicate. DR4 and DR5 protein was detected by western blot. The data are one representative of three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4148114/&orig_host=www.ncbi.nlm.nih.gov'>24970806</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00410-3-IHC-anti-dr5-picoband-antibody.jpgAnti-DR5/TNFRSF10B Antibody Picoband® IHC analysis of DR5 using anti-DR5 antibody (A00410). <br>
DR5 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-DR5 Antibody (A00410) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00410-4-IHC-anti-dr5-picoband-antibody.jpgAnti-DR5/TNFRSF10B Antibody Picoband® IHC analysis of DR5 using anti-DR5 antibody (A00410). <br>
DR5 was detected in a paraffin-embedded section of human intetsinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-DR5 Antibody (A00410) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-5.pngAnti-DR5/TNFRSF10B Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-DR5 antibody (A00410). <br> Overlay histogram showing A549 cells stained with A00410 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DR5 Antibody (A00410,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-6.pngAnti-DR5/TNFRSF10B Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-DR5 antibody (A00410). <br> Overlay histogram showing U87 cells stained with A00410 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DR5 Antibody (A00410,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-7.pngAnti-DR5/TNFRSF10B Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-DR5 antibody (A00410). Overlay histogram showing THP-1 cells stained with A00410 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DR5 Antibody (A00410,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. FITC conjugated goat anti-rabbit IgG (BA1105, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00410-8.pngAnti-DR5/TNFRSF10B Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-DR5 antibody (A00410). Overlay histogram showing PC-3 cells stained with A00410 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DR5 Antibody (A00410,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. FITC conjugated goat anti-rabbit IgG (BA1105, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-treml1-picoband-trade-antibody-a07682-2-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07682-2-1-western-blotting_1.jpgAnti-TREML1 Antibody Picoband® Western blot analysis of TREML1 using anti-TREML1 antibody (A07682-2).<br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br> Lane 1: human THP-1 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TREML1 antigen affinity purified polyclonal antibody (Catalog # A07682-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TREML1 at approximately 33KD. The expected band size for TREML1 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tub-1-picoband-trade-antibody-a02917-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02917-1-1-WB-anti-tub-1-picoband-antibody.jpgAnti-TUB 1 Antibody Picoband® Western blot analysis of TUB 1 using anti-TUB 1 antibody (A02917-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human COLO320 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUB 1 antigen affinity purified polyclonal antibody (Catalog # A02917-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TUB 1 at approximately 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02917-1-2.pngAnti-TUB 1 Antibody Picoband® Flow Cytometry analysis of HeLa cells using anti-TUB 1 antibody (A02917-1). <br> Overlay histogram showing HeLa cells stained with A02917-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TUB 1 Antibody (A02917-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-antibody-a00045-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00045-1-WB-anti-vegf-antibody.jpgAnti-VEGF/Vegfa Antibody Picoband® Western blot analysis of VEGF using anti-VEGF antibody (A00045). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF antigen affinity purified polyclonal antibody (Catalog # A00045) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF at approximately 27 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-aprt-picoband-trade-antibody-a02721-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02721-aprt-primary-antibodies-if-testing-2.jpgAnti-APRT Antibody Picoband® IF analysis of APRT using anti-APRT antibody (A02721). <br>
APRT was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-APRT Antibody (A02721) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02721-aprt-primary-antibodies-fcm-testing-3.jpgAnti-APRT Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-APRT antibody (A02721). <br>Overlay histogram showing A549 cells stained with A02721 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-APRT Antibody (A02721, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02721-aprt-primary-antibodies-wb-testing-1.jpgAnti-APRT Antibody Picoband® Western blot analysis of APRT using anti-APRT antibody (A02721). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates, <br>
Lane 2: human A549 whole cell lysates, <br>
Lane 3: human K562 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APRT antigen affinity purified polyclonal antibody (Catalog # A02721) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APRT at approximately 20 kDa. The expected band size for APRT is at 19 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-dbi-picoband-trade-antibody-a01267-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-dbi-primary-antibodies-wb-testing-1.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® Western blot analysis of DBI using anti-DBI antibody (A01267). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human COLO320 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DBI antigen affinity purified polyclonal antibody (Catalog # A01267) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DBI at approximately 10 kDa. The expected band size for DBI is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01267-2_1-IHC-anti-dbi-picoband-antibody.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® IHC analysis of DBI using anti-DBI antibody (A01267). <br> DBI was detected in paraffin-embedded section of human prostatic cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-DBI Antibody (A01267) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01267-3_1-IHC-anti-dbi-picoband-antibody.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® IHC analysis of DBI using anti-DBI antibody (A01267).<br> DBI was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-DBI Antibody (A01267) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-dbi-primary-antibodies-fc-testing-4.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-DBI antibody (A01267). <br>Overlay histogram showing MCF-7 cells stained with A01267 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DBI Antibody (A01267,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-dbi-primary-antibodies-fc-testing-5.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-DBI antibody (A01267). <br>Overlay histogram showing PC-3 cells stained with A01267 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DBI Antibody (A01267,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-dbi-primary-antibodies-fc-testing-6.pngAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-DBI antibody (A01267). <br> Overlay histogram showing THP-1 cells stained with A01267 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DBI Antibody (A01267,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-dbi-primary-antibodies-if-testing-7.jpgAnti-Diazepam Binding Inhibitor/DBI Antibody Picoband® IF analysis of DBI using anti-DBI antibody (A01267). <br> DBI was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-DBI Antibody (A01267) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-gaa-picoband-trade-antibody-a01548-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01548-1.jpgAnti-GAA Antibody Picoband® Western blot analysis of GAA using anti-GAA antibody (A01548). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human A549 whole cell lysates, <br> Lane 2: human HepG2 whole cell lysates, <br> Lane 3: human HEK293 whole cell lysates, <br> Lane 4: human PC-3 whole cell lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAA antigen affinity purified polyclonal antibody (Catalog # A01548) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAA at approximately 110,95,76,70KD. The expected band size for GAA is at 110,95,76,70KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01548-2_1-IHC-anti-gaa-lyag-picoband-antibody.jpgAnti-GAA Antibody Picoband® IHC analysis of GAA using anti-GAA antibody (A01548).<br>
GAA was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAA Antibody (A01548) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01548-3_1-IHC-anti-gaa-lyag-picoband-antibody.jpgAnti-GAA Antibody Picoband® IHC analysis of GAA using anti-GAA antibody (A01548).<br>
GAA was detected in paraffin-embedded section of human prostatic cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAA Antibody (A01548) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-fibrinogen-alpha-chain-picoband-trade-antibody-a00816-1-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00816-1-1_1-WB-anti-fibrinogen-alpha-chain-picoband-antibody.jpgAnti-Fibrinogen alpha chain/FGA Antibody Picoband® Western blot analysis of FGA using anti-FGA antibody (A00816-1).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat skeletal muscle tissue lysates,<br>
Lane 2: HEPG2 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGA antigen affinity purified polyclonal antibody (Catalog # A00816-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGA at approximately 95KD. The expected band size for FGA is at 95KD.
https://www.bosterbio.com/products/primary-antibodies/anti-gla-picoband-trade-antibody-a01135-boster.html2026-03-24T05:07:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01135-gla-primary-antibodies-wb-testing-1.jpgAnti-Galactosidase alpha/Gla Antibody Picoband® Western blot analysis of Gla using anti-Gla antibody (A01135). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: rat C6 whole cell lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Gla antigen affinity purified polyclonal antibody (Catalog # A01135) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Gla at approximately 49 kDa. The expected band size for Gla is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01135-gla-primary-antibodies-wb-testing-2.jpgAnti-Galactosidase alpha/Gla Antibody Picoband® Western blot analysis of Gla using anti-Gla antibody (A01135). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: rat C6 whole cell lysates, <br>
Lane 3: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Gla antigen affinity purified polyclonal antibody (A01135) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for Gla at approximately 49 kDa. The expected band size for Gla is at 49 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-l-picoband-trade-antibody-a03769-boster.html2026-03-24T05:07:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-wb-testing-1.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® Western blot analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human U87 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse RAW264.7 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HNRNPL antigen affinity purified polyclonal antibody (Catalog # A03769) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HNRNPL at approximately 64 kDa. The expected band size for HNRNPL is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-2.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-3.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-4.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-5.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-6.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-7.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-ihc-testing-8.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IHC analysis of HNRNPL using anti-HNRNPL antibody (A03769). <br>
HNRNPL was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03769-hnrnpl-primary-antibodies-if-testing-9.jpgAnti-HnRNP L/HNRNPL Antibody Picoband® IF analysis of HNRNPL using anti-HNRNPL antibody (A03769).<br>
HNRNPL was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HNRNPL Antibody (A03769) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-irf9-picoband-trade-antibody-a04485-boster.html2026-03-24T05:07:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04485-irf9-primary-antibodies-wb-testing-1.jpgAnti-Interferon regulatory factor 9/IRF9 Antibody Picoband®Western blot analysis of IRF9 using anti-IRF9 antibody (A04485). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human PC-3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF9 antigen affinity purified polyclonal antibody (A04485) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IRF9 at approximately 44 kDa. The expected band size for IRF9 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04485-irf9-primary-antibodies-ihc-testing-1.jpgAnti-Interferon regulatory factor 9/IRF9 Antibody Picoband®IHC analysis of IRF9 using anti-IRF9 antibody (A04485). <br>IRF9 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF9 Antibody (A04485) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04485-irf9-primary-antibodies-if-testing-1.jpgAnti-Interferon regulatory factor 9/IRF9 Antibody Picoband®IF analysis of IRF9 using anti-IRF9 antibody (A04485) and anti-Tubulin Alpha antibody (M03989-3).<br>
IRF9 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IRF9 Antibody (A04485) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04485-irf9-primary-antibodies-fcm-testing-1.jpgAnti-Interferon regulatory factor 9/IRF9 Antibody Picoband®Flow Cytometry analysis of PC-3 cells using anti-IRF9 antibody (A04485). <br>
Overlay histogram showing PC-3 cells stained with A04485 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRF9 Antibody (A04485, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp13-picoband-trade-antibody-a00420-boster.html2026-03-24T05:07:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00420-1.jpgAnti-MMP13 Antibody Picoband® Western blot analysis of MMP13 using anti-MMP13 antibody (A00420). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: HELA whole cell lysates.<br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP13 antigen affinity purified polyclonal antibody (Catalog # A00420) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP13 at approximately 54KD. The expected band size for MMP13 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00420-2_1.jpgAnti-MMP13 Antibody Picoband® Western blot analysis of MMP13 using anti-MMP13 antibody (A00420). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human PC-3 whole cell lysates, <br> Lane 2: human U20S whole cell lysates, <br> Lane 3: human A549 whole cell lysates, <br> Lane 4: human HEK293 whole cell lysates. <br> Lane 5: Rabbit IgG(55KD), <br> Lane 6: Marker 1113 <br> Lane 7: human MDA-MB-453 whole cell lysates, <br> Lane 8: monkey COS-7 whole cell lysates, <br> Lane 9: rat lung tissue lysates, <br> Lane 10: mouse lung tissue lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP13 antigen affinity purified polyclonal antibody (Catalog # A00420) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP13 at approximately 54KD. The expected band size for MMP13 is at 54KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mut-picoband-trade-antibody-a01065-boster.html2026-03-24T05:07:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-wb-testing-1_1.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®Western blot analysis of MUT using anti-MUT antibody (A01065). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
lane 1: human Hela whole cell lysates,<br>
lane 2: human PC-3 whole cell lysates,<br>
lane 3: human A431 whole cell lysates,<br>
lane 4: human A564 whole cell lysates,<br>
lane 5: rat liver tissue lysates,<br>
lane 6: rat PC-12 whole cell lysates,<br>
lane 7: mouse liver tissue lysates,<br>
lane 8: mouse SP2/0 whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUT antigen affinity purified polyclonal antibody (Catalog # A01065) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MUT at approximately 83 kDa. The expected band size for MUT is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-ihc-testing-1.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®IHC analysis of MUT using anti-MUT antibody (A01065). <br>
MUT was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUT Antibody (A01065) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-ihc-testing-2.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®IHC analysis of MUT using anti-MUT antibody (A01065). <br>
MUT was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUT Antibody (A01065) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-ihc-testing-3.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®IHC analysis of MUT using anti-MUT antibody (A01065). <br>
MUT was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUT Antibody (A01065) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-ihc-testing-4.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®IHC analysis of MUT using anti-MUT antibody (A01065). <br>
MUT was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUT Antibody (A01065) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-ihc-testing-5.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®IHC analysis of MUT using anti-MUT antibody (A01065). <br>
MUT was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUT Antibody (A01065) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-fcm-testing-1_1.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®Flow Cytometry analysis of SiHa cells using anti-MUT antibody (A01065). <br>
Overlay histogram showing SiHa cells stained with A01065 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MUT Antibody (A01065, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01065-mut-primary-antibodies-fcm-testing-2_1.jpgAnti-Methylmalonyl Coenzyme A mutase Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-MUT antibody (A01065). <br>
Overlay histogram showing HepG2 cells stained with A01065 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MUT Antibody (A01065, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-dok-2-y299-antibody-p07956-1-boster.html2026-03-24T05:07:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07956-1-dok2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-Dok-2 (Y299) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using p56 Dok-2 (Phospho-Tyr299) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07956-1-dok2-primary-antibodies-wb-testing-2.jpgAnti-Phospho-Dok-2 (Y299) AntibodyWestern Blot analysis of various cells using Phospho-Dok-2 (Y299) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07956-1-dok2-primary-antibodies-wb-testing-3.jpgAnti-Phospho-Dok-2 (Y299) AntibodyWestern blot analysis of lysates from COS7 cells treated with insulin 0.01U/ml 15', Jurkat cells treated with insulin 0.01U/ml 15' and 293 cells treated with serum 20% 15', using p56 Dok-2 (Phospho-Tyr299) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tensin-2-y483-antibody-p07021-boster.html2026-03-24T05:07:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07021-tns2-primary-antibodies-wb-testing-2.jpgAnti-Phospho-Tensin-2 (Y483) AntibodyWestern Blot analysis of 3T3 cells using Phospho-Tensin-2 (Y483) Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07021-tns2-primary-antibodies-wb-testing-3.jpgAnti-Phospho-Tensin-2 (Y483) AntibodyWestern blot analysis of lysate from K562 cells, using phospho-Thrensin-2 (Phospho-Tyr483) antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p07021-tns2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-Tensin-2 (Y483) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Tensin-2 (Phospho-Tyr483) Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tob1-s164-antibody-p04119-boster.html2026-03-24T05:07:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04119-tob1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-TOB1 (S164) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using TOB1 (Phospho-Ser164) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04119-tob1-primary-antibodies-wb-testing-2.jpgAnti-Phospho-TOB1 (S164) AntibodyWestern Blot analysis of JK cells using Phospho-TOB1 (S164) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04119-tob1-primary-antibodies-wb-testing-3.jpgAnti-Phospho-TOB1 (S164) AntibodyWestern blot analysis of lysates from HT29 cells treated with serum 20% 15', using TOB1 (Phospho-Ser164) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-glycogen-synthase-1-s645-antibody-p03512-1-boster.html2026-03-24T05:07:47+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-dapk3-t265-antibody-p03300-boster.html2026-03-24T05:07:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-DAPK3 (T265) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using DAPK3 (Phospho-Thr265) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-wb-testing-2.jpgAnti-Phospho-DAPK3 (T265) AntibodyWestern Blot analysis of HuvEc cells using Phospho-DAPK3 (T265) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-wb-testing-3.jpgAnti-Phospho-DAPK3 (T265) AntibodyWestern blot analysis of lysates from HUVEC cells, using DAPK3 (Phospho-Thr265) Antibody. The lane on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-DAPK3 (T265) AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-if-testing-5.jpgAnti-Phospho-DAPK3 (T265) AntibodyImmunofluorescence analysis of Hela cell. 1,DAPK3 (phospho Thr265) Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). α-tubulin Monoclonal Antibody (8F11) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03300-dapk3-primary-antibodies-if-testing-6.jpgAnti-Phospho-DAPK3 (T265) AntibodyImmunofluorescence analysis of A549 cells, using DAPK3 (Phospho-Thr265) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-g3bp1-s232-antibody-p02199-1-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02199-1-g3bp1-primary-antibodies-wb-testing-2.jpgAnti-Phospho-G3BP1 (S232) AntibodyWestern Blot analysis of various cells using Phospho-G3BP1 (S232) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02199-1-g3bp1-primary-antibodies-wb-testing-3.jpgAnti-Phospho-G3BP1 (S232) AntibodyWestern blot analysis of extracts from HeLa cells, using G3BP-1 (Phospho-Ser232) Antibody. The lane on the right is treated with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02199-1-g3bp1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-G3BP1 (S232) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast cancer, using G3BP-1 (Phospho-Ser232) Antibody. The picture on the right is blocked with the G3BP-1 (Phospho-Ser232) peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-smc1-s966-antibody-p02148-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02148-smc1a-primary-antibodies-wb-testing-2.jpgAnti-Phospho-SMC1 (S966) SMC1A AntibodyWestern blot analysis of K562 using p-SMC1 (S966) antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02148-smc1a-primary-antibodies-wb-testing-3.jpgAnti-Phospho-SMC1 (S966) SMC1A AntibodyWestern blot analysis of lysates from HUVEC cells treated with etoposide 24uM 24h, using SMC1 (Phospho-Ser966) Antibody. The lane on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02148-smc1a-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-SMC1 (S966) SMC1A AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma, using SMC1 (Phospho-Ser966) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-rpa-p32-s33-antibody-p02067-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02067-rpa2-primary-antibodies-wb-testing-2.jpgAnti-Phospho-RPA p32 (S33) AntibodyWestern Blot analysis of MCF-7 cells using Phospho-RPA p32 (S33) Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02067-rpa2-primary-antibodies-wb-testing-3.jpgAnti-Phospho-RPA p32 (S33) AntibodyWestern blot analysis of lysates from NIH/3T3 cells treated with Adriamycin 0.5ug/ml 24h, using RFA2 (Phospho-Ser33) Antibody. The lane on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02067-rpa2-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-RPA p32 (S33) AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-perk-t981-antibody-p01992-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-wb-testing-2.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyWestern blot analysis of lysates from 1) 453, 2) AD293 , 3) Hela cells, (Green） primary antibody was diluted at 1:1000, 4°over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red） Actin β Monoclonal Antibody (5B7) antibody was diluted at 1:5000 as loading control, 4° over night, secondary antibody was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-lung tissue. 1, PERK (phospho Thr981) Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1, PERK (phospho Thr981) Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-ihc-testing-5.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-kidney tissue. 1, PERK (phospho Thr981) Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-ihc-testing-6.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma, using PEK/PERK (Phospho-Thr981) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-if-testing-7.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyImmunofluorescence analysis of Hela cell. 1, PERK (phospho Thr981) Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). 3 DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01992-eif2ak3-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-PERK (T981) Rabbit Polyclonal AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PEK/PERK (Phospho-Thr981) Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-epha4-y596-antibody-p01860-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01860-epha4-primary-antibodies-wb-testing-1.jpgAnti-Phospho-EphA4 (Y596) AntibodyWestern Blot analysis of JK cells using Phospho-EphA4 (Y596) Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-eps15-y849-antibody-p01681-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01681-eps15-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Eps15 (Y849) AntibodyWestern Blot analysis of JK cells using Phospho-Eps15 (Y849) Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tip60-s86-antibody-p01393-boster.html2026-03-24T05:07:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01393-kat5-primary-antibodies-wb-testing-2.jpgAnti-Phospho-TIP60 (S86) KAT5 AntibodyWestern Blot analysis of Jurkat cells using Phospho-TIP60 (S86) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01393-kat5-primary-antibodies-wb-testing-3.jpgAnti-Phospho-TIP60 (S86) KAT5 AntibodyWestern blot analysis of lysates from Jurkat cells, using TIP60 (Phospho-Ser86) Antibody. The lane on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01393-kat5-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-TIP60 (S86) KAT5 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01393-kat5-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-TIP60 (S86) KAT5 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using TIP60 (Phospho-Ser86) Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-c-kit-y721-antibody-p01335-boster.html2026-03-24T05:07:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01335-kit-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-c-Kit (Y721) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using c-Kit (Phospho-Tyr721) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01335-kit-primary-antibodies-wb-testing-2.jpgAnti-Phospho-c-Kit (Y721) AntibodyWestern Blot analysis of various cells using Phospho-c-Kit (Y721) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01335-kit-primary-antibodies-wb-testing-3.jpgAnti-Phospho-c-Kit (Y721) AntibodyWestern blot analysis of lysates from HepG2 cells treated with EGF 200ng/ml 30', using c-Kit (Phospho-Tyr721) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-ddr1-y513-antibody-p00905-boster.html2026-03-24T05:07:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00905-ddr1-primary-antibodies-wb-testing-2.jpgAnti-Phospho-DDR1 (Y513) AntibodyWestern Blot analysis of various cells using Phospho-DDR1 (Y513) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00905-ddr1-primary-antibodies-wb-testing-3.jpgAnti-Phospho-DDR1 (Y513) AntibodyWestern blot analysis of lysates from HepG2 cells treated with Na3VO4 0.3mM 40', using DDR1 (Phospho-Tyr513) Antibody. The lane on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00905-ddr1-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-DDR1 (Y513) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using DDR1 (Phospho-Tyr513) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00905-ddr1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho-DDR1 (Y513) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using DDR1 (Phospho-Tyr513) Antibody
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-cdk9-t186-antibody-p00794-boster.html2026-03-24T05:07:49+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-fadd-s194-antibody-p00237-boster.html2026-03-24T05:07:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00237-fadd-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-FADD (S194) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using FADD (Phospho-Ser194) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00237-fadd-primary-antibodies-wb-testing-2.jpgAnti-Phospho-FADD (S194) AntibodyWestern blot analysis of MOUSE-KIDNEY MOUSE-BRAIN MOUSE-SPLEEN MOUSE-LUNG using p-FADD (S194) antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00237-fadd-primary-antibodies-wb-testing-3.jpgAnti-Phospho-FADD (S194) AntibodyWestern blot analysis of lysates from HeLa cells treated with Paclitaxel 1uM 60', using FADD (Phospho-Ser194) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5d3-antibody-a30429-boster.html2026-03-24T05:07:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30429-or5d3-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 5D3 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 5D3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cyp2a6v2-antibody-a30427-boster.html2026-03-24T05:07:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30427-cyp2a6v2-primary-antibodies-wb-testing-2.jpgAnti-CYP2A6V2 AntibodyWestern Blot analysis of L929 cells using CYP2A6V2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30427-cyp2a6v2-primary-antibodies-ihc-testing-1.jpgAnti-CYP2A6V2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2a42-antibody-a19549-boster.html2026-03-24T05:07:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19549-or2a1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2A42 OR2A1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2A42 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19549-or2a1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2A42 OR2A1 AntibodyWestern Blot analysis of COLO cells using Olfactory receptor 2A42 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2ap1-antibody-a18886-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18886-or2ap1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2AP1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 2AP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18886-or2ap1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2AP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR2AP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8s1-antibody-a18882-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18882-or8s1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8S1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 8S1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18882-or8s1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8S1 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR8S1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18882-or8s1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 8S1 AntibodyWestern blot analysis of the lysates from HeLa cells using OR8S1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-9q2-antibody-a18881-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18881-or9q2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 9Q2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 9Q2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18881-or9q2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 9Q2 AntibodyWestern blot analysis of lysates from HeLa and HT-29 cells, using OR9Q2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4p4-antibody-a18866-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18866-or4p4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4P4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4P4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18866-or4p4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4P4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR4P4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18866-or4p4-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4P4 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR4P4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18866-or4p4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4P4 AntibodyImmunofluorescence analysis of A549 cells, using OR4P4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8k3-antibody-a18812-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18812-or8k3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8K3 AntibodyWestern Blot analysis of LOVO cells using Olfactory receptor 8K3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18812-or8k3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8K3 AntibodyWestern blot analysis of lysates from LOVO cells, using OR8K3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18812-or8k3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8K3 AntibodyImmunofluorescence analysis of HUVEC cells, using OR8K3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6c68-antibody-a18803-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18803-or6c68-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6C68 AntibodyWestern Blot analysis of various cells using Olfactory receptor 6C68 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18803-or6c68-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 6C68 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR6C68 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18803-or6c68-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6C68 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR6C68 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5h15-antibody-a18797-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18797-or5h15-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5H15 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5H15 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18797-or5h15-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5H15 AntibodyWestern Blot analysis of COLO cells using Olfactory receptor 5H15 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18797-or5h15-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5H15 AntibodyWestern blot analysis of lysates from COLO cells, using OR5H15 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18797-or5h15-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 5H15 AntibodyWestern blot analysis of the lysates from HeLa cells using OR5H15 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5ap2-antibody-a18792-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18792-or5ap2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5AP2 AntibodyWestern Blot analysis of 3T3 cells using Olfactory receptor 5AP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18792-or5ap2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5AP2 AntibodyImmunofluorescence analysis of HeLa cells, using OR5AP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5ak3-antibody-a18791-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18791-or5ak3p-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5AK3 OR5AK3P AntibodyWestern Blot analysis of various cells using Olfactory receptor 5AK3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18791-or5ak3p-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5AK3 OR5AK3P AntibodyWestern blot analysis of lysates from HUVEC and COS7 cells, using OR5AK3P Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18791-or5ak3p-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5AK3 OR5AK3P AntibodyWestern blot analysis of the lysates from HepG2 cells using OR5AK3P antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52e5-antibody-a18783-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18783-or52e5-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E5 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52E5 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18783-or52e5-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E5 AntibodyWestern blot analysis of lysates from COLO, MCF-7, and HeLa cells, using OR52E5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18783-or52e5-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52E5 AntibodyWestern blot analysis of the lysates from HeLa cells using OR52E5 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52e4-antibody-a18782-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18782-or52e4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 52E4 AntibodyImmunofluorescence analysis of LOVO cells, using OR52E4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18782-or52e4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52E4 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18782-or52e4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E4 AntibodyWestern blot analysis of lysates from HepG2 and HeLa cells, using OR52E4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52e2-antibody-a18781-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18781-or52e2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52E2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR52E2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18781-or52e2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E2 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 52E2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18781-or52e2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR52E2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4a16-antibody-a18771-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18771-or4a16-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4A16 AntibodyImmunofluorescence analysis of A549 cells, using OR4A16 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18771-or4a16-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4A16 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4A16 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18771-or4a16-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4A16 AntibodyWestern blot analysis of lysates from COLO cells, using OR4A16 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18771-or4a16-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4A16 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR4A16 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2t2-35-antibody-a18769-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18769-or2t35-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2T2/35 OR2T35 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR2T2/2T35 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18769-or2t35-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2T2/35 OR2T35 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2T2/35 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18769-or2t35-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2T2/35 OR2T35 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR2T2/2T35 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2t11-antibody-a18767-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18767-or2t11-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 2T11 AntibodyWestern Blot (WB) analysis of MCF-7 cells using Olfactory receptor 2T11 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2l5-antibody-a18766-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18766-or2l5-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 2L5 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 2L5 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2aj1-antibody-a18763-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18763-or2aj1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2AJ1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 2AJ1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18763-or2aj1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2AJ1 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using OR2AJ1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18763-or2aj1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2AJ1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR2AJ1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2ag1-2-antibody-a18762-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18762-or2ag2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2AG1/2 OR2AG2 AntibodyWestern Blot analysis of 293 cells using Olfactory receptor 2AG1/2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18762-or2ag2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2AG1/2 OR2AG2 AntibodyWestern blot analysis of lysates from LOVO cells, using OR2AG1/2AG2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18762-or2ag2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 2AG1/2 OR2AG2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR2AG1/2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18762-or2ag2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2AG1/2 OR2AG2 AntibodyImmunofluorescence analysis of LOVO cells, using OR2AG1/2AG2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10g6-antibody-a18753-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18753-or10g6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10G6 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10G6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18753-or10g6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10G6 AntibodyWestern blot analysis of lysates from COLO cells, using OR10G6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18753-or10g6-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10G6 AntibodyImmunofluorescence analysis of A549 cells, using OR10G6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10d4-antibody-a18752-boster.html2026-03-24T05:07:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18752-or10d4p-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10D4 OR10D4P AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 10D4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10a6-antibody-a18750-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18750-or10a6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10A6 AntibodyWestern Blot analysis of A549 cells using Olfactory receptor 10A6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18750-or10a6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10A6 AntibodyWestern blot analysis of lysates from A549 cells, using OR10A6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18750-or10a6-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10A6 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR10A6 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgg-antibody-a18678-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18678-mrgprg-primary-antibodies-wb-testing-2.jpgAnti-MRGG MRGPRG AntibodyWestern Blot analysis of various cells using MRGG Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18678-mrgprg-primary-antibodies-wb-testing-3.jpgAnti-MRGG MRGPRG AntibodyWestern blot analysis of lysates from HUVEC cells, using MRGRG Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18678-mrgprg-primary-antibodies-ihc-testing-4.jpgAnti-MRGG MRGPRG AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18678-mrgprg-primary-antibodies-if-testing-1.jpgAnti-MRGG MRGPRG AntibodyImmunofluorescence analysis of A549 cells, using MRGRG Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tmem145-antibody-a18552-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18552-tmem145-primary-antibodies-wb-testing-2.jpgAnti-TMEM145 AntibodyWestern Blot analysis of various cells using TMEM145 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18552-tmem145-primary-antibodies-wb-testing-1.jpgAnti-TMEM145 AntibodyWestern blot analysis of lysates from HepG2 cells, using TMEM145 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-s-100a7l2-antibody-a18516-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18516-s100a7l2-primary-antibodies-wb-testing-2.jpgAnti-S-100A7L2 AntibodyWestern Blot analysis of HuvEc cells using S-100A7L2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18516-s100a7l2-primary-antibodies-wb-testing-1.jpgAnti-S-100A7L2 AntibodyWestern blot analysis of the lysates from HepG2 cells using S100A7L2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-pote-14-22-antibody-a18244-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18244-poteh-primary-antibodyes-wb-testing-1.jpgAnti-POTE-14/22 AntibodyWestern Blot (WB) analysis of AD293 using POTE-14/22 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf113b-antibody-a18242-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18242-rnf113b-primary-antibodies-ihc-testing-1.jpgAnti-RING finger protein 113B RNF113B AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18242-rnf113b-primary-antibodies-wb-testing-2.jpgAnti-RING finger protein 113B RNF113B AntibodyWestern Blot analysis of 293 cells using RNF113B Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10g2-antibody-a18230-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18230-or10g2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10G2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10G2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18230-or10g2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10G2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10G2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18230-or10g2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10G2 AntibodyWestern blot analysis of lysates from HUVEC, HeLa, MCF-7, Jurkat, and COLO cells, using OR10G2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-c1ql2-antibody-a18194-1-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18194-1-c1ql2-primary-antibodyes-wb-testing-1.jpgAnti-C1qL2/C1Qtnf10 AntibodyWestern Blot (WB) analysis of specific cells using C1qL2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gusbp1-antibody-a18107-boster.html2026-03-24T05:07:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18107-gusbp1-primary-antibodies-wb-testing-2.jpgAnti-GUSBP1 AntibodyWestern Blot analysis of K562 cells using GUSBP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18107-gusbp1-primary-antibodies-wb-testing-1.jpgAnti-GUSBP1 AntibodyWestern blot analysis of the lysates from HT-29 cells using GUSBL1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l54-antibody-a17999-1-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17999-1-mrpl54-primary-antibodyes-wb-testing-1.jpgAnti-MRP-L54 AntibodyWestern Blot (WB) analysis of specific cells using MRP-L54 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr137c-antibody-a17969-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17969-gpr137c-primary-antibodies-wb-testing-2.jpgAnti-GPR137C AntibodyWestern Blot analysis of various cells using GPR137C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17969-gpr137c-primary-antibodies-wb-testing-3.jpgAnti-GPR137C AntibodyWestern blot analysis of lysates from HepG2 cells, using GPR137C Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17969-gpr137c-primary-antibodies-ihc-testing-4.jpgAnti-GPR137C AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR137C Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17969-gpr137c-primary-antibodies-if-testing-1.jpgAnti-GPR137C AntibodyImmunofluorescence analysis of MCF7 cells, using GPR137C Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-taar3-antibody-a17858-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17858-taar3-primary-antibodies-wb-testing-2.jpgAnti-TAAR3 AntibodyWestern Blot analysis of various cells using TAAR3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17858-taar3-primary-antibodies-wb-testing-3.jpgAnti-TAAR3 AntibodyWestern blot analysis of lysates from COLO and HepG2 cells, using TAAR3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17858-taar3-primary-antibodies-wb-testing-1.jpgAnti-TAAR3 AntibodyWestern blot analysis of the lysates from HepG2 cells using TAAR3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tubulin-alpha-3c-d-e-antibody-a17842-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17842-tuba3c-primary-antibodies-wb-testing-2.jpgAnti-Tubulin alpha-3C/D/E AntibodyWestern Blot analysis of various cells using Tubulin α-3C/D/E Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17842-tuba3c-primary-antibodies-wb-testing-1.jpgAnti-Tubulin alpha-3C/D/E AntibodyWestern Blot analysis of HEPG2 HELA cells using Antibody diluted at 2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10g4-antibody-a17776-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17776-or10g4-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10G4 AntibodyWestern blot analysis of lysates from HeLa, COLO, and MCF-7 cells, using OR10G4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17776-or10g4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10G4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10G4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17776-or10g4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10G4 AntibodyWestern Blot analysis of MCF7 cells using Olfactory receptor 10G4 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4x1-antibody-a17774-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17774-or4x1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4X1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4X1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17774-or4x1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4X1 AntibodyWestern Blot analysis of COLO205 cells using Olfactory receptor 4X1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17774-or4x1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4X1 AntibodyWestern blot analysis of lysates from HeLa, Jurkat, HUVEC, MCF-7, and COLO cells, using OR4X1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17774-or4x1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4X1 AntibodyImmunofluorescence analysis of A549 cells, using OR4X1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5w2-antibody-a17771-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17771-or5w2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5W2 AntibodyWestern Blot analysis of 293T-UV cells using Olfactory receptor 5W2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17771-or5w2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5W2 AntibodyWestern blot analysis of lysates from HeLa cells, using OR5W2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17771-or5w2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 5W2 AntibodyWestern blot analysis of the lysates from 293 cells using OR5W2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17771-or5w2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5W2 AntibodyImmunofluorescence analysis of A549 cells, using OR5W2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4q3-antibody-a17768-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17768-or4q3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4Q3 AntibodyImmunofluorescence analysis of A549 cells, using OR4Q3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17768-or4q3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4Q3 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4Q3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17768-or4q3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4Q3 AntibodyWestern blot analysis of lysates from HeLa, Jurkat, and HepG2 cells, using OR4Q3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4l1-antibody-a17765-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17765-or4l1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 4L1 AntibodyWestern Blot (WB) analysis of K562 cells using Olfactory receptor 4L1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10g7-antibody-a17758-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17758-or10g7-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10G7 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10G7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17758-or10g7-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10G7 AntibodyWestern blot analysis of lysates from HepG2 cells, using OR10G7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17758-or10g7-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10G7 AntibodyImmunofluorescence analysis of A549 cells, using OR10G7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10z1-antibody-a17739-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17739-or10z1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10Z1 AntibodyWestern Blot analysis of COS-7 cells using Olfactory receptor 10Z1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17739-or10z1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10Z1 AntibodyWestern blot analysis of lysates from COS7 cells, using OR10Z1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17739-or10z1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 10Z1 AntibodyWestern blot analysis of the lysates from HeLa cells using OR10Z1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17739-or10z1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10Z1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10Z1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5m11-antibody-a17733-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17733-or5m11-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5M11 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR5M11 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17733-or5m11-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5M11 AntibodyWestern Blot analysis of various cells using Olfactory receptor 5M11 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-9q1-antibody-a17732-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17732-or9q1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 9Q1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 9Q1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17732-or9q1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 9Q1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR9Q1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17732-or9q1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 9Q1 AntibodyWestern blot analysis of the lysates from HeLa cells using OR9Q1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17732-or9q1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 9Q1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR9Q1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-saf-a2-antibody-a17701-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17701-hnrnpul2-primary-antibodyes-wb-testing-1.jpgAnti-SAF-A2 HNRNPUL2 AntibodyWestern Blot (WB) analysis of K562 cells using SAF-A2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-1d4-1d5-antibody-a17690-boster.html2026-03-24T05:07:53+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-mrge-antibody-a17659-boster.html2026-03-24T05:07:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17659-mrgpre-primary-antibodyes-wb-testing-1.jpgAnti-MRGE MRGPRE AntibodyWestern Blot (WB) analysis of specific cells using MRGE Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8j3-antibody-a17588-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17588-or8j3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8J3 AntibodyWestern Blot analysis of various cells using Olfactory receptor 8J3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17588-or8j3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 8J3 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and HUVEC cells, using OR8J3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6t1-antibody-a17581-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17581-or6t1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6T1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 6T1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17581-or6t1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 6T1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR6T1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17581-or6t1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6T1 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR6T1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6p1-antibody-a17580-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17580-or6p1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6P1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 6P1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17580-or6p1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6P1 AntibodyWestern blot analysis of lysates from Jurkat and COLO cells, using OR6P1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6c3-antibody-a17576-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17576-or6c3-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 6C3 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 6C3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-56b4-antibody-a17564-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17564-or56b4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 56B4 AntibodyImmunofluorescence analysis of MCF7 cells, using OR56B4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17564-or56b4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 56B4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 56B4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17564-or56b4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 56B4 AntibodyWestern blot analysis of lysates from COLO cells, using OR56B4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52e6-antibody-a17559-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17559-or52e6-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 52E6 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 52E6 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-51t1-antibody-a17557-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17557-or51t1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 51T1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 51T1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-51a7-antibody-a17554-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17554-or51a7-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 51A7 AntibodyWestern Blot (WB) analysis of COLO205 cells using Olfactory receptor 51A7 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4k14-antibody-a17551-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17551-or4k14-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4K14 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4K14 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17551-or4k14-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4K14 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and HUVEC cells, using OR4K14 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17551-or4k14-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4K14 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR4K14 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17551-or4k14-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4K14 AntibodyImmunofluorescence analysis of A549 cells, using OR4K14 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4c15-antibody-a17546-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17546-or4c15-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4C15 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4C15 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17546-or4c15-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4C15 AntibodyWestern blot analysis of lysates from Jurkat and HepG2 cells, using OR4C15 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17546-or4c15-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4C15 AntibodyImmunofluorescence analysis of A549 cells, using OR4C15 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10v1-antibody-a17530-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17530-or10v1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10V1 AntibodyImmunofluorescence analysis of A549 cells, using OR10V1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17530-or10v1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10V1 AntibodyWestern Blot analysis of A549 cells using Olfactory receptor 10V1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17530-or10v1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10V1 AntibodyWestern blot analysis of lysates from A549 and Jurkat cells, using OR10V1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10h4-antibody-a17528-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17528-or10h4-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10H4 AntibodyWestern Blot (WB) analysis of Raw 264.7 cells using Olfactory receptor 10H4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10ag1-antibody-a17524-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17524-or10ag1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10AG1 AntibodyWestern Blot (WB) analysis of HuvEc cells using Olfactory receptor 10AG1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17524-or10ag1-primary-antibodyes-wb-testing-2.jpgAnti-Olfactory receptor 10AG1 AntibodyWestern Blot (WB) analysis of Jurkat and K562 cells using Olfactory receptor 10AG1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10ad1-antibody-a17523-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17523-or10ad1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10AD1 AntibodyImmunofluorescence analysis of A549 cells, using OR10AD1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17523-or10ad1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10AD1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10AD1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17523-or10ad1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10AD1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR10AD1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17523-or10ad1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 10AD1 AntibodyWestern blot analysis of the lysates from 293 cells using OR10AD1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10a7-antibody-a17522-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17522-or10a7-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10A7 AntibodyWestern Blot (WB) analysis of K562 cells using Olfactory receptor 10A7 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-calpain-12-antibody-a17322-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17322-capn12-primary-antibodies-wb-testing-1.jpgAnti-Calpain 12 CAPN12 AntibodyWestern blot analysis of the lysates from K562 cells using CAPN12 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17322-capn12-primary-antibodies-wb-testing-2.jpgAnti-Calpain 12 CAPN12 AntibodyWestern Blot analysis of various cells using Calpain 12 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17322-capn12-primary-antibodies-wb-testing-3.jpgAnti-Calpain 12 CAPN12 AntibodyWestern Blot analysis of 293 cells using Calpain 12 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4c6-antibody-a17267-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17267-or4c6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4C6 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4C6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17267-or4c6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4C6 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using OR4C6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17267-or4c6-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4C6 AntibodyImmunofluorescence analysis of A549 cells, using OR4C6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mage-a5-antibody-a17180-boster.html2026-03-24T05:07:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17180-magea5-primary-antibodyes-wb-testing-1.jpgAnti-MAGE-A5 AntibodyWestern Blot (WB) analysis of 3T3 cells using MAGE-A5 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr108-antibody-a17169-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17169-gpr108-primary-antibodies-if-testing-1.jpgAnti-GPR108 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR108 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17169-gpr108-primary-antibodies-wb-testing-2.jpgAnti-GPR108 AntibodyWestern Blot analysis of various cells using GPR108 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17169-gpr108-primary-antibodies-wb-testing-3.jpgAnti-GPR108 AntibodyWestern blot analysis of lysates from A549 cells, using GPR108 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nrip3-antibody-a17131-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17131-nrip3-primary-antibodies-wb-testing-2.jpgAnti-NRIP3 AntibodyWestern Blot analysis of various cells using NRIP3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17131-nrip3-primary-antibodies-wb-testing-3.jpgAnti-NRIP3 AntibodyWestern blot analysis of lysates from COLO cells, using NRIP3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17131-nrip3-primary-antibodies-ihc-testing-1.jpgAnti-NRIP3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2t2-35-antibody-a17070-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17070-or2t2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2T2/35 AntibodyImmunofluorescence analysis of A549 cells, using OR2T2/2T35 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17070-or2t2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2T2/35 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2T2/35 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17070-or2t2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2T2/35 AntibodyWestern blot analysis of lysates from HepG2 cells, using OR2T2/2T35 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17070-or2t2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 2T2/35 AntibodyWestern blot analysis of the lysates from HeLa cells using OR2T2/35 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ccdc4-antibody-a17039-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17039-bend4-primary-antibodyes-wb-testing-1.jpgAnti-CCDC4 AntibodyWestern Blot (WB) analysis of specific cells using CCDC4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2m7-antibody-a17018-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17018-or2m7-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2M7 AntibodyWestern blot analysis of lysates from HUVEC, COLO, MCF-7, Jurkat, and HepG2 cells, using OR2M7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17018-or2m7-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2M7 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2M7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5a1-antibody-a17016-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17016-or5a1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5A1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR5A1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17016-or5a1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5A1 AntibodyWestern Blot analysis of MCF-7 cells using Olfactory receptor 5A1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-znf227-antibody-a16995-boster.html2026-03-24T05:07:55+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8i2-antibody-a16910-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16910-or8i2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8I2 AntibodyWestern Blot analysis of HeLa cells using Olfactory receptor 8I2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16910-or8i2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8I2 AntibodyWestern blot analysis of lysates from HeLa and HT-29 cells, using OR8I2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16910-or8i2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 8I2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR8I2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8g5-antibody-a16909-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16909-or8g5-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 8G5 AntibodyWestern Blot (WB) analysis of HeLa cells using Olfactory receptor 8G5 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6k2-antibody-a16904-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16904-or6k2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6K2 AntibodyWestern blot analysis of lysates from HeLa cells, using OR6K2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16904-or6k2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6K2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 6K2 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5m3-antibody-a16899-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16899-or5m3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5M3 AntibodyWestern Blot analysis of HEPG2 cells using Olfactory receptor 5M3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16899-or5m3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5M3 AntibodyWestern blot analysis of lysates from HepG2, HUVEC, and MCF-7 cells, using OR5M3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16899-or5m3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5M3 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5M3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5a2-antibody-a16891-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16891-or5a2-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 5A2 AntibodyWestern Blot (WB) analysis of 3T3 cells using Olfactory receptor 5A2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52w1-antibody-a16889-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16889-or52w1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52W1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52W1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16889-or52w1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52W1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR52W1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52k1-antibody-a16887-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16887-or52k1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52K1 AntibodyWestern Blot analysis of 293T cells using Olfactory receptor 52K1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16887-or52k1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52K1 AntibodyWestern blot analysis of lysates from 293 cells, using OR52K1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52b2-antibody-a16885-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16885-or52b2-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 52B2 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 52B2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-51f2-antibody-a16883-boster.html2026-03-24T05:07:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16883-or51f2-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 51F2 AntibodyWestern Blot (WB) analysis of K562 cells using Olfactory receptor 51F2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2d3-antibody-a16876-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16876-or2d3-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 2D3 AntibodyWestern Blot (WB) analysis of HeLa cells using Olfactory receptor 2D3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10h3-4-antibody-a16868-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16868-or10h3-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10H3/4 AntibodyWestern Blot (WB) analysis of HeLa using Olfactory receptor 10H3/4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rhophilin-antibody-a16728-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16728-rhpn1-primary-antibodies-wb-testing-2.jpgAnti-Rhophilin AntibodyWestern Blot analysis of A549 cells using Rhophilin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16728-rhpn1-primary-antibodies-wb-testing-3.jpgAnti-Rhophilin AntibodyWestern blot analysis of the lysates from HepG2 cells using RHPN1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16728-rhpn1-primary-antibodies-ihc-testing-1.jpgAnti-Rhophilin AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-gpr152-antibody-a16638-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16638-gpr152-primary-antibodies-wb-testing-2.jpgAnti-GPR152 AntibodyWestern Blot analysis of k562 cells using GPR152 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16638-gpr152-primary-antibodies-wb-testing-1.jpgAnti-GPR152 AntibodyWestern blot analysis of lysates from Jurkat cells, using GPR152 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-13c4-antibody-a16636-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16636-or13c4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 13C4 AntibodyImmunofluorescence analysis of LOVO cells, using OR13C4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16636-or13c4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 13C4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 13C4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16636-or13c4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 13C4 AntibodyWestern blot analysis of lysates from COS7 cells, using OR13C4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16636-or13c4-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 13C4 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR13C4 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4c12-antibody-a16635-boster.html2026-03-24T05:07:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16635-or4c12-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 4C12 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 4C12 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-csrnp2-antibody-a16562-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16562-csrnp2-primary-antibodies-wb-testing-2.jpgAnti-CSRNP2/Fam130A1 AntibodyWestern Blot analysis of A549 cells using CSRNP2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16562-csrnp2-primary-antibodies-wb-testing-3.jpgAnti-CSRNP2/Fam130A1 AntibodyWestern blot analysis of the lysates from 293 cells using TAIP-12 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16562-csrnp2-primary-antibodies-ihc-testing-1.jpgAnti-CSRNP2/Fam130A1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5p2-antibody-a16533-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16533-or5p2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5P2 AntibodyWestern Blot analysis of HUVEC cells using Olfactory receptor 5P2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16533-or5p2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5P2 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR5P2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16533-or5p2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 5P2 AntibodyWestern blot analysis of the lysates from K562 cells using OR5P2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16533-or5p2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5P2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5P2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5ar1-antibody-a16528-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16528-or5ar1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5AR1 AntibodyImmunofluorescence analysis of A549 cells, using OR5AR1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16528-or5ar1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5AR1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 5AR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16528-or5ar1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5AR1 AntibodyWestern blot analysis of lysates from Jurkat, COLO, and MCF-7 cells, using OR5AR1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4c16-antibody-a16523-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16523-or4c16-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 4C16 AntibodyWestern Blot (WB) analysis of SH-SY5Y cells using Olfactory receptor 4C16 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-1s1-2-antibody-a16516-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16516-or1s2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 1S1/2 OR1S2 AntibodyWestern blot analysis of the lysates from HUVECcells using OR1S1/1S2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16516-or1s2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 1S1/2 OR1S2 AntibodyWestern Blot analysis of HuvEc cells using Olfactory receptor 1S1/2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16516-or1s2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 1S1/2 OR1S2 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using OR1S1/1S2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10t2-antibody-a16511-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16511-or10t2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10T2 AntibodyWestern Blot analysis of 293T-UV cells using Olfactory receptor 10T2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16511-or10t2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10T2 AntibodyWestern blot analysis of lysates from HUVEC and COLO cells, using OR10T2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-photomedin-2-antibody-a16481-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16481-olfml2b-primary-antibodies-ihc-testing-1.jpgAnti-Photomedin-2 OLFML2B AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16481-olfml2b-primary-antibodies-wb-testing-2.jpgAnti-Photomedin-2 OLFML2B AntibodyWestern Blot analysis of various cells using Photomedin-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16481-olfml2b-primary-antibodies-wb-testing-3.jpgAnti-Photomedin-2 OLFML2B AntibodyWestern blot analysis of lysates from HUVEC cells, using OLFML2B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10h1-antibody-a16480-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16480-or10h1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10H1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10H1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16480-or10h1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10H1 AntibodyWestern blot analysis of lysates from HeLa and MCF-7 cells, using OR10H1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-13h1-antibody-a16479-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16479-or13h1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 13H1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 13H1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16479-or13h1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 13H1 AntibodyWestern blot analysis of lysates from HepG2 and Jurkat cells, using OR13H1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sh2d5-antibody-a16472-1-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16472-1-sh2d5-primary-antibodies-wb-testing-2.jpgAnti-SH2D5 AntibodyWestern Blot analysis of various cells using SH2D5 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16472-1-sh2d5-primary-antibodies-ihc-testing-1.jpgAnti-SH2D5 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-mrgx4-antibody-a16446-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16446-mrgprx4-primary-antibodies-wb-testing-2.jpgAnti-MRGX4 MRGPRX4 AntibodyWestern blot analysis of lysates from HUVEC and COLO cells, using MRGX4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16446-mrgprx4-primary-antibodies-ihc-testing-3.jpgAnti-MRGX4 MRGPRX4 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16446-mrgprx4-primary-antibodies-if-testing-1.jpgAnti-MRGX4 MRGPRX4 AntibodyImmunofluorescence analysis of A549 cells, using MRGX4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-v1rl2-antibody-a16434-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16434-vn1r2-primary-antibodies-wb-testing-2.jpgAnti-V1RL2 AntibodyWestern Blot analysis of various cells using V1RL2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16434-vn1r2-primary-antibodies-wb-testing-1.jpgAnti-V1RL2 AntibodyWestern blot analysis of lysates from HUVEC, COLO, and MCF-7 cells, using VN1R2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5k1-antibody-a16375-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16375-or5k1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5K1 AntibodyImmunofluorescence analysis of HUVEC cells, using OR5K1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16375-or5k1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5K1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 5K1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16375-or5k1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5K1 AntibodyWestern blot analysis of lysates from COLO and Jurkat cells, using OR5K1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4c13-antibody-a16372-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16372-or4c13-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4C13 AntibodyWestern blot analysis of lysates from HeLa, Jurkat, HepG2, and MCF-7 cells, using OR4C13 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16372-or4c13-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4C13 AntibodyImmunofluorescence analysis of A549 cells, using OR4C13 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2t1-antibody-a16371-boster.html2026-03-24T05:07:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16371-or2t1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2T1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2T1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16371-or2t1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2T1 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR2T1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16371-or2t1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2T1 AntibodyImmunofluorescence analysis of A549 cells, using OR2T1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2a4-7-antibody-a16369-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16369-or2a7-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2A4/7 OR2A7 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2A4/7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16369-or2a7-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2A4/7 OR2A7 AntibodyWestern blot analysis of lysates from HeLa cells, using OR2A4/2A7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16369-or2a7-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2A4/7 OR2A7 AntibodyImmunofluorescence analysis of HepG2 cells, using OR2A4/2A7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-histone-h2a-antibody-a16318-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16318-hist1h2ag-primary-antibodies-wb-testing-2.jpgAnti-Histone H2A HIST1H2AG AntibodyWestern Blot analysis of HeLa cells using Histone H2A Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16318-hist1h2ag-primary-antibodies-ihc-testing-1.jpgAnti-Histone H2A HIST1H2AG AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-abhd7-antibody-a16314-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16314-ephx4-primary-antibodies-wb-testing-2.jpgAnti-ABHD7 AntibodyWestern Blot analysis of various cells using ABHD7 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16314-ephx4-primary-antibodies-wb-testing-3.jpgAnti-ABHD7 AntibodyWestern blot analysis of lysates from HT-29 cells, using ABHD7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16314-ephx4-primary-antibodies-wb-testing-1.jpgAnti-ABHD7 AntibodyWestern blot analysis of the lysates from HeLa cells using ABHD7 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl11-antibody-a16260-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16260-klhl11-primary-antibodies-wb-testing-2.jpgAnti-KLHL11 Monoclonal Antibody Western Blot analysis using KLHL11 Monoclonal Antibody against HeLa (1) and MCF-7 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16260-klhl11-primary-antibodies-ihc-testing-3.jpgAnti-KLHL11 Monoclonal Antibody Immunohistochemistry analysis of paraffin-embedded liver cancer (right) and colon cancer tissues (left) with DAB staining using KLHL11 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16260-klhl11-primary-antibodies-if-testing-1.jpgAnti-KLHL11 Monoclonal Antibody Immunofluorescence analysis of NIH/3T3 cells using KLHL11 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/anti-mob3a-b-antibody-a16079-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16079-mob3a-primary-antibodyes-wb-testing-1.jpgAnti-Mob3A/B AntibodyWestern Blot (WB) analysis of 3T3 using Mob3A/B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16079-mob3a-primary-antibodyes-ihc-testing-2.jpgAnti-Mob3A/B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Skin, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-epsilon-tubulin-antibody-a16034-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16034-tube1-primary-antibodies-ihc-testing-1.jpgAnti-Epsilon Tubulin Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Colon Carcinoma Tissue using Epsilon Tubulin Mouse mAb diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/anti-grtp1-antibody-a15959-boster.html2026-03-24T05:07:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15959-grtp1-primary-antibodies-wb-testing-2.jpgAnti-GRTP1 AntibodyWestern Blot analysis of various cells using GRTP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15959-grtp1-primary-antibodies-wb-testing-3.jpgAnti-GRTP1 AntibodyWestern blot analysis of lysates from 293 cells, using GRTP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15959-grtp1-primary-antibodies-ihc-testing-1.jpgAnti-GRTP1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-nacad-antibody-a15919-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15919-nacad-primary-antibodies-wb-testing-2.jpgAnti-NACAD AntibodyWestern blot analysis of lysates from Jurkat cells, using NACAD Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15919-nacad-primary-antibodies-wb-testing-3.jpgAnti-NACAD AntibodyWestern blot analysis of the lysates from HeLa cells using NACAD antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15919-nacad-primary-antibodies-ihc-testing-1.jpgAnti-NACAD AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-rsad1-antibody-a15914-1-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15914-1-rsad1-primary-antibodyes-wb-testing-1.jpgAnti-RSAD1 AntibodyWestern Blot (WB) analysis of specific cells using RSAD1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4d6-antibody-a15901-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15901-or4d6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4D6 AntibodyWestern Blot analysis of LOVO cells using Olfactory receptor 4D6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15901-or4d6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4D6 AntibodyWestern blot analysis of lysates from LOVO and NIH/3T3 cells, using OR4D6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15901-or4d6-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 4D6 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR4D6 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8d1-antibody-a15899-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15899-or8d1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8D1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 8D1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15899-or8d1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8D1 AntibodyWestern blot analysis of lysates from Jurkat, HepG2, MCF-7, and COLO cells, using OR8D1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15899-or8d1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8D1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR8D1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-akap-14-antibody-a15886-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15886-akap14-primary-antibodies-wb-testing-2.jpgAnti-AKAP 14 AntibodyWestern Blot analysis of Jurkat cells using AKAP 14 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15886-akap14-primary-antibodies-wb-testing-3.jpgAnti-AKAP 14 AntibodyWestern blot analysis of lysates from Jurkat, K562, and HUVEC cells, using AKAP14 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15886-akap14-primary-antibodies-wb-testing-4.jpgAnti-AKAP 14 AntibodyWestern blot analysis of the lysates from RAW264.7cells using AKAP14 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15886-akap14-primary-antibodies-ihc-testing-5.jpgAnti-AKAP 14 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15886-akap14-primary-antibodies-if-testing-1.jpgAnti-AKAP 14 AntibodyImmunofluorescence analysis of HeLa cells, using AKAP14 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dcamkl3-antibody-a15882-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15882-dclk3-primary-antibodies-wb-testing-2.jpgAnti-DCAMKL3 DCLK3 AntibodyWestern Blot analysis of various cells using DCAMKL3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15882-dclk3-primary-antibodies-wb-testing-3.jpgAnti-DCAMKL3 DCLK3 AntibodyWestern Blot analysis of Jurkat cells using DCAMKL3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15882-dclk3-primary-antibodies-ihc-testing-1.jpgAnti-DCAMKL3 DCLK3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using DCLK3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-1b1-antibody-a15873-boster.html2026-03-24T05:07:59+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-51b2-antibody-a15871-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15871-or51b2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51B2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 51B2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15871-or51b2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 51B2 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR51B2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15871-or51b2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 51B2 AntibodyWestern blot analysis of the lysates from K562 cells using OR51B2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15871-or51b2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51B2 AntibodyImmunofluorescence analysis of LOVO cells, using OR51B2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52d1-antibody-a15870-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15870-or52d1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 52D1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 52D1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-pote15-antibody-a15855-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15855-poteb-primary-antibodies-wb-testing-2.jpgAnti-POTE15 POTEB AntibodyWestern blot analysis of Mouse-kidney 3T3 lysis using POTE15 antibody. Antibody was diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15855-poteb-primary-antibodies-wb-testing-3.jpgAnti-POTE15 POTEB AntibodyWestern blot analysis of lysates from Jurkat cells, using A26B1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15855-poteb-primary-antibodies-ihc-testing-1.jpgAnti-POTE15 POTEB AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-7a10-antibody-a15826-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15826-or7a10-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 7A10 AntibodyWestern Blot analysis of various cells using Olfactory receptor 7A10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15826-or7a10-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 7A10 AntibodyWestern blot analysis of lysates from COS7 cells, using OR7A10 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15826-or7a10-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 7A10 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR7A10 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5b12-antibody-a15823-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15823-or5b12-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5B12 AntibodyImmunofluorescence analysis of COS7 cells, using OR5B12 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15823-or5b12-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5B12 AntibodyWestern Blot analysis of A549 cells using Olfactory receptor 5B12 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4a15-antibody-a15816-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15816-or4a15-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4A15 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4A15 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15816-or4a15-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4A15 AntibodyWestern blot analysis of lysates from COLO and HepG2 cells, using OR4A15 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15816-or4a15-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4A15 AntibodyWestern blot analysis of the lysates from HeLa cells using OR4A15 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15816-or4a15-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4A15 AntibodyImmunofluorescence analysis of A549 cells, using OR4A15 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2j2-antibody-a15815-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15815-or2j2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2J2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2J2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15815-or2j2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2J2 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR2J2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15815-or2j2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2J2 AntibodyImmunofluorescence analysis of A549 cells, using OR2J2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-1l6-antibody-a15811-boster.html2026-03-24T05:07:59+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-11g2-antibody-a15808-boster.html2026-03-24T05:07:59+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10x1-antibody-a15807-boster.html2026-03-24T05:07:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15807-or10x1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10X1 AntibodyWestern Blot analysis of COLO cells using Olfactory receptor 10X1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15807-or10x1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10X1 AntibodyWestern blot analysis of lysates from COLO cells, using OR10X1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15807-or10x1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10X1 AntibodyImmunofluorescence analysis of A549 cells, using OR10X1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10r2-antibody-a15806-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15806-or10r2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10R2 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR10R2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15806-or10r2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10R2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10R2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15806-or10r2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10R2 AntibodyWestern blot analysis of lysates from HeLa cells, using OR10R2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tcr-beta-antibody-a15765-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15765-trbc1-primary-antibodies-wb-testing-2.jpgAnti-TCR beta AntibodyWestern Blot analysis of various cells using TCR β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15765-trbc1-primary-antibodies-wb-testing-1.jpgAnti-TCR beta AntibodyWestern blot analysis of lysate from COLO205 cells treated with Forskolin, using TCR β antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l21-antibody-a15741-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15741-mrpl21-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L21 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MRPL21 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15741-mrpl21-primary-antibodies-wb-testing-2.jpgAnti-MRP-L21 AntibodyWestern Blot analysis of various cells using MRP-L21 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15741-mrpl21-primary-antibodies-wb-testing-3.jpgAnti-MRP-L21 AntibodyWestern blot analysis of lysates from COLO cells, using MRPL21 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15741-mrpl21-primary-antibodies-wb-testing-4.jpgAnti-MRP-L21 AntibodyWestern blot analysis of the lysates from HeLa cells using MRPL21 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-trmt11-antibody-a15724-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15724-trmt11-primary-antibodies-wb-testing-1.jpgAnti-TRMT11/Trm11 AntibodyWestern blot analysis of HepG2 JK Colo Hela using TRMT11 antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-pabp3-antibody-a15710-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15710-pabpc3-primary-antibodies-wb-testing-2.jpgAnti-PABP3 PABPC3 AntibodyWestern Blot analysis of 3T3 cells using PABP3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15710-pabpc3-primary-antibodies-wb-testing-3.jpgAnti-PABP3 PABPC3 AntibodyWestern blot analysis of PABPC3 Antibody. The lane on the right is blocked with the PABPC3 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15710-pabpc3-primary-antibodies-ihc-testing-1.jpgAnti-PABP3 PABPC3 AntibodyImmunohistochemistryt analysis of paraffin-embedded human testis, using PABPC3 Antibody. The lane on the right is blocked with the PABPC3 peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcng2-antibody-a15685-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15685-kcng2-primary-antibodies-wb-testing-2.jpgAnti-KCNG2/Kv6.2 AntibodyWestern Blot analysis of various cells using KCNG2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15685-kcng2-primary-antibodies-wb-testing-3.jpgAnti-KCNG2/Kv6.2 AntibodyWestern blot analysis of lysates from COLO cells, using KCNG2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15685-kcng2-primary-antibodies-ihc-testing-1.jpgAnti-KCNG2/Kv6.2 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-foxd4l1-antibody-a15665-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15665-foxd4l1-primary-antibodies-wb-testing-1.jpgAnti-Forkhead box protein D4-like 1 FoxD4L1 AntibodyWestern blot analysis of FOXD4L1 Antibody. The lane on the right is blocked with the FOXD4L1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15665-foxd4l1-primary-antibodies-wb-testing-2.jpgAnti-Forkhead box protein D4-like 1 FoxD4L1 AntibodyWestern Blot analysis of HuvEc cells using FoxD4L1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/anti-rrp7a-antibody-a15583-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15583-rrp7a-primary-antibodies-wb-testing-2.jpgAnti-RRP7A AntibodyWestern Blot analysis of K562, 293, SK-HEP-1, SHSY5Y, M21, mouse eye cells using RRP7A Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15583-rrp7a-primary-antibodies-ihc-testing-1.jpgAnti-RRP7A AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l24-antibody-a15563-1-boster.html2026-03-24T05:08:00+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-egfl5-antibody-a15544-1-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15544-1-megf9-primary-antibodies-wb-testing-2.jpgAnti-EGFL5 MEGF9 AntibodyWestern Blot analysis of various cells using EGFL5 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15544-1-megf9-primary-antibodies-wb-testing-1.jpgAnti-EGFL5 MEGF9 AntibodyWestern blot analysis of lysates from COLO cells, using MEGF9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5i1-antibody-a15527-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15527-or5i1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5I1 AntibodyWestern Blot analysis of 293T cells using Olfactory receptor 5I1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15527-or5i1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5I1 AntibodyWestern blot analysis of lysates from HepG2 cells, using OR5I1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15527-or5i1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 5I1 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR5I1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15527-or5i1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5I1 AntibodyImmunofluorescence analysis of A549 cells, using OR5I1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-suhw1-antibody-a15519-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15519-znf280a-primary-antibodies-ihc-testing-1.jpgAnti-SUHW1 ZNF280A AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15519-znf280a-primary-antibodies-wb-testing-2.jpgAnti-SUHW1 ZNF280A AntibodyWestern blot analysis of lysates from HeLa cells, using ZNF280A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr180-antibody-a15497-boster.html2026-03-24T05:08:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15497-gpr180-primary-antibodies-if-testing-1.jpgAnti-GPR180 AntibodyImmunofluorescence analysis of A549 cells, using GPR180 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15497-gpr180-primary-antibodies-wb-testing-2.jpgAnti-GPR180 AntibodyWestern Blot analysis of LOVO cells using GPR180 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15497-gpr180-primary-antibodies-wb-testing-3.jpgAnti-GPR180 AntibodyWestern blot analysis of the lysates from Jurkat cells using GPR180 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15497-gpr180-primary-antibodies-ihc-testing-4.jpgAnti-GPR180 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR180 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr146-antibody-a15465-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15465-gpr146-primary-antibodies-wb-testing-2.jpgAnti-GPR146 AntibodyWestern Blot analysis of LOVO cells using GPR146 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15465-gpr146-primary-antibodies-wb-testing-1.jpgAnti-GPR146 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR146 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ran-bp-6-antibody-a15427-1-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15427-1-ranbp6-primary-antibodies-wb-testing-2.jpgAnti-Ran BP-6 AntibodyWestern Blot analysis of various cells using Ran BP-6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15427-1-ranbp6-primary-antibodies-wb-testing-3.jpgAnti-Ran BP-6 AntibodyWestern blot analysis of lysates from COS7, K562, and COLO cells, using RANBP6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15427-1-ranbp6-primary-antibodies-wb-testing-4.jpgAnti-Ran BP-6 AntibodyWestern Blot analysis of Various cells using primary antibody at 1:1000 dilution 4°C, overnight. Secondary antibody was diluted at 1:10000 25°C, 1.5hourshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15427-1-ranbp6-primary-antibodies-ihc-testing-1.jpgAnti-Ran BP-6 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-7c2-antibody-a15405-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15405-or7c2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 7C2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 7C2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15405-or7c2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 7C2 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR7C2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15405-or7c2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 7C2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR7C2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rim4-antibody-a15404-1-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15404-1-rims4-primary-antibodies-wb-testing-2.jpgAnti-Rim4 RIMS4 AntibodyWestern Blot analysis of various cells using Rim4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15404-1-rims4-primary-antibodies-ihc-testing-1.jpgAnti-Rim4 RIMS4 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RIMS4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-5f1-antibody-a15375-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15375-or5f1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5F1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 5F1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15375-or5f1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5F1 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using OR5F1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15375-or5f1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5F1 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR5F1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52n4-antibody-a15373-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15373-or52n4-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52N4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR52N4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-4d1-antibody-a15371-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15371-or4d1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4D1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 4D1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15371-or4d1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4D1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR4D1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15371-or4d1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 4D1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR4D1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15371-or4d1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4D1 AntibodyImmunofluorescence analysis of A549 cells, using OR4D1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10s1-antibody-a15362-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15362-or10s1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10S1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10S1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15362-or10s1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10S1 AntibodyWestern blot analysis of lysates from COS7 and LOVO cells, using OR10S1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15362-or10s1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10S1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10S1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr176-antibody-a15335-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15335-gpr176-primary-antibodies-wb-testing-2.jpgAnti-GPR176 AntibodyWestern Blot analysis of various cells using GPR176 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15335-gpr176-primary-antibodies-wb-testing-3.jpgAnti-GPR176 AntibodyWestern blot analysis of lysates from COLO205 cells, using GPR176 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15335-gpr176-primary-antibodies-if-testing-1.jpgAnti-GPR176 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR176 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pdik1l-antibody-a15324-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15324-pdik1l-primary-antibodies-wb-testing-2.jpgAnti-PDIK1L AntibodyWestern Blot analysis of K562 cells using PDIK1L Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15324-pdik1l-primary-antibodies-wb-testing-3.jpgAnti-PDIK1L AntibodyWestern blot analysis of lysates from K562 cells, using PDIK1L Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15324-pdik1l-primary-antibodies-ihc-testing-1.jpgAnti-PDIK1L AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PDIK1L Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cripto-3-antibody-a15317-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15317-tdgf1p3-primary-antibodies-wb-testing-1.jpgAnti-Cripto-3 TDGF1P3 AntibodyWestern blot analysis of HepG2 293T AD293 Hela lysis using TDGF1P3 antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2a25-antibody-a15315-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15315-or2a25-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2A25 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2A25 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15315-or2a25-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2A25 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR2A25 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15315-or2a25-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 2A25 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR2A25 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15315-or2a25-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2A25 AntibodyImmunofluorescence analysis of A549 cells, using OR2A25 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr62-antibody-a15290-boster.html2026-03-24T05:08:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15290-gpr62-primary-antibodies-wb-testing-1.jpgAnti-G-protein coupled receptor 62 GPR62 AntibodyWestern blot analysis of lysates from COLO cells, using GPR62 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15290-gpr62-primary-antibodies-wb-testing-2.jpgAnti-G-protein coupled receptor 62 GPR62 AntibodyWestern Blot analysis of various cells using GPR62 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-foxr1-antibody-a15179-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15179-foxr1-primary-antibodies-wb-testing-2.jpgAnti-FoxR1 AntibodyWestern Blot analysis of various cells using FoxR1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15179-foxr1-primary-antibodies-wb-testing-3.jpgAnti-FoxR1 AntibodyWestern blot analysis of lysates from HeLa cells, using FOXR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15179-foxr1-primary-antibodies-ihc-testing-1.jpgAnti-FoxR1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-twik-3-antibody-a15165-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15165-kcnk7-primary-antibodies-wb-testing-1.jpgAnti-TWIK-3 AntibodyWestern Blot analysis of JK cells using TWIK-3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-cabp7-antibody-a15152-1-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15152-1-cabp7-primary-antibodies-ihc-testing-1.jpgAnti-Calcium-binding protein 7 CaBP7 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15152-1-cabp7-primary-antibodies-wb-testing-2.jpgAnti-Calcium-binding protein 7 CaBP7 AntibodyWestern Blot analysis of COLO cells using CaBP7 Polyclonal Antibody diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/anti-photomedin-1-antibody-a15100-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15100-olfml2a-primary-antibodyes-wb-testing-1.jpgAnti-Photomedin-1 AntibodyWestern blot analysis of RAW264.7 cells using Photomedin-1 Polyclonal Antibody
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15100-olfml2a-primary-antibodyes-wb-testing-2.jpgAnti-Photomedin-1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OLFML2A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15100-olfml2a-primary-antibodyes-ihc-testing-3.jpgAnti-Photomedin-1 AntibodyImmunofluorescence analysis of A549 cells, using OLFML2A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-7c1-antibody-a15095-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15095-or7c1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 7C1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 7C1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15095-or7c1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 7C1 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and COLO cells, using OR7C1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mct14-antibody-a15084-boster.html2026-03-24T05:08:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15084-slc16a14-primary-antibodyes-wb-testing-1.jpgAnti-MCT14 SLC16A14 AntibodyWestern Blot (WB) analysis of HepG2 cells using MCT14 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-10j1-antibody-a15013-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15013-or10j1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 10J1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 10J1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2k2-antibody-a14987-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14987-or2k2-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 2K2 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 2K2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-als2cr13-antibody-a14981-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14981-fam117b-primary-antibodies-wb-testing-2.jpgAnti-ALS2CR13 FAM117B AntibodyWestern Blot analysis of HELA cells using ALS2CR13 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14981-fam117b-primary-antibodies-wb-testing-1.jpgAnti-ALS2CR13 FAM117B AntibodyWestern Blot analysis of HELA cells using ALS2CR13 Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/anti-tnfaip8l3-antibody-a14951-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14951-tnfaip8l3-primary-antibodies-wb-testing-1.jpgAnti-TNFAIP8L3 AntibodyWestern Blot analysis of 1, 293T 2, mouse-brain cells using primary antibody diluted at 1:1000 (4°C overnight). Secondary antibody:Goat Anti-rabbit IgG IRDye 800 ( diluted at 1:5000, 25°C, 1 hour)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14951-12943_2022_1626_fig1_html.pngAnti-TNFAIP8L3 AntibodyT1: The expression and clinical significance of TIPE3 in PC. A Representative IHC staining of TIPE3. B IHC sum scores were applied to assess TIPE3 in PC specimens. C ) IHC staining of TIPE3 in PC tissues with or without lymph node metastasis. D IHC sum scores were applied to assess TIPE3 in PC specimens with or without lymph node metastasis. E TIPE3 expression in negative lymph node and metastatic lymph node. F Survival analysis according to TIPE3 expression in 188 PC patients. G Prognostic Nomogram of 188 PC patients. H Calibration curves of the OS nomogram. (I-K) DCA for the OS nomogram at 1-year I 2-year J and 3-year K . ***, P < 0.001. T2. The clinical significance of TIPE3 A IHC sum scores were applied to determine TIPE3 in PC. B IHC sum scores were applied to assess TIPE3 expression in PC specimens. C Survival analysis using TIPE3 in 66 PC patients. *, P < 0.05; ***, P < 0.001. T3. TIPE3 promoted malignant biological behaviors of PC cells. A Detection of TIPE3 mRNA expression using qRT-PCR. B TIPE3 expression were detected after TIPE3 silencing or overexpression using qRT-PCR. C CCK8 analysis was conducted after TIPE3 silencing in AsPC-1 and PANC-1 cells. D CCK8 analysis was conducted after TIPE3 overexpression in PC cells. E Trans-well assays were performed after TIPE3 silencing or overexpression in AsPC-1 cells. F Trans-well assays were performed after TIPE3 silencing or overexpression in PANC-1 cells. *, P < 0.05; **, P < 0.01; ***, P < 0.001. T4. TIPE3 promoted tumor progression and metastasis in mice. A Tumor growth curve of orthotopic xenograft mouse. B Representative pictures of primary tumors in pancreas. B Tumor volume in NC, shTIPE3 and TIPE3 group, respectively. D Tumor weight in NC, shTIPE3 and TIPE3 group, respectively. E Survival curves of different groups. F The representative of bioluminescent images in metastatic mouse model. G Number of liver metastatic foci were recorded. H Number of peritoneal metastatic tumors were recorded. *, P < 0.05; **, P < 0.01; ***, P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-022-01626-5'>35941647</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14951-12943_2022_1626_fig2_html.pngAnti-TNFAIP8L3 AntibodyT1: TIPE3 increased RAC1 in PC. A IHC staining of RAC1. B IHC sum scores were applied to determine RAC1 expression. C IHC sum scores of RAC1 in PC tissues with low or high TIPE3 expression. D Western-blot was conducted to detected RAC1 expression after TIPE3 silencing or overexpression. E Quantified results of western-blot for RAC1 expression in PC cells. F IHC staining of TIPE3, RAC1, RhoA and MMP9 in orthotopic xenograft tumors. G IHC sum scores of TIPE3, RAC1, RhoA and MMP9 expression in orthotopic xenograft tumors. *, P < 0.05; **, P < 0.01; ***, P < 0.001. T2. TIPE3 accelerated the malignant behaviors of PC cells in a RAC1-dependent manner. A NSC23766 (50 μM) was used in CCK8 analysis. B CCK8 assays was measurement after RAC1 silencing in PC cells. C Trans-well assays after treatment of NSC23766 (50 μM). D Trans-well assays were measurement after RAC1 silencing in PC cells. E CCK8 assays were measurement in TIPE3 silencing PC cells that pretreated with NSC23766 (50 μM) or transfection with RAC1 siRNA. F CCK8 assays were conducted in TIPE3 overexpressed PC cells that pretreated with NSC23766 (50 μM) or transfection with RAC1 siRNA. G Trans-well assays were conducted in TIPE3 silenced PC cells that pretreated with NSC23766 (50 μM). H Trans-well assays were conducted in TIPE3 silenced PC cells that transfected with RAC1 siRNA. I Trans-well assays were conducted in TIPE3 overexpressed PC cells that pretreated with NSC23766 (50 μM). J Trans-well migration and invasion assays were conducted in TIPE3 overexpressed PC cells that transfected with RAC1 siRNA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-022-01626-5'>35941647</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-gpr82-antibody-a14949-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14949-gpr82-primary-antibodies-wb-testing-2.jpgAnti-GPR82 AntibodyWestern Blot analysis of various cells using GPR82 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14949-gpr82-primary-antibodies-wb-testing-1.jpgAnti-GPR82 AntibodyWestern blot analysis of lysates from A549, K562, and HT-29 cells, using GPR82 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-mrp-s34-antibody-a14945-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14945-mrps34-primary-antibodies-ihc-testing-1.jpgAnti-MRP-S34 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14945-mrps34-primary-antibodies-wb-testing-2.jpgAnti-MRP-S34 AntibodyWestern Blot analysis of Jurkat cells using MRP-S34 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14945-mrps34-primary-antibodies-wb-testing-3.jpgAnti-MRP-S34 AntibodyWestern blot analysis of lysates from HeLa, HUVEC, HT-29, A549, and Jurkat cells, using MRPS34 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-1a1-antibody-a14933-boster.html2026-03-24T05:08:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14933-or1a1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 1A1 AntibodyWestern blot analysis of lysates from COLO cells, using OR1A1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14933-or1a1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 1A1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 1A1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-gpr156-antibody-a14916-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14916-gpr156-primary-antibodyes-wb-testing-1.jpgAnti-GPR156 AntibodyWestern Blot (WB) analysis of specific cells using GPR156 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-hsp77-76-antibody-a14896-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14896-hspa7-primary-antibodies-wb-testing-1.jpgAnti-HSP77/76 AntibodyWestern Blot analysis of K562 cells using HSP77/76 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-cadherin-26-antibody-a14851-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14851-cdh26-primary-antibodies-wb-testing-2.jpgAnti-Cadherin-26 AntibodyWestern Blot analysis of various cells using Cadherin-26 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14851-cdh26-primary-antibodies-if-testing-1.jpgAnti-Cadherin-26 AntibodyImmunofluorescence analysis of MCF7 cells, using CDH26 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr115-antibody-a14764-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14764-adgrf4-primary-antibodies-wb-testing-2.jpgAnti-GPR115 ADGRF4 AntibodyWestern Blot analysis of RAW264.7 cells using GPR115 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14764-adgrf4-primary-antibodies-wb-testing-3.jpgAnti-GPR115 ADGRF4 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using GPR115 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14764-adgrf4-primary-antibodies-if-testing-1.jpgAnti-GPR115 ADGRF4 AntibodyImmunofluorescence analysis of LOVO cells, using GPR115 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ccdc45-antibody-a14760-1-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14760-1-cep95-primary-antibodyes-wb-testing-1.jpgAnti-CCDC45 CEP95 AntibodyWestern Blot (WB) analysis of specific cells using CCDC45 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-6q1-antibody-a14742-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14742-or6q1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6Q1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 6Q1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14742-or6q1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 6Q1 AntibodyWestern blot analysis of lysates from Jurkat and HT-29 cells, using OR6Q1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14742-or6q1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6Q1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR6Q1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-usp43-antibody-a14739-1-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14739-1-usp43-primary-antibodies-wb-testing-1.jpgAnti-USP43 AntibodyWestern Blot analysis of JK cells using USP43 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbl1y-antibody-a14704-boster.html2026-03-24T05:08:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14704-tbl1y-primary-antibodies-wb-testing-1.jpgAnti-TBL1Y Monoclonal AntibodyWestern Blot analysis using TBL1Y Monoclonal Antibody against Y79, HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-kdel-receptor-3-antibody-a14682-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14682-kdelr3-primary-antibodies-wb-testing-2.jpgAnti-KDEL Receptor 3 KDELR3 AntibodyWestern Blot analysis of 3T3 cells using KDEL Receptor 3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14682-kdelr3-primary-antibodies-wb-testing-1.jpgAnti-KDEL Receptor 3 KDELR3 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using ERD23 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-actin-kappa-antibody-a14672-1-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14672-1-actbl2-primary-antibodyes-wb-testing-1.jpgAnti-Actin- kappa ACTBL2 AntibodyWestern Blot (WB) analysis of specific cells using Actin-kappa Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-kv-beta-3-antibody-a14634-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14634-kcnab3-primary-antibodies-ihc-testing-1.jpgAnti-KV beta.3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using KCNAB3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14634-kcnab3-primary-antibodies-wb-testing-2.jpgAnti-KV beta.3 AntibodyWestern Blot analysis of various cells using KVβ.3 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-cd306-antibody-a14618-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14618-lair2-primary-antibodies-wb-testing-2.jpgAnti-CD306 AntibodyWestern blot analysis of RAT-KIDNEY lysis using LAIR2 antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14618-lair2-primary-antibodies-wb-testing-1.jpgAnti-CD306 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-neurexophilin-3-antibody-a14597-1-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-1-nxph3-primary-antibodies-wb-testing-2.jpgAnti-Neurexophilin-3 NXPH3 AntibodyWestern Blot analysis of various cells using Neurexophilin-3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-1-nxph3-primary-antibodies-wb-testing-3.jpgAnti-Neurexophilin-3 NXPH3 AntibodyWestern blot analysis of lysates from HT-29 cells, using NXPH3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-1-nxph3-primary-antibodies-wb-testing-4.jpgAnti-Neurexophilin-3 NXPH3 AntibodyWestern blot analysis of the lysates from HepG2 cells using NXPH3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-1-nxph3-primary-antibodies-ihc-testing-1.jpgAnti-Neurexophilin-3 NXPH3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-gpr19-antibody-a14590-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14590-gpr19-primary-antibodyes-wb-testing-1.jpgAnti-GPR19 AntibodyWestern Blot (WB) analysis of specific cells using GPR19 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dgat2l3-antibody-a14578-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14578-awat1-primary-antibodies-wb-testing-2.jpgAnti-DGAT2L3 AWAT1 AntibodyWestern Blot analysis of 293 cells using DGAT2L3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14578-awat1-primary-antibodies-wb-testing-3.jpgAnti-DGAT2L3 AWAT1 AntibodyWestern blot analysis of mouse-kidney KB lysis using DGAT2L3 antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14578-awat1-primary-antibodies-wb-testing-4.jpgAnti-DGAT2L3 AWAT1 AntibodyWestern blot analysis of lysates from 293 cells, using AWAT1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14578-awat1-primary-antibodies-wb-testing-1.jpgAnti-DGAT2L3 AWAT1 AntibodyWestern blot analysis of the lysates from HT-29 cells using AWAT1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rab-l2a-antibody-a14567-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14567-rabl2a-primary-antibodies-wb-testing-2.jpgAnti-Rab L2A AntibodyWestern Blot analysis of COLO205 cells using Rab L2A Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14567-rabl2a-primary-antibodies-ihc-testing-1.jpgAnti-Rab L2A AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-pig-x-antibody-a14557-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14557-pigx-primary-antibodies-wb-testing-2.jpgAnti-PIG-X AntibodyWestern Blot analysis of various cells using PIG-X Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14557-pigx-primary-antibodies-wb-testing-3.jpgAnti-PIG-X AntibodyWestern blot analysis of lysates from 293, COLO, HUVEC, and Jurkat cells, using PIGX Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14557-pigx-primary-antibodies-ihc-testing-1.jpgAnti-PIG-X AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr113-antibody-a14528-boster.html2026-03-24T05:08:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14528-adgrf3-primary-antibodies-wb-testing-2.jpgAnti-GPR113 AntibodyWestern Blot analysis of Hela cells using GPR113 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14528-adgrf3-primary-antibodies-wb-testing-1.jpgAnti-GPR113 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR113 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l35-antibody-a14506-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14506-mrpl35-primary-antibodyes-wb-testing-1.jpgAnti-MRP-L35 AntibodyWestern Blot (WB) analysis of 293T COLO205 using MRP-L35 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14506-mrpl35-primary-antibodyes-wb-testing-2.jpgAnti-MRP-L35 AntibodyWestern Blot (WB) analysis of 293 using MRP-L35 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cdyl2-antibody-a14503-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14503-cdyl2-primary-antibodies-wb-testing-2.jpgAnti-Chromodomain Y-like protein 2 CDYL2 AntibodyWestern Blot analysis of various cells using CDYL2 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14503-cdyl2-primary-antibodies-wb-testing-3.jpgAnti-Chromodomain Y-like protein 2 CDYL2 AntibodyWestern Blot analysis of HEPG2 cells using CDYL2 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14503-cdyl2-primary-antibodies-ihc-testing-1.jpgAnti-Chromodomain Y-like protein 2 CDYL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using CDYL2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dleu7-antibody-a14500-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14500-dleu7-primary-antibodyes-ihc-testing-1.jpgAnti-Leukemia-associated protein 7 DLEU7 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14500-dleu7-primary-antibodyes-ihc-testing-2.jpgAnti-Leukemia-associated protein 7 DLEU7 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr171-antibody-a14498-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14498-gpr171-primary-antibodyes-wb-testing-1.jpgAnti-GPR171 AntibodyWestern blot analysis of various cells using GPR171 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l51-antibody-a14477-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14477-mrpl51-primary-antibodies-wb-testing-2.jpgAnti-MRP-L51 AntibodyWestern Blot analysis of 293T cells using MRP-L51 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14477-mrpl51-primary-antibodies-wb-testing-3.jpgAnti-MRP-L51 AntibodyWestern blot analysis of the lysates from HUVECcells using MRPL51 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14477-mrpl51-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L51 AntibodyImmunohistochemistry analysis of paraffin-embedded human tonsil tissue, using MRPL51 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ppp1r14d-antibody-a14433-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14433-ppp1r14d-primary-antibodies-wb-testing-2.jpgAnti-PPP1R14D/Gbpi 1 AntibodyWestern Blot analysis of various cells using PPP1R14D Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14433-ppp1r14d-primary-antibodies-wb-testing-3.jpgAnti-PPP1R14D/Gbpi 1 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and COLO cells, using PPP1R14D Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14433-ppp1r14d-primary-antibodies-ihc-testing-1.jpgAnti-PPP1R14D/Gbpi 1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-thap4-antibody-a14419-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14419-thap4-primary-antibodies-wb-testing-2.jpgAnti-THAP4 AntibodyWestern Blot analysis of various cells using THAP4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14419-thap4-primary-antibodies-wb-testing-3.jpgAnti-THAP4 AntibodyWestern blot analysis of the lysates from HT-29 cells using THAP4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14419-thap4-primary-antibodies-ihc-testing-1.jpgAnti-THAP4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52a1-antibody-a14417-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14417-or52a1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 52A1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 52A1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgf-antibody-a14393-boster.html2026-03-24T05:08:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14393-mrgprf-primary-antibodyes-wb-testing-1.jpgAnti-MRGF MRGPRF AntibodyWestern Blot (WB) analysis of specific cells using MRGF Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-sre-zbp-antibody-a14317-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14317-zscan26-primary-antibodies-wb-testing-2.jpgAnti-SRE-ZBP ZSCAN26 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using ZNF187 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14317-zscan26-primary-antibodies-ihc-testing-3.jpgAnti-SRE-ZBP ZSCAN26 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14317-zscan26-primary-antibodies-if-testing-1.jpgAnti-SRE-ZBP ZSCAN26 AntibodyImmunofluorescence analysis of A549 cells, using ZNF187 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l46-antibody-a14284-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14284-mrpl46-primary-antibodies-wb-testing-2.jpgAnti-MRP-L46 AntibodyWestern Blot analysis of various cells using MRP-L46 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14284-mrpl46-primary-antibodies-wb-testing-3.jpgAnti-MRP-L46 AntibodyWestern blot analysis of lysates from HeLa cells, using MRPL46 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14284-mrpl46-primary-antibodies-wb-testing-4.jpgAnti-MRP-L46 AntibodyWestern blot analysis of the lysates from HUVECcells using MRPL46 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14284-mrpl46-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L46 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using MRPL46 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-acetyl-nf-e4-k43-antibody-a14260-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14260-nfe4-primary-antibodyes-wb-testing-1.jpgAnti-Acetyl-NF-E4 (K43) AntibodyWestern Blot (WB) analysis of AD-293 cells using Acetyl-NF-E4 (K43) Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14260-nfe4-primary-antibodyes-wb-testing-2.jpgAnti-Acetyl-NF-E4 (K43) AntibodyWestern Blot (WB) analysis of AD-293 cells using Acetyl-NF-E4 (K43) Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rbm34-antibody-a14178-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14178-rbm34-primary-antibodies-ihc-testing-1.jpgAnti-RBM34 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RBM34 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14178-rbm34-primary-antibodies-wb-testing-2.jpgAnti-RBM34 AntibodyWestern Blot analysis of 3T3 cells using RBM34 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/anti-septin-8-antibody-a14166-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14166-sept8-primary-antibodies-wb-testing-2.jpgAnti-Septin 8 SEPT8; AntibodyWestern Blot analysis of various cells using Septin 8 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14166-sept8-primary-antibodies-wb-testing-3.jpgAnti-Septin 8 SEPT8; AntibodyWestern blot analysis of lysates from HeLa cells, using SEPT8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14166-sept8-primary-antibodies-ihc-testing-1.jpgAnti-Septin 8 SEPT8; AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-fam80b-antibody-a14138-boster.html2026-03-24T05:08:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14138-rimklb-primary-antibodies-wb-testing-2.jpgAnti-FAM80B RIMKLB AntibodyWestern Blot analysis of various cells using FAM80B Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14138-rimklb-primary-antibodies-wb-testing-1.jpgAnti-FAM80B RIMKLB AntibodyWestern blot analysis of lysates from HepG2 and COS cells, using RIMKB Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr173-antibody-a14126-boster.html2026-03-24T05:08:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14126-gpr173-primary-antibodies-wb-testing-1.jpgAnti-GPR173/Sreb3 AntibodyWestern blot analysis of the lysates from COLO205 cells using GPR173 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14126-gpr173-primary-antibodies-wb-testing-2.jpgAnti-GPR173/Sreb3 AntibodyWestern Blot analysis of 3T3 cells using GPR173 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14126-gpr173-primary-antibodies-wb-testing-3.jpgAnti-GPR173/Sreb3 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using GPR173 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cmtm4-antibody-a14124-boster.html2026-03-24T05:08:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14124-cmtm4-primary-antibodies-wb-testing-2.jpgAnti-CMTM4 AntibodyWestern Blot analysis of HELA cells using CMTM4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14124-cmtm4-primary-antibodies-wb-testing-3.jpgAnti-CMTM4 AntibodyWestern blot analysis of CKLF4 Antibody. The lane on the right is blocked with the CKLF4 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14124-cmtm4-primary-antibodies-ihc-testing-4.jpgAnti-CMTM4 AntibodyImmunohistochemistryt analysis of paraffin-embedded human breast carcinoma, using CKLF4 Antibody. The lane on the right is blocked with the CKLF4 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14124-cmtm4-primary-antibodies-if-testing-1.jpgAnti-CMTM4 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/anti-cmtm6-antibody-a14107-boster.html2026-03-24T05:08:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14107-cmtm6-primary-antibodies-ihc-testing-1.jpgAnti-CMTM6 AntibodyImmunohistochemical analysis of paraffin-embedded human-oophoroma, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14107-cmtm6-primary-antibodies-wb-testing-2.jpgAnti-CMTM6 AntibodyWestern Blot analysis of 293 cells using CMTM6 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-mrp-s25-antibody-a14080-1-boster.html2026-03-24T05:08:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14080-1-mrps25-primary-antibodies-ihc-testing-1.jpgAnti-MRP-S25 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14080-1-mrps25-primary-antibodies-wb-testing-2.jpgAnti-MRP-S25 AntibodyWestern Blot analysis of various cells using MRP-S25 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14080-1-mrps25-primary-antibodies-wb-testing-3.jpgAnti-MRP-S25 AntibodyWestern blot analysis of lysates from 293 cells, using MRPS25 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14080-1-mrps25-primary-antibodies-wb-testing-4.jpgAnti-MRP-S25 AntibodyWestern blot analysis of the lysates from HepG2 cells using MRPS25 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-s9-antibody-a14072-1-boster.html2026-03-24T05:08:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14072-1-mrps9-primary-antibodies-ihc-testing-1.jpgAnti-MRP-S9 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14072-1-mrps9-primary-antibodies-wb-testing-2.jpgAnti-MRP-S9 AntibodyWestern Blot analysis of various cells using MRP-S9 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14072-1-mrps9-primary-antibodies-wb-testing-3.jpgAnti-MRP-S9 AntibodyWestern blot analysis of lysates from A549 cells, using MRPS9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nek5-antibody-a14002-1-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14002-1-nek5-primary-antibodies-wb-testing-2.jpgAnti-Nek5 AntibodyWestern Blot analysis of various cells using Nek5 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14002-1-nek5-primary-antibodies-wb-testing-1.jpgAnti-Nek5 AntibodyWestern blot analysis of NEK5 Antibody. The lane on the right is blocked with the NEK5 peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-adam32-antibody-a13911-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13911-adam32-primary-antibodyes-wb-testing-1.jpgAnti-ADAM32 AntibodyWestern Blot (WB) analysis of specific cells using ADAM32 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-bsx-antibody-a13902-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13902-bsx-primary-antibodies-wb-testing-1.jpgAnti-BSX AntibodyWestern Blot analysis of 293T cells using BSX Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/anti-gsc2-antibody-a13871-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13871-gsc2-primary-antibodyes-wb-testing-1.jpgAnti-Homeobox protein goosecoid-2 GSC2 AntibodyWestern Blot (WB) analysis of specific cells using GSC2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-plasminogen-receptor-antibody-a13829-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13829-plgrkt-primary-antibodyes-wb-testing-1.jpgAnti-Plasminogen receptor PLGRKT AntibodyWestern Blot (WB) analysis of HepG2 cells using Plasminogen receptor Polyclonal antibody diluted at 1:500.
https://www.bosterbio.com/products/primary-antibodies/anti-pdrg1-antibody-a13826-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13826-pdrg1-primary-antibodies-wb-testing-2.jpgAnti-PDRG1/Pdrg AntibodyWestern Blot analysis of various cells using PDRG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13826-pdrg1-primary-antibodies-wb-testing-3.jpgAnti-PDRG1/Pdrg AntibodyWestern blot analysis of lysates from Jurkat, COLO, MCF-7, and HepG2 cells, using PDRG1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13826-pdrg1-primary-antibodies-ihc-testing-1.jpgAnti-PDRG1/Pdrg AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-s35-antibody-a13823-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-mrps35-primary-antibodies-wb-testing-2.jpgAnti-MRP-S35 AntibodyWestern Blot analysis of K562 cells using MRP-S35 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-mrps35-primary-antibodies-wb-testing-3.jpgAnti-MRP-S35 AntibodyWestern blot analysis of lysates from Jurkat, COLO, and A549 cells, using MRPS35 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-mrps35-primary-antibodies-ihc-testing-4.jpgAnti-MRP-S35 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-mrps35-primary-antibodies-if-testing-1.jpgAnti-MRP-S35 AntibodyImmunofluorescence analysis of MCF7 cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/anti-fgf-11-antibody-a13819-boster.html2026-03-24T05:08:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13819-fgf11-primary-antibodies-wb-testing-1.jpgAnti-FGF-11 AntibodyWestern Blot analysis of NIH-3T3, Hela cells using FGF-11 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-13g1-antibody-a13790-boster.html2026-03-24T05:08:10+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-cdc50b-antibody-a13764-1-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13764-1-tmem30b-primary-antibodyes-wb-testing-1.jpgAnti-Cdc50B TMEM30B AntibodyWestern Blot (WB) analysis of K562 cells using Cdc50B Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tryptase-3-antibody-a13747-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13747-tpsd1-primary-antibodies-wb-testing-2.jpgAnti-Tryptase-3 Antibody Western Blot analysis of HEPG2 cells using Tryptase-3 Polyclonal Antibody diluted at 1:800. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13747-tpsd1-primary-antibodies-ihc-testing-3.jpgAnti-Tryptase-3 Antibody Immunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13747-tpsd1-primary-antibodies-ihc-testing-4.jpgAnti-Tryptase-3 Antibody Immunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13747-tpsd1-primary-antibodies-ihc-testing-1.jpgAnti-Tryptase-3 Antibody Immunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-cep78-antibody-a13706-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13706-cep78-primary-antibodies-wb-testing-2.jpgAnti-CEP78 AntibodyWestern Blot analysis of various cells using CEP78 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13706-cep78-primary-antibodies-wb-testing-3.jpgAnti-CEP78 AntibodyWestern blot analysis of lysates from HeLa cells, using CEP78 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13706-cep78-primary-antibodies-ihc-testing-1.jpgAnti-CEP78 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using CEP78 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prpf18-antibody-a13674-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13674-prpf18-primary-antibodies-wb-testing-2.jpgAnti-PRPF18/Prp18 AntibodyWestern Blot analysis of HuvEc cells using PRPF18 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13674-prpf18-primary-antibodies-wb-testing-3.jpgAnti-PRPF18/Prp18 AntibodyWestern blot analysis of lysates from 293, MCF-7, and HUVEC cells, using PRPF18 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13674-prpf18-primary-antibodies-ihc-testing-1.jpgAnti-PRPF18/Prp18 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-aarsd1-antibody-a13651-1-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13651-1-aarsd1-primary-antibodies-wb-testing-2.jpgAnti-AARSD1 AntibodyWestern Blot analysis of various cells using AARSD1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13651-1-aarsd1-primary-antibodies-wb-testing-3.jpgAnti-AARSD1 AntibodyWestern blot analysis of lysates from A549, 293, and HepG2 cells, using AARSD1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13651-1-aarsd1-primary-antibodies-wb-testing-1.jpgAnti-AARSD1 AntibodyWestern blot analysis of the lysates from HUVECcells using AARSD1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs14-antibody-a13641-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13641-sugp2-primary-antibodies-wb-testing-2.jpgAnti-SFRS14 AntibodyWestern blot analysis of SFRS14 Antibody. The lane on the right is blocked with the SFRS14 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13641-sugp2-primary-antibodies-ihc-testing-1.jpgAnti-SFRS14 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-lrrc41-antibody-a13640-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13640-lrrc41-primary-antibodyes-wb-testing-1.jpgAnti-LRRC41 AntibodyWestern Blot (WB) analysis of specific cells using LRRC41 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13640-lrrc41-primary-antibodyes-wb-testing-2.jpgAnti-LRRC41 AntibodyWestern Blot (WB) analysis of K562 cells using LRRC41 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-usp40-antibody-a13619-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13619-usp40-primary-antibodies-wb-testing-2.jpgAnti-USP40 AntibodyWestern Blot analysis of 293 cells using USP40 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13619-usp40-primary-antibodies-ihc-testing-1.jpgAnti-USP40 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using USP40 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr175-antibody-a13599-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13599-tpra1-primary-antibodies-wb-testing-2.jpgAnti-GPR175 TPRA1 AntibodyWestern Blot analysis of various cells using GPR175 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13599-tpra1-primary-antibodies-wb-testing-1.jpgAnti-GPR175 TPRA1 AntibodyWestern blot analysis of lysates from 293 cells, using GPR175 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-emr4-antibody-a13581-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13581-adgre4p-primary-antibodies-wb-testing-2.jpgAnti-EMR4 ADGRE4P AntibodyWestern Blot analysis of various cells using EMR4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13581-adgre4p-primary-antibodies-wb-testing-3.jpgAnti-EMR4 ADGRE4P AntibodyWestern Blot analysis of COLO205 cells using EMR4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13581-adgre4p-primary-antibodies-wb-testing-1.jpgAnti-EMR4 ADGRE4P AntibodyWestern blot analysis of lysates from HUVEC cells, COS7 cells, HeLa cells, and COLO205 cells, using EMR4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-serpin-b12-antibody-a13578-boster.html2026-03-24T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13578-serpinb12-primary-antibodies-ihc-testing-1.jpgAnti-Serpin B12 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13578-serpinb12-primary-antibodies-wb-testing-2.jpgAnti-Serpin B12 AntibodyWestern Blot analysis of various cells using Serpin B12 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13578-serpinb12-primary-antibodies-wb-testing-3.jpgAnti-Serpin B12 AntibodyWestern blot analysis of the lysates from HeLa cells using SERPINB12 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l13-antibody-a13508-1-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13508-1-mrpl13-primary-antibodies-wb-testing-2.jpgAnti-MRP-L13 AntibodyWestern Blot analysis of various cells using MRP-L13 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13508-1-mrpl13-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L13 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using MRPL13 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2ag1-2-antibody-a13455-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13455-or2ag1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 2AG1/2 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 2AG1/2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cd300d-antibody-a13423-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13423-cd300ld-primary-antibodies-wb-testing-2.jpgAnti-CD300d AntibodyWestern Blot analysis of NIH-3T3 cells using CD300d Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13423-cd300ld-primary-antibodies-wb-testing-1.jpgAnti-CD300d AntibodyWestern Blot analysis of 3T3 cells using CD300d Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-brp16-antibody-a13420-1-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13420-1-hgh1-primary-antibodies-ihc-testing-1.jpgAnti-Brp16 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using BRP16 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13420-1-hgh1-primary-antibodies-wb-testing-2.jpgAnti-Brp16 AntibodyWestern Blot analysis of various cells using Brp16 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13420-1-hgh1-primary-antibodies-wb-testing-3.jpgAnti-Brp16 AntibodyWestern blot analysis of lysates from COLO cells, using BRP16 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cyp4z1-2-antibody-a13386-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13386-cyp4z1-primary-antibodies-wb-testing-2.jpgAnti-CYP4Z1/2 AntibodyWestern Blot analysis of various cells using CYP4Z1/2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13386-cyp4z1-primary-antibodies-ihc-testing-1.jpgAnti-CYP4Z1/2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-gpr75-antibody-a13384-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13384-gpr75-primary-antibodies-if-testing-1.jpgAnti-GPR75 AntibodyImmunofluorescence analysis of LOVO cells, using GPR75 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13384-gpr75-primary-antibodies-wb-testing-2.jpgAnti-GPR75 AntibodyWestern Blot analysis of HT-29 cells using GPR75 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13384-gpr75-primary-antibodies-wb-testing-3.jpgAnti-GPR75 AntibodyWestern blot analysis of lysates from HT-29 and K562 cells, using GPR75 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-zfp106-antibody-a13343-boster.html2026-03-24T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13343-znf106-primary-antibodies-wb-testing-2.jpgAnti-ZFP106 ZNF106 AntibodyWestern Blot analysis of COS7 cells using ZFP106 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13343-znf106-primary-antibodies-wb-testing-1.jpgAnti-ZFP106 ZNF106 AntibodyWestern blot analysis of lysate from COS7 cells, using ZFP106 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cpa5-antibody-a13307-1-boster.html2026-03-24T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13307-1-cpa5-primary-antibodies-wb-testing-2.jpgAnti-CPA5 AntibodyWestern Blot analysis of various cells using CPA5 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13307-1-cpa5-primary-antibodies-wb-testing-1.jpgAnti-CPA5 AntibodyWestern blot analysis of the lysates from COLO205 cells using CPA5 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zadh2-antibody-a13201-1-boster.html2026-03-24T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13201-1-zadh2-primary-antibodies-ihc-testing-1.jpgAnti-ZADH2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13201-1-zadh2-primary-antibodies-wb-testing-2.jpgAnti-ZADH2 AntibodyWestern blot analysis of lysates from HUVEC, HT-29, and COLO cells, using ZADH2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pmp24-antibody-a13147-boster.html2026-03-24T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13147-pxmp4-primary-antibodies-wb-testing-2.jpgAnti-Pmp24 AntibodyWestern Blot analysis of COS-7 cells using Pmp24 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13147-pxmp4-primary-antibodies-wb-testing-3.jpgAnti-Pmp24 AntibodyWestern blot analysis of lysates from COS7 and COLO cells, using PXMP4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13147-pxmp4-primary-antibodies-ihc-testing-1.jpgAnti-Pmp24 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-52e1-antibody-a13120-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13120-or52e1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 52E1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 52E1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zip9-antibody-a13097-1-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13097-1-slc39a9-primary-antibodies-wb-testing-2.jpgAnti-ZIP9 SLC39A9 AntibodyWestern Blot analysis of various cells using ZIP9 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13097-1-slc39a9-primary-antibodies-wb-testing-3.jpgAnti-ZIP9 SLC39A9 AntibodyWestern blot analysis of SLC39A9 Antibody. The lane on the right is blocked with the SLC39A9 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13097-1-slc39a9-primary-antibodies-wb-testing-1.jpgAnti-ZIP9 SLC39A9 AntibodyWestern blot analysis of the lysates from HeLa cells using SLC39A9 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-eif4e3-antibody-a13024-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13024-eif4e3-primary-antibodies-wb-testing-2.jpgAnti-eIF4E3 AntibodyWestern Blot analysis of 3T3 cells using eIF4E3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13024-eif4e3-primary-antibodies-wb-testing-3.jpgAnti-eIF4E3 AntibodyWestern blot analysis of lysates from LOVO cells, using EIF4E3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13024-eif4e3-primary-antibodies-wb-testing-1.jpgAnti-eIF4E3 AntibodyWestern blot analysis of the lysates from HepG2 cells using EIF4E3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cd85f-antibody-a13016-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13016-lilra5-primary-antibodyes-wb-testing-1.jpgAnti-CD85f LILRA5 AntibodyWestern Blot (WB) analysis of HeLa cells using CD85f Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr52-antibody-a13015-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13015-gpr52-primary-antibodies-wb-testing-2.jpgAnti-G-protein coupled receptor 52 GPR52 AntibodyWestern Blot analysis of various cells using GPR52 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13015-gpr52-primary-antibodies-wb-testing-3.jpgAnti-G-protein coupled receptor 52 GPR52 AntibodyWestern blot analysis of 293T 3T3 lysis using GPR52 antibody. Antibody was diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13015-gpr52-primary-antibodies-wb-testing-1.jpgAnti-G-protein coupled receptor 52 GPR52 AntibodyWestern blot analysis of lysates from COLO, HUVEC, HeLa, and HepG2 cells, using GPR52 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-septin-3-antibody-a12961-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12961-sept3-primary-antibodies-wb-testing-2.jpgAnti-Septin 3 AntibodyWestern Blot analysis of various cells using Septin 3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12961-sept3-primary-antibodies-wb-testing-3.jpgAnti-Septin 3 AntibodyWestern blot analysis of lysates from 293 cells, using SEPT3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12961-sept3-primary-antibodies-ihc-testing-1.jpgAnti-Septin 3 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2w3-antibody-a12959-boster.html2026-03-24T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12959-or2w3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2W3 AntibodyWestern Blot analysis of 3T3 cells using Olfactory receptor 2W3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12959-or2w3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2W3 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using OR2W3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf420-antibody-a12954-1-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12954-1-znf420-primary-antibodies-wb-testing-2.jpgAnti-Zinc finger protein 420 ZNF420 AntibodyWestern Blot analysis of K562 cells using ZNF420 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12954-1-znf420-primary-antibodies-wb-testing-3.jpgAnti-Zinc finger protein 420 ZNF420 AntibodyWestern blot analysis of ZNF420 Antibody. The lane on the right is blocked with the ZNF420 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12954-1-znf420-primary-antibodies-wb-testing-1.jpgAnti-Zinc finger protein 420 ZNF420 AntibodyWestern blot analysis of the lysates from COLO205 cells using ZNF420 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-8j1-antibody-a12941-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12941-or8j1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8J1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 8J1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12941-or8j1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8J1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR8J1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12941-or8j1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 8J1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR8J1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12941-or8j1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8J1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR8J1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr114-antibody-a12882-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12882-adgrg5-primary-antibodies-wb-testing-1.jpgAnti-GPR114 AntibodyWestern blot analysis of lysates from COLO205 cells, using GPR114 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12882-adgrg5-primary-antibodies-wb-testing-2.jpgAnti-GPR114 AntibodyWestern Blot analysis of COLO205 cells using GPR114 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-ankrd30a-antibody-a12867-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12867-ankrd30a-primary-antibodies-wb-testing-2.jpgAnti-ANKRD30A/Ny Br 1 AntibodyWestern Blot analysis of various cells using ANKRD30A Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12867-ankrd30a-primary-antibodies-wb-testing-3.jpgAnti-ANKRD30A/Ny Br 1 AntibodyWestern blot analysis of lysates from 293 and COLO cells, using AN30A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12867-ankrd30a-primary-antibodies-ihc-testing-1.jpgAnti-ANKRD30A/Ny Br 1 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-npdc-1-antibody-a12846-1-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12846-1-npdc1-primary-antibodies-wb-testing-2.jpgAnti-NPDC-1 AntibodyWestern Blot analysis of various cells using NPDC-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12846-1-npdc1-primary-antibodies-wb-testing-3.jpgAnti-NPDC-1 AntibodyWestern blot analysis of lysates from HepG2 and LOVO cells, using NPDC1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12846-1-npdc1-primary-antibodies-wb-testing-1.jpgAnti-NPDC-1 AntibodyWestern blot analysis of the lysates from K562 cells using NPDC1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-egfl4-antibody-a12840-boster.html2026-03-24T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12840-megf8-primary-antibodies-wb-testing-2.jpgAnti-EGFL4 AntibodyWestern Blot analysis of various cells using EGFL4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12840-megf8-primary-antibodies-wb-testing-3.jpgAnti-EGFL4 AntibodyWestern blot analysis of lysates from COLO cells, using MEGF8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12840-megf8-primary-antibodies-wb-testing-1.jpgAnti-EGFL4 AntibodyWestern blot analysis of the lysates from COLO205 cells using MEGF8 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cadherin-18-antibody-a12825-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12825-cdh18-primary-antibodies-wb-testing-1.jpgAnti-Cadherin-18 AntibodyWestern blot analysis of lysates from HeLa, A549, and COLO205 cells, using CDH18 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12825-cdh18-primary-antibodies-wb-testing-2.jpgAnti-Cadherin-18 AntibodyWestern Blot analysis of various cells using Cadherin-18 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-rrp22-antibody-a12803-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12803-rasl10a-primary-antibodies-wb-testing-2.jpgAnti-RRP22 RASL10A AntibodyWestern blot analysis of lysates from HeLa cells, using RASL10A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12803-rasl10a-primary-antibodies-wb-testing-1.jpgAnti-RRP22 RASL10A AntibodyWestern blot analysis of the lysates from 293 cells using RASL10A antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl21-antibody-a12797-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12797-klhl21-primary-antibodyes-wb-testing-1.jpgAnti-KLHL21 Monoclonal Antibody Western Blot (WB) analysis using KLHL21 Monoclonal antibody against recombinant KLHL21 protein (1).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12797-klhl21-primary-antibodyes-ihc-testing-2.jpgAnti-KLHL21 Monoclonal Antibody Immunohistochemistry (IHC) analysis of paraffin-embedded Human Brain tissues with DAB staining using KLHL21 Monoclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-asah3-antibody-a12775-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12775-acer1-primary-antibodyes-wb-testing-1.jpgAnti-ASAH3 AntibodyWestern Blot (WB) analysis of HepG2 using ASAH3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-znf608-antibody-a12737-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12737-znf608-primary-antibodies-wb-testing-2.jpgAnti-Zinc finger protein 608 ZNF608 AntibodyWestern Blot analysis of various cells using ZNF608 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12737-znf608-primary-antibodies-ihc-testing-1.jpgAnti-Zinc finger protein 608 ZNF608 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ZNF608 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ntt4-antibody-a12725-boster.html2026-03-24T05:08:15+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-adamts-19-antibody-a12646-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12646-adamts19-primary-antibodyes-wb-testing-1.jpgAnti-ADAMTS-19 AntibodyWestern Blot (WB) analysis of 293 cells using ADAMTS-19 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-s12-antibody-a12643-boster.html2026-03-24T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12643-mrps12-primary-antibodies-wb-testing-2.jpgAnti-MRP-S12 AntibodyWestern Blot analysis of SH-SY5Y cells using MRP-S12 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12643-mrps12-primary-antibodies-wb-testing-3.jpgAnti-MRP-S12 AntibodyWestern blot analysis of the lysates from HepG2 cells using MRPS12 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12643-mrps12-primary-antibodies-ihc-testing-1.jpgAnti-MRP-S12 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-histone-h2b-antibody-a12594-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12594-h2bfs-primary-antibodies-if-testing-1.jpgAnti-Histone H2B H2BFS AntibodyImmunofluorescence analysis of HeLa cells, using Histone H2B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12594-h2bfs-primary-antibodies-wb-testing-2.jpgAnti-Histone H2B H2BFS AntibodyWestern Blot analysis of COS7 cells using Histone H2B Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12594-h2bfs-primary-antibodies-ihc-testing-3.jpgAnti-Histone H2B H2BFS AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Histone H2B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-l-type-ca-cp-gamma7-antibody-a12584-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12584-cacng7-primary-antibodyes-wb-testing-1.jpgAnti-L-type Ca++ CP gamma7 CACNG7 AntibodyWestern Blot (WB) analysis of specific cells using L-type Ca++ CP gamma7 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-n4bp1-antibody-a12575-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12575-n4bp1-primary-antibodies-wb-testing-2.jpgAnti-NEDD4-binding protein 1 N4BP1 AntibodyWestern Blot analysis of K562 cells using N4BP1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12575-n4bp1-primary-antibodies-wb-testing-3.jpgAnti-NEDD4-binding protein 1 N4BP1 AntibodyWestern blot analysis of lysates from MCF-7 and Jurkat/293 cells, using N4BP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12575-n4bp1-primary-antibodies-ihc-testing-1.jpgAnti-NEDD4-binding protein 1 N4BP1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl13-antibody-a12505-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12505-klhl13-primary-antibodies-wb-testing-2.jpgAnti-KLHL13 Monoclonal AntibodyWestern Blot analysis using KLHL13 Monoclonal Antibody against HeLa (1) and MCF-7 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12505-klhl13-primary-antibodies-ihc-testing-3.jpgAnti-KLHL13 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded brain tissues (left) and pancreas tissues (right) with DAB staining using KLHL13 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12505-klhl13-primary-antibodies-if-testing-4.jpgAnti-KLHL13 Monoclonal AntibodyImmunofluorescence analysis of NTERA-2 cells (left) and U251 (right) cells using KLHL13 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12505-klhl13-primary-antibodies-fcm-testing-1.jpgAnti-KLHL13 Monoclonal AntibodyFlow cytometric analysis of 3T3/L1 cells using KLHL13 Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/anti-rnf130-antibody-a12501-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12501-rnf130-primary-antibodyes-wb-testing-1.jpgAnti-RNF130 AntibodyWestern Blot (WB) analysis of specific cells using RNF130 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl22-antibody-a12497-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12497-klhl22-primary-antibodies-wb-testing-2.jpgAnti-KLHL22 Monoclonal AntibodyWestern Blot analysis using KLHL22 Monoclonal Antibody against mouse brain tissues lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12497-klhl22-primary-antibodies-if-testing-1.jpgAnti-KLHL22 Monoclonal AntibodyImmunofluorescence analysis of U251 cells using KLHL22 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/anti-paf65-alpha-antibody-a12489-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12489-taf6l-primary-antibodies-ihc-testing-1.jpgAnti-PAF65 alpha AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12489-taf6l-primary-antibodies-wb-testing-2.jpgAnti-PAF65 alpha AntibodyWestern Blot analysis of 293 cells using PAF65α Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12489-taf6l-primary-antibodies-wb-testing-3.jpgAnti-PAF65 alpha AntibodyWestern blot analysis of lysates from 293 cells, using TAF6L Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pdp2-antibody-a12472-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12472-pdp2-primary-antibodyes-wb-testing-1.jpgAnti-PDP2 AntibodyWestern Blot (WB) analysis of extracts from K562 cells, using PDP2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-alpha-1-xxviii-antibody-a12439-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12439-col28a1-primary-antibodies-wb-testing-1.jpgAnti-Collagen alpha-1(XXVIII) COL28A1 AntibodyWestern Blot analysis of 3T3 HEPG2 cells using Collagen alpha-1 (XXVIII)Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-t2r8-antibody-a12428-boster.html2026-03-24T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12428-tas2r8-primary-antibodies-wb-testing-2.jpgAnti-T2R8 TAS2R8 AntibodyWestern Blot analysis of various cells using T2R8 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12428-tas2r8-primary-antibodies-wb-testing-1.jpgAnti-T2R8 TAS2R8 AntibodyWestern blot analysis of lysates from COLO cells, using TAS2R8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd158f1-2-antibody-a12423-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12423-kir2dl5a-primary-antibodyes-ihc-testing-1.jpgAnti-CD158f1/2 KIR2DL5A AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fucokinase-antibody-a12417-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12417-fuk-primary-antibodies-wb-testing-2.jpgAnti-Fucokinase FUK Monoclonal AntibodyWestern Blot analysis using Fucokinase Monoclonal Antibody against HeLa (1), HepG2 (2), Jurkat (3), A431 (4), HEK293 (5), MCF-7 (6), PC-12 (7), Cos7 (8), and NIH/3T3 (9) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12417-fuk-primary-antibodies-fcm-testing-1.jpgAnti-Fucokinase FUK Monoclonal AntibodyFlow cytometric analysis of Hela cells using Fucokinase Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/anti-gmf-gamma-antibody-a12403-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12403-gmfg-primary-antibodies-ihc-testing-1.jpgAnti-GMF- gamma AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-2h2-antibody-a12353-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12353-or2h2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2H2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2H2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12353-or2h2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2H2 AntibodyWestern blot analysis of lysates from Jurkat and MCF-7 cells, using OR2H2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tesk2-antibody-a12351-1-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12351-1-tesk2-primary-antibodyes-wb-testing-1.jpgAnti-TESK2 AntibodyWestern Blot (WB) analysis of specific cells using TESK2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-vps26b-antibody-a12325-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12325-vps26b-primary-antibodies-wb-testing-2.jpgAnti-VPS26B AntibodyWestern Blot analysis of LOVO cells using VPS26B Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12325-vps26b-primary-antibodies-wb-testing-1.jpgAnti-VPS26B AntibodyWestern blot analysis of lysates from LOVO cells, using VPS26B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-noxin-antibody-a12306-boster.html2026-03-24T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12306-ddias-primary-antibodyes-wb-testing-1.jpgAnti-NOXIN DDIAS AntibodyWestern Blot (WB) analysis of 823, 293T, AD293, HeLa, HepG2 cells using NOXIN Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-hrp-3-antibody-a12283-1-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12283-1-hdgfl3-primary-antibodies-wb-testing-1.jpgAnti-HRP-3 HDGFL3 AntibodyWestern Blot analysis of NIH-3T3, PC12 cells using HRP-3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-phkg1-antibody-a12257-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12257-phkg1-primary-antibodies-wb-testing-2.jpgAnti-PHKG1 AntibodyWestern Blot analysis of various cells using PHKG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12257-phkg1-primary-antibodies-wb-testing-3.jpgAnti-PHKG1 AntibodyWestern Blot analysis of HepG2 cells using PHKG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12257-phkg1-primary-antibodies-ihc-testing-1.jpgAnti-PHKG1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-crmp-3-antibody-a12176-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12176-dpysl4-primary-antibodies-wb-testing-2.jpgAnti-CRMP-3 DPYSL4 AntibodyWestern Blot analysis of LOVO cells using CRMP-3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12176-dpysl4-primary-antibodies-wb-testing-3.jpgAnti-CRMP-3 DPYSL4 AntibodyWestern blot analysis of lysates from LOVO and HT-29 cells, using DPYSL4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12176-dpysl4-primary-antibodies-wb-testing-1.jpgAnti-CRMP-3 DPYSL4 AntibodyWestern blot analysis of the lysates from RAW264.7cells using DPYSL4 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zkscan4-antibody-a12174-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12174-zkscan4-primary-antibodies-wb-testing-2.jpgAnti-ZKSCAN4/Znf307 AntibodyWestern Blot analysis of MCF7, HepG2, 293, mouse brain, mouse lung cells using ZKSCAN4 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12174-zkscan4-primary-antibodies-ihc-testing-1.jpgAnti-ZKSCAN4/Znf307 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-machr-m5-antibody-a12171-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12171-chrm5-primary-antibodies-wb-testing-2.jpgAnti-mAChR M5 AntibodyWestern blot analysis of lysates from LOVO and RAW264.7 cells, using CHRM5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12171-chrm5-primary-antibodies-wb-testing-3.jpgAnti-mAChR M5 AntibodyWestern blot analysis of the lysates from K562 cells using CHRM5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12171-chrm5-primary-antibodies-if-testing-1.jpgAnti-mAChR M5 AntibodyImmunofluorescence analysis of A549 cells, using CHRM5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-olfactory-receptor-51d1-antibody-a12133-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12133-or51d1-primary-antibodyes-wb-testing-1.jpgAnti-Olfactory receptor 51D1 AntibodyWestern Blot (WB) analysis of specific cells using Olfactory receptor 51D1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ribosomal-protein-s27l-antibody-a12106-boster.html2026-03-24T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12106-rps27l-primary-antibodies-wb-testing-2.jpgAnti-Ribosomal Protein S27L RPS27L AntibodyWestern Blot analysis of various cells using Ribosomal Protein S27L Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12106-rps27l-primary-antibodies-wb-testing-3.jpgAnti-Ribosomal Protein S27L RPS27L AntibodyWestern blot analysis of lysates from COLO cells, using RPS27L Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12106-rps27l-primary-antibodies-wb-testing-4.jpgAnti-Ribosomal Protein S27L RPS27L AntibodyWestern blot analysis of the lysates from COLO205 cells using RPS27L antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12106-rps27l-primary-antibodies-ihc-testing-1.jpgAnti-Ribosomal Protein S27L RPS27L AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-dhhc-15-antibody-a12099-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12099-zdhhc15-primary-antibodies-wb-testing-1.jpgAnti-DHHC-15 ZDHHC15 AntibodyWestern blot analysis of the lysates from 293 cells using ZDHHC15 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12099-zdhhc15-primary-antibodies-wb-testing-2.jpgAnti-DHHC-15 ZDHHC15 AntibodyWestern Blot analysis of Jurkat cells using DHHC-15 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12099-zdhhc15-primary-antibodies-wb-testing-3.jpgAnti-DHHC-15 ZDHHC15 AntibodyWestern blot analysis of lysates from Jurkat cells, using ZDHHC15 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-myomesin-2-antibody-a12094-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12094-myom2-primary-antibodies-wb-testing-2.jpgAnti-Myomesin-2 MYOM2 AntibodyWestern blot analysis of lysates from COS7 and HT-29 cells, using MYOM2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12094-myom2-primary-antibodies-ihc-testing-1.jpgAnti-Myomesin-2 MYOM2 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-pgbd1-antibody-a12083-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12083-pgbd1-primary-antibodies-wb-testing-2.jpgAnti-PGBD1 AntibodyWestern Blot analysis of various cells using PGBD1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12083-pgbd1-primary-antibodies-wb-testing-3.jpgAnti-PGBD1 AntibodyWestern blot analysis of lysates from HeLa cells, using PGBD1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12083-pgbd1-primary-antibodies-ihc-testing-1.jpgAnti-PGBD1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-apool-antibody-a12075-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12075-apool-primary-antibodies-wb-testing-2.jpgAnti-ApoOL/Apolipoprotein O Like AntibodyWestern blot analysis of SH-SY5Y 293T 3T3 lysis using ApoOL antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12075-apool-primary-antibodies-wb-testing-1.jpgAnti-ApoOL/Apolipoprotein O Like AntibodyWestern blot analysis of lysates from COLO and NIH/3T3 cells, using APOOL Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-d-gpcr-antibody-a12058-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12058-or51e1-primary-antibodies-wb-testing-2.jpgAnti-D-GPCR OR51E1 AntibodyWestern Blot analysis of various cells using D-GPCR Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12058-or51e1-primary-antibodies-wb-testing-3.jpgAnti-D-GPCR OR51E1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR51E1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12058-or51e1-primary-antibodies-wb-testing-4.jpgAnti-D-GPCR OR51E1 AntibodyWestern blot analysis of the lysates from K562 cells using OR51E1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12058-or51e1-primary-antibodies-if-testing-1.jpgAnti-D-GPCR OR51E1 AntibodyImmunofluorescence analysis of A549 cells, using OR51E1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rcl1-antibody-a12027-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12027-rcl1-primary-antibodyes-wb-testing-1.jpgAnti-RCL1 AntibodyWestern Blot (WB) analysis of HuvEc cells using RCL1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-znhit1-antibody-a12010-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12010-znhit1-primary-antibodies-wb-testing-1.jpgAnti-ZNHIT1 AntibodyWestern Blot analysis of various cells using ZNHIT1 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-tfiiic102-antibody-a12003-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12003-gtf3c3-primary-antibodies-wb-testing-2.jpgAnti-TFIIIC102 GTF3C3 AntibodyWestern Blot analysis of various cells using TFIIIC102 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12003-gtf3c3-primary-antibodies-wb-testing-3.jpgAnti-TFIIIC102 GTF3C3 AntibodyWestern Blot analysis of 293 cells using TFIIIC102 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12003-gtf3c3-primary-antibodies-wb-testing-4.jpgAnti-TFIIIC102 GTF3C3 AntibodyWestern blot analysis of the lysates from Jurkat cells using TF3C3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12003-gtf3c3-primary-antibodies-ihc-testing-1.jpgAnti-TFIIIC102 GTF3C3 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-zzz3-antibody-a12002-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12002-zzz3-primary-antibodies-wb-testing-2.jpgAnti-ZZZ3 AntibodyWestern Blot analysis of various cells using ZZZ3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12002-zzz3-primary-antibodies-wb-testing-1.jpgAnti-ZZZ3 AntibodyWestern blot analysis of lysates from HepG2 cells, using ZZZ3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ca-vb-antibody-a11974-1-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11974-1-ca5b-primary-antibodies-wb-testing-2.jpgAnti-CA VB CA5B AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using CA5B Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11974-1-ca5b-primary-antibodies-wb-testing-3.jpgAnti-CA VB CA5B AntibodyWestern blot analysis of the lysates from HT-29 cells using CA5B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11974-1-ca5b-primary-antibodies-ihc-testing-4.jpgAnti-CA VB CA5B AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11974-1-ca5b-primary-antibodies-if-testing-1.jpgAnti-CA VB CA5B AntibodyImmunofluorescence analysis of MCF7 cells, using CA5B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-polr3e-antibody-a11932-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11932-polr3e-primary-antibodyes-wb-testing-1.jpgAnti-POLR3E AntibodyWestern Blot (WB) analysis of JK cells using POLR3E Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11932-polr3e-primary-antibodyes-wb-testing-2.jpgAnti-POLR3E AntibodyWestern Blot (WB) analysis of specific cells using POLR3E Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-efhd1-antibody-a11920-boster.html2026-03-24T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11920-efhd1-primary-antibodies-if-testing-1.jpgAnti-EFHD1 Monoclonal AntibodyIF analysis of Hela with antibody (Left) and DAPI (Right) diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11920-efhd1-primary-antibodies-wb-testing-2.jpgAnti-EFHD1 Monoclonal AntibodyWestern blot analysis of 1) Mouse spleen tissue, 2) Rat spleen tissue, diluted at 1:3000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11920-efhd1-primary-antibodies-if-testing-3.jpgAnti-EFHD1 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-heart tissue. 1,EFHD1 Monoclonal Antibody (3G2) was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11920-efhd1-primary-antibodies-ihc-testing-4.jpgAnti-EFHD1 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-testis tissue. 1,EFHD1 Monoclonal Antibody (3G2) was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.
https://www.bosterbio.com/products/primary-antibodies/anti-ppp2r3c-antibody-a11897-1-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11897-1-ppp2r3c-primary-antibodies-wb-testing-2.jpgAnti-PPP2R3C/G5Pr AntibodyWestern blot analysis of PPP2R3C Antibody. The lane on the right is blocked with the PPP2R3C peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11897-1-ppp2r3c-primary-antibodies-wb-testing-3.jpgAnti-PPP2R3C/G5Pr AntibodyWestern blot analysis of the lysates from HepG2 cells using PPP2R3C antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11897-1-ppp2r3c-primary-antibodies-ihc-testing-1.jpgAnti-PPP2R3C/G5Pr AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-ndufb10-antibody-a11886-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11886-ndufb10-primary-antibodyes-wb-testing-1.jpgAnti-NDUFB10 AntibodyWestern Blot (WB) analysis of specific cells using NDUFB10 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ube4a-antibody-a11871-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11871-ube4a-primary-antibodies-wb-testing-2.jpgAnti-UBE4A AntibodyWestern Blot analysis of extracts from Jurkat cells, using UBE4A Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11871-ube4a-primary-antibodies-ihc-testing-3.jpgAnti-UBE4A AntibodyImmunohistochemical analysis of paraffin-embedded rat-muscle, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11871-ube4a-primary-antibodies-ihc-testing-1.jpgAnti-UBE4A AntibodyImmunohistochemical analysis of paraffin-embedded mouse-muscle, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-nanog-p8-antibody-a11849-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11849-nanogp8-primary-antibodies-ihc-testing-1.jpgAnti-Nanog P8 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11849-nanogp8-primary-antibodies-wb-testing-2.jpgAnti-Nanog P8 AntibodyWestern blot analysis of lysates from HUVEC, HT-29, HepG2, and Jurkat cells, using NANOGP8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tfiiic110-antibody-a11837-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11837-gtf3c2-primary-antibodies-ihc-testing-1.jpgAnti-TFIIIC110 GTF3C2 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11837-gtf3c2-primary-antibodies-wb-testing-2.jpgAnti-TFIIIC110 GTF3C2 AntibodyWestern blot analysis of lysates from HepG2, COLO205, and HUVEC cells, using TF3C2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-endoglycan-antibody-a11824-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11824-podxl2-primary-antibodyes-wb-testing-1.jpgAnti-Endoglycan PODXL2 AntibodyWestern Blot (WB) analysis of HeLa using Endoglycan antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ddx8-antibody-a11805-1-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11805-1-dhx8-primary-antibodies-wb-testing-2.jpgAnti-DDX8 DHX8 AntibodyWestern Blot analysis of various cells using DDX8 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11805-1-dhx8-primary-antibodies-wb-testing-1.jpgAnti-DDX8 DHX8 AntibodyWestern blot analysis of the lysates from HeLa cells using DHX8 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cmtm8-antibody-a11789-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11789-cmtm8-primary-antibodyes-wb-testing-1.jpgAnti-CMTM8/Cklfsf8 AntibodyWestern Blot (WB) analysis of HeLa lysis using CMTM8 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11789-cmtm8-primary-antibodyes-ihc-testing-2.jpgAnti-CMTM8/Cklfsf8 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Tonsils, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11789-cmtm8-primary-antibodyes-ihc-testing-3.jpgAnti-CMTM8/Cklfsf8 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Tonsils, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11789-cmtm8-primary-antibodyes-ihc-testing-4.jpgAnti-CMTM8/Cklfsf8 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Tonsils2, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/anti-psmd12-antibody-a11756-boster.html2026-03-24T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11756-psmd12-primary-antibodyes-wb-testing-1.jpgAnti-PSMD12 AntibodyWestern Blot (WB) analysis of HepG2 cells using PSMD12 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11756-psmd12-primary-antibodyes-wb-testing-2.jpgAnti-PSMD12 AntibodyWestern Blot (WB) analysis of specific cells using PSMD12 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-endophilin-b2-antibody-a11736-1-boster.html2026-03-24T05:08:21+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-mpr-alpha-antibody-a11720-boster.html2026-03-24T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11720-paqr7-primary-antibodies-ihc-testing-1.jpgAnti-mPR alpha PAQR7 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11720-paqr7-primary-antibodies-wb-testing-2.jpgAnti-mPR alpha PAQR7 AntibodyWestern blot analysis of lysates from 293 and COLO cells, using MPRA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr158-antibody-a11699-boster.html2026-03-24T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11699-gpr158-primary-antibodies-if-testing-1.jpgAnti-GPR158 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR158 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11699-gpr158-primary-antibodies-wb-testing-2.jpgAnti-GPR158 AntibodyWestern Blot analysis of COLO 293T HELA cells using GPR158 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11699-gpr158-primary-antibodies-wb-testing-3.jpgAnti-GPR158 AntibodyWestern blot analysis of lysates from K562 cells, using GPR158 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11699-gpr158-primary-antibodies-ihc-testing-4.jpgAnti-GPR158 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR158 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sr-3d-antibody-a11687-boster.html2026-03-24T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11687-htr3d-primary-antibodies-wb-testing-1.jpgAnti-SR-3D HTR3D AntibodyWestern Blot analysis of HT-29 cells using SR-3D Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-rap-2c-antibody-a11672-boster.html2026-03-24T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11672-rap2c-primary-antibodies-ihc-testing-1.jpgAnti-Rap 2C AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11672-rap2c-primary-antibodies-wb-testing-2.jpgAnti-Rap 2C AntibodyWestern Blot analysis of various cells using Rap 2C Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11672-rap2c-primary-antibodies-wb-testing-3.jpgAnti-Rap 2C AntibodyWestern blot analysis of lysates from Jurkat and MCF-7 cells, using RAP2C Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11672-rap2c-primary-antibodies-wb-testing-4.jpgAnti-Rap 2C AntibodyWestern blot analysis of the lysates from K562 cells using RAP2C antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ubce7ip4-antibody-a11625-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11625-rnf144a-primary-antibodies-wb-testing-2.jpgAnti-UBCE7IP4 RNF144A AntibodyWestern Blot analysis of various cells using UBCE7IP4 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11625-rnf144a-primary-antibodies-wb-testing-1.jpgAnti-UBCE7IP4 RNF144A AntibodyWestern blot analysis of lysates from COLO cells, using RNF144A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ssh3-antibody-a11609-1-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-1-ssh3-primary-antibodies-ihc-testing-1.jpgAnti-SSH3 AntibodyImmunohistochemistryt analysis of paraffin-embedded human lung carcinoma, using SSH3 Antibody. The lane on the right is blocked with the SSH3 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-1-ssh3-primary-antibodies-wb-testing-2.jpgAnti-SSH3 AntibodyWestern blot analysis of SSH3 Antibody. The lane on the right is blocked with the SSH3 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-1-ssh3-primary-antibodies-wb-testing-3.jpgAnti-SSH3 AntibodyWestern blot analysis of the lysates from K562 cells using SSH3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gk2-antibody-a11596-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11596-gk2-primary-antibodyes-wb-testing-1.jpgAnti-Glycerol kinase 2 GK2 AntibodyWestern Blot (WB) analysis of HeLa cells using GK2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11596-gk2-primary-antibodyes-wb-testing-2.jpgAnti-Glycerol kinase 2 GK2 AntibodyWestern Blot (WB) analysis of specific cells using GK2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-p2ry8-antibody-a11574-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11574-p2ry8-primary-antibodyes-wb-testing-1.jpgAnti-P2RY8/P2Y8 AntibodyWestern Blot (WB) analysis of specific cells using P2RY8 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-grp1-antibody-a11548-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11548-cyth3-primary-antibodyes-wb-testing-1.jpgAnti-GRP1 CYTH3 AntibodyWestern Blot (WB) analysis of specific cells using GRP1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ss-56-antibody-a11532-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11532-trim68-primary-antibodies-wb-testing-2.jpgAnti-SS-56 TRIM68 AntibodyWestern Blot analysis of extracts from Jurkat, K562 cells, using SS-56 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11532-trim68-primary-antibodies-ihc-testing-1.jpgAnti-SS-56 TRIM68 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-luc7l2-antibody-a11514-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11514-luc7l2-primary-antibodies-wb-testing-2.jpgAnti-LUC7L2 AntibodyWestern Blot analysis of various cells using LUC7L2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11514-luc7l2-primary-antibodies-ihc-testing-1.jpgAnti-LUC7L2 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using LUC7L2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l40-antibody-a11512-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11512-mrpl40-primary-antibodyes-wb-testing-1.jpgAnti-MRP-L40 AntibodyWestern Blot (WB) analysis of specific cells using MRP-L40 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mpp10-antibody-a11510-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11510-mphosph10-primary-antibodyes-wb-testing-1.jpgAnti-MPP10 MPHOSPH10 AntibodyWestern Blot (WB) analysis of extracts from Jurkat cells, using MPP10 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-vps72-antibody-a11502-boster.html2026-03-24T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11502-vps72-primary-antibodies-wb-testing-2.jpgAnti-VPS72 AntibodyWestern blot analysis of lysates from RAW264.7 and NIH/3T3 cells, using VPS72 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11502-vps72-primary-antibodies-ihc-testing-1.jpgAnti-VPS72 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using VPS72 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kanadaptin-antibody-a11461-1-boster.html2026-03-24T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11461-1-slc4a1ap-primary-antibodies-wb-testing-2.jpgAnti-Kanadaptin SLC4A1AP AntibodyWestern Blot analysis of various cells using Kanadaptin Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11461-1-slc4a1ap-primary-antibodies-wb-testing-3.jpgAnti-Kanadaptin SLC4A1AP AntibodyWestern blot analysis of lysates from HUVEC cells, using NADAP Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11461-1-slc4a1ap-primary-antibodies-ihc-testing-1.jpgAnti-Kanadaptin SLC4A1AP AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-fam48a-antibody-a11433-boster.html2026-03-24T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11433-supt20h-primary-antibodies-wb-testing-1.jpgAnti-FAM48A SUPT20H AntibodyWestern Blot analysis of mouse-kidney cells using Antibody diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-ifn-epsilon-antibody-a11425-boster.html2026-03-24T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11425-ifne-primary-antibodyes-wb-testing-1.jpgAnti-IFN- epsilon AntibodyWestern blot analysis of Jurkat cells using IFN-Epsilon Polyclonal Antibody.. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11425-ifne-primary-antibodyes-wb-testing-2.jpgAnti-IFN- epsilon AntibodyWestern blot analysis of lysate from Jurkat cells, using IFNE Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ak5-antibody-a11378-boster.html2026-03-24T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11378-ak5-primary-antibodies-ihc-testing-1.jpgAnti-Adenylate kinase isoenzyme 5 AK5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using AK5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11378-ak5-primary-antibodies-wb-testing-2.jpgAnti-Adenylate kinase isoenzyme 5 AK5 AntibodyWestern Blot analysis of various cells using AK5 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-t2r39-antibody-a11356-boster.html2026-03-24T05:08:23+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/anti-mpp9-antibody-a11350-boster.html2026-03-24T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-mphosph9-primary-antibodies-wb-testing-2.jpgAnti-MPP9 MPHOSPH9 AntibodyWestern Blot analysis of various cells using MPP9 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-mphosph9-primary-antibodies-wb-testing-3.jpgAnti-MPP9 MPHOSPH9 AntibodyWestern blot analysis of the lysates from COLO205 cells using MPHOSPH9 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-mphosph9-primary-antibodies-ihc-testing-1.jpgAnti-MPP9 MPHOSPH9 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-gdf-7-antibody-a11336-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11336-gdf7-primary-antibodies-ihc-testing-1.jpgAnti-GDF-7 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11336-gdf7-primary-antibodies-wb-testing-2.jpgAnti-GDF-7 AntibodyWestern Blot analysis of Hela cells using GDF-7 Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-raftlin-antibody-a11324-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11324-rftn1-primary-antibodies-ihc-testing-1.jpgAnti-Raftlin RFTN1 AntibodyImmunohistochemical analysis of paraffin-embedded human uterus. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11324-rftn1-primary-antibodies-wb-testing-2.jpgAnti-Raftlin RFTN1 AntibodyWestern Blot analysis of 3T3 cells using Raftlin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11324-rftn1-primary-antibodies-wb-testing-3.jpgAnti-Raftlin RFTN1 AntibodyWestern blot analysis of the lysates from RAW264.7cells using RFTN1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-pitp-beta-antibody-a11315-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11315-pitpnb-primary-antibodies-wb-testing-2.jpgAnti-PITP beta PITPNB AntibodyWestern Blot analysis of HepG2 cells using PITPβ Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11315-pitpnb-primary-antibodies-wb-testing-3.jpgAnti-PITP beta PITPNB AntibodyWestern blot analysis of the lysates from K562 cells using PITPNB antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11315-pitpnb-primary-antibodies-ihc-testing-1.jpgAnti-PITP beta PITPNB AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-ccp2-antibody-a11275-1-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11275-1-agbl2-primary-antibodies-wb-testing-2.jpgAnti-CCP2 AGBL2 AntibodyWestern Blot analysis of various cells using CCP2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11275-1-agbl2-primary-antibodies-wb-testing-3.jpgAnti-CCP2 AGBL2 AntibodyWestern blot analysis of lysates from HUVEC cells, using CBCP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11275-1-agbl2-primary-antibodies-wb-testing-4.jpgAnti-CCP2 AGBL2 AntibodyWestern blot analysis of the lysates from Jurkat cells using CBCP2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11275-1-agbl2-primary-antibodies-ihc-testing-1.jpgAnti-CCP2 AGBL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using CBCP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd300e-antibody-a11226-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11226-cd300e-primary-antibodyes-ihc-testing-1.jpgAnti-CD300e/Lmir6 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11226-cd300e-primary-antibodyes-ihc-testing-2.jpgAnti-CD300e/Lmir6 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/anti-if3-antibody-a11221-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11221-mtif3-primary-antibodies-wb-testing-2.jpgAnti-IF3 MTIF3 AntibodyWestern Blot analysis of HuvEC cells using IF3 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11221-mtif3-primary-antibodies-ihc-testing-1.jpgAnti-IF3 MTIF3 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-rassf4-antibody-a11193-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11193-rassf4-primary-antibodyes-wb-testing-1.jpgAnti-RASSF4 AntibodyWestern Blot (WB) analysis of specific cells using RASSF4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zbtb40-antibody-a11168-1-boster.html2026-03-24T05:08:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11168-1-zbtb40-primary-antibodies-wb-testing-2.jpgAnti-ZBTB40 AntibodyWestern Blot analysis of various cells using ZBTB40 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11168-1-zbtb40-primary-antibodies-wb-testing-3.jpgAnti-ZBTB40 AntibodyWestern blot analysis of ZBTB40 Antibody. The lane on the right is blocked with the ZBTB40 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11168-1-zbtb40-primary-antibodies-wb-testing-4.jpgAnti-ZBTB40 AntibodyWestern blot analysis of the lysates from HUVECcells using ZBTB40 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11168-1-zbtb40-primary-antibodies-ihc-testing-1.jpgAnti-ZBTB40 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ZBTB40 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr34-antibody-a11157-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11157-gpr34-primary-antibodyes-wb-testing-1.jpgAnti-GPR34 AntibodyWestern Blot (WB) analysis of specific cells using GPR34 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cleaved-mmp-27-y99-antibody-a11153-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11153-mmp27-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-MMP-27 (Y99) AntibodyWestern Blot analysis of various cells using Cleaved-MMP-27 (Y99) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11153-mmp27-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-MMP-27 (Y99) AntibodyWestern blot analysis of lysates from COS7 cells, treated with etoposide 25uM 1h, using MMP27 (Cleaved-Tyr99) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sr-6-antibody-a11122-1-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11122-1-htr6-primary-antibodies-wb-testing-1.jpgAnti-SR-6 HTR6 AntibodyWestern Blot analysis of A549 cells using SR-6 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-zfp91-antibody-a11088-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11088-zfp91-primary-antibodies-wb-testing-1.jpgAnti-ZFP91 AntibodyWestern Blot analysis of hepg2, NT28 cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-gmf-beta-antibody-a11087-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11087-gmfb-primary-antibodies-wb-testing-2.jpgAnti-GMF- beta AntibodyWestern Blot analysis of HeLa cells using GMF-β Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11087-gmfb-primary-antibodies-ihc-testing-1.jpgAnti-GMF- beta AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-lir-7-antibody-a11081-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11081-lilra2-primary-antibodies-wb-testing-2.jpgAnti-LIR-7 LILRA2 AntibodyWestern Blot analysis of HepG2 cells using LIR-7 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11081-lilra2-primary-antibodies-ihc-testing-1.jpgAnti-LIR-7 LILRA2 AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-angptl7-antibody-a11067-1-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11067-1-angptl7-primary-antibodyes-wb-testing-1.jpgAnti-Angptl7/Angiopoietin Like 7 AntibodyWestern Blot (WB) analysis of SH-SY5Y cells using Angptl7 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-kctd7-antibody-a11066-boster.html2026-03-24T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11066-kctd7-primary-antibodyes-wb-testing-1.jpgAnti-KCTD7 AntibodyWestern Blot analysis of 1) mouse brain, 2) mouse heart cells using primary antibody diluted at 1: 1000 (4℃ overnight) . Secondary antibody: Goat Anti-rabbit IgG IRDye 800 (diluted at 1: 5000, 25℃, 1 hour).
https://www.bosterbio.com/products/primary-antibodies/anti-abhd2-antibody-a11055-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11055-abhd2-primary-antibodies-wb-testing-2.jpgAnti-Monoacylglycerol lipase ABHD2 ABHD2 AntibodyWestern Blot analysis of various cells using ABHD2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11055-abhd2-primary-antibodies-wb-testing-3.jpgAnti-Monoacylglycerol lipase ABHD2 ABHD2 AntibodyWestern blot analysis of lysates from HT29 cells, using ABHD2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11055-abhd2-primary-antibodies-if-testing-1.jpgAnti-Monoacylglycerol lipase ABHD2 ABHD2 AntibodyImmunofluorescence analysis of MCF-7 cells, using ABHD2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pp2c-epsilon-antibody-a11054-1-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11054-1-ppm1l-primary-antibodies-wb-testing-2.jpgAnti-PP2C epsilon PPM1L AntibodyWestern Blot analysis of Jurkat cells using PP2Cε Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11054-1-ppm1l-primary-antibodies-wb-testing-3.jpgAnti-PP2C epsilon PPM1L AntibodyWestern blot analysis of lysates from Jurkat cells, using PPM1L Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11054-1-ppm1l-primary-antibodies-wb-testing-4.jpgAnti-PP2C epsilon PPM1L AntibodyWestern blot analysis of the lysates from HepG2 cells using PPM1L antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11054-1-ppm1l-primary-antibodies-ihc-testing-1.jpgAnti-PP2C epsilon PPM1L AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-scp-2-antibody-a11028-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11028-sycp2-primary-antibodyes-wb-testing-1.jpgAnti-SCP-2 SYCP2 AntibodyWestern Blot (WB) analysis of SKOV3, BT474, Jurkat, PC-3, U937, MCF7 cells using SCP-2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zc3h13-antibody-a11022-1-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11022-1-zc3h13-primary-antibodies-wb-testing-1.jpgAnti-ZC3H13 AntibodyWestern blot analysis of the lysates from HUVECcells using ZC3H13 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11022-1-zc3h13-primary-antibodies-wb-testing-2.jpgAnti-ZC3H13 AntibodyWestern Blot analysis of various cells using ZC3H13 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11022-1-zc3h13-primary-antibodies-wb-testing-3.jpgAnti-ZC3H13 AntibodyWestern blot analysis of lysates from A549, Jurkat, HepG2 cells, using ZC3H13 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab-20-antibody-a11018-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11018-rab20-primary-antibodies-wb-testing-2.jpgAnti-Rab 20 AntibodyWestern Blot analysis of A549 cells using Rab 20 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11018-rab20-primary-antibodies-wb-testing-3.jpgAnti-Rab 20 AntibodyWestern blot analysis of lysates from HeLa, MCF-7, HUVEC, and A549 cells, using RAB20 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11018-rab20-primary-antibodies-wb-testing-4.jpgAnti-Rab 20 AntibodyWestern blot analysis of the lysates from HeLa cells using RAB20 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11018-rab20-primary-antibodies-ihc-testing-1.jpgAnti-Rab 20 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-gbp4-antibody-a11011-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11011-gbp4-primary-antibodies-wb-testing-2.jpgAnti-Guanylate-binding protein 4 GBP4 AntibodyWestern Blot analysis of RAW cells using GBP4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11011-gbp4-primary-antibodies-ihc-testing-1.jpgAnti-Guanylate-binding protein 4 GBP4 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using GBP4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl1-antibody-a11010-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11010-klhl1-primary-antibodies-wb-testing-2.jpgAnti-KLHL1 Monoclonal AntibodyWestern Blot analysis using KLHL1 Monoclonal Antibody antiobdy against KLHL1 recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11010-klhl1-primary-antibodies-if-testing-1.jpgAnti-KLHL1 Monoclonal AntibodyImmunofluorescence analysis of NIH/3T3 cells using KLHL1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/anti-v-atpase-h-antibody-a11008-1-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11008-1-atp6v1h-primary-antibodies-wb-testing-2.jpgAnti-V-ATPase H ATP6V1H AntibodyWestern Blot analysis of various cells using V-ATPase H Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11008-1-atp6v1h-primary-antibodies-ihc-testing-1.jpgAnti-V-ATPase H ATP6V1H AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ATP6V1H Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pkr1-antibody-a10986-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10986-prokr1-primary-antibodies-wb-testing-2.jpgAnti-PKR1 PROKR1 AntibodyWestern Blot analysis of COLO205 cells using PKR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10986-prokr1-primary-antibodies-wb-testing-3.jpgAnti-PKR1 PROKR1 AntibodyWestern blot analysis of lysates from COLO cells, using PKR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10986-prokr1-primary-antibodies-ihc-testing-1.jpgAnti-PKR1 PROKR1 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-nop132-antibody-a10985-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10985-nol8-primary-antibodyes-wb-testing-1.jpgAnti-Nop132 NOL8 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using Nop132 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10985-nol8-primary-antibodyes-wb-testing-2.jpgAnti-Nop132 NOL8 AntibodyWestern Blot (WB) analysis of 3T3 cells using Nop132 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cd85c-antibody-a10961-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10961-lilrb5-primary-antibodies-wb-testing-2.jpgAnti-CD85c LILRB5 AntibodyWestern Blot analysis of HepG2 cells using CD85c Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10961-lilrb5-primary-antibodies-ihc-testing-1.jpgAnti-CD85c LILRB5 AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-sv2c-antibody-a10958-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10958-sv2c-primary-antibodyes-wb-testing-1.jpgAnti-SV2C AntibodyWestern Blot (WB) analysis of extracts from Jurkat cells, using SV2C Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10958-sv2c-primary-antibodyes-ihc-testing-2.jpgAnti-SV2C AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/anti-septin-6-antibody-a10957-1-boster.html2026-03-24T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10957-1-sept6-primary-antibodies-wb-testing-2.jpgAnti-Septin 6 SEPT6; AntibodyWestern Blot analysis of JK cells using Septin 6 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10957-1-sept6-primary-antibodies-wb-testing-3.jpgAnti-Septin 6 SEPT6; AntibodyWestern blot analysis of the lysates from HeLa cells using SEPT6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10957-1-sept6-primary-antibodies-ihc-testing-1.jpgAnti-Septin 6 SEPT6; AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/anti-gpr87-95-antibody-a10952-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10952-gpr87-primary-antibodies-ihc-testing-1.jpgAnti-GPR87/95 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10952-gpr87-primary-antibodies-wb-testing-2.jpgAnti-GPR87/95 AntibodyWestern Blot analysis of K562 cells using GPR87/95 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-cd232-antibody-a10941-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10941-plxnc1-primary-antibodies-wb-testing-2.jpgAnti-CD232 PLXNC1 AntibodyWestern Blot analysis of 3T3 cells using CD232 Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10941-plxnc1-primary-antibodies-wb-testing-1.jpgAnti-CD232 PLXNC1 AntibodyWestern Blot analysis of 3T3 cells using CD232 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-abcf2-antibody-a10873-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10873-abcf2-primary-antibodies-wb-testing-2.jpgAnti-ABCF2 AntibodyWestern Blot analysis of various cells using ABCF2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10873-abcf2-primary-antibodies-wb-testing-3.jpgAnti-ABCF2 AntibodyWestern Blot analysis of HeLa cells using ABCF2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10873-abcf2-primary-antibodies-wb-testing-4.jpgAnti-ABCF2 AntibodyWestern blot analysis of ABCF2 Antibody. The lane on the right is blocked with the ABCF2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10873-abcf2-primary-antibodies-wb-testing-1.jpgAnti-ABCF2 AntibodyWestern blot analysis of the lysates from HepG2 cells using ABCF2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-kir5-1-antibody-a10858-1-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10858-1-kcnj16-primary-antibodyes-wb-testing-1.jpgAnti-KIR5.1 KCNJ16 AntibodyWestern Blot (WB) analysis of HeLa cells using KIR5.1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-il-17b-antibody-a10846-1-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10846-1-il17b-primary-antibodies-ihc-testing-1.jpgAnti-IL-17B AntibodyImmunohistochemical analysis of paraffin-embedded human-small-intestine, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-gcp3-antibody-a10799-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10799-tubgcp3-primary-antibodies-ihc-testing-1.jpgAnti-GCP3 TUBGCP3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TUBGCP3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10799-tubgcp3-primary-antibodies-wb-testing-2.jpgAnti-GCP3 TUBGCP3 AntibodyWestern Blot analysis of K562 cells using GCP3 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-pi-3-kinase-c2-gamma-antibody-a10773-boster.html2026-03-24T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10773-pik3c2g-primary-antibodies-wb-testing-2.jpgAnti-PI 3-Kinase C2 gamma PIK3C2G AntibodyWestern blot analysis of A549 using PI 3-Kinase C2γ antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10773-pik3c2g-primary-antibodies-ihc-testing-1.jpgAnti-PI 3-Kinase C2 gamma PIK3C2G AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-scaf1-antibody-a10769-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10769-scaf1-primary-antibodyes-wb-testing-1.jpgAnti-SCAF1 AntibodyWestern Blot (WB) analysis of specific cells using SCAF1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cmtm5-antibody-a10739-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10739-cmtm5-primary-antibodies-ihc-testing-1.jpgAnti-CMTM5 AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10739-cmtm5-primary-antibodies-wb-testing-2.jpgAnti-CMTM5 AntibodyWestern Blot analysis of PC12 cells using CMTM5 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-synaptotagmin-xi-antibody-a10695-1-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10695-1-syt11-primary-antibodies-wb-testing-2.jpgAnti-Synaptotagmin XI SYT11 AntibodyWestern Blot analysis of various cells using Synaptotagmin XI Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10695-1-syt11-primary-antibodies-wb-testing-1.jpgAnti-Synaptotagmin XI SYT11 AntibodyWestern blot analysis of SYT11 Antibody. The lane on the right is blocked with the SYT11 peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l10-antibody-a10693-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10693-mrpl10-primary-antibodies-wb-testing-2.jpgAnti-MRP-L10 AntibodyWestern Blot analysis of various cells using MRP-L10 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10693-mrpl10-primary-antibodies-wb-testing-3.jpgAnti-MRP-L10 AntibodyWestern blot analysis of lysates from 293, HepG2, and COLO cells, using MRPL10 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10693-mrpl10-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L10 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-polr3g-antibody-a10669-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10669-polr3g-primary-antibodyes-ihc-testing-1.jpgAnti-POLR3G AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10669-polr3g-primary-antibodyes-wb-testing-2.jpgAnti-POLR3G AntibodyWestern Blot (WB) analysis of PC12 cells using POLR3G Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10669-polr3g-primary-antibodyes-ihc-testing-3.jpgAnti-POLR3G AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/anti-mdfi-antibody-a10664-1-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10664-1-mdfi-primary-antibodies-wb-testing-1.jpgAnti-MyoD family inhibitor MDFI AntibodyWestern blot analysis of lysates from Jurkat cells, using MDFI Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10664-1-mdfi-primary-antibodies-wb-testing-2.jpgAnti-MyoD family inhibitor MDFI AntibodyWestern Blot analysis of various cells using MDFI Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-v-atpase-d1-antibody-a10658-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10658-atp6v0d1-primary-antibodies-wb-testing-2.jpgAnti-V-ATPase D1 ATP6V0D1 AntibodyWestern Blot analysis of extracts from NIH-3T3, K562 cells, using V-ATPase D1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10658-atp6v0d1-primary-antibodies-wb-testing-1.jpgAnti-V-ATPase D1 ATP6V0D1 AntibodyWestern blot analysis of lysates from HeLa cells, using V-ATPase D1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cd300g-antibody-a10652-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10652-cd300lg-primary-antibodies-wb-testing-2.jpgAnti-CD300g CD300LG AntibodyWestern Blot analysis of L929 cells using CD300g Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10652-cd300lg-primary-antibodies-wb-testing-1.jpgAnti-CD300g CD300LG AntibodyWestern blot analysis of lysate from L929 cells, using CD300LG Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-slc17a2-antibody-a10637-1-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10637-1-slc17a2-primary-antibodies-ihc-testing-1.jpgAnti-SLC17A2 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10637-1-slc17a2-primary-antibodies-wb-testing-2.jpgAnti-SLC17A2 AntibodyWestern Blot analysis of various cells using SLC17A2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10637-1-slc17a2-primary-antibodies-wb-testing-3.jpgAnti-SLC17A2 AntibodyWestern blot analysis of the lysates from RAW264.7cells using SLC17A2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-atp5f1-antibody-a10633-1-boster.html2026-03-24T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10633-1-atp5f1-primary-antibodies-wb-testing-1.jpgAnti-ATP5F1 AntibodyWestern Blot analysis of 3T3 cells using ATP5F1 Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l41-antibody-a10631-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10631-mrpl41-primary-antibodyes-wb-testing-1.jpgAnti-MRP-L41 AntibodyWestern Blot (WB) analysis of specific cells using MRP-L41 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-med18-antibody-a10600-1-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10600-1-med18-primary-antibodies-wb-testing-2.jpgAnti-Med18 AntibodyWestern Blot analysis of various cells using Med18 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10600-1-med18-primary-antibodies-wb-testing-1.jpgAnti-Med18 AntibodyWestern blot analysis of lysates from COLO and Jurkat cells, using MED18 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-p39-antibody-a10584-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10584-cdk5r2-primary-antibodyes-wb-testing-1.jpgAnti-p39 CDK5R2 AntibodyWestern Blot (WB) analysis of specific cells using p39 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-inhibin-beta-c-antibody-a10556-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10556-inhbc-primary-antibodyes-wb-testing-1.jpgAnti-Inhibin beta-C INHBC AntibodyWestern Blot (WB) analysis of specific cells using Inhibin beta-C Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr116-antibody-a10539-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10539-adgrf5-primary-antibodies-wb-testing-2.jpgAnti-GPR116 ADGRF5 AntibodyWestern Blot analysis of various cells using GPR116 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10539-adgrf5-primary-antibodies-wb-testing-3.jpgAnti-GPR116 ADGRF5 AntibodyWestern blot analysis of lysates from A549 cells, using GPR116 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10539-adgrf5-primary-antibodies-ihc-testing-4.jpgAnti-GPR116 ADGRF5 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10539-adgrf5-primary-antibodies-if-testing-1.jpgAnti-GPR116 ADGRF5 AntibodyImmunofluorescence analysis of HeLa cells, using GPR116 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-col5a3-antibody-a10525-boster.html2026-03-24T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10525-col5a3-primary-antibodies-wb-testing-2.jpgAnti-Collagen alpha-3(V) chain COL5A3 AntibodyWestern Blot analysis of various cells using COL5A3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10525-col5a3-primary-antibodies-wb-testing-3.jpgAnti-Collagen alpha-3(V) chain COL5A3 AntibodyWestern Blot analysis of K562 cells using COL5A3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10525-col5a3-primary-antibodies-ihc-testing-4.jpgAnti-Collagen alpha-3(V) chain COL5A3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Collagen V alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10525-col5a3-primary-antibodies-if-testing-1.jpgAnti-Collagen alpha-3(V) chain COL5A3 AntibodyImmunofluorescence analysis of HeLa cells, using Collagen V alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tcf-19-antibody-a10508-1-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10508-1-tcf19-primary-antibodies-wb-testing-1.jpgAnti-TCF-19 AntibodyWestern Blot analysis of extracts from Jurkat cells, using TCF-19 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/anti-cyp2a7-antibody-a10507-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10507-cyp2a7-primary-antibodies-wb-testing-2.jpgAnti-Cytochrome P450 2A7 CYP2A7 AntibodyWestern Blot analysis of 22RV1 cells using CYP2A7 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10507-cyp2a7-primary-antibodies-ihc-testing-1.jpgAnti-Cytochrome P450 2A7 CYP2A7 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-rnf144b-antibody-a10490-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10490-rnf144b-primary-antibodies-wb-testing-2.jpgAnti-RNF144b/Ibrdc2 AntibodyWestern Blot analysis of various cells using p53RFP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10490-rnf144b-primary-antibodies-wb-testing-1.jpgAnti-RNF144b/Ibrdc2 AntibodyWestern Blot analysis of HeLa cells using p53RFP Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-sr-1f-antibody-a10463-1-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10463-1-htr1f-primary-antibodies-ihc-testing-1.jpgAnti-SR-1F HTR1F AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10463-1-htr1f-primary-antibodies-wb-testing-2.jpgAnti-SR-1F HTR1F AntibodyWestern Blot analysis of various cells using SR-1F Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10463-1-htr1f-primary-antibodies-wb-testing-3.jpgAnti-SR-1F HTR1F AntibodyWestern blot analysis of lysates from COS7 cells, using 5-HT-1F Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tssk-4-antibody-a10441-1-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10441-1-tssk4-primary-antibodies-wb-testing-2.jpgAnti-TSSK 4 AntibodyWestern Blot analysis of various cells using TSSK 4 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10441-1-tssk4-primary-antibodies-wb-testing-3.jpgAnti-TSSK 4 AntibodyWestern blot analysis of lysates from HT-29 cells, using TSSK4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10441-1-tssk4-primary-antibodies-wb-testing-1.jpgAnti-TSSK 4 AntibodyWestern blot analysis of the lysates from HT-29 cells using TSSK4 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ifn-omega-antibody-a10413-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10413-ifnw1-primary-antibodies-ihc-testing-1.jpgAnti-IFN- omega IFNW1 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10413-ifnw1-primary-antibodies-wb-testing-2.jpgAnti-IFN- omega IFNW1 AntibodyWestern Blot analysis of HeLa cells using IFN-ω Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10413-ifnw1-primary-antibodies-wb-testing-3.jpgAnti-IFN- omega IFNW1 AntibodyWestern blot analysis of lysate from HeLa cells, using IFNW1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-17-beta-hsd11-antibody-a10397-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10397-hsd17b11-primary-antibodies-wb-testing-2.jpgAnti-17 beta-HSD11 HSD17B11 AntibodyWestern Blot analysis of various cells using 17β-HSD11 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10397-hsd17b11-primary-antibodies-wb-testing-3.jpgAnti-17 beta-HSD11 HSD17B11 AntibodyWestern blot analysis of lysates from 293 cells, using DHRS8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10397-hsd17b11-primary-antibodies-wb-testing-4.jpgAnti-17 beta-HSD11 HSD17B11 AntibodyWestern blot analysis of the lysates from RAW264.7cells using DHRS8 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10397-hsd17b11-primary-antibodies-if-testing-1.jpgAnti-17 beta-HSD11 HSD17B11 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/anti-mrp-l12-antibody-a10395-1-boster.html2026-03-24T05:08:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10395-1-mrpl12-primary-antibodies-wb-testing-2.jpgAnti-MRP-L12 AntibodyWestern Blot analysis of various cells using MRP-L12 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10395-1-mrpl12-primary-antibodies-wb-testing-3.jpgAnti-MRP-L12 AntibodyWestern blot analysis of lysates from COLO cells, using MRPL12 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10395-1-mrpl12-primary-antibodies-ihc-testing-1.jpgAnti-MRP-L12 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-cadherin-7-antibody-a10388-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10388-cdh7-primary-antibodies-wb-testing-2.jpgAnti-Cadherin-7 CDH7 AntibodyWestern Blot analysis of various cells using Cadherin-7 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10388-cdh7-primary-antibodies-wb-testing-1.jpgAnti-Cadherin-7 CDH7 AntibodyWestern blot analysis of lysates from A549 cells, using CDH7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-chid1-antibody-a10376-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10376-chid1-primary-antibodies-wb-testing-1.jpgAnti-CHID1/Si Clp AntibodyWestern Blot analysis of 3T3 cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-serinc1-antibody-a10374-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-serinc1-primary-antibodies-ihc-testing-1.jpgAnti-Serine incorporator 1 Serinc1 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-serinc1-primary-antibodies-wb-testing-2.jpgAnti-Serine incorporator 1 Serinc1 AntibodyWestern Blot analysis of various cells using Serinc1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-serinc1-primary-antibodies-wb-testing-3.jpgAnti-Serine incorporator 1 Serinc1 AntibodyWestern blot analysis of lysates from HepG2 cells, using SERC1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr107-antibody-a10357-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10357-gpr107-primary-antibodies-ihc-testing-1.jpgAnti-Protein GPR107 GPR107 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10357-gpr107-primary-antibodies-wb-testing-2.jpgAnti-Protein GPR107 GPR107 AntibodyWestern blot analysis of lysates from HUVEC, Jurkat, and COLO205 cells, using GPR107 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdc42ep2-antibody-a10345-1-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10345-1-cdc42ep2-primary-antibodies-wb-testing-2.jpgAnti-Cdc42 effector protein 2 Cdc42EP2 AntibodyWestern Blot analysis of K562 cells using Cdc42EP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10345-1-cdc42ep2-primary-antibodies-wb-testing-3.jpgAnti-Cdc42 effector protein 2 Cdc42EP2 AntibodyWestern blot analysis of lysates from K562 cells, using BORG1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10345-1-cdc42ep2-primary-antibodies-ihc-testing-1.jpgAnti-Cdc42 effector protein 2 Cdc42EP2 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-rbm16-antibody-a10330-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10330-scaf8-primary-antibodies-wb-testing-2.jpgAnti-RBM16 SCAF8 AntibodyWestern Blot analysis of JK cells using RBM16 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10330-scaf8-primary-antibodies-ihc-testing-1.jpgAnti-RBM16 SCAF8 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-cd300c-antibody-a10291-boster.html2026-03-24T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10291-cd300c-primary-antibodies-wb-testing-2.jpgAnti-CD300c/Lmir2 AntibodyWestern Blot analysis of rat kidney cells using CD300c Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10291-cd300c-primary-antibodies-wb-testing-1.jpgAnti-CD300c/Lmir2 AntibodyWestern Blot analysis of RAT-kidney cells using CD300c Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-rabphilin-3a-antibody-a10247-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10247-rph3a-primary-antibodies-wb-testing-2.jpgAnti-Rabphilin-3A RPH3A AntibodyWestern Blot analysis of various cells using Rabphilin-3A Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10247-rph3a-primary-antibodies-wb-testing-3.jpgAnti-Rabphilin-3A RPH3A AntibodyWestern blot analysis of lysates from HeLa cells, treated with TNF-a 20ng/ml 2', using Rabphilin 3A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10247-rph3a-primary-antibodies-ihc-testing-4.jpgAnti-Rabphilin-3A RPH3A AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Rabphilin 3A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10247-rph3a-primary-antibodies-if-testing-1.jpgAnti-Rabphilin-3A RPH3A AntibodyImmunofluorescence analysis of HeLa cells, using Rabphilin 3A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr172b-antibody-a10245-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10245-slc52a1-primary-antibodies-wb-testing-2.jpgAnti-GPR172B SLC52A1 AntibodyWestern Blot analysis of 293T cells using GPR172B Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10245-slc52a1-primary-antibodies-wb-testing-3.jpgAnti-GPR172B SLC52A1 AntibodyWestern blot analysis of lysates from LOVO cells, using PEVR2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10245-slc52a1-primary-antibodies-if-testing-1.jpgAnti-GPR172B SLC52A1 AntibodyImmunofluorescence analysis of MCF7 cells, using PEVR2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr101-antibody-a10226-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10226-gpr101-primary-antibodies-wb-testing-2.jpgAnti-GPR101 AntibodyWestern Blot analysis of various cells using GPR101 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10226-gpr101-primary-antibodies-wb-testing-3.jpgAnti-GPR101 AntibodyWestern blot analysis of lysates from COS7 cells, using GPR101 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10226-gpr101-primary-antibodies-if-testing-1.jpgAnti-GPR101 AntibodyImmunofluorescence analysis of HeLa cells, using GPR101 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs15-antibody-a10224-1-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10224-1-scaf4-primary-antibodyes-wb-testing-1.jpgAnti-SFRS15 SCAF4 AntibodyWestern Blot (WB) analysis of COLO205 cells using SFRS15 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rhobtb3-antibody-a10214-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10214-rhobtb3-primary-antibodies-wb-testing-2.jpgAnti-RHOBTB3 AntibodyWestern Blot analysis of K562 cells using RHOBTB3 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10214-rhobtb3-primary-antibodies-wb-testing-3.jpgAnti-RHOBTB3 AntibodyWestern blot analysis of customer's lysis using RHOBTB3 antibody. Antibody was diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10214-rhobtb3-primary-antibodies-ihc-testing-1.jpgAnti-RHOBTB3 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using RHOBTB3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-phf3-antibody-a10188-1-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10188-1-phf3-primary-antibodies-wb-testing-2.jpgAnti-PHD finger protein 3 PHF3 AntibodyWestern Blot analysis of various cells using PHF3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10188-1-phf3-primary-antibodies-ihc-testing-1.jpgAnti-PHD finger protein 3 PHF3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PHF3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd300b-antibody-a10132-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10132-cd300lb-primary-antibodyes-ihc-testing-1.jpgAnti-CD300b CD300LB AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10132-cd300lb-primary-antibodyes-ihc-testing-2.jpgAnti-CD300b CD300LB AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr38-antibody-a10124-boster.html2026-03-24T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10124-mlnr-primary-antibodies-wb-testing-1.jpgAnti-GPR38 MLNR AntibodyWestern Blot analysis of various cells using GPR38 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/anti-hnk-1st-antibody-a10117-1-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10117-1-chst10-primary-antibodies-wb-testing-2.jpgAnti-HNK-1ST CHST10 AntibodyWestern Blot analysis of various cells using HNK-1ST Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10117-1-chst10-primary-antibodies-wb-testing-3.jpgAnti-HNK-1ST CHST10 AntibodyWestern blot analysis of lysates from HUVEC cells, using CHST10 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10117-1-chst10-primary-antibodies-ihc-testing-1.jpgAnti-HNK-1ST CHST10 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using CHST10 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nut-antibody-a10092-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10092-nutm1-primary-antibodies-wb-testing-1.jpgAnti-NUT NUTM1 AntibodyWestern Blot analysis of 293T cells using primary antibody diluted at 1:1000 (4°C overnight). Secondary antibody:Goat Anti-rabbit IgG IRDye 800 (diluted at 1:5000, 25°C, 1 hour)
https://www.bosterbio.com/products/primary-antibodies/anti-erk-8-antibody-a10088-1-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10088-1-mapk15-primary-antibodies-wb-testing-2.jpgAnti-ERK 8 MAPK15 AntibodyWestern Blot analysis of various cells using ERK 8 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10088-1-mapk15-primary-antibodies-wb-testing-3.jpgAnti-ERK 8 MAPK15 AntibodyWestern blot analysis of lysates from HepG2 cells, using ERK8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10088-1-mapk15-primary-antibodies-ihc-testing-4.jpgAnti-ERK 8 MAPK15 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10088-1-mapk15-primary-antibodies-if-testing-1.jpgAnti-ERK 8 MAPK15 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using ERK8 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdca3-antibody-a10074-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10074-cdca3-primary-antibodies-wb-testing-2.jpgAnti-CdcA3 AntibodyWestern Blot analysis of various cells using CdcA3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10074-cdca3-primary-antibodies-wb-testing-3.jpgAnti-CdcA3 AntibodyWestern blot analysis of lysates from HepG2 cells, using CDCA3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10074-cdca3-primary-antibodies-ihc-testing-1.jpgAnti-CdcA3 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using CDCA3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdnf-antibody-a10069-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10069-cdnf-primary-antibodies-ihc-testing-1.jpgAnti-CDNF AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-casein-kinase-i-gamma2-antibody-a10048-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10048-csnk1g2-primary-antibodies-wb-testing-2.jpgAnti-Casein Kinase I gamma2 CSNK1G2 AntibodyWestern Blot analysis of HeLa cells using Casein Kinase Iγ2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10048-csnk1g2-primary-antibodies-wb-testing-3.jpgAnti-Casein Kinase I gamma2 CSNK1G2 AntibodyWestern blot analysis of lysates from HeLa and 293 cells, using CKI-gamma2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10048-csnk1g2-primary-antibodies-ihc-testing-1.jpgAnti-Casein Kinase I gamma2 CSNK1G2 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-usp42-antibody-a10046-1-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10046-1-usp42-primary-antibodies-wb-testing-2.jpgAnti-USP42 AntibodyWestern Blot analysis of various cells using USP42 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10046-1-usp42-primary-antibodies-wb-testing-3.jpgAnti-USP42 AntibodyWestern blot analysis of lysates from HT-29 cells, using USP42 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10046-1-usp42-primary-antibodies-wb-testing-1.jpgAnti-USP42 AntibodyWestern blot analysis of the lysates from HeLa cells using USP42 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gcp5-antibody-a10040-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10040-tubgcp5-primary-antibodies-ihc-testing-1.jpgAnti-GCP5 TUBGCP5 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10040-tubgcp5-primary-antibodies-wb-testing-2.jpgAnti-GCP5 TUBGCP5 AntibodyWestern blot analysis of lysates from HT-29, Jurkat, and 293 cells, using TUBGCP5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-inhibin-beta-e-antibody-a10030-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10030-inhbe-primary-antibodies-wb-testing-2.jpgAnti-Inhibin beta-E INHBE AntibodyWestern Blot analysis of L929 cells using Inhibin β-E Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10030-inhbe-primary-antibodies-ihc-testing-3.jpgAnti-Inhibin beta-E INHBE AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10030-inhbe-primary-antibodies-ihc-testing-1.jpgAnti-Inhibin beta-E INHBE AntibodyImmunohistochemical analysis of paraffin-embedded mouse-muscle, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/anti-epigen-antibody-a10011-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-epgn-primary-antibodies-wb-testing-2.jpgAnti-Epigen EPGN AntibodyWestern Blot analysis of 293T, 823 cells using Epigen Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-epgn-primary-antibodies-wb-testing-1.jpgAnti-Epigen EPGN AntibodyWestern Blot analysis of 293T cells using Epigen Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-lyar-antibody-a09986-boster.html2026-03-24T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-lyar-primary-antibodies-wb-testing-2.jpgAnti-LYAR AntibodyWestern Blot analysis of SH-SY5Y cells using LYAR Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-lyar-primary-antibodies-wb-testing-3.jpgAnti-LYAR AntibodyWestern blot analysis of lysates from Jurkat, HepG2, and LOVO cells, using LYAR Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-lyar-primary-antibodies-wb-testing-4.jpgAnti-LYAR AntibodyWestern blot analysis of the lysates from K562 cells using LYAR antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-lyar-primary-antibodies-ihc-testing-1.jpgAnti-LYAR AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-cacna2d4-antibody-a09975-1-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09975-1-cacna2d4-primary-antibodyes-wb-testing-1.jpgAnti-Cacna2d4 AntibodyWestern Blot (WB) analysis of specific cells using Cacna2d4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-acetyl-histone-h2b-k126-antibody-a09942-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09942-hist1h2ba-primary-antibodies-wb-testing-1.jpgAnti-Acetyl-Histone H2B (K126) HIST1H2BA AntibodyWestern Blot analysis of A549 cells using Acetyl-Histone H2B (K126) Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-gnl1-antibody-a09923-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09923-gnl1-primary-antibodyes-wb-testing-1.jpgAnti-GNL1 AntibodyWestern Blot (WB) analysis of K562 cells using GNL1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09923-gnl1-primary-antibodyes-wb-testing-2.jpgAnti-GNL1 AntibodyWestern Blot (WB) analysis of specific cells using GNL1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mdm1-antibody-a09897-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09897-mdm1-primary-antibodies-wb-testing-1.jpgAnti-Nuclear protein MDM1 MDM1 AntibodyWestern blot analysis of the lysates from HepG2 cells using MDM1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09897-mdm1-primary-antibodies-wb-testing-2.jpgAnti-Nuclear protein MDM1 MDM1 AntibodyWestern Blot analysis of 3T3 cells using MDM1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/anti-kv3-4-antibody-a09889-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09889-kcnc4-primary-antibodies-wb-testing-2.jpgAnti-Kv3.4 KCNC4 AntibodyWestern Blot analysis of SH-SY5Y cells using Kv3.4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09889-kcnc4-primary-antibodies-wb-testing-3.jpgAnti-Kv3.4 KCNC4 AntibodyWestern blot analysis of lysates from COS7 cells treated with Anisomycin 25ug/ml 30', using Kv3.4/KCNC4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09889-kcnc4-primary-antibodies-ihc-testing-4.jpgAnti-Kv3.4 KCNC4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using Kv3.4/KCNC4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09889-kcnc4-primary-antibodies-if-testing-1.jpgAnti-Kv3.4 KCNC4 AntibodyImmunofluorescence analysis of HeLa cells, using Kv3.4/KCNC4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nrf3-antibody-a09888-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09888-nfe2l3-primary-antibodies-wb-testing-1.jpgAnti-Nrf3 NFE2L3 AntibodyWestern Blot analysis of HeLa cells using Nrf3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09888-nfe2l3-primary-antibodies-wb-testing-2.jpgAnti-Nrf3 NFE2L3 AntibodyWestern Blot analysis of various cells using Nrf3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-apoo-antibody-a09879-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09879-apoo-primary-antibodies-wb-testing-2.jpgAnti-ApoO Monoclonal AntibodyWestern Blot analysis using ApoO Monoclonal Antibody against HepG2 (1) and 3T3L1 (2) cell lysatehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09879-apoo-primary-antibodies-ihc-testing-1.jpgAnti-ApoO Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human Testis tissues with AEC staining using ApoO Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rbak-antibody-a09876-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09876-rbak-primary-antibodies-wb-testing-2.jpgAnti-RBAK AntibodyWestern Blot analysis of various cells using RBAK Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09876-rbak-primary-antibodies-wb-testing-3.jpgAnti-RBAK AntibodyWestern blot analysis of lysates from HepG2 cells, using RBAK Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09876-rbak-primary-antibodies-ihc-testing-1.jpgAnti-RBAK AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-cd163b-antibody-a09845-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09845-cd163l1-primary-antibodies-ihc-testing-1.jpgAnti-CD163b CD163L1 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09845-cd163l1-primary-antibodies-wb-testing-2.jpgAnti-CD163b CD163L1 AntibodyWestern Blot analysis of HeLa cells using CD163b Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09845-cd163l1-primary-antibodies-wb-testing-3.jpgAnti-CD163b CD163L1 AntibodyWestern blot analysis of lysate from HeLa cells, using CD163L1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-znf384-antibody-a09826-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09826-znf384-primary-antibodies-wb-testing-1.jpgAnti-Zinc finger protein 384 ZNF384 AntibodyWestern Blot analysis of VEC cells using ZNF384 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/anti-il-1f6-antibody-a09802-boster.html2026-03-24T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09802-il36a-primary-antibodies-ihc-testing-1.jpgAnti-IL-1F6 IL36A AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-lzk-antibody-a09780-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09780-map3k13-primary-antibodies-wb-testing-2.jpgAnti-LZK MAP3K13 AntibodyWestern Blot analysis of HepG2 cells using LZK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09780-map3k13-primary-antibodies-wb-testing-3.jpgAnti-LZK MAP3K13 AntibodyWestern blot analysis of lysates from HeLa, HUVEC, and HepG2 cells, using M3K13 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09780-map3k13-primary-antibodies-ihc-testing-1.jpgAnti-LZK MAP3K13 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-trp14-antibody-a09772-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09772-txndc17-primary-antibodies-wb-testing-1.jpgAnti-TRP14 TXNDC17 AntibodyWestern Blot analysis of HL-60, Raji, K562, SW480, A549, 22RV-1 cells using TRP14 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-grin1-antibody-a09764-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09764-gprin1-primary-antibodies-wb-testing-1.jpgAnti-GRIN1 GPRIN1 AntibodyWestern blot analysis of lysates from HT-29 cells, using GPRIN1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09764-gprin1-primary-antibodies-wb-testing-2.jpgAnti-GRIN1 GPRIN1 AntibodyWestern Blot analysis of HT29 cells using GRIN1 Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/anti-myoz2-antibody-a09739-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09739-myoz2-primary-antibodies-ihc-testing-1.jpgAnti-MYOZ2 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09739-myoz2-primary-antibodies-wb-testing-2.jpgAnti-MYOZ2 AntibodyWestern Blot analysis of hepg2 cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-mrrf-antibody-a09708-1-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09708-1-mrrf-primary-antibodyes-wb-testing-1.jpgAnti-MRRF AntibodyWestern Blot (WB) analysis of 293T 3T3 lysis using MRRF antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09708-1-mrrf-primary-antibodyes-wb-testing-2.jpgAnti-MRRF AntibodyWestern Blot (WB) analysis of specific cells using MRRF Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-asah3l-antibody-a09706-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09706-acer2-primary-antibodies-wb-testing-2.jpgAnti-ASAH3L ACER2 AntibodyWestern blot analysis of COS7 using ASAH3L antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09706-acer2-primary-antibodies-ihc-testing-3.jpgAnti-ASAH3L ACER2 AntibodyImmunohistochemical analysis of paraffin-embedded human-breast-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09706-acer2-primary-antibodies-ihc-testing-4.jpgAnti-ASAH3L ACER2 AntibodyImmunohistochemical analysis of paraffin-embedded human-breast-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09706-acer2-primary-antibodies-ihc-testing-1.jpgAnti-ASAH3L ACER2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/anti-cactin-antibody-a09699-1-boster.html2026-03-24T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09699-1-cactin-primary-antibodies-wb-testing-1.jpgAnti-CACTIN AntibodyWestern Blot analysis of hepg2 cells using Antibody diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-mov10l1-antibody-a09677-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09677-mov10l1-primary-antibodies-ihc-testing-1.jpgAnti-RNA helicase Mov10l1 MOV10L1 AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1,primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09677-mov10l1-primary-antibodies-wb-testing-2.jpgAnti-RNA helicase Mov10l1 MOV10L1 AntibodyWestern Blot analysis of various cells using MOV10L1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09677-mov10l1-primary-antibodies-wb-testing-3.jpgAnti-RNA helicase Mov10l1 MOV10L1 AntibodyWestern blot analysis of lysates from HeLa and RAW264.7 cells, using MOV10L1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-armcx1-antibody-a09670-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09670-armcx1-primary-antibodies-wb-testing-2.jpgAnti-ARMCX1 AntibodyWestern Blot analysis of various cells using ARMCX1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09670-armcx1-primary-antibodies-wb-testing-3.jpgAnti-ARMCX1 AntibodyWestern Blot analysis of mouse-brain cells using ARMCX1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09670-armcx1-primary-antibodies-wb-testing-4.jpgAnti-ARMCX1 AntibodyWestern blot analysis of lysates from rat brain cells, using ARMX1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09670-armcx1-primary-antibodies-ihc-testing-1.jpgAnti-ARMCX1 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-cgi-43-antibody-a09666-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09666-ccz1-primary-antibodyes-wb-testing-1.jpgAnti-CGI-43 CCZ1 AntibodyWestern Blot (WB) analysis of Jurkat cells using CGI-43 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nectin-3-antibody-a09633-1-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09633-1-nectin3-primary-antibodyes-wb-testing-1.jpgAnti-Nectin 3 AntibodyWestern Blot (WB) analysis of specific cells using Nectin 3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nectin-3-antibody-a09633-2-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09633-2-nectin3-primary-antibodies-wb-testing-2.jpgAnti-Nectin 3 AntibodyWestern Blot analysis of HeLa cells using Nectin 3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09633-2-nectin3-primary-antibodies-wb-testing-1.jpgAnti-Nectin 3 AntibodyWestern blot analysis of lysate from HeLa cells, using PVRL3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-grk-7-antibody-a09628-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09628-grk7-primary-antibodyes-wb-testing-1.jpgAnti-GRK 7 AntibodyWestern Blot (WB) analysis of specific cells using GRK 7 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd315-antibody-a09624-boster.html2026-03-24T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09624-ptgfrn-primary-antibodies-wb-testing-2.jpgAnti-CD315 PTGFRN AntibodyWestern Blot analysis of 293 cells using CD315 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09624-ptgfrn-primary-antibodies-ihc-testing-3.jpgAnti-CD315 PTGFRN AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09624-ptgfrn-primary-antibodies-if-testing-1.jpgAnti-CD315 PTGFRN AntibodyImmunofluorescence analysis of A549. 1, primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd85g-antibody-a09611-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09611-lilra4-primary-antibodies-wb-testing-2.jpgAnti-CD85g LILRA4 AntibodyWestern Blot analysis of MCF7 cells using CD85g Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09611-lilra4-primary-antibodies-wb-testing-3.jpgAnti-CD85g LILRA4 AntibodyWestern blot analysis of lysate from MCF7 cells, using LILRA4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09611-lilra4-primary-antibodies-ihc-testing-1.jpgAnti-CD85g LILRA4 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ifn-alpha1-antibody-a09608-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09608-ifna1-primary-antibodies-wb-testing-1.jpgAnti-IFN- alpha1 IFNA1 AntibodyWestern Blot analysis of BT474, A549 cells using IFN-α1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr105-antibody-a09607-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09607-p2ry14-primary-antibodies-wb-testing-2.jpgAnti-GPR105 P2RY14 AntibodyWestern Blot analysis of various cells using GPR105 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09607-p2ry14-primary-antibodies-wb-testing-3.jpgAnti-GPR105 P2RY14 AntibodyWestern blot analysis of lysates from 293, COLO205, and HepG2 cells, using GPR105 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09607-p2ry14-primary-antibodies-if-testing-1.jpgAnti-GPR105 P2RY14 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR105 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-iqgap3-antibody-a09547-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09547-iqgap3-primary-antibodyes-wb-testing-1.jpgAnti-IQGAP3 AntibodyWestern blot analysis of various cells using IQGAP3 Polyclonal Antibody diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rpap2-antibody-a09543-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09543-rpap2-primary-antibodies-wb-testing-2.jpgAnti-RPAP2 AntibodyWestern Blot analysis of various cells using RPAP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09543-rpap2-primary-antibodies-wb-testing-1.jpgAnti-RPAP2 AntibodyWestern blot analysis of RPAP2 Antibody. The lane on the right is blocked with the RPAP2 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scfd1-antibody-a09509-1-boster.html2026-03-24T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09509-1-scfd1-primary-antibodies-wb-testing-2.jpgAnti-SCFD1 AntibodyWestern Blot analysis of various cells using SCFD1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09509-1-scfd1-primary-antibodies-wb-testing-3.jpgAnti-SCFD1 AntibodyWestern blot analysis of SCFD1 Antibody. The lane on the right is blocked with the SCFD1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09509-1-scfd1-primary-antibodies-wb-testing-4.jpgAnti-SCFD1 AntibodyWestern blot analysis of the lysates from 293 cells using SCFD1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09509-1-scfd1-primary-antibodies-ihc-testing-1.jpgAnti-SCFD1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp2s1-antibody-a09468-boster.html2026-03-24T05:08:37+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-doc-1-antibody-a09467-1-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09467-1-cdk2ap1-primary-antibodies-wb-testing-2.jpgAnti-DOC-1 CDK2AP1 AntibodyWestern Blot analysis of various cells using DOC-1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09467-1-cdk2ap1-primary-antibodies-wb-testing-3.jpgAnti-DOC-1 CDK2AP1 AntibodyWestern blot analysis of lysates from HeLa cells, using CDKPA1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09467-1-cdk2ap1-primary-antibodies-wb-testing-1.jpgAnti-DOC-1 CDK2AP1 AntibodyWestern blot analysis of the lysates from HeLa cells using CDKAP1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ntf2-antibody-a09424-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09424-nutf2-primary-antibodyes-wb-testing-1.jpgAnti-NTF2 NUTF2 AntibodyWestern Blot (WB) analysis of HeLa cells using NTF2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09424-nutf2-primary-antibodyes-wb-testing-2.jpgAnti-NTF2 NUTF2 AntibodyWestern Blot (WB) analysis of HeLa cells using NTF2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-insl4-antibody-a09422-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09422-insl4-primary-antibodies-if-testing-1.jpgAnti-INSL4 AntibodyImmunofluorescence analysis of A549 cells, using INSL4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09422-insl4-primary-antibodies-wb-testing-2.jpgAnti-INSL4 AntibodyWestern Blot analysis of various cells using INSL4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09422-insl4-primary-antibodies-wb-testing-3.jpgAnti-INSL4 AntibodyWestern blot analysis of lysates from HT-29 cells, using INSL4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gnl3l-antibody-a09415-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09415-gnl3l-primary-antibodies-wb-testing-2.jpgAnti-GNL3L AntibodyWestern Blot analysis of HT29 cells using GNL3L Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09415-gnl3l-primary-antibodies-wb-testing-3.jpgAnti-GNL3L AntibodyWestern Blot analysis of customer's (cat sample) using GNL3L Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09415-gnl3l-primary-antibodies-wb-testing-4.jpgAnti-GNL3L AntibodyWestern blot analysis of lysates from 293, HeLa, and HT-29 cells, using GNL3L Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09415-gnl3l-primary-antibodies-ihc-testing-1.jpgAnti-GNL3L AntibodyImmunohistochemical analysis of paraffin-embedded human brain. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dc-lamp-antibody-a09406-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09406-lamp3-primary-antibodies-wb-testing-2.jpgAnti-DC-LAMP LAMP3 AntibodyWestern blot analysis of mouse-lung mouse-heart 293T Hela 3T3 lysate, antibody was diluted at 500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09406-lamp3-primary-antibodies-ihc-testing-1.jpgAnti-DC-LAMP LAMP3 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung-cancer, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-cathepsin-l2-l114-antibody-a09374-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09374-ctsv-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Cathepsin L2 (L114) CTSV AntibodyWestern Blot analysis of various cells using Cleaved-Cathepsin L2 (L114) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09374-ctsv-primary-antibodies-wb-testing-3.jpgAnti-Cleaved-Cathepsin L2 (L114) CTSV AntibodyWestern blot analysis of lysates from 293 and COS cells, treated with etoposide 25uM 1h, using CATL2 (Cleaved-Leu114) Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09374-ctsv-primary-antibodies-if-testing-1.jpgAnti-Cleaved-Cathepsin L2 (L114) CTSV AntibodyImmunofluorescence analysis of Siha cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 488 Secondary antibody was diluted at 1:500 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tcp-1-zeta-antibody-a09373-1-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09373-1-cct6a-primary-antibodies-ihc-testing-1.jpgAnti-TCP-1 zeta CCT6A AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using CCT6A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09373-1-cct6a-primary-antibodies-wb-testing-2.jpgAnti-TCP-1 zeta CCT6A AntibodyWestern Blot analysis of various cells using TCP-1 ζ Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09373-1-cct6a-primary-antibodies-wb-testing-3.jpgAnti-TCP-1 zeta CCT6A AntibodyWestern blot analysis of CCT6A Antibody. The lane on the right is blocked with the CCT6A peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr100-antibody-a09371-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09371-rxfp4-primary-antibodies-wb-testing-2.jpgAnti-GPR100 RXFP4 AntibodyWestern Blot analysis of A549 cells using GPR100 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09371-rxfp4-primary-antibodies-wb-testing-3.jpgAnti-GPR100 RXFP4 AntibodyWestern blot analysis of lysates from A549 cells, using GPR100 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09371-rxfp4-primary-antibodies-if-testing-1.jpgAnti-GPR100 RXFP4 AntibodyImmunofluorescence analysis of A549 cells, using GPR100 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-beta-1-4-gal-t5-antibody-a09370-boster.html2026-03-24T05:08:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09370-b4galt5-primary-antibodies-wb-testing-2.jpgAnti-beta-1,4-Gal-T5 B4GALT5 AntibodyWestern Blot analysis of various cells using β-1, 4-Gal-T5 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09370-b4galt5-primary-antibodies-wb-testing-1.jpgAnti-beta-1,4-Gal-T5 B4GALT5 AntibodyWestern Blot analysis of 293 cells using β-1, 4-Gal-T5 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gabaa-r-epsilon-antibody-a09362-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09362-gabre-primary-antibodyes-wb-testing-1.jpgAnti-GABAA R epsilon GABRE AntibodyWestern Blot (WB) analysis of extracts from Jurkat cells, using GABAA Repsilon Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-encephalopsin-antibody-a09353-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09353-opn3-primary-antibodies-wb-testing-2.jpgAnti-Encephalopsin OPN3 AntibodyWestern blot analysis of various cell Lysate, antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09353-opn3-primary-antibodies-wb-testing-3.jpgAnti-Encephalopsin OPN3 AntibodyWestern blot analysis of lysates from mouse brain, using Encephalopsin Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09353-opn3-primary-antibodies-ihc-testing-4.jpgAnti-Encephalopsin OPN3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09353-opn3-primary-antibodies-if-testing-1.jpgAnti-Encephalopsin OPN3 AntibodyImmunofluorescence analysis of MCF7 cells, using Encephalopsin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hgfa-antibody-a09351-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09351-hgfac-primary-antibodies-wb-testing-1.jpgAnti-HGFA HGFAC AntibodyWestern Blot analysis of extracts from K562, Jurkat cells, using HGFA Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab11-fip4-antibody-a09318-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09318-rab11fip4-primary-antibodies-ihc-testing-1.jpgAnti-Rab11-FIP4 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09318-rab11fip4-primary-antibodies-wb-testing-2.jpgAnti-Rab11-FIP4 AntibodyWestern Blot analysis of various cells using Rab11-FIP4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09318-rab11fip4-primary-antibodies-wb-testing-3.jpgAnti-Rab11-FIP4 AntibodyWestern blot analysis of lysates from 293, COLO, HUVEC, HepG2, and HT-29 cells, using RAB11FIP4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rabenosyn-5-antibody-a09291-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09291-rbsn-primary-antibodies-ihc-testing-1.jpgAnti-Rabenosyn-5 RBSN AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09291-rbsn-primary-antibodies-wb-testing-2.jpgAnti-Rabenosyn-5 RBSN AntibodyWestern Blot analysis of various cells using Rabenosyn-5 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09291-rbsn-primary-antibodies-wb-testing-3.jpgAnti-Rabenosyn-5 RBSN AntibodyWestern blot analysis of lysates from HUVEC and Jurkat cells, using ZFYVE20 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09291-rbsn-primary-antibodies-wb-testing-4.jpgAnti-Rabenosyn-5 RBSN AntibodyWestern blot analysis of the lysates from COLO205 cells using ZFYVE20 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-integrin-alphad-antibody-a09283-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09283-itgad-primary-antibodies-wb-testing-1.jpgAnti-Integrin alphaD ITGAD AntibodyWestern blot analysis of lysate from 4T1 cells, using ITGAD Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09283-itgad-primary-antibodies-wb-testing-2.jpgAnti-Integrin alphaD ITGAD AntibodyWestern Blot analysis of 4T1, 293 cells using Integrin αD Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bdh1-antibody-a09277-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09277-bdh1-primary-antibodies-wb-testing-2.jpgAnti-BDH1 Monoclonal AntibodyWestern Blot analysis using BDH1 Monoclonal Antibody against HepG2 (1) and NIH/3T3 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09277-bdh1-primary-antibodies-ihc-testing-1.jpgAnti-BDH1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human liver cancer (left) and colorectal cancer tissues (right) with DAB staining using BDH1 Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ndufa4-antibody-a09276-1-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09276-1-ndufa4-primary-antibodyes-wb-testing-1.jpgAnti-NDUFA4 AntibodyWestern Blot (WB) analysis of specific cells using NDUFA4 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-1f10-antibody-a09268-boster.html2026-03-24T05:08:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09268-il1f10-primary-antibodies-wb-testing-1.jpgAnti-IL-1F10 AntibodyWestern blot analysis of MOUSE-KIDNEY MOUSE-HEART MOUSE-BRAIN MOUSE-SPLEEN RAT-SPLEEN using IL1F10 antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nmur1-antibody-a09256-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09256-nmur1-primary-antibodyes-wb-testing-1.jpgAnti-NMUR1/Neuromedin U R1 AntibodyWestern Blot (WB) analysis of K562 cells using NMUR1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p2y4-antibody-a09252-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09252-p2ry4-primary-antibodies-wb-testing-1.jpgAnti-P2Y4 P2RY4 AntibodyWestern blot analysis of the lysates from COLO205 cells using P2RY4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09252-p2ry4-primary-antibodies-wb-testing-2.jpgAnti-P2Y4 P2RY4 AntibodyWestern Blot analysis of various cells using P2Y4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09252-p2ry4-primary-antibodies-wb-testing-3.jpgAnti-P2Y4 P2RY4 AntibodyWestern blot analysis of lysates from HeLa cells, using P2RY4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-28-antibody-a09233-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09233-ifnl2-primary-antibodies-wb-testing-2.jpgAnti-IL-28 IFNL2 AntibodyWestern Blot analysis of MCF7 cells using IL-28 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09233-ifnl2-primary-antibodies-wb-testing-3.jpgAnti-IL-28 IFNL2 AntibodyWestern blot analysis of lysate from MCF7 cells, using IL28A Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09233-ifnl2-primary-antibodies-ihc-testing-4.jpgAnti-IL-28 IFNL2 AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09233-ifnl2-primary-antibodies-ihc-testing-1.jpgAnti-IL-28 IFNL2 AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ephrin-a4-antibody-a09230-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09230-efna4-primary-antibodies-wb-testing-2.jpgAnti-Ephrin-A4 EFNA4 AntibodyWestern Blot analysis of various cells using Ephrin-A4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09230-efna4-primary-antibodies-wb-testing-1.jpgAnti-Ephrin-A4 EFNA4 AntibodyWestern blot analysis of lysates from HepG2 cells, using EFNA4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fast-antibody-a09199-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09199-fastk-primary-antibodyes-wb-testing-1.jpgAnti-FAST FASTK AntibodyWestern Blot (WB) analysis of specific cells using FAST Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ca-xiii-antibody-a09186-1-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09186-1-ca13-primary-antibodyes-wb-testing-1.jpgAnti-CA XIII CA13 AntibodyWestern Blot (WB) analysis of specific cells using CA XIII Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cerebellin-1-antibody-a09176-1-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09176-1-cbln1-primary-antibodyes-wb-testing-1.jpgAnti-Cerebellin 1 CBLN1 AntibodyWestern Blot (WB) analysis of specific cells using Cerebellin 1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09176-1-fnins-19-1556570-g008.jpgAnti-Cerebellin 1 CBLN1 AntibodyNEXMIF overexpression results in transcriptional dysregulation in the brain. (A) RNA sequencing bar chart showing the normalized (Log2) fold changes of the top 44 of 161 total differentially expressed genes (DEGs) in the hippocampus (HPC) of P70 NEX OX mice. In total, 131 DEGs (81%) were downregulated and 30 DEGs (19%) were upregulated by at least a 1.3-fold change in the NEX OX mouse brain, relative to CTRL. (B) Gene Ontology (GO) enrichment analysis bar chart depicting the most enriched biological processes. The “# of DEGs” refers to the number of genes from the RNA sequencing dataset within each predefined Mus musculus GO biological process. Each bar reflects the percentage of upregulated (red) and/or downregulated (green) DEGs within each GO biological process. The False Discovery Rate (FDR) is a statistical measure of true nulls. For example, an FDR of 3% means that, among all genes considered significant, 3% of these genes are truly null. (C) Selected list of top hippocampal DEGs indicating their associated GO term, fold change in expression (NEX OX / CTRL), and adjusted p value. (D) Western blot showing the protein expression of CBLN1 (top panel), BAIAP3 (middle panel), and SGK1 (bottom panel) in the brain lysates of P70 CTRL and NEX OX mice. (E) Quantification of the western blots in (D) showed a significant reduction in CBLN1 and BAIAP3 protein in P70 NEX OX brains, in addition to an increase in SGK1 protein, consistent with RNA sequencing data. N = 3–4 mice/group. Data are represented as average ± SEM. Two-tailed student’s t test (E) : * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2025.1556570/abstract'>40606839</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aps-antibody-a09167-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09167-sh2b2-primary-antibodies-wb-testing-1.jpgAnti-APS SH2B2 AntibodyWestern Blot analysis of HuvEc cells using APS Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ccrl2-antibody-a09152-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09152-ccrl2-primary-antibodyes-wb-testing-1.jpgAnti-CCRL2/Cram A AntibodyWestern Blot (WB) analysis of specific cells using CCRL2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nrbf-2-antibody-a09144-boster.html2026-03-24T05:08:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09144-nrbf2-primary-antibodies-wb-testing-1.jpgAnti-NRBF-2 AntibodyWestern blot analysis of the lysates from RAW264.7cells using NRBF2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09144-nrbf2-primary-antibodies-wb-testing-2.jpgAnti-NRBF-2 AntibodyWestern Blot analysis of various cells using NRBF-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09144-nrbf2-primary-antibodies-wb-testing-3.jpgAnti-NRBF-2 AntibodyWestern blot analysis of lysates from A549 cells, using NRBF2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab3ip-antibody-a09085-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-rab3ip-primary-antibodyes-wb-testing-1.jpgAnti-Rab-3A-interacting protein RAB3IP AntibodyWestern Blot (WB) analysis of K562 cells using RAB3IP Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scgf-antibody-a09076-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09076-clec11a-primary-antibodies-wb-testing-2.jpgAnti-SCGF CLEC11A AntibodyWestern blot analysis of MOUSE-SPLEEN RAT-SPLEEN using CLEC11A antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09076-clec11a-primary-antibodies-ihc-testing-1.jpgAnti-SCGF CLEC11A AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-septin-7-antibody-a09070-1-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09070-1-sept7-primary-antibodies-wb-testing-2.jpgAnti-Septin 7 SEPT7; AntibodyWestern Blot analysis of various cells using Septin 7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09070-1-sept7-primary-antibodies-wb-testing-3.jpgAnti-Septin 7 SEPT7; AntibodyWestern blot analysis of lysates from HeLa, HUVEC, and MCF-7 cells, using SEPT7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09070-1-sept7-primary-antibodies-ihc-testing-1.jpgAnti-Septin 7 SEPT7; AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ny-co-1-antibody-a09039-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09039-nemf-primary-antibodies-ihc-testing-1.jpgAnti-NY-CO-1 NEMF AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09039-nemf-primary-antibodies-wb-testing-2.jpgAnti-NY-CO-1 NEMF AntibodyWestern Blot analysis of 3T3 cells using NY-CO-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09039-nemf-primary-antibodies-wb-testing-3.jpgAnti-NY-CO-1 NEMF AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using SDCG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ak6-antibody-a09025-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09025-ak6-primary-antibodies-wb-testing-2.jpgAnti-Adenylate kinase isoenzyme 6 AK6 AntibodyWestern Blot analysis of various cells using AK6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09025-ak6-primary-antibodies-wb-testing-3.jpgAnti-Adenylate kinase isoenzyme 6 AK6 AntibodyWestern blot analysis of lysates from Jurkat cells, using KAD6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09025-ak6-primary-antibodies-ihc-testing-1.jpgAnti-Adenylate kinase isoenzyme 6 AK6 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-xpln-antibody-a09012-1-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09012-1-arhgef3-primary-antibodies-wb-testing-2.jpgAnti-XPLN ARHGEF3 AntibodyWestern Blot analysis of various cells using XPLN Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09012-1-arhgef3-primary-antibodies-wb-testing-3.jpgAnti-XPLN ARHGEF3 AntibodyWestern blot analysis of lysates from COLO cells, using ARHGEF3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09012-1-arhgef3-primary-antibodies-wb-testing-4.jpgAnti-XPLN ARHGEF3 AntibodyWestern blot analysis of the lysates from HeLa cells using ARHGEF3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09012-1-arhgef3-primary-antibodies-ihc-testing-1.jpgAnti-XPLN ARHGEF3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lambda-5-antibody-a08965-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08965-igll1-primary-antibodies-wb-testing-1.jpgAnti-Lambda 5 IGLL1 AntibodyWestern Blot analysis of KB cells using Lambda 5 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arylsulfatase-g-antibody-a08962-boster.html2026-03-24T05:08:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08962-arsg-primary-antibodyes-wb-testing-1.jpgAnti-Arylsulfatase G ARSG AntibodyWestern Blot (WB) analysis of mouse cells using Arylsulfatase G Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scml2-antibody-a08958-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08958-scml2-primary-antibodies-wb-testing-2.jpgAnti-SCML2 AntibodyWestern Blot analysis of extracts from 293 cells, using SCML2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08958-scml2-primary-antibodies-ihc-testing-1.jpgAnti-SCML2 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-psmd11-antibody-a08940-1-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08940-1-psmd11-primary-antibodyes-wb-testing-1.jpgAnti-PSMD11 AntibodyWestern Blot (WB) analysis of specific cells using PSMD11 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gremlin-2-antibody-a08939-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08939-grem2-primary-antibodies-ihc-testing-1.jpgAnti-Gremlin-2 GREM2 AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08939-grem2-primary-antibodies-wb-testing-2.jpgAnti-Gremlin-2 GREM2 AntibodyWestern blot analysis of RAT-brain lysate, antibody was diluted at 1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08939-grem2-primary-antibodies-if-testing-3.jpgAnti-Gremlin-2 GREM2 AntibodyImmunohistochemical analysis of paraffin-embedded human-small-intestine, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-paox-antibody-a08936-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08936-paox-primary-antibodies-wb-testing-1.jpgAnti-PAOX AntibodyWestern Blot analysis of extracts from rat stomach, K562 cells, using PAOX Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-l36-antibody-a08922-1-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08922-1-rpl36-primary-antibodyes-wb-testing-1.jpgAnti-Ribosomal Protein L36 RPL36 AntibodyWestern Blot (WB) analysis of specific cells using Ribosomal Protein L36 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nnt-1-antibody-a08886-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08886-clcf1-primary-antibodies-ihc-testing-1.jpgAnti-NNT-1 CLCF1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-neuropsin-antibody-a08880-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08880-opn5-primary-antibodies-if-testing-1.jpgAnti-Neuropsin OPN5 AntibodyImmunofluorescence analysis of HeLa cells, using OPN5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08880-opn5-primary-antibodies-wb-testing-2.jpgAnti-Neuropsin OPN5 AntibodyWestern Blot analysis of Jurkat cells using Neuropsin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08880-opn5-primary-antibodies-wb-testing-3.jpgAnti-Neuropsin OPN5 AntibodyWestern blot analysis of lysates from Jurkat cells, using OPN5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08880-opn5-primary-antibodies-wb-testing-4.jpgAnti-Neuropsin OPN5 AntibodyWestern blot analysis of the lysates from HUVECcells using OPN5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08880-opn5-primary-antibodies-ihc-testing-5.jpgAnti-Neuropsin OPN5 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peroxin-11-beta-antibody-a08864-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08864-pex11b-primary-antibodies-wb-testing-2.jpgAnti-Peroxin 11 beta PEX11B AntibodyWestern Blot analysis of various cells using Peroxin 11β Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08864-pex11b-primary-antibodies-wb-testing-3.jpgAnti-Peroxin 11 beta PEX11B AntibodyWestern blot analysis of lysates from COLO, HUVEC, COS7, and Jurkat cells, using PEX11B Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08864-pex11b-primary-antibodies-ihc-testing-1.jpgAnti-Peroxin 11 beta PEX11B AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tab182-antibody-a08836-1-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08836-1-tnks1bp1-primary-antibodies-wb-testing-2.jpgAnti-TAB182 TNKS1BP1 AntibodyWestern Blot analysis of various cells using TAB182 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08836-1-tnks1bp1-primary-antibodies-wb-testing-1.jpgAnti-TAB182 TNKS1BP1 AntibodyWestern blot analysis of lysates from 293 cells, using TNKS1BP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-epha6-antibody-a08818-boster.html2026-03-24T05:08:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08818-epha6-primary-antibodyes-wb-testing-1.jpgAnti-EphA6/Eph Receptor A6 Monoclonal AntibodyWestern Blot (WB) analysis using EphA6 Monoclonal antibody against truncated MBP-EphA6 recombinant protein (1) and truncated GST-EphA6(aa695-795) recombinant protein (2).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tetranectin-antibody-a08805-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08805-clec3b-primary-antibodies-ihc-testing-1.jpgAnti-Tetranectin CLEC3B AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acsm3-antibody-a08748-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08748-acsm3-primary-antibodies-wb-testing-1.jpgAnti-ACSM3 Monoclonal AntibodyWestern Blot analysis using ACSM3 Monoclonal Antibody against K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-drak2-antibody-a08711-2-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08711-2-stk17b-primary-antibodies-wb-testing-2.jpgAnti-DRAK2 STK17B AntibodyWestern Blot analysis of various cells using DRAK2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08711-2-stk17b-primary-antibodies-wb-testing-3.jpgAnti-DRAK2 STK17B AntibodyWestern Blot analysis of brain cells using DRAK2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08711-2-stk17b-primary-antibodies-wb-testing-4.jpgAnti-DRAK2 STK17B AntibodyWestern blot analysis of STK17B Antibody. The lane on the right is blocked with the STK17B peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08711-2-stk17b-primary-antibodies-ihc-testing-1.jpgAnti-DRAK2 STK17B AntibodyImmunohistochemistryt analysis of paraffin-embedded human tonsil, using STK17B Antibody. The lane on the right is blocked with the STK17B peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fundc1-antibody-a08688-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-fundc1-primary-antibodies-wb-testing-2.jpgAnti-FUNDC1 AntibodyWestern Blot analysis of AD293 cells using FUNDC1 Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-fundc1-primary-antibodies-wb-testing-3.jpgAnti-FUNDC1 AntibodyWestern Blot analysis of AD293 cells using FUNDC1 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-fundc1-primary-antibodies-if-testing-1.jpgAnti-FUNDC1 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pja2-antibody-a08677-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08677-pja2-primary-antibodyes-wb-testing-1.jpgAnti-PJA2/Praja2 AntibodyWestern Blot (WB) analysis of Jurkat cells using PJA2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08677-pja2-primary-antibodyes-wb-testing-2.jpgAnti-PJA2/Praja2 AntibodyWestern Blot (WB) analysis of specific cells using PJA2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nac-1-antibody-a08675-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08675-nacc1-primary-antibodies-wb-testing-2.jpgAnti-NAC-1 NACC1 Monoclonal AntibodyWestern Blot analysis using NAC-1 Monoclonal Antibody against HEK293 (1) and NACC1-hIgGFc transfected HEK293 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08675-nacc1-primary-antibodies-ihc-testing-1.jpgAnti-NAC-1 NACC1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded mammary cancer tissues (left) and ovarian cancer tissues (right) with DAB staining using NAC-1 Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-stathmin-3-antibody-a08661-1-boster.html2026-03-24T05:08:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08661-1-stmn3-primary-antibodies-wb-testing-2.jpgAnti-Stathmin-3 STMN3 AntibodyWestern Blot analysis of various cells using Stathmin-3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08661-1-stmn3-primary-antibodies-wb-testing-3.jpgAnti-Stathmin-3 STMN3 AntibodyWestern blot analysis of the lysates from K562 cells using STMN3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08661-1-stmn3-primary-antibodies-ihc-testing-1.jpgAnti-Stathmin-3 STMN3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-braf35-antibody-a08646-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08646-hmg20b-primary-antibodyes-wb-testing-1.jpgAnti-BRAF35 HMG20B AntibodyWestern Blot (WB) analysis of AD293 cells using BRAF35 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08646-hmg20b-primary-antibodyes-wb-testing-2.jpgAnti-BRAF35 HMG20B AntibodyWestern Blot (WB) analysis of specific cells using BRAF35 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-1f8-antibody-a08643-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08643-il36b-primary-antibodyes-ihc-testing-1.jpgAnti-IL-1F8 IL36B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08643-il36b-primary-antibodyes-wb-testing-2.jpgAnti-IL-1F8 IL36B AntibodyWestern Blot (WB) analysis of HepG2 cells using IL-1F8 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08643-il36b-primary-antibodyes-ihc-testing-3.jpgAnti-IL-1F8 IL36B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-liprin-beta1-antibody-a08629-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08629-ppfibp1-primary-antibodies-wb-testing-2.jpgAnti-Liprin beta1 PPFIBP1 AntibodyWestern Blot analysis of various cells using Liprin β1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08629-ppfibp1-primary-antibodies-ihc-testing-1.jpgAnti-Liprin beta1 PPFIBP1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ndufb9-antibody-a08623-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08623-ndufb9-primary-antibodies-wb-testing-2.jpgAnti-NDUFB9 AntibodyWestern blot analysis of lysates from COLO205 cells and 293 cells, using NDUFB9 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08623-ndufb9-primary-antibodies-wb-testing-3.jpgAnti-NDUFB9 AntibodyWestern blot analysis of the lysates from COLO205 cells using NDUFB9 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08623-ndufb9-primary-antibodies-ihc-testing-1.jpgAnti-NDUFB9 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sr-1e-antibody-a08598-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08598-htr1e-primary-antibodies-wb-testing-2.jpgAnti-SR-1E HTR1E AntibodyWestern Blot analysis of various cells using SR-1E Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08598-htr1e-primary-antibodies-wb-testing-3.jpgAnti-SR-1E HTR1E AntibodyWestern blot analysis of lysates from HeLa cells, using 5-HT-1E Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08598-htr1e-primary-antibodies-ihc-testing-1.jpgAnti-SR-1E HTR1E AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tyrrs-antibody-a08583-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08583-yars-primary-antibodies-wb-testing-2.jpgAnti-TyrRS YARS AntibodyWestern Blot analysis of Hela cells using TyrRS Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08583-yars-primary-antibodies-ihc-testing-3.jpgAnti-TyrRS YARS AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08583-yars-primary-antibodies-ihc-testing-1.jpgAnti-TyrRS YARS AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-brs-3-antibody-a08571-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08571-brs3-primary-antibodies-wb-testing-2.jpgAnti-BRS-3 AntibodyWestern blot analysis of lysates from HUVEC cells, using BRS3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08571-brs3-primary-antibodies-wb-testing-3.jpgAnti-BRS-3 AntibodyWestern blot analysis of the lysates from HT-29 cells using BRS3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08571-brs3-primary-antibodies-if-testing-1.jpgAnti-BRS-3 AntibodyImmunofluorescence analysis of A549 cells, using BRS3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klhl12-antibody-a08568-boster.html2026-03-24T05:08:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08568-klhl12-primary-antibodyes-wb-testing-1.jpgAnti-KLHL12/C3Ip1 Monoclonal AntibodyWestern Blot (WB) analysis using KLHL12 Monoclonal antibody against HeLa (1) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gz-alpha-antibody-a08513-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08513-gnaz-primary-antibodyes-wb-testing-1.jpgAnti-Gz- alpha GNAZ AntibodyWestern Blot (WB) analysis of specific cells using Gz-alpha Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kv8-2-antibody-a08497-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08497-kcnv2-primary-antibodies-ihc-testing-1.jpgAnti-KV8.2 KCNV2 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08497-kcnv2-primary-antibodies-wb-testing-2.jpgAnti-KV8.2 KCNV2 AntibodyWestern Blot analysis of MCF-7 cells using KV8.2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08497-kcnv2-primary-antibodies-wb-testing-3.jpgAnti-KV8.2 KCNV2 AntibodyWestern blot analysis of lysates from MCF-7 cells, using KCNV2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-abca8-antibody-a08490-1-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08490-1-abca8-primary-antibodies-wb-testing-1.jpgAnti-ABCA8 AntibodyWestern blot analysis of lysates from HUVEC cells, using ABCA8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08490-1-abca8-primary-antibodies-wb-testing-2.jpgAnti-ABCA8 AntibodyWestern Blot analysis of various cells using ABCA8 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08490-1-abca8-primary-antibodies-wb-testing-3.jpgAnti-ABCA8 AntibodyWestern Blot analysis of HuvEc cells using ABCA8 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-achr-alpha10-antibody-a08482-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08482-chrna10-primary-antibodies-wb-testing-2.jpgAnti-AChR alpha10 CHRNA10 AntibodyWestern Blot analysis of various cells using AChRα10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08482-chrna10-primary-antibodies-wb-testing-3.jpgAnti-AChR alpha10 CHRNA10 AntibodyWestern Blot analysis of A549 cells using AChRα10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08482-chrna10-primary-antibodies-wb-testing-1.jpgAnti-AChR alpha10 CHRNA10 AntibodyWestern blot analysis of lysates from HeLa, 293, COLO, and A549 cells, using CHRNA10 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nhe-8-antibody-a08467-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08467-slc9a8-primary-antibodyes-wb-testing-1.jpgAnti-NHE-8 SLC9A8 AntibodyWestern Blot (WB) analysis of Jurkat cells using NHE-8 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mipp-antibody-a08462-1-boster.html2026-03-24T05:08:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-1-minpp1-primary-antibodies-ihc-testing-1.jpgAnti-MIPP MINPP1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-1-minpp1-primary-antibodies-wb-testing-2.jpgAnti-MIPP MINPP1 AntibodyWestern Blot analysis of various cells using MIPP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-1-minpp1-primary-antibodies-wb-testing-3.jpgAnti-MIPP MINPP1 AntibodyWestern blot analysis of the lysates from HepG2 cells using MINPP1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-7l1-antibody-a08450-1-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08450-1-rab29-primary-antibodies-wb-testing-2.jpgAnti-Rab 7L1 RAB29 AntibodyWestern Blot analysis of various cells using Rab 7L1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08450-1-rab29-primary-antibodies-wb-testing-3.jpgAnti-Rab 7L1 RAB29 AntibodyWestern blot analysis of lysates from HT-29 cells, using RAB7L1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08450-1-rab29-primary-antibodies-wb-testing-4.jpgAnti-Rab 7L1 RAB29 AntibodyWestern blot analysis of the lysates from HepG2 cells using RAB7L1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08450-1-rab29-primary-antibodies-ihc-testing-1.jpgAnti-Rab 7L1 RAB29 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lmtk3-antibody-a08432-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08432-lmtk3-primary-antibodies-wb-testing-1.jpgAnti-LMTK3 AntibodyWestern blot analysis of the lysates from HeLa cells using LMTK3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clptm1-antibody-a08423-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08423-clptm1-primary-antibodies-wb-testing-2.jpgAnti-CLPTM1 AntibodyWestern Blot analysis of COS-7 cells using CLPTM1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08423-clptm1-primary-antibodies-wb-testing-1.jpgAnti-CLPTM1 AntibodyWestern blot analysis of lysates from COS7 cells, using CLPT1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arhgap18-antibody-a08418-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08418-arhgap18-primary-antibodies-wb-testing-2.jpgAnti-ARHGAP18 AntibodyWestern Blot analysis of various cells using ARHGAP18 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08418-arhgap18-primary-antibodies-wb-testing-3.jpgAnti-ARHGAP18 AntibodyWestern Blot analysis of Jurkat cells using ARHGAP18 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08418-arhgap18-primary-antibodies-wb-testing-4.jpgAnti-ARHGAP18 AntibodyWestern blot analysis of RHG18 Antibody. The lane on the right is blocked with the RHG18 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08418-arhgap18-primary-antibodies-wb-testing-5.jpgAnti-ARHGAP18 AntibodyWestern blot analysis of the lysates from HepG2 cells using RHG18 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08418-arhgap18-primary-antibodies-ihc-testing-1.jpgAnti-ARHGAP18 AntibodyImmunohistochemistryt analysis of paraffin-embedded human brain, using RHG18 Antibody. The lane on the right is blocked with the RHG18 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-usp44-antibody-a08401-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08401-usp44-primary-antibodies-wb-testing-2.jpgAnti-USP44 AntibodyWestern blot analysis of mouse-kidney lysis using USP44 antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08401-usp44-primary-antibodies-wb-testing-1.jpgAnti-USP44 AntibodyWestern blot analysis of lysates from LOVO and NIH/3T3 cells, using USP44 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr172a-antibody-a08399-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08399-slc52a2-primary-antibodyes-wb-testing-1.jpgAnti-GPR172A SLC52A2 AntibodyWestern Blot (WB) analysis of A549 cells using GPR172A Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pfk-2-liv-antibody-a08398-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08398-pfkfb1-primary-antibodies-wb-testing-2.jpgAnti-PFK-2 liv PFKFB1 AntibodyWestern Blot analysis of Jurkat cells using PFK-2 liv Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08398-pfkfb1-primary-antibodies-wb-testing-3.jpgAnti-PFK-2 liv PFKFB1 AntibodyWestern blot analysis of lysates from HUVEC cells and Jurkat cells, using PFKFB1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08398-pfkfb1-primary-antibodies-ihc-testing-1.jpgAnti-PFK-2 liv PFKFB1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ccrl1-antibody-a08326-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08326-ackr4-primary-antibodyes-wb-testing-1.jpgAnti-CCRL1 ACKR4 AntibodyWestern Blot (WB) analysis of specific cells using CCRL1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mia2-antibody-a08319-boster.html2026-03-24T05:08:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08319-mia2-primary-antibodies-ihc-testing-1.jpgAnti-MIA2 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08319-mia2-primary-antibodies-wb-testing-2.jpgAnti-MIA2 AntibodyWestern Blot analysis of HEPG2 cells using MIA2 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08319-mia2-primary-antibodies-if-testing-3.jpgAnti-MIA2 AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ip3ka-antibody-a08296-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08296-itpka-primary-antibodyes-wb-testing-1.jpgAnti-IP3KA ITPKA AntibodyWestern Blot (WB) analysis of specific cells using IP3KA Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pacap-antibody-a08281-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-mzb1-primary-antibodies-ihc-testing-1.jpgAnti-PACAP MZB1 AntibodyImmunohistochemical analysis of paraffin-embedded human-testis, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aven-antibody-a08274-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08274-aven-primary-antibodies-wb-testing-2.jpgAnti-Cell death regulator Aven Aven AntibodyWestern Blot analysis of various cells using Aven Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08274-aven-primary-antibodies-wb-testing-3.jpgAnti-Cell death regulator Aven Aven AntibodyWestern blot analysis of lysates from COS7 and LOVO cells, using AVEN Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08274-aven-primary-antibodies-ihc-testing-1.jpgAnti-Cell death regulator Aven Aven AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-drs-1-antibody-a08254-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08254-eci2-primary-antibodies-ihc-testing-1.jpgAnti-DRS-1 ECI2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PECI Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08254-eci2-primary-antibodies-wb-testing-2.jpgAnti-DRS-1 ECI2 AntibodyWestern Blot analysis of various cells using DRS-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08254-eci2-primary-antibodies-wb-testing-3.jpgAnti-DRS-1 ECI2 AntibodyWestern Blot analysis of 293 cells using DRS-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08254-eci2-primary-antibodies-wb-testing-4.jpgAnti-DRS-1 ECI2 AntibodyWestern blot analysis of lysates from 293 cells, using PECI Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08254-eci2-primary-antibodies-wb-testing-5.jpgAnti-DRS-1 ECI2 AntibodyWestern blot analysis of the lysates from COLO205 cells using PECI antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sapap1-antibody-a08230-1-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08230-1-dlgap1-primary-antibodies-if-testing-1.jpgAnti-SAPAP1 DLGAP1 AntibodyImmunofluorescence analysis of HeLa cells, using DLGP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08230-1-dlgap1-primary-antibodies-wb-testing-2.jpgAnti-SAPAP1 DLGAP1 AntibodyWestern Blot analysis of various cells using SAPAP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08230-1-dlgap1-primary-antibodies-wb-testing-3.jpgAnti-SAPAP1 DLGAP1 AntibodyWestern blot analysis of lysates from HepG2 cells, using DLGP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08230-1-dlgap1-primary-antibodies-ihc-testing-4.jpgAnti-SAPAP1 DLGAP1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cep170-antibody-a08211-boster.html2026-03-24T05:08:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08211-cep170-primary-antibodies-wb-testing-2.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern Blot analysis of various cells using CEP170 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08211-cep170-primary-antibodies-wb-testing-3.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern Blot analysis of AD293 cells using CEP170 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08211-cep170-primary-antibodies-wb-testing-4.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern blot analysis of lysates from HepG2 and Jurkat cells, using CEP170 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08211-cep170-primary-antibodies-ihc-testing-1.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CEP170 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-alpha-protein-kinase-1-antibody-a08171-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08171-alpk1-primary-antibodies-wb-testing-2.jpgAnti-alpha-protein Kinase 1 ALPK1 AntibodyWestern Blot analysis of various cells using α-protein Kinase 1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08171-alpk1-primary-antibodies-wb-testing-3.jpgAnti-alpha-protein Kinase 1 ALPK1 AntibodyWestern blot analysis of lysates from COLO and HepG2 cells, using ALPK1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08171-alpk1-primary-antibodies-ihc-testing-1.jpgAnti-alpha-protein Kinase 1 ALPK1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tcp-1-eta-antibody-a08169-1-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08169-1-cct7-primary-antibodyes-wb-testing-1.jpgAnti-TCP-1 eta CCT7 AntibodyWestern Blot (WB) analysis of HeLa cells using TCP-1 eta Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clecsf6-antibody-a08158-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08158-clec4a-primary-antibodies-wb-testing-2.jpgAnti-CLECSF6 CLEC4A AntibodyWestern Blot analysis of HEPG2 cells using CLECSF6 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08158-clec4a-primary-antibodies-ihc-testing-3.jpgAnti-CLECSF6 CLEC4A AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08158-clec4a-primary-antibodies-ihc-testing-1.jpgAnti-CLECSF6 CLEC4A AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ataxin-2l-antibody-a08149-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08149-atxn2l-primary-antibodies-wb-testing-2.jpgAnti-Ataxin-2L ATXN2L AntibodyWestern Blot analysis of 293T cells using Ataxin-2L Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08149-atxn2l-primary-antibodies-wb-testing-3.jpgAnti-Ataxin-2L ATXN2L AntibodyWestern blot analysis of lysates from NIH/3T3 and RAW264.7 cells, using ATXN2L Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08149-atxn2l-primary-antibodies-wb-testing-1.jpgAnti-Ataxin-2L ATXN2L AntibodyWestern blot analysis of the lysates from 293 cells using ATXN2L antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eif2b-gamma-antibody-a08134-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08134-eif2b3-primary-antibodies-wb-testing-2.jpgAnti-eIF2B gamma EIF2B3 AntibodyWestern Blot analysis of various cells using eIF2Bγ Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08134-eif2b3-primary-antibodies-wb-testing-1.jpgAnti-eIF2B gamma EIF2B3 AntibodyWestern Blot analysis of K562 cells using eIF2Bγ Polyclonal Antibody diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p140cap-antibody-a08110-boster.html2026-03-24T05:08:48+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-claudin-19-antibody-a08096-1-boster.html2026-03-24T05:08:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08096-1-cldn19-primary-antibodies-wb-testing-2.jpgAnti-Claudin-19 CLDN19 AntibodyWestern Blot analysis of various cells using Claudin-19 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08096-1-cldn19-primary-antibodies-wb-testing-1.jpgAnti-Claudin-19 CLDN19 AntibodyWestern blot analysis of lysates from Jurkat and HepG2 cells, using CLDN19 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-mmp-17-q129-antibody-a08090-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08090-mmp17-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-MMP-17 (Q129) AntibodyWestern Blot analysis of various cells using Cleaved-MMP-17 (Q129) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08090-mmp17-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-MMP-17 (Q129) AntibodyWestern blot analysis of lysates from A549 cells, treated with etoposide 25uM 1h, using MMP17 (Cleaved-Gln129) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nectin-2-antibody-a08081-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08081-nectin2-primary-antibodies-wb-testing-2.jpgAnti-Nectin 2 AntibodyWestern Blot analysis of mouse brain cells using Nectin 2 Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08081-nectin2-primary-antibodies-wb-testing-1.jpgAnti-Nectin 2 AntibodyWestern Blot analysis of MOUSE-BRAIN cells using Nectin 2 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col25a1-antibody-a08068-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08068-col25a1-primary-antibodies-wb-testing-1.jpgAnti-COL25A1/Clacp AntibodyWestern Blot analysis of HEPG2 cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chrdl1-antibody-a08014-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08014-chrdl1-primary-antibodies-wb-testing-1.jpgAnti-CHRDL1/Chordin Like 1 Monoclonal AntibodyWestern Blot analysis using CHRDL1 Monoclonal Antibody against rat kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hormad1-antibody-a08011-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08011-hormad1-primary-antibodies-wb-testing-2.jpgAnti-HORMAD1 AntibodyWestern Blot analysis of various cells using HORMAD1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08011-hormad1-primary-antibodies-wb-testing-1.jpgAnti-HORMAD1 AntibodyWestern blot analysis of lysates from HeLa, HUVEC, and COLO cells, using HORMAD1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dgk-beta-antibody-a07973-1-boster.html2026-03-24T05:08:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07973-1-dgkb-primary-antibodies-wb-testing-2.jpgAnti-DGK- beta AntibodyWestern Blot analysis of HuvEC cells using DGK-β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07973-1-dgkb-primary-antibodies-wb-testing-1.jpgAnti-DGK- beta AntibodyWestern blot analysis of the lysates from HUVECcells using DGKB antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acss1-antibody-a07972-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07972-acss1-primary-antibodyes-wb-testing-1.jpgAnti-ACSS1 AntibodyWestern Blot (WB) analysis of HT29 cells using ACSS1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07972-acss1-primary-antibodyes-wb-testing-2.jpgAnti-ACSS1 AntibodyWestern Blot (WB) analysis of specific cells using ACSS1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gli-1-antibody-a07972-1-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07972-1-acss1-primary-antibodies-wb-testing-1.jpgAnti-GLI-1 ACSS1 AntibodyWestern Blot analysis of 1, mouse-liver 2, hela cells using primary antibody diluted at 1:1000 (4°C overnight). Secondary antibody:Goat Anti-rabbit IgG IRDye 800 ( diluted at 1:5000, 25°C, 1 hour)
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lpaat-theta-antibody-a07965-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07965-gpat3-primary-antibodies-if-testing-1.jpgAnti-LPAAT- theta GPAT3 AntibodyImmunofluorescence analysis of HepG2 cells, using PLCH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07965-gpat3-primary-antibodies-wb-testing-2.jpgAnti-LPAAT- theta GPAT3 AntibodyWestern blot analysis of lysates from Jurkat cells, COLO205 cells, HeLa cells, and HUVEC cells, using PLCH Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07965-gpat3-primary-antibodies-if-testing-3.jpgAnti-LPAAT- theta GPAT3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mkp-4-antibody-a07919-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07919-dusp9-primary-antibodies-wb-testing-2.jpgAnti-MKP-4 DUSP9 AntibodyWestern Blot analysis of COLO cells using MKP-4 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07919-dusp9-primary-antibodies-wb-testing-3.jpgAnti-MKP-4 DUSP9 AntibodyWestern blot analysis of lysates from HeLa cells, using DUSP9 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07919-dusp9-primary-antibodies-ihc-testing-4.jpgAnti-MKP-4 DUSP9 AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using DUSP9 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07919-dusp9-primary-antibodies-if-testing-1.jpgAnti-MKP-4 DUSP9 AntibodyImmunofluorescence analysis of HeLa cells, using DUSP9 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd300f-antibody-a07913-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07913-cd300lf-primary-antibodies-wb-testing-2.jpgAnti-CD300f CD300LF AntibodyWestern Blot analysis of HeLa, PC12 cells using CD300f Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07913-cd300lf-primary-antibodies-ihc-testing-1.jpgAnti-CD300f CD300LF AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cng-2-antibody-a07901-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-cnga2-primary-antibodies-wb-testing-2.jpgAnti-CNG-2 CNGA2 AntibodyWestern Blot analysis of various cells using CNG-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-cnga2-primary-antibodies-wb-testing-3.jpgAnti-CNG-2 CNGA2 AntibodyWestern Blot analysis of K562 cells using CNG-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-cnga2-primary-antibodies-if-testing-1.jpgAnti-CNG-2 CNGA2 AntibodyImmunofluorescence analysis of A549 cells, using CNGA2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gbp3-antibody-a07900-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07900-gbp3-primary-antibodies-ihc-testing-1.jpgAnti-Guanylate-binding protein 3 GBP3 AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1,primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07900-gbp3-primary-antibodies-wb-testing-2.jpgAnti-Guanylate-binding protein 3 GBP3 AntibodyWestern blot analysis of lysates from HT-29 and COLO cells, using GBP3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-spt3-antibody-a07858-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07858-supt3h-primary-antibodyes-wb-testing-1.jpgAnti-SPT3 SUPT3H AntibodyWestern Blot (WB) analysis of specific cells using SPT3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-s8-antibody-a07839-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07839-rps8-primary-antibodies-wb-testing-2.jpgAnti-Ribosomal Protein S8 RPS8 AntibodyWestern Blot analysis of various cells using Ribosomal Protein S8 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07839-rps8-primary-antibodies-wb-testing-3.jpgAnti-Ribosomal Protein S8 RPS8 AntibodyWestern blot analysis of lysates from A549, 293, and COLO cells, using RPS8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07839-rps8-primary-antibodies-wb-testing-4.jpgAnti-Ribosomal Protein S8 RPS8 AntibodyWestern blot analysis of the lysates from Jurkat cells using RPS8 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07839-rps8-primary-antibodies-ihc-testing-1.jpgAnti-Ribosomal Protein S8 RPS8 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr50-antibody-a07827-boster.html2026-03-24T05:08:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07827-gpr50-primary-antibodies-if-testing-1.jpgAnti-Melatonin-related receptor GPR50 AntibodyImmunofluorescence analysis of LOVO cells, using MTR1L Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07827-gpr50-primary-antibodies-wb-testing-2.jpgAnti-Melatonin-related receptor GPR50 AntibodyWestern Blot analysis of various cells using GPR50 Polyclonal Antibody diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-stip1-antibody-a07823-boster.html2026-03-24T05:08:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07823-elp2-primary-antibodyes-wb-testing-1.jpgAnti-StIp1 ELP2 AntibodyWestern Blot (WB) analysis of specific cells using StIp1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acsl6-antibody-a07813-1-boster.html2026-03-24T05:08:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07813-1-acsl6-primary-antibodyes-wb-testing-1.jpgAnti-ACSL6 AntibodyWestern Blot (WB) analysis of specific cells using ACSL6 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gm2-gd2-synthase-antibody-a07778-1-boster.html2026-03-24T05:08:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07778-1-b4galnt1-primary-antibodies-wb-testing-2.jpgAnti-GM2/GD2 synthase B4GALNT1 AntibodyWestern Blot analysis of various cells using GM2/GD2 synthase Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07778-1-b4galnt1-primary-antibodies-wb-testing-1.jpgAnti-GM2/GD2 synthase B4GALNT1 AntibodyWestern blot analysis of the lysates from COLO205 cells using B4GALNT1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-erf3a-antibody-a07761-boster.html2026-03-24T05:08:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07761-gspt1-primary-antibodies-wb-testing-2.jpgAnti-eRF3a GSPT1 AntibodyWestern Blot analysis of 3T3 cells using eRF3a Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07761-gspt1-primary-antibodies-ihc-testing-1.jpgAnti-eRF3a GSPT1 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using GSPT1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pmch-antibody-a07730-boster.html2026-03-24T05:08:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07730-pmch-primary-antibodies-ihc-testing-1.jpgAnti-Pro-MCH PMCH AntibodyImmunohistochemical analysis of paraffin-embedded human-testis, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd231-antibody-a07727-boster.html2026-03-24T05:08:51+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-zip7-antibody-a07719-1-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07719-1-slc39a7-primary-antibodies-wb-testing-2.jpgAnti-ZIP7 SLC39A7 AntibodyWestern Blot analysis of various cells using ZIP7 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07719-1-slc39a7-primary-antibodies-wb-testing-3.jpgAnti-ZIP7 SLC39A7 AntibodyWestern blot analysis of lysates from 293 and COLO cells, using SLC39A7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07719-1-slc39a7-primary-antibodies-wb-testing-1.jpgAnti-ZIP7 SLC39A7 AntibodyWestern blot analysis of the lysates from HUVECcells using SLC39A7 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hnrnp-h-antibody-a07691-1-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07691-1-hnrnph1-primary-antibodyes-wb-testing-1.jpgAnti-hnRNP H HNRNPH1 AntibodyWestern Blot (WB) analysis of specific cells using hnRNP H Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-card-10-antibody-a07686-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-card10-primary-antibodyes-wb-testing-1.jpgAnti-CARD 10 AntibodyWestern Blot (WB) analysis of specific cells using CARD 10 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-6-antibody-a07685-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07685-fgf6-primary-antibodies-wb-testing-2.jpgAnti-FGF-6 AntibodyWestern Blot analysis of 293, HepG2, PC-3, M21 cells using FGF-6 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07685-fgf6-primary-antibodies-wb-testing-1.jpgAnti-FGF-6 AntibodyWestern blot analysis of lysate from 293 cells, using FGF6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rfx3-antibody-a07674-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07674-rfx3-primary-antibodies-wb-testing-2.jpgAnti-Transcription factor RFX3 RFX3 AntibodyWestern Blot analysis of various cells using RFX3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07674-rfx3-primary-antibodies-wb-testing-3.jpgAnti-Transcription factor RFX3 RFX3 AntibodyWestern blot analysis of lysates from COLO and RAW264.7 cells, using RFX3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07674-rfx3-primary-antibodies-ihc-testing-1.jpgAnti-Transcription factor RFX3 RFX3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RFX3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ef-1-beta-antibody-a07669-boster.html2026-03-24T05:08:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07669-eef1b2-primary-antibodies-wb-testing-2.jpgAnti-EF-1 beta EEF1B2 AntibodyWestern Blot analysis of extracts from K562 cells, using EF-1β Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07669-eef1b2-primary-antibodies-wb-testing-1.jpgAnti-EF-1 beta EEF1B2 AntibodyWestern blot analysis of lysates from K562 cells , using EF-1β antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-adi1-antibody-a07662-boster.html2026-03-24T05:08:52+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-vangl1-antibody-a07587-1-boster.html2026-03-24T05:08:53+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chsy1-antibody-a07580-1-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07580-1-chsy1-primary-antibodies-wb-testing-2.jpgAnti-Chondroitin sulfate synthase 1 CHSY1 AntibodyWestern Blot analysis of various cells using CHSY1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07580-1-chsy1-primary-antibodies-wb-testing-3.jpgAnti-Chondroitin sulfate synthase 1 CHSY1 AntibodyWestern blot analysis of CHSY1 Antibody. The lane on the right is blocked with the CHSY1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07580-1-chsy1-primary-antibodies-wb-testing-4.jpgAnti-Chondroitin sulfate synthase 1 CHSY1 AntibodyWestern blot analysis of the lysates from HepG2 cells using CHSY1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07580-1-chsy1-primary-antibodies-ihc-testing-1.jpgAnti-Chondroitin sulfate synthase 1 CHSY1 AntibodyImmunohistochemistryt analysis of paraffin-embedded human brain, using CHSY1 Antibody. The lane on the right is blocked with the CHSY1 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p2y11-antibody-a07573-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07573-p2ry11-primary-antibodies-wb-testing-2.jpgAnti-P2Y11 P2RY11 AntibodyWestern Blot analysis of various cells using P2Y11 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07573-p2ry11-primary-antibodies-wb-testing-3.jpgAnti-P2Y11 P2RY11 AntibodyWestern blot analysis of lysates from HepG2, Jurkat, and COLO cells, using P2RY11 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07573-p2ry11-primary-antibodies-wb-testing-1.jpgAnti-P2Y11 P2RY11 AntibodyWestern blot analysis of the lysates from K562 cells using P2RY11 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-26-antibody-a07565-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07565-il26-primary-antibodies-wb-testing-1.jpgAnti-IL-26 AntibodyWestern blot analysis of RAT-MUSLE RAT-SPLEEN 293T SH-SY5Y using IL26 antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-slu7-antibody-a07557-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07557-slu7-primary-antibodies-wb-testing-2.jpgAnti-Pre-mRNA-splicing factor SLU7 SLU7 AntibodyWestern blot analysis of lysates from HeLa cells, using SLU7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07557-slu7-primary-antibodies-wb-testing-3.jpgAnti-Pre-mRNA-splicing factor SLU7 SLU7 AntibodyWestern blot analysis of the lysates from HepG2 cells using SLU7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07557-slu7-primary-antibodies-ihc-testing-1.jpgAnti-Pre-mRNA-splicing factor SLU7 SLU7 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hoxd3-antibody-a07544-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07544-hoxd3-primary-antibodies-ihc-testing-1.jpgAnti-Homeobox protein Hox-D3 HoxD3 AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07544-hoxd3-primary-antibodies-wb-testing-2.jpgAnti-Homeobox protein Hox-D3 HoxD3 AntibodyWestern blot analysis of lysate from HepG2 cells, using HOXD3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07544-hoxd3-primary-antibodies-if-testing-3.jpgAnti-Homeobox protein Hox-D3 HoxD3 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07544-hoxd3-primary-antibodies-ihc-testing-4.jpgAnti-Homeobox protein Hox-D3 HoxD3 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cadherin-16-antibody-a07518-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07518-cdh16-primary-antibodies-wb-testing-2.jpgAnti-Cadherin-16 CDH16 AntibodyWestern Blot analysis of various cells using Cadherin-16 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07518-cdh16-primary-antibodies-wb-testing-3.jpgAnti-Cadherin-16 CDH16 AntibodyWestern Blot analysis of A549 cells using Cadherin-16 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07518-cdh16-primary-antibodies-wb-testing-4.jpgAnti-Cadherin-16 CDH16 AntibodyWestern blot analysis of lysates from A549 cells, using CDH16 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07518-cdh16-primary-antibodies-wb-testing-5.jpgAnti-Cadherin-16 CDH16 AntibodyWestern blot analysis of the lysates from HepG2 cells using Cytochrome P450 24A1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07518-cdh16-primary-antibodies-ihc-testing-1.jpgAnti-Cadherin-16 CDH16 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-iga-antibody-a07514-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07514-igha1-primary-antibodyes-wb-testing-1.jpgAnti-IgA IGHA1 AntibodyWestern Blot (WB) analysis of specific cells using IgA Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tusc2-antibody-a07508-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07508-tusc2-primary-antibodies-ihc-testing-1.jpgAnti-Tumor suppressor candidate 2 TUSC2 AntibodyImmunohistochemical analysis of paraffin-embedded Human heart. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07508-tusc2-primary-antibodies-wb-testing-2.jpgAnti-Tumor suppressor candidate 2 TUSC2 AntibodyWestern Blot analysis of 293T cells using TUSC2 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07508-tusc2-primary-antibodies-wb-testing-3.jpgAnti-Tumor suppressor candidate 2 TUSC2 AntibodyWestern blot analysis of lysates from HeLa cells, using TUSC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clc-6-antibody-a07500-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07500-clcn6-primary-antibodies-wb-testing-2.jpgAnti-CLC-6 CLCN6 AntibodyWestern Blot analysis of various cells using CLC-6 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07500-clcn6-primary-antibodies-wb-testing-3.jpgAnti-CLC-6 CLCN6 AntibodyWestern Blot analysis of L929 cells using CLC-6 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07500-clcn6-primary-antibodies-wb-testing-1.jpgAnti-CLC-6 CLCN6 AntibodyWestern blot analysis of lysates from COS7 and HT-29 cells, using CLCN6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-9r-antibody-a07490-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07490-il9r-primary-antibodyes-wb-testing-1.jpgAnti-IL-9R AntibodyWestern Blot (WB) analysis of KB cells using IL-9R Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07490-il9r-primary-antibodyes-wb-testing-2.jpgAnti-IL-9R AntibodyWestern Blot (WB) analysis of KB, NIH-3T3 cells using IL-9R Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p52-s6-kinase-antibody-a07473-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07473-rps6kc1-primary-antibodies-wb-testing-2.jpgAnti-p52 S6 kinase RPS6KC1 AntibodyWestern blot analysis of HELA 293T lysis using p52 S6 kinase antibody. Antibody was diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07473-rps6kc1-primary-antibodies-wb-testing-3.jpgAnti-p52 S6 kinase RPS6KC1 AntibodyWestern blot analysis of lysates from K562 cells, using RPS6KC1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07473-rps6kc1-primary-antibodies-wb-testing-4.jpgAnti-p52 S6 kinase RPS6KC1 AntibodyWestern blot analysis of the lysates from HT-29 cells using RPS6KC1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07473-rps6kc1-primary-antibodies-if-testing-1.jpgAnti-p52 S6 kinase RPS6KC1 AntibodyImmunofluorescence analysis of LOVO cells, using RPS6KC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-igm-chain-c-antibody-a07469-boster.html2026-03-24T05:08:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07469-ighm-primary-antibodies-wb-testing-2.jpgAnti-IgM Chain C IGHM AntibodyWestern Blot analysis of HEPG2 cells using IgM Chain C Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07469-ighm-primary-antibodies-ihc-testing-1.jpgAnti-IgM Chain C IGHM AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jtb-antibody-a07448-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07448-jtb-primary-antibodies-wb-testing-2.jpgAnti-Protein JTB JTB AntibodyWestern blot analysis of JTB Antibody. The lane on the right is blocked with the JTB peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07448-jtb-primary-antibodies-wb-testing-3.jpgAnti-Protein JTB JTB AntibodyWestern blot analysis of the lysates from HUVECcells using JTB antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07448-jtb-primary-antibodies-ihc-testing-1.jpgAnti-Protein JTB JTB AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gdi-2-antibody-a07443-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07443-gdi2-primary-antibodies-ihc-testing-1.jpgAnti-GDI-2 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07443-gdi2-primary-antibodies-wb-testing-2.jpgAnti-GDI-2 AntibodyWestern Blot analysis of A549, HT29, K562, mouse kidney, mouse lung cells using GDI-2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07443-gdi2-primary-antibodies-if-testing-3.jpgAnti-GDI-2 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-topo-iii-alpha-antibody-a07428-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07428-top3a-primary-antibodies-wb-testing-1.jpgAnti-Topo III alpha TOP3A AntibodyWestern blot analysis of 293T using Topo IIIα antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dematin-antibody-a07422-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07422-dmtn-primary-antibodies-if-testing-1.jpgAnti-Dematin DMTN AntibodyImmunofluorescence analysis of HUVEC cells, using Dematin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07422-dmtn-primary-antibodies-wb-testing-2.jpgAnti-Dematin DMTN AntibodyWestern Blot analysis of various cells using Dematin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07422-dmtn-primary-antibodies-wb-testing-3.jpgAnti-Dematin DMTN AntibodyWestern blot analysis of lysates from 293 cells, using Dematin Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07422-dmtn-primary-antibodies-ihc-testing-4.jpgAnti-Dematin DMTN AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Dematin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cytokeratin-4-antibody-a07410-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07410-krt4-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 4 KRT4 AntibodyWestern blot analysis of SKOV3 293T lysate, antibody was diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr119-antibody-a07391-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07391-gpr119-primary-antibodyes-wb-testing-1.jpgAnti-GPR119 AntibodyWestern Blot (WB) analysis of SH-SY5Y Mouse Kidney lysis using GPR119 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07391-gpr119-primary-antibodyes-wb-testing-2.jpgAnti-GPR119 AntibodyWestern Blot (WB) analysis of COLO205 cells using GPR119 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-stk33-antibody-a07375-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07375-stk33-primary-antibodies-ihc-testing-1.jpgAnti-STK33 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07375-stk33-primary-antibodies-wb-testing-2.jpgAnti-STK33 AntibodyWestern Blot analysis of 293 cells using STK33 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ssx-antibody-a07363-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07363-ssx1-primary-antibodies-wb-testing-2.jpgAnti-SSX SSX1 AntibodyWestern Blot analysis of 22RV-1, SW480 cells using SSX Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07363-ssx1-primary-antibodies-wb-testing-3.jpgAnti-SSX SSX1 AntibodyWestern blot analysis of lysate from 22RV-1 cells, using SSX1/2/3/4/5/6/7/8/9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07363-ssx1-primary-antibodies-ihc-testing-1.jpgAnti-SSX SSX1 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rsk-4-antibody-a07352-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07352-rps6ka6-primary-antibodies-wb-testing-2.jpgAnti-Rsk-4 RPS6KA6 AntibodyWestern Blot analysis of various cells using Rsk-4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07352-rps6ka6-primary-antibodies-wb-testing-3.jpgAnti-Rsk-4 RPS6KA6 AntibodyWestern blot analysis of lysates from K562 and HT-29 cells, using S6K-alpha6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07352-rps6ka6-primary-antibodies-ihc-testing-1.jpgAnti-Rsk-4 RPS6KA6 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using S6K-alpha6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-adamts-18-antibody-a07341-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07341-adamts18-primary-antibodies-ihc-testing-1.jpgAnti-ADAMTS-18 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07341-adamts18-primary-antibodies-wb-testing-2.jpgAnti-ADAMTS-18 AntibodyWestern blot analysis of 3T3 using ADAMTS-18 antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pfk-c-antibody-a07337-boster.html2026-03-24T05:08:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-pfkp-primary-antibodies-ihc-testing-1.jpgAnti-PFK-C PFKP AntibodyImmunohistochemical analysis of paraffin-embedded Human testis. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-pfkp-primary-antibodies-wb-testing-2.jpgAnti-PFK-C PFKP AntibodyWestern Blot analysis of HuvEc cells using PFK-C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-pfkp-primary-antibodies-wb-testing-3.jpgAnti-PFK-C PFKP AntibodyWestern blot analysis of lysates from A549 and COS7 cells, using K6PP Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bnip-2-antibody-a07336-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07336-bnip2-primary-antibodies-wb-testing-2.jpgAnti-BNIP-2 AntibodyWestern Blot analysis of various cells using BNIP-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07336-bnip2-primary-antibodies-wb-testing-3.jpgAnti-BNIP-2 AntibodyWestern Blot analysis of K562 cells using BNIP-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07336-bnip2-primary-antibodies-wb-testing-4.jpgAnti-BNIP-2 AntibodyWestern blot analysis of lysate from Jurkat cells, using BNIP-2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07336-bnip2-primary-antibodies-ihc-testing-1.jpgAnti-BNIP-2 AntibodyImmunohistochemistry analysis of BNIP-2 antibody in paraffin-embedded human breast carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-12-antibody-a07326-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07326-fgf12-primary-antibodies-wb-testing-2.jpgAnti-FGF-12 AntibodyWestern Blot analysis of 22RV-1, BT474, SHSY5Y cells using FGF-12 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07326-fgf12-primary-antibodies-wb-testing-3.jpgAnti-FGF-12 AntibodyWestern blot analysis of lysate from 22RV-1 cells, using FGF12 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07326-fgf12-primary-antibodies-ihc-testing-4.jpgAnti-FGF-12 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07326-fgf12-primary-antibodies-ihc-testing-1.jpgAnti-FGF-12 AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rgs12-antibody-a07317-1-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07317-1-rgs12-primary-antibodyes-wb-testing-1.jpgAnti-RGS12 AntibodyWestern Blot (WB) analysis of 3T3 cells using RGS12 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-psg1-antibody-a07308-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07308-psg1-primary-antibodies-wb-testing-2.jpgAnti-PSG1 AntibodyWestern Blot analysis of K562 cells using PSG1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07308-psg1-primary-antibodies-ihc-testing-3.jpgAnti-PSG1 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07308-psg1-primary-antibodies-ihc-testing-1.jpgAnti-PSG1 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aass-antibody-a07302-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07302-aass-primary-antibodyes-wb-testing-1.jpgAnti-AASS AntibodyWestern Blot (WB) analysis of specific cells using AASS Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07302-aass-primary-antibodyes-wb-testing-2.jpgAnti-AASS AntibodyWestern Blot (WB) analysis of 293 cells using AASS Polyclonal antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mesp1-antibody-a07301-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07301-mesp1-primary-antibodies-wb-testing-1.jpgAnti-MESP1 Monoclonal AntibodyWestern Blot analysis using MESP1 Monoclonal Antibody against MESP1-hIgGFc transfected HEK293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-a1bg-antibody-a07289-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07289-a1bg-primary-antibodies-wb-testing-2.jpgAnti-Alpha-1B-glycoprotein A1BG AntibodyWestern Blot analysis of extracts from K562 cells, using A1BG Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07289-a1bg-primary-antibodies-ihc-testing-3.jpgAnti-Alpha-1B-glycoprotein A1BG AntibodyImmunohistochemical analysis of paraffin-embedded human-ovary, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07289-a1bg-primary-antibodies-ihc-testing-1.jpgAnti-Alpha-1B-glycoprotein A1BG AntibodyImmunohistochemical analysis of paraffin-embedded human-uterus, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clip-115-antibody-a07287-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07287-clip2-primary-antibodies-wb-testing-1.jpgAnti-CLIP-115 CLIP2 AntibodyWestern Blot analysis of A549 cells using CLIP-115 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07287-clip2-primary-antibodies-wb-testing-2.jpgAnti-CLIP-115 CLIP2 AntibodyWestern Blot analysis of various cells using CLIP-115 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-spindlin-1-antibody-a07281-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-spin1-primary-antibodies-wb-testing-2.jpgAnti-Spindlin-1 SPIN1 AntibodyWestern blot analysis of lysates from HeLa cells, using SPIN1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-spin1-primary-antibodies-wb-testing-3.jpgAnti-Spindlin-1 SPIN1 AntibodyWestern blot analysis of the lysates from K562 cells using SPIN1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-spin1-primary-antibodies-ihc-testing-4.jpgAnti-Spindlin-1 SPIN1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-spin1-primary-antibodies-if-testing-1.jpgAnti-Spindlin-1 SPIN1 AntibodyImmunofluorescence analysis of Hela cell. 1, Spindlin-1 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). Bcl-2 Monoclonal Antibody (6B5) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-3-gap-p150-antibody-a07244-1-boster.html2026-03-24T05:08:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07244-1-rab3gap2-primary-antibodies-wb-testing-2.jpgAnti-Rab 3 GAP p150 RAB3GAP2 AntibodyWestern Blot analysis of various cells using Rab 3 GAP p150 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07244-1-rab3gap2-primary-antibodies-wb-testing-3.jpgAnti-Rab 3 GAP p150 RAB3GAP2 AntibodyWestern blot analysis of lysates from COS cells, using RAB3GAP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07244-1-rab3gap2-primary-antibodies-ihc-testing-1.jpgAnti-Rab 3 GAP p150 RAB3GAP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RAB3GAP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-d54-antibody-a07219-1-boster.html2026-03-24T05:08:55+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cnt2-antibody-a07211-1-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07211-1-slc28a2-primary-antibodies-wb-testing-2.jpgAnti-CNT2 SLC28A2 AntibodyWestern Blot analysis of various cells using CNT2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07211-1-slc28a2-primary-antibodies-wb-testing-3.jpgAnti-CNT2 SLC28A2 AntibodyWestern Blot analysis of 3T3 cells using CNT2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07211-1-slc28a2-primary-antibodies-wb-testing-4.jpgAnti-CNT2 SLC28A2 AntibodyWestern blot analysis of lysates from Jurkat cells, using SLC28A2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07211-1-slc28a2-primary-antibodies-wb-testing-5.jpgAnti-CNT2 SLC28A2 AntibodyWestern blot analysis of the lysates from HepG2 cells using SLC28A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07211-1-slc28a2-primary-antibodies-ihc-testing-1.jpgAnti-CNT2 SLC28A2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using SLC28A2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gcn5-antibody-a07210-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07210-kat2a-primary-antibodies-ihc-testing-1.jpgAnti-GCN5 KAT2A AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07210-kat2a-primary-antibodies-wb-testing-2.jpgAnti-GCN5 KAT2A AntibodyWestern Blot analysis of Hela cells using GCN5 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07210-kat2a-primary-antibodies-wb-testing-3.jpgAnti-GCN5 KAT2A AntibodyWestern blot analysis of the lysates from RAW264.7cells using GCN5L2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-iti-h2-d702-antibody-a07196-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07196-itih2-primary-antibodyes-wb-testing-1.jpgAnti-Cleaved-ITI-H2 (D702) AntibodyWestern Blot (WB) analysis of specific cells using Cleaved-ITI-H2 (D702) Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nice4-antibody-a07183-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07183-ubap2l-primary-antibodies-wb-testing-1.jpgAnti-NICE4 UBAP2L AntibodyWestern blot analysis of the lysates from Jurkat cells using UBAP2L antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07183-ubap2l-primary-antibodies-wb-testing-2.jpgAnti-NICE4 UBAP2L AntibodyWestern Blot analysis of NIH-3T3 K562 NIH-3T3 293T cells using NICE4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07183-ubap2l-primary-antibodies-wb-testing-3.jpgAnti-NICE4 UBAP2L AntibodyWestern blot analysis of lysates from HT-29 and 293 cells, using UBAP2L Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-g2a-antibody-a07182-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07182-gpr132-primary-antibodies-wb-testing-2.jpgAnti-G2A GPR132 AntibodyWestern Blot analysis of 293T cells using G2A Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07182-gpr132-primary-antibodies-wb-testing-3.jpgAnti-G2A GPR132 AntibodyWestern blot analysis of lysates from COS7 cells, using GPR132 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07182-gpr132-primary-antibodies-if-testing-1.jpgAnti-G2A GPR132 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hoxb5-antibody-a07156-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07156-hoxb5-primary-antibodies-wb-testing-1.jpgAnti-Homeobox protein Hox-B5 HoxB5 AntibodyWestern blot analysis of lysate from HUVEC cells, using HoxB5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07156-hoxb5-primary-antibodies-wb-testing-2.jpgAnti-Homeobox protein Hox-B5 HoxB5 AntibodyWestern Blot analysis of various cells using HoxB5 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c8-beta-antibody-a07152-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07152-c8b-primary-antibodies-wb-testing-1.jpgAnti-C8 beta AntibodyWestern Blot analysis of 3T3 HEPG2 cells using C8 β Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ccl14-antibody-a07151-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07151-ccl14-primary-antibodyes-ihc-testing-1.jpgAnti-CCL14/Hcc 1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07151-ccl14-primary-antibodyes-ihc-testing-2.jpgAnti-CCL14/Hcc 1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-atp1al1-antibody-a07149-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07149-atp12a-primary-antibodies-wb-testing-1.jpgAnti-ATP1AL1 ATP12A AntibodyWestern Blot analysis of extracts from rat stomach, using ATP1AL1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nipa-antibody-a07135-boster.html2026-03-24T05:08:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07135-zc3hc1-primary-antibodyes-wb-testing-1.jpgAnti-NIPA ZC3HC1 AntibodyWestern Blot (WB) analysis of specific cells using NIPA Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bcas3-antibody-a07120-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07120-bcas3-primary-antibodies-wb-testing-1.jpgAnti-BCAS3 AntibodyWestern Blot analysis of 293 cells using BCAS3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nephrocystin-5-antibody-a07108-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07108-iqcb1-primary-antibodies-wb-testing-2.jpgAnti-Nephrocystin-5 IQCB1 AntibodyWestern Blot analysis of SH-SY5Y cells using Nephrocystin-5 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07108-iqcb1-primary-antibodies-wb-testing-3.jpgAnti-Nephrocystin-5 IQCB1 AntibodyWestern blot analysis of lysates from K562 cells, using IQCB1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07108-iqcb1-primary-antibodies-wb-testing-4.jpgAnti-Nephrocystin-5 IQCB1 AntibodyWestern blot analysis of the lysates from HepG2 cells using IQCB1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07108-iqcb1-primary-antibodies-ihc-testing-1.jpgAnti-Nephrocystin-5 IQCB1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-zis-antibody-a07103-1-boster.html2026-03-24T05:08:57+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-osteoglycin-antibody-a07061-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07061-ogn-primary-antibodyes-wb-testing-1.jpgAnti-Osteoglycin OGN AntibodyWestern blot analysis of L929 cells using Osteoglycin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07061-ogn-primary-antibodyes-wb-testing-2.jpgAnti-Osteoglycin OGN AntibodyWestern blot analysis of lysate from L929 cells, using OGN Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-l18-antibody-a07057-1-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-1-rpl18-primary-antibodyes-wb-testing-1.jpgAnti-Ribosomal Protein L18 RPL18 AntibodyWestern Blot (WB) analysis of specific cells using Ribosomal Protein L18 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peropsin-antibody-a07038-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07038-rrh-primary-antibodies-wb-testing-1.jpgAnti-Peropsin RRH AntibodyWestern blot analysis of lysates from Jurkat and COLO cells, using RRH Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07038-rrh-primary-antibodies-wb-testing-2.jpgAnti-Peropsin RRH AntibodyWestern Blot analysis of Jurkat cells using Peropsin Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mc5-r-antibody-a07019-1-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07019-1-mc5r-primary-antibodies-if-testing-1.jpgAnti-MC5-R AntibodyImmunofluorescence analysis of MCF7 cells, using MC5R Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07019-1-mc5r-primary-antibodies-wb-testing-2.jpgAnti-MC5-R AntibodyWestern Blot analysis of 3T3 cells using MC5-R Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07019-1-mc5r-primary-antibodies-wb-testing-3.jpgAnti-MC5-R AntibodyWestern blot analysis of lysates from K562 cells, using MC5R Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07019-1-mc5r-primary-antibodies-wb-testing-4.jpgAnti-MC5-R AntibodyWestern blot analysis of the lysates from HeLa cells using MC5R antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07019-1-mc5r-primary-antibodies-ihc-testing-5.jpgAnti-MC5-R AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd158z-antibody-a07017-boster.html2026-03-24T05:08:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07017-kir3dl3-primary-antibodyes-wb-testing-1.jpgAnti-CD158z KIR3DL3 AntibodyWestern Blot (WB) analysis of K562, L929, A549 cells using CD158z Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07017-kir3dl3-primary-antibodyes-ihc-testing-2.jpgAnti-CD158z KIR3DL3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07017-kir3dl3-primary-antibodyes-ihc-testing-3.jpgAnti-CD158z KIR3DL3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07017-kir3dl3-primary-antibodyes-ihc-testing-4.jpgAnti-CD158z KIR3DL3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung Cancer, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07017-kir3dl3-primary-antibodyes-ihc-testing-5.jpgAnti-CD158z KIR3DL3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung Cancer, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-17-antibody-a07009-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07009-fgf17-primary-antibodyes-ihc-testing-1.jpgAnti-FGF-17 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07009-fgf17-primary-antibodyes-wb-testing-2.jpgAnti-FGF-17 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using FGF-17 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07009-fgf17-primary-antibodyes-ihc-testing-3.jpgAnti-FGF-17 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-l30-antibody-a06994-1-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06994-1-rpl30-primary-antibodyes-wb-testing-1.jpgAnti-Ribosomal Protein L30 RPL30 AntibodyWestern Blot (WB) analysis of specific cells using Ribosomal Protein L30 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bmp-10-antibody-a06968-1-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06968-1-bmp10-primary-antibodies-wb-testing-1.jpgAnti-BMP-10 AntibodyWestern Blot analysis of mouse-brain mouse-lung cells using BMP-10 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arhgef10-antibody-a06958-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06958-arhgef10-primary-antibodyes-wb-testing-1.jpgAnti-ARHGEF10 AntibodyWestern Blot (WB) analysis of specific cells using ARHGEF10 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bmp-6-antibody-a06924-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06924-bmp6-primary-antibodies-wb-testing-1.jpgAnti-BMP-6 AntibodyWestern Blot analysis of 4T1 cells using BMP-6 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd297-antibody-a06913-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06913-art4-primary-antibodyes-ihc-testing-1.jpgAnti-CD297 ART4 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06913-art4-primary-antibodyes-ihc-testing-2.jpgAnti-CD297 ART4 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-casein-kinase-i-gamma1-antibody-a06904-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06904-csnk1g1-primary-antibodies-ihc-testing-1.jpgAnti-Casein Kinase I gamma1 CSNK1G1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06904-csnk1g1-primary-antibodies-wb-testing-2.jpgAnti-Casein Kinase I gamma1 CSNK1G1 AntibodyWestern Blot analysis of various cells using Casein Kinase Iγ1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06904-csnk1g1-primary-antibodies-wb-testing-3.jpgAnti-Casein Kinase I gamma1 CSNK1G1 AntibodyWestern blot analysis of lysates from COS7 cells, using CKI-gamma1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cysltr2-antibody-a06895-boster.html2026-03-24T05:08:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06895-cysltr2-primary-antibodies-wb-testing-2.jpgAnti-CysLTR2/Cyslt2 AntibodyWestern Blot analysis of HeLa cells using CysLTR2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06895-cysltr2-primary-antibodies-wb-testing-1.jpgAnti-CysLTR2/Cyslt2 AntibodyWestern blot analysis of lysates from HeLa and COLO cells, using CLTR2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tmc8-antibody-a06892-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06892-tmc8-primary-antibodies-wb-testing-2.jpgAnti-TMC8/Ever2 AntibodyWestern Blot analysis of HeLa cells using TMC8 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06892-tmc8-primary-antibodies-ihc-testing-1.jpgAnti-TMC8/Ever2 AntibodyImmunohistochemistry analysis of paraffin-embedded human tonsil, using TMC8 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-recoverin-antibody-a06882-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06882-rcvrn-primary-antibodies-wb-testing-2.jpgAnti-Recoverin RCVRN AntibodyWestern Blot analysis of 3T3 cells using Recoverin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06882-rcvrn-primary-antibodies-wb-testing-3.jpgAnti-Recoverin RCVRN AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using Recoverin Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06882-rcvrn-primary-antibodies-ihc-testing-1.jpgAnti-Recoverin RCVRN AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gdf-3-antibody-a06869-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06869-gdf3-primary-antibodyes-wb-testing-1.jpgAnti-GDF-3 AntibodyWestern Blot (WB) analysis of L929 cells using GDF-3 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06869-gdf3-primary-antibodyes-wb-testing-2.jpgAnti-GDF-3 AntibodyWestern Blot (WB) analysis of K562 KB using GDF-3 Polyclonal antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06869-gdf3-primary-antibodyes-wb-testing-3.jpgAnti-GDF-3 AntibodyWestern Blot (WB) analysis of L929 cells using GDF-3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nfr-kappab-antibody-a06867-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06867-nfrkb-primary-antibodyes-wb-testing-1.jpgAnti-NFR kappaB NFRKB AntibodyWestern Blot (WB) analysis of COS7 cells using NFRkappaB Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06867-nfrkb-primary-antibodyes-wb-testing-2.jpgAnti-NFR kappaB NFRKB AntibodyWestern Blot (WB) analysis of specific cells using NFRkappaB Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dp-2-antibody-a06850-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06850-tfdp2-primary-antibodies-wb-testing-2.jpgAnti-DP-2 TFDP2 AntibodyWestern Blot analysis of various cells using DP-2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06850-tfdp2-primary-antibodies-wb-testing-1.jpgAnti-DP-2 TFDP2 AntibodyWestern blot analysis of lysate from COS7 cells, using DP-2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd316-antibody-a06844-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06844-igsf8-primary-antibodies-wb-testing-1.jpgAnti-CD316 IGSF8 AntibodyWestern Blot analysis of NIH-3T3 cells using CD316 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-na-cp-type-ii-beta-antibody-a06842-1-boster.html2026-03-24T05:08:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06842-1-scn2b-primary-antibodies-wb-testing-2.jpgAnti-Na+ CP type II beta SCN2B AntibodyWestern Blot analysis of various cells using Na+ CP type IIβ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06842-1-scn2b-primary-antibodies-wb-testing-3.jpgAnti-Na+ CP type II beta SCN2B AntibodyWestern blot analysis of the lysates from HepG2 cells using SCN2B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06842-1-scn2b-primary-antibodies-ihc-testing-1.jpgAnti-Na+ CP type II beta SCN2B AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-larg-antibody-a06802-1-boster.html2026-03-24T05:09:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-1-arhgef12-primary-antibodies-ihc-testing-1.jpgAnti-LARG ARHGEF12 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-1-arhgef12-primary-antibodies-wb-testing-2.jpgAnti-LARG ARHGEF12 AntibodyWestern Blot analysis of RAW264.7 cells using LARG Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-1-arhgef12-primary-antibodies-wb-testing-3.jpgAnti-LARG ARHGEF12 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using ARHGEF12 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-1-arhgef12-primary-antibodies-wb-testing-4.jpgAnti-LARG ARHGEF12 AntibodyWestern blot analysis of the lysates from HUVECcells using ARHGEF12 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cytokeratin-15-antibody-a06791-1-boster.html2026-03-24T05:09:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-1-krt15-primary-antibodyes-wb-testing-1.jpgAnti-Cytokeratin 15 KRT15 Monoclonal AntibodyWestern Blot (WB) analysis using Cytokeratin 15 Monoclonal antibody against A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-1-krt15-primary-antibodyes-if-testing-2.jpgAnti-Cytokeratin 15 KRT15 Monoclonal AntibodyImmunofluorescence (IF) analysis of HepG2(left) and PACN-1 (right) cells using Cytokeratin 15 Monoclonal antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-1-krt15-primary-antibodyes-ihc-testing-3.jpgAnti-Cytokeratin 15 KRT15 Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Tonsil tissues with AEC staining using Cytokeratin 15 Monoclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-1-krt15-primary-antibodyes-fcm-testing-4.jpgAnti-Cytokeratin 15 KRT15 Monoclonal AntibodyFlow cytometric (FCM) analysis of PACN-1 cells using Cytokeratin 15 Monoclonal antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sema4a-antibody-a06779-1-boster.html2026-03-24T05:09:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06779-1-sema4a-primary-antibodies-wb-testing-2.jpgAnti-SEMA4A/Semaphorin 4A AntibodyWestern blot analysis of lysates from COS7 and Jurkat cells, using SEMA4A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06779-1-sema4a-primary-antibodies-ihc-testing-1.jpgAnti-SEMA4A/Semaphorin 4A AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using SEMA4A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-inhibin-beta-a-antibody-a06777-boster.html2026-03-24T05:09:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06777-inhba-primary-antibodies-ihc-testing-1.jpgAnti-Inhibin beta-A INHBA AntibodyImmunohistochemical analysis of paraffin-embedded Human liver. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06777-inhba-primary-antibodies-wb-testing-2.jpgAnti-Inhibin beta-A INHBA AntibodyWestern Blot analysis of MCF-7, 293 cells using Inhibin β-A Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06777-inhba-primary-antibodies-wb-testing-3.jpgAnti-Inhibin beta-A INHBA AntibodyWestern blot analysis of lysate from 293, MCF-7 cells, using INHBA Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ndr2-antibody-a06774-boster.html2026-03-24T05:09:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06774-stk38l-primary-antibodies-wb-testing-2.jpgAnti-NDR2 STK38L AntibodyWestern Blot analysis of mouse cells using NDR2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06774-stk38l-primary-antibodies-ihc-testing-1.jpgAnti-NDR2 STK38L AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-irtks-antibody-a06770-1-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06770-1-baiap2l1-primary-antibodyes-wb-testing-1.jpgAnti-IRTKS BAIAP2L1 AntibodyWestern Blot (WB) analysis of specific cells using IRTKS Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-g-beta-5-antibody-a06754-1-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06754-1-gnb5-primary-antibodies-wb-testing-1.jpgAnti-G beta 5 GNB5 AntibodyWestern Blot analysis of HepG2 cells using Gβ 5 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-epha8-antibody-a06731-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06731-epha8-primary-antibodies-wb-testing-1.jpgAnti-EphA8 Monoclonal AntibodyWestern Blot analysis using EphA8 Monoclonal Antibody against truncated Trx-EphA8 recombinant protein (1) and truncated MBP-EphA8 (aa70-150) recombinant protein (2).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-negr1-antibody-a06730-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06730-negr1-primary-antibodies-wb-testing-2.jpgAnti-NEGR1/Kilon AntibodyWestern Blot analysis of various cells using NEGR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06730-negr1-primary-antibodies-wb-testing-3.jpgAnti-NEGR1/Kilon AntibodyWestern blot analysis of lysates from COLO cells, using NEGR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06730-negr1-primary-antibodies-wb-testing-1.jpgAnti-NEGR1/Kilon AntibodyWestern blot analysis of the lysates from COLO205 cells using NEGR1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bag-4-antibody-a06722-1-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06722-1-bag4-primary-antibodies-wb-testing-2.jpgAnti-Bag-4 AntibodyWestern Blot analysis of various cells using Bag-4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06722-1-bag4-primary-antibodies-wb-testing-3.jpgAnti-Bag-4 AntibodyWestern Blot analysis of K562 cells using Bag-4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06722-1-bag4-primary-antibodies-ihc-testing-1.jpgAnti-Bag-4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr92-antibody-a06721-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06721-lpar5-primary-antibodies-wb-testing-2.jpgAnti-GPR92 LPAR5 AntibodyWestern Blot analysis of various cells using GPR92 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06721-lpar5-primary-antibodies-wb-testing-1.jpgAnti-GPR92 LPAR5 AntibodyWestern blot analysis of lysates from HT-29 and K562 cells, using GPR92 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-histone-h1-antibody-a06717-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06717-hist1h1b-primary-antibodies-if-testing-1.jpgAnti-Histone H1 HIST1H1B AntibodyImmunofluorescence analysis of HUVEC cells, using Histone H1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06717-hist1h1b-primary-antibodies-wb-testing-2.jpgAnti-Histone H1 HIST1H1B AntibodyWestern Blot analysis of 3T3 cells using Histone H1 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06717-hist1h1b-primary-antibodies-wb-testing-3.jpgAnti-Histone H1 HIST1H1B AntibodyWestern blot analysis of lysates from COLO cells, using Histone H1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06717-hist1h1b-primary-antibodies-ihc-testing-4.jpgAnti-Histone H1 HIST1H1B AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using Histone H1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06717-hist1h1b-primary-antibodies-if-testing-5.jpgAnti-Histone H1 HIST1H1B AntibodyImmunofluorescence analysis of Hela cell. 1,Histone H1 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). α-SMA Monoclonal Antibody (6A12) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nf-yb-antibody-a06714-2-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06714-2-nfyb-primary-antibodies-wb-testing-2.jpgAnti-NF-YB AntibodyWestern Blot analysis of various cells using NF-YB Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06714-2-nfyb-primary-antibodies-wb-testing-3.jpgAnti-NF-YB AntibodyWestern blot analysis of lysates from 293 cells, using NFYB Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06714-2-nfyb-primary-antibodies-ihc-testing-1.jpgAnti-NF-YB AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp4b1-antibody-a06690-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06690-cyp4b1-primary-antibodyes-wb-testing-1.jpgAnti-Cytochrome P450 4B1 CYP4B1 AntibodyWestern Blot (WB) analysis of COLO205 cells using CYP4B1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col14a1-antibody-a06685-boster.html2026-03-24T05:09:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06685-col14a1-primary-antibodyes-ihc-testing-1.jpgAnti-Collagen alpha-1(XIV) chain COL14A1 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tlk2-antibody-a06645-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06645-tlk2-primary-antibodies-wb-testing-2.jpgAnti-TLK2 AntibodyWestern Blot analysis of various cells using TLK2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06645-tlk2-primary-antibodies-wb-testing-3.jpgAnti-TLK2 AntibodyWestern blot analysis of lysates from COLO cells, using TLK2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06645-tlk2-primary-antibodies-wb-testing-4.jpgAnti-TLK2 AntibodyWestern blot analysis of the lysates from HeLa cells using TLK2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06645-tlk2-primary-antibodies-ihc-testing-1.jpgAnti-TLK2 AntibodyImmunohistochemical analysis of paraffin-embedded human meningioma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-urotensin-ii-antibody-a06633-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06633-uts2-primary-antibodies-wb-testing-2.jpgAnti-Urotensin II UTS2 AntibodyWestern Blot analysis of various cells using Urotensin II Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06633-uts2-primary-antibodies-wb-testing-1.jpgAnti-Urotensin II UTS2 AntibodyWestern blot analysis of lysate from 293 cells, using Urotensin II antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kir2-3-antibody-a06605-1-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06605-1-kcnj4-primary-antibodies-wb-testing-2.jpgAnti-KIR2.3 KCNJ4 AntibodyWestern Blot analysis of 293 cells using KIR2.3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06605-1-kcnj4-primary-antibodies-wb-testing-3.jpgAnti-KIR2.3 KCNJ4 AntibodyWestern blot analysis of KCNJ4 Antibody. The lane on the right is blocked with the KCNJ4 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06605-1-kcnj4-primary-antibodies-ihc-testing-1.jpgAnti-KIR2.3 KCNJ4 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-edg-7-antibody-a06597-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-lpar3-primary-antibodies-wb-testing-2.jpgAnti-EDG-7 LPAR3 AntibodyWestern Blot analysis of 3T3 cells using EDG-7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-lpar3-primary-antibodies-wb-testing-3.jpgAnti-EDG-7 LPAR3 AntibodyWestern blot analysis of lysates from Jurkat cells, using EDG7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-lpar3-primary-antibodies-ihc-testing-4.jpgAnti-EDG-7 LPAR3 AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-lpar3-primary-antibodies-if-testing-1.jpgAnti-EDG-7 LPAR3 AntibodyImmunofluorescence analysis of A549 cells, using EDG7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gps2-antibody-a06569-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06569-gps2-primary-antibodies-wb-testing-2.jpgAnti-GPS2 AntibodyWestern Blot analysis of RAW264.7 cells using GPS2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06569-gps2-primary-antibodies-wb-testing-1.jpgAnti-GPS2 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using GPS2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyfip2-antibody-a06562-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06562-cyfip2-primary-antibodies-wb-testing-2.jpgAnti-CYFIP2 AntibodyWestern Blot analysis of HEPG2 Hela cells using CYFIP2 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06562-cyfip2-primary-antibodies-ihc-testing-3.jpgAnti-CYFIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06562-cyfip2-primary-antibodies-ihc-testing-4.jpgAnti-CYFIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06562-cyfip2-primary-antibodies-ihc-testing-1.jpgAnti-CYFIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-colon, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd328-antibody-a06553-boster.html2026-03-24T05:09:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06553-siglec7-primary-antibodies-wb-testing-2.jpgAnti-CD328 SIGLEC7 AntibodyWestern Blot analysis of K562 cells using CD328 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06553-siglec7-primary-antibodies-wb-testing-3.jpgAnti-CD328 SIGLEC7 AntibodyWestern blot analysis of lysate from K562 cells, using SIGLEC7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06553-siglec7-primary-antibodies-ihc-testing-1.jpgAnti-CD328 SIGLEC7 AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-siglec-5-14-antibody-a06510-1-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06510-1-siglec5-primary-antibodies-wb-testing-2.jpgAnti-Siglec-5/14 AntibodyWestern Blot analysis of L929 cells using Siglec-5/14 Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06510-1-siglec5-primary-antibodies-ihc-testing-1.jpgAnti-Siglec-5/14 AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdk10-antibody-a06507-1-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06507-1-cdk10-primary-antibodies-wb-testing-2.jpgAnti-Cyclin-dependent kinase 10 Cdk10 AntibodyWestern Blot analysis of various cells using Cdk10 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06507-1-cdk10-primary-antibodies-wb-testing-3.jpgAnti-Cyclin-dependent kinase 10 Cdk10 AntibodyWestern Blot analysis of 293 cells using Cdk10 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06507-1-cdk10-primary-antibodies-wb-testing-4.jpgAnti-Cyclin-dependent kinase 10 Cdk10 AntibodyWestern blot analysis of lysates from 293 cells, using CDK10 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06507-1-cdk10-primary-antibodies-ihc-testing-1.jpgAnti-Cyclin-dependent kinase 10 Cdk10 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mysm1-antibody-a06500-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06500-mysm1-primary-antibodies-ihc-testing-1.jpgAnti-MYSM1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using MYSM1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06500-mysm1-primary-antibodies-wb-testing-2.jpgAnti-MYSM1 AntibodyWestern Blot analysis of MCF7 cells using MYSM1 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06500-mysm1-primary-antibodies-wb-testing-3.jpgAnti-MYSM1 AntibodyWestern blot analysis of Hela lysis using MYSM1 antibody. Antibody was diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-protein-z-antibody-a06491-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06491-proz-primary-antibodies-wb-testing-1.jpgAnti-Protein Z PROZ Monoclonal AntibodyWestern Blot analysis using Protein Z Monoclonal Antibody against human plasma (1).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cerberus-antibody-a06475-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06475-cer1-primary-antibodies-wb-testing-2.jpgAnti-Cerberus CER1 AntibodyWestern Blot analysis of MCF-7 cells using Cerberus Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06475-cer1-primary-antibodies-wb-testing-3.jpgAnti-Cerberus CER1 AntibodyWestern Blot analysis of Rat-heart Rat-brain using Cerberus Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06475-cer1-primary-antibodies-ihc-testing-1.jpgAnti-Cerberus CER1 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-a-cyclase-i-antibody-a06460-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06460-adcy1-primary-antibodies-wb-testing-2.jpgAnti-A Cyclase I ADCY1 AntibodyWestern Blot analysis of COLO205 cells using A Cyclase I Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06460-adcy1-primary-antibodies-wb-testing-1.jpgAnti-A Cyclase I ADCY1 AntibodyWestern blot analysis of lysates from COLO205 cells, using ADCY1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd218b-antibody-a06457-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06457-il18rap-primary-antibodies-ihc-testing-2.jpgAnti-CD218b IL18RAP AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06457-il18rap-primary-antibodies-ihc-testing-1.jpgAnti-CD218b IL18RAP AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scn4b-antibody-a06453-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06453-scn4b-primary-antibodyes-wb-testing-1.jpgAnti-Sodium channel subunit beta-4 Scn4b AntibodyWestern Blot (WB) analysis of specific cells using Scn4b Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rfc3-antibody-a06442-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06442-rfc3-primary-antibodies-wb-testing-2.jpgAnti-Replication factor C subunit 3 RFC3 AntibodyWestern Blot analysis of various cells using RFC3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06442-rfc3-primary-antibodies-wb-testing-3.jpgAnti-Replication factor C subunit 3 RFC3 AntibodyWestern blot analysis of lysate from HepG2 cells, using RFC3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06442-rfc3-primary-antibodies-ihc-testing-1.jpgAnti-Replication factor C subunit 3 RFC3 AntibodyImmunohistochemistry analysis of RFC3 antibody in paraffin-embedded human brain tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd307-antibody-a06435-boster.html2026-03-24T05:09:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06435-fcrl5-primary-antibodies-wb-testing-2.jpgAnti-CD307 FCRL5 AntibodyWestern Blot analysis of HepG2 cells using CD307 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ca-xiv-antibody-a06411-1-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06411-1-ca14-primary-antibodies-wb-testing-2.jpgAnti-CA XIV CA14 AntibodyWestern Blot analysis of various cells using CA XIV Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06411-1-ca14-primary-antibodies-wb-testing-1.jpgAnti-CA XIV CA14 AntibodyWestern blot analysis of lysates from Jurkat, COLO, and 293 cells, using CA14 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lok-antibody-a06406-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06406-stk10-primary-antibodies-ihc-testing-1.jpgAnti-LOK STK10 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06406-stk10-primary-antibodies-wb-testing-2.jpgAnti-LOK STK10 AntibodyWestern Blot analysis of HuvEc cells using LOK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06406-stk10-primary-antibodies-wb-testing-3.jpgAnti-LOK STK10 AntibodyWestern blot analysis of the lysates from HT-29 cells using STK10 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-usp30-antibody-a06403-1-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06403-1-usp30-primary-antibodies-wb-testing-2.jpgAnti-USP30 AntibodyWestern Blot analysis of various cells using USP30 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06403-1-usp30-primary-antibodies-wb-testing-1.jpgAnti-USP30 AntibodyWestern blot analysis of lysates from HeLa cells, using USP30 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ppx-antibody-a06390-1-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06390-1-ppp4c-primary-antibodies-if-testing-1.jpgAnti-PPX PPP4C Monoclonal AntibodyImmunofluorescence analysis of HeLa cells using PPX Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06390-1-ppp4c-primary-antibodies-wb-testing-2.jpgAnti-PPX PPP4C Monoclonal AntibodyWestern Blot analysis using PPX Monoclonal Antibody against HeLa, 293, Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06390-1-ppp4c-primary-antibodies-ihc-testing-3.jpgAnti-PPX PPP4C Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human breast cancer using PPX Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-uba5-antibody-a06385-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06385-uba5-primary-antibodies-wb-testing-2.jpgAnti-Uba5/Ufm1 Activating Enzyme AntibodyWestern Blot analysis of various cells using Uba5 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06385-uba5-primary-antibodies-wb-testing-3.jpgAnti-Uba5/Ufm1 Activating Enzyme AntibodyWestern blot analysis of lysates from HepG2 and 293 cells, using UBA5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06385-uba5-primary-antibodies-ihc-testing-1.jpgAnti-Uba5/Ufm1 Activating Enzyme AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-snm1b-antibody-a06378-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06378-dclre1b-primary-antibodyes-wb-testing-1.jpgAnti-SNM1B DCLRE1B AntibodyWestern Blot (WB) analysis of extracts from K562, Jurkat cells, using SNM1B Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd296-antibody-a06376-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06376-art1-primary-antibodies-wb-testing-2.jpgAnti-CD296 ART1 AntibodyWestern blot analysis of MOUSE-BRAIN lysis using ART1 antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06376-art1-primary-antibodies-wb-testing-1.jpgAnti-CD296 ART1 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-baf170-antibody-a06370-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06370-smarcc2-primary-antibodies-wb-testing-2.jpgAnti-BAF170 SMARCC2 AntibodyWestern Blot analysis of various cells using BAF170 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06370-smarcc2-primary-antibodies-wb-testing-3.jpgAnti-BAF170 SMARCC2 AntibodyWestern Blot analysis of COLO205 cells using BAF170 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06370-smarcc2-primary-antibodies-wb-testing-1.jpgAnti-BAF170 SMARCC2 AntibodyWestern blot analysis of lysates from HUVEC and COLO205 cells, using SMRC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dgk-alpha-antibody-a06354-boster.html2026-03-24T05:09:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-dgka-primary-antibodies-if-testing-1.jpgAnti-DGK- alpha AntibodyImmunofluorescence analysis of MCF7 cell. 1,primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-dgka-primary-antibodies-wb-testing-2.jpgAnti-DGK- alpha AntibodyWestern Blot analysis of various cells using DGK-α Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-dgka-primary-antibodies-wb-testing-3.jpgAnti-DGK- alpha AntibodyWestern Blot analysis of Lovo cells using DGK-α Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-dgka-primary-antibodies-wb-testing-4.jpgAnti-DGK- alpha AntibodyWestern blot analysis of lysates from Jurkat cells, using DGKA Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-dgka-primary-antibodies-ihc-testing-5.jpgAnti-DGK- alpha AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-k-cadherin-antibody-a06353-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06353-cdh6-primary-antibodies-wb-testing-1.jpgAnti-K-Cadherin-6 CDH6-AntibodyWestern Blot analysis of BT474, A549, SHSY5Y, 293 cells using K-cadherin Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mybpc1-antibody-a06339-1-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06339-1-mybpc1-primary-antibodies-wb-testing-2.jpgAnti-MYBPC1 AntibodyWestern Blot analysis of 293 cells using MYBPC1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06339-1-mybpc1-primary-antibodies-ihc-testing-1.jpgAnti-MYBPC1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gamma-tubulin-antibody-a06313-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06313-tubg1-primary-antibodies-wb-testing-1.jpgAnti-Gamma Tubulin TUBG1 Monoclonal AntibodyWestern Blot analysis of paraffin-embedded Jurkat\Hela\Mouse-brain\Rat-brain using Gamma Tubulin Mouse mAb diluted at 1:1000.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-emx1-antibody-a06307-1-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06307-1-emx1-primary-antibodies-wb-testing-2.jpgAnti-Homeobox protein EMX1 Emx1 AntibodyWestern Blot analysis of HuvEC cells using Emx1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06307-1-emx1-primary-antibodies-wb-testing-1.jpgAnti-Homeobox protein EMX1 Emx1 AntibodyWestern blot analysis of the lysates from Jurkat cells using EMX1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgl2-antibody-a06303-1-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06303-1-fgl2-primary-antibodies-wb-testing-2.jpgAnti-Fgl2/Fibroleukin AntibodyWestern Blot analysis of various cells using Fgl2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06303-1-fgl2-primary-antibodies-wb-testing-1.jpgAnti-Fgl2/Fibroleukin AntibodyWestern blot analysis of lysate from 293 cells treated with insulin, using Fgl2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nprl2-antibody-a06286-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06286-nprl2-primary-antibodies-wb-testing-1.jpgAnti-NPRL2/Npr2L AntibodyWestern Blot analysis of extracts from Jurkat, K562 cells, using NPRL2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sec22b-antibody-a06284-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06284-sec22b-primary-antibodies-wb-testing-2.jpgAnti-SEC22B/Sec22L1 AntibodyWestern blot analysis of JK using SEC22B antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06284-sec22b-primary-antibodies-ihc-testing-1.jpgAnti-SEC22B/Sec22L1 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-granzyme-k-antibody-a06281-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06281-gzmk-primary-antibodyes-wb-testing-1.jpgAnti-Granzyme K GZMK AntibodyWestern Blot (WB) analysis of specific cells using Granzyme K Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-intestinal-cell-kinase-antibody-a06270-1-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06270-1-ick-primary-antibodies-ihc-testing-1.jpgAnti-Intestinal Cell Kinase ICK AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1,primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06270-1-ick-primary-antibodies-wb-testing-2.jpgAnti-Intestinal Cell Kinase ICK AntibodyWestern Blot analysis of 3T3 cells using Intestinal Cell Kinase Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06270-1-ick-primary-antibodies-wb-testing-3.jpgAnti-Intestinal Cell Kinase ICK AntibodyWestern blot analysis of lysates from NIH/3T3 cells, treated with PBS 10uM 60', using ICK Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd53-antibody-a06249-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06249-cd53-primary-antibodyes-wb-testing-1.jpgAnti-Leukocyte surface antigen CD53 CD53 AntibodyWestern Blot (WB) analysis of KB cells using CD53 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06249-cd53-primary-antibodyes-wb-testing-2.jpgAnti-Leukocyte surface antigen CD53 CD53 AntibodyWestern Blot (WB) analysis of KB cells using CD53 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-wdhd1-antibody-a06240-boster.html2026-03-24T05:09:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06240-wdhd1-primary-antibodies-wb-testing-2.jpgAnti-WDHD1 AntibodyWestern blot analysis of lysates from Jurkat and HepG2 cells, using WDHD1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06240-wdhd1-primary-antibodies-ihc-testing-1.jpgAnti-WDHD1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hub-d-antibody-a06194-1-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06194-1-elavl2-primary-antibodies-if-testing-1.jpgAnti-HuB/D ELAVL2 AntibodyImmunofluorescence analysis of HepG2 cells, using ELAV2/4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06194-1-elavl2-primary-antibodies-wb-testing-2.jpgAnti-HuB/D ELAVL2 AntibodyWestern Blot analysis of Hela cells using HuB/D Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06194-1-elavl2-primary-antibodies-wb-testing-3.jpgAnti-HuB/D ELAVL2 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using ELAV2/4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06194-1-elavl2-primary-antibodies-ihc-testing-4.jpgAnti-HuB/D ELAVL2 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pd2r-antibody-a06190-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06190-ptgdr-primary-antibodies-wb-testing-2.jpgAnti-PD2R PTGDR AntibodyWestern Blot analysis of 293 cells using PD2R Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06190-ptgdr-primary-antibodies-wb-testing-3.jpgAnti-PD2R PTGDR AntibodyWestern blot analysis of lysates from HepG2 cells, using PTGDR Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06190-ptgdr-primary-antibodies-ihc-testing-4.jpgAnti-PD2R PTGDR AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06190-ptgdr-primary-antibodies-if-testing-1.jpgAnti-PD2R PTGDR AntibodyImmunofluorescence analysis of A549 cells, using PTGDR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd1e-antibody-a06184-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06184-cd1e-primary-antibodies-wb-testing-2.jpgAnti-CD1E AntibodyWestern Blot analysis of K562 cells using CD1E Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06184-cd1e-primary-antibodies-wb-testing-3.jpgAnti-CD1E AntibodyWestern blot analysis of lysate from K562 cells, using CD1E Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06184-cd1e-primary-antibodies-ihc-testing-1.jpgAnti-CD1E AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hlx1-antibody-a06177-1-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06177-1-hlx-primary-antibodyes-wb-testing-1.jpgAnti-HLX/Hlx11 AntibodyWestern Blot (WB) analysis of specific cells using HLX1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hlx1-antibody-a06177-2-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06177-2-hlx-primary-antibodies-wb-testing-1.jpgAnti-HLX1 Monoclonal AntibodyWestern Blot analysis using HLX1 Monoclonal Antibody against Mouse pancreas cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hox-a7-antibody-a06154-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06154-hoxa7-primary-antibodies-wb-testing-1.jpgAnti-Hox-A7 AntibodyWestern blot analysis of lysates from COLO205 and Jurkat cells, using HOXA7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06154-hoxa7-primary-antibodies-wb-testing-2.jpgAnti-Hox-A7 AntibodyWestern Blot analysis of various cells using Hox-A7 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nf-yc-antibody-a06128-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06128-nfyc-primary-antibodies-wb-testing-2.jpgAnti-NF-YC AntibodyWestern Blot analysis of 293 cells using NF-YC Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06128-nfyc-primary-antibodies-wb-testing-3.jpgAnti-NF-YC AntibodyWestern blot analysis of lysates from HeLa and 293 cells, using NFYC Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06128-nfyc-primary-antibodies-ihc-testing-1.jpgAnti-NF-YC AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rag-c-antibody-a06127-boster.html2026-03-24T05:09:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06127-rragc-primary-antibodies-wb-testing-2.jpgAnti-Rag C RRAGC AntibodyWestern blot analysis of lysates from HepG2, A549, and LOVO cells, using RRAGC Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06127-rragc-primary-antibodies-ihc-testing-1.jpgAnti-Rag C RRAGC AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-maxik-beta-antibody-a06117-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06117-kcnmb4-primary-antibodies-ihc-testing-1.jpgAnti-MaxiK beta KCNMB4 AntibodyImmunohistochemistry analysis of MaxiKβ antibody in paraffin-embedded human brain tissue.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06117-kcnmb4-primary-antibodies-wb-testing-2.jpgAnti-MaxiK beta KCNMB4 AntibodyWestern Blot analysis of various cells using MaxiKβ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06117-kcnmb4-primary-antibodies-wb-testing-3.jpgAnti-MaxiK beta KCNMB4 AntibodyWestern blot analysis of lysate from HepG2 cells, using MaxiKβ antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nckx4-antibody-a06104-1-boster.html2026-03-24T05:09:07+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-v-atpase-b1-antibody-a06073-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06073-atp6v1b1-primary-antibodies-wb-testing-2.jpgAnti-V-ATPase B1 ATP6V1B1 AntibodyWestern Blot analysis of various cells using V-ATPase B1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06073-atp6v1b1-primary-antibodies-wb-testing-3.jpgAnti-V-ATPase B1 ATP6V1B1 AntibodyWestern blot analysis of ATP6V1B1 Antibody. The lane on the right is blocked with the ATP6V1B1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06073-atp6v1b1-primary-antibodies-ihc-testing-1.jpgAnti-V-ATPase B1 ATP6V1B1 AntibodyImmunohistochemistryt analysis of paraffin-embedded human breast carcinoma, using ATP6V1B1 Antibody. The lane on the right is blocked with the ATP6V1B1 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-polr3a-antibody-a06059-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06059-polr3a-primary-antibodies-wb-testing-2.jpgAnti-POLR3A AntibodyWestern Blot analysis of various cells using POLR3A Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06059-polr3a-primary-antibodies-wb-testing-3.jpgAnti-POLR3A AntibodyWestern blot analysis of lysates from COS and HUVEC cells, using RPC1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06059-polr3a-primary-antibodies-wb-testing-4.jpgAnti-POLR3A AntibodyWestern blot analysis of the lysates from 293 cells using RPC1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06059-polr3a-primary-antibodies-ihc-testing-1.jpgAnti-POLR3A AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sr-1d-antibody-a06046-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06046-htr1d-primary-antibodyes-wb-testing-1.jpgAnti-SR-1D HTR1D AntibodyWestern Blot (WB) analysis of HepG2 823 293T AD293 HeLa using SR-1D antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06046-htr1d-primary-antibodyes-ihc-testing-2.jpgAnti-SR-1D HTR1D AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbx15-18-antibody-a06044-1-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06044-1-tbx18-primary-antibodyes-wb-testing-1.jpgAnti-TBX15/18 AntibodyWestern Blot (WB) analysis of specific cells using TBX15/18 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eif3-alpha-antibody-a06040-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06040-eif3j-primary-antibodies-wb-testing-1.jpgAnti-eIF3 alpha EIF3J AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-l7-antibody-a06025-boster.html2026-03-24T05:09:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06025-rpl7-primary-antibodies-wb-testing-2.jpgAnti-Ribosomal Protein L7 RPL7 AntibodyWestern Blot analysis of various cells using Ribosomal Protein L7 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06025-rpl7-primary-antibodies-wb-testing-3.jpgAnti-Ribosomal Protein L7 RPL7 AntibodyWestern Blot analysis of customer's (cat sample) using Ribosomal Protein L7 Polyclonal Antibody. Antibody was diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06025-rpl7-primary-antibodies-wb-testing-4.jpgAnti-Ribosomal Protein L7 RPL7 AntibodyWestern blot analysis of lysates from 293 and HeLa cells, using RPL7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06025-rpl7-primary-antibodies-wb-testing-5.jpgAnti-Ribosomal Protein L7 RPL7 AntibodyWestern blot analysis of the lysates from K562 cells using RPL7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06025-rpl7-primary-antibodies-ihc-testing-1.jpgAnti-Ribosomal Protein L7 RPL7 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rit1-antibody-a06008-1-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06008-1-rit1-primary-antibodies-wb-testing-2.jpgAnti-GTP-binding protein Rit1 Rit1 AntibodyWestern Blot analysis of various cells using Rit1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06008-1-rit1-primary-antibodies-wb-testing-3.jpgAnti-GTP-binding protein Rit1 Rit1 AntibodyWestern blot analysis of lysates from Jurkat cells, using RIT1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06008-1-rit1-primary-antibodies-ihc-testing-1.jpgAnti-GTP-binding protein Rit1 Rit1 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-elovl6-antibody-a06004-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06004-elovl6-primary-antibodies-wb-testing-2.jpgAnti-ELOVL6 AntibodyWestern blot analysis of the lysates from K562 cells using ELOVL6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06004-elovl6-primary-antibodies-wb-testing-1.jpgAnti-ELOVL6 AntibodyWestern Blot analysis of various cells using ELOVL6 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cpa1-antibody-a05985-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05985-cpa1-primary-antibodies-wb-testing-2.jpgAnti-CPA1/Carboxypeptidase A1 AntibodyWestern Blot analysis of various cells using CPA1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05985-cpa1-primary-antibodies-wb-testing-3.jpgAnti-CPA1/Carboxypeptidase A1 AntibodyWestern Blot analysis of K562 cells using CPA1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05985-cpa1-primary-antibodies-ihc-testing-1.jpgAnti-CPA1/Carboxypeptidase A1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-vamp-1-2-3-antibody-a05982-boster.html2026-03-24T05:09:08+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd236-antibody-a05974-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05974-gypc-primary-antibodyes-ihc-testing-1.jpgAnti-CD236 GYPC AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05974-gypc-primary-antibodyes-ihc-testing-2.jpgAnti-CD236 GYPC AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05974-gypc-primary-antibodyes-ihc-testing-3.jpgAnti-CD236 GYPC AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-trypsin-3-antibody-a05961-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05961-prss3-primary-antibodies-wb-testing-2.jpgAnti-Trypsin-3 PRSS3 AntibodyWestern Blot analysis of various cells using Trypsin-3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05961-prss3-primary-antibodies-wb-testing-1.jpgAnti-Trypsin-3 PRSS3 AntibodyWestern blot analysis of lysate from A549 cells, using Trypsin-3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-npt1-antibody-a05923-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05923-slc17a1-primary-antibodyes-wb-testing-1.jpgAnti-NPT1 SLC17A1 Monoclonal AntibodyWestern Blot (WB) analysis using NPT1 Monoclonal antibody against truncated NPT1 recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lefty-antibody-a05889-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05889-lefty1-primary-antibodies-ihc-testing-1.jpgAnti-Lefty LEFTY1 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05889-lefty1-primary-antibodies-wb-testing-2.jpgAnti-Lefty LEFTY1 AntibodyWestern Blot analysis of HepG2-UV cells using Lefty Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05889-lefty1-primary-antibodies-wb-testing-3.jpgAnti-Lefty LEFTY1 AntibodyWestern Blot analysis of HEPG2-UV cells using Lefty Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ube2t-antibody-a05874-1-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05874-1-ube2t-primary-antibodies-wb-testing-1.jpgAnti-UBE2T/Hspc150 AntibodyWestern Blot analysis of various cells using UBE2T Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-usp19-antibody-a05870-1-boster.html2026-03-24T05:09:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05870-1-usp19-primary-antibodies-wb-testing-2.jpgAnti-USP19 AntibodyWestern Blot analysis of NIH-3T3 cells using USP19 Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05870-1-usp19-primary-antibodies-wb-testing-3.jpgAnti-USP19 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using USP19 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05870-1-usp19-primary-antibodies-ihc-testing-1.jpgAnti-USP19 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using USP19 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-striatin-antibody-a05855-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05855-strn-primary-antibodyes-ihc-testing-1.jpgAnti-Striatin STRN AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05855-strn-primary-antibodyes-wb-testing-2.jpgAnti-Striatin STRN AntibodyWestern Blot (WB) analysis of extracts from K562 cells, using Striatin Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05855-strn-primary-antibodyes-ihc-testing-3.jpgAnti-Striatin STRN AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-klf12-antibody-a05848-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05848-klf12-primary-antibodies-wb-testing-2.jpgAnti-Krueppel-like factor 12 KLF12 AntibodyWestern Blot analysis of rat muscle cells using KLF12 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05848-klf12-primary-antibodies-ihc-testing-1.jpgAnti-Krueppel-like factor 12 KLF12 AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sec23b-antibody-a05847-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05847-sec23b-primary-antibodies-ihc-testing-1.jpgAnti-Sec23B AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05847-sec23b-primary-antibodies-wb-testing-2.jpgAnti-Sec23B AntibodyWestern Blot analysis of COLO205 cells using Sec23B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05847-sec23b-primary-antibodies-wb-testing-3.jpgAnti-Sec23B AntibodyWestern blot analysis of lysate from COLO205 cells, using Sec23B antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p70-s6-kinase-beta-antibody-a05845-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05845-rps6kb2-primary-antibodies-ihc-testing-1.jpgAnti-p70 S6 kinase beta RPS6KB2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05845-rps6kb2-primary-antibodies-wb-testing-2.jpgAnti-p70 S6 kinase beta RPS6KB2 AntibodyWestern Blot analysis of various cells using p70 S6 kinase β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05845-rps6kb2-primary-antibodies-wb-testing-3.jpgAnti-p70 S6 kinase beta RPS6KB2 AntibodyWestern Blot analysis of 293 cells using p70 S6 kinase β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05845-rps6kb2-primary-antibodies-wb-testing-4.jpgAnti-p70 S6 kinase beta RPS6KB2 AntibodyWestern blot analysis of lysates from 293 cells, using p70 S6 Kinase beta Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05845-rps6kb2-primary-antibodies-wb-testing-5.jpgAnti-p70 S6 kinase beta RPS6KB2 AntibodyWestern blot analysis of the lysates from HUVECcells using p70 S6 Kinase β antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-n33-antibody-a05834-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05834-tusc3-primary-antibodies-if-testing-1.jpgAnti-N33 TUSC3 AntibodyImmunofluorescence analysis of HeLa cells using TUSC3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05834-tusc3-primary-antibodies-wb-testing-2.jpgAnti-N33 TUSC3 AntibodyWestern Blot analysis of HeLa cells using N33 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05834-tusc3-primary-antibodies-wb-testing-3.jpgAnti-N33 TUSC3 AntibodyWestern blot analysis of lysates from COLO205 and HeLa cells, using TUSC3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05834-tusc3-primary-antibodies-ihc-testing-4.jpgAnti-N33 TUSC3 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd229-antibody-a05830-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05830-ly9-primary-antibodies-wb-testing-2.jpgAnti-CD229 LY9 AntibodyWestern Blot analysis of HepG2 cells using CD229 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05830-ly9-primary-antibodies-wb-testing-3.jpgAnti-CD229 LY9 AntibodyWestern blot analysis of lysate from HepG2 cells, using LY9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05830-ly9-primary-antibodies-ihc-testing-1.jpgAnti-CD229 LY9 AntibodyImmunohistochemical analysis of paraffin-embedded human-prostate-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ampd2-antibody-a05817-1-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05817-1-ampd2-primary-antibodies-wb-testing-2.jpgAnti-AMP deaminase 2 AMPD2 AntibodyWestern Blot analysis of various cells using AMPD2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05817-1-ampd2-primary-antibodies-wb-testing-1.jpgAnti-AMP deaminase 2 AMPD2 AntibodyWestern blot analysis of the lysates from HeLa cells using AMPD2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdc23-antibody-a05798-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05798-cdc23-primary-antibodies-wb-testing-1.jpgAnti-Cdc23 AntibodyWestern Blot analysis of COS7 cells using Cdc23 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05798-cdc23-primary-antibodies-wb-testing-2.jpgAnti-Cdc23 AntibodyWestern Blot analysis of various cells using Cdc23 Polyclonal Antibody diluted at 1:2000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pbfe-antibody-a05757-1-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05757-1-ehhadh-primary-antibodies-ihc-testing-1.jpgAnti-PBFE EHHADH AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using EHHADH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05757-1-ehhadh-primary-antibodies-wb-testing-2.jpgAnti-PBFE EHHADH AntibodyWestern Blot analysis of various cells using PBFE Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05757-1-ehhadh-primary-antibodies-wb-testing-3.jpgAnti-PBFE EHHADH AntibodyWestern Blot analysis of A549 cells using PBFE Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05757-1-ehhadh-primary-antibodies-wb-testing-4.jpgAnti-PBFE EHHADH AntibodyWestern blot analysis of lysates from A549 cells, using EHHADH Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05757-1-ehhadh-primary-antibodies-wb-testing-5.jpgAnti-PBFE EHHADH AntibodyWestern blot analysis of the lysates from HepG2 cells using EHHADH antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp2a-a-beta-antibody-a05756-1-boster.html2026-03-24T05:09:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05756-1-ppp2r1b-primary-antibodyes-wb-testing-1.jpgAnti-PP2A-A beta PPP2R1B AntibodyWestern Blot (WB) analysis of specific cells using PP2A-Abeta Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chd1l-antibody-a05749-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05749-chd1l-primary-antibodies-wb-testing-2.jpgAnti-CHD1L AntibodyWestern Blot analysis of extracts from NIH-3T3, Jurkat, A549 cells, using CHD1L Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05749-chd1l-primary-antibodies-wb-testing-1.jpgAnti-CHD1L AntibodyWestern blot analysis of lysates from HepG2 cells, using CHD1L antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-melanopsin-antibody-a05740-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05740-opn4-primary-antibodies-wb-testing-2.jpgAnti-Melanopsin OPN4 AntibodyWestern Blot analysis of COLO205 cells using Melanopsin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05740-opn4-primary-antibodies-wb-testing-3.jpgAnti-Melanopsin OPN4 AntibodyWestern blot analysis of various lysis using Melanopsin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05740-opn4-primary-antibodies-wb-testing-4.jpgAnti-Melanopsin OPN4 AntibodyWestern blot analysis of lysates from COLO cells, using OPN4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05740-opn4-primary-antibodies-ihc-testing-1.jpgAnti-Melanopsin OPN4 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scp-3-antibody-a05718-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05718-sycp3-primary-antibodies-wb-testing-2.jpgAnti-SCP-3 SYCP3 AntibodyWestern Blot analysis of K562, 22RV-1, H460 cells using SCP-3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05718-sycp3-primary-antibodies-ihc-testing-1.jpgAnti-SCP-3 SYCP3 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-abin-2-antibody-a05716-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05716-tnip2-primary-antibodyes-ihc-testing-1.jpgAnti-Abin-2 TNIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-cervical-cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05716-tnip2-primary-antibodyes-ihc-testing-2.jpgAnti-Abin-2 TNIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-cervical-cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05716-tnip2-primary-antibodyes-ihc-testing-3.jpgAnti-Abin-2 TNIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05716-tnip2-primary-antibodyes-ihc-testing-4.jpgAnti-Abin-2 TNIP2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nox3-antibody-a05715-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05715-nox3-primary-antibodies-ihc-testing-1.jpgAnti-NADPH oxidase 3 Nox3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using NOX3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05715-nox3-primary-antibodies-wb-testing-2.jpgAnti-NADPH oxidase 3 Nox3 AntibodyWestern Blot analysis of various cells using Nox3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05715-nox3-primary-antibodies-wb-testing-3.jpgAnti-NADPH oxidase 3 Nox3 AntibodyWestern blot analysis of various cell Lysate, antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cox10-antibody-a05710-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05710-cox10-primary-antibodies-wb-testing-2.jpgAnti-COX10 AntibodyWestern blot analysis of mouse-kidney mouse-brain Hela KB 293T lysis using COX10 antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05710-cox10-primary-antibodies-wb-testing-1.jpgAnti-COX10 AntibodyWestern blot analysis of lysate from HeLa cells, using COX10 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cpn-cat-antibody-a05704-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05704-cpn1-primary-antibodies-wb-testing-1.jpgAnti-CPN cat CPN1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using CPN1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05704-cpn1-primary-antibodies-wb-testing-2.jpgAnti-CPN cat CPN1 AntibodyWestern Blot analysis of Hela cells using CPN cat Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gprc6a-antibody-a05697-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05697-gprc6a-primary-antibodies-wb-testing-2.jpgAnti-GPRC6A AntibodyWestern Blot analysis of Jurkat cells using GPRC6A Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05697-gprc6a-primary-antibodies-wb-testing-3.jpgAnti-GPRC6A AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05697-gprc6a-primary-antibodies-wb-testing-4.jpgAnti-GPRC6A AntibodyWestern blot analysis of lysates from Jurkat cells, using GPRC6A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05697-gprc6a-primary-antibodies-if-testing-1.jpgAnti-GPRC6A AntibodyImmunofluorescence analysis of MCF7 cells, using GPRC6A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pipk-i-gamma-antibody-a05687-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05687-pip5k1c-primary-antibodies-wb-testing-2.jpgAnti-PIPK I gamma PIP5K1C AntibodyWestern Blot analysis of A549 cells using PIPK I γ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05687-pip5k1c-primary-antibodies-wb-testing-3.jpgAnti-PIPK I gamma PIP5K1C AntibodyWestern blot analysis of lysates from A549 cells, using PIP5K1C Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05687-pip5k1c-primary-antibodies-wb-testing-1.jpgAnti-PIPK I gamma PIP5K1C AntibodyWestern blot analysis of the lysates from HepG2 cells using PIP5K1C antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-m-rip-antibody-a05678-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05678-mprip-primary-antibodies-ihc-testing-1.jpgAnti-M-RIP MPRIP AntibodyImmunohistochemical analysis of paraffin-embedded human meningioma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05678-mprip-primary-antibodies-wb-testing-2.jpgAnti-M-RIP MPRIP AntibodyWestern Blot analysis of 293 cells using M-RIP Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-keratin-pan-antibody-a05667-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05667-krt2-primary-antibodies-wb-testing-2.jpgAnti-Keratin-pan KRT2 AntibodyWestern Blot analysis of Jurkat cells using Keratin-pan Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05667-krt2-primary-antibodies-wb-testing-3.jpgAnti-Keratin-pan KRT2 AntibodyWestern blot analysis of lysate from Jurkat cells, using Keratin-pan Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05667-krt2-primary-antibodies-ihc-testing-1.jpgAnti-Keratin-pan KRT2 AntibodyImmunohistochemical analysis of paraffin-embedded human-mammary-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tis11b-antibody-a05651-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05651-zfp36l1-primary-antibodies-wb-testing-2.jpgAnti-TIS11B ZFP36L1 AntibodyWestern Blot analysis of various cells using TIS11B Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05651-zfp36l1-primary-antibodies-wb-testing-3.jpgAnti-TIS11B ZFP36L1 AntibodyWestern blot analysis of lysates from Jurkat, HeLa, A549, and LOVO cells, using TISB Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05651-zfp36l1-primary-antibodies-ihc-testing-1.jpgAnti-TIS11B ZFP36L1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TISB Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-plakophilin-4-antibody-a05639-boster.html2026-03-24T05:09:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05639-pkp4-primary-antibodyes-wb-testing-1.jpgAnti-Plakophilin 4 PKP4 AntibodyWestern Blot (WB) analysis of Mouse Heart lysis using Plakophilin 4 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nup160-antibody-a05629-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05629-nup160-primary-antibodies-wb-testing-2.jpgAnti-Nup160 AntibodyWestern Blot analysis of Hela cells using Nup160 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05629-nup160-primary-antibodies-wb-testing-1.jpgAnti-Nup160 AntibodyWestern blot analysis of lysates from NIH/3T3, A549, and HepG2 cells, using NUP160 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd203c-antibody-a05615-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-wb-testing-1.jpgAnti-CD203c ENPP3 AntibodyWestern Blot (WB) analysis of Mouse Kidney lysis using CD203c antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-wb-testing-2.jpgAnti-CD203c ENPP3 AntibodyWestern Blot (WB) analysis of Rat Kidney HeLa 293T SH-SY5Y Mouse Kidney, Mouse Spleen, Mouse Lung, using ENPP3 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-wb-testing-3.jpgAnti-CD203c ENPP3 AntibodyWestern Blot (WB) analysis of K562, MCF7 cells using CD203c Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-ihc-testing-4.jpgAnti-CD203c ENPP3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Testis, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-ihc-testing-5.jpgAnti-CD203c ENPP3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Testis, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-enpp3-primary-antibodyes-ihc-testing-6.jpgAnti-CD203c ENPP3 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Prostate Cancer, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g003.jpgAnti-CD203c ENPP3 AntibodySRSF1 regulated alternative splicing of ENPP3 pre-mRNA. (A) StarBase and RBPDB databases were used to predict the potential RNA-binding protein (RBP) of ENPP3. (B) Illustration of two transcripts of ENPP3 gene and the potential binding sites of SRSF1 to the exon 21 of ENPP3 gene. H9C2 and AC-16 cells were transfected with shSRSF1. (C) RT-qPCR analysis of ENPP3 mRNA and lncRNA ENPP3 expression in cardiomyocytes. (D) The protein level of SRSF1 and ENPP3 was assessed by Western blotting. (E)&(F) The protein level of ENPP3 in the in vivo and in vitro models of CME was measured by Western blotting. (G)&(H) RIP assay validated the endogenous and exogenous binding of SRSF1 to ENPP3 pre-mRNA. (I) The wild type (WT) and mutant (MUT) ENPP3 splicing reporters containing SRSF1 binding sites were transfected into 293T cells. TRAP assay determined the interplay between SRSF1 and ENPP3 pre-mRNA. (J) H9C2 cells were transfected with shSRSF1 together with ENPP3 reporter-WT or ENPP3 reporter-MUT, and expression of ENPP3 mRNA/lncRNA and SRSF1 was assessed by RT-qPCR and Western blotting, respectively. H9C2 cells were transfected with SRSF1 overexpression plasmid together with ENPP3 reporter-WT or ENPP3 reporter-MUT. (K) The interaction between SRSF1 and ENPP3 mRNA was detected by RIP. (L) RT-qPCR and Western blotting analysis of ENPP3 mRNA/lncRNA and SRSF1 levels, respectively. For C, D, F-K, n=3. For E, n=6. Student's t test (for E, G) and one-way ANOVA (for C-F) were performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g004.jpgAnti-CD203c ENPP3 AntibodySRSF1 regulated alternative splicing of ENPP3 pre-mRNA. (A) StarBase and RBPDB databases were used to predict the potential RNA-binding protein (RBP) of ENPP3. (B) Illustration of two transcripts of ENPP3 gene and the potential binding sites of SRSF1 to the exon 21 of ENPP3 gene. H9C2 and AC-16 cells were transfected with shSRSF1. (C) RT-qPCR analysis of ENPP3 mRNA and lncRNA ENPP3 expression in cardiomyocytes. (D) The protein level of SRSF1 and ENPP3 was assessed by Western blotting. (E)&(F) The protein level of ENPP3 in the in vivo and in vitro models of CME was measured by Western blotting. (G)&(H) RIP assay validated the endogenous and exogenous binding of SRSF1 to ENPP3 pre-mRNA. (I) The wild type (WT) and mutant (MUT) ENPP3 splicing reporters containing SRSF1 binding sites were transfected into 293T cells. TRAP assay determined the interplay between SRSF1 and ENPP3 pre-mRNA. (J) H9C2 cells were transfected with shSRSF1 together with ENPP3 reporter-WT or ENPP3 reporter-MUT, and expression of ENPP3 mRNA/lncRNA and SRSF1 was assessed by RT-qPCR and Western blotting, respectively. H9C2 cells were transfected with SRSF1 overexpression plasmid together with ENPP3 reporter-WT or ENPP3 reporter-MUT. (K) The interaction between SRSF1 and ENPP3 mRNA was detected by RIP. (L) RT-qPCR and Western blotting analysis of ENPP3 mRNA/lncRNA and SRSF1 levels, respectively. For C, D, F-K, n=3. For E, n=6. Student's t test (for E, G) and one-way ANOVA (for C-F) were performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g005.jpgAnti-CD203c ENPP3 AntibodySRSF1 silencing suppressed cardiac inflammation in CME via modulation of ENPP3 splicing. H9C2 and AC-16 cells were transfected with shSRSF1, followed by stimulation with OGD. (A) Western blotting detected SRSF1 protein level. (B) Apoptosis of cardiomyocytes was detected by flow cytometry. (C) The production of TNF-α, IL-1β, and IL-6 was measured by ELISA. (D) RT-qPCR analysis of ENPP3 mRNA and lncRNA ENPP3 levels in each group. (E) The protein level of ENPP3 was determined by Western blotting. n=3 for A-E. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g006.jpgAnti-CD203c ENPP3 AntibodySRSF1 enhanced ENPP3 mRNA expression to trigger NF-κB p65-mediated transcription of pro-inflammatory cytokines. H9C2 and AC-16 cells were transfected with overexpression plasmid for ENPP3 or lncRNA ENPP3. (A) ENPP3 mRNA and lncRNA ENPP3 levels were evaluated by RT-qPCR. (B) Western blotting measured ENPP3 protein level in each group. (C) The mRNA levels of TNF-α, IL-1β, and IL-6 were assessed by RT-qPCR. (D) ELISA detected the release of TNF-α, IL-1β, and IL-6 from cardiomyocytes. (E) The binding of NF-κB p65 to the promoters of TNF-α, IL-1β, and IL-6 was determined by dual-luciferase reporter assay. H9C2 and AC-16 cells were transfected with shSRSF1, overexpression plasmid for ENPP3, or a combination of them. (F) ENPP3 mRNA and lncRNA ENPP3 levels were measured by RT-qPCR. (G) Western blotting analysis of ENPP3 protein level in cardiomyocytes. (H)&(I) The levels of TNF-α, IL-1β, and IL-6 in cardiomyocytes were evaluated by RT-qPCR and ELISA. (J) Dual-luciferase reporter assay analyzed the interaction between NF-κB p65 and the promoters of TNF-α, IL-1β, and IL-6. n=3 for A-J. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g007.jpgAnti-CD203c ENPP3 AntibodySRSF1 enhanced ENPP3 mRNA expression to trigger NF-κB p65-mediated transcription of pro-inflammatory cytokines. H9C2 and AC-16 cells were transfected with overexpression plasmid for ENPP3 or lncRNA ENPP3. (A) ENPP3 mRNA and lncRNA ENPP3 levels were evaluated by RT-qPCR. (B) Western blotting measured ENPP3 protein level in each group. (C) The mRNA levels of TNF-α, IL-1β, and IL-6 were assessed by RT-qPCR. (D) ELISA detected the release of TNF-α, IL-1β, and IL-6 from cardiomyocytes. (E) The binding of NF-κB p65 to the promoters of TNF-α, IL-1β, and IL-6 was determined by dual-luciferase reporter assay. H9C2 and AC-16 cells were transfected with shSRSF1, overexpression plasmid for ENPP3, or a combination of them. (F) ENPP3 mRNA and lncRNA ENPP3 levels were measured by RT-qPCR. (G) Western blotting analysis of ENPP3 protein level in cardiomyocytes. (H)&(I) The levels of TNF-α, IL-1β, and IL-6 in cardiomyocytes were evaluated by RT-qPCR and ELISA. (J) Dual-luciferase reporter assay analyzed the interaction between NF-κB p65 and the promoters of TNF-α, IL-1β, and IL-6. n=3 for A-J. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g010.jpgAnti-CD203c ENPP3 AntibodyENPP3 contributed to inflammation by inhibiting O-GlcNAcylation of BRD4. H9C2 and AC-16 cells were transfected with shENPP3, followed by exposure to OGD. (A) ENPP3 and BRD4 protein levels were measured by Western blotting. (B) The O-GlcNAc level of BRD4 protein was assessed. (C) The production of TNF-α, IL-1β, and IL-6 was determined by ELISA. (D) Dual-luciferase reporter assay evaluated the binding of NF-κB p65 to TNF-α, IL-1β, and IL-6 promoters. n=3 for A-D. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g011.jpgAnti-CD203c ENPP3 AntibodySRSF1/ENPP3 axis suppressed BRD4 O-GlcNAcylation to promote inflammation in CME. The OGD-stimulated cardiomyocytes were transfected with shSRSF1, ENPP3 overexpression plasmid, or a combination of them. (A) ENPP3 mRNA and lncRNA ENPP3 expression levels were detected by RT-qPCR. (B) The protein abundance of ENPP3 and BRD4 was assessed by Western blotting. (C) The O-GlcNAc level of BRD4 was determined. (D) ELISA was carried out to measure TNF-α, IL-1β, and IL-6 concentrations. n=3 for A-D. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05615-thnov15p6839g012.jpgAnti-CD203c ENPP3 AntibodyMyocardium-specific SRSF1 knockout alleviated CME-induced inflammation via inactivation of the ENPP3/BRD4/NF-κB pathway. SRSF1 flox/flox and SRSF1-KO rats were injected with microspheres into the left ventricle to induce CME. (A) LVEF, LVFS, LVEDd, and CO were detected to evaluate cardiac function. (B) The serum cTnl level in different groups was measured by ELISA. (C) Pathological alterations in myocardial tissues were observed by HE staining (scale bar = 100 μm). (D) Myocardial infarct size was measured by HBFP staining (scale bar = 100 μm). (E) SRSF1, ENPP3, and BRD4 expression in myocardial tissues was evaluated by immunohistochemical staining (scale bar = 100 μm). (F) The protein abundance of SRSF1, ENPP3, BRD4, p65, and O-GlcNAcylation of BRD4 was detected by Western blotting or Co-IP, respectively. (G) ELISA was carried out to measure TNF-α, IL-1β, and IL-6 concentrations. n=6 for A-G. ANOVA for repeated measurement (for A, B), and one-way ANOVA (for F, G) was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dfna5-antibody-a05604-1-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05604-1-dfna5-primary-antibodyes-wb-testing-1.jpgAnti-DFNA5 AntibodyWestern blot analysis of extracts from rat stomach, 293 cells, using DFNA5 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-qsk-antibody-a05580-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05580-sik3-primary-antibodyes-wb-testing-1.jpgAnti-QSK SIK3 AntibodyWestern blot analysis of LOVO cells using QSK Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05580-sik3-primary-antibodyes-ihc-testing-2.jpgAnti-QSK SIK3 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using QSK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr56-antibody-a05578-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05578-adgrg1-primary-antibodies-wb-testing-2.jpgAnti-GPR56 ADGRG1 AntibodyWestern Blot analysis of NIH-3T3 cells using GPR56 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05578-adgrg1-primary-antibodies-wb-testing-3.jpgAnti-GPR56 ADGRG1 AntibodyWestern blot analysis of lysates from K562 cells, using GPR56 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05578-adgrg1-primary-antibodies-if-testing-1.jpgAnti-GPR56 ADGRG1 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR56 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kid-antibody-a05570-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05570-kif22-primary-antibodies-wb-testing-2.jpgAnti-KID KIF22 Monoclonal AntibodyWestern Blot analysis using KID Monoclonal Antibody against HEK293 (1) and KID-hIgGFc transfected HEK293 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05570-kif22-primary-antibodies-ihc-testing-3.jpgAnti-KID KIF22 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded rectum cancer tissues with DAB staining using KID Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05570-kif22-primary-antibodies-fcm-testing-1.jpgAnti-KID KIF22 Monoclonal AntibodyFlow cytometric analysis of NIH/3T3 cells using KID Monoclonal Antibody (blue) and negative control (red).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tis11d-antibody-a05565-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05565-zfp36l2-primary-antibodies-wb-testing-2.jpgAnti-TIS11D ZFP36L2 AntibodyWestern Blot analysis of various cells using TIS11D Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05565-zfp36l2-primary-antibodies-wb-testing-3.jpgAnti-TIS11D ZFP36L2 AntibodyWestern blot analysis of lysates from A549 cells, using TISD Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05565-zfp36l2-primary-antibodies-ihc-testing-1.jpgAnti-TIS11D ZFP36L2 AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mip-5-antibody-a05563-boster.html2026-03-24T05:09:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05563-ccl15-primary-antibodyes-ihc-testing-1.jpgAnti-MIP-5 CCL15 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gdf-6-antibody-a05536-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05536-gdf6-primary-antibodyes-wb-testing-1.jpgAnti-GDF-6 AntibodyWestern Blot (WB) analysis of Rat Kidney cells using GDF-6 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05536-gdf6-primary-antibodyes-wb-testing-2.jpgAnti-GDF-6 AntibodyWestern Blot (WB) analysis of 293T using GDF-6 Polyclonal antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05536-gdf6-primary-antibodyes-wb-testing-3.jpgAnti-GDF-6 AntibodyWestern Blot (WB) analysis of Rat Kidney cells using GDF-6 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp8b1-antibody-a05518-1-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05518-1-cyp8b1-primary-antibodies-wb-testing-2.jpgAnti-CYP8B1 AntibodyWestern Blot analysis of various cells using CYP8B1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05518-1-cyp8b1-primary-antibodies-wb-testing-3.jpgAnti-CYP8B1 AntibodyWestern blot analysis of Cytochrome P450 8B1 Antibody. The lane on the right is blocked with the Cytochrome P450 8B1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05518-1-cyp8b1-primary-antibodies-wb-testing-4.jpgAnti-CYP8B1 AntibodyWestern blot analysis of the lysates from HT-29 cells using Cytochrome P450 8B1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05518-1-cyp8b1-primary-antibodies-ihc-testing-1.jpgAnti-CYP8B1 AntibodyImmunohistochemistryt analysis of paraffin-embedded human liver, using Cytochrome P450 8B1 Antibody. The lane on the right is blocked with the Cytochrome P450 8B1 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mct4-antibody-a05510-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05510-slc16a3-primary-antibodies-wb-testing-2.jpgAnti-MCT4 SLC16A3 AntibodyWestern Blot analysis of PC-3 cells using MCT4 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05510-slc16a3-primary-antibodies-wb-testing-1.jpgAnti-MCT4 SLC16A3 AntibodyWestern blot analysis of lysates from LOVO cells, using MOT4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-neil3-antibody-a05497-1-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05497-1-neil3-primary-antibodies-ihc-testing-1.jpgAnti-NEIL3/Nei3 AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05497-1-neil3-primary-antibodies-wb-testing-2.jpgAnti-NEIL3/Nei3 AntibodyWestern Blot analysis of various cells using NEIL3 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05497-1-neil3-primary-antibodies-wb-testing-3.jpgAnti-NEIL3/Nei3 AntibodyWestern blot analysis of lysates from HeLa, HepG2, HUVEC, and COLO cells, using NEIL3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cng-1-antibody-a05494-1-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05494-1-cnga1-primary-antibodies-wb-testing-1.jpgAnti-CNG-1 CNGA1 AntibodyWestern blot analysis of the lysates from HepG2 cells using CNGA1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05494-1-cnga1-primary-antibodies-wb-testing-2.jpgAnti-CNG-1 CNGA1 AntibodyWestern Blot analysis of HepG2 cells using CNG-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05494-1-cnga1-primary-antibodies-wb-testing-3.jpgAnti-CNG-1 CNGA1 AntibodyWestern blot analysis of CNGA1 Antibody. The lane on the right is blocked with the CNGA1 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chemokine-receptor-d6-antibody-a05491-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05491-ackr2-primary-antibodies-if-testing-1.jpgAnti-Chemokine Receptor D6 ACKR2 AntibodyImmunofluorescence analysis of COS7 cells, using CCBP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05491-ackr2-primary-antibodies-wb-testing-2.jpgAnti-Chemokine Receptor D6 ACKR2 AntibodyWestern Blot analysis of various cells using Chemokine Receptor D6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05491-ackr2-primary-antibodies-wb-testing-3.jpgAnti-Chemokine Receptor D6 ACKR2 AntibodyWestern blot analysis of lysates from HepG2 cells, using CCBP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05491-ackr2-primary-antibodies-wb-testing-4.jpgAnti-Chemokine Receptor D6 ACKR2 AntibodyWestern blot analysis of the lysates from HT-29 cells using CCBP2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05491-ackr2-primary-antibodies-ihc-testing-5.jpgAnti-Chemokine Receptor D6 ACKR2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hri-antibody-a05465-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05465-eif2ak1-primary-antibodies-wb-testing-2.jpgAnti-HRI EIF2AK1 AntibodyWestern Blot analysis of various cells using HRI Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05465-eif2ak1-primary-antibodies-wb-testing-3.jpgAnti-HRI EIF2AK1 AntibodyWestern blot analysis of lysates from A549 and COS7 cells, using EIF2AK1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05465-eif2ak1-primary-antibodies-wb-testing-4.jpgAnti-HRI EIF2AK1 AntibodyWestern blot analysis of the lysates from COLO205 cells using EIF2AK1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05465-eif2ak1-primary-antibodies-ihc-testing-5.jpgAnti-HRI EIF2AK1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05465-eif2ak1-primary-antibodies-if-testing-1.jpgAnti-HRI EIF2AK1 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nvl-antibody-a05446-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-nvl-primary-antibodies-wb-testing-1.jpgAnti-NVL AntibodyWestern Blot analysis of extracts from rat stomach, 293 cells, using NVL Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tef-antibody-a05436-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05436-tef-primary-antibodyes-wb-testing-1.jpgAnti-Thyrotroph embryonic factor TEF AntibodyWestern Blot (WB) analysis of specific cells using TEF Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgfr-5-antibody-a05416-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05416-fgfrl1-primary-antibodies-wb-testing-1.jpgAnti-FGFR-5 FGFRL1 AntibodyWestern Blot analysis of 3T3 cells using FGFR-5 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tfiih-p62-antibody-a05408-1-boster.html2026-03-24T05:09:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05408-1-gtf2h1-primary-antibodies-wb-testing-1.jpgAnti-TFIIH p62 GTF2H1 Monoclonal AntibodyWestern Blot analysis using TFIIH p62 Monoclonal Antibody against LNCAP, K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cysltr1-antibody-a05393-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05393-cysltr1-primary-antibodies-wb-testing-2.jpgAnti-CysLTR1/Cyslt1 AntibodyWestern Blot analysis of HeLa cells using CysLTR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05393-cysltr1-primary-antibodies-wb-testing-3.jpgAnti-CysLTR1/Cyslt1 AntibodyWestern blot analysis of lysates from COLO205, HT-29, and HeLa cells, using CYSLTR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05393-cysltr1-primary-antibodies-wb-testing-4.jpgAnti-CysLTR1/Cyslt1 AntibodyWestern blot analysis of the lysates from HT-29 cells using CYSLTR1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05393-cysltr1-primary-antibodies-if-testing-1.jpgAnti-CysLTR1/Cyslt1 AntibodyImmunofluorescence analysis of COS7 cells, using CYSLTR1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nup88-antibody-a05382-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05382-nup88-primary-antibodies-wb-testing-1.jpgAnti-Nup88 AntibodyWestern Blot analysis of extracts from K562 cells, using Nup88 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peroxin-7-antibody-a05365-1-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05365-1-pex7-primary-antibodies-wb-testing-2.jpgAnti-Peroxin 7 PEX7 AntibodyWestern Blot analysis of 3T3 cells using Peroxin 7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05365-1-pex7-primary-antibodies-wb-testing-3.jpgAnti-Peroxin 7 PEX7 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using PEX7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05365-1-pex7-primary-antibodies-ihc-testing-1.jpgAnti-Peroxin 7 PEX7 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PEX7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chordin-antibody-a05363-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05363-chrd-primary-antibodies-ihc-testing-1.jpgAnti-Chordin CHRD AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gabp-alpha-antibody-a05350-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05350-gabpa-primary-antibodies-if-testing-1.jpgAnti-GABP- alpha Monoclonal AntibodyConfocal immunofluorescence analysis of Hela cells using GABP-α Monoclonal Antibody (green). Red: Actin filaments have been labeled using DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05350-gabpa-primary-antibodies-wb-testing-2.jpgAnti-GABP- alpha Monoclonal AntibodyWestern Blot analysis using GABP-α Monoclonal Antibody against HeLa (1), A549 (2), MCF-7 (3), NIH/3T3 (4) and SMMC-7721 (5) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mena-antibody-a05337-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05337-enah-primary-antibodies-wb-testing-2.jpgAnti-Mena ENAH AntibodyWestern Blot analysis of 293 cells using Mena Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05337-enah-primary-antibodies-wb-testing-3.jpgAnti-Mena ENAH AntibodyWestern blot analysis of lysates from HepG2 cells, using ENAH Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05337-enah-primary-antibodies-ihc-testing-1.jpgAnti-Mena ENAH AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ENAH Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mage-c2-antibody-a05335-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05335-magec2-primary-antibodies-wb-testing-1.jpgAnti-MAGE-C2 AntibodyWestern blot analysis of MAGEC2 Antibody. The lane on the right is blocked with the MAGEC2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05335-magec2-primary-antibodies-wb-testing-2.jpgAnti-MAGE-C2 AntibodyWestern Blot analysis of 293 cells using MAGE-C2 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05335-magec2-primary-antibodies-wb-testing-3.jpgAnti-MAGE-C2 AntibodyWestern blot analysis of mouse-brain HELA KB SH-SY5Y 293T 3T3 lysis using MAGE-C2 antibody. Antibody was diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aldolase-c-antibody-a05296-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05296-aldoc-primary-antibodies-wb-testing-2.jpgAnti-Aldolase C ALDOC AntibodyWestern Blot analysis of mouse liver, mouse spinal cord cells using Aldolase C Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05296-aldoc-primary-antibodies-wb-testing-3.jpgAnti-Aldolase C ALDOC AntibodyWestern blot analysis of lysate from mouse liver cells, using ALDOC Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05296-aldoc-primary-antibodies-ihc-testing-1.jpgAnti-Aldolase C ALDOC AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ctack-antibody-a05293-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05293-ccl27-primary-antibodies-wb-testing-2.jpgAnti-CTACK CCL27 AntibodyWestern blot analysis of mouse-kidney lysis using CCL27 antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05293-ccl27-primary-antibodies-wb-testing-3.jpgAnti-CTACK CCL27 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05293-ccl27-primary-antibodies-ihc-testing-1.jpgAnti-CTACK CCL27 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-achr-alpha9-antibody-a05280-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05280-chrna9-primary-antibodies-wb-testing-1.jpgAnti-AChR alpha9 CHRNA9 AntibodyWestern blot analysis of 293T lysis using CHRNA9 antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd37-antibody-a05276-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05276-cd37-primary-antibodies-wb-testing-1.jpgAnti-Leukocyte antigen CD37 CD37 AntibodyWestern Blot analysis of HeLa cells using CD37 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd37-antibody-a05276-1-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05276-1-cd37-primary-antibodies-if-testing-1.jpgAnti-CD37 Monoclonal AntibodyConfocal immunofluorescence analysis of methanol-fixed BCBL-1 (left) and L1210 (right) cells using CD37 Monoclonal Antibody (green), showing membrane localization. Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-31r-alpha-antibody-a05256-boster.html2026-03-24T05:09:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05256-il31ra-primary-antibodies-wb-testing-1.jpgAnti-IL-31R alpha AntibodyWestern Blot analysis of extracts from Jurkat cells, using IL-31R Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-helios-antibody-a05228-1-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05228-1-ikzf2-primary-antibodyes-wb-testing-1.jpgAnti-Helios IKZF2 AntibodyWestern blot analysis of Hela cells using Helios Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003, Inventbiotech, MN, USA).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05228-1-ikzf2-primary-antibodyes-wb-testing-2.jpgAnti-Helios IKZF2 AntibodyWestern blot analysis of the lysates from HeLa cells using IKZF2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-usp11-antibody-a05225-1-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05225-1-usp11-primary-antibodies-wb-testing-2.jpgAnti-USP11 AntibodyWestern Blot analysis of 293 cells using USP11 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05225-1-usp11-primary-antibodies-if-testing-3.jpgAnti-USP11 AntibodyImmunofluorescence analysis of human-uterus tissue. 1, USP11 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05225-1-usp11-primary-antibodies-if-testing-1.jpgAnti-USP11 AntibodyImmunofluorescence analysis of human-lung tissue. 1, USP11 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ulk2-antibody-a05219-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05219-ulk2-primary-antibodies-wb-testing-1.jpgAnti-ULK2 AntibodyWestern Blot analysis of HELA cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clk2-antibody-a05206-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05206-clk2-primary-antibodies-wb-testing-2.jpgAnti-CLK2 AntibodyWestern Blot analysis of various cells using CLK2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05206-clk2-primary-antibodies-wb-testing-3.jpgAnti-CLK2 AntibodyWestern Blot analysis of A549 cells using CLK2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05206-clk2-primary-antibodies-wb-testing-4.jpgAnti-CLK2 AntibodyWestern blot analysis of lysates from COLO205 and A549 cells, using CLK2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05206-clk2-primary-antibodies-ihc-testing-1.jpgAnti-CLK2 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rgs10-antibody-a05197-1-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05197-1-rgs10-primary-antibodies-ihc-testing-1.jpgAnti-RGS10 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05197-1-rgs10-primary-antibodies-wb-testing-2.jpgAnti-RGS10 AntibodyWestern Blot analysis of various cells using RGS10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05197-1-rgs10-primary-antibodies-wb-testing-3.jpgAnti-RGS10 AntibodyWestern blot analysis of RGS10 Antibody. The lane on the right is blocked with the RGS10 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-igd-antibody-a05183-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05183-ighd-primary-antibodyes-ihc-testing-1.jpgAnti-IgD IGHD AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-csh1-antibody-a05177-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05177-csh1-primary-antibodyes-wb-testing-1.jpgAnti-CSH1/Placental Lactogen AntibodyWestern Blot (WB) analysis of Mouse Brain cells using antibody diluted at 1:800.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mmp-19-antibody-a05171-1-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-1-mmp19-primary-antibodies-ihc-testing-1.jpgAnti-MMP-19 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using MMP-19 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-1-mmp19-primary-antibodies-wb-testing-2.jpgAnti-MMP-19 AntibodyWestern Blot analysis of various cells using MMP-19 Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ar-alpha2c-antibody-a05170-boster.html2026-03-24T05:09:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05170-adra2c-primary-antibodies-wb-testing-2.jpgAnti-AR alpha2C ADRA2C AntibodyWestern Blot analysis of various cells using AR α2C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05170-adra2c-primary-antibodies-wb-testing-3.jpgAnti-AR alpha2C ADRA2C AntibodyWestern blot analysis of lysates from HepG2 cells, using Adrenergic Receptor alpha-2C Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05170-adra2c-primary-antibodies-wb-testing-1.jpgAnti-AR alpha2C ADRA2C AntibodyWestern blot analysis of the lysates from HeLa cells using Adrenergic Receptor α-2C antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tug-antibody-a05168-1-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05168-1-aspscr1-primary-antibodyes-wb-testing-1.jpgAnti-TUG ASPSCR1 Monoclonal AntibodyWestern Blot (WB) analysis using TUG Monoclonal antibody against NIH/3T3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mox-2-antibody-a05167-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05167-meox2-primary-antibodies-ihc-testing-1.jpgAnti-MOX-2 MEOX2 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05167-meox2-primary-antibodies-wb-testing-2.jpgAnti-MOX-2 MEOX2 AntibodyWestern Blot analysis of various cells using MOX-2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05167-meox2-primary-antibodies-wb-testing-3.jpgAnti-MOX-2 MEOX2 AntibodyWestern Blot analysis of COLO205 cells using MOX-2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05167-meox2-primary-antibodies-wb-testing-4.jpgAnti-MOX-2 MEOX2 AntibodyWestern blot analysis of lysates from COLO205 cells, using MEOX2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-daam1-antibody-a05163-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05163-daam1-primary-antibodies-wb-testing-1.jpgAnti-DAAM1 AntibodyWestern blot analysis of SW480 MCF7 lysate, antibody was diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cabc1-antibody-a05162-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05162-adck3-primary-antibodies-wb-testing-2.jpgAnti-CABC1 ADCK3 AntibodyWestern Blot analysis of various cells using CABC1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05162-adck3-primary-antibodies-wb-testing-3.jpgAnti-CABC1 ADCK3 AntibodyWestern Blot analysis of COLO205 cells using CABC1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05162-adck3-primary-antibodies-wb-testing-4.jpgAnti-CABC1 ADCK3 AntibodyWestern blot analysis of lysates from HepG2 and mouse muscle cells, using ADCK3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05162-adck3-primary-antibodies-ihc-testing-1.jpgAnti-CABC1 ADCK3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdkn3-antibody-a05157-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05157-cdkn3-primary-antibodies-wb-testing-2.jpgAnti-CDKN3 AntibodyWestern Blot analysis of SH-SY5Y cells using CDKN3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05157-cdkn3-primary-antibodies-wb-testing-3.jpgAnti-CDKN3 AntibodyWestern blot analysis of lysates from LOVO cells, using CDKN3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05157-cdkn3-primary-antibodies-ihc-testing-1.jpgAnti-CDKN3 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-20-antibody-a05124-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05124-il20-primary-antibodies-ihc-testing-1.jpgAnti-IL-20 AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-25-antibody-a05115-boster.html2026-03-24T05:09:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05115-rab25-primary-antibodies-wb-testing-2.jpgAnti-Rab 25 Monoclonal AntibodyWestern Blot analysis using Rab 25 Monoclonal Antibody against MCF-7 (1), T47D (2) and GC7901 (3) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05115-rab25-primary-antibodies-ihc-testing-3.jpgAnti-Rab 25 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded esophagus tissues (left) and human lung cancer (right) with DAB staining using Rab 25 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05115-rab25-primary-antibodies-if-testing-4.jpgAnti-Rab 25 Monoclonal AntibodyImmunofluorescence analysis of A549 cells using Rab 25 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05115-rab25-primary-antibodies-fcm-testing-1.jpgAnti-Rab 25 Monoclonal AntibodyFlow cytometric analysis of NIH/3T3 cells using Rab 25 Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hurp-antibody-a05112-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05112-dlgap5-primary-antibodies-wb-testing-1.jpgAnti-HURP DLGAP5 AntibodyWestern blot analysis of the lysates from HT-29 cells using DLGAP5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05112-dlgap5-primary-antibodies-wb-testing-2.jpgAnti-HURP DLGAP5 AntibodyWestern Blot analysis of A549 cells using HURP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05112-dlgap5-primary-antibodies-wb-testing-3.jpgAnti-HURP DLGAP5 AntibodyWestern blot analysis of lysates from A549, 293, and HUVEC cells, using DLGAP5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-pol-delta3-antibody-a05111-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05111-pold3-primary-antibodies-wb-testing-2.jpgAnti-DNA pol delta3 POLD3 AntibodyWestern Blot analysis of hela cells using DNA pol δ3 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05111-pold3-primary-antibodies-wb-testing-1.jpgAnti-DNA pol delta3 POLD3 AntibodyWestern blot analysis of lysates from LOVO, HepG2, and mouse brain cells, using POLD3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-adducin-beta-antibody-a05106-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05106-add2-primary-antibodies-wb-testing-2.jpgAnti-Adducin beta ADD2 AntibodyWestern Blot analysis of various cells using Adducin β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05106-add2-primary-antibodies-wb-testing-3.jpgAnti-Adducin beta ADD2 AntibodyWestern Blot analysis of 293 cells using Adducin β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05106-add2-primary-antibodies-wb-testing-4.jpgAnti-Adducin beta ADD2 AntibodyWestern blot analysis of lysates from 293 cells, using ADD2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05106-add2-primary-antibodies-if-testing-1.jpgAnti-Adducin beta ADD2 AntibodyImmunofluorescence analysis of HeLa cells, using ADD2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cgkii-antibody-a05103-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05103-prkg2-primary-antibodies-wb-testing-2.jpgAnti-cGKII PRKG2 AntibodyWestern Blot analysis of various cells using cGKII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05103-prkg2-primary-antibodies-wb-testing-3.jpgAnti-cGKII PRKG2 AntibodyWestern Blot analysis of HuvEc cells using cGKII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05103-prkg2-primary-antibodies-wb-testing-4.jpgAnti-cGKII PRKG2 AntibodyWestern blot analysis of lysates from HUVEC cells, using CGK 2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05103-prkg2-primary-antibodies-ihc-testing-1.jpgAnti-cGKII PRKG2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd180-antibody-a05085-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05085-cd180-primary-antibodies-wb-testing-2.jpgAnti-CD180/Rp105 AntibodyWestern Blot analysis of mouse brain cells using CD180 Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05085-cd180-primary-antibodies-wb-testing-1.jpgAnti-CD180/Rp105 AntibodyWestern Blot analysis of MOUSE-BRAIN cells using CD180 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jip-1-antibody-a05068-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05068-mapk8ip1-primary-antibodies-wb-testing-2.jpgAnti-JIP-1 MAPK8IP1 AntibodyWestern Blot analysis of COLO205 cells using JIP-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05068-mapk8ip1-primary-antibodies-wb-testing-3.jpgAnti-JIP-1 MAPK8IP1 AntibodyWestern blot analysis of lysates from COLO205 cells, treated with Serum 20% 15', using JIP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05068-mapk8ip1-primary-antibodies-ihc-testing-4.jpgAnti-JIP-1 MAPK8IP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using JIP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05068-mapk8ip1-primary-antibodies-if-testing-1.jpgAnti-JIP-1 MAPK8IP1 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using JIP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-actin-alpha3-antibody-a05066-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05066-actg2-primary-antibodies-ihc-testing-1.jpgAnti-Actin alpha3 ACTG2 AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using Actin-gamma2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05066-actg2-primary-antibodies-wb-testing-2.jpgAnti-Actin alpha3 ACTG2 AntibodyWestern Blot analysis of various cells using Actin α3 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05066-actg2-primary-antibodies-wb-testing-3.jpgAnti-Actin alpha3 ACTG2 AntibodyWestern Blot analysis of COLO205 cells using Actin α3 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05066-actg2-primary-antibodies-wb-testing-4.jpgAnti-Actin alpha3 ACTG2 AntibodyWestern blot analysis of lysates from COLO205 cells, using Actin-gamma2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-adducin-gamma-antibody-a05046-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05046-add3-primary-antibodyes-wb-testing-1.jpgAnti-Adducin gamma ADD3 AntibodyWestern Blot (WB) analysis of HepG2 cells using Adducin gamma Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05046-add3-primary-antibodyes-wb-testing-2.jpgAnti-Adducin gamma ADD3 AntibodyWestern Blot (WB) analysis of specific cells using Adducin gamma Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mylip-antibody-a05031-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05031-mylip-primary-antibodies-ihc-testing-1.jpgAnti-MYLIP AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MYLIP Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05031-mylip-primary-antibodies-wb-testing-2.jpgAnti-MYLIP AntibodyWestern Blot analysis of Jurkat cells using MYLIP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05031-mylip-primary-antibodies-wb-testing-3.jpgAnti-MYLIP AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using MYLIP Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hps-1-antibody-a05026-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05026-hps1-primary-antibodies-wb-testing-1.jpgAnti-HPS-1 Monoclonal AntibodyWestern Blot analysis using HPS-1 Monoclonal Antibody against truncated HPS1 recombinant protein (1) and HPS1-hIgGFc transfected CHO-K1 cell lysate (2).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-thrombospondin-4-antibody-a05024-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05024-thbs4-primary-antibodies-ihc-testing-1.jpgAnti-Thrombospondin 4 THBS4 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nhe-6-antibody-a05023-1-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05023-1-slc9a6-primary-antibodies-wb-testing-1.jpgAnti-NHE-6 SLC9A6 AntibodyWestern blot analysis of the lysates from COLO205 cells using SLC9A6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05023-1-slc9a6-primary-antibodies-wb-testing-2.jpgAnti-NHE-6 SLC9A6 AntibodyWestern Blot analysis of RAW cells using NHE-6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05023-1-slc9a6-primary-antibodies-wb-testing-3.jpgAnti-NHE-6 SLC9A6 AntibodyWestern blot analysis of SLC9A6 Antibody. The lane on the right is blocked with the SLC9A6 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-oatp1-antibody-a05001-boster.html2026-03-24T05:09:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05001-slco1a2-primary-antibodies-wb-testing-1.jpgAnti-OATP1 SLCO1A2 AntibodyWestern blot analysis of lysates from HeLa, MCF-7, and HepG2 cells, using SLCO1A2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05001-slco1a2-primary-antibodies-wb-testing-2.jpgAnti-OATP1 SLCO1A2 AntibodyWestern Blot analysis of various cells using OATP1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05001-slco1a2-primary-antibodies-wb-testing-3.jpgAnti-OATP1 SLCO1A2 AntibodyWestern Blot analysis of A549 AD293 HEPG2 using OATP1 Polyclonal Antibody. Antibody was diluted at 1:2000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-plasma-kallikrein-hc-r390-antibody-a04995-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04995-klkb1-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Plasma Kallikrein HC (R390) KLKB1 AntibodyWestern Blot analysis of HeLa cells using Cleaved-Plasma Kallikrein HC (R390) Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04995-klkb1-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-Plasma Kallikrein HC (R390) KLKB1 AntibodyWestern blot analysis of lysates from HeLa cells, using KLKB1 (heavy chain, Cleaved-Arg390) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nectin-1-antibody-a04988-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04988-nectin1-primary-antibodies-wb-testing-2.jpgAnti-Nectin 1 AntibodyWestern Blot analysis of KB cells using Nectin 1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04988-nectin1-primary-antibodies-wb-testing-1.jpgAnti-Nectin 1 AntibodyWestern Blot analysis of KB cells using Nectin 1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nlrx1-antibody-a04980-1-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04980-1-nlrx1-primary-antibodies-wb-testing-2.jpgAnti-NLRX1/Nod9 AntibodyWestern Blot analysis of HEPG2 Hela cells using NLRX1 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04980-1-nlrx1-primary-antibodies-ihc-testing-3.jpgAnti-NLRX1/Nod9 AntibodyImmunohistochemical analysis of paraffin-embedded human-heart, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04980-1-nlrx1-primary-antibodies-ihc-testing-1.jpgAnti-NLRX1/Nod9 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ifitm2-antibody-a04964-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04964-ifitm2-primary-antibodyes-wb-testing-1.jpgAnti-IFITM2 AntibodyWestern Blot (WB) analysis of HeLa cells using IFITM2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd93-antibody-a04939-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04939-cd93-primary-antibodies-wb-testing-2.jpgAnti-CD93/C1Q R1 AntibodyWestern Blot analysis of KB cells using CD93 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04939-cd93-primary-antibodies-wb-testing-1.jpgAnti-CD93/C1Q R1 AntibodyWestern Blot analysis of KB cells using CD93 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-faim2-antibody-a04900-boster.html2026-03-24T05:09:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04900-faim2-primary-antibodies-wb-testing-1.jpgAnti-Protein lifeguard 2 FAIM2 AntibodyWestern Blot analysis of extracts from Jurkat cells, using FAIM2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cln5-antibody-a04893-1-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04893-1-cln5-primary-antibodies-wb-testing-2.jpgAnti-CLN5 AntibodyWestern Blot analysis of 293T cells using CLN5 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04893-1-cln5-primary-antibodies-wb-testing-3.jpgAnti-CLN5 AntibodyWestern blot analysis of CLN5 Antibody. The lane on the right is blocked with the CLN5 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04893-1-cln5-primary-antibodies-wb-testing-1.jpgAnti-CLN5 AntibodyWestern blot analysis of the lysates from COLO205 cells using CLN5 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cnot7-antibody-a04884-1-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04884-1-cnot7-primary-antibodies-wb-testing-2.jpgAnti-CNOT7 AntibodyWestern Blot analysis of various cells using CNOT7 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04884-1-cnot7-primary-antibodies-wb-testing-3.jpgAnti-CNOT7 AntibodyWestern blot analysis of lysates from HeLa and HUVEC cells, using CNOT7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04884-1-cnot7-primary-antibodies-wb-testing-4.jpgAnti-CNOT7 AntibodyWestern blot analysis of the lysates from HUVECcells using CNOT7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04884-1-cnot7-primary-antibodies-ihc-testing-1.jpgAnti-CNOT7 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cathepsin-e-antibody-a04874-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04874-ctse-primary-antibodies-ihc-testing-1.jpgAnti-Cathepsin E CTSE AntibodyImmunohistochemistry analysis of Cathepsin E antibody in paraffin-embedded human lung carcinoma tissue.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04874-ctse-primary-antibodies-wb-testing-2.jpgAnti-Cathepsin E CTSE AntibodyWestern Blot analysis of various cells using Cathepsin E Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04874-ctse-primary-antibodies-wb-testing-3.jpgAnti-Cathepsin E CTSE AntibodyWestern blot analysis of lysate from HUVEC cells, using Cathepsin E antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd84-antibody-a04872-1-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04872-1-cd84-primary-antibodies-wb-testing-2.jpgAnti-CD84/Slamf5 AntibodyWestern Blot analysis of K562, L929 cells using CD84 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04872-1-cd84-primary-antibodies-wb-testing-3.jpgAnti-CD84/Slamf5 AntibodyWestern blot analysis of lysate from K562 cells, using CD84 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04872-1-cd84-primary-antibodies-ihc-testing-4.jpgAnti-CD84/Slamf5 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04872-1-cd84-primary-antibodies-ihc-testing-1.jpgAnti-CD84/Slamf5 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jdp2-antibody-a04870-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04870-jdp2-primary-antibodyes-wb-testing-1.jpgAnti-Jun dimerization protein 2 JDP2 AntibodyWestern Blot (WB) analysis of Jurkat cells using JDP2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lrrfip1-antibody-a04854-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04854-lrrfip1-primary-antibodies-wb-testing-1.jpgAnti-LRRFIP1 Monoclonal AntibodyWestern Blot analysis using LRRFIP1 Monoclonal Antibody against Raji, C2C12, MCF7, Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-relaxin-receptor-2-antibody-a04848-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04848-rxfp2-primary-antibodies-wb-testing-2.jpgAnti-Relaxin Receptor 2 RXFP2 AntibodyWestern blot analysis of lysates from Jurkat cells, using RXFP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04848-rxfp2-primary-antibodies-wb-testing-3.jpgAnti-Relaxin Receptor 2 RXFP2 AntibodyWestern blot analysis of the lysates from HUVECcells using RXFP2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04848-rxfp2-primary-antibodies-ihc-testing-1.jpgAnti-Relaxin Receptor 2 RXFP2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cop1-antibody-a04843-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04843-rfwd2-primary-antibodies-wb-testing-1.jpgAnti-COP1 RFWD2 AntibodyWestern blot analysis of 293T lysis using COP1 antibody. Antibody was diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-psd-93-antibody-a04826-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04826-dlg2-primary-antibodies-ihc-testing-1.jpgAnti-PSD-93 DLG2 AntibodyImmunohistochemistryt analysis of paraffin-embedded human brain, using DLG2 Antibody. The lane on the right is blocked with the DLG2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04826-dlg2-primary-antibodies-wb-testing-2.jpgAnti-PSD-93 DLG2 AntibodyWestern Blot analysis of 293T-UV cells using PSD-93 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04826-dlg2-primary-antibodies-wb-testing-3.jpgAnti-PSD-93 DLG2 AntibodyWestern blot analysis of DLG2 Antibody. The lane on the right is blocked with the DLG2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04826-dlg2-primary-antibodies-wb-testing-4.jpgAnti-PSD-93 DLG2 AntibodyWestern blot analysis of the lysates from HeLa cells using DLG2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clasp1-antibody-a04813-1-boster.html2026-03-24T05:09:18+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-3-gap-p130-antibody-a04789-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04789-rab3gap1-primary-antibodies-wb-testing-2.jpgAnti-Rab 3 GAP p130 RAB3GAP1 AntibodyWestern Blot analysis of various cells using Rab 3 GAP p130 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04789-rab3gap1-primary-antibodies-wb-testing-3.jpgAnti-Rab 3 GAP p130 RAB3GAP1 AntibodyWestern blot analysis of lysates from 293 cells, using RAB3GAP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04789-rab3gap1-primary-antibodies-ihc-testing-1.jpgAnti-Rab 3 GAP p130 RAB3GAP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using RAB3GAP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-snrp116-antibody-a04780-boster.html2026-03-24T05:09:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04780-eftud2-primary-antibodies-wb-testing-2.jpgAnti-Snrp116 EFTUD2 AntibodyWestern Blot analysis of various cells using Snrp116 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04780-eftud2-primary-antibodies-wb-testing-3.jpgAnti-Snrp116 EFTUD2 AntibodyWestern blot analysis of lysates from 293 and HUVEC cells, using EFTUD2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04780-eftud2-primary-antibodies-ihc-testing-1.jpgAnti-Snrp116 EFTUD2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using EFTUD2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aralar-antibody-a04746-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04746-slc25a12-primary-antibodies-wb-testing-2.jpgAnti-ARALAR SLC25A12 AntibodyWestern Blot analysis of various cells using ARALAR Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04746-slc25a12-primary-antibodies-wb-testing-3.jpgAnti-ARALAR SLC25A12 AntibodyWestern Blot analysis of HEPG2 cells using ARALAR Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04746-slc25a12-primary-antibodies-ihc-testing-1.jpgAnti-ARALAR SLC25A12 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using CMC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hnrnp-g-antibody-a04738-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-rbmx-primary-antibodies-wb-testing-2.jpgAnti-hnRNP G RBMX AntibodyWestern Blot analysis of various cells using hnRNP G Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-rbmx-primary-antibodies-wb-testing-3.jpgAnti-hnRNP G RBMX AntibodyWestern blot analysis of lysates from HeLa cells, using hnRNP G Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-rbmx-primary-antibodies-ihc-testing-4.jpgAnti-hnRNP G RBMX AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-rbmx-primary-antibodies-if-testing-1.jpgAnti-hnRNP G RBMX AntibodyImmunofluorescence analysis of HepG2 cells, using hnRNP G Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chp-antibody-a04737-1-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04737-1-chp1-primary-antibodies-wb-testing-1.jpgAnti-CHP CHP1 AntibodyWestern Blot analysis of HeLa cells using CHP Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp5-antibody-a04723-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04723-ppp5c-primary-antibodies-wb-testing-1.jpgAnti-PP5 PPP5C Monoclonal AntibodyWestern Blot analysis using PP5 Monoclonal Antibody against HeLa, Jurkat, 293T, A431, MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd238-antibody-a04711-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04711-kel-primary-antibodies-ihc-testing-1.jpgAnti-CD238 KEL AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04711-kel-primary-antibodies-wb-testing-2.jpgAnti-CD238 KEL AntibodyWestern Blot analysis of mouse-heart cells using CD238 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gpr120-antibody-a04709-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04709-ffar4-primary-antibodyes-wb-testing-1.jpgAnti-GPR120 FFAR4 AntibodyWestern blot analysis of HEPG2-UV cells using GPR120 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04709-ffar4-primary-antibodyes-wb-testing-2.jpgAnti-GPR120 FFAR4 AntibodyWestern blot analysis of various cells using GPR120 Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rpa14-antibody-a04696-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04696-rpa3-primary-antibodies-wb-testing-2.jpgAnti-RPA14 RPA3 AntibodyWestern blot analysis of lysate, antibody was diluted at 2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04696-rpa3-primary-antibodies-ihc-testing-1.jpgAnti-RPA14 RPA3 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-factor-xiii-b-antibody-a04664-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04664-f13b-primary-antibodies-wb-testing-2.jpgAnti-Factor XIII B F13B AntibodyWestern blot analysis of varias lysis using F13B antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04664-f13b-primary-antibodies-ihc-testing-1.jpgAnti-Factor XIII B F13B AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hic-5-antibody-a04630-boster.html2026-03-24T05:09:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04630-tgfb1i1-primary-antibodies-if-testing-1.jpgAnti-Hic-5 TGFB1I1 AntibodyImmunofluorescence analysis of HeLa cells, using Hic-5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04630-tgfb1i1-primary-antibodies-wb-testing-2.jpgAnti-Hic-5 TGFB1I1 AntibodyWestern Blot analysis of NIH-3T3 cells using Hic-5 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04630-tgfb1i1-primary-antibodies-ihc-testing-3.jpgAnti-Hic-5 TGFB1I1 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using Hic-5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdz-rhogef-antibody-a04614-1-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04614-1-arhgef11-primary-antibodyes-wb-testing-1.jpgAnti-PDZ-RhoGEF ARHGEF11 AntibodyWestern Blot (WB) analysis of specific cells using PDZ-RhoGEF Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-g-alpha-t1-antibody-a04598-1-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04598-1-gnat1-primary-antibodies-wb-testing-1.jpgAnti-G alpha t1 AntibodyWestern blot analysis of lysates from COLO cells, using GNAT1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04598-1-gnat1-primary-antibodies-wb-testing-2.jpgAnti-G alpha t1 AntibodyWestern Blot analysis of various cells using Gα t1 Polyclonal Antibody diluted at 1:2000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-igg1-antibody-a04575-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04575-ighg1-primary-antibodies-wb-testing-2.jpgAnti-IgG1 AntibodyWestern Blot analysis of colo cells using IgG1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04575-ighg1-primary-antibodies-wb-testing-3.jpgAnti-IgG1 AntibodyWestern blot analysis of lysate from LOVO cells, using IgG1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04575-ighg1-primary-antibodies-ihc-testing-1.jpgAnti-IgG1 AntibodyImmunohistochemistry analysis of IgG1 antibody in paraffin-embedded human lung carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-torc3-antibody-a04568-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04568-crtc3-primary-antibodies-wb-testing-2.jpgAnti-TORC3 CRTC3 Monoclonal AntibodyWestern Blot analysis using TORC3 Monoclonal Antibody against HeLa (1), Jurkat (2), Cos7 (3) and MCF-7 (4) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04568-crtc3-primary-antibodies-ihc-testing-3.jpgAnti-TORC3 CRTC3 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded breast cancer (left) and ovarian cancer (right) with DAB staining using TORC3 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04568-crtc3-primary-antibodies-if-testing-4.jpgAnti-TORC3 CRTC3 Monoclonal AntibodyImmunofluorescence analysis of NTERA-2 cells using TORC3 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-thc2-antibody-a04567-1-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04567-1-mastl-primary-antibodyes-wb-testing-1.jpgAnti-THC2 MASTL AntibodyWestern Blot (WB) analysis of specific cells using THC2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col9a1-antibody-a04554-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04554-col9a1-primary-antibodyes-wb-testing-1.jpgAnti-COL9A1 AntibodyWestern Blot (WB) analysis of HepG2 cells using COL9A1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-myh14-antibody-a04528-1-boster.html2026-03-24T05:09:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-1-myh14-primary-antibodyes-wb-testing-1.jpgAnti-MYH14/Myosin Heavy Chain AntibodyWestern Blot (WB) analysis of specific cells using MYH14 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-13r-alpha1-antibody-a04527-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04527-il13ra1-primary-antibodyes-wb-testing-1.jpgAnti-IL-13R alpha1 IL13RA1 AntibodyWestern Blot (WB) analysis of specific cells using IL-13Ralpha1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbl1xr1-antibody-a04524-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04524-tbl1xr1-primary-antibodyes-ihc-testing-1.jpgAnti-TBL1XR1/Tblr1 Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded huma breast cancer using TBL1XR1 Monoclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04524-tbl1xr1-primary-antibodyes-wb-testing-2.jpgAnti-TBL1XR1/Tblr1 Monoclonal AntibodyWestern Blot (WB) analysis using TBL1XR1 Monoclonal antibody against Mouse Brain, Mouse Heart, K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04524-tbl1xr1-primary-antibodyes-if-testing-3.jpgAnti-TBL1XR1/Tblr1 Monoclonal AntibodyImmunofluorescence (IF) analysis of HeLa cells using TBL1XR1 Monoclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lunatic-fringe-antibody-a04513-1-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04513-1-lfng-primary-antibodies-wb-testing-2.jpgAnti-Lunatic Fringe LFNG AntibodyWestern Blot analysis of 3T3 cells using Lunatic Fringe Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04513-1-lfng-primary-antibodies-wb-testing-1.jpgAnti-Lunatic Fringe LFNG AntibodyWestern blot analysis of lysates from HUVEC and MCF-7 cells, using LFNG Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cas-antibody-a04496-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04496-cse1l-primary-antibodyes-wb-testing-1.jpgAnti-CAS CSE1L AntibodyWestern Blot (WB) analysis of specific cells using CAS Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-wdr79-antibody-a04484-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04484-wrap53-primary-antibodies-wb-testing-1.jpgAnti-WDR79 WRAP53 Monoclonal AntibodyWestern Blot analysis using WDR79 Monoclonal Antibody against HeLa, U2OS cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdc-e2-antibody-a04469-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04469-dlat-primary-antibodies-wb-testing-1.jpgAnti-PDC-E2 Monoclonal Antibody Western Blot analysis using PDC-E2 Monoclonal Antibody against Jurkat, A549, U251, F9, LNCAP, HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bmp-3a-antibody-a04449-1-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04449-1-bmp3-primary-antibodies-wb-testing-2.jpgAnti-BMP-3A AntibodyWestern Blot analysis of Jurkat cells using BMP-3A Polyclonal Antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04449-1-bmp3-primary-antibodies-wb-testing-3.jpgAnti-BMP-3A AntibodyWestern blot analysis of lysate from Jurkat cells, using BMP3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04449-1-bmp3-primary-antibodies-ihc-testing-1.jpgAnti-BMP-3A AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-git2-antibody-a04441-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04441-git2-primary-antibodyes-wb-testing-1.jpgAnti-GIT2 AntibodyWestern Blot (WB) analysis of HepG2 cells using GIT2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04441-git2-primary-antibodyes-wb-testing-2.jpgAnti-GIT2 AntibodyWestern Blot (WB) analysis of specific cells using GIT2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-19-antibody-a04434-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04434-il19-primary-antibodies-ihc-testing-1.jpgAnti-IL-19 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04434-il19-primary-antibodies-wb-testing-2.jpgAnti-IL-19 AntibodyWestern blot analysis of 293T Hela VEC KB mouse-kidney lysate, antibody was diluted at 500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd116-antibody-a04432-boster.html2026-03-24T05:09:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04432-csf2ra-primary-antibodies-ihc-testing-1.jpgAnti-CD116 CSF2RA AntibodyImmunohistochemical analysis of paraffin-embedded human-lymph, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04432-csf2ra-primary-antibodies-wb-testing-2.jpgAnti-CD116 CSF2RA AntibodyWestern Blot analysis of L929 cells using CD116 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04432-csf2ra-primary-antibodies-wb-testing-3.jpgAnti-CD116 CSF2RA AntibodyWestern blot analysis of lysate from L929 cells, using CSF2RA Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-pol-alpha-antibody-a04421-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04421-pola1-primary-antibodyes-wb-testing-1.jpgAnti-DNA pol alpha AntibodyWestern Blot (WB) analysis of specific cells using DNA pol alpha Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rrs1-antibody-a04418-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04418-rrs1-primary-antibodies-wb-testing-2.jpgAnti-RRS1 AntibodyWestern Blot analysis of various cells using RRS1 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04418-rrs1-primary-antibodies-wb-testing-3.jpgAnti-RRS1 AntibodyWestern blot analysis of lysates from HUVEC and 293 cells, using RRS1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04418-rrs1-primary-antibodies-wb-testing-4.jpgAnti-RRS1 AntibodyWestern blot analysis of the lysates from HT-29 cells using RRS1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04418-rrs1-primary-antibodies-ihc-testing-1.jpgAnti-RRS1 AntibodyImmunohistochemical analysis of paraffin-embedded human brain. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fig4-antibody-a04403-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04403-fig4-primary-antibodies-wb-testing-1.jpgAnti-FIG4 AntibodyWestern Blot analysis of 1, mouse-liver 2, hela 3, mouse-brain cells using primary antibody diluted at 1:1000 (4°C overnight). Secondary antibody:Goat Anti-rabbit IgG IRDye 800 ( diluted at 1:5000, 25°C, 1 hour)
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-vasohibin-antibody-a04402-1-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04402-1-vash1-primary-antibodies-wb-testing-2.jpgAnti-Vasohibin VASH1 AntibodyWestern Blot analysis of various cells using Vasohibin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04402-1-vash1-primary-antibodies-wb-testing-3.jpgAnti-Vasohibin VASH1 AntibodyWestern blot analysis of VASH1 Antibody. The lane on the right is blocked with the VASH1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04402-1-vash1-primary-antibodies-ihc-testing-4.jpgAnti-Vasohibin VASH1 AntibodyImmunohistochemical analysis of paraffin-embedded human colon. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, EDTA pH 9.0 was used for antigen retrieval. 3 Reday to use Secondary antibody was used at 37°C, 30minhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04402-1-vash1-primary-antibodies-ihc-testing-1.jpgAnti-Vasohibin VASH1 AntibodyImmunohistochemical analysis of paraffin-embedded human brain. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, EDTA pH 9.0 was used for antigen retrieval 3 Reday to use Secondary antibody was used at 37°C, 30min
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pa28-gamma-antibody-a04375-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04375-psme3-primary-antibodies-wb-testing-1.jpgAnti-PA28 gamma PSME3 Monoclonal AntibodyWestern Blot analysis using PA28γ Monoclonal Antibody against HepG2, Jurkat, K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pfkm-antibody-a04370-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04370-pfkm-primary-antibodies-wb-testing-2.jpgAnti-PFKM/Pfk 1 AntibodyWestern Blot analysis of various cells using PFKM Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04370-pfkm-primary-antibodies-wb-testing-3.jpgAnti-PFKM/Pfk 1 AntibodyWestern blot analysis of lysate from Hela cells, using PFK-1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04370-pfkm-primary-antibodies-ihc-testing-4.jpgAnti-PFKM/Pfk 1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04370-pfkm-primary-antibodies-ihc-testing-1.jpgAnti-PFKM/Pfk 1 AntibodyImmunohistochemistry analysis of PFK-1 antibody in paraffin-embedded human brain tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ara70-antibody-a04368-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04368-ncoa4-primary-antibodyes-wb-testing-1.jpgAnti-ARA70 NCOA4 AntibodyWestern Blot (WB) analysis of specific cells using ARA70 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04368-ncoa4-primary-antibodyes-wb-testing-2.jpgAnti-ARA70 NCOA4 AntibodyWestern blot analysis of NCOA4 Antibody. The lane on the right is blocked with the NCOA4 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04368-ncoa4-primary-antibodyes-ihc-testing-3.jpgAnti-ARA70 NCOA4 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using NCOA4 Antibody. The lane on the right is blocked with the NCOA4 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lrg1-antibody-a04365-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-lrg1-primary-antibodies-ihc-testing-1.jpgAnti-LRG1 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-lrg1-primary-antibodies-wb-testing-2.jpgAnti-LRG1 AntibodyWestern Blot analysis of various cells using LRG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-lrg1-primary-antibodies-wb-testing-3.jpgAnti-LRG1 AntibodyWestern Blot analysis of hela cells using LRG1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-separase-antibody-a04364-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04364-espl1-primary-antibodies-wb-testing-2.jpgAnti-Separase AntibodyWestern Blot analysis of A431 cells using Separase Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04364-espl1-primary-antibodies-ihc-testing-3.jpgAnti-Separase AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using SEPARASE Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04364-espl1-primary-antibodies-if-testing-1.jpgAnti-Separase AntibodyImmunofluorescence analysis of HUVEC cells, using SEPARASE Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nop56-antibody-a04335-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04335-nop56-primary-antibodies-wb-testing-1.jpgAnti-NOP56 AntibodyWestern Blot analysis of HEPG2 Hela cells using NOP56 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kif-7-antibody-a04321-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04321-kif7-primary-antibodies-ihc-testing-2.jpgAnti-Kif 7 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04321-kif7-primary-antibodies-if-testing-1.jpgAnti-Kif 7 Monoclonal AntibodyImmunofluorescence analysis of Hela cell. 1, C/EBP β Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). Kif 7 Monoclonal Antibody (3F8) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp2c-kappa-antibody-a04319-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-ppm1k-primary-antibodies-wb-testing-2.jpgAnti-PP2C kappa PPM1K AntibodyWestern Blot analysis of various cells using PP2Cκ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-ppm1k-primary-antibodies-wb-testing-3.jpgAnti-PP2C kappa PPM1K AntibodyWestern blot analysis of the lysates from HeLa cells using PPM1K antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-ppm1k-primary-antibodies-ihc-testing-1.jpgAnti-PP2C kappa PPM1K AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas tissue, using PPM1K Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fog-2-antibody-a04312-boster.html2026-03-24T05:09:22+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hsp70-antibody-a04286-boster.html2026-03-24T05:09:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-wb-testing-2.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyWestern blot analysis of lysates from HT-29, NIH/3T3, and HepG2 cells, primary antibody was diluted at 1:1000, 4° over night, secondary antibody was diluted at 1:10000, 37° 1hour. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-wb-testing-3.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyWestern blot analysis of 1) Hela, 2) Mouse Brain, diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-ihc-testing-4.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human-uterus-cancer tissue. 1, HSP70 Monoclonal Antibody (3G10) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-ihc-testing-5.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-testis tissue. 1, HSP70 Monoclonal Antibody (3G10) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-if-testing-6.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyImmunofluorescence analysis of Hela cell. 1, AIM2 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). HSP70 Monoclonal Antibody (3G10) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-if-testing-7.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyImmunofluorescence analysis of Mouse-lung tissue. 1, HSP70 Monoclonal Antibody (3G10) (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-hspa1l-primary-antibodies-if-testing-1.jpgAnti-HSP70 HSPA1L Monoclonal AntibodyIF analysis of Hela with antibody (Left) and DAPI (Right) diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-smyd2-antibody-a04281-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04281-smyd2-primary-antibodies-ihc-testing-1.jpgAnti-SMYD2/Kmt3C AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04281-smyd2-primary-antibodies-wb-testing-2.jpgAnti-SMYD2/Kmt3C AntibodyWestern Blot analysis of various cells using SMYD2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04281-smyd2-primary-antibodies-wb-testing-3.jpgAnti-SMYD2/Kmt3C AntibodyWestern blot analysis of lysate from HT29 cells, using SMYD2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-20-antibody-a04273-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04273-fgf20-primary-antibodyes-ihc-testing-1.jpgAnti-FGF-20 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04273-fgf20-primary-antibodyes-wb-testing-2.jpgAnti-FGF-20 AntibodyWestern Blot (WB) analysis of SW480, MCF-7, HL-60, BT474, mouse colon cells using FGF-20 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04273-fgf20-primary-antibodyes-ihc-testing-3.jpgAnti-FGF-20 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-btn3a1-2-3-antibody-a04257-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04257-btn3a1-primary-antibodyes-ihc-testing-1.jpgAnti-BTN3A1/2/3 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04257-btn3a1-primary-antibodyes-ihc-testing-2.jpgAnti-BTN3A1/2/3 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-habp2-antibody-a04235-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04235-habp2-primary-antibodies-wb-testing-1.jpgAnti-Hyaluronan-binding protein 2 HABP2 AntibodyWestern Blot analysis of various cells using HABP2 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-akap-79-antibody-a04234-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04234-akap5-primary-antibodies-wb-testing-2.jpgAnti-AKAP 79 AKAP5 AntibodyWestern Blot analysis of various cells using AKAP 79 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04234-akap5-primary-antibodies-wb-testing-3.jpgAnti-AKAP 79 AKAP5 AntibodyWestern blot analysis of lysates from HepG2, HeLa, and COLO205 cells, using AKAP5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04234-akap5-primary-antibodies-ihc-testing-4.jpgAnti-AKAP 79 AKAP5 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04234-akap5-primary-antibodies-if-testing-1.jpgAnti-AKAP 79 AKAP5 AntibodyImmunofluorescence analysis of HeLa cells, using AKAP5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ghrh-r-antibody-a04230-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04230-ghrhr-primary-antibodies-wb-testing-2.jpgAnti-GHRH-R AntibodyWestern Blot analysis of L929 COLO 293T HELA MOUSE-brain cells using GHRH-R Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04230-ghrhr-primary-antibodies-wb-testing-3.jpgAnti-GHRH-R AntibodyWestern blot analysis of various lysis using GHRH-R Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04230-ghrhr-primary-antibodies-wb-testing-4.jpgAnti-GHRH-R AntibodyWestern blot analysis of lysates from LOVO cells, using GHRHR Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04230-ghrhr-primary-antibodies-if-testing-1.jpgAnti-GHRH-R AntibodyImmunofluorescence analysis of HUVEC cells, using GHRHR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-a-cyclase-v-vi-antibody-a04197-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04197-adcy5-primary-antibodies-wb-testing-2.jpgAnti-A Cyclase V/VI ADCY5 AntibodyWestern Blot analysis of COLO205 cells using A Cyclase V/VI Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04197-adcy5-primary-antibodies-wb-testing-3.jpgAnti-A Cyclase V/VI ADCY5 AntibodyWestern blot analysis of lysates from COLO205 cells, using ADCY5/6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04197-adcy5-primary-antibodies-wb-testing-4.jpgAnti-A Cyclase V/VI ADCY5 AntibodyWestern blot analysis of the lysates from HUVECcells using Collagen V α1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04197-adcy5-primary-antibodies-ihc-testing-1.jpgAnti-A Cyclase V/VI ADCY5 AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-qm-antibody-a04190-1-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04190-1-rpl10-primary-antibodyes-wb-testing-1.jpgAnti-QM RPL10 AntibodyWestern Blot (WB) analysis of cat sample using QM Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-18-antibody-a04181-1-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04181-1-fgf18-primary-antibodies-wb-testing-2.jpgAnti-FGF-18 AntibodyWestern Blot analysis of SW480, SKOV3, BT474, mouse heart cells using FGF-18 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04181-1-fgf18-primary-antibodies-ihc-testing-3.jpgAnti-FGF-18 AntibodyImmunohistochemical analysis of paraffin-embedded rat-lung, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04181-1-fgf18-primary-antibodies-ihc-testing-1.jpgAnti-FGF-18 AntibodyImmunohistochemical analysis of paraffin-embedded mouse-lung, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gdi-1-antibody-a04179-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04179-gdi1-primary-antibodyes-wb-testing-1.jpgAnti-GDI-1 AntibodyWestern Blot (WB) analysis of extracts from K562 cells, using GDI-1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd159a-c-antibody-a04175-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04175-klrc1-primary-antibodies-wb-testing-2.jpgAnti-CD159a/c KLRC1 AntibodyWestern blot analysis of lysate from L929 cells, using KLRC1/2/3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04175-klrc1-primary-antibodies-ihc-testing-1.jpgAnti-CD159a/c KLRC1 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peroxin-3-antibody-a04166-boster.html2026-03-24T05:09:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04166-pex3-primary-antibodies-ihc-testing-1.jpgAnti-Peroxin 3 PEX3 AntibodyImmunohistochemical analysis of paraffin-embedded human uterus. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04166-pex3-primary-antibodies-wb-testing-2.jpgAnti-Peroxin 3 PEX3 AntibodyWestern Blot analysis of various cells using Peroxin 3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04166-pex3-primary-antibodies-wb-testing-3.jpgAnti-Peroxin 3 PEX3 AntibodyWestern blot analysis of lysates from HeLa cells, using PEX3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nf-1c-antibody-a04154-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04154-nfic-primary-antibodies-wb-testing-1.jpgAnti-NF-1C NFIC Monoclonal AntibodyWestern Blot analysis using NF-1C Monoclonal Antibody against HeLa nuclear extract.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd85d-antibody-a04141-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04141-lilrb2-primary-antibodies-wb-testing-1.jpgAnti-CD85d LILRB2 AntibodyWestern Blot analysis of Hela cells using CD85d Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mst-3-antibody-a04112-1-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04112-1-stk24-primary-antibodies-ihc-testing-1.jpgAnti-MST-3 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using STK24 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04112-1-stk24-primary-antibodies-wb-testing-2.jpgAnti-MST-3 AntibodyWestern Blot analysis of various cells using MST-3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04112-1-stk24-primary-antibodies-wb-testing-3.jpgAnti-MST-3 AntibodyWestern blot analysis of lysates from COLO cells, using STK24 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04112-1-stk24-primary-antibodies-wb-testing-4.jpgAnti-MST-3 AntibodyWestern blot analysis of the lysates from COLO205 cells using STK24 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-btf-antibody-a04100-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04100-bclaf1-primary-antibodies-wb-testing-2.jpgAnti-BTF AntibodyWestern Blot analysis of various cells using BTF Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04100-bclaf1-primary-antibodies-wb-testing-3.jpgAnti-BTF AntibodyWestern Blot analysis of A549 cells using BTF Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04100-bclaf1-primary-antibodies-wb-testing-1.jpgAnti-BTF AntibodyWestern blot analysis of the lysates from HeLa cells using BCLAF1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fbxo7-antibody-a04086-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-fbxo7-primary-antibodies-wb-testing-1.jpgAnti-FBXO7 Antibody Western Blot analysis of mouse-kidney cells using Antibody diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pinch-1-antibody-a04072-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04072-lims1-primary-antibodyes-wb-testing-1.jpgAnti-Pinch-1 LIMS1 Monoclonal AntibodyWestern Blot (WB) analysis using Pinch-1 Monoclonal antibody against A549 (1), Jurkat (2), and HeLa (3) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04072-lims1-primary-antibodyes-fcm-testing-2.jpgAnti-Pinch-1 LIMS1 Monoclonal AntibodyFlow cytometric (FCM) analysis of HeLa cells using Pinch-1 Monoclonal antibody (blue) and negative control (red).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04072-lims1-primary-antibodyes-if-testing-3.jpgAnti-Pinch-1 LIMS1 Monoclonal AntibodyImmunofluorescence (IF) analysis of HepG2 cells using Pinch-1 Monoclonal antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04072-lims1-primary-antibodyes-elisa-testing-4.jpgAnti-Pinch-1 LIMS1 Monoclonal AntibodyELISA analysis of Pinch-1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-scca1-2-antibody-a04067-boster.html2026-03-24T05:09:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04067-serpinb3-primary-antibodies-wb-testing-2.jpgAnti-SCCA1/2 SERPINB3 AntibodyWestern Blot analysis of Jurkat, 293 cells using SCCA1/2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04067-serpinb3-primary-antibodies-wb-testing-3.jpgAnti-SCCA1/2 SERPINB3 AntibodyWestern blot analysis of lysate from Jurkat cells, using SERPINB3/4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04067-serpinb3-primary-antibodies-ihc-testing-1.jpgAnti-SCCA1/2 SERPINB3 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-prk2-antibody-a04066-boster.html2026-03-24T05:09:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04066-pkn2-primary-antibodies-wb-testing-2.jpgAnti-PRK2 PKN2 Monoclonal AntibodyWestern Blot analysis using PRK2 Monoclonal Antibody against PC-12 (1), Cos7 (2), K562 (3), Jurkat (4), HeLa (5), A431 (6), C6 (7), NIH/3T3 (8) and HEK293 (9) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04066-pkn2-primary-antibodies-ihc-testing-3.jpgAnti-PRK2 PKN2 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded prostate tissues with DAB staining using PRK2 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04066-pkn2-primary-antibodies-fcm-testing-1.jpgAnti-PRK2 PKN2 Monoclonal AntibodyFlow cytometric analysis of NIH/3T3 cells using PRK2 Monoclonal Antibody (blue) and negative control (red).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ca-xii-antibody-a04063-boster.html2026-03-24T05:09:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04063-ca12-primary-antibodies-wb-testing-2.jpgAnti-CA XII CA12 AntibodyWestern Blot analysis of NIH-3T3 293T cells using CA XII Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04063-ca12-primary-antibodies-wb-testing-3.jpgAnti-CA XII CA12 AntibodyWestern blot analysis of lysates from MCF-7 cells, using CA12 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04063-ca12-primary-antibodies-wb-testing-4.jpgAnti-CA XII CA12 AntibodyWestern blot analysis of the lysates from COLO205 cells using CA12 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04063-ca12-primary-antibodies-ihc-testing-1.jpgAnti-CA XII CA12 AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dcr3-antibody-a04048-boster.html2026-03-24T05:09:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04048-tnfrsf6b-primary-antibodies-wb-testing-2.jpgAnti-DcR3 AntibodyWestern Blot analysis of various cells using DcR3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04048-tnfrsf6b-primary-antibodies-wb-testing-3.jpgAnti-DcR3 AntibodyWestern blot analysis of TNFRSF6B Antibody. The lane on the right is blocked with the TNFRSF6B peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04048-tnfrsf6b-primary-antibodies-wb-testing-4.jpgAnti-DcR3 AntibodyWestern blot analysis of the lysates from HT-29 cells using TNFRSF6B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04048-tnfrsf6b-primary-antibodies-ihc-testing-5.jpgAnti-DcR3 AntibodyImmunohistochemistryt analysis of paraffin-embedded human colon t carcinoma, using TNFRSF6B Antibody. The lane on the right is blocked with the TNFRSF6B peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04048-tnfrsf6b-primary-antibodies-if-testing-1.jpgAnti-DcR3 AntibodyImmunofluorescence analysis of TNFRSF6B Antibody. The lane on the right is blocked with the TNFRSF6B peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-camkii-beta-gamma-antibody-a04046-boster.html2026-03-24T05:09:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04046-camk2b-primary-antibodyes-wb-testing-1.jpgAnti-CaMKII beta/ gamma AntibodyWestern Blot (WB) analysis of specific cells using CaMKIIbeta/gamma Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-brd3-antibody-a04044-boster.html2026-03-24T05:09:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04044-brd3-primary-antibodies-wb-testing-2.jpgAnti-BRD3 AntibodyWestern Blot analysis of various cells using BRD3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04044-brd3-primary-antibodies-wb-testing-3.jpgAnti-BRD3 AntibodyWestern Blot analysis of A549 cells using BRD3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04044-brd3-primary-antibodies-ihc-testing-1.jpgAnti-BRD3 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tom20-antibody-a04039-1-boster.html2026-03-24T05:09:25+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp1-beta-antibody-a04022-1-boster.html2026-03-25T05:22:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04022-1-ppp1cb-primary-antibodies-wb-testing-1.jpgAnti-PP1 beta PPP1CB Monoclonal AntibodyWestern Blot analysis using PP1β Monoclonal Antibody against Mouse brain, F9, MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jmjd1a-antibody-a03994-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03994-kdm3a-primary-antibodies-wb-testing-2.jpgAnti-JMJD1A KDM3A Monoclonal AntibodyWestern Blot analysis using JMJD1A Monoclonal Antibody against HeLa (1) and HepG2 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03994-kdm3a-primary-antibodies-if-testing-1.jpgAnti-JMJD1A KDM3A Monoclonal AntibodyImmunofluorescence analysis of Hela cells using JMJD1A Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ube2d2-antibody-a03971-1-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03971-1-ube2d2-primary-antibodies-wb-testing-2.jpgAnti-UBE2D2/Ubch5B AntibodyWestern Blot analysis of various cells using UBE2D2 Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03971-1-ube2d2-primary-antibodies-wb-testing-1.jpgAnti-UBE2D2/Ubch5B AntibodyWestern blot analysis of the lysates from K562 cells using UBE2D2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-wave2-antibody-a03969-1-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03969-1-wasf2-primary-antibodies-wb-testing-2.jpgAnti-WAVE2 WASF2 AntibodyWestern blot analysis of WASF2 Antibody. The lane on the right is blocked with the WASF2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03969-1-wasf2-primary-antibodies-wb-testing-3.jpgAnti-WAVE2 WASF2 AntibodyWestern blot analysis of the lysates from K562 cells using WASF2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03969-1-wasf2-primary-antibodies-ihc-testing-1.jpgAnti-WAVE2 WASF2 AntibodyImmunohistochemistryt analysis of paraffin-embedded human pancreas, using WASF2 Antibody. The lane on the right is blocked with the WASF2 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd177-antibody-a03958-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03958-cd177-primary-antibodies-wb-testing-2.jpgAnti-CD177 antigen CD177 AntibodyWestern Blot analysis of K562 cells using CD177 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03958-cd177-primary-antibodies-wb-testing-3.jpgAnti-CD177 antigen CD177 AntibodyWestern blot analysis of lysate from K562 cells, using CD177 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03958-cd177-primary-antibodies-ihc-testing-1.jpgAnti-CD177 antigen CD177 AntibodyImmunohistochemical analysis of paraffin-embedded human-colon, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-npt2b-antibody-a03957-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03957-slc34a2-primary-antibodies-wb-testing-1.jpgAnti-NPT2b SLC34A2 AntibodyWestern Blot analysis of extracts from rat kidney, K562 cells, using NPT2b Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-syt-antibody-a03947-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03947-ss18-primary-antibodies-wb-testing-2.jpgAnti-SYT SS18 AntibodyWestern Blot analysis of various cells using SYT Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03947-ss18-primary-antibodies-wb-testing-3.jpgAnti-SYT SS18 AntibodyWestern blot analysis of lysates from HepG2, Jurkat, and COLO205 cells, using SSXT Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03947-ss18-primary-antibodies-ihc-testing-1.jpgAnti-SYT SS18 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-grk-1-antibody-a03924-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03924-grk1-primary-antibodies-ihc-testing-1.jpgAnti-GRK 1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GRK1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03924-grk1-primary-antibodies-wb-testing-2.jpgAnti-GRK 1 AntibodyWestern Blot analysis of various cells using GRK 1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03924-grk1-primary-antibodies-wb-testing-3.jpgAnti-GRK 1 AntibodyWestern blot analysis of lysates from COLO205 cells, using GRK1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03924-grk1-primary-antibodies-wb-testing-4.jpgAnti-GRK 1 AntibodyWestern blot analysis of the lysates from Jurkat cells using GRK1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pka-ii-alpha-reg-antibody-a03911-1-boster.html2026-03-24T05:09:26+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdc27-antibody-a03905-1-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03905-1-cdc27-primary-antibodies-wb-testing-2.jpgAnti-Cdc27 AntibodyWestern Blot analysis of various cells using Cdc27 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03905-1-cdc27-primary-antibodies-wb-testing-3.jpgAnti-Cdc27 AntibodyWestern blot analysis of lysates from HUVEC, HepG2, and COLO205 cells, using H-NUC Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03905-1-cdc27-primary-antibodies-ihc-testing-1.jpgAnti-Cdc27 AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-14-3-3-theta-tau-antibody-a03904-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03904-ywhaq-primary-antibodies-wb-testing-2.jpgAnti-14-3-3 theta/ tau YWHAQ AntibodyWestern Blot analysis of Hela cells using 14-3-3 θ/τ Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03904-ywhaq-primary-antibodies-wb-testing-3.jpgAnti-14-3-3 theta/ tau YWHAQ AntibodyWestern blot analysis of lysates from HeLa cells, using 14-3-3 thet/tau Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03904-ywhaq-primary-antibodies-ihc-testing-4.jpgAnti-14-3-3 theta/ tau YWHAQ AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03904-ywhaq-primary-antibodies-if-testing-1.jpgAnti-14-3-3 theta/ tau YWHAQ AntibodyImmunofluorescence analysis of MCF7 cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lal-antibody-a03895-boster.html2026-03-24T05:09:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03895-lipa-primary-antibodies-wb-testing-1.jpgAnti-LAL LIPA Monoclonal AntibodyWestern Blot analysis using LAL Monoclonal Antibody against LAL recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aldolase-b-antibody-a03893-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03893-aldob-primary-antibodies-wb-testing-2.jpgAnti-Aldolase B ALDOB AntibodyWestern Blot analysis of HuvEc cells using Aldolase B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03893-aldob-primary-antibodies-wb-testing-3.jpgAnti-Aldolase B ALDOB AntibodyWestern blot analysis of lysates from MCF-7 and HUVEC cells, using ALDOB Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03893-aldob-primary-antibodies-wb-testing-4.jpgAnti-Aldolase B ALDOB AntibodyWestern blot analysis of the lysates from 293 cells using ALDOB antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03893-aldob-primary-antibodies-ihc-testing-1.jpgAnti-Aldolase B ALDOB AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyclin-a-antibody-a03889-1-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03889-1-ccna1-primary-antibodyes-wb-testing-1.jpgAnti-Cyclin A AntibodyWestern Blot (WB) analysis of COS7 cells using Cyclin A Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03889-1-ccna1-primary-antibodyes-wb-testing-2.jpgAnti-Cyclin A AntibodyWestern Blot (WB) analysis of specific cells using Cyclin A Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyclin-a1-antibody-a03889-2-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03889-2-ccna1-primary-antibodies-wb-testing-2.jpgAnti-Cyclin A1 AntibodyWestern Blot analysis of HeLa cells using Cyclin A1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03889-2-ccna1-primary-antibodies-ihc-testing-1.jpgAnti-Cyclin A1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Cyclin A1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c-ebp-epsilon-antibody-a03884-1-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03884-1-cebpe-primary-antibodies-wb-testing-2.jpgAnti-C/EBP epsilon CEBPE AntibodyWestern Blot analysis of Jurkat cells using C/EBP ε Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03884-1-cebpe-primary-antibodies-wb-testing-3.jpgAnti-C/EBP epsilon CEBPE AntibodyWestern blot analysis of lysates from JurKat cells, treated with Insulin 0.01U/ml 15', using C/EBP-epsilon Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03884-1-cebpe-primary-antibodies-ihc-testing-4.jpgAnti-C/EBP epsilon CEBPE AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using C/EBP-epsilon Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03884-1-cebpe-primary-antibodies-if-testing-1.jpgAnti-C/EBP epsilon CEBPE AntibodyImmunofluorescence analysis of HeLa cells, using C/EBP-epsilon Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ncx1-antibody-a03876-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03876-slc8a1-primary-antibodies-wb-testing-1.jpgAnti-NCX1 SLC8A1 AntibodyWestern Blot analysis of extracts from 293 cells, using NCX1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col5a2-antibody-a03869-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03869-col5a2-primary-antibodies-wb-testing-2.jpgAnti-Collagen alpha-2(V) chain COL5A2 AntibodyWestern Blot analysis of HepG2 cells using COL5A2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03869-col5a2-primary-antibodies-ihc-testing-1.jpgAnti-Collagen alpha-2(V) chain COL5A2 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-atrip-antibody-a03862-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03862-atrip-primary-antibodies-wb-testing-2.jpgAnti-ATRIP AntibodyWestern Blot analysis of various cells using ATRIP Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03862-atrip-primary-antibodies-wb-testing-3.jpgAnti-ATRIP AntibodyWestern Blot analysis of 3T3 cells using ATRIP Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03862-atrip-primary-antibodies-wb-testing-4.jpgAnti-ATRIP AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using ATRIP Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03862-atrip-primary-antibodies-ihc-testing-5.jpgAnti-ATRIP AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using ATRIP Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03862-atrip-primary-antibodies-if-testing-1.jpgAnti-ATRIP AntibodyImmunofluorescence analysis of HeLa cells, using ATRIP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-crsp130-antibody-a03859-1-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03859-1-med23-primary-antibodies-wb-testing-2.jpgAnti-CRSP130 AntibodyWestern Blot analysis of various cells using CRSP130 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03859-1-med23-primary-antibodies-ihc-testing-3.jpgAnti-CRSP130 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using MED23 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03859-1-med23-primary-antibodies-if-testing-1.jpgAnti-CRSP130 AntibodyImmunofluorescence analysis of A549 cells, using MED23 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-inhibin-beta-b-antibody-a03838-boster.html2026-03-24T05:09:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03838-inhbb-primary-antibodyes-wb-testing-1.jpgAnti-Inhibin beta-B AntibodyWestern Blot (WB) analysis of HeLa cells using Inhibin beta-B Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03838-inhbb-primary-antibodyes-wb-testing-2.jpgAnti-Inhibin beta-B AntibodyWestern Blot (WB) analysis of Mouse Heart and Mouse Brain using Inhibin beta-B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03838-inhbb-primary-antibodyes-ihc-testing-3.jpgAnti-Inhibin beta-B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Skin, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03838-inhbb-primary-antibodyes-ihc-testing-4.jpgAnti-Inhibin beta-B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03838-inhbb-primary-antibodyes-ihc-testing-5.jpgAnti-Inhibin beta-B AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Skin, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-spectrin-alpha-ii-d1185-antibody-a03831-boster.html2026-03-24T05:09:27+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-atrophin-1-antibody-a03828-1-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03828-1-atn1-primary-antibodies-wb-testing-1.jpgAnti-Atrophin-1 ATN1 AntibodyWestern Blot analysis of various cells using Atrophin-1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arp-antibody-a03825-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03825-manf-primary-antibodies-ihc-testing-1.jpgAnti-ARP AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03825-manf-primary-antibodies-wb-testing-2.jpgAnti-ARP AntibodyWestern Blot analysis of 293 cells using ARP Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03825-manf-primary-antibodies-wb-testing-3.jpgAnti-ARP AntibodyWestern blot analysis of lysate from 293 cells, using MANF Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mda-7-antibody-a03793-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03793-il24-primary-antibodyes-ihc-testing-1.jpgAnti-MDA-7 IL24 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03793-il24-primary-antibodyes-wb-testing-2.jpgAnti-MDA-7 IL24 AntibodyWestern Blot (WB) analysis of 293 cells using MDA-7 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03793-il24-primary-antibodyes-ihc-testing-3.jpgAnti-MDA-7 IL24 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Lung, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-shank-2-antibody-a03782-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03782-shank2-primary-antibodies-wb-testing-2.jpgAnti-Shank 2 AntibodyWestern Blot analysis of RAW264.7 cells using Shank 2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03782-shank2-primary-antibodies-wb-testing-3.jpgAnti-Shank 2 AntibodyWestern blot analysis of lysates from RAW264.7, Jurkat, HepG2, and COLO cells, using SHANK2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03782-shank2-primary-antibodies-wb-testing-4.jpgAnti-Shank 2 AntibodyWestern blot analysis of the lysates from HT-29 cells using SHANK2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03782-shank2-primary-antibodies-ihc-testing-1.jpgAnti-Shank 2 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd241-antibody-a03778-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03778-rhag-primary-antibodies-wb-testing-2.jpgAnti-CD241 RHAG AntibodyWestern Blot analysis of K562 cells using CD241 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03778-rhag-primary-antibodies-wb-testing-3.jpgAnti-CD241 RHAG AntibodyWestern blot analysis of lysate from K562 cells, using RHAG Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03778-rhag-primary-antibodies-ihc-testing-4.jpgAnti-CD241 RHAG AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03778-rhag-primary-antibodies-ihc-testing-5.jpgAnti-CD241 RHAG AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03778-rhag-primary-antibodies-ihc-testing-1.jpgAnti-CD241 RHAG AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tra-2-alpha-antibody-a03770-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03770-tra2a-primary-antibodies-wb-testing-2.jpgAnti-Tra-2 alpha AntibodyWestern Blot analysis of various cells using Tra-2α Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03770-tra2a-primary-antibodies-wb-testing-3.jpgAnti-Tra-2 alpha AntibodyWestern blot analysis of lysates from HUVEC cells, using TRA-2 alpha Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03770-tra2a-primary-antibodies-ihc-testing-4.jpgAnti-Tra-2 alpha AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TRA-2 alpha Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03770-tra2a-primary-antibodies-if-testing-1.jpgAnti-Tra-2 alpha AntibodyImmunofluorescence analysis of HeLa cells, using TRA-2 alpha Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bap31-antibody-a03767-1-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-1-bcap31-primary-antibodyes-wb-testing-1.jpgAnti-BAP31 BCAP31 AntibodyWestern Blot (WB) analysis of 293T cells using BAP31 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-1-bcap31-primary-antibodyes-wb-testing-2.jpgAnti-BAP31 BCAP31 AntibodyWestern Blot (WB) analysis of specific cells using BAP31 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tfiiib90-1-antibody-a03761-1-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03761-1-brf1-primary-antibodies-wb-testing-2.jpgAnti-TFIIIB90-1 AntibodyWestern Blot analysis of various cells using TFIIIB90-1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03761-1-brf1-primary-antibodies-wb-testing-3.jpgAnti-TFIIIB90-1 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using TF3B Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03761-1-brf1-primary-antibodies-ihc-testing-4.jpgAnti-TFIIIB90-1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TF3B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03761-1-brf1-primary-antibodies-if-testing-1.jpgAnti-TFIIIB90-1 AntibodyImmunofluorescence analysis of MCF7 cells, using TF3B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bptf-antibody-a03754-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03754-bptf-primary-antibodies-wb-testing-1.jpgAnti-BPTF/Falz Monoclonal AntibodyWestern Blot analysis using BPTF Monoclonal Antibody against HEK293 (1) and BPTF (AA: 503-670)-hIgGFc transfected HEK293 (2) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-18-antibody-a03719-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03719-rab18-primary-antibodyes-wb-testing-1.jpgAnti-Rab 18 AntibodyWestern Blot (WB) analysis of MCF-7 cells using Rab 18 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-4-1g-antibody-a03718-boster.html2026-03-24T05:09:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03718-epb41l2-primary-antibodies-ihc-testing-1.jpgAnti-4.1G AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03718-epb41l2-primary-antibodies-wb-testing-2.jpgAnti-4.1G AntibodyWestern Blot analysis of K562 cells using 4.1G Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-elf-4-antibody-a03714-1-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03714-1-elf4-primary-antibodies-wb-testing-1.jpgAnti-Elf-4 AntibodyWestern blot analysis of the lysates from RAW264.7cells using ELF4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03714-1-elf4-primary-antibodies-wb-testing-2.jpgAnti-Elf-4 AntibodyWestern Blot analysis of 22RV1 cells using Elf-4 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ox2r-antibody-a03707-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03707-cd200r1-primary-antibodies-wb-testing-2.jpgAnti-OX2R AntibodyWestern Blot analysis of HepG2 cells using OX2R Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03707-cd200r1-primary-antibodies-wb-testing-1.jpgAnti-OX2R AntibodyWestern blot analysis of lysates from K562 cells, using MOX2R Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dream-antibody-a03700-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03700-kcnip3-primary-antibodies-wb-testing-2.jpgAnti-DREAM AntibodyWestern Blot analysis of various cells using DREAM Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03700-kcnip3-primary-antibodies-wb-testing-3.jpgAnti-DREAM AntibodyWestern blot analysis of SH-SY5Y 293T 3T3 lysis using DREAM antibody. Antibody was diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03700-kcnip3-primary-antibodies-wb-testing-4.jpgAnti-DREAM AntibodyWestern blot analysis of lysates from MCF-7, Jurkat, and A549 cells, using Calsenilin/KCNIP3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03700-kcnip3-primary-antibodies-ihc-testing-5.jpgAnti-DREAM AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Calsenilin/KCNIP3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03700-kcnip3-primary-antibodies-if-testing-1.jpgAnti-DREAM AntibodyImmunofluorescence analysis of HeLa cells, using Calsenilin/KCNIP3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hnrnp-u-antibody-a03691-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03691-hnrnpu-primary-antibodies-wb-testing-1.jpgAnti-hnRNP U Monoclonal AntibodyWestern Blot analysis using hnRNP U Monoclonal Antibody against K562, Jurkat, HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-psr-antibody-a03690-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03690-jmjd6-primary-antibodies-wb-testing-2.jpgAnti-PSR JMJD6 Monoclonal AntibodyWestern Blot analysis using PSR Monoclonal Antibody against HeLa, HL-60 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03690-jmjd6-primary-antibodies-if-testing-1.jpgAnti-PSR JMJD6 Monoclonal AntibodyImmunofluorescence analysis of HeLa cells using PSR Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sr-4-antibody-a03681-1-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03681-1-htr4-primary-antibodies-wb-testing-2.jpgAnti-SR-4 HTR4 AntibodyWestern Blot analysis of various cells using SR-4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03681-1-htr4-primary-antibodies-wb-testing-3.jpgAnti-SR-4 HTR4 AntibodyWestern blot analysis of lysates from Jurkat/COLO205, using 5-HT-4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03681-1-htr4-primary-antibodies-wb-testing-4.jpgAnti-SR-4 HTR4 AntibodyWestern blot analysis of the lysates from 293 cells using Collagen I α2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03681-1-htr4-primary-antibodies-if-testing-1.jpgAnti-SR-4 HTR4 AntibodyImmunofluorescence analysis of HeLa cells, using 5-HT-4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-surf-1-antibody-a03678-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03678-surf1-primary-antibodies-wb-testing-2.jpgAnti-SURF-1 AntibodyWestern Blot analysis of Jurkat cells using SURF-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03678-surf1-primary-antibodies-wb-testing-3.jpgAnti-SURF-1 AntibodyWestern blot analysis of lysates from Jurkat cells, using SURF1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03678-surf1-primary-antibodies-ihc-testing-1.jpgAnti-SURF-1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd158k-antibody-a03677-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03677-kir3dl2-primary-antibodies-ihc-testing-2.jpgAnti-CD158k AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03677-kir3dl2-primary-antibodies-ihc-testing-1.jpgAnti-CD158k AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pept1-antibody-a03672-1-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03672-1-slc15a1-primary-antibodies-wb-testing-2.jpgAnti-PEPT1 SLC15A1 AntibodyWestern blot analysis of the lysates from HeLa cells using SLC15A1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03672-1-slc15a1-primary-antibodies-ihc-testing-1.jpgAnti-PEPT1 SLC15A1 AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-icad-antibody-a03671-1-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03671-1-dffa-primary-antibodies-ihc-testing-1.jpgAnti-ICAD DFFA AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using DFFA Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03671-1-dffa-primary-antibodies-wb-testing-2.jpgAnti-ICAD DFFA AntibodyWestern Blot analysis of 3T3 cells using ICAD Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03671-1-dffa-primary-antibodies-wb-testing-3.jpgAnti-ICAD DFFA AntibodyWestern blot analysis of lysates from Jurkat, 293, and HeLa cells, using DFFA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kcnq4-antibody-a03659-1-boster.html2026-03-24T05:09:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03659-1-kcnq4-primary-antibodies-wb-testing-2.jpgAnti-KCNQ4/Kv7.4 AntibodyWestern Blot analysis of various cells using KCNQ4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03659-1-kcnq4-primary-antibodies-ihc-testing-1.jpgAnti-KCNQ4/Kv7.4 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp26a1-antibody-a03646-1-boster.html2026-03-24T05:09:29+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mnk2-antibody-a03619-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03619-mknk2-primary-antibodyes-wb-testing-1.jpgAnti-Mnk2 MKNK2 AntibodyWestern Blot (WB) analysis of HeLa cells using Mnk2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-alr-antibody-a03595-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03595-gfer-primary-antibodyes-wb-testing-1.jpgAnti-ALR GFER AntibodyWestern Blot (WB) analysis of HBE cells using ALR Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03595-gfer-primary-antibodyes-ihc-testing-2.jpgAnti-ALR GFER AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aly-antibody-a03580-1-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03580-1-alyref-primary-antibodies-wb-testing-2.jpgAnti-ALY ALYREF AntibodyWestern Blot analysis of LOVO cells using ALY Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03580-1-alyref-primary-antibodies-wb-testing-3.jpgAnti-ALY ALYREF AntibodyWestern blot analysis of THOC4 Antibody. The lane on the right is blocked with the THOC4 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03580-1-alyref-primary-antibodies-wb-testing-1.jpgAnti-ALY ALYREF AntibodyWestern blot analysis of the lysates from HepG2 cells using THOC4 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-creb3-antibody-a03564-1-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03564-1-creb3-primary-antibodies-wb-testing-1.jpgAnti-CREB3 AntibodyWestern Blot analysis of 3T3 cells using CREB3 Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rap1gap-antibody-a03561-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03561-rap1gap-primary-antibodyes-wb-testing-1.jpgAnti-Rap1GAP AntibodyWestern Blot (WB) analysis of COLO205 cells using Rap1GAP Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03561-rap1gap-primary-antibodyes-wb-testing-2.jpgAnti-Rap1GAP AntibodyWestern Blot (WB) analysis of specific cells using Rap1GAP Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp2r1-antibody-a03557-boster.html2026-03-24T05:09:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03557-cyp2r1-primary-antibodies-wb-testing-2.jpgAnti-Vitamin D 25-hydroxylase CYP2R1 AntibodyWestern Blot analysis of HT-29 cells using CYP2R1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03557-cyp2r1-primary-antibodies-wb-testing-3.jpgAnti-Vitamin D 25-hydroxylase CYP2R1 AntibodyWestern blot analysis of lysates from HT29 cells, using Cytochrome P450 2R1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03557-cyp2r1-primary-antibodies-wb-testing-4.jpgAnti-Vitamin D 25-hydroxylase CYP2R1 AntibodyWestern blot analysis of the lysates from HT-29 cells using Cytochrome P450 2R1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03557-cyp2r1-primary-antibodies-ihc-testing-1.jpgAnti-Vitamin D 25-hydroxylase CYP2R1 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using Cytochrome P450 2R1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-s2-antibody-a03548-1-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03548-1-rps2-primary-antibodies-wb-testing-2.jpgAnti-Ribosomal Protein S2 RPS2 AntibodyWestern Blot analysis of various cells using Ribosomal Protein S2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03548-1-rps2-primary-antibodies-ihc-testing-1.jpgAnti-Ribosomal Protein S2 RPS2 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arpp-21-antibody-a03525-1-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03525-1-arpp21-primary-antibodies-wb-testing-2.jpgAnti-ARPP-21 AntibodyWestern Blot analysis of HeLa cells using ARPP-21 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03525-1-arpp21-primary-antibodies-wb-testing-3.jpgAnti-ARPP-21 AntibodyWestern blot analysis of lysates from HeLa cells, using ARPP21 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03525-1-arpp21-primary-antibodies-ihc-testing-1.jpgAnti-ARPP-21 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using ARPP21 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-synuclein-gamma-antibody-a03523-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03523-sncg-primary-antibodies-wb-testing-2.jpgAnti-Synuclein-gamma SNCG Monoclonal AntibodyWestern Blot analysis using Synuclein-γ Monoclonal Antibody against truncated Synuclein-γ recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03523-sncg-primary-antibodies-ihc-testing-1.jpgAnti-Synuclein-gamma SNCG Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human ovary carcinoma (left) and breast carcinoma (right), showing cytoplasmic (ovary carcinoma) localization, cytoplasmic and nuclear (breast carcinoma) localization with DAB staining using Synuclein-γ Mo
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ptp-zeta-antibody-a03510-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03510-ptprz1-primary-antibodies-wb-testing-2.jpgAnti-PTP zeta PTPRZ1 AntibodyWestern Blot analysis of various cells using PTPζ Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03510-ptprz1-primary-antibodies-wb-testing-3.jpgAnti-PTP zeta PTPRZ1 AntibodyWestern Blot analysis of A549 cells using PTPζ Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03510-ptprz1-primary-antibodies-wb-testing-4.jpgAnti-PTP zeta PTPRZ1 AntibodyWestern blot analysis of PTPRZ1 Antibody. The lane on the right is blocked with the PTPRZ1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03510-ptprz1-primary-antibodies-ihc-testing-1.jpgAnti-PTP zeta PTPRZ1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mkp-2-antibody-a03486-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03486-dusp4-primary-antibodies-wb-testing-2.jpgAnti-MKP-2 DUSP4 AntibodyWestern Blot analysis of HEPG2-UV cells using MKP-2 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03486-dusp4-primary-antibodies-wb-testing-3.jpgAnti-MKP-2 DUSP4 AntibodyWestern blot analysis of lysates from RAW264.7, A549, COS7, and NIH/3T3 cells, using DUSP4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03486-dusp4-primary-antibodies-ihc-testing-1.jpgAnti-MKP-2 DUSP4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using DUSP4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-1f5-antibody-a03455-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03455-il36rn-primary-antibodies-wb-testing-1.jpgAnti-IL-1F5 IL36RN AntibodyWestern blot analysis of RAT-KIDNEY 293T lysis using IL36RN antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bmp-9-antibody-a03443-1-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03443-1-gdf2-primary-antibodyes-ihc-testing-1.jpgAnti-BMP-9 GDF2 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03443-1-gdf2-primary-antibodyes-ihc-testing-2.jpgAnti-BMP-9 GDF2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03443-1-gdf2-primary-antibodyes-ihc-testing-3.jpgAnti-BMP-9 GDF2 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03443-1-gdf2-primary-antibodyes-ihc-testing-4.jpgAnti-BMP-9 GDF2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver-cancer, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sp-b-antibody-a03441-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03441-sftpb-primary-antibodies-wb-testing-2.jpgAnti-SP-B SFTPB AntibodyWestern Blot analysis of various cells using SP-B Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03441-sftpb-primary-antibodies-wb-testing-3.jpgAnti-SP-B SFTPB AntibodyWestern blot analysis of lysate from A549 cells, using SP-B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03441-sftpb-primary-antibodies-ihc-testing-1.jpgAnti-SP-B SFTPB AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd42d-antibody-a03425-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03425-gp5-primary-antibodies-ihc-testing-2.jpgAnti-CD42d GP5 AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsils, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03425-gp5-primary-antibodies-wb-testing-1.jpgAnti-CD42d GP5 AntibodyWestern Blot analysis of Hela cells using CD42d Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-galectin-9-antibody-a03415-boster.html2026-03-24T05:09:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03415-lgals9-primary-antibodies-if-testing-1.jpgAnti-Galectin-9 LGALS9 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using LEG9 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03415-lgals9-primary-antibodies-if-testing-2.jpgAnti-Galectin-9 LGALS9 AntibodyImmunofluorescence analysis of Hela cell. 1,Galectin-9 Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). 3 DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03415-lgals9-primary-antibodies-wb-testing-3.jpgAnti-Galectin-9 LGALS9 AntibodyWestern blot analysis of lysates from 1) VEC, 2) HepG2 cells, (Green) primary antibody was diluted at 1:1000, 4°over night, Dylight 800 secondary antibody was diluted at 1:10000, 37° 1hour. (Red) Tubulin β Monoclonal Antibody (5G3) antibody was diluted at 1:5000 as loading control, 4° over night,Dylight 680 secondary antibody was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03415-lgals9-primary-antibodies-ihc-testing-4.jpgAnti-Galectin-9 LGALS9 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-erf-antibody-a03411-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03411-erf-primary-antibodies-wb-testing-2.jpgAnti-ERF AntibodyWestern Blot analysis of HepG2 cells using ERF Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03411-erf-primary-antibodies-ihc-testing-3.jpgAnti-ERF AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using ERF Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03411-erf-primary-antibodies-if-testing-1.jpgAnti-ERF AntibodyImmunofluorescence analysis of HeLa cells, using ERF Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-calnexin-antibody-a03372-1-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-wb-testing-2.jpgAnti-Calnexin CANX AntibodyWestern blot analysis of lysates from 1) HCT116, 2) HEK293, 3) MCF-7, 4) A549 cells, (Green） primary antibody was diluted at 1:1000, 4°over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red） Actin β Monoclonal Antibody (5B7) antibody was diluted at 1:5000 as loading control, 4° over night, secondary antibody was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-wb-testing-3.jpgAnti-Calnexin CANX AntibodyWestern blot analysis of lysates from HT-29, NIH/3T3, and HepG2 cells, primary antibody was diluted at 1:1000, 4° over night, secondary antibody was diluted at 1:10000, 37° 1hour. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-wb-testing-4.jpgAnti-Calnexin CANX AntibodyWestern Blot analysis of 293 cells using Calnexin Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-5.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Human-liver tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-6.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Human-liver-cancer tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-7.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Human-lung-cancer tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-8.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-9.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-liver tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-10.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-colon tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-11.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-lung tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-12.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-kidney tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-13.jpgAnti-Calnexin CANX AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-spleen tissue. 1, Calnexin Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-ihc-testing-14.jpgAnti-Calnexin CANX AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using Calnexin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-if-testing-15.jpgAnti-Calnexin CANX AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-if-testing-16.jpgAnti-Calnexin CANX AntibodyImmunofluorescence analysis of Hela cell. 1, Calnexin Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). (red) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-if-testing-17.jpgAnti-Calnexin CANX AntibodyImmunofluorescence analysis of rat-lung tissue. 1, Calnexin Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-if-testing-18.jpgAnti-Calnexin CANX AntibodyImmunofluorescence analysis of rat-kidney tissue. 1, Calnexin Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03372-1-canx-primary-antibodies-if-testing-1.jpgAnti-Calnexin CANX AntibodyImmunofluorescence analysis of rat-spleen tissue. 1, Calnexin Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mnt-antibody-a03357-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03357-mnt-primary-antibodyes-wb-testing-1.jpgAnti-MNT/Max Binding Protein AntibodyWestern Blot (WB) analysis of A549 cells using MNT Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03357-mnt-primary-antibodyes-wb-testing-2.jpgAnti-MNT/Max Binding Protein AntibodyWestern Blot (WB) analysis of specific cells using MNT Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ik-antibody-a03341-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03341-ik-primary-antibodyes-wb-testing-1.jpgAnti-Protein Red IK AntibodyWestern Blot (WB) analysis of HeLa, KB, SH-SY5Y, 293T, 3T3 lysis using IK antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03341-ik-primary-antibodyes-wb-testing-2.jpgAnti-Protein Red IK AntibodyWestern Blot (WB) analysis of specific cells using IK Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dra-antibody-a03335-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03335-41522_2023_433_fig6_html.pngAnti-DRA SLC26A3 AntibodyPhosphocholine decreases fluid absorption by increasing cAMP levels via the activation of adenylyl cyclase. The levels of cAMP a and cGMP b in the colon, and the activity of adenylyl cyclase c and guanylyl cyclase d ; data were analyzed with two-tailed Student’s t-test and presented as mean ± SEM. n = 6. * P < 0.05. e Western blots showing the protein expression of SLC9A3, SLC5A1, SLC26A3, and GAPDH in the colon; cAMP content f , adenylyl cyclase activity g , cGMP content h , and guanylyl cyclase activity i in the primary colonocytes; j Western blots showing the protein expression of SLC9A3, SLC5A1, SLC26A3 and GAPDH in the primary colonocytes; Relative level of Na + k and Cl - l in the culture medium. Data were analyzed using one-way analysis of variance (ANOVA) and presented as the mean ± SEM. n = 4. * P < 0.05, ** P < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41522-023-00433-0'>37666845</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-crabp-ii-antibody-a03297-1-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03297-1-crabp2-primary-antibodies-wb-testing-2.jpgAnti-CRABP-II CRABP2 AntibodyWestern Blot analysis of various cells using CRABP-II Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03297-1-crabp2-primary-antibodies-wb-testing-3.jpgAnti-CRABP-II CRABP2 AntibodyWestern blot analysis of lysates from HT-29 cells, using CRABP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03297-1-crabp2-primary-antibodies-ihc-testing-1.jpgAnti-CRABP-II CRABP2 AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-calpain-10-antibody-a03289-boster.html2026-03-24T05:09:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03289-capn10-primary-antibodies-wb-testing-1.jpgAnti-Calpain 10 CAPN10 AntibodyWestern Blot analysis of LOVO cells using Calpain 10 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-phf8-antibody-a03288-boster.html2026-03-24T05:09:33+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clk1-antibody-a03271-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03271-clk1-primary-antibodies-wb-testing-2.jpgAnti-CLK1 AntibodyWestern Blot analysis of various cells using CLK1 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03271-clk1-primary-antibodies-wb-testing-3.jpgAnti-CLK1 AntibodyWestern blot analysis of KB lysis using CLK1 antibody. Antibody was diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03271-clk1-primary-antibodies-wb-testing-4.jpgAnti-CLK1 AntibodyWestern blot analysis of lysates from 293 cells, using CLK1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03271-clk1-primary-antibodies-ihc-testing-5.jpgAnti-CLK1 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03271-clk1-primary-antibodies-if-testing-1.jpgAnti-CLK1 AntibodyImmunofluorescence analysis of HUVEC cells, using CLK1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-parp-2-antibody-a03270-1-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03270-1-parp2-primary-antibodies-wb-testing-1.jpgAnti-PARP-2 AntibodyWestern Blot analysis of K562 cells using PARP-2 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-claudin-5-antibody-a03260-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-wb-testing-2.jpgAnti-Claudin-5 CLDN5 AntibodyWestern Blot analysis of A549 cells using Claudin-5 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-wb-testing-3.jpgAnti-Claudin-5 CLDN5 AntibodyWestern blot analysis of lysates from A549 cells, using Claudin 5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-ihc-testing-4.jpgAnti-Claudin-5 CLDN5 AntibodyImmunohistochemical analysis of paraffin-embedded Human-lung-cancer tissue. 1, Claudin-5 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-ihc-testing-5.jpgAnti-Claudin-5 CLDN5 AntibodyImmunohistochemical analysis of paraffin-embedded Human-stomach-cancer tissue. 1, Claudin-5 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-ihc-testing-6.jpgAnti-Claudin-5 CLDN5 AntibodyImmunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1, Claudin-5 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-ihc-testing-7.jpgAnti-Claudin-5 CLDN5 AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-testis tissue. 1, Claudin-5 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-ihc-testing-8.jpgAnti-Claudin-5 CLDN5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Claudin 5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-if-testing-9.jpgAnti-Claudin-5 CLDN5 AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-if-testing-10.jpgAnti-Claudin-5 CLDN5 AntibodyImmunofluorescence analysis of human-lung tissue. 1, Claudin-5 Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03260-cldn5-primary-antibodies-if-testing-1.jpgAnti-Claudin-5 CLDN5 AntibodyImmunofluorescence analysis of human-stomach tissue. 1, Claudin-5 Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd94-antibody-a03257-1-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03257-1-klrd1-primary-antibodies-wb-testing-2.jpgAnti-CD94 KLRD1 Monoclonal AntibodyWestern Blot analysis using CD94 Monoclonal Antibody against recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03257-1-klrd1-primary-antibodies-fcm-testing-1.jpgAnti-CD94 KLRD1 Monoclonal AntibodyFlow cytometric analysis of RAJI cells using CD94 Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lekti-antibody-a03254-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03254-spink5-primary-antibodies-wb-testing-2.jpgAnti-LEKTI AntibodyWestern blot analysis of SPINK5 Antibody. The lane on the right is blocked with the SPINK5 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03254-spink5-primary-antibodies-wb-testing-3.jpgAnti-LEKTI AntibodyWestern blot analysis of the lysates from COLO205 cells using SPINK5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03254-spink5-primary-antibodies-ihc-testing-1.jpgAnti-LEKTI AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-thrombospondin-2-antibody-a03253-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03253-thbs2-primary-antibodyes-wb-testing-1.jpgAnti-Thrombospondin 2 AntibodyWestern blot analysis of mouse-heart lysis using THBS2 antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03253-thbs2-primary-antibodyes-ihc-testing-2.jpgAnti-Thrombospondin 2 AntibodyImmunohistochemical analysis of paraffin-embedded rat-testis, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peg10-antibody-a03240-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03240-peg10-primary-antibodyes-ihc-testing-1.jpgAnti-PEG10 Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded human Placenta tissues with AEC staining using PEG10 Monoclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03240-peg10-primary-antibodyes-wb-testing-2.jpgAnti-PEG10 Monoclonal AntibodyWestern Blot (WB) analysis using PEG10 Monoclonal antibody against truncated Trx-PEG10 recombinant protein (1),truncated GST-PEG10 (aa1-120) recombinant protein (2) and full-length PEG10 (aa1-325)-hIgGFc transfected CHO-K1 cell lysate (3).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03240-peg10-primary-antibodyes-if-testing-3.jpgAnti-PEG10 Monoclonal AntibodyConfocal Immunofluorescence (IF) analysis of methanol-fixed HepG2 cells using PEG10 Monoclonal antibody (green), showing cytoplasmic localization. Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-peg10-antibody-a03240-1-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03240-1-peg10-primary-antibodies-wb-testing-1.jpgAnti-PEG10 Monoclonal AntibodyWestern Blot analysis using PEG10 Monoclonal Antibody against HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-myl2-antibody-a03215-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03215-myl2-primary-antibodies-wb-testing-1.jpgAnti-MYL2 Monoclonal Antibody Western Blot analysis using MYL2 Monoclonal Antibody against rat fetal heart tissue lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lir-1-antibody-a03208-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03208-lilrb1-primary-antibodyes-wb-testing-1.jpgAnti-LIR-1 LILRB1 AntibodyWestern Blot (WB) analysis of SKOV3 cells using LIR-1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mi2-alpha-antibody-a03200-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03200-chd3-primary-antibodies-wb-testing-2.jpgAnti-Mi2- alpha Monoclonal Antibody Western Blot analysis using Mi2-α Monoclonal Antibody against Y7P, Raji cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03200-chd3-primary-antibodies-ihc-testing-3.jpgAnti-Mi2- alpha Monoclonal Antibody Immunohistochemistry analysis of paraffin-embedded human colon using Mi2-α Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03200-chd3-primary-antibodies-if-testing-4.jpgAnti-Mi2- alpha Monoclonal Antibody Immunofluorescence analysis of HeLa cells using Mi2-α Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03200-chd3-primary-antibodies-fcm-testing-1.jpgAnti-Mi2- alpha Monoclonal Antibody Flow cytometric analysis of K562 cells stained with Mi2-α Monoclonal Antibody (red), followed by FITC-conjugated goat anti-mouse IgG. Blue line histogram represents the isotype control, normal mouse IgG.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd39-antibody-a03196-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03196-entpd1-primary-antibodies-wb-testing-1.jpgAnti-CD39 AntibodyWestern Blot analysis of Hela cells using CD39 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col6a2-antibody-a03194-boster.html2026-03-24T05:09:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03194-col6a2-primary-antibodyes-wb-testing-1.jpgAnti-Collagen alpha-2(VI) chain COL6A2 AntibodyWestern Blot (WB) analysis of K562 cells using COL6A2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ecp-antibody-a03115-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03115-rnase3-primary-antibodies-wb-testing-2.jpgAnti-ECP AntibodyWestern Blot analysis of various cells using ECP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03115-rnase3-primary-antibodies-wb-testing-1.jpgAnti-ECP AntibodyWestern blot analysis of lysate from 293 cells, usiung ECP antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdgf-c-antibody-a03092-boster.html2026-03-24T05:09:34+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gsc-antibody-a03084-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03084-gsc-primary-antibodies-ihc-testing-2.jpgAnti-GSC/Goosecoid AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03084-gsc-primary-antibodies-ihc-testing-1.jpgAnti-GSC/Goosecoid AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-reg-i-alpha-antibody-a03075-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03075-reg1a-primary-antibodies-if-testing-1.jpgAnti-Reg I alpha REG1A Monoclonal AntibodyConfocal immunofluorescence analysis of PC12 cells using Reg Iα Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03075-reg1a-primary-antibodies-ihc-testing-2.jpgAnti-Reg I alpha REG1A Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human Pancreas tissues with AEC staining using Reg Iα Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dok-1-antibody-a03039-1-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03039-1-dok1-primary-antibodyes-wb-testing-1.jpgAnti-Dok-1 AntibodyWestern Blot (WB) analysis of Jurkat cells using Dok-1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col17a1-antibody-a03031-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03031-col17a1-primary-antibodies-if-testing-1.jpgAnti-COL17A1/Collagen Xvii AntibodyImmunofluorescence analysis of A549. 1,primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03031-col17a1-primary-antibodies-wb-testing-2.jpgAnti-COL17A1/Collagen Xvii AntibodyWestern Blot analysis of 3T3, hepg2 cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03031-col17a1-primary-antibodies-if-testing-3.jpgAnti-COL17A1/Collagen Xvii AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp2b-a-alpha-antibody-a03026-1-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03026-1-ppp3ca-primary-antibodies-wb-testing-1.jpgAnti-PP2B-A alpha PPP3CA Monoclonal AntibodyWestern Blot analysis using PP2B-Aα Monoclonal Antibody against A431, HeLa cell lysate .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ascl1-antibody-a03023-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03023-ascl1-primary-antibodies-ihc-testing-1.jpgAnti-ASCL1/Mash1 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rac-gap1-antibody-a03018-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03018-racgap1-primary-antibodies-wb-testing-2.jpgAnti-Rac GAP1 AntibodyWestern Blot analysis of various cells using Rac GAP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03018-racgap1-primary-antibodies-wb-testing-3.jpgAnti-Rac GAP1 AntibodyWestern blot analysis of lysates from COS7 cells, using GTPase Activating Protein Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03018-racgap1-primary-antibodies-ihc-testing-4.jpgAnti-Rac GAP1 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03018-racgap1-primary-antibodies-if-testing-1.jpgAnti-Rac GAP1 AntibodyImmunofluorescence analysis of HeLa cells, using GTPase Activating Protein Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-15r-alpha-antibody-a03016-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-il15ra-primary-antibodies-wb-testing-2.jpgAnti-IL-15R alpha AntibodyWestern Blot analysis of COLO cells using IL-15Rα Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-il15ra-primary-antibodies-wb-testing-3.jpgAnti-IL-15R alpha AntibodyWestern blot analysis of lysates from COLO cells, using IL15RA Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-il15ra-primary-antibodies-wb-testing-1.jpgAnti-IL-15R alpha AntibodyWestern blot analysis of the lysates from HeLa cells using IL15RA antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pitx1-antibody-a02993-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02993-pitx1-primary-antibodyes-wb-testing-1.jpgAnti-Pituitary homeobox 1 Pitx1 AntibodyWestern Blot (WB) analysis of Jurkat cells using Pitx1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02993-pitx1-primary-antibodyes-wb-testing-2.jpgAnti-Pituitary homeobox 1 Pitx1 AntibodyWestern Blot (WB) analysis of specific cells using Pitx1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02993-pitx1-primary-antibodyes-wb-testing-3.jpgAnti-Pituitary homeobox 1 Pitx1 AntibodyWestern blot analysis of lysates from Jurkat and COLO cells, using PITX1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chemr23-antibody-a02960-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-if-testing-1.jpgAnti-ChemR23 CMKLR1 AntibodyImmunofluorescence analysis of A549. 1,primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-wb-testing-2.jpgAnti-ChemR23 CMKLR1 AntibodyWestern Blot analysis of various cells using ChemR23 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-wb-testing-3.jpgAnti-ChemR23 CMKLR1 AntibodyWestern Blot analysis of COLO205 cells using ChemR23 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-wb-testing-4.jpgAnti-ChemR23 CMKLR1 AntibodyWestern blot analysis of 293T lysis using ChemR23 antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-wb-testing-5.jpgAnti-ChemR23 CMKLR1 AntibodyWestern blot analysis of lysates from HeLa and HUVEC cells, using CMKLR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02960-cmklr1-primary-antibodies-ihc-testing-6.jpgAnti-ChemR23 CMKLR1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cytochrome-c1-antibody-a02958-boster.html2026-03-24T05:09:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02958-cyc1-primary-antibodies-wb-testing-2.jpgAnti-Cytochrome c1 CYC1 AntibodyWestern Blot analysis of various cells using Cytochrome c1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02958-cyc1-primary-antibodies-wb-testing-3.jpgAnti-Cytochrome c1 CYC1 AntibodyWestern Blot analysis of rat-musle cells using Cytochrome c1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02958-cyc1-primary-antibodies-wb-testing-1.jpgAnti-Cytochrome c1 CYC1 AntibodyWestern blot analysis of the lysates from HUVECcells using CYC1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cck-4-antibody-a02957-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02957-ptk7-primary-antibodies-wb-testing-2.jpgAnti-CCK-4 PTK7 Monoclonal AntibodyWestern Blot analysis using CCK-4 Monoclonal Antibody against HeLa (1), A431 (2), HCT116 (3), Caco2 (4), HepG2 (5) and MCF-7 (6) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02957-ptk7-primary-antibodies-ihc-testing-1.jpgAnti-CCK-4 PTK7 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded lung cancer tissues with DAB staining using CCK-4 Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gcsm-gamma-antibody-a02948-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02948-gclm-primary-antibodyes-wb-testing-1.jpgAnti-GCSm- gamma GCLM AntibodyWestern Blot (WB) analysis of COS7 cells using GCSm-gamma Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02948-gclm-primary-antibodyes-wb-testing-2.jpgAnti-GCSm- gamma GCLM AntibodyWestern Blot (WB) analysis of Mouse Kidney Mouse Brain lysis using GCSm-gamma antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02948-gclm-primary-antibodyes-wb-testing-3.jpgAnti-GCSm- gamma GCLM AntibodyWestern Blot (WB) analysis of specific cells using GCSm-gamma Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rab-6a-antibody-a02911-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02911-rab6a-primary-antibodies-wb-testing-2.jpgAnti-Rab 6A AntibodyWestern Blot analysis of COLO cells using Rab 6A Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02911-rab6a-primary-antibodies-wb-testing-3.jpgAnti-Rab 6A AntibodyWestern blot analysis of lysates from A549 cells, using RAB6A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02911-rab6a-primary-antibodies-wb-testing-4.jpgAnti-Rab 6A AntibodyWestern blot analysis of the lysates from HT-29 cells using RAB6A antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02911-rab6a-primary-antibodies-ihc-testing-1.jpgAnti-Rab 6A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dio3-antibody-a02903-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02903-dio3-primary-antibodies-wb-testing-2.jpgAnti-Thyroxine 5-deiodinase DIO3 AntibodyWestern Blot analysis of various cells using DIO3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02903-dio3-primary-antibodies-wb-testing-1.jpgAnti-Thyroxine 5-deiodinase DIO3 AntibodyWestern blot analysis of lysate from HUVEC cells, using DIO3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hnrnp-d0-antibody-a02895-2-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02895-2-hnrnpd-primary-antibodies-if-testing-1.jpgAnti-hnRNP D0 AntibodyImmunofluorescence analysis of HeLa cells, using hnRPD Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02895-2-hnrnpd-primary-antibodies-wb-testing-2.jpgAnti-hnRNP D0 AntibodyWestern blot analysis of lysates from 293, Jurkat, 3T3, and COLO205 cells, using hnRPD Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02895-2-hnrnpd-primary-antibodies-ihc-testing-3.jpgAnti-hnRNP D0 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using hnRPD Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nab2-antibody-a02873-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-nab2-primary-antibodies-wb-testing-2.jpgAnti-NGFI-A-binding protein 2 NAB2 AntibodyWestern blot analysis of lysates from HT-29 and RAW264.7 cells, using NAB2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-nab2-primary-antibodies-wb-testing-3.jpgAnti-NGFI-A-binding protein 2 NAB2 AntibodyWestern blot analysis of the lysates from HeLa cells using NAB2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-nab2-primary-antibodies-ihc-testing-1.jpgAnti-NGFI-A-binding protein 2 NAB2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NAB2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-crmp-2-antibody-a02860-1-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02860-1-dpysl2-primary-antibodies-if-testing-1.jpgAnti-CRMP-2 DPYSL2 AntibodyImmunofluorescence analysis of HeLa cells, using DRP-2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02860-1-dpysl2-primary-antibodies-wb-testing-2.jpgAnti-CRMP-2 DPYSL2 AntibodyWestern Blot analysis of mouse brain cells using CRMP-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02860-1-dpysl2-primary-antibodies-wb-testing-3.jpgAnti-CRMP-2 DPYSL2 AntibodyWestern blot analysis of lysates from A549 cells, treated with EGF 200ng/ml 30', using DRP-2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02860-1-dpysl2-primary-antibodies-wb-testing-4.jpgAnti-CRMP-2 DPYSL2 AntibodyWestern blot analysis of the lysates from HepG2 cells using DRP-2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02860-1-dpysl2-primary-antibodies-ihc-testing-5.jpgAnti-CRMP-2 DPYSL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using DRP-2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-r-spondin-antibody-a02857-boster.html2026-03-24T05:09:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02857-rspo1-primary-antibodies-wb-testing-1.jpgAnti-R-Spondin RSPO1 Monoclonal AntibodyWestern Blot analysis using R-Spondin Monoclonal Antibody against recombinant R-spondin1 protein (1) and R-spondin1 (aa21-263)-hIgGFc transfected HEK293 cell lysate (2).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-smcx-antibody-a02849-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02849-kdm5c-primary-antibodies-if-testing-1.jpgAnti-SmcX KDM5C Monoclonal AntibodyImmunofluorescence analysis of HeLa cells using SmcX Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02849-kdm5c-primary-antibodies-wb-testing-2.jpgAnti-SmcX KDM5C Monoclonal AntibodyWestern Blot analysis using SmcX Monoclonal Antibody against HeLa, 293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd299-antibody-a02814-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02814-clec4m-primary-antibodies-wb-testing-1.jpgAnti-CD299 CLEC4M AntibodyWestern blot analysis of mouse-lung mouse-lung lysate, antibody was diluted at 2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pp1-alpha-antibody-a02801-boster.html2026-03-24T05:09:36+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-xrn2-antibody-a02797-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02797-xrn2-primary-antibodies-wb-testing-2.jpgAnti-5'-3' exoribonuclease 2 XRN2 AntibodyWestern Blot analysis of various cells using XRN2 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02797-xrn2-primary-antibodies-wb-testing-3.jpgAnti-5'-3' exoribonuclease 2 XRN2 AntibodyWestern blot analysis of lysates from COS7 cells, using XRN2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02797-xrn2-primary-antibodies-ihc-testing-1.jpgAnti-5'-3' exoribonuclease 2 XRN2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using XRN2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-s-100a10-antibody-a02787-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02787-s100a10-primary-antibodyes-wb-testing-1.jpgAnti-S-100A10 AntibodyWestern Blot (WB) analysis of specific cells using S-100A10 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-s-100a10-antibody-a02787-1-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02787-1-s100a10-primary-antibodies-wb-testing-2.jpgAnti-S-100A10 Monoclonal AntibodyWestern Blot analysis using S-100A10 Monoclonal Antibody against MCF-7 (1), HepG2 (2) and HeLa (3).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02787-1-s100a10-primary-antibodies-ihc-testing-3.jpgAnti-S-100A10 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human nerve and ganglion cells with AEC staining using S-100A10 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02787-1-s100a10-primary-antibodies-if-testing-1.jpgAnti-S-100A10 Monoclonal AntibodyConfocal immunofluorescence analysis of Hela (left) and L-02 (right) cells using S-100A10 Monoclonal Antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tradd-antibody-a02785-1-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02785-1-tradd-primary-antibodies-wb-testing-2.jpgAnti-TRADD AntibodyWestern Blot analysis of various cells using TRADD Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02785-1-tradd-primary-antibodies-wb-testing-3.jpgAnti-TRADD AntibodyWestern Blot analysis of COS7 cells using TRADD Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02785-1-tradd-primary-antibodies-wb-testing-4.jpgAnti-TRADD AntibodyWestern blot analysis of lysates from COS7 cells, using TRADD Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02785-1-tradd-primary-antibodies-ihc-testing-1.jpgAnti-TRADD AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using TRADD Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hp1-alpha-antibody-a02780-boster.html2026-03-24T05:09:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02780-cbx5-primary-antibodies-wb-testing-1.jpgAnti-HP1 alpha CBX5 Monoclonal AntibodyWestern Blot analysis using HP1α Monoclonal Antibody against HeLa nuclear extract, 3T3, MCF7 whole cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ephrin-b1-2-antibody-a02767-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02767-efnb1-primary-antibodies-wb-testing-2.jpgAnti-Ephrin-B1/2 EFNB1 AntibodyWestern Blot analysis of 293 cells using Ephrin-B1/2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02767-efnb1-primary-antibodies-wb-testing-3.jpgAnti-Ephrin-B1/2 EFNB1 AntibodyWestern blot analysis of lysates from 293 cells, treated with EGF 200ng/ml 5', using EFNB1/2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02767-efnb1-primary-antibodies-ihc-testing-1.jpgAnti-Ephrin-B1/2 EFNB1 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using EFNB1/2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tgf-beta-riii-antibody-a02765-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02765-tgfbr3-primary-antibodyes-wb-testing-1.jpgAnti-TGF beta RIII TGFBR3 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using TGFbeta RIII Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ampk-gamma2-antibody-a02758-1-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02758-1-prkag2-primary-antibodies-wb-testing-2.jpgAnti-AMPK gamma2 PRKAG2 AntibodyWestern Blot analysis of K562 using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02758-1-prkag2-primary-antibodies-ihc-testing-3.jpgAnti-AMPK gamma2 PRKAG2 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using PRKAG2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02758-1-prkag2-primary-antibodies-if-testing-1.jpgAnti-AMPK gamma2 PRKAG2 AntibodyImmunofluorescence analysis of A549 cells, using PRKAG2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mof-antibody-a02757-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02757-kat8-primary-antibodies-wb-testing-2.jpgAnti-MOF KAT8 Monoclonal AntibodyWestern Blot analysis using MOF Monoclonal Antibody against HeLa (1), HepG2 (2) and SMMC-7721 (3) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02757-kat8-primary-antibodies-ihc-testing-3.jpgAnti-MOF KAT8 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human esophageal squamous cell carcinoma (A), normal esophagus epithelium (B), rectum adenocarcinoma (C), lung squamous cell carcinoma (D), breast infiltrating carcinoma (E), and breast infiltrating carcihttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02757-kat8-primary-antibodies-if-testing-1.jpgAnti-MOF KAT8 Monoclonal AntibodyConfocal immunofluorescence analysis of Eca 109 cells using MOF Monoclonal Antibody (green), showing nuclear localization.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-ligase-iii-antibody-a02741-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02741-lig3-primary-antibodies-wb-testing-2.jpgAnti-DNA Ligase III LIG3 AntibodyWestern Blot analysis of various cells using DNA Ligase III Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02741-lig3-primary-antibodies-wb-testing-1.jpgAnti-DNA Ligase III LIG3 AntibodyWestern Blot analysis of MCF7 cells using DNA Ligase III Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-orc1-antibody-a02735-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02735-orc1-primary-antibodies-wb-testing-1.jpgAnti-ORC1 AntibodyWestern blot analysis of the lysates from HepG2 cells using ORC1L antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02735-orc1-primary-antibodies-wb-testing-2.jpgAnti-ORC1 AntibodyWestern Blot analysis of 3T3 cells using ORC1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-caf-1-p150-antibody-a02732-1-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02732-1-chaf1a-primary-antibodies-wb-testing-1.jpgAnti-CAF-1 p150 CHAF1A AntibodyWestern Blot analysis of K562 cells using CAF-1 p150 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nfatc3-antibody-a02727-1-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-1-nfatc3-primary-antibodies-ihc-testing-1.jpgAnti-NFATc3/Nfat4 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-1-nfatc3-primary-antibodies-wb-testing-2.jpgAnti-NFATc3/Nfat4 AntibodyWestern Blot analysis of various cells using NFATc3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-1-nfatc3-primary-antibodies-wb-testing-3.jpgAnti-NFATc3/Nfat4 AntibodyWestern blot analysis of lysates from HeLa cells, treated with Ca+ 40nM 30', using NFAT4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd158a-antibody-a02724-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02724-kir2dl1-primary-antibodyes-wb-testing-1.jpgAnti-CD158a KIR2DL1 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using CD158a Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02724-kir2dl1-primary-antibodyes-wb-testing-2.jpgAnti-CD158a KIR2DL1 AntibodyWestern Blot (WB) analysis of 3T3 cells using CD158a Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-clc-7-antibody-a02720-1-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02720-1-clcn7-primary-antibodies-wb-testing-1.jpgAnti-CLC-7 CLCN7 AntibodyWestern blot analysis of the lysates from COLO205 cells using CLCN7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02720-1-clcn7-primary-antibodies-wb-testing-2.jpgAnti-CLC-7 CLCN7 AntibodyWestern Blot analysis of A549 cells using CLC-7 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02720-1-clcn7-primary-antibodies-wb-testing-3.jpgAnti-CLC-7 CLCN7 AntibodyWestern blot analysis of CLCN7 Antibody. The lane on the right is blocked with the CLCN7 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-arg-antibody-a02715-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02715-abl2-primary-antibodyes-wb-testing-1.jpgAnti-Arg ABL2 AntibodyWestern Blot (WB) analysis of AD293 cells using Arg Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02715-abl2-primary-antibodyes-ihc-testing-2.jpgAnti-Arg ABL2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02715-abl2-primary-antibodyes-ihc-testing-3.jpgAnti-Arg ABL2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02715-abl2-primary-antibodyes-ihc-testing-4.jpgAnti-Arg ABL2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Mouse Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02715-abl2-primary-antibodyes-ihc-testing-5.jpgAnti-Arg ABL2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nkx-3-1-antibody-a02709-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02709-nkx3-1-primary-antibodyes-ihc-testing-1.jpgAnti-Nkx-3.1 Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded human prostata tissues (A, B) with DAB staining using Nkx-3.1 Monoclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02709-nkx3-1-primary-antibodyes-wb-testing-2.jpgAnti-Nkx-3.1 Monoclonal AntibodyWestern Blot (WB) analysis using Nkx-3.1 Monoclonal antibody against LNCaP (1) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02709-nkx3-1-primary-antibodyes-fcm-testing-3.jpgAnti-Nkx-3.1 Monoclonal AntibodyFlow cytometric (FCM) analysis of PC-3 cells using Nkx-3.1 Monoclonal antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-npas2-antibody-a02688-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02688-npas2-primary-antibodyes-wb-testing-1.jpgAnti-NPAS2 AntibodyWestern Blot (WB) analysis of extracts from rat stomach, 293 cells, using NPAS2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kv1-5-antibody-a02673-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02673-kcna5-primary-antibodies-wb-testing-2.jpgAnti-KV1.5 KCNA5 AntibodyWestern Blot analysis of various cells using KV1.5 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02673-kcna5-primary-antibodies-wb-testing-3.jpgAnti-KV1.5 KCNA5 AntibodyWestern blot analysis of KCNA5 Antibody. The lane on the right is blocked with the KCNA5 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02673-kcna5-primary-antibodies-ihc-testing-1.jpgAnti-KV1.5 KCNA5 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ing4-antibody-a02664-1-boster.html2026-03-24T05:09:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02664-1-ing4-primary-antibodies-wb-testing-2.jpgAnti-Inhibitor of growth protein 4 ING4 AntibodyWestern Blot analysis of extracts from Jurkat, K562 cells, using ING4 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02664-1-ing4-primary-antibodies-wb-testing-1.jpgAnti-Inhibitor of growth protein 4 ING4 AntibodyWestern blot analysis of lysates from 293 cells, using ING4 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dsg1-antibody-a02655-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02655-1-dsg1-primary-antibodies-ihc-testing-1.jpgAnti-Dsg1/Desmoglein 1 AntibodyImmunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02655-1-dsg1-primary-antibodies-wb-testing-2.jpgAnti-Dsg1/Desmoglein 1 AntibodyWestern blot analysis of 293T lysate, antibody was diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fyb-antibody-a02630-1-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02630-1-fyb-primary-antibodies-wb-testing-1.jpgAnti-Fyb/Adap AntibodyWestern blot analysis of FYB Antibody. The lane on the right is blocked with the FYB peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02630-1-fyb-primary-antibodies-wb-testing-2.jpgAnti-Fyb/Adap AntibodyWestern Blot analysis of COLO205 cells using Fyb Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-myosin-vi-antibody-a02627-1-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-1-myo6-primary-antibodyes-wb-testing-1.jpgAnti-Myosin VI MYO6 AntibodyWestern Blot (WB) analysis of extracts from Jurkat cells, using Myosin VI Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-1-myo6-primary-antibodyes-ihc-testing-2.jpgAnti-Myosin VI MYO6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-1-myo6-primary-antibodyes-ihc-testing-3.jpgAnti-Myosin VI MYO6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-1-myo6-primary-antibodyes-ihc-testing-4.jpgAnti-Myosin VI MYO6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pde10a-antibody-a02605-boster.html2026-03-24T05:09:38+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tudorsn-antibody-a02602-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02602-snd1-primary-antibodies-wb-testing-2.jpgAnti-TudorSN SND1 AntibodyWestern Blot analysis of extracts from Jurkat cells, using TudorSN Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02602-snd1-primary-antibodies-ihc-testing-1.jpgAnti-TudorSN SND1 AntibodyImmunohistochemical analysis of paraffin-embedded mouse-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jak3-antibody-a02598-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-wb-testing-2.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyWestern Blot analysis of 293T cells using JAK3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-wb-testing-3.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyWestern blot analysis of lysates from Jurkat cells, using JAK3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-ihc-testing-4.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyImmunohistochemical analysis of paraffin-embedded Human-stomach tissue. 1, JAK3 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-ihc-testing-5.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using JAK3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-if-testing-6.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyImmunofluorescence analysis of Hela cell. 1, JAK3 Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). 3 DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-jak3-primary-antibodies-if-testing-1.jpgAnti-Tyrosine-protein kinase JAK3 JAK3 AntibodyImmunofluorescence analysis of rat-kidney tissue. 1, JAK3 Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-jak3-antibody-a02598-1-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-1-jak3-primary-antibodyes-if-testing-1.jpgAnti-JAK3 Monoclonal AntibodyConfocal Immunofluorescence (IF) analysis of HeLa (left) and HepG2 (right) cells using JAK3 Monoclonal antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-1-jak3-primary-antibodyes-wb-testing-2.jpgAnti-JAK3 Monoclonal AntibodyWestern Blot (WB) analysis using JAK3 Monoclonal antibody against Jurkat cell lysate (1).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02598-1-jak3-primary-antibodyes-fcm-testing-3.jpgAnti-JAK3 Monoclonal AntibodyFlow cytometric (FCM) analysis of HeLa cells using JAK3 Monoclonal antibody (blue) and negative control (red).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lfc-antibody-a02572-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-arhgef2-primary-antibodies-wb-testing-2.jpgAnti-Lfc ARHGEF2 AntibodyWestern Blot analysis of HT29 cells using Lfc Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-arhgef2-primary-antibodies-wb-testing-3.jpgAnti-Lfc ARHGEF2 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using Rho/Rac Guanine Nucleotide Exchange Factor 2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-arhgef2-primary-antibodies-ihc-testing-1.jpgAnti-Lfc ARHGEF2 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ox40l-antibody-a02554-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02554-tnfsf4-primary-antibodies-wb-testing-2.jpgAnti-Ox40L TNFSF4 AntibodyWestern Blot analysis of KB cells using Ox40L Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02554-tnfsf4-primary-antibodies-wb-testing-1.jpgAnti-Ox40L TNFSF4 AntibodyWestern Blot analysis of KB cells using Ox40L Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-histamine-h4-receptor-antibody-a02549-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02549-hrh4-primary-antibodies-wb-testing-2.jpgAnti-Histamine H4 Receptor HRH4 AntibodyWestern Blot analysis of COLO cells using Histamine H4 Receptor Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02549-hrh4-primary-antibodies-if-testing-1.jpgAnti-Histamine H4 Receptor HRH4 AntibodyImmunofluorescence analysis of LOVO cells, using HRH4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mum1-antibody-a02544-1-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02544-1-mum1-primary-antibodies-wb-testing-2.jpgAnti-MUM1 AntibodyWestern Blot analysis of mouse-kidney mouse-heart mouse-brain cells using MUM1 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02544-1-mum1-primary-antibodies-ihc-testing-1.jpgAnti-MUM1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dynamin-i-antibody-a02536-boster.html2026-03-24T05:09:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-dnm1-primary-antibodies-wb-testing-2.jpgAnti-Dynamin I DNM1 AntibodyWestern Blot analysis of 3T3 cells using Dynamin I Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-dnm1-primary-antibodies-wb-testing-3.jpgAnti-Dynamin I DNM1 AntibodyWestern blot analysis of lysates from mouse brain, using Dynamin-1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-dnm1-primary-antibodies-ihc-testing-1.jpgAnti-Dynamin I DNM1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Dynamin-1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dynamin-i-antibody-a02536-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-1-dnm1-primary-antibodies-wb-testing-2.jpgAnti-Dynamin I DNM1 Monoclonal AntibodyWestern Blot analysis using Dynamin I Monoclonal Antibody against C6 (1), NIH/3T3 (2), SKN-SH (3), LN18 (4), SHSY5Y (5) cell lysate and rat brain tiisues lysate (6).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-1-dnm1-primary-antibodies-ihc-testing-1.jpgAnti-Dynamin I DNM1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human lymph tissue (A), glioma tissue (B) and cerebellum tissue (C), showing membrane localization with DAB staining using Dynamin I Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd100-antibody-a02512-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02512-1-sema4d-primary-antibodies-wb-testing-1.jpgAnti-CD100 AntibodyWestern blot analysis of lysate from MCF7 cells, using SEMA4D Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02512-1-sema4d-primary-antibodies-wb-testing-2.jpgAnti-CD100 AntibodyWestern Blot analysis of MCF7, L929 cells using CD100 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hspb8-hsp22-antibody-a02492-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02492-1-hspb8-primary-antibodies-wb-testing-1.jpgAnti-HSPB8/HSP22 Monoclonal AntibodyWestern blot analysis of 293T with HSPB8/HSP22 Mouse mAb diluted at 1:2, 000.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lysrs-antibody-a02479-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02479-kars-primary-antibodies-ihc-testing-1.jpgAnti-LysRS KARS Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human cervical carcinoma, showing cytoplasmic localization with DAB staining using LysRS Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02479-kars-primary-antibodies-wb-testing-2.jpgAnti-LysRS KARS Monoclonal AntibodyWestern Blot analysis using LysRS Monoclonal Antibody against truncated Trx-LysRS recombinant protein (1), truncated MBP-LysRS (aa90-174) and full length LysRS (aa1-188) transfected CHO-K1 cell lysate (3).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-syntenin-1-antibody-a02475-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02475-1-sdcbp-primary-antibodies-wb-testing-1.jpgAnti-Syntenin-1 SDCBP Monoclonal AntibodyWestern Blot analysis using Syntenin-1 Monoclonal Antibody against HeLa nuclear extract, HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tle1-2-3-4-antibody-a02460-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02460-tle1-primary-antibodies-wb-testing-2.jpgAnti-TLE1/2/3/4 AntibodyWestern Blot analysis of A549 3T3 mouse-liver SH-SY5Y K562 Hela 293T cells using TLE1/2/3/4 Polyclonal Antibody diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02460-tle1-primary-antibodies-ihc-testing-3.jpgAnti-TLE1/2/3/4 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02460-tle1-primary-antibodies-ihc-testing-1.jpgAnti-TLE1/2/3/4 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eklf-cklf-uklf-antibody-a02450-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02450-1-klf1-primary-antibodies-wb-testing-1.jpgAnti-EKLF/CKLF/UKLF AntibodyWestern blot analysis of lysates from Jurkat cells, treated with serum 20% 15', using KLF Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02450-1-klf1-primary-antibodies-wb-testing-2.jpgAnti-EKLF/CKLF/UKLF AntibodyWestern Blot analysis of VEC cells using EKLF/CKLF/UKLF Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-prp19-antibody-a02434-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02434-prpf19-primary-antibodies-ihc-testing-1.jpgAnti-PRP19 PRPF19 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02434-prpf19-primary-antibodies-wb-testing-2.jpgAnti-PRP19 PRPF19 AntibodyWestern Blot analysis of various cells using PRP19 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02434-prpf19-primary-antibodies-wb-testing-3.jpgAnti-PRP19 PRPF19 AntibodyWestern blot analysis of lysates from COLO and Jurkat cells, using PRPF19 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-14-3-3-beta-antibody-a02431-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02431-ywhab-primary-antibodies-wb-testing-2.jpgAnti-14-3-3 beta YWHAB AntibodyWestern Blot analysis of various cells using 14-3-3 β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02431-ywhab-primary-antibodies-wb-testing-3.jpgAnti-14-3-3 beta YWHAB AntibodyWestern Blot analysis of Jurkat cells using 14-3-3 β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02431-ywhab-primary-antibodies-wb-testing-4.jpgAnti-14-3-3 beta YWHAB AntibodyWestern blot analysis of lysates from HepG2 and Jurkat cells, using 14-3-3 beta Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02431-ywhab-primary-antibodies-wb-testing-5.jpgAnti-14-3-3 beta YWHAB AntibodyWestern blot analysis of the lysates from HepG2 cells using 14-3-3 β antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02431-ywhab-primary-antibodies-ihc-testing-1.jpgAnti-14-3-3 beta YWHAB AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd64-antibody-a02428-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02428-fcgr1a-primary-antibodyes-ihc-testing-1.jpgAnti-CD64 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02428-fcgr1a-primary-antibodyes-wb-testing-2.jpgAnti-CD64 AntibodyWestern blot analysis of mouse-kidney, mouse lung, mouse heart, 293T lysate, antibody was diluted at 2000. Secondary antibody was diluted at 1:20000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02428-fcgr1a-primary-antibodyes-ihc-testing-3.jpgAnti-CD64 AntibodyImmunohistochemical analysis of paraffin-embedded human-stomach-cancer, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pcaf-antibody-a02403-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02403-kat2b-primary-antibodies-ihc-testing-1.jpgAnti-PCAF KAT2B AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using p300/CBP Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02403-kat2b-primary-antibodies-wb-testing-2.jpgAnti-PCAF KAT2B AntibodyWestern Blot analysis of various cells using PCAF Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02403-kat2b-primary-antibodies-wb-testing-3.jpgAnti-PCAF KAT2B AntibodyWestern blot analysis of lysates from COLO205 cells, using p300/CBP Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acetyl-pcaf-k428-antibody-a02403-1-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02403-1-kat2b-primary-antibodies-wb-testing-2.jpgAnti-Acetyl-PCAF (K428) KAT2B AntibodyWestern Blot analysis of HepG2 cells using Acetyl-PCAF (K428) Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02403-1-kat2b-primary-antibodies-ihc-testing-1.jpgAnti-Acetyl-PCAF (K428) KAT2B AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mcad-antibody-a02383-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02383-acadm-primary-antibodies-ihc-testing-1.jpgAnti-MCAD ACADM AntibodyImmunohistochemical analysis of paraffin-embedded human uterus. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02383-acadm-primary-antibodies-wb-testing-2.jpgAnti-MCAD ACADM AntibodyWestern Blot analysis of extracts from A549 cells, using MCAD Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02383-acadm-primary-antibodies-wb-testing-3.jpgAnti-MCAD ACADM AntibodyWestern blot analysis of lysates from HeLa cells, using MCAD antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-atp-citrate-synthase-antibody-a02372-boster.html2026-03-24T05:09:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02372-acly-primary-antibodies-wb-testing-2.jpgAnti-ATP-citrate synthase ACLY Monoclonal AntibodyWestern Blot analysis using ATP-citrate synthase Monoclonal Antibody against K562, HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02372-acly-primary-antibodies-if-testing-3.jpgAnti-ATP-citrate synthase ACLY Monoclonal AntibodyImmunofluorescence analysis of HeLa cells using ATP-citrate synthase Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02372-acly-primary-antibodies-fcm-testing-1.jpgAnti-ATP-citrate synthase ACLY Monoclonal AntibodyFlow cytometric analysis of HeLa cells stained with ATP-citrate synthase Monoclonal Antibody (red), followed by FITC-conjugated goat anti-mouse IgG. Black line histogram represents the isotype control, normal mouse IgG.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nsd1-antibody-a02327-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02327-nsd1-primary-antibodies-wb-testing-1.jpgAnti-NSD1/Kmt3B Monoclonal AntibodyWestern Blot analysis using NSD1 Monoclonal Antibody against HepG2 cell lysate .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nf90-antibody-a02313-1-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02313-1-ilf3-primary-antibodies-wb-testing-2.jpgAnti-NF90 ILF3 AntibodyWestern Blot analysis of extracts from A549, K562, NIH-3T3 cells, using NF90 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02313-1-ilf3-primary-antibodies-wb-testing-3.jpgAnti-NF90 ILF3 AntibodyWestern blot analysis of lysates from HeLa cells, using NF90 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02313-1-ilf3-primary-antibodies-if-testing-1.jpgAnti-NF90 ILF3 AntibodyImmunofluorescence analysis of MCF7 cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cytokeratin-10-antibody-a02305-1-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02305-1-krt10-primary-antibodies-wb-testing-2.jpgAnti-Cytokeratin 10 KRT10 AntibodyWestern Blot analysis of various cells using Cytokeratin 10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02305-1-krt10-primary-antibodies-wb-testing-3.jpgAnti-Cytokeratin 10 KRT10 AntibodyWestern Blot analysis of HeLa cells using Cytokeratin 10 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02305-1-krt10-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 10 KRT10 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02305-1-krt10-primary-antibodies-if-testing-1.jpgAnti-Cytokeratin 10 KRT10 AntibodyImmunofluorescence analysis of A549 cells, using Keratin 10 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fibulin-3-antibody-a02302-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02302-efemp1-primary-antibodies-wb-testing-2.jpgAnti-Fibulin-3 EFEMP1 AntibodyWestern Blot analysis of rat cells using Fibulin-3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02302-efemp1-primary-antibodies-wb-testing-3.jpgAnti-Fibulin-3 EFEMP1 AntibodyWestern blot analysis of lysates from rat lung, using EFEMP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02302-efemp1-primary-antibodies-ihc-testing-1.jpgAnti-Fibulin-3 EFEMP1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd206-antibody-a02285-1-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02285-1-mrc1-primary-antibodyes-wb-testing-1.jpgAnti-CD206 MRC1 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using CD206 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02285-1-mrc1-primary-antibodyes-wb-testing-2.jpgAnti-CD206 MRC1 AntibodyWestern Blot (WB) analysis of 3T3 cells using CD206 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02285-1-mrc1-primary-antibodyes-ihc-testing-3.jpgAnti-CD206 MRC1 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Heart, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eef2k-antibody-a02277-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02277-eef2k-primary-antibodies-wb-testing-2.jpgAnti-eEF2K AntibodyWestern Blot analysis of HeLa cells using eEF2K Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02277-eef2k-primary-antibodies-wb-testing-3.jpgAnti-eEF2K AntibodyWestern blot analysis of lysates from HeLa cells, treated with serum 10% 15', using eEF2K Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02277-eef2k-primary-antibodies-ihc-testing-1.jpgAnti-eEF2K AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using eEF2K Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eif3l-antibody-a02238-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02238-eif3l-primary-antibodies-wb-testing-2.jpgAnti-eIF3L/Eif3S6Ip AntibodyWestern Blot analysis of various cells using eIF3L Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02238-eif3l-primary-antibodies-wb-testing-1.jpgAnti-eIF3L/Eif3S6Ip AntibodyWestern blot analysis of lysates from HUVEC cells, using IF3EI Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd276-antibody-a02220-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02220-cd276-primary-antibodies-wb-testing-2.jpgAnti-CD276/B7 H3 AntibodyWestern blot analysis of lysate from 293 cells, using CD276 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02220-cd276-primary-antibodies-ihc-testing-1.jpgAnti-CD276/B7 H3 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-3r-beta-antibody-a02219-1-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02219-1-csf2rb-primary-antibodyes-wb-testing-1.jpgAnti-IL-3R beta CSF2RB AntibodyWestern Blot (WB) analysis of specific cells using IL-3Rbeta Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-g3bp1-antibody-a02199-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02199-g3bp1-primary-antibodies-ihc-testing-1.jpgAnti-G3BP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using G3BP-1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02199-g3bp1-primary-antibodies-wb-testing-2.jpgAnti-G3BP1 AntibodyWestern Blot analysis of various cells using G3BP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02199-g3bp1-primary-antibodies-wb-testing-3.jpgAnti-G3BP1 AntibodyWestern blot analysis of lysates from HeLa cells, using G3BP-1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd158e-antibody-a02187-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02187-kir3dl1-primary-antibodies-wb-testing-2.jpgAnti-CD158e KIR3DL1 AntibodyWestern blot analysis of mouse-lung lysis using KIR3DL1 antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02187-kir3dl1-primary-antibodies-wb-testing-3.jpgAnti-CD158e KIR3DL1 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02187-kir3dl1-primary-antibodies-ihc-testing-1.jpgAnti-CD158e KIR3DL1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-probetacellulin-antibody-a02171-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02171-btc-primary-antibodies-wb-testing-2.jpgAnti-Probetacellulin BTC AntibodyWestern Blot analysis of KB cells using Probetacellulin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02171-btc-primary-antibodies-wb-testing-3.jpgAnti-Probetacellulin BTC AntibodyWestern Blot analysis of KB cells using Probetacellulin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02171-btc-primary-antibodies-ihc-testing-1.jpgAnti-Probetacellulin BTC AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd1b-antibody-a02158-boster.html2026-03-24T05:09:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02158-cd1b-primary-antibodies-ihc-testing-2.jpgAnti-CD1B AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02158-cd1b-primary-antibodies-ihc-testing-3.jpgAnti-CD1B AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02158-cd1b-primary-antibodies-ihc-testing-1.jpgAnti-CD1B AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-senp1-antibody-a02156-1-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02156-1-senp1-primary-antibodies-wb-testing-2.jpgAnti-Sentrin-specific protease 1 SENP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using SENP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02156-1-senp1-primary-antibodies-ihc-testing-1.jpgAnti-Sentrin-specific protease 1 SENP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using SENP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-smc1-antibody-a02148-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02148-smc1a-primary-antibodyes-wb-testing-1.jpgAnti-SMC1 AntibodyWestern Blot (WB) analysis of 293 cells using SMC1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-smc1-antibody-a02148-2-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02148-2-smc1a-primary-antibodyes-ihc-testing-1.jpgAnti-SMC1 SMC1A Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Colon using SMC1 Monoclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02148-2-smc1a-primary-antibodyes-wb-testing-2.jpgAnti-SMC1 SMC1A Monoclonal AntibodyWestern Blot (WB) analysis using SMC1 Monoclonal antibody against HeLa nuclear extract.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02148-2-smc1a-primary-antibodyes-fcm-testing-3.jpgAnti-SMC1 SMC1A Monoclonal AntibodyFlow cytometric (FCM) analysis of HeLa cells stained with SMC1 Monoclonal antibody (red), followed by FITC-conjugated goat anti-Mouse IgG. Black line histogram represents the isotype control, normal Mouse IgG.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aox1-antibody-a02144-1-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02144-1-aox1-primary-antibodies-wb-testing-2.jpgAnti-AOX1/Aldehyde Oxidase AntibodyWestern Blot analysis of various cells using AOX1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02144-1-aox1-primary-antibodies-wb-testing-3.jpgAnti-AOX1/Aldehyde Oxidase AntibodyWestern blot analysis of lysates from HeLa cells, using AOX1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02144-1-aox1-primary-antibodies-ihc-testing-1.jpgAnti-AOX1/Aldehyde Oxidase AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using AOX1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-git1-antibody-a02140-1-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02140-1-git1-primary-antibodies-ihc-testing-1.jpgAnti-GIT1 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen tissue. 1,primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02140-1-git1-primary-antibodies-wb-testing-2.jpgAnti-GIT1 AntibodyWestern Blot analysis of HepG2 cells using GIT1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02140-1-git1-primary-antibodies-wb-testing-3.jpgAnti-GIT1 AntibodyWestern blot analysis of the lysates from 293 cells using GIT1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-trem-1-antibody-a02135-boster.html2026-03-24T05:09:41+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dhs-antibody-a02106-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02106-dhps-primary-antibodies-wb-testing-2.jpgAnti-DHS DHPS AntibodyWestern Blot analysis of various cells using DHS Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02106-dhps-primary-antibodies-wb-testing-3.jpgAnti-DHS DHPS AntibodyWestern Blot analysis of K562 cells using DHS Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02106-dhps-primary-antibodies-wb-testing-4.jpgAnti-DHS DHPS AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using DHPS Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02106-dhps-primary-antibodies-wb-testing-1.jpgAnti-DHS DHPS AntibodyWestern blot analysis of the lysates from HUVECcells using DHPS antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp2c19-antibody-a02102-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02102-cyp2c19-primary-antibodies-wb-testing-2.jpgAnti-CYP2C19/Cytochrome P450 2C19 AntibodyWestern Blot analysis of MOUSE-BRAIN cells using CYP2C19 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02102-cyp2c19-primary-antibodies-wb-testing-3.jpgAnti-CYP2C19/Cytochrome P450 2C19 AntibodyWestern blot analysis of lysates from 293 cells, using Cytochrome P450 2C19 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02102-cyp2c19-primary-antibodies-ihc-testing-1.jpgAnti-CYP2C19/Cytochrome P450 2C19 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd42b-antibody-a02073-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02073-gp1ba-primary-antibodies-ihc-testing-1.jpgAnti-CD42b GP1BA AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02073-gp1ba-primary-antibodies-wb-testing-2.jpgAnti-CD42b GP1BA AntibodyWestern Blot analysis of HeLa cells using CD42b Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-a-raf-antibody-a02061-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02061-araf-primary-antibodies-wb-testing-2.jpgAnti-A-Raf AntibodyWestern blot analysis in MCF-7 cells transfected with siA-Raf.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02061-araf-primary-antibodies-wb-testing-3.jpgAnti-A-Raf AntibodyWestern Blot analysis of various cells using A-Raf Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02061-araf-primary-antibodies-ihc-testing-1.jpgAnti-A-Raf AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using A-RAF Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ifn-alphar2-antibody-a02056-1-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02056-1-ifnar2-primary-antibodies-wb-testing-2.jpgAnti-IFN- alphaR2 IFNAR2 AntibodyWestern Blot analysis of AD293 cells using IFN-αR2 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02056-1-ifnar2-primary-antibodies-wb-testing-3.jpgAnti-IFN- alphaR2 IFNAR2 AntibodyWestern blot analysis of lysate from AD293 cells, using IFNAR2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02056-1-ifnar2-primary-antibodies-ihc-testing-1.jpgAnti-IFN- alphaR2 IFNAR2 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fnk-antibody-a02054-1-boster.html2026-03-24T05:09:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02054-1-plk3-primary-antibodies-wb-testing-1.jpgAnti-Fnk PLK3 AntibodyWestern blot analysis of the lysates from RAW264.7cells using PLK3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02054-1-plk3-primary-antibodies-wb-testing-2.jpgAnti-Fnk PLK3 AntibodyWestern Blot analysis of various cells using Fnk Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02054-1-plk3-primary-antibodies-wb-testing-3.jpgAnti-Fnk PLK3 AntibodyWestern blot analysis of lysates from HepG2 cells, using PLK3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lsk-antibody-a02050-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-matk-primary-antibodies-wb-testing-2.jpgAnti-Lsk MATK Monoclonal AntibodyWestern Blot analysis using Lsk Monoclonal Antibody against K562 cell lysate (1).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-matk-primary-antibodies-fcm-testing-1.jpgAnti-Lsk MATK Monoclonal AntibodyFlow cytometric analysis of K562 cells using Lsk Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ocrl-antibody-a02042-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02042-ocrl-primary-antibodies-wb-testing-2.jpgAnti-OCRL/Inpp5F AntibodyWestern Blot analysis of various cells using OCRL Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02042-ocrl-primary-antibodies-wb-testing-1.jpgAnti-OCRL/Inpp5F AntibodyWestern blot analysis of lysate from COLO205 cells treated with Forskolin, using OCRL antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ifn-beta-antibody-a02041-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02041-ifnb1-primary-antibodyes-ihc-testing-1.jpgAnti-IFN- beta IFNB1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02041-ifnb1-primary-antibodyes-ihc-testing-2.jpgAnti-IFN- beta IFNB1 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02041-ifnb1-primary-antibodyes-ihc-testing-3.jpgAnti-IFN- beta IFNB1 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02041-ifnb1-primary-antibodyes-ihc-testing-4.jpgAnti-IFN- beta IFNB1 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-spop-antibody-a02032-boster.html2026-03-24T05:09:42+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ercc4-antibody-a01993-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01993-ercc4-primary-antibodies-wb-testing-2.jpgAnti-ERCC4/Xpf AntibodyWestern Blot analysis of various cells using ERCC4 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01993-ercc4-primary-antibodies-wb-testing-3.jpgAnti-ERCC4/Xpf AntibodyWestern Blot analysis of 293 cells using ERCC4 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01993-ercc4-primary-antibodies-wb-testing-1.jpgAnti-ERCC4/Xpf AntibodyWestern blot analysis of lysates from 293 cells, using XPF Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-achr-alpha3-antibody-a01981-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01981-chrna3-primary-antibodies-wb-testing-2.jpgAnti-AChR alpha3 CHRNA3 AntibodyWestern Blot analysis of various cells using AChRα3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01981-chrna3-primary-antibodies-wb-testing-1.jpgAnti-AChR alpha3 CHRNA3 AntibodyWestern blot analysis of lysate from HeLa cells, using AChRα3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ledgf-antibody-a01960-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-psip1-primary-antibodies-ihc-testing-2.jpgAnti-LEDGF PSIP1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded breast cancer tissues (left) and ovarian cancer tissues (right) with DAB staining using LEDGF Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-psip1-primary-antibodies-if-testing-3.jpgAnti-LEDGF PSIP1 Monoclonal AntibodyImmunofluorescence analysis of NIH/3T3 cells using LEDGF Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-psip1-primary-antibodies-wb-testing-1.jpgAnti-LEDGF PSIP1 Monoclonal AntibodyWestern Blot analysis using LEDGF Monoclonal Antibody against HepG2 (1), Jurkat (2), K562 (3), Cos7 (4), PC-12 (5), HeLa (6), and NIH/3T3 (7) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-batf3-antibody-a01957-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01957-batf3-primary-antibodies-wb-testing-2.jpgAnti-BATF3/Snft AntibodyWestern blot analysis of mouse-lung mouse-spleen lysis using BATF3 antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01957-batf3-primary-antibodies-ihc-testing-1.jpgAnti-BATF3/Snft AntibodyImmunohistochemical analysis of paraffin-embedded human-breast-cancer, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-pol-beta-antibody-a01946-1-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01946-1-polb-primary-antibodies-wb-testing-2.jpgAnti-DNA pol beta AntibodyWestern Blot analysis of various cells using DNA pol β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01946-1-polb-primary-antibodies-wb-testing-3.jpgAnti-DNA pol beta AntibodyWestern Blot analysis of K562 cells using DNA pol β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01946-1-polb-primary-antibodies-wb-testing-4.jpgAnti-DNA pol beta AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using DNA Polymerase beta Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01946-1-polb-primary-antibodies-ihc-testing-1.jpgAnti-DNA pol beta AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using DNA Polymerase beta Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-integrin-alpha2-antibody-a01933-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01933-itga2-primary-antibodyes-wb-testing-1.jpgAnti-Integrin alpha2 ITGA2 AntibodyWestern Blot (WB) analysis of NIH-3T3 cells using Integrin alpha2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01933-itga2-primary-antibodyes-wb-testing-2.jpgAnti-Integrin alpha2 ITGA2 AntibodyWestern Blot (WB) analysis of 3T3 cells using Integrin alpha2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01933-itga2-primary-antibodyes-ihc-testing-3.jpgAnti-Integrin alpha2 ITGA2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Colon, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gabarap-antibody-a01927-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01927-gabarapl2-primary-antibodies-wb-testing-1.jpgAnti-GABARAP GABARAPL2 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-glypican-3-antibody-a01922-boster.html2026-03-24T05:09:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01922-gpc3-primary-antibodies-wb-testing-2.jpgAnti-Glypican-3 GPC3 AntibodyWestern Blot analysis of HepG2 cells using Glypican-3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01922-gpc3-primary-antibodies-wb-testing-3.jpgAnti-Glypican-3 GPC3 AntibodyWestern blot analysis of lysate from HepG2 cells, using GPC3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01922-gpc3-primary-antibodies-ihc-testing-1.jpgAnti-Glypican-3 GPC3 AntibodyImmunohistochemical analysis of paraffin-embedded rat-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-neuromedin-u-antibody-a01919-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-nmu-primary-antibodies-ihc-testing-1.jpgAnti-Neuromedin-U NMU AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using NMU Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-nmu-primary-antibodies-wb-testing-2.jpgAnti-Neuromedin-U NMU AntibodyWestern Blot analysis of various cells using Neuromedin-U Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-nmu-primary-antibodies-wb-testing-3.jpgAnti-Neuromedin-U NMU AntibodyWestern blot analysis of lysates from HepG2 cells, using NMU Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdha1-antibody-a01906-1-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-1-pdha1-primary-antibodyes-wb-testing-1.jpgAnti-PDHA1/Pdh E1Alpha AntibodyWestern blot analysis of various cells using PDHA1 Polyclonal Antibody diluted at 1：2000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdh-e1-alpha-antibody-a01906-2-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-2-pdha1-primary-antibodies-wb-testing-2.jpgAnti-PDH-E1 alpha PDHA1 Monoclonal AntibodyWestern Blot analysis using PDH-E1α Monoclonal Antibody against A549, HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-2-pdha1-primary-antibodies-if-testing-1.jpgAnti-PDH-E1 alpha PDHA1 Monoclonal AntibodyImmunofluorescence analysis of HeLa cells using PDH-E1α Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd88-antibody-a01898-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01898-c5ar1-primary-antibodies-wb-testing-1.jpgAnti-CD88 C5AR1 AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01898-c5ar1-primary-antibodies-wb-testing-2.jpgAnti-CD88 C5AR1 AntibodyWestern blot analysis of MOUSE-BRAIN RAT-SPLEEN lysis using C5AR1 antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-micu1-antibody-a01895-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01895-micu1-primary-antibodies-ihc-testing-2.jpgAnti-MICU1/Cbara1 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-testis tissue. 1, MICU1 Monoclonal Antibody (Mix) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01895-micu1-primary-antibodies-if-testing-3.jpgAnti-MICU1/Cbara1 Monoclonal AntibodyImmunofluorescence analysis of Hela cell. 1, c-Myc Polyclonal Antibody (red) was diluted at 1:200 (4° overnight). MICU1 Monoclonal Antibody (Mix) (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01895-micu1-primary-antibodies-if-testing-1.jpgAnti-MICU1/Cbara1 Monoclonal AntibodyImmunofluorescence analysis of Human-appendix tissue. 1, MICU1 Monoclonal Antibody (Mix) (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cep290-antibody-a01894-1-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01894-1-cep290-primary-antibodies-wb-testing-2.jpgAnti-Centrosomal protein of 290 kDa CEP290 AntibodyWestern Blot analysis of various cells using CEP290 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01894-1-cep290-primary-antibodies-wb-testing-1.jpgAnti-Centrosomal protein of 290 kDa CEP290 AntibodyWestern blot analysis of lysates from K562 cells, using CEP290 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mdmx-antibody-a01889-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01889-mdm4-primary-antibodies-wb-testing-2.jpgAnti-MDMX MDM4 AntibodyWestern Blot analysis of 293T cells using MDMX Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01889-mdm4-primary-antibodies-wb-testing-3.jpgAnti-MDMX MDM4 AntibodyWestern blot analysis of lysates from rat muscle cells, using MDM4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01889-mdm4-primary-antibodies-ihc-testing-1.jpgAnti-MDMX MDM4 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using MDM4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-brm-antibody-a01888-1-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01888-1-smarca2-primary-antibodies-wb-testing-2.jpgAnti-Brm SMARCA2 AntibodyWestern Blot analysis of extracts from A549 cells, using Brm Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01888-1-smarca2-primary-antibodies-wb-testing-1.jpgAnti-Brm SMARCA2 AntibodyWestern blot analysis of lysates from K562 cells, using Brm antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fsh-beta-antibody-a01885-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01885-fshb-primary-antibodies-ihc-testing-1.jpgAnti-FSH beta AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdgf-d-antibody-a01875-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01875-pdgfd-primary-antibodies-wb-testing-2.jpgAnti-PDGF-D AntibodyWestern Blot analysis of L929 cells using PDGF-D Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01875-pdgfd-primary-antibodies-wb-testing-3.jpgAnti-PDGF-D AntibodyWestern blot analysis of lysate from L929 cells, using PDGFD Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01875-pdgfd-primary-antibodies-ihc-testing-1.jpgAnti-PDGF-D AntibodyImmunohistochemical analysis of paraffin-embedded human-mammary-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tmem173-antibody-a01871-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01871-tmem173-primary-antibodies-wb-testing-2.jpgAnti-TMEM173/Sting AntibodyWestern Blot analysis of HeLa, K562, 4T1 cells using TMEM173 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01871-tmem173-primary-antibodies-ihc-testing-1.jpgAnti-TMEM173/Sting AntibodyImmunohistochemical analysis of paraffin-embedded human-Breast-cancer, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-epsin-1-antibody-a01870-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01870-epn1-primary-antibodies-wb-testing-1.jpgAnti-Epsin 1 EPN1 AntibodyWestern Blot analysis of MOuse-brain cells using Epsin 1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01870-epn1-primary-antibodies-wb-testing-2.jpgAnti-Epsin 1 EPN1 AntibodyWestern Blot analysis of various cells using Epsin 1 Polyclonal Antibody diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fgf-16-antibody-a01859-boster.html2026-03-24T05:09:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01859-fgf16-primary-antibodies-wb-testing-1.jpgAnti-FGF-16 AntibodyWestern Blot analysis of K562 cells using FGF-16 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kir2-1-antibody-a01850-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01850-kcnj2-primary-antibodies-wb-testing-2.jpgAnti-KIR2.1 KCNJ2 AntibodyWestern Blot analysis of various cells using KIR2.1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01850-kcnj2-primary-antibodies-ihc-testing-1.jpgAnti-KIR2.1 KCNJ2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using KCNJ2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-galactosidase-beta-antibody-a01829-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01829-glb1-primary-antibodyes-ihc-testing-1.jpgAnti-Galactosidase beta GLB1 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Breast Cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01829-glb1-primary-antibodyes-wb-testing-2.jpgAnti-Galactosidase beta GLB1 AntibodyWestern Blot (WB) analysis of 3T3 using Galactosidase beta antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01829-glb1-primary-antibodyes-ihc-testing-3.jpgAnti-Galactosidase beta GLB1 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Colont-cancer, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-etar-antibody-a01828-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01828-ednra-primary-antibodies-wb-testing-2.jpgAnti-ETAR EDNRA AntibodyWestern Blot analysis of various cells using ETAR Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01828-ednra-primary-antibodies-wb-testing-3.jpgAnti-ETAR EDNRA AntibodyWestern blot analysis of lysates from COS7 cells, using EDNRA Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01828-ednra-primary-antibodies-ihc-testing-4.jpgAnti-ETAR EDNRA AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01828-ednra-primary-antibodies-if-testing-1.jpgAnti-ETAR EDNRA AntibodyImmunofluorescence analysis of LOVO cells, using EDNRA Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acc-alpha-antibody-a01802-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01802-acaca-primary-antibodies-ihc-testing-1.jpgAnti-ACC alpha ACACA AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using ACC1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01802-acaca-primary-antibodies-ihc-testing-2.jpgAnti-ACC alpha ACACA AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01802-acaca-primary-antibodies-wb-testing-3.jpgAnti-ACC alpha ACACA AntibodyWestern blot analysis of lysates from 1) Hela, 2) 293T ,3) NIH/3T3 cells, (Green） primary antibody was diluted at 1:1000, 4°over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red） GAPDH Monoclonal Antibody (2B8) antibody was diluted at 1:5000 as loading control, 4° over night,secondary antibody was diluted at 1:10000, 37° 1hour.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd98-antibody-a01794-1-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-1-slc3a2-primary-antibodies-wb-testing-1.jpgAnti-CD98 SLC3A2 AntibodyWestern Blot analysis of HEB cells using CD98 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd166-antibody-a01788-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-alcam-primary-antibodies-wb-testing-2.jpgAnti-CD166 ALCAM AntibodyWestern Blot analysis of K562 cells using CD166 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-alcam-primary-antibodies-wb-testing-3.jpgAnti-CD166 ALCAM AntibodyWestern blot analysis of lysate from K562 cells, using ALCAM Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-alcam-primary-antibodies-ihc-testing-4.jpgAnti-CD166 ALCAM AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-alcam-primary-antibodies-ihc-testing-5.jpgAnti-CD166 ALCAM AntibodyImmunohistochemical analysis of paraffin-embedded Human Liver. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-alcam-primary-antibodies-ihc-testing-1.jpgAnti-CD166 ALCAM AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach. 1, Antibody was diluted at 1:100 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ucp3-antibody-a01769-1-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01769-1-ucp3-primary-antibodies-wb-testing-2.jpgAnti-UCP3 AntibodyWestern Blot analysis of various cells using UCP3 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01769-1-ucp3-primary-antibodies-wb-testing-1.jpgAnti-UCP3 AntibodyWestern blot analysis of lysate from Jurkat cells, using UCP3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cyp4f2-antibody-a01737-boster.html2026-03-24T05:09:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01737-cyp4f2-primary-antibodies-ihc-testing-1.jpgAnti-CYP4F2 AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma, using Cytochrome P450 4F2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01737-cyp4f2-primary-antibodies-wb-testing-2.jpgAnti-CYP4F2 AntibodyWestern Blot analysis of various cells using CYP4F2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01737-cyp4f2-primary-antibodies-wb-testing-3.jpgAnti-CYP4F2 AntibodyWestern Blot analysis of Hela cells using CYP4F2 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rfc1-antibody-a01730-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01730-rfc1-primary-antibodies-wb-testing-2.jpgAnti-Replication factor C subunit 1 RFC1 AntibodyWestern Blot analysis of mouse liver, mouse kidney cells using RFC1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01730-rfc1-primary-antibodies-ihc-testing-1.jpgAnti-Replication factor C subunit 1 RFC1 AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-parafibromin-antibody-a01726-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01726-cdc73-primary-antibodyes-wb-testing-1.jpgAnti-Parafibromin CDC73 AntibodyWestern Blot analysis of 1) mouse heart, 2) mouse spleen cells using primary antibody diluted at 1: 500 (4℃ overnight) . Secondary antibody: Goat Anti-rabbit IgG IRDye 800 (diluted at 1: 5000, 25℃, 1 hour).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-alpp-alppl2-antibody-a01718-1-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-1-alpp-primary-antibodyes-wb-testing-1.jpgAnti-ALPP/ALPPL2 AntibodyWestern Blot (WB) analysis of 293 cells using ALPP/ALPPL2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01718-1-alpp-primary-antibodyes-wb-testing-2.jpgAnti-ALPP/ALPPL2 AntibodyWestern Blot (WB) analysis of sample using ALPP/ALPPL2 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ghrelin-antibody-a01710-1-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01710-1-ghrl-primary-antibodies-if-testing-1.jpgAnti-Ghrelin GHRL AntibodyImmunofluorescence analysis of A549. 1,primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01710-1-ghrl-primary-antibodies-wb-testing-2.jpgAnti-Ghrelin GHRL AntibodyWestern Blot analysis of 293 cells using Ghrelin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01710-1-ghrl-primary-antibodies-if-testing-3.jpgAnti-Ghrelin GHRL AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01710-1-ghrl-primary-antibodies-ihc-testing-4.jpgAnti-Ghrelin GHRL AntibodyImmunohistochemistry analysis of Ghrelin antibody in paraffin-embedded human lung carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ddr2-antibody-a01698-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01698-ddr2-primary-antibodyes-ihc-testing-1.jpgAnti-DDR2/Tyro10 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung-cancer, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01698-ddr2-primary-antibodyes-ihc-testing-2.jpgAnti-DDR2/Tyro10 AntibodyImmunohistochemical analysis of paraffin-embedded human-lung-cancer, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cot-antibody-a01696-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01696-map3k8-primary-antibodyes-wb-testing-1.jpgAnti-COT MAP3K8 AntibodyWestern Blot (WB) analysis of specific cells using COT Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-14-3-3-epsilon-antibody-a01687-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01687-ywhae-primary-antibodies-wb-testing-2.jpgAnti-14-3-3 epsilon YWHAE AntibodyWestern Blot analysis of various cells using 14-3-3 ε Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01687-ywhae-primary-antibodies-wb-testing-3.jpgAnti-14-3-3 epsilon YWHAE AntibodyWestern blot analysis of lysates from HepG2 and Jurkat cells, using 14-3-3 epsilon Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01687-ywhae-primary-antibodies-ihc-testing-1.jpgAnti-14-3-3 epsilon YWHAE AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1, primary Antibody was diluted at 1:200 (4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-ligase-iv-antibody-a01685-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01685-lig4-primary-antibodies-ihc-testing-1.jpgAnti-DNA Ligase IV LIG4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01685-lig4-primary-antibodies-wb-testing-2.jpgAnti-DNA Ligase IV LIG4 AntibodyWestern Blot analysis of various cells using DNA Ligase IV Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01685-lig4-primary-antibodies-wb-testing-3.jpgAnti-DNA Ligase IV LIG4 AntibodyWestern Blot analysis of VEC cells using DNA Ligase IV Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01685-lig4-primary-antibodies-wb-testing-4.jpgAnti-DNA Ligase IV LIG4 AntibodyWestern blot analysis of lysates from Jurkat cells, using DNL4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-udg-antibody-a01672-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01672-ung-primary-antibodies-wb-testing-2.jpgAnti-UDG UNG AntibodyWestern Blot analysis of COLO205 cells using UDG Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01672-ung-primary-antibodies-wb-testing-3.jpgAnti-UDG UNG AntibodyWestern blot analysis of lysates from HepG2 and COLO cells, using UNG Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01672-ung-primary-antibodies-wb-testing-4.jpgAnti-UDG UNG AntibodyWestern blot analysis of the lysates from HepG2 cells using UNG antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01672-ung-primary-antibodies-ihc-testing-1.jpgAnti-UDG UNG AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sox-17-antibody-a01665-1-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01665-1-sox17-primary-antibodies-wb-testing-2.jpgAnti-Sox-17 AntibodyWestern Blot analysis of extracts from Jurkat cells, using Sox-17 Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01665-1-sox17-primary-antibodies-ihc-testing-1.jpgAnti-Sox-17 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cux1-antibody-a01653-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01653-cux1-primary-antibodyes-wb-testing-1.jpgAnti-CUX1/Cdp AntibodyWestern Blot (WB) analysis of 293T cells using CUX1 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01653-cux1-primary-antibodyes-wb-testing-2.jpgAnti-CUX1/Cdp AntibodyWestern Blot (WB) analysis of specific cells using CUX1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-glcne-antibody-a01647-1-boster.html2026-03-24T05:09:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01647-1-gne-primary-antibodies-ihc-testing-1.jpgAnti-GLCNE GNE AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01647-1-gne-primary-antibodies-wb-testing-2.jpgAnti-GLCNE GNE AntibodyWestern Blot analysis of 3T3 cells using GLCNE Polyclonal Antibody diluted at 1:500
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-trypsin-1-antibody-a01637-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01637-prss1-primary-antibodies-wb-testing-1.jpgAnti-Trypsin-1 PRSS1 AntibodyWestern blot analysis of lysate from 293 cells, using Trypsin-1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01637-prss1-primary-antibodies-wb-testing-2.jpgAnti-Trypsin-1 PRSS1 AntibodyWestern Blot analysis of various cells using Trypsin-1 Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd21-antibody-a01632-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-cr2-primary-antibodies-ihc-testing-2.jpgAnti-CD21 CR2 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1, CD21 Monoclonal Antibody (2C5) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-cr2-primary-antibodies-ihc-testing-3.jpgAnti-CD21 CR2 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-kidney tissue. 1, CD21 Monoclonal Antibody (2C5) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-cr2-primary-antibodies-if-testing-1.jpgAnti-CD21 CR2 Monoclonal AntibodyImmunofluorescence analysis of Mouse-liver tissue. 1, CD21 Monoclonal Antibody (2C5) (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd21-antibody-a01632-1-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-1-cr2-primary-antibodyes-wb-testing-1.jpgAnti-CD21 CR2 AntibodyWestern Blot (WB) analysis of NIH-3T3, KB cells using CD21 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-1-cr2-primary-antibodyes-wb-testing-2.jpgAnti-CD21 CR2 AntibodyWestern Blot (WB) analysis of 3T3 cells using CD21 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-1-cr2-primary-antibodyes-ihc-testing-3.jpgAnti-CD21 CR2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Tonsils, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fer-antibody-a01630-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01630-fer-primary-antibodies-if-testing-1.jpgAnti-Fer Monoclonal AntibodyConfocal immunofluorescence analysis of Hela cells using Fer Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01630-fer-primary-antibodies-wb-testing-2.jpgAnti-Fer Monoclonal AntibodyWestern Blot analysis using Fer Monoclonal Antibody against NIH/3T3 (1), A549 (2) and SK-MEL-5 (3) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01630-fer-primary-antibodies-ihc-testing-3.jpgAnti-Fer Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human kidney tissues with AEC staining using Fer Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dynamin-ii-antibody-a01629-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01629-dnm2-primary-antibodies-wb-testing-2.jpgAnti-Dynamin II DNM2 Monoclonal AntibodyWestern Blot analysis using Dynamin II Monoclonal Antibody against truncated Dynamin-2 recombinant protein (1), SKN-SH cell lysate (2) and NIH/3T3 cell lysate (3).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01629-dnm2-primary-antibodies-ihc-testing-1.jpgAnti-Dynamin II DNM2 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human cerebrum tissue (left) and myelencephalon tissue (right), showing cytoplasmic localization with DAB staining using Dynamin II Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pgd-antibody-a01623-1-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-1-pgd-primary-antibodies-ihc-testing-1.jpgAnti-PGD AntibodyImmunohistochemical analysis of paraffin-embedded Human Right kidney. 1, Antibody was diluted at 1:400 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-1-pgd-primary-antibodies-wb-testing-2.jpgAnti-PGD AntibodyWestern Blot analysis of A549 cells using PGD Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-1-pgd-primary-antibodies-if-testing-3.jpgAnti-PGD AntibodyImmunohistochemical analysis of paraffin-embedded Human colon. 1, Antibody was diluted at 1:100 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rad18-antibody-a01622-boster.html2026-03-24T05:09:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01622-rad18-primary-antibodyes-wb-testing-1.jpgAnti-Rad18 AntibodyWestern Blot (WB) analysis of Jurkat cells using Rad18 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01622-rad18-primary-antibodyes-wb-testing-2.jpgAnti-Rad18 AntibodyWestern Blot (WB) analysis of specific cells using Rad18 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bubr1-antibody-a01564-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01564-bub1b-primary-antibodies-wb-testing-2.jpgAnti-BubR1 BUB1B AntibodyWestern Blot analysis of various cells using BubR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01564-bub1b-primary-antibodies-wb-testing-1.jpgAnti-BubR1 BUB1B AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, treated with H2O2 100uM 30', using BUB1B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ribosomal-protein-s3-antibody-a01542-1-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01542-1-rps3-primary-antibodies-ihc-testing-1.jpgAnti-Ribosomal Protein S3 RPS3 AntibodyImmunohistochemistry analysis of paraffin-embedded human tonsil tissue, using RPS3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01542-1-rps3-primary-antibodies-wb-testing-2.jpgAnti-Ribosomal Protein S3 RPS3 AntibodyWestern Blot analysis of various cells using Ribosomal Protein S3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01542-1-rps3-primary-antibodies-wb-testing-3.jpgAnti-Ribosomal Protein S3 RPS3 AntibodyWestern blot analysis of lysates from HepG2 cells, using RPS3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01542-1-rps3-primary-antibodies-wb-testing-4.jpgAnti-Ribosomal Protein S3 RPS3 AntibodyWestern blot analysis of the lysates from RAW264.7cells using RPS3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ca-iv-antibody-a01523-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01523-ca4-primary-antibodies-wb-testing-1.jpgAnti-CA IV CA4 AntibodyWestern Blot analysis of rat muscle cells using CA IV Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd200-antibody-a01512-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01512-cd200-primary-antibodies-wb-testing-2.jpgAnti-OX-2 membrane glycoprotein CD200 AntibodyWestern Blot analysis of PC12 cells using CD200 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01512-cd200-primary-antibodies-ihc-testing-1.jpgAnti-OX-2 membrane glycoprotein CD200 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hxk-i-antibody-a01504-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01504-hk1-primary-antibodies-wb-testing-2.jpgAnti-HXK I HK1 Monoclonal AntibodyWestern Blot analysis using HXK I Monoclonal Antibody against Jurkat (1), HeLa (2), HepG2 (3) and NIH/3T3 (4) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01504-hk1-primary-antibodies-ihc-testing-3.jpgAnti-HXK I HK1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded kidney tissues with DAB staining using HXK I Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01504-hk1-primary-antibodies-if-testing-4.jpgAnti-HXK I HK1 Monoclonal AntibodyImmunofluorescence analysis of NIH/3T3 cells using HXK I Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01504-hk1-primary-antibodies-fcm-testing-1.jpgAnti-HXK I HK1 Monoclonal AntibodyFlow cytometric analysis of K562 cells using HXK I Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-edg-1-antibody-a01502-1-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01502-1-s1pr1-primary-antibodies-wb-testing-2.jpgAnti-EDG-1 S1PR1 AntibodyWestern Blot analysis of various cells using EDG-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01502-1-s1pr1-primary-antibodies-wb-testing-3.jpgAnti-EDG-1 S1PR1 AntibodyWestern Blot analysis of A549 cells using EDG-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01502-1-s1pr1-primary-antibodies-wb-testing-4.jpgAnti-EDG-1 S1PR1 AntibodyWestern blot analysis of lysates from HT-29, LOVO, and A549 cells, using S1P Receptor EDG1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01502-1-s1pr1-primary-antibodies-wb-testing-5.jpgAnti-EDG-1 S1PR1 AntibodyWestern blot analysis of the lysates from HUVECcells using S1P Receptor EDG1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01502-1-s1pr1-primary-antibodies-if-testing-1.jpgAnti-EDG-1 S1PR1 AntibodyImmunofluorescence analysis of A549 cells, using S1P Receptor EDG1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cdk8-antibody-a01493-boster.html2026-03-24T05:09:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01493-cdk8-primary-antibodies-wb-testing-2.jpgAnti-Cyclin-dependent kinase 8 Cdk8 AntibodyWestern Blot analysis of various cells using Cdk8 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01493-cdk8-primary-antibodies-wb-testing-3.jpgAnti-Cyclin-dependent kinase 8 Cdk8 AntibodyWestern blot analysis of lysates from 293 cells, using CDK8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01493-cdk8-primary-antibodies-ihc-testing-1.jpgAnti-Cyclin-dependent kinase 8 Cdk8 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gsta1-antibody-a01462-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-gsta1-primary-antibodies-ihc-testing-1.jpgAnti-Glutathione S-transferase A1 GSTA1 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cathepsin-b-antibody-a01456-1-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-wb-testing-2.jpgAnti-Cathepsin B CTSB AntibodyWestern Blot analysis of various cells using Cathepsin B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-wb-testing-3.jpgAnti-Cathepsin B CTSB AntibodyWestern blot analysis of lysate from COLO cells, using Cathepsin B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-ihc-testing-4.jpgAnti-Cathepsin B CTSB AntibodyImmunohistochemical analysis of paraffin-embedded Human colon. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-ihc-testing-5.jpgAnti-Cathepsin B CTSB AntibodyImmunohistochemical analysis of paraffin-embedded Human colon. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-ihc-testing-6.jpgAnti-Cathepsin B CTSB AntibodyImmunohistochemical analysis of paraffin-embedded Human colon. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01456-1-ctsb-primary-antibodies-ihc-testing-1.jpgAnti-Cathepsin B CTSB AntibodyImmunohistochemistry analysis of Cathepsin B antibody in paraffin-embedded human brain tissue.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pak-gamma-antibody-a01419-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-pak2-primary-antibodies-ihc-testing-1.jpgAnti-PAK gamma PAK2 AntibodyImmunohistochemistryt analysis of paraffin-embedded human brain, using PAK2 Antibody. The lane on the right is blocked with the PAK2 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-pak2-primary-antibodies-wb-testing-2.jpgAnti-PAK gamma PAK2 AntibodyWestern Blot analysis of 3T3 cells using PAKγ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-pak2-primary-antibodies-wb-testing-3.jpgAnti-PAK gamma PAK2 AntibodyWestern blot analysis of the lysates from COLO205 cells using PAK2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pak-gamma-antibody-a01419-1-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-1-pak2-primary-antibodies-wb-testing-2.jpgAnti-PAK gamma PAK2 Monoclonal AntibodyWestern Blot analysis using PAKγ Monoclonal Antibody against HeLa (1), Jurkat (2), A549 (3), HEK293 (4) and K562 (5) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-1-pak2-primary-antibodies-ihc-testing-3.jpgAnti-PAK gamma PAK2 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human lung cancer (left) and gastric cancer (right) with DAB staining using PAKγ Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01419-1-pak2-primary-antibodies-if-testing-1.jpgAnti-PAK gamma PAK2 Monoclonal AntibodyConfocal immunofluorescence analysis of Hela cells using PAKγ Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-prmt1-antibody-a01417-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01417-prmt1-primary-antibodies-wb-testing-1.jpgAnti-PRMT1 Monoclonal AntibodyWestern Blot analysis using PRMT1 Monoclonal Antibody against HeLa, A549 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cpe-antibody-a01407-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01407-cpe-primary-antibodyes-wb-testing-1.jpgAnti-CPE/Carboxypeptidase E AntibodyWestern Blot (WB) analysis of Mouse Brain cells using CPE Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01407-cpe-primary-antibodyes-ihc-testing-2.jpgAnti-CPE/Carboxypeptidase E AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Rat Brain, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tip60-antibody-a01393-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01393-kat5-primary-antibodies-ihc-testing-1.jpgAnti-TIP60 KAT5 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01393-kat5-primary-antibodies-wb-testing-2.jpgAnti-TIP60 KAT5 AntibodyWestern Blot analysis of 3T3 cells using TIP60 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01393-kat5-primary-antibodies-wb-testing-3.jpgAnti-TIP60 KAT5 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, treated with starved 24h, using Tip60 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tip60-antibody-a01393-1-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01393-1-kat5-primary-antibodies-ihc-testing-1.jpgAnti-TIP60 KAT5 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma (A), recturn carcinoma (B), normal medulla tissue (C) and normal interbrain tissues (D), showing nuclear localization with DAB staining using TIP60 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01393-1-kat5-primary-antibodies-wb-testing-2.jpgAnti-TIP60 KAT5 Monoclonal AntibodyWestern Blot analysis using TIP60 Monoclonal Antibody against truncated TIP60 recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-sphk2-antibody-a01382-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01382-sphk2-primary-antibodies-wb-testing-2.jpgAnti-Sphingosine kinase 2 SphK2 AntibodyWestern Blot analysis of 22RV1 cells using SphK2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01382-sphk2-primary-antibodies-wb-testing-3.jpgAnti-Sphingosine kinase 2 SphK2 AntibodyWestern blot analysis of lysates from 293 cells, using SPHK2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01382-sphk2-primary-antibodies-ihc-testing-1.jpgAnti-Sphingosine kinase 2 SphK2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using SPHK2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-pol-iota-antibody-a01376-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01376-poli-primary-antibodies-wb-testing-1.jpgAnti-DNA pol iota AntibodyWestern blot analysis of the lysates from HeLa cells using POLI antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01376-poli-primary-antibodies-wb-testing-2.jpgAnti-DNA pol iota AntibodyWestern Blot analysis of HeLa cells using DNA pol ι Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gdf-5-antibody-a01356-1-boster.html2026-03-24T05:09:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01356-1-gdf5-primary-antibodies-wb-testing-2.jpgAnti-GDF-5 AntibodyWestern Blot analysis of 293 cells using GDF-5 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01356-1-gdf5-primary-antibodies-wb-testing-3.jpgAnti-GDF-5 AntibodyWestern blot analysis of lysate from 293 cells, using GDF5 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01356-1-gdf5-primary-antibodies-ihc-testing-4.jpgAnti-GDF-5 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01356-1-gdf5-primary-antibodies-ihc-testing-1.jpgAnti-GDF-5 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aladin-antibody-a01336-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01336-aaas-primary-antibodies-wb-testing-1.jpgAnti-Aladin AAAS AntibodyWestern Blot analysis of extracts from rat kidney, using Aladin Polyclonal Antibody. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c-kit-antibody-a01335-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01335-kit-primary-antibodies-wb-testing-2.jpgAnti-c-Kit AntibodyWestern Blot analysis of 453 cells using c-Kit Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01335-kit-primary-antibodies-wb-testing-3.jpgAnti-c-Kit AntibodyWestern blot analysis of the lysates from K562 cells using KIT antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01335-kit-primary-antibodies-ihc-testing-1.jpgAnti-c-Kit AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pth-rp-antibody-a01321-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01321-pthlh-primary-antibodyes-wb-testing-1.jpgAnti-PTH-rP PTHLH AntibodyWestern Blot (WB) analysis of HeLa cells using PTH-rP Polyclonal antibody diluted at 1:800.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tcf-1-antibody-a01315-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01315-tcf7-primary-antibodies-wb-testing-2.jpgAnti-TCF-1 TCF7 AntibodyWestern blot analysis of lysates from HUVEC, COLO205, and 293 cells, using TCF7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01315-tcf7-primary-antibodies-ihc-testing-1.jpgAnti-TCF-1 TCF7 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA, pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd81-antibody-a01281-1-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-1-cd81-primary-antibodyes-wb-testing-1.jpgAnti-CD81 antigen CD81 AntibodyWestern Blot (WB) analysis of 4T1 cells using CD81 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-1-13287_2020_1639_fig1_html.pngAnti-CD81 antigen CD81 AntibodyMorphology and characterization of hucMSCs and hucMSC-exosomes. a The fibroblast-like morphology of hucMSCs shown in light microscopy images (× 40). b Surface markers of hucMSCs analysed by flow cytometry. hucMSCs were positive for CD29, CD44, and CD90 and were negative for CD34 and CD45. c MSCs displayed the ability of adipogenic differentiation (× 40). d MSCs displayed the ability of chondrogenic differentiation (× 40). e Morphology of exosomes under transmission electron microscopy. Scale bar, 100 nm. f The size distribution of exosomes measured by Image-Pro Plus software. g Western blotting analyses of the exosome surface markers (CD9, CD81, and CD63) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://stemcellres.biomedcentral.com/articles/10.1186/s13287-020-01639-1'>32293542</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-flt-4-antibody-a01276-1-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-1-flt4-primary-antibodyes-wb-testing-1.jpgAnti-Flt-4 AntibodyWestern blot analysis of 293T and mouse kidney lysate, antibody was diluted at 500. Secondary antibody was diluted at 1:20000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-1-flt4-primary-antibodyes-ihc-testing-2.jpgAnti-Flt-4 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pdk1-antibody-a01268-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01268-pdk1-primary-antibodies-ihc-testing-1.jpgAnti-PDK1 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01268-pdk1-primary-antibodies-wb-testing-2.jpgAnti-PDK1 AntibodyWestern Blot analysis of Hela cells using PDK1 Polyclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acbp-antibody-a01267-1-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-1-dbi-primary-antibodies-wb-testing-2.jpgAnti-ACBP DBI AntibodyWestern Blot analysis of MCF7, U251, mouse liver, mouse kidney cells using ACBP Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01267-1-dbi-primary-antibodies-wb-testing-1.jpgAnti-ACBP DBI AntibodyWestern blot analysis of lysate from MCF7 cells, using DBI Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p57-antibody-a01244-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01244-cdkn1c-primary-antibodies-ihc-testing-1.jpgAnti-p57 CDKN1C AntibodyImmunohistochemical analysis of paraffin-embedded human-mammary-cancer, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01244-cdkn1c-primary-antibodies-wb-testing-2.jpgAnti-p57 CDKN1C AntibodyWestern Blot analysis of Jurkat cells using p57 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01244-cdkn1c-primary-antibodies-wb-testing-3.jpgAnti-p57 CDKN1C AntibodyWestern blot analysis of extracts from Jurkat cells, using p57Kip2 (Ab-278) Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-lpp-antibody-a01240-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01240-lpp-primary-antibodies-wb-testing-2.jpgAnti-LPP Monoclonal AntibodyWestern Blot analysis using LPP Monoclonal Antibody against HeLa (1), NIH/3T3 (2), COS (3), Caki (4), MCF-7 (5), HepG2 (6) and SMMC-7721 (7) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01240-lpp-primary-antibodies-ihc-testing-3.jpgAnti-LPP Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human small intestine with DAB staining using LPP Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01240-lpp-primary-antibodies-if-testing-1.jpgAnti-LPP Monoclonal AntibodyConfocal immunofluorescence analysis of COS cells using LPP Monoclonal Antibody (green). Red: Actin filaments have been labeled using DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-factor-xii-hc-r372-antibody-a01226-boster.html2026-03-24T05:09:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01226-f12-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Factor XII HC (R372) F12 AntibodyWestern Blot analysis of various cells using Cleaved-Factor XII HC (R372) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01226-f12-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-Factor XII HC (R372) F12 AntibodyWestern blot analysis of lysates from 293 cells, treated with etoposide 25uM 1h, using FA12 (heavy chain, Cleaved-Arg372) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c1inh-antibody-a01221-boster.html2026-03-24T05:09:50+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd1c-antibody-a01188-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01188-cd1c-primary-antibodyes-wb-testing-1.jpgAnti-CD1C/Bdca 1 AntibodyWestern Blot (WB) analysis of K562 cells using CD1C Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-xpa-antibody-a01182-1-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01182-1-xpa-primary-antibodies-wb-testing-2.jpgAnti-XPA AntibodyWestern Blot analysis of various cells using XPA Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01182-1-xpa-primary-antibodies-wb-testing-3.jpgAnti-XPA AntibodyWestern blot analysis of lysates from COLO205 cells, using XPA Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01182-1-xpa-primary-antibodies-ihc-testing-1.jpgAnti-XPA AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using XPA Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-serca2-antibody-a01176-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01176-atp2a2-primary-antibodyes-wb-testing-1.jpgAnti-SERCA2 ATP2A2 AntibodyWestern Blot (WB) analysis of 293 cells using SERCA2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01176-atp2a2-primary-antibodyes-ihc-testing-2.jpgAnti-SERCA2 ATP2A2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Muscle, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd201-antibody-a01166-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01166-procr-primary-antibodies-ihc-testing-1.jpgAnti-CD201 PROCR AntibodyImmunohistochemical analysis of paraffin-embedded mouse-spleen, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01166-procr-primary-antibodies-wb-testing-2.jpgAnti-CD201 PROCR AntibodyWestern blot analysis of Rat-barin lysis using CD201 antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01166-procr-primary-antibodies-if-testing-3.jpgAnti-CD201 PROCR AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-11-antibody-a01160-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01160-il11-primary-antibodies-wb-testing-1.jpgAnti-IL-11 Monoclonal AntibodyWestern Blot analysis using IL-11 Monoclonal Antibody against truncated IL-11 recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aldh3a1-antibody-a01121-1-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01121-1-aldh3a1-primary-antibodies-wb-testing-1.jpgAnti-ALDH3A1 AntibodyWestern blot analysis of lysates from A549 cells, using ALDH3A1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01121-1-aldh3a1-primary-antibodies-wb-testing-2.jpgAnti-ALDH3A1 AntibodyWestern Blot analysis of extracts from A549, K562 cells, using ALDH3A1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbx3-antibody-a01107-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01107-tbx3-primary-antibodies-wb-testing-2.jpgAnti-TBX3 AntibodyWestern Blot analysis of KB cells using TBX3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01107-tbx3-primary-antibodies-wb-testing-1.jpgAnti-TBX3 AntibodyWestern blot analysis of mouse-kidney mouse-brain KB 293T lysis using TBX3 antibody. Antibody was diluted at 1:1000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c4a-b-antibody-a01095-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01095-c4a-primary-antibodyes-wb-testing-1.jpgAnti-C4a/b AntibodyWestern Blot (WB) analysis of AD293 cells using C4a/b Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01095-c4a-primary-antibodyes-ihc-testing-2.jpgAnti-C4a/b AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01095-c4a-primary-antibodyes-ihc-testing-3.jpgAnti-C4a/b AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Brain, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01095-c4a-primary-antibodyes-ihc-testing-4.jpgAnti-C4a/b AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dnam-1-antibody-a01094-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01094-cd226-primary-antibodies-if-testing-1.jpgAnti-DNAM-1 CD226 AntibodyImmunofluorescence analysis of HeLa cells, using CD226/DNAM-1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01094-cd226-primary-antibodies-wb-testing-2.jpgAnti-DNAM-1 CD226 AntibodyWestern Blot analysis of COS7 cells using DNAM-1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01094-cd226-primary-antibodies-wb-testing-3.jpgAnti-DNAM-1 CD226 AntibodyWestern blot analysis of lysates from COS7 and K562 cells, treated with PMA 125ng/ml 30' , using CD226/DNAM-1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01094-cd226-primary-antibodies-wb-testing-4.jpgAnti-DNAM-1 CD226 AntibodyWestern blot analysis of the lysates from HUVECcells using CD226/DNAM-1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01094-cd226-primary-antibodies-ihc-testing-5.jpgAnti-DNAM-1 CD226 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd240d-antibody-a01082-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01082-rhd-primary-antibodyes-wb-testing-1.jpgAnti-CD240d RHD AntibodyWestern Blot (WB) analysis of Mouse Brain cells using CD240d Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01082-rhd-primary-antibodyes-wb-testing-2.jpgAnti-CD240d RHD AntibodyWestern Blot (WB) analysis of Mouse Brain cells using CD240d Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hck-antibody-a01073-boster.html2026-03-24T05:09:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01073-hck-primary-antibodies-wb-testing-2.jpgAnti-Tyrosine-protein kinase HCK Hck AntibodyWestern Blot analysis of various cells using Hck Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01073-hck-primary-antibodies-ihc-testing-3.jpgAnti-Tyrosine-protein kinase HCK Hck AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using HCK Antibody . The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01073-hck-primary-antibodies-if-testing-1.jpgAnti-Tyrosine-protein kinase HCK Hck AntibodyImmunofluorescence analysis of HepG2 cells, using HCK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hck-antibody-a01073-1-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01073-1-hck-primary-antibodies-ihc-testing-1.jpgAnti-Hck Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human colon cancer (left) and ancreas cancer (right), showing cytoplasmic localization with DAB staining using Hck Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01073-1-hck-primary-antibodies-wb-testing-2.jpgAnti-Hck Monoclonal AntibodyWestern Blot analysis using Hck Monoclonal Antibody against truncated HCK recombinant protein (1) and full-length HCK-GFP transfected CHO-K1 cell lysate (2).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-acta2-antibody-a01072-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01072-acta2-primary-antibodies-fcm-testing-1.jpgAnti-ACTA2/Alpha Smooth Muscle Actin Monoclonal AntibodyFlow cytometric analysis of Hela cells using ACTA2 Monoclonal Antibody (green) and negative control (purple).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01072-acta2-primary-antibodies-wb-testing-2.jpgAnti-ACTA2/Alpha Smooth Muscle Actin Monoclonal AntibodyWestern Blot analysis using ACTA2 Monoclonal Antibody against HeLa (1), A431 (2), Jurkat (3), K562 (4), HEK293 (5), HepG2 (6), NIH/3T3 (7), PC-12 (8) and Cos7 (9) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01072-acta2-primary-antibodies-ihc-testing-3.jpgAnti-ACTA2/Alpha Smooth Muscle Actin Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human duodenum tissues (left) and human esophagus tissues (right) with DAB staining using ACTA2 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01072-acta2-primary-antibodies-if-testing-4.jpgAnti-ACTA2/Alpha Smooth Muscle Actin Monoclonal AntibodyImmunofluorescence analysis of HepG2 cells using ACTA2 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Blue: DRAQ5 fluorescent DNA dye.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-kcnh1-antibody-a01036-1-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01036-1-kcnh1-primary-antibodies-ihc-testing-1.jpgAnti-KCNH1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01036-1-kcnh1-primary-antibodies-wb-testing-2.jpgAnti-KCNH1 AntibodyWestern blot analysis of KCNH1 Antibody. The lane on the right is blocked with the KCNH1 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01036-1-kcnh1-primary-antibodies-wb-testing-3.jpgAnti-KCNH1 AntibodyWestern blot analysis of the lysates from COLO205 cells using KCNH1 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd209-antibody-a01025-1-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01025-1-cd209-primary-antibodies-wb-testing-1.jpgAnti-CD209/Dc Sign AntibodyWestern Blot analysis of mouse brain cells using CD209 Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd35-antibody-a01022-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01022-cr1-primary-antibodies-wb-testing-1.jpgAnti-CD35 CR1 AntibodyWestern Blot analysis of A549 3T3 mouse-liver mouse-brain cells using CD35 Polyclonal Antibody diluted at 1:800. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mbl-c-antibody-a01000-1-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-1-mbl2-primary-antibodies-wb-testing-2.jpgAnti-MBL-C MBL2 AntibodyWestern Blot analysis of mouse-kidney cells using Antibody diluted at 500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-1-mbl2-primary-antibodies-ihc-testing-3.jpgAnti-MBL-C MBL2 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-1-mbl2-primary-antibodies-ihc-testing-4.jpgAnti-MBL-C MBL2 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-1-mbl2-primary-antibodies-ihc-testing-1.jpgAnti-MBL-C MBL2 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-d4dr-antibody-a00998-1-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00998-1-drd4-primary-antibodies-if-testing-1.jpgAnti-D4DR DRD4 AntibodyImmunofluorescence analysis of MCF7 cells, using DRD4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00998-1-drd4-primary-antibodies-wb-testing-2.jpgAnti-D4DR DRD4 AntibodyWestern Blot analysis of various cells using D4DR Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00998-1-drd4-primary-antibodies-wb-testing-3.jpgAnti-D4DR DRD4 AntibodyWestern Blot analysis of K562 cells using D4DR Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00998-1-drd4-primary-antibodies-wb-testing-4.jpgAnti-D4DR DRD4 AntibodyWestern blot analysis of lysates from MCF-7 and HUVEC cells, using DRD4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00998-1-drd4-primary-antibodies-wb-testing-5.jpgAnti-D4DR DRD4 AntibodyWestern blot analysis of the lysates from RAW264.7cells using DRD4 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ampk-alpha1-antibody-a00994-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-prkaa1-primary-antibodies-wb-testing-2.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyWestern blot analysis of 1)Hela, 2) 293T, 3)3T3, 4) PC12 with AMPK a1 Mouse mAb diluted at 1:2, 000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-prkaa1-primary-antibodies-ihc-testing-1.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse ColonTissue using AMPK a1 Mouse mAb diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ampk-alpha1-antibody-a00994-2-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-2-prkaa1-primary-antibodies-fcm-testing-1.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyFlow cytometric analysis of PC-2 cells using AMPKα1 Monoclonal Antibody (green) and negative control (purple).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-2-prkaa1-primary-antibodies-wb-testing-2.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyWestern Blot analysis using AMPKα1 Monoclonal Antibody against Jurkat (1), HeLa (2), HepG2 (3), MCF-7 (4), Cos7 (5), NIH/3T3 (6), K562 (7), HEK293 (8), and PC-12 (9) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-2-prkaa1-primary-antibodies-ihc-testing-3.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded ovarian cancer (left) and brain tissues (right) with DAB staining using AMPKα1 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00994-2-prkaa1-primary-antibodies-if-testing-4.jpgAnti-AMPK alpha1 PRKAA1 Monoclonal AntibodyImmunofluorescence analysis of NTERA-2 cells using AMPKα1 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eomes-antibody-a00992-boster.html2026-03-24T05:09:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00992-eomes-primary-antibodies-wb-testing-1.jpgAnti-EOMES/Tbr2 AntibodyWestern blot analysis of lysate from HT29 cells, using EOMES antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00992-eomes-primary-antibodies-wb-testing-2.jpgAnti-EOMES/Tbr2 AntibodyWestern Blot analysis of various cells using EOMES Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-22-antibody-a00963-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-il22-primary-antibodies-wb-testing-1.jpgAnti-IL-22 AntibodyWestern blot analysis of MOUSE-KIDNEY lysis using IL22 antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-foxc1-2-antibody-a00962-1-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00962-1-foxc1-primary-antibodies-ihc-testing-1.jpgAnti-FoxC1/2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200 (4° overnight.3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00962-1-foxc1-primary-antibodies-wb-testing-2.jpgAnti-FoxC1/2 AntibodyWestern Blot analysis of hela cells using FoxC1/2 Polyclonal Antibody diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00962-1-foxc1-primary-antibodies-wb-testing-3.jpgAnti-FoxC1/2 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using FOXC1/2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00962-1-foxc1-primary-antibodies-wb-testing-4.jpgAnti-FoxC1/2 AntibodyWestern blot analysis of the lysates from Jurkat cells using FOXC1/2 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cystatin-c-antibody-a00961-1-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00961-1-cst3-primary-antibodies-wb-testing-2.jpgAnti-Cystatin C CST3 AntibodyWestern Blot analysis of various cells using Cystatin C Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00961-1-cst3-primary-antibodies-wb-testing-1.jpgAnti-Cystatin C CST3 AntibodyWestern Blot analysis of 293T cells using Cystatin C Polyclonal Antibody diluted at 1:2000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-na-k-atpase-alpha1-antibody-a00956-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00956-atp1a1-primary-antibodies-if-testing-1.jpgAnti-Na+/K+-ATPase alpha1 AntibodyImmunofluorescence analysis of COS7 cells, using ATPase Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00956-atp1a1-primary-antibodies-wb-testing-2.jpgAnti-Na+/K+-ATPase alpha1 AntibodyWestern Blot analysis of 293 cells using Na+/K+-ATPase α1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00956-atp1a1-primary-antibodies-wb-testing-3.jpgAnti-Na+/K+-ATPase alpha1 AntibodyWestern blot analysis of lysates from 293 cells, treated with PMA 125ng/ml 30', using ATPase Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00956-atp1a1-primary-antibodies-ihc-testing-4.jpgAnti-Na+/K+-ATPase alpha1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ATPase Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00956-fphar-11-01255-g004.jpgAnti-Na+/K+-ATPase alpha1 AntibodyTrimetazidine treatment promotes the protein expression related to myocardial substrate uptake and utilization in myocardial tissues of isoproterenol-induced heart failure rats. (A) Cytosolic protein was extracted and expression levels of cellular localization of GLUT4 were determined using Western blot. β-actin was choice as an internal control. (B) Membrane protein was extracted and expression levels of cellular localization of GLUT4 were determined using Western blot. ATP1A1 was chosen as an internal control. (C) Western blot was used to evaluate metabolism-related protein expression. AMPK, p-AMPK, PPARα, p-ACC, LDH, CPT1, BDH1, MCT1, ACAT1, and OXCT1 were included. (D) Immunoblotting analysis was conducted to detect the ratio of p-AMPK/AMPK protein expression within myocardial tissues (n = 3). (E) The histogram indicated the specific relevant quantitative results (n = 3). Data are represented as means ± SD, # P < 0.05, ## P < 0.01 compared with ISO group, *P < 0.05, **P < 0.01 compared with control group. p-AMPK, phospho-AMPK; AMPK, adenosine monophosphate-activated protein kinase; PPARα, peroxisome proliferator activated receptorα; p-ACC, phospho-acetyl-CoA carboxylase; LDH, lactate dehydrogenase;CPT1, carnitine palmitoyltransferase 1; BDH1,β-hydroxybutyrate dehydrogenase 1; MCT1, monocarboxylate transporter 1; ACAT1, acetoacetyl-CoA thiolase 1; OXCT1(SCOT1), succinyl-CoA:3-ketoacid-CoA transferase1.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2020.01255/full'>32922293</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ena-78-antibody-a00946-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00946-cxcl5-primary-antibodies-ihc-testing-1.jpgAnti-ENA-78 CXCL5 AntibodyImmunohistochemical analysis of paraffin-embedded human-pancreas-cancer, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tal1-2-acetyl-lys221-acetyl-lys222-acetyl-lys36-acetyl-lys37-antibody-a00944-1-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00944-1-tal1-primary-antibodies-wb-testing-1.jpgAnti-TAL1/2 (Acetyl Lys221/Acetyl Lys222/Acetyl Lys36/Acetyl Lys37) AntibodyWestern blot analysis of MOUSE-HEART MOUSE-BRAIN using Acetyl-TAL1/2 (K221/K222/K36/K37) antibody. Antibody was diluted at 1:500. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ets1-antibody-a00931-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-ets1-primary-antibodies-if-testing-1.jpgAnti-Protein C-ets-1 ETS1 AntibodyImmunofluorescence analysis of HeLa cells, using ETS1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-ets1-primary-antibodies-wb-testing-2.jpgAnti-Protein C-ets-1 ETS1 AntibodyWestern Blot analysis of 293T cells using ETS1 Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-ets1-primary-antibodies-if-testing-3.jpgAnti-Protein C-ets-1 ETS1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-ets1-primary-antibodies-ihc-testing-4.jpgAnti-Protein C-ets-1 ETS1 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ETS1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ets1-antibody-a00931-1-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-1-ets1-primary-antibodies-wb-testing-2.jpgAnti-ETS1 Monoclonal AntibodyWestern Blot analysis using ETS1 Monoclonal Antibody against Jurkat (1), HepG2 (2) and ETS1-hIgGFc transfected HEK293 (3) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-1-ets1-primary-antibodies-ihc-testing-3.jpgAnti-ETS1 Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human Colon, Adipocytes tissues with AEC staining using ETS1 Monoclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-1-ets1-primary-antibodies-if-testing-4.jpgAnti-ETS1 Monoclonal AntibodyImmunofluorescence analysis of NIH/3T3 cells using ETS1 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-1-ets1-primary-antibodies-fcm-testing-1.jpgAnti-ETS1 Monoclonal AntibodyFlow cytometric analysis of Jurkat cells using ETS1 Monoclonal Antibody (green) and negative control (purple).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ask-1-antibody-a00929-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00929-map3k5-primary-antibodies-wb-testing-2.jpgAnti-ASK 1 MAP3K5 AntibodyWestern Blot analysis of 293 cells using ASK 1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00929-map3k5-primary-antibodies-wb-testing-3.jpgAnti-ASK 1 MAP3K5 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using ASK1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00929-map3k5-primary-antibodies-ihc-testing-1.jpgAnti-ASK 1 MAP3K5 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ASK1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-12a-antibody-a00918-boster.html2026-03-24T05:09:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-wb-testing-1.jpgAnti-IL-12A AntibodyWestern Blot (WB) analysis of HeLa cells using IL-12A Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-wb-testing-2.jpgAnti-IL-12A AntibodyWestern blot analysis of lysate from HeLa cells, using IL-12A antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-ihc-testing-3.jpgAnti-IL-12A AntibodyImmunohistochemistry analysis of IL-12A antibody in paraffin-embedded human brain tissue.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-ihc-testing-4.jpgAnti-IL-12A AntibodyImmunohistochemical analysis of paraffin-embedded Human Amygdala. 1, Antibody was diluted at 1:200 (4°C overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-ihc-testing-5.jpgAnti-IL-12A AntibodyImmunohistochemical analysis of paraffin-embedded Human Amygdala. 1, Antibody was diluted at 1:200 (4°C overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-il12a-primary-antibodyes-ihc-testing-6.jpgAnti-IL-12A AntibodyImmunohistochemical analysis of paraffin-embedded Human Amygdala. 1, Antibody was diluted at 1:200 (4°C overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-flk-1-antibody-a00901-1-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-if-testing-1.jpgAnti-Flk-1 KDR AntibodyImmunofluorescence analysis of rat-kidney tissue. 1,Flk-1 Polyclonal Antibody (red) was diluted at 1:200 (4°C,overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-wb-testing-2.jpgAnti-Flk-1 KDR AntibodyWestern Blot analysis of Hela cells using Flk-1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-wb-testing-3.jpgAnti-Flk-1 KDR AntibodyWestern blot analysis of lysates from SK-OV3 cells, using VEGFR2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-ihc-testing-4.jpgAnti-Flk-1 KDR AntibodyImmunohistochemical analysis of paraffin-embedded Human-stomach-cancer tissue. 1,Flk-1 Polyclonal Antibody was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-ihc-testing-5.jpgAnti-Flk-1 KDR AntibodyImmunohistochemical analysis of paraffin-embedded Rat-spinal-cord tissue. 1,Flk-1 Polyclonal Antibody was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-ihc-testing-6.jpgAnti-Flk-1 KDR AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using VEGFR2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-1-kdr-primary-antibodies-if-testing-7.jpgAnti-Flk-1 KDR AntibodyImmunofluorescence analysis of rat-lung tissue. 1,Flk-1 Polyclonal Antibody (red) was diluted at 1:200 (4°C,overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tgf-beta2-antibody-a00892-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00892-tgfb2-primary-antibodyes-ihc-testing-1.jpgAnti-TGF beta2 TGFB2 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00892-tgfb2-primary-antibodyes-ihc-testing-2.jpgAnti-TGF beta2 TGFB2 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00892-tgfb2-primary-antibodyes-ihc-testing-3.jpgAnti-TGF beta2 TGFB2 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00892-tgfb2-primary-antibodyes-ihc-testing-4.jpgAnti-TGF beta2 TGFB2 AntibodyImmunohistochemical analysis of paraffin-embedded human-placenta, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gfi-1-antibody-a00888-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00888-gfi1-primary-antibodies-wb-testing-1.jpgAnti-Gfi-1 Monoclonal AntibodyWestern Blot analysis using Gfi-1 Monoclonal Antibody against HEK293 (1) and GFI1-hIgGFc transfected HEK293 (2) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-eset-antibody-a00881-1-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00881-1-setdb1-primary-antibodies-if-testing-1.jpgAnti-ESET SETDB1 Monoclonal AntibodyImmunofluorescence analysis of LOVO cells using ESET Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00881-1-setdb1-primary-antibodies-wb-testing-2.jpgAnti-ESET SETDB1 Monoclonal AntibodyWestern Blot analysis using ESET Monoclonal Antibody against MCF-7 (1),T47D (2), HEK293 (3), JURKAT (4), NIH/3T3 (5), F9 (6), RAW246.7 (7) and Cos7 (8) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-il-27a-antibody-a00857-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00857-il27-primary-antibodyes-ihc-testing-1.jpgAnti-IL-27A AntibodyImmunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-musk-antibody-a00815-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00815-musk-primary-antibodies-if-testing-1.jpgAnti-MuSK Monoclonal AntibodyConfocal immunofluorescence analysis of HEK293 cells trasfected with extracellular MUSK (aa24-209)-hIgGFc using MuSK Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00815-musk-primary-antibodies-ihc-testing-2.jpgAnti-MuSK Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded human lung cancer (A), muscles (B) and breast cancer (C) with DAB staining using MuSK Monoclonal Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tbx5-antibody-a00803-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00803-tbx5-primary-antibodies-wb-testing-1.jpgAnti-TBX5 Monoclonal AntibodyWestern Blot analysis using TBX5 Monoclonal Antibody against HepG2 cell lysate (1).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dmpk-antibody-a00797-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00797-dmpk-primary-antibodies-wb-testing-2.jpgAnti-Myotonin-protein kinase DMPK AntibodyWestern Blot analysis of various cells using DMPK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00797-dmpk-primary-antibodies-wb-testing-3.jpgAnti-Myotonin-protein kinase DMPK AntibodyWestern Blot analysis of Jurkat cells using DMPK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00797-dmpk-primary-antibodies-wb-testing-4.jpgAnti-Myotonin-protein kinase DMPK AntibodyWestern blot analysis of lysates from Jurkat and COLO205 cells, using DMPK Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00797-dmpk-primary-antibodies-wb-testing-1.jpgAnti-Myotonin-protein kinase DMPK AntibodyWestern blot analysis of the lysates from HT-29 cells using DMPK antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ddx3-antibody-a00751-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-ddx3x-primary-antibodyes-wb-testing-1.jpgAnti-DDX3 DDX3X AntibodyWestern Blot (WB) analysis of specific cells using DDX3 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-neurotensin-antibody-a00726-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00726-nts-primary-antibodies-wb-testing-1.jpgAnti-Neurotensin NTS AntibodyWestern Blot analysis of HeLa, HepG2 cells using Neurotensin Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-plasminogen-hc-a-short-form-v98-antibody-a00702-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00702-plg-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Plasminogen HC A short form (V98) PLG AntibodyWestern Blot analysis of various cells using Cleaved-Plasminogen HC A short form (V98) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00702-plg-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-Plasminogen HC A short form (V98) PLG AntibodyWestern blot analysis of PLMN (heavy chain A short form, Cleaved-Val98) Antibody. The lane on the right is blocked with the PLMN (heavy chain A short form, Cleaved-Val98) peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pka-i-alpha-reg-antibody-a00699-2-boster.html2026-03-24T05:09:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00699-2-prkar1a-primary-antibodies-ihc-testing-1.jpgAnti-PKA I alpha reg PRKAR1A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00699-2-prkar1a-primary-antibodies-wb-testing-2.jpgAnti-PKA I alpha reg PRKAR1A AntibodyWestern Blot analysis of 293 cells using PKA Iα reg Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00699-2-prkar1a-primary-antibodies-wb-testing-3.jpgAnti-PKA I alpha reg PRKAR1A AntibodyWestern blot analysis of lysates from HepG2 cells, using KAP0 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-vav1-antibody-a00691-1-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00691-1-vav1-primary-antibodies-wb-testing-2.jpgAnti-Proto-oncogene vav VAV1 AntibodyWestern Blot analysis of extracts from NIH-3T3 cells, using VAV1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00691-1-vav1-primary-antibodies-if-testing-1.jpgAnti-Proto-oncogene vav VAV1 AntibodyImmunofluorescence analysis of HeLa cells, using VAV1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ephb4-antibody-a00690-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-ephb4-primary-antibodies-wb-testing-2.jpgAnti-Ephrin type-B receptor 4 EphB4 AntibodyWestern Blot analysis of HY926 cells using EphB4 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-ephb4-primary-antibodies-wb-testing-3.jpgAnti-Ephrin type-B receptor 4 EphB4 AntibodyWestern blot analysis of lysates from Jurkat and 293 cells, using EPHB4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-ephb4-primary-antibodies-ihc-testing-1.jpgAnti-Ephrin type-B receptor 4 EphB4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-12860_2020_273_fig3_html.pngAnti-Ephrin type-B receptor 4 EphB4 AntibodyThe effect of the lentivirus-mediated shRNA interference of TNFR2 on TNF-α-stimulated EphB4 expression and osteogenic differentiation. a MC3T3-E1 cells stably transduced with lentiviral particles were selected with puromycin and named as pHBLV-TNFR2siRNA1 cells, pHBLV-TNFR2siRNA2 cells, pHBLV-TNFR2siRNA3 cells and pHBLV-NC cells, respectively. The mRNA levels of Tnfr2 were determined in these cells, among which the pHBLV-TNFR2siRNA1 cells displayed the highest TNFR2 gene silencing efficiency and were selected to continue the following studies. b TNFR2 protein levels in pHBLV-TNFR2siRNA1 cells and pHBLV-NC cells. c , d mRNA levels of Ephb4 , Runx2 and Bsp in pHBLV-TNFR2siRNA1 cells and pHBLV-NC cells cultured in the osteogenic induction medium supplemented with 0.5 ng/ml TNF-α for 24 h ( c ) or 48 h ( d ). e , f Protein levels of EphB4, RUNX2 and BSP in pHBLV-TNFR2siRNA1 cells and pHBLV-NC cells cultured in the osteogenic induction medium supplemented with 0.5 ng/ml TNF-α for 24 h ( e ) or 48 h ( f ). *, p < 0.05 vs. the pHBLV-NC group; **, p < 0.01 vs. the pHBLV-NC group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12860-020-00273-2'>32299362</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-12860_2020_273_fig4_html.pngAnti-Ephrin type-B receptor 4 EphB4 AntibodyThe effect of the impaired binding between TNF-α and TNFR2 on TNF-α-stimulated EphB4 expression and osteogenic differentiation. MC3T3-E1 cells were treated with an anti-mouse TNFR2/ CD120b/TNFRSF1B neutralizing antibody (TNFR2 NAb) at the concentration of 0.2 μg/ml, and were cultured in the osteogenic induction medium supplemented with or without 0.5 ng/ml TNF-α. Cells treated with 0.2 μg/ml of the normal rabbit IgG negative control antibody (control Ab) served as negative controls. (a) ALP activities were determined 7d or 14d after the treatment. (b, c) mRNA levels of Ephb4 , Runx2 and Bsp were determined after 24 h (b) or 48 h (c). (d, e) Protein levels of EphB4, RUNX2 and BSP were determined after 24 h (d) or 48 h (e). a, p < 0.05 vs. the control Ab group; b, p < 0.05 vs. the TNFR2 NAb group; c, p < 0.05 vs. the TNF-α + control Ab group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12860-020-00273-2'>32299362</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-12860_2020_273_fig5_html.pngAnti-Ephrin type-B receptor 4 EphB4 AntibodyThe effect of inhibited EphB4 forward signaling on TNF-α-stimulated TNFR2 expression and osteogenic differentiation. (a) A potent inhibitor of EphB4 auto-phosphorylation, NVP-BHG712, was used to suppress EphB4 forward signaling. MC3T3-E1 cells were pretreated with 200 nM NVP-BHG712 in the regular culture medium for 1 h. Cells were then incubated in osteogenic induction medium supplemented with 200 nM NVP-BHG712 and/or 0.5 ng/ml TNF-α for 7d or 14d. MC3T3-E1 cells cultured in osteogenic induction medium served as controls. The ALP activities were determined. (b, c) MC3T3-E1 cells were pretreated with 200 nM NVP-BHG712 for 1 h in the regular culture medium, and then incubated in osteogenic induction medium supplemented with 200 nM NVP-BHG712 and/or 0.5 ng/ml TNF-α. Cells cultured in osteogenic induction medium served as controls. mRNA levels of Tnfr2 , Runx2 and Bsp were determined after 24 h (b) or 48 h (c) of incubation. (d, e) MC3T3-E1 cells were pretreated with 200 nM NVP-BHG712 for 1 h in the regular culture medium, and then incubated in osteogenic induction medium supplemented with 200 nM NVP-BHG712 and/or 0.5 ng/ml TNF-α. Cells cultured in osteogenic induction medium served as controls. Protein levels of TNFR2, RUNX2 and BSP were determined after 24 h (d) or 48 h (e) of incubation. a, p < 0.05 vs. the control group; b, p < 0.05 vs. the NVP-BHG712 group; c, p < 0.05 vs. the TNF-α group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12860-020-00273-2'>32299362</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-12860_2020_273_fig6_html.pngAnti-Ephrin type-B receptor 4 EphB4 AntibodyEphB4, TNFR2 and MAPK signaling pathways comprise a signaling axis to mediate the positive effect of TNF-α on osteogenic differentiation. a Levels of p38, p -p38, ERK1/2, p -ERK1/2, JNK1 + 2 + 3 and p -JNK1 + 2 + 3 in MC3T3-E1 cells treated with TNF-α for 0 min, 5 min, 15 min, 30 min and 60 min. b Levels of p38, p -p38, ERK1/2, p -ERK1/2, JNK1 + 2 + 3 and p -JNK1 + 2 + 3 in the pHBLV-TNFR2siRNA1 cells and the pHBLV-NC cells treated with or without 0.5 ng/ml TNF-α in regular culture medium for 15 min. c MC3T3-E1 cells were pretreated with or without 200 nM NVP-BHG712 in the regular culture medium for 1 h, and then 0.5 ng/ml TNF-α was added into the medium. The cells were incubated for another 15 min. Levels of ERK1/2 and p -ERK1/2 were determined. d-f MC3T3-E1 cells were cultured in the regular culture medium and pretreated with the ERK inhibitor U0126 (10 μM) for 1 h. The culture medium was then switched to the osteogenic induction medium supplemented with 0.5 ng/ml TNF-α and U0126 (10 μM). Cells treated without U0126 (10 μM) served as controls. ALP activities were determined 7d or 14d after the treatment ( d ). mRNA levels ( e ) and protein levels ( f ) of BSP and RUNX2 were determined 3 days after the treatment. *, p < 0.05 vs. the control group; **, p < 0.01 vs. the control group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12860-020-00273-2'>32299362</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd155-antibody-a00664-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00664-pvr-primary-antibodies-if-testing-1.jpgAnti-CD155 PVR AntibodyImmunofluorescence analysis of A549. 1,primary Antibody was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 488 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00664-pvr-primary-antibodies-wb-testing-2.jpgAnti-CD155 PVR AntibodyWestern Blot analysis of KB cells using CD155 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-pka-alpha-beta-gamma-cat-antibody-a00653-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00653-prkaca-primary-antibodies-wb-testing-2.jpgAnti-PKA alpha/ beta/ gamma cat PRKACA AntibodyWestern blot analysis of lysates from 1) 22RV1, 2) Hela , 3) COLO205 cells, (Green） primary antibody was diluted at 1:1000, 4°over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red） Tubulin β Monoclonal Antibody (5G3) antibody was diluted at 1:5000 as loading control, 4° over night, secondary antibody was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00653-prkaca-primary-antibodies-ihc-testing-3.jpgAnti-PKA alpha/ beta/ gamma cat PRKACA AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using PKA alpha/beta CAT Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00653-prkaca-primary-antibodies-if-testing-1.jpgAnti-PKA alpha/ beta/ gamma cat PRKACA AntibodyImmunofluorescence analysis of Hela cell. 1, PKAα/β/γ cat Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). 3 DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-dna-pkcs-antibody-a00645-1-boster.html2026-03-24T05:09:54+00:00daily0.9
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-factor-xa-activated-hc-i235-antibody-a00641-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00641-f10-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Factor Xa activated HC (I235) F10 AntibodyWestern Blot analysis of rat cells using Cleaved-Factor Xa activated HC (I235) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00641-f10-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-Factor Xa activated HC (I235) F10 AntibodyWestern blot analysis of lysates from rat liver cells, using FA10 (activated heavy chain, Cleaved-Ile235) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-col1a2-g1102-antibody-a00624-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-col1a2-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-COL1A2 (G1102) AntibodyWestern Blot analysis of VEC cells using Cleaved-COL1A2 (G1102) Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-col1a2-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-COL1A2 (G1102) AntibodyWestern blot analysis of lysates from Jurkat cells, treated with etoposide 25uM 24h, using Collagen I alpha2 (Cleaved-Gly1102) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-col1a2-antibody-a00624-1-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-1-col1a2-primary-antibodies-wb-testing-2.jpgAnti-Collagen alpha-2(I) chain COL1A2 AntibodyWestern Blot analysis of various cells using COL1A2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-1-col1a2-primary-antibodies-ihc-testing-3.jpgAnti-Collagen alpha-2(I) chain COL1A2 AntibodyImmunohistochemical analysis of paraffin-embedded Rat-lung tissue. 1, COL1A2 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-1-col1a2-primary-antibodies-ihc-testing-4.jpgAnti-Collagen alpha-2(I) chain COL1A2 AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-liver tissue. 1, COL1A2 Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-1-col1a2-primary-antibodies-if-testing-5.jpgAnti-Collagen alpha-2(I) chain COL1A2 AntibodyImmunofluorescence analysis of rat-lung tissue. 1, COL1A2 Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00624-1-col1a2-primary-antibodies-if-testing-1.jpgAnti-Collagen alpha-2(I) chain COL1A2 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using Collagen I Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-vegf-c-antibody-a00623-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00623-vegfc-primary-antibodies-wb-testing-2.jpgAnti-VEGF-C AntibodyWestern Blot analysis of L929 cells using VEGF-C Polyclonal Antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00623-vegfc-primary-antibodies-wb-testing-3.jpgAnti-VEGF-C AntibodyWestern blot analysis of lysate from L929 cells, using VEGFC Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00623-vegfc-primary-antibodies-ihc-testing-1.jpgAnti-VEGF-C AntibodyImmunohistochemical analysis of paraffin-embedded Human Liver. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00623-41598_2015_article_bfsrep12807_fig3_html.jpgAnti-VEGF-C AntibodyEffects of HMGB1 down-regulation on NF-κB/p65, IκBα and VEGF-C in T24 cells. A1, A2 and A3: The expression of NF-κB/p65 and VEGF-C in the shRNA group was lower than in the other two groups transfected with shNC plasmids or the untransfected controls (all P < 0.05). On the contrary, the expression of IκBα showed an opposite tendency, while no significant differences in the expression of NF-κB/p65, IκBα and VEGF-C in T24 cells were found between the CON and NC groups (all P > 0.05). The display of cropped gels is used to improve the clarity and conciseness of the presentation and all the cropped gels have been run under the same experimental conditions. : The blue areas indicate nuclei stained using 4, 6-diamidino-2-phenylindole (DAPI) and the green areas indicate the nuclear translocation of NF-κB/p65 in T24 cells transfected with shNC plasmids or untransfected and cytoplasmic localization of NF-κB/p65 in cells transfected with shRNA plasmids. The results showed that knockdown of HMGB1 expression inhibited the translocation of NF-κB/p65 from the cytoplasm to the nucleus. : EMSA revealed that the DNA-binding activity of NF-κB/p65 in T24 cells was decreased by HMGB1 knockdown. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fsrep12807'>26239046</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-adm-antibody-a00594-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00594-adm-primary-antibodies-ihc-testing-1.jpgAnti-ADM/Adrenomedullin AntibodyImmunohistochemical analysis of paraffin-embedded rat-kidney, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00594-adm-primary-antibodies-wb-testing-2.jpgAnti-ADM/Adrenomedullin AntibodyWestern Blot analysis of mouse kidney, mouse lung, mouse heart cells using ADM Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00594-adm-primary-antibodies-wb-testing-3.jpgAnti-ADM/Adrenomedullin AntibodyWestern blot analysis of lysate from mouse kidney cells, using ADM Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00594-adm-primary-antibodies-ihc-testing-4.jpgAnti-ADM/Adrenomedullin AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00594-adm-primary-antibodies-ihc-testing-5.jpgAnti-ADM/Adrenomedullin AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-irf-1-antibody-a00580-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00580-irf1-primary-antibodyes-wb-testing-1.jpgAnti-IRF-1 AntibodyWestern Blot (WB) analysis of PC12 cells using IRF-1 Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd156c-antibody-a00566-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00566-adam10-primary-antibodies-wb-testing-2.jpgAnti-CD156c ADAM10 AntibodyWestern blot analysis of K562 using CD156c antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00566-adam10-primary-antibodies-ihc-testing-1.jpgAnti-CD156c ADAM10 AntibodyImmunohistochemical analysis of paraffin-embedded human-lymph, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fancd2-antibody-a00563-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00563-fancd2-primary-antibodies-wb-testing-2.jpgAnti-FANCD2 AntibodyWestern Blot analysis of various cells using FANCD2 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00563-fancd2-primary-antibodies-ihc-testing-3.jpgAnti-FANCD2 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100 (4° overnight). High-pressure and temperature Tris-EDTA, pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00563-fancd2-primary-antibodies-ihc-testing-1.jpgAnti-FANCD2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using FANCD2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd45-antibody-a00555-boster.html2026-03-24T05:09:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00555-ptprc-primary-antibodies-wb-testing-2.jpgAnti-CD45 PTPRC AntibodyWestern Blot analysis of Jurkat cells using CD45 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00555-ptprc-primary-antibodies-ihc-testing-3.jpgAnti-CD45 PTPRC AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using CD45 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00555-ptprc-primary-antibodies-if-testing-1.jpgAnti-CD45 PTPRC AntibodyImmunofluorescence analysis of A549. 1, primary Antibody (red) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000 (room temperature, 50min).3, Picture B: DAPI (blue) 10min.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-gtbp-antibody-a00553-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00553-msh6-primary-antibodies-wb-testing-2.jpgAnti-GTBP MSH6 AntibodyWestern Blot analysis of various cells using GTBP Polyclonal Antibody diluted at 1:1000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00553-msh6-primary-antibodies-wb-testing-3.jpgAnti-GTBP MSH6 AntibodyWestern blot analysis of lysates from HUVEC cells, using MSH6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00553-msh6-primary-antibodies-ihc-testing-1.jpgAnti-GTBP MSH6 AntibodyImmunohistochemical analysis of paraffin-embedded Human Lymph gland. 1, Antibody was diluted at 1:100 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ttn-antibody-a00540-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00540-ttn-primary-antibodies-ihc-testing-2.jpgAnti-TTN/Titin AntibodyImmunohistochemical analysis of paraffin-embedded human-heart, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00540-ttn-primary-antibodies-ihc-testing-1.jpgAnti-TTN/Titin AntibodyImmunohistochemical analysis of paraffin-embedded human-skeletal-muscle, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-exo1-antibody-a00536-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00536-exo1-primary-antibodyes-wb-testing-1.jpgAnti-Exonuclease 1 Exo1 AntibodyWestern blot analysis of various cells using Exo1 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003, Inventbiotech, MN, USA).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00536-exo1-primary-antibodyes-if-testing-2.jpgAnti-Exonuclease 1 Exo1 AntibodyImmunofluorescence analysis of A549 cells, using EXO1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hfe-antibody-a00506-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00506-hfe-primary-antibodyes-if-testing-1.jpgAnti-HFE Monoclonal AntibodyImmunofluorescence (IF) analysis of HepG2 cells using HFE Monoclonal antibody (green). Blue: DRAQ5 fluorescent DNA dye.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00506-hfe-primary-antibodyes-wb-testing-2.jpgAnti-HFE Monoclonal AntibodyWestern Blot (WB) analysis using HFE Monoclonal antibody against HEK293 (1) and HFE-hIgGFc transfected HEK293 (2) cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00506-hfe-primary-antibodyes-elisa-testing-3.jpgAnti-HFE Monoclonal AntibodyELISA analysis of HFE antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-nrl-antibody-a00505-1-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00505-1-nrl-primary-antibodies-wb-testing-2.jpgAnti-Nrl AntibodyWestern Blot analysis of various cells using Nrl Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00505-1-nrl-primary-antibodies-wb-testing-3.jpgAnti-Nrl AntibodyWestern blot analysis of NRL Antibody. The lane on the right is blocked with the NRL peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00505-1-nrl-primary-antibodies-wb-testing-1.jpgAnti-Nrl AntibodyWestern blot analysis of the lysates from HUVECcells using NRL antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd110-antibody-a00483-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00483-mpl-primary-antibodies-ihc-testing-1.jpgAnti-CD110 MPL AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00483-mpl-primary-antibodies-wb-testing-2.jpgAnti-CD110 MPL AntibodyWestern Blot analysis of MCF7 cells using CD110 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-skp1-p19-antibody-a00476-1-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00476-1-skp1-primary-antibodies-wb-testing-2.jpgAnti-Skp1 p19 AntibodyWestern Blot analysis of various cells using Skp1 p19 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00476-1-skp1-primary-antibodies-wb-testing-3.jpgAnti-Skp1 p19 AntibodyWestern blot analysis of lysates from COS7 cells, using SKP1A/p19 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00476-1-skp1-primary-antibodies-ihc-testing-1.jpgAnti-Skp1 p19 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using SKP1A/p19 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-apoa-antibody-a00472-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00472-lpa-primary-antibodyes-wb-testing-1.jpgAnti-ApoA LPA Monoclonal AntibodyWestern Blot (WB) analysis using ApoA Monoclonal antibody against truncated LPA-His recombinant protein (1) and truncated Trx-LPA(aa4330-4521) recombinant protein (2).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00472-lpa-primary-antibodyes-ihc-testing-2.jpgAnti-ApoA LPA Monoclonal AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver Tissues with AEC staining using ApoA Monoclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tank-antibody-a00445-1-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00445-1-tank-primary-antibodies-ihc-testing-1.jpgAnti-TANK AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00445-1-tank-primary-antibodies-wb-testing-2.jpgAnti-TANK AntibodyWestern Blot analysis of HT-29 cells using TANK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00445-1-tank-primary-antibodies-wb-testing-3.jpgAnti-TANK AntibodyWestern blot analysis of lysates from HT29 cells, using I-TRAF Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-amylin-antibody-a00414-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00414-iapp-primary-antibodies-wb-testing-2.jpgAnti-Amylin IAPP AntibodyWestern Blot analysis of various cells using Amylin Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00414-iapp-primary-antibodies-wb-testing-3.jpgAnti-Amylin IAPP AntibodyWestern blot analysis of lysates from HeLa cells, treated with EGF 200ng/ml 30', using Amylin Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00414-iapp-primary-antibodies-ihc-testing-1.jpgAnti-Amylin IAPP AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Amylin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-mll-antibody-a00402-boster.html2026-03-24T05:09:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00402-kmt2a-primary-antibodies-ihc-testing-2.jpgAnti-MLL KMT2A AntibodyImmunohistochemical analysis of paraffin-embedded human-lung-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00402-kmt2a-primary-antibodies-ihc-testing-3.jpgAnti-MLL KMT2A AntibodyImmunohistochemical analysis of paraffin-embedded human-lung-cancer, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00402-kmt2a-primary-antibodies-ihc-testing-4.jpgAnti-MLL KMT2A AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00402-kmt2a-primary-antibodies-ihc-testing-1.jpgAnti-MLL KMT2A AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd1-antibody-a00375-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00375-cd1a-primary-antibodies-if-testing-1.jpgAnti-CD1 CD1A Monoclonal AntibodyImmunofluorescence analysis of Mouse-heart tissue. 1,CD1 Monoclonal Antibody (9H6) (red) was diluted at 1:200 (4°C,overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+Bhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00375-cd1a-primary-antibodies-ihc-testing-2.jpgAnti-CD1 CD1A Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human-Tonsil tissue. 1,CD1 Monoclonal Antibody (9H6) was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00375-cd1a-primary-antibodies-if-testing-3.jpgAnti-CD1 CD1A Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat-heart tissue. 1,CD1 Monoclonal Antibody (9H6) was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00375-cd1a-primary-antibodies-ihc-testing-4.jpgAnti-CD1 CD1A Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse-heart tissue. 1,CD1 Monoclonal Antibody (9H6) was diluted at 1:200 (4°C,overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C,20min). 3,Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-factor-viii-antibody-a00367-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00367-f8-primary-antibodies-wb-testing-2.jpgAnti-Factor VIII F8 AntibodyWestern Blot analysis of various cells using Factor VIII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00367-f8-primary-antibodies-wb-testing-3.jpgAnti-Factor VIII F8 AntibodyWestern blot analysis of lysates from HUVEC cells, using Factor VIII Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00367-f8-primary-antibodies-ihc-testing-1.jpgAnti-Factor VIII F8 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-tel-antibody-a00361-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-etv6-primary-antibodies-wb-testing-2.jpgAnti-TEL ETV6 AntibodyWestern Blot analysis of various cells using TEL Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-etv6-primary-antibodies-wb-testing-3.jpgAnti-TEL ETV6 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and Jurkat cells, using ETV6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-etv6-primary-antibodies-ihc-testing-4.jpgAnti-TEL ETV6 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-etv6-primary-antibodies-if-testing-1.jpgAnti-TEL ETV6 AntibodyImmunofluorescence analysis of HeLa cells, using ETV6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-c6-antibody-a00317-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00317-c6-primary-antibodies-ihc-testing-1.jpgAnti-Complement component C6 C6 AntibodyImmunohistochemistryt analysis of paraffin-embedded human heart, using C6 Antibody. The lane on the right is blocked with the C6 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00317-c6-primary-antibodies-wb-testing-2.jpgAnti-Complement component C6 C6 AntibodyWestern Blot analysis of various cells using C6 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00317-c6-primary-antibodies-wb-testing-3.jpgAnti-Complement component C6 C6 AntibodyWestern blot analysis of C6 Antibody. The lane on the right is blocked with the C6 peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chop-antibody-a00311-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-ddit3-primary-antibodyes-wb-testing-1.jpgAnti-CHOP DDIT3 AntibodyWestern Blot (WB) analysis of specific lysis using CHOP Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-ddit3-primary-antibodyes-wb-testing-2.jpgAnti-CHOP DDIT3 AntibodyWestern Blot (WB) analysis of VEC cells using CHOP Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-ddit3-primary-antibodyes-wb-testing-3.jpgAnti-CHOP DDIT3 AntibodyWestern Blot (WB) analysis of specific lysis using CHOP Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-ddit3-primary-antibodyes-wb-testing-4.jpgAnti-CHOP DDIT3 AntibodyWestern Blot (WB) analysis of specific cells using CHOP Polyclonal antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-chop-antibody-a00311-1-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-1-ddit3-primary-antibodies-ihc-testing-2.jpgAnti-CHOP DDIT3 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human-stomach tissue. 1, CHOP Mouse Monoclonal Antibody (2B1) was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-1-ddit3-primary-antibodies-ihc-testing-3.jpgAnti-CHOP DDIT3 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Stomach Carcinoma Tissue using CHOP Mouse mAb diluted at 1:200.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00311-1-ddit3-primary-antibodies-ihc-testing-1.jpgAnti-CHOP DDIT3 Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Pancreas Carcinoma Tissue using CHOP Mouse mAb diluted at 1:200.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fractalkine-receptor-antibody-a00280-1-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00280-1-cx3cr1-primary-antibodies-ihc-testing-1.jpgAnti-Fractalkine Receptor CX3CR1 AntibodyImmunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00280-1-cx3cr1-primary-antibodies-wb-testing-2.jpgAnti-Fractalkine Receptor CX3CR1 AntibodyWestern Blot analysis of U87 cells using Fractalkine Receptor Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00280-1-12931_2024_3058_fig10_html.pngAnti-Fractalkine Receptor CX3CR1 AntibodyIL-21 induced M2 macrophage polarization in primary alveolar macrophage isolated and cultured from mice. ( a ) The percentage of F4/80 + CD11c + Fizz1 + M2 macrophages in bronchoalveolar lavage. ( b ) Percentage of F4/80 + CD11c + Fizz1 + M2 macrophages in bronchoalveolar lavage was analysed by histogram. ( c ) Expression of Fizz1 in bronchoalveolar lavage analysed by western blot. ( d ) Quantitative analysis of Fizz1. ( e , f ) Identification of PASMCs, the expression of α-SMA was verified by immunocytochemistry and immunofluorescence staining. Scale bar = 50 μm. ( g , h ) CX3CL1 and CX3CR1 concentrations were measured using ELISA. Values were means ± SD, n = 6. Comparisons were made using the one-way ANOVA with Bonferroni’s post hoc tests. Scale bar = 50 μm. * P < 0.05, ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-024-03058-9'>39633343</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-aid-antibody-a00267-1-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00267-1-aicda-primary-antibodies-ihc-testing-1.jpgAnti-AID AICDA AntibodyImmunohistochemical analysis of paraffin-embedded human-colon-cancer, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00267-1-aicda-primary-antibodies-wb-testing-2.jpgAnti-AID AICDA AntibodyWestern Blot analysis of Hela, HepG2 cells using AID Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-crp-antibody-a00249-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-crp-primary-antibodies-ihc-testing-1.jpgAnti-CRP/C Reactive Protein AntibodyImmunohistochemical analysis of paraffin-embedded Human Liver. 1, Antibody was diluted at 1:200 (4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-crp-primary-antibodies-wb-testing-2.jpgAnti-CRP/C Reactive Protein AntibodyWestern Blot analysis of mouse liver cells using CRP Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-crp-primary-antibodies-wb-testing-3.jpgAnti-CRP/C Reactive Protein AntibodyWestern blot analysis of lysate from mouse liver cells, using CRP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-crp-primary-antibodies-ihc-testing-4.jpgAnti-CRP/C Reactive Protein AntibodyImmunohistochemical analysis of paraffin-embedded rat-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-crp-primary-antibodies-ihc-testing-5.jpgAnti-CRP/C Reactive Protein AntibodyImmunohistochemical analysis of paraffin-embedded rat-liver, antibody was diluted at 1:100
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-fadd-antibody-a00237-1-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00237-1-fadd-primary-antibodies-wb-testing-2.jpgAnti-FADD AntibodyWestern Blot analysis of HeLa cells using FADD Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00237-1-fadd-primary-antibodies-ihc-testing-1.jpgAnti-FADD AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA, pH9.0 was used for antigen retrieval. 3, Secondary antibody was diluted at 1:200 (room temperature, 30min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cbp-antibody-a00205-1-boster.html2026-03-24T05:09:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00205-1-crebbp-primary-antibodies-wb-testing-2.jpgAnti-CBP CREBBP AntibodyWestern Blot analysis of various cells using CBP Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00205-1-crebbp-primary-antibodies-wb-testing-3.jpgAnti-CBP CREBBP AntibodyWestern blot analysis of lysates from HT-29 cells, treated with calyculinA 50ng/ml 30', using CBP Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00205-1-crebbp-primary-antibodies-ihc-testing-4.jpgAnti-CBP CREBBP AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using CBP Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00205-1-crebbp-primary-antibodies-if-testing-1.jpgAnti-CBP CREBBP AntibodyImmunofluorescence analysis of HeLa cells, using CBP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-flt3-antibody-a00188-1-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00188-1-flt3-primary-antibodies-wb-testing-2.jpgAnti-Flt3/Cd135 AntibodyWestern blot analysis of lysates from LOVO cells, using FLT3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00188-1-flt3-primary-antibodies-wb-testing-1.jpgAnti-Flt3/Cd135 AntibodyWestern blot analysis of the lysates from K562 cells using FLT3 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd192-antibody-a00158-1-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00158-1-ccr2-primary-antibodies-wb-testing-2.jpgAnti-CD192 CCR2 AntibodyWestern Blot analysis of NIH-3T3 cells using CD192 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00158-1-ccr2-primary-antibodies-wb-testing-1.jpgAnti-CD192 CCR2 AntibodyWestern Blot analysis of 3T3 cells using CD192 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-ryr-2-antibody-a00155-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00155-ryr2-primary-antibodies-wb-testing-2.jpgAnti-RyR-2 AntibodyWestern Blot analysis of HepG2-UV MOUSE-BRAIN AD293 PC-3 cells using RyR-2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00155-ryr2-primary-antibodies-ihc-testing-1.jpgAnti-RyR-2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RyR2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-bcl-6-antibody-a00142-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-bcl6-primary-antibodyes-wb-testing-1.jpgAnti-Bcl-6 AntibodyWestern Blot (WB) analysis of 293 cells using Bcl-6 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-bcl6-primary-antibodyes-ihc-testing-2.jpgAnti-Bcl-6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-bcl6-primary-antibodyes-ihc-testing-3.jpgAnti-Bcl-6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-bcl6-primary-antibodyes-ihc-testing-4.jpgAnti-Bcl-6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-bcl6-primary-antibodyes-ihc-testing-5.jpgAnti-Bcl-6 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Liver, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rnase-iii-drosha-antibody-a00111-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00111-drosha-primary-antibodies-wb-testing-2.jpgAnti-RNase III Drosha AntibodyWestern blot analysis of SH-SY5Y K562 HELA using RNase III Drosha antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00111-drosha-primary-antibodies-wb-testing-3.jpgAnti-RNase III Drosha AntibodyWestern blot analysis of lysates from brain tissue, using RNase III Drosha antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00111-drosha-primary-antibodies-ihc-testing-1.jpgAnti-RNase III Drosha AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-hla-dqb1-2-antibody-a00106-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-hla-dqb1-primary-antibodyes-wb-testing-1.jpgAnti-HLA-DQB1/2 AntibodyWestern Blot (WB) analysis of PC12 cells using HLA-DQB1/2 Polyclonal antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-hla-dqb1-primary-antibodyes-ihc-testing-2.jpgAnti-HLA-DQB1/2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Colon, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-hla-dqb1-primary-antibodyes-ihc-testing-3.jpgAnti-HLA-DQB1/2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Colon, antibody was diluted at 1:100.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-hla-dqb1-primary-antibodyes-ihc-testing-4.jpgAnti-HLA-DQB1/2 AntibodyImmunohistochemistry (IHC) analysis of paraffin-embedded Human Spleen, antibody was diluted at 1:100.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-n-h-k-ras-antibody-a00099-1-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-1-nras-primary-antibodies-wb-testing-2.jpgAnti-N/H/K-Ras NRAS AntibodyWestern Blot analysis of various cells using N/H/K-Ras Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-1-nras-primary-antibodies-wb-testing-3.jpgAnti-N/H/K-Ras NRAS AntibodyWestern Blot analysis of 293 cells using N/H/K-Ras Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-1-nras-primary-antibodies-ihc-testing-4.jpgAnti-N/H/K-Ras NRAS AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RASH/RASK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-1-nras-primary-antibodies-if-testing-5.jpgAnti-N/H/K-Ras NRAS AntibodyImmunofluorescence analysis of Siha cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 488 Secondary antibody was diluted at 1:500 (room temperature, 50min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-1-nras-primary-antibodies-if-testing-1.jpgAnti-N/H/K-Ras NRAS AntibodyImmunofluorescence analysis of Siha cell. 1, primary Antibody was diluted at 1:100 (4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rhodopsin-antibody-a00083-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00083-rho-primary-antibodies-wb-testing-2.jpgAnti-Rhodopsin AntibodyWestern Blot analysis of various cells using Rhodopsin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00083-rho-primary-antibodies-wb-testing-3.jpgAnti-Rhodopsin AntibodyWestern blot analysis of lysates from COLO cells, using Rhodopsin Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00083-rho-primary-antibodies-ihc-testing-1.jpgAnti-Rhodopsin AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Rhodopsin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-neurofibromin-antibody-a00043-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00043-nf1-primary-antibodies-if-testing-1.jpgAnti-Neurofibromin NF1 AntibodyImmunofluorescence analysis of HepG2 cells, using NF1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00043-nf1-primary-antibodies-wb-testing-2.jpgAnti-Neurofibromin NF1 AntibodyWestern Blot analysis of various cells using Neurofibromin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00043-nf1-primary-antibodies-wb-testing-3.jpgAnti-Neurofibromin NF1 AntibodyWestern Blot analysis of HepG2 cells using Neurofibromin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00043-nf1-primary-antibodies-wb-testing-4.jpgAnti-Neurofibromin NF1 AntibodyWestern blot analysis of lysates from HepG2 cells, using NF1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00043-nf1-primary-antibodies-ihc-testing-5.jpgAnti-Neurofibromin NF1 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200 (4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200 (room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cleaved-notch-1-v1754-antibody-a00033-1-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00033-1-notch1-primary-antibodies-wb-testing-1.jpgAnti-Cleaved-Notch 1 (V1754) AntibodyWestern Blot analysis of various cells using Cleaved-Notch 1 (V1754) Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00033-1-notch1-primary-antibodies-wb-testing-2.jpgAnti-Cleaved-Notch 1 (V1754) AntibodyWestern Blot analysis of KB cells using Cleaved-Notch 1 (V1754) Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00033-1-notch1-primary-antibodies-if-testing-3.jpgAnti-Cleaved-Notch 1 (V1754) AntibodyImmunofluorescence analysis of Hela cell. 1,Cleaved-Notch 1 (V1754) Polyclonal Antibody (green) was diluted at 1:200 (4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000 (room temperature, 50min). 3 DAPI (blue) 10min. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00033-1-notch1-primary-antibodies-if-testing-4.jpgAnti-Cleaved-Notch 1 (V1754) AntibodyImmunofluorescence analysis of Human-lung-cancer tissue. 1,Cleaved-Notch 1 (V1754) Polyclonal Antibody (red) was diluted at 1:200 (4°C,overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd152-antibody-a00020-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00020-ctla4-primary-antibodies-ihc-testing-2.jpgAnti-CD152 CTLA4 AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00020-ctla4-primary-antibodies-ihc-testing-1.jpgAnti-CD152 CTLA4 AntibodyImmunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00020-40164_2022_275_fig3_html.pngAnti-CD152 CTLA4 AntibodyImmunohistochemical staining and analysis of subcutaneous tumors. Immunohistochemical staining was conducted on subcutaneous tumor tissue microarray. H-score were calculated to quantify the expression levels of marker proteins. Representative images captured at 40 ×. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. Foxp3 forkhead box protein p3, CTLA4 cytotoxic T-lymphocyte-associated protein 4, TIGIT T cell immunoreceptor with Ig and ITIM domains, TIM3 T-cell immunoglobulin mucin-3, VISTA V domain-containing Ig suppressor of T-cell activation <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s40164-022-00275-0'>35379324</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-p16-antibody-a00016-3-boster.html2026-03-24T05:09:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00016-3-cdkn2a-primary-antibodyes-wb-testing-1.jpgAnti-p16 CDKN2A Monoclonal AntibodyWestern blot analysis using p16 monoclonal antibody against truncated p16 recombinant protein.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00016-3-cdkn2a-primary-antibodyes-ihc-testing-2.jpgAnti-p16 CDKN2A Monoclonal AntibodyImmunohistochemistry analysis of paraffin-embedded rat liver tissue (A) , human brain tumor (B) , breast cancer (C) , esophageal epithelium tissue (D) , mouse brain tissue (E) and stomach tisue (F) , showing nuclear localization with DAB staining using p16 Mon
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00016-3-41419_2020_2238_fig3_html.pngAnti-p16 CDKN2A Monoclonal AntibodyAccumulation of damaged mitochondria led to stress-induced apoptosis and senescence. a , b 2′,7′-Dichlorofluorescin diacetate (DCFH-DA) detection of reactive oxygen species (ROS; n = 4). c , d TUNEL–DAPI detection of deoxyribonucleic acid (DNA) damage and apoptosis ( n = 4). e , f Annexin V–FITC and propidium iodide (PI) detection of apoptosis ( n = 4). g , h Detection of β-gal activity by β-gal staining ( n = 4). i – k Western blot analysis of P16 and P21 expression ( n = 3). In ( b ), ( d ), ( f ), ( h ), and ( j – k ), data are presented as means ± SD. Statistical significances were calculated by Student’s t test. Data were compared with the control group: * P < 0.05. H 2 O 2 was used to simulate OS; L-DMEM was used as control. TUNEL = terminal deoxynucleotidyl transferase deoxyuridine-5′-triphosphate nick end labeling; DAPI = 4′,6-diamidino-2-phenylindole; FITC = fluorescein isothiocyanate; P16 = protein 16; P21 = protein 21; β-gal = β-galactosidase. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-2238-1'>31959744</a></b>
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-apc-antibody-a00008-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00008-apc-primary-antibodyes-wb-testing-1.jpgAnti-APC AntibodyWestern blot analysis of COLO205 cells using APC Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00008-apc-primary-antibodyes-wb-testing-2.jpgAnti-APC AntibodyWestern blot analysis of various cells using APC Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00008-apc-primary-antibodyes-wb-testing-3.jpgAnti-APC AntibodyWestern blot analysis of lysates from COLO205 cells, using APC Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00008-apc-primary-antibodyes-ihc-testing-4.jpgAnti-APC AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using APC Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00008-apc-primary-antibodyes-if-testing-5.jpgAnti-APC AntibodyImmunofluorescence analysis of Hela cell. 1, APC Polyclonal Antibody (red) was diluted at 1:200 (4°C overnight). Galectin-3 monoclonal antibody (6G2) (green) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit Alexa Fluor 594 Catalog: (NA was diluted at 1:1000 (room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 Catalog: (NA was diluted at 1:1000 (room temperature, 50min).
https://www.bosterbio.com/products/primary-antibodies/anti-cord2-picoband-trade-antibody-a02202-1-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02202-1-1-WB-anti-cord2-picoband-antibody.jpgAnti-CORD2/CRX Antibody Picoband®<b> Western blot analysis of CORD2 using anti-CORD2 antibody (A02202-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CORD2 antigen affinity purified polyclonal antibody (Catalog # A02202-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CORD2 at approximately 37KD. The expected band size for CORD2 is at 32KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ngf-ngf-beta-picoband-trade-antibody-a00341-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00341-1-WB-anti-ngf-ngf-beta-picoband-antibody.jpgAnti-NGF/NGF Beta Antibody Picoband®<b> Western blot analysis of NGF/NGF Beta using anti-NGF/NGF Beta antibody (A00341). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>
Lane 1: Recombinant Human NGF/NGF Beta Protein 0.5ng <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NGF/NGF Beta antigen affinity purified polyclonal antibody (Catalog # A00341) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NGF/NGF Beta at approximately 13KD. The expected band size for NGF/NGF Beta is at 13KD.
https://www.bosterbio.com/products/primary-antibodies/anti-crp-picoband-trade-antibody-a00249-1-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00249-1-2-IHC-anti-crp-c-reactive-protein-picoband-antibody.jpgAnti-C Reactive Protein/Crp Antibody Picoband®<b> IHC analysis of Crp using anti-Crp antibody (A00249-1).</b><br>
Crp was detected in paraffin-embedded section of mouse kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Crp Antibody (A00249-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00249-1-3-IHC-anti-crp-c-reactive-protein-picoband-antibody.jpgAnti-C Reactive Protein/Crp Antibody Picoband®<b> IHC analysis of Crp using anti-Crp antibody (A00249-1).</b><br>
Crp was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Crp Antibody (A00249-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00249-1-1_1.jpgAnti-C Reactive Protein/Crp Antibody Picoband® Western blot analysis of Crp using anti-Crp antibody (A00249-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysates, <br>Lane 2: rat brain tissue lysates, <br>Lane 3: rat thymus tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Crp antigen affinity purified polyclonal antibody (Catalog # A00249-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Crp at approximately 25KD. The expected band size for Crp is at 25KD.
https://www.bosterbio.com/products/primary-antibodies/anti-otc-picoband-trade-antibody-a00721-1-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00721-1-1-WB-anti-otc-ornithine-carbamoyltransferase-picoband-antibody.jpgAnti-Ornithine Carbamoyltransferase/OTC Antibody Picoband®<b> Western blot analysis of OTC using anti-OTC antibody (A00721-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>
Lane 1: rat liver tissue lysates, <br>
Lane 2: mouse liver tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OTC antigen affinity purified polyclonal antibody (Catalog # A00721-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OTC at approximately 40KD. The expected band size for OTC is at 40KD.
https://www.bosterbio.com/products/primary-antibodies/anti-pdgf-beta-picoband-trade-antibody-a00348-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00348-1_1.jpgAnti-PDGF beta/PDGFB Antibody Picoband® Western blot analysis of PDGF beta using anti-PDGF beta antibody (A00348). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates, <br>Lane 2: mouse brain tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDGF beta antigen affinity purified polyclonal antibody (Catalog # A00348) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDGF beta at approximately 27KD. The expected band size for PDGF beta is at 27KD.
https://www.bosterbio.com/products/primary-antibodies/anti-akr1b10-picoband-trade-antibody-a02976-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02976-akr1b10-primary-antibodies-wb-testing-1.jpgAnti-AKR1B10 Antibody Picoband® Western blot analysis of AKR1B10 using anti-AKR1B10 antibody (A02976). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AKR1B10 antigen affinity purified polyclonal antibody (Catalog # A02976) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AKR1B10 at approximately 36 kDa. The expected band size for AKR1B10 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02976-2-IHC-anti-akr1b10-picoband-antibody.jpgAnti-AKR1B10 Antibody Picoband®<b> IHC analysis of AKR1B10 using anti-AKR1B10 antibody (A02976).</b><br>
AKR1B10 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-AKR1B10 Antibody (A02976) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02976-3-IHC-anti-akr1b10-picoband-antibody.jpgAnti-AKR1B10 Antibody Picoband®<b> IHC analysis of AKR1B10 using anti-AKR1B10 antibody (A02976).</b><br>
AKR1B10 was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-AKR1B10 Antibody (A02976) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02976-akr1b10-primary-antibodies-if-testing-4.jpgAnti-AKR1B10 Antibody Picoband® IF analysis of AKR1B10 using anti-AKR1B10 antibody (A02976). <br>
AKR1B10 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AKR1B10 Antibody (A02976) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-hemoglobin-picoband-trade-antibody-a00233-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00233-1-hemoglobin-primary-antibodies-wb-testing-1.jpgAnti-Hemoglobin/HBA1/HBA2 Antibody Picoband® Western blot analysis of Hemoglobin using anti-Hemoglobin antibody (A00233-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hemoglobin antigen affinity purified polyclonal antibody (Catalog # A00233-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hemoglobin at approximately 15 kDa. The expected band size for Hemoglobin is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00233-1-hemoglobin-primary-antibodies-ihc-testing-2.jpgAnti-Hemoglobin/HBA1/HBA2 Antibody Picoband® IHC analysis of Hemoglobin using anti-Hemoglobin antibody (A00233-1). <br>
Hemoglobin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hemoglobin Antibody (A00233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00233-1-hemoglobin-primary-antibodies-ihc-testing-3.jpgAnti-Hemoglobin/HBA1/HBA2 Antibody Picoband® IHC analysis of Hemoglobin using anti-Hemoglobin antibody (A00233-1). <br>
Hemoglobin was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hemoglobin Antibody (A00233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00233-1-hemoglobin-primary-antibodies-fcm-testing-4_1.jpgAnti-Hemoglobin/HBA1/HBA2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-Hemoglobin antibody (A00233-1). <br>
Overlay histogram showing K562 cells stained with A00233-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Hemoglobin Antibody (A00233-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-chk1-picoband-trade-antibody-a01060-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01060-chk1-primary-antibodies-wb-testing-1.jpgAnti-Chk1/CHEK1 Antibody Picoband® Western blot analysis of Chk1/CHEK1 using anti-Chk1/CHEK1 antibody (A01060). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Chk1/CHEK1 antigen affinity purified polyclonal antibody (Catalog # A01060) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Chk1/CHEK1 at approximately 54 kDa. The expected band size for Chk1/CHEK1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01060-chk1-primary-antibodies-fcm-testing-2.jpgAnti-Chk1/CHEK1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-Chk1/CHEK1 antibody (A01060). <br>
Overlay histogram showing K562 cells stained with A01060 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Chk1/CHEK1 Antibody (A01060, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-pik3cb-picoband-trade-antibody-a01091-1-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01091-1-3-IHC-anti-pik3cb-pi-3-kinase-p110-beta-picoband-antibody.jpgAnti-PI3 Kinase p110 beta/PIK3CB Antibody Picoband®<b> IHC analysis of PIK3CB using anti-PIK3CB antibody (A01091-1).</b><br>
PIK3CB was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PIK3CB Antibody (A01091-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01091-1-2-IHC-anti-pik3cb-pi-3-kinase-p110-beta-picoband-antibody.jpgAnti-PI3 Kinase p110 beta/PIK3CB Antibody Picoband®<b> IHC analysis of PIK3CB using anti-PIK3CB antibody (A01091-1).</b><br>
PIK3CB was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PIK3CB Antibody (A01091-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01091-1-1_1.jpgAnti-PI3 Kinase p110 beta/PIK3CB Antibody Picoband® Western blot analysis of PIK3CB using anti-PIK3CB antibody (A01091-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates, <br>Lane 2: rat kidney tissue lysates, <br>Lane 3: mouse spleen tissue lysates, <br>Lane 4: mouse thymus tissue lysates, <br>Lane 5: MCF-7 whole Cell lysates, <br>Lane 6: K562 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3CB antigen affinity purified polyclonal antibody (Catalog # A01091-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIK3CB at approximately 110KD. The expected band size for PIK3CB is at 123KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cxcr4-picoband-trade-antibody-a00031-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00031-1_1-WB-anti-cxcr4-picoband-antibody.jpgAnti-CXCR4 Antibody Picoband®<b> Western blot analysis of CXCR4 using anti-CXCR4 antibody (A00031). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HELA whole Cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CXCR4 antigen affinity purified polyclonal antibody (Catalog # A00031) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CXCR4 at approximately 40KD. The expected band size for CXCR4 is at 40KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd166-alcam-picoband-trade-antibody-a01788-1-boster.html2026-03-27T05:07:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-wb-testing-1_1.jpgAnti-CD166/ALCAM Antibody Picoband® Western blot analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates, <br>
Lane 2: human Hela whole cell lysates, <br>
Lane 3: rat liver tissue lysates, <br>
Lane 4: rat brain tissue lysates, <br>
Lane 5: rat lung tissue lysates, <br>
Lane 6: mouse liver tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD166/ALCAM antigen affinity purified polyclonal antibody (Catalog # A01788-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD166/ALCAM at approximately 100-110 kDa. The expected band size for CD166/ALCAM is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-2.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-3.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-4_1.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-5_1.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-6_1.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-ihc-testing-7.jpgAnti-CD166/ALCAM Antibody Picoband® IHC analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-if-testing-8.jpgAnti-CD166/ALCAM Antibody Picoband® IF analysis of CD166/ALCAM using anti-CD166/ALCAM antibody (A01788-1). <br>
CD166/ALCAM was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-CD166/ALCAM Antibody (A01788-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01788-1-cd166-primary-antibodies-fcm-testing-9.jpgAnti-CD166/ALCAM Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-CD166/ALCAM antibody (A01788-1). <br>
Overlay histogram showing SH-SY5Y cells stained with A01788-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD166/ALCAM Antibody (A01788-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-cytochrome-p450-2d6-picoband-trade-antibody-a00498-1-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00498-1-4-IHC-anti-cytochrome-p450-2d6-picoband-antibody.jpgAnti-Cytochrome P450 2D6/CYP2D6 Antibody Picoband®<b> IHC analysis of Cytochrome P450 2D6 using anti-Cytochrome P450 2D6 antibody (A00498-1).</b><br>
Cytochrome P450 2D6 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome P450 2D6 Antibody (A00498-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00498-1-3-IHC-anti-cytochrome-p450-2d6-picoband-antibody.jpgAnti-Cytochrome P450 2D6/CYP2D6 Antibody Picoband®<b> IHC analysis of Cytochrome P450 2D6 using anti-Cytochrome P450 2D6 antibody (A00498-1).</b><br>
Cytochrome P450 2D6 was detected in paraffin-embedded section of mouse liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome P450 2D6 Antibody (A00498-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00498-1-5-IHC-anti-cytochrome-p450-2d6-picoband-antibody.jpgAnti-Cytochrome P450 2D6/CYP2D6 Antibody Picoband®<b> IHC analysis of Cytochrome P450 2D6 using anti-Cytochrome P450 2D6 antibody (A00498-1).</b><br>
Cytochrome P450 2D6 was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome P450 2D6 Antibody (A00498-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00498-1-2-IHC-anti-cytochrome-p450-2d6-picoband-antibody.jpgAnti-Cytochrome P450 2D6/CYP2D6 Antibody Picoband®<b> IHC analysis of Cytochrome P450 2D6 using anti-Cytochrome P450 2D6 antibody (A00498-1).</b><br>
Cytochrome P450 2D6 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome P450 2D6 Antibody (A00498-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00498-1-1_1.jpgAnti-Cytochrome P450 2D6/CYP2D6 Antibody Picoband® Western blot analysis of Cytochrome P450 2D6 using anti-Cytochrome P450 2D6 antibody (A00498-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates, <br>Lane 2: mouse liver tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytochrome P450 2D6 antigen affinity purified polyclonal antibody (Catalog # A00498-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytochrome P450 2D6 at approximately 56KD. The expected band size for Cytochrome P450 2D6 is at 56KD.
https://www.bosterbio.com/products/primary-antibodies/anti-aldh1a3-picoband-trade-antibody-a03030-boster.html2026-03-24T05:09:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030_41598_2024_82460_fig2_html.pngAnti-ALDH1A3 Antibody Picoband®IHC analysis to check the expression of ALDH1/2 and ALDH1A3 in MIBC tumors and distant normal urothelium. Asterisks in the graphs denote statistical significance as “*” p < 0.05. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-82460-1'>40595790</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030_41598_2024_82460_fig3_html.pngAnti-ALDH1A3 Antibody Picoband®Photomicrographs showing negative, weak and strong staining patterns of ALDH1/2 and ALDH1A3 proteins in distant normal bladder urothelium and MIBC tumor tissues. Bottom panel shows the representative results from the ImageJ based IHC profiler plugin to validate the accuracy of our scoring. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-82460-1'>40595790</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030_41598_2024_82460_fig4_html.pngAnti-ALDH1A3 Antibody Picoband®( a. ) Overall survival analysis and Kaplan Meier’s estimate for IHC cohort of MIBC patients. ( b. ) and ( c. ) represent survival analysis of high and low expressor groups of ALDH1/2 and ALDH1A3 proteins, respectively. Asterisks in the graphs denote statistical significance as “*” p < 0.05, “**” p < 0.01, “***” p < 0.001, “****” p < 0.0001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-82460-1'>40595790</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030_41598_2024_82460_fig7_html.pngAnti-ALDH1A3 Antibody Picoband®Association of transcript expression of ALDH1A1 and 1A3 mRNA with patient’s survival in TCGA database. ( a ) overall survival curve of high and low ALDH1A1 expression, ( b ) disease free survival curve of high and low ALDH1A1 expression, ( c ) overall survival of high and low ALDH1A3 expression and ( d ) disease free survival curve of high and low ALDH1A3 expression. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-82460-1'>40595790</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-wb-testing-1_1.jpgAnti-ALDH1A3 Antibody Picoband®Western blot analysis of ALDH1A3 using anti-ALDH1A3 antibody (A03030). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALDH1A3 antigen affinity purified polyclonal antibody (Catalog # A03030) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALDH1A3 at approximately 50-56 kDa. The expected band size for ALDH1A3 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-ihc-testing-1.jpgAnti-ALDH1A3 Antibody Picoband®IHC analysis of ALDH1A3 using anti-ALDH1A3 antibody (A03030). <br>
ALDH1A3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ALDH1A3 Antibody (A03030) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-ihc-testing-2.jpgAnti-ALDH1A3 Antibody Picoband®IHC analysis of ALDH1A3 using anti-ALDH1A3 antibody (A03030). <br>
ALDH1A3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ALDH1A3 Antibody (A03030) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-ihc-testing-3.jpgAnti-ALDH1A3 Antibody Picoband®IHC analysis of ALDH1A3 using anti-ALDH1A3 antibody (A03030). <br>
ALDH1A3 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ALDH1A3 Antibody (A03030) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-if-testing-1.jpgAnti-ALDH1A3 Antibody Picoband®IF analysis of ALDH1A3 using anti-ALDH1A3 antibody (A03030). <br>
ALDH1A3 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ALDH1A3 Antibody (A03030) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03030-aldh1a3-primary-antibodies-fcm-testing-1.jpgAnti-ALDH1A3 Antibody Picoband®Flow Cytometry analysis of PC-3 cells using anti-ALDH1A3 antibody (A03030). <br>
Overlay histogram showing PC-3 cells stained with A03030 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ALDH1A3 Antibody (A03030, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-amh-picoband-trade-antibody-a00763-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00763-1-WB-anti-amh-mis-picoband-antibody.jpgAnti-AMH Antibody Picoband®<b> Western blot analysis of AMH using anti-AMH antibody (A00763).</b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: 293T whole Cell lysates, <br>
Lane 2: COLO320 whole Cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AMH antigen affinity purified polyclonal antibody (Catalog # A00763) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AMH4 at approximately 65KD. The expected band size for AMH is at 59KD.
https://www.bosterbio.com/products/primary-antibodies/anti-dishevelled-2-picoband-trade-antibody-a02404-3-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02404-3-1-WB-anti-dishevelled-2-picoband-antibody.jpgAnti-Dishevelled 2/DVL2 Antibody Picoband®<b> Western blot analysis of Dishevelled 2 using anti-Dishevelled 2 antibody (A02404-3). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates, <br>
Lane 2: mouse kidney tissue lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dishevelled 2 antigen affinity purified polyclonal antibody (Catalog # A02404-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Dishevelled 2 at approximately 79KD. The expected band size for Dishevelled 2 is at 79KD.
https://www.bosterbio.com/products/primary-antibodies/anti-amylase-picoband-trade-antibody-a12967-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a12967-2-IHC-anti-alpha-amylase-1-picoband-antibody.jpgAnti-Amylase/AMY1A/AMY1B/AMY1C Antibody Picoband®<b> IHC analysis of Amylase using anti-Amylase antibody (A12967).</b><br>
Amylase was detected in paraffin-embedded section of human pancreatic cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Amylase Antibody (A12967) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12967-1_1.jpgAnti-Amylase/AMY1A/AMY1B/AMY1C Antibody Picoband® Western blot analysis of Amylase using anti-Amylase antibody (A12967). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat pancreas tissue lysates, <br>Lane 2: mouse pancreas tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Amylase antigen affinity purified polyclonal antibody (Catalog # A12967) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Amylase at approximately 58KD. The expected band size for Amylase is at 58KD.
https://www.bosterbio.com/products/primary-antibodies/anti-dishevelled-3-picoband-trade-antibody-a03577-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03577-1-WB-anti-dishevelled-3-picoband-antibody.jpgAnti-Dishevelled 3/DVL3 Antibody Picoband®<b> Western blot analysis of Dishevelled 3 using anti-Dishevelled 3 antibody (A03577). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: mouse brain tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dishevelled 3 antigen affinity purified polyclonal antibody (Catalog # A03577) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Dishevelled 3 at approximately 78KD. The expected band size for Dishevelled 3 is at 78KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ece1-picoband-trade-antibody-a02519-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02519-1-ece1-primary-antibodies-wb-testing-1.jpgAnti-ECE1 Antibody Picoband®Western blot analysis of ECE1 using anti-ECE1 antibody (A02519-1). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human HUVEC whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ECE1 antigen affinity purified polyclonal antibody (Catalog # A02519-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ECE1 at approximately 120-130 kDa. The expected band size for ECE1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02519-1-ece1-primary-antibodies-ihc-testing-1.jpgAnti-ECE1 Antibody Picoband®IHC analysis of ECE1 using anti-ECE1 antibody (A02519-1. <br>ECE1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ECE1 Antibody (A02519-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02519-1-ece1-primary-antibodies-ihc-testing-2.jpgAnti-ECE1 Antibody Picoband®IHC analysis of ECE1 using anti-ECE1 antibody (A02519-1. <br>ECE1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ECE1 Antibody (A02519-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-eif3e-picoband-trade-antibody-a00481-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00481-1-eif3e-primary-antibodies-wb-testing-1.jpgAnti-EIF3e Antibody Picoband®Western blot analysis of EIF3e using anti-EIF3e antibody (A00481-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF3e antigen affinity purified polyclonal antibody (A00481-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF3e at approximately 52 kDa. The expected band size for EIF3e is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00481-1-eif3e-primary-antibodies-ihc-testing-1.jpgAnti-EIF3e Antibody Picoband®IHC analysis of EIF3e using anti-EIF3e antibody (A00481-1). <br>EIF3e was detected in a paraffin-embedded section of human cerebral cortex tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3e Antibody (A00481-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00481-1-eif3e-primary-antibodies-ihc-testing-2.jpgAnti-EIF3e Antibody Picoband®IHC analysis of EIF3e using anti-EIF3e antibody (A00481-1). <br>EIF3e was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3e Antibody (A00481-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00481-1-eif3e-primary-antibodies-ip-testing-1.jpgAnti-EIF3e Antibody Picoband®Immunoprecipitating (IP) EIF3e in HepG2 whole cell lysate.<br>
Western blot analysis of EIF3e using anti-EIF3e antibody (A00481-1); <br>
Lane 1: HepG2 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-EIF3e antibody in HepG2 whole cell lysate;<br>
Lane 3: anti-EIF3e antibody (2μg) + HepG2 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EIF3e antigen affinity purified polyclonal antibody (A00481-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for EIF3e at approximately 52 kDa. The expected band size for EIF3e is at 52 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-annexin-iv-picoband-trade-antibody-a04840-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-wb-testing-1.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® Western blot analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human A549 whole cell lysates, <br>
Lane 3: human THP-1 whole cell lysates, <br>
Lane 4: human Hacat whole cell lysates, <br>
Lane 5: rat stomach tissue lysates, <br>
Lane 6: rat lung tissue lysates, <br>
Lane 7: mouse stomach tissue lysates, <br>
Lane 8: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANXA4 antigen affinity purified polyclonal antibody (Catalog # A04840) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANXA4 at approximately 36 kDa. The expected band size for ANXA4 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-2.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-fcm-testing-8.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-ANXA4 antibody (A04840). <br>Overlay histogram showing HEL cells stained with A04840 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ANXA4 Antibody (A04840, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-3.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of human colonic adenom tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-4.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-5.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-6.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04840-anxa4-primary-antibodies-ihc-testing-7.jpgAnti-Annexin IV/ANXA4 Antibody Picoband® IHC analysis of ANXA4 using anti-ANXA4 antibody (A04840). <br>
ANXA4 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANXA4 Antibody (A04840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-erbb-2-picoband-trade-antibody-a00010-2-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00010-2-erbb-2-primary-antibodies-wb-testing-1.jpgAnti-ErbB 2/ERBB2 Antibody Picoband® Western blot analysis of ErbB 2 using anti-ErbB 2 antibody (A00010-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ErbB 2 antigen affinity purified polyclonal antibody (Catalog # A00010-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ErbB 2 at approximately 185 kDa. The expected band size for ErbB 2 is at 138 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00010-2-erbb-2-primary-antibodies-ihc-testing-2.jpgAnti-ErbB 2/ERBB2 Antibody Picoband® IHC analysis of ErbB 2 using anti-ErbB 2 antibody (A00010-2). <br>
ErbB 2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ErbB 2 Antibody (A00010-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ets1-picoband-trade-antibody-a00931-2-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00931-2-1_1.jpgAnti-ETS1 Antibody Picoband® Western blot analysis of ETS1 using anti-ETS1 antibody (A00931-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: NIH3T3 whole Cell lysates, <br>Lane 2: A375 whole cell lysates.<br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ETS1 antigen affinity purified polyclonal antibody (Catalog # A00931-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ETS1 at approximately 54KD. The expected band size for ETS1 is at 54KD.
https://www.bosterbio.com/products/primary-antibodies/anti-aquaporin-3-picoband-trade-antibody-a02181-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02181-1_1.jpgAnti-Aquaporin 3/Aqp3 Antibody Picoband®<b> Western blot analysis of Aquaporin 3 using anti-Aquaporin 3 antibody (A02181). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse kidney tissue lysates, <br>Lane 2: mouse brain tissue lysates, <br>Lane 3: rat kidney tissue lysates, <br>Lane 4: rat brain tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Aquaporin 3 antigen affinity purified polyclonal antibody (Catalog # A02181) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Aquaporin 3 at approximately 32KD. The expected band size for Aquaporin 3 is at 32KD.
https://www.bosterbio.com/products/primary-antibodies/anti-fabp2-i-fabp-picoband-trade-antibody-a02378-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02378-fabp2-primary-antibodies-wb-testing-1.jpgAnti-FABP2/I-FABP Antibody Picoband® Western blot analysis of FABP2/I-FABP using anti-FABP2/I-FABP antibody (A02378). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat small intestine tissue lysates,<br>
Lane 3: mouse liver tissue lysates,<br>
Lane 4: mouse small intestine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FABP2/I-FABP antigen affinity purified polyclonal antibody (Catalog # A02378) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FABP2/I-FABP at approximately 15 kDa. The expected band size for FABP2/I-FABP is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02378-2-IHC-anti-fabp2-i-fabp-picoband-antibody.jpgAnti-FABP2/I-FABP Antibody Picoband®<b> IHC analysis of FABP2/I-FABP using anti-FABP2/I-FABP antibody (A02378).</b><br>
FABP2/I-FABP was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FABP2/I-FABP Antibody (A02378) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02378-3-IHC-anti-fabp2-i-fabp-picoband-antibody.jpgAnti-FABP2/I-FABP Antibody Picoband®<b> IHC analysis of FABP2/I-FABP using anti-FABP2/I-FABP antibody (A02378).</b><br>
FABP2/I-FABP was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FABP2/I-FABP Antibody (A02378) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02378-4-IHC-anti-fabp2-i-fabp-picoband-antibody.jpgAnti-FABP2/I-FABP Antibody Picoband®<b> IHC analysis of FABP2/I-FABP using anti-FABP2/I-FABP antibody (A02378).</b><br>
FABP2/I-FABP was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FABP2/I-FABP Antibody (A02378) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-fdcsp-picoband-trade-antibody-a13093-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a13093-1-1-IHC-anti-fdcsp-picoband-antibody.jpgAnti-FDCSP Antibody<b> IHC analysis of FDCSP using anti-FDCSP antibody (A13093-1).</b><br>
FDCSP was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FDCSP Antibody (A13093-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17067-1-fdcsp-primary-antibodies-if-testing-2.jpgAnti-FDCSP Antibody IF analysis of FDCSP using anti-FDCSP antibody (A13093-1). <br>
FDCSP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-FDCSP Antibody (A13093-1) overnight at 4°C. FITC Conjugated Goat Anti-Rabbit IgG (BA1105) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-fsh-receptor-picoband-trade-antibody-a00897-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00897-1-WB-anti-fsh-receptor-picoband-antibody.jpgAnti-FSH Receptor/FSHR Antibody Picoband®<b> Western blot analysis of FSH Receptor using anti-FSH Receptor antibody (A00897). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: mouse ovary tissue lysates, <br>
Lane 2: HELA whole Cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FSH Receptor antigen affinity purified polyclonal antibody (Catalog # A00897) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FSH Receptor at approximately 78KD. The expected band size for FSH Receptor is at 78KD.
https://www.bosterbio.com/products/primary-antibodies/anti-aquaporin-6-picoband-trade-antibody-a10607-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngAnti-Aquaporin 6/AQP6 Antibody Picoband®Boster Kit Box
https://www.bosterbio.com/products/primary-antibodies/anti-gabbr1-picoband-trade-antibody-a07297-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07297-1-gabbr1-primary-antibodies-wb-testing-1.jpgAnti-GABA B Receptor 1/GABBR1 Antibody Picoband® Western blot analysis of GABBR1 using anti-GABBR1 antibody (A07297-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GABBR1 antigen affinity purified polyclonal antibody (Catalog # A07297-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GABBR1 at approximately 108 kDa. The expected band size for GABBR1 is at 108,130 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bmal1-arntl-picoband-trade-antibody-a00260-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00260-1-arntl-primary-antibodies-wb-testing-1.jpgAnti-BMAL1/ARNTL Antibody Picoband® Western blot analysis of BMAL1/ARNTL using anti-BMAL1/ARNTL antibody (A00260-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HT1080 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMAL1/ARNTL antigen affinity purified polyclonal antibody (Catalog # A00260-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BMAL1/ARNTL at approximately 75 kDa. The expected band size for BMAL1/ARNTL is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00260-1-arntl-primary-antibodies-fcm-testing-2.jpgAnti-BMAL1/ARNTL Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-BMAL1/ARNTL antibody (A00260-1). <br>
Overlay histogram showing MCF-7 cells stained with A00260-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BMAL1/ARNTL Antibody (A00260-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-gas-6-picoband-trade-antibody-a00608-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00608-1-gas6-primary-antibody-wb-testing-1.jpgAnti-GAS 6/GAS6 Antibody Picoband® Western blot analysis of GAS6 using anti-GAS6 antibody (A00608-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAS6 antigen affinity purified polyclonal antibody (A00608-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GAS6 at approximately 55, 79 kDa. The expected band size for GAS6 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00608-1-gas6-primary-antibody-ihc-testing-2.jpgAnti-GAS 6/GAS6 Antibody Picoband® IHC analysis of GAS6 using anti-GAS6 antibody (A00608-1). <br>
GAS6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAS6 Antibody (A00608-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00608-1-gas6-primary-antibody-fcm-testing-3.jpgAnti-GAS 6/GAS6 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-GAS6 antibody (A00608-1). <br>
Overlay histogram showing THP-1 cells stained with A00608-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GAS6 Antibody (A00608-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-gdf15-picoband-trade-antibody-a01583-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01583-1-1-WB-anti-gdf15-picoband-antibody.jpgAnti-GDF15 Antibody Picoband®<b> Western blot analysis of GDF15 using anti-GDF15 antibody (A01583-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: 22RV whole Cell lysates, <br>
Lane 2: human placenta tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GDF15 antigen affinity purified polyclonal antibody (Catalog # A01583-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GDF15 at approximately 34KD. The expected band size for GDF15 is at 34KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01583-1-gdf-15-primary-antibodies-elisa-testing-2.jpgAnti-GDF15 Antibody Picoband® Sandwich ELISA - Recombinant human GDF-15 protein standard curve.<br>
Use in combination with reagents from Human GDF-15 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0767).
https://www.bosterbio.com/products/primary-antibodies/anti-atf6-picoband-trade-antibody-a00655-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00655-2-IHC-anti-atf6-picoband-antibody.jpgAnti-ATF6 Antibody Picoband®<b> IHC analysis of ATF6 using anti-ATF6 antibody (A00655).</b><br>
ATF6 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ATF6 Antibody (A00655) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00655-1-WB-anti-atf6-picoband-antibody.jpgAnti-ATF6 Antibody Picoband®<b> Western blot analysis of ATF6 using anti-ATF6 antibody (A00655).</b> <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates, <br>
Lane 2: mouse liver tissue lysates, <br>
Lane 3: MCF-7 whole Cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF6 antigen affinity purified polyclonal antibody (Catalog # A00655) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF6 at approximately 90 KD,100KD. The expected band size for ATF6 is at 75KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00655-41419_2020_2930_fig3_html.pngAnti-ATF6 Antibody Picoband®BCAT1 regulates autophagy through the endoplasmic reticulum stress pathway. a Expression of BCAT1 and ER-Tracker Red staining in PASMCs exposed to NOR or HYP for 24 h. Scale bar = 50 μm ( n = 3). b Western blot analysis of PERK, IRE1, ATF6, and GRP78 protein expression in the ERs pathway in PASMCs treated with gabapentin ( n = 8). c Western blot analysis of IRE1, PERK, ATF6, and GRP78 expression in PASMCs transfected with BCAT1 siRNA ( n = 8). d Western blot analysis of BECN1 and Atg5 in PASMCs treated with the ERs pathway inhibitor 4-PBA and BCAT1 plasmid ( n = 8). e Coimmunoprecipitation of the whole-cell lysates of PASMCs exposed to normoxia or hypoxia for 24 h with anti-IRE1, followed by probing with anti-BCAT1 ( n = 3). Nor normoxia, Hyp hypoxia, H + G hypoxia plus gabapentin, H + NC hypoxia plus control siRNA, H + SI hypoxia plus BCAT1 siRNA, N + Con normoxia plus control vector, H + Con hypoxia plus control vector, H + B hypoxia plus BCAT1 plasmid, H + Con+4 hypoxia plus control vector plus 4-phenylbutyric acid, H + B + 4 hypoxia plus BCAT1 plasmid plus 4-phenylbutyric acid, IP immunoprecipitation, IB immunoblotting. Statistical analysis was performed with one-way ANOVA. All values are presented as the mean ± SEM. ** p < 0.01; *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02930-y'>32938905</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-hcn2-picoband-trade-antibody-a02804-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02804-2-IHC-anti-hcn2-picoband-antibody.jpgAnti-HCN2 Antibody Picoband®<b> IHC analysis of HCN2 using anti-HCN2 antibody (A02804).</b><br>
HCN2 was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HCN2 Antibody (A02804) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02804-1-WB-anti-hcn2-picoband-antibody.jpgAnti-HCN2 Antibody Picoband®<b> Western blot analysis of HCN2 using anti-HCN2 antibody (A02804). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: mouse brain tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HCN2 antigen affinity purified polyclonal antibody (Catalog # A02804) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HCN2 at approximately 97KD. The expected band size for HCN2 is at 97KD.
https://www.bosterbio.com/products/primary-antibodies/anti-plaur-picoband-trade-antibody-a00993-1-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00993-1-1-WB-anti-plaur-upar-picoband-antibody.jpgAnti-uPA Receptor/PLAUR Antibody Picoband®<b> Western blot analysis of PLAUR using anti-PLAUR antibody (A00993-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HELA whole Cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLAUR antigen affinity purified polyclonal antibody (Catalog # A00993-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLAUR at approximately 39KD, 55KD. The expected band size for PLAUR is at 37KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cyclophilin-a-picoband-trade-antibody-a01308-boster.html2026-03-24T05:09:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin-a-primary-antibodies-wb-testing-1.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® Western blot analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human MOLT-4 whole cell lysates, <br>
Lane 4: human Daudi whole cell lysates, <br>
Lane 5: rat lung tissue lysates, <br>
Lane 6: rat brain tissue lysates, <br>
Lane 7: mouse lung tissue lysates, <br>
Lane 8: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclophilin A antigen affinity purified polyclonal antibody (Catalog # A01308) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclophilin A at approximately 185 kDa. The expected band size for Cyclophilin A is at 185 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01308-2-IHC-anti-cyclophilin-a-picoband-antibody.jpgAnti-Cyclophilin A/PPIA Antibody Picoband®<b> IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308).</b><br>
Cyclophilin A was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01308-3-IHC-anti-cyclophilin-a-picoband-antibody.jpgAnti-Cyclophilin A/PPIA Antibody Picoband®<b> IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308).</b><br>
Cyclophilin A was detected in paraffin-embedded section of rat spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01308-4-IHC-anti-cyclophilin-a-picoband-antibody.jpgAnti-Cyclophilin A/PPIA Antibody Picoband®<b> IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308).</b><br>
Cyclophilin A was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-ppia-primary-antibodies-fc-testing-5.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PPIA antibody (A01308).<br>Overlay histogram showing THP-1 cells stained with A01308 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPIA Antibody (A01308,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-ppia-primary-antibodies-fc-testing-6.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-PPIA antibody (A01308).<br>Overlay histogram showing U937 cells stained with A01308 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPIA Antibody (A01308,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-ppia-primary-antibodies-fc-testing-7.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PPIA antibody (A01308).<br>Overlay histogram showing K562 cells stained with A01308 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPIA Antibody (A01308,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin_a-primary-antibodies-icc-testing-8.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br> Cyclophilin A was detected in immunocytochemical section of THP-1 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin_a-primary-antibodies-icc-testing-9.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br> Cyclophilin A was detected in immunocytochemical section of THP-1 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin_a-primary-antibodies-icc-testing-10.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br> Cyclophilin A was detected in immunocytochemical section of THP-1 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin_a-primary-antibodies-icc-testing-11.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® IHC analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br> Cyclophilin A was detected in immunocytochemical section of THP-1 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/ml rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was developed using DyLight®488 Conjugated Avidin (BA1128). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01308-cyclophilin_a-primary-antibodies-if-testing-12.jpg.jpgAnti-Cyclophilin A/PPIA Antibody Picoband® IF analysis of Cyclophilin A using anti-Cyclophilin A antibody (A01308). <br> Cyclophilin A was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Cyclophilin A Antibody (A01308) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-connexin-45-gja7-picoband-trade-antibody-a08562-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08562-4-IHC-anti-connexin-45-gja7-picoband-antibody.jpgAnti-Connexin 45/GJA7/GJC1 Antibody Picoband®<b> IHC analysis of Connexin 45/GJA7 using anti-Connexin 45/GJA7 antibody (A08562).</b><br>
Connexin 45/GJA7 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Connexin 45/GJA7 Antibody (A08562) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08562-3-IHC-anti-connexin-45-gja7-picoband-antibody.jpgAnti-Connexin 45/GJA7/GJC1 Antibody Picoband®<b> IHC analysis of Connexin 45/GJA7 using anti-Connexin 45/GJA7 antibody (A08562).</b><br>
Connexin 45/GJA7 was detected in paraffin-embedded section of rat skeletal muscle tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Connexin 45/GJA7 Antibody (A08562) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08562-2-IHC-anti-connexin-45-gja7-picoband-antibody.jpgAnti-Connexin 45/GJA7/GJC1 Antibody Picoband®<b> IHC analysis of Connexin 45/GJA7 using anti-Connexin 45/GJA7 antibody (A08562).</b><br>
Connexin 45/GJA7 was detected in paraffin-embedded section of mouse cardiac muscle tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Connexin 45/GJA7 Antibody (A08562) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a08562-5-IHC-anti-connexin-45-gja7-picoband-antibody.jpgAnti-Connexin 45/GJA7/GJC1 Antibody Picoband®<b> IHC analysis of Connexin 45/GJA7 using anti-Connexin 45/GJA7 antibody (A08562).</b><br>
Connexin 45/GJA7 was detected in paraffin-embedded section of human placneta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Connexin 45/GJA7 Antibody (A08562) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08562-1_1.jpgAnti-Connexin 45/GJA7/GJC1 Antibody Picoband® Western blot analysis of Connexin 45/GJA7 using anti-Connexin 45/GJA7 antibody (A08562). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Connexin 45/GJA7 antigen affinity purified polyclonal antibody (Catalog # A08562) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Connexin 45/GJA7 at approximately 45KD. The expected band size for Connexin 45/GJA7 is at 45KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cpi17-alpha-picoband-trade-antibody-a05752-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05752-1-2-IHC-anti-cpi17-alpha-picoband-antibody.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband®<b> IHC analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1).</b><br>
CPI17 alpha was detected in paraffin-embedded section of mouse testis tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05752-1-1_1.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband® Western blot analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates, <br>Lane 2: mouse brain tissue lysates, <br>Lane 3: PANC-1 whole Cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CPI17 alpha antigen affinity purified polyclonal antibody (Catalog # A05752-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CPI17 alpha at approximately 20KD. The expected band size for CPI17 alpha is at 20KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05752-1-3-IHC-anti-cpi17-alpha-picoband-antibody.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband®<b> IHC analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1).</b><br>
CPI17 alpha was detected in paraffin-embedded section of rat lung tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05752-1-4-IHC-anti-cpi17-alpha-picoband-antibody.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband®<b> IHC analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1).</b><br>
CPI17 alpha was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05752-1-5-IHC-anti-cpi17-alpha-picoband-antibody.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband®<b> IHC analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1).</b><br>
CPI17 alpha was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05752-1-6-IHC-anti-cpi17-alpha-picoband-antibody.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband®<b> IHC analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1).</b><br>
CPI17 alpha was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05752-1-cpi17_alpha-primary-antibodies-fc-testing-7.jpg.pngAnti-CPI17 alpha/PPP1R14A Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-CPI17 alpha antibody (A05752-1). <br> Overlay histogram showing U20S cells stained with A05752-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CPI17 alpha Antibody (A05752-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05752-1-cpi17_alpha-primary-antibodies-if-testing-8.jpgAnti-CPI17 alpha/PPP1R14A Antibody Picoband® IF analysis of CPI17 alpha using anti-CPI17 alpha antibody (A05752-1). <br>
CPI17 alpha was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-CPI17 alpha Antibody (A05752-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-bag1-picoband-trade-antibody-a02423-2-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-wb-testing-1.jpgAnti-Bag1 Antibody Picoband® Western blot analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bag1 antigen affinity purified polyclonal antibody (Catalog # A02423-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bag1 at approximately 33, 46, 56 kDa. The expected band size for Bag1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-ihc-testing-2.jpgAnti-Bag1 Antibody Picoband® IHC analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Bag1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bag1 Antibody (A02423-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-ihc-testing-3.jpgAnti-Bag1 Antibody Picoband® IHC analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Bag1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bag1 Antibody (A02423-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-ihc-testing-4.jpgAnti-Bag1 Antibody Picoband® IHC analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Bag1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bag1 Antibody (A02423-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-ihc-testing-5.jpgAnti-Bag1 Antibody Picoband® IHC analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Bag1 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bag1 Antibody (A02423-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02423-2-bag1-primary-antibodies-ihc-testing-6.jpgAnti-Bag1 Antibody Picoband® IHC analysis of Bag1 using anti-Bag1 antibody (A02423-2). <br>
Bag1 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bag1 Antibody (A02423-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ptger4-picoband-trade-antibody-a02153-2-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02153-2-ptger4-primary-antibodies-wb-testing-1.jpgAnti-Prostaglandin E Receptor EP4/PTGER4 Antibody Picoband®Western blot analysis of PTGER4 using anti-PTGER4 antibody (A02153-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTGER4 antigen affinity purified polyclonal antibody (Catalog # A02153-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PTGER4 at approximately 53 kDa. The expected band size for PTGER4 is at 53 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-hdac4-picoband-trade-antibody-a00971-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-hdac4-primary-antibody-wb-testing-1.jpgAnti-HDAC4 Antibody Picoband® Western blot analysis of HDAC4 using anti-HDAC4 antibody (A00971-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: human HEK293 whole cell lysates, <br>
Lane 2: human HELA whole cell lysates, <br>
Lane 3: human THP-1 whole cell lysates, <br>
Lane 4: human HEPG2 whole cell lysates, <br>
Lane 5: human U87 whole cell lysates, <br>
Lane 6: rat testis tissue lysates, <br>
Lane 7: mouse testis tissue lysates, <br>
Lane 8: mouse NIH/3T3 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDAC4 antigen affinity purified polyclonal antibody (Catalog # A00971-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDAC4 at approximately 140KD. The expected band size for HDAC4 is at 119KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-2.pngAnti-HDAC4 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-HDAC4 antibody (A00971-1). <br> Overlay histogram showing THP-1 cells stained with A00971-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDAC4 Antibody (A00971-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-3.pngAnti-HDAC4 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-HDAC4 antibody (A00971-1). <br> Overlay histogram showing SiHa cells stained with A00971-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDAC4 Antibody (A00971-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-hdac4-primary-antibody-ihc-testing-4.jpgAnti-HDAC4 Antibody Picoband® IHC analysis of HDAC4 using anti-HDAC4 antibody (A00971-1). <br>
HDAC4 was detected in paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-HDAC4 Antibody (A00971-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-hdac4-primary-antibody-ihc-testing-5.jpgAnti-HDAC4 Antibody Picoband® IHC analysis of HDAC4 using anti-HDAC4 antibody (A00971-1). <br>
HDAC4 was detected in paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-HDAC4 Antibody (A00971-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00971-1-hdac4-primary-antibody-if-testing-6.jpgAnti-HDAC4 Antibody Picoband® IF analysis of HDAC4 using anti-HDAC4 antibody (A00971-1). <br>
HDAC4 was detected in immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-HDAC4 Antibody (A00971-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-ranbp1-picoband-trade-antibody-a04000-2-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04000-2-ranbp1-primary-antibodies-wb-testing-1.jpgAnti-RanBP1 Antibody Picoband® Western blot analysis of RanBP1 using anti-RanBP1 antibody (A04000-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates, <br>
Lane 2: human HEK293 whole cell lysates, <br>
Lane 3: human HL-60 whole cell lysates, <br>
Lane 4: human U20S whole cell lysates, <br>
Lane 5: human A431 whole cell lysates, <br>
Lane 6: human HEPG2 whole cell lysates, <br>
Lane 7: human U937 whole cell lysates, <br>
Lane 8: rat testis tissue lysates, <br>
Lane 9: rat C6 whole cell lysates, <br>
Lane 10: mouse testis tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RanBP1 antigen affinity purified polyclonal antibody (Catalog # A04000-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RanBP1 at approximately 27KD. The expected band size for RanBP1 is at 23KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04000-2-2-IHC-anti-ranbp1-picoband-antibody.jpgAnti-RanBP1 Antibody Picoband® IHC analysis of RanBP1 using anti-RanBP1 antibody (A04000-2).</b><br>
RanBP1 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RanBP1 Antibody (A04000-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04000-2-3-IHC-anti-ranbp1-picoband-antibody.jpgAnti-RanBP1 Antibody Picoband® IHC analysis of RanBP1 using anti-RanBP1 antibody (A04000-2).</b><br>
RanBP1 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RanBP1 Antibody (A04000-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04000-2-4-IHC-anti-ranbp1-picoband-antibody.jpgAnti-RanBP1 Antibody Picoband® IHC analysis of RanBP1 using anti-RanBP1 antibody (A04000-2).</b><br>
RanBP1 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RanBP1 Antibody (A04000-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04000-2-5-IHC-anti-ranbp1-picoband-antibody.jpgAnti-RanBP1 Antibody Picoband® IHC analysis of RanBP1 using anti-RanBP1 antibody (A04000-2).</b><br>
RanBP1 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RanBP1 Antibody (A04000-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04000-2-6.jpgAnti-RanBP1 Antibody Picoband® IF analysis of RanBP1 using anti-RanBP1 antibody (A04000-2). <br>
RanBP1 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-RanBP1 Antibody (A04000-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04000-2-7.jpgAnti-RanBP1 Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-RanBP1 antibody (A04000-2). <br>Overlay histogram showing U937 cells stained with A04000-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RanBP1 Antibody (A04000-2, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-hfe-picoband-trade-antibody-a00506-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00506-1-1_1-WB-anti-hfe-picoband-antibody.jpgAnti-HFE Antibody Picoband®<b> Western blot analysis of HFE using anti-HFE antibody (A00506-1).</b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HELA whole Cell lysates, <br>
Lane 2: HEPG2 whole Cell lysates, <br>
Lane 3: A431 whole Cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HFE antigen affinity purified polyclonal antibody (Catalog # A00506-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HFE at approximately 40KD. The expected band size for HFE is at 40KD.
https://www.bosterbio.com/products/primary-antibodies/anti-rps6-picoband-trade-antibody-a01567-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01567-1-1-WB-anti-rps6-ribosomal-protein-s6-picoband-antibody.jpgAnti-RPS6 Antibody Picoband®<b> Western blot analysis of RPS6 using anti-RPS6 antibody (A01567-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat testis tissue lysates, <br>
Lane 2: mouse testis tissue lysates, <br>
Lane 3: MCF-7 whole Cell lysates, <br>
Lane 4: A549 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS6 antigen affinity purified polyclonal antibody (Catalog # A01567-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPS6 at approximately 32KD. The expected band size for RPS6 is at 29KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01567-1-2-IHC-anti-rps6-ribosomal-protein-s6-picoband-antibody.jpgAnti-RPS6 Antibody Picoband®<b> IHC analysis of RPS6 using anti-RPS6 antibody (A01567-1).</b><br>
RPS6 was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RPS6 Antibody (A01567-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01567-1-4-IHC-anti-rps6-ribosomal-protein-s6-picoband-antibody.jpgAnti-RPS6 Antibody Picoband®<b> IHC analysis of RPS6 using anti-RPS6 antibody (A01567-1).</b><br>
RPS6 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RPS6 Antibody (A01567-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01567-1-5-IHC-anti-rps6-ribosomal-protein-s6-picoband-antibody.jpgAnti-RPS6 Antibody Picoband®<b> IHC analysis of RPS6 using anti-RPS6 antibody (A01567-1).</b><br>
RPS6 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RPS6 Antibody (A01567-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01567-1-3-IHC-anti-rps6-ribosomal-protein-s6-picoband-antibody.jpgAnti-RPS6 Antibody Picoband®<b> IHC analysis of RPS6 using anti-RPS6 antibody (A01567-1).</b><br>
RPS6 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RPS6 Antibody (A01567-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ptgs2-picoband-trade-antibody-a00084-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00084-fphar-14-1181133-g006.jpgAnti-COX2/Cyclooxygenase 2/PTGS2 Antibody Picoband®The pretreatment of RD-6 inhibited the IL-17 signaling pathway in indomethacin-induced GU rats. The expression of IL17RA, FOS, IL1B, and PTGS2 determined in gastric tissue by qRT-PCR (A) and western bloting (B) . Data are expressed as mean ± S.E.M ( n = 3). One-way ANOVA with the uncorrected Fisher’s LSD test was used to evaluate multiple comparisons. # p < 0.05, ## p < 0.01 vs. NC group; * p < 0.05, ** p < 0.01 vs. IND group. NC, normal control; IND, indomethacin; RD-6-L, M, and H represent Ruda-6 at low, medium and high doses, respectively.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10449537/&orig_host=www.ncbi.nlm.nih.gov'>37637418</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00084-cox2-primary-antibodies-wb-testing-1.jpgAnti-COX2/Cyclooxygenase 2/PTGS2 Antibody Picoband® Western blot analysis of PTGS2 using anti-PTGS2 antibody (A00084). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: human U87 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTGS2 antigen affinity purified polyclonal antibody (Catalog # A00084) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTGS2 at approximately 75 kDa. The expected band size for PTGS2 is at 69 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bag5-picoband-trade-antibody-a07402-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07402-bag5-primary-antibodies-wb-testing-1_1.jpgAnti-Bag5 Antibody Picoband® Western blot analysis of Bag5 using anti-Bag5 antibody (A07402). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates, <br>
Lane 2: human U-87 whole cell lysates, <br>
Lane 3: human Hela whole cell lysates, <br>
Lane 4: human K562 whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat stomach tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse stomach tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bag5 antigen affinity purified polyclonal antibody (Catalog # A07402) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bag5 at approximately 51 kDa. The expected band size for Bag5 is at 51 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07402-bag5-primary-antibodies-fcm-testing-3.pngAnti-Bag5 Antibody Picoband® Flow Cytometry analysis of HL-60 cells using anti-Bag5 antibody (A07402). <br>Overlay histogram showing HL-60 cells stained with A07402 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Bag5 Antibody (A07402, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07402-bag5-primary-antibodies-if-testing-2_1.jpgAnti-Bag5 Antibody Picoband® IF analysis of Bag5 using anti-Bag5 antibody (A07402). <br>
Bag5 was detected in an immunocytochemical section of T-47D cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Bag5 Antibody (A07402) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-sparc-picoband-trade-antibody-a00862-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00862-1-sparc-primary-antibodies-wb-testing-1_1.jpgAnti-SPARC Antibody Picoband® Western blot analysis of SPARC using anti-SPARC antibody (A00862-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30ug of sample under reducing conditions. <br>
Lane 1: human HUVEC whole cell lysates, <br>
Lane 2: human placenta tissue lysates, <br>
Lane 3: human A375 whole cell lysates, <br>
Lane 4: human U20S whole cell lysates, <br>
Lane 5: human U87 whole cell lysates, <br>
Lane 6: rat testis tissue lysates, <br>
Lane 7: rat kidney tissue lysates, <br>
Lane 8: mouse testis tissue lysates, <br>
Lane 9: mouse kidney tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPARC antigen affinity purified polyclonal antibody (Catalog # A00862-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SPARC at approximately 35 kDa. The expected band size for SPARC is at 35 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00862-1-sparc-primary-antibodies-wb-testing-2.jpgAnti-SPARC Antibody Picoband®Western blot analysis of SPARC using anti-SPARC antibody (A00862-1).<br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: Zebrafish head tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPARC antigen affinity purified polyclonal antibody (A00862-1) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SPARC at approximately 35 kDa.The expected band size for SPARC is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-stat1-picoband-trade-antibody-a00036-2-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00036-2-stat1-primary-antibodies-wb-testing-1.jpgAnti-STAT1 Antibody Picoband® Western blot analysis of STAT1 using anti-STAT1 antibody (A00036-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: human Raji whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT1 antigen affinity purified polyclonal antibody (Catalog # A00036-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT1 at approximately 91 kDa. The expected band size for STAT1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00036-2-2-IHC-anti-stat1-picoband-antibody.jpgAnti-STAT1 Antibody Picoband® IHC analysis of STAT1 using anti-STAT1 antibody (A00036-2).<br>STAT1 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-STAT1 Antibody (A00036-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00036-2-3.jpgAnti-STAT1 Antibody Picoband® IF analysis of STAT1 using anti-STAT1 antibody (A00036-2) <br> STAT1 was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-STAT1 Antibody (A00036-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00036-2-4.jpgAnti-STAT1 Antibody Picoband® IF analysis of STAT1 using anti-STAT1 antibody (A00036-2) <br> STAT1 was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-STAT1 Antibody (A00036-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00036-2-5.pngAnti-STAT1 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-STAT1 antibody (A00036-2). <br> Overlay histogram showing A431 cells stained with A00036-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STAT1 Antibody (A00036-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-heparanase-1-picoband-trade-antibody-a01313-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01313-1_1.jpgAnti-Heparanase 1/Hpse Antibody Picoband®<b> Western blot analysis of Heparanase 1 using anti-Heparanase 1 antibody (A01313). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse spleen tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Heparanase 1 antigen affinity purified polyclonal antibody (Catalog # A01313) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Heparanase 1 at approximately 65KD. The expected band size for Heparanase 1 is at 61KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hsd17b4-picoband-trade-antibody-a02923-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02923-hsd17b4-primary-antibodies-wb-testing-1.jpgAnti-Hydroxysteroid (17-beta) Dehydrogenase 4/HSD17B4 Antibody Picoband® Western blot analysis of HSD17B4 using anti-HSD17B4 antibody (A02923). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates, <br>
Lane 2: rat liver tissue lysates, <br>
Lane 3: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSD17B4 antigen affinity purified polyclonal antibody (Catalog # A02923) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo
r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSD17B4 at approximately 80 kDa. The expected band size for HSD17B4 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02923-2-IHC-anti-hsd17b4-picoband-antibody.jpgAnti-Hydroxysteroid (17-beta) Dehydrogenase 4/HSD17B4 Antibody Picoband®<b> IHC analysis of HSD17B4 using anti-HSD17B4 antibody (A02923).</b><br>
HSD17B4 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSD17B4 Antibody (A02923) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02923-3-IHC-anti-hsd17b4-picoband-antibody.jpgAnti-Hydroxysteroid (17-beta) Dehydrogenase 4/HSD17B4 Antibody Picoband®<b> IHC analysis of HSD17B4 using anti-HSD17B4 antibody (A02923).</b><br>
HSD17B4 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSD17B4 Antibody (A02923) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02923-4-IHC-anti-hsd17b4-picoband-antibody.jpgAnti-Hydroxysteroid (17-beta) Dehydrogenase 4/HSD17B4 Antibody Picoband®<b> IHC analysis of HSD17B4 using anti-HSD17B4 antibody (A02923).</b><br>
HSD17B4 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSD17B4 Antibody (A02923) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tfpi-picoband-trade-antibody-a01052-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01052-1-WB-anti-tfpi-picoband-antibody.jpgAnti-TFPI Antibody Picoband®<b> Western blot analysis of TFPI using anti-TFPI antibody (A01052). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HELA whole Cell lysates, <br>
Lane 2: MCF-7 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFPI antigen affinity purified polyclonal antibody (Catalog # A01052) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFPI at approximately 45KD. The expected band size for TFPI is at 35KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tfpi2-picoband-trade-antibody-a03697-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03697-1-1-WB-anti-tfpi2-picoband-antibody.jpgAnti-TFPI2 Antibody Picoband®<b> Western blot analysis of TFPI2 using anti-TFPI2 antibody (A03697-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: mouse spleen tissue lysates, <br>
Lane 2: HELA whole Cell lysates, <br>
Lane 3: human placenta tissue lysates, <br>
Lane 4: MCF-7 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFPI2 antigen affinity purified polyclonal antibody (Catalog # A03697-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFPI2 at approximately 27KD, 35KD. The expected band size for TFPI2 is at 27KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03697-1-2-IHC-anti-tfpi2-picoband-antibody.jpgAnti-TFPI2 Antibody Picoband®<b> IHC analysis of TFPI2 using anti-TFPI2 antibody (A03697-1).</b><br>
TFPI2 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TFPI2 Antibody (A03697-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03697-1-3.pngAnti-TFPI2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-TFPI2 antibody (A03697-1). <br> Overlay histogram showing U87 cells stained with A03697-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TFPI2 Antibody (A03697-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03697-1-4.pngAnti-TFPI2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-TFPI2 antibody (A03697-1). <br> Overlay histogram showing A549 cells stained with A03697-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TFPI2 Antibody (A03697-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-hspb8-hsp22-picoband-trade-antibody-a02492-2-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02492-2-hspb8-primary-antibodies-wb-testing-1_1.jpgAnti-HSPB8/Hsp22 Antibody Picoband® Western blot analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: rat H9C2 whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: mouse C2C12 whole cell lysates,<br>
Lane 6: mouse skeletal muscle tissue lysates,<br>
Lane 7: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPB8/Hsp22 antigen affinity purified polyclonal antibody (Catalog # A02492-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPB8/Hsp22 at approximately 22 kDa. The expected band size for HSPB8/Hsp22 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02492-2-2-IHC-anti-hspb8-hsp22-picoband-antibody.jpgAnti-HSPB8/Hsp22 Antibody Picoband®<b> IHC analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2).</b><br>
HSPB8/Hsp22 was detected in paraffin-embedded section of mouse pancreas tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSPB8/Hsp22 Antibody (A02492-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02492-2-3-IHC-anti-hspb8-hsp22-picoband-antibody.jpgAnti-HSPB8/Hsp22 Antibody Picoband®<b> IHC analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2).</b><br>
HSPB8/Hsp22 was detected in paraffin-embedded section of rat pancreas tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSPB8/Hsp22 Antibody (A02492-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02492-2-4-IHC-anti-hspb8-hsp22-picoband-antibody.jpgAnti-HSPB8/Hsp22 Antibody Picoband®<b> IHC analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2).</b><br>
HSPB8/Hsp22 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSPB8/Hsp22 Antibody (A02492-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a02492-2-5-IHC-anti-hspb8-hsp22-picoband-antibody.jpgAnti-HSPB8/Hsp22 Antibody Picoband®<b> IHC analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2).</b><br>
HSPB8/Hsp22 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HSPB8/Hsp22 Antibody (A02492-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02492-2-6.jpgAnti-HSPB8/Hsp22 Antibody Picoband® IF analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2). <br>
HSPB8/Hsp22 was detected in immunocytochemical section of MCF7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HSPB8/Hsp22 Antibody (A02492-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02492-2-hspb8-primary-antibodies-fcm-testing-7.jpgAnti-HSPB8/Hsp22 Antibody Picoband® Flow Cytometry analysis of U2OS cells using anti-HSPB8/Hsp22 antibody (A02492-2). <br>
Overlay histogram showing U2OS cells stained with A02492-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPB8/Hsp22 Antibody (A02492-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02492-2-hspb8-primary-antibodies-ip-testing-8.jpgAnti-HSPB8/Hsp22 Antibody Picoband® Immunoprecipitating HSPB8/Hsp22 in MCF-7 whole cell lysate.<br>
Western blot analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (A02492-2); <br>
Lane 1: MCF-7 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-HSPB8/Hsp22 antibody in MCF-7 whole cell lysate;<br>
Lane 3: anti-HSPB8/Hsp22 antibody (2μg) + MCF-7 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSPB8/Hsp22 antigen affinity purified polyclonal antibody (A02492-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for HSPB8/Hsp22 at approximately 22 kDa. The expected band size for HSPB8/Hsp22 is at 22 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-htra3-picoband-trade-antibody-a05478-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05478-1-WB-anti-htra3-picoband-antibody.jpgAnti-HtrA3 Antibody Picoband®<b> Western blot analysis of HtrA3 using anti-HtrA3 antibody (A05478). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: PANC-1 whole Cell lysates, <br>
Lane 2: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HtrA3 antigen affinity purified polyclonal antibody (Catalog # A05478) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HtrA3 at approximately 49KD. The expected band size for HtrA3 is at 49KD.
https://www.bosterbio.com/products/primary-antibodies/anti-survivin-picoband-trade-antibody-a00379-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00379-survivin-primary-antibodies-wb-testing-1.jpgAnti-Survivin/BIRC5 Antibody Picoband® Western blot analysis of Survivin using anti-Survivin antibody (A00379). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Survivin antigen affinity purified polyclonal antibody (Catalog # A00379) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Survivin at approximately 16 kDa. The expected band size for Survivin is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00379-survivin-primary-antibodies-ihc-testing-2.jpgAnti-Survivin/BIRC5 Antibody Picoband® IHC analysis of Survivin using anti-Survivin antibody (A00379). <br>
Survivin was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Survivin Antibody (A00379) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00379-survivin-primary-antibodies-ihc-testing-3.jpgAnti-Survivin/BIRC5 Antibody Picoband® IHC analysis of Survivin using anti-Survivin antibody (A00379). <br>
Survivin was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Survivin Antibody (A00379) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-thrombospondin-picoband-trade-antibody-a00667-1-boster.html2026-03-24T05:10:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00667-1-1_1.jpgAnti-Thrombospondin/THBS1 Antibody Picoband® Western blot analysis of Thrombospondin using anti-Thrombospondin antibody (A00667-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates, <br>Lane 2: mouse liver tissue lysates, <br>Lane 3: HELA whole Cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Thrombospondin antigen affinity purified polyclonal antibody (Catalog # A00667-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Thrombospondin at approximately 165KD, 180KD. The expected band size for Thrombospondin is at 130KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00667-1-41420_2024_1837_fig3_html.pngAnti-Thrombospondin/THBS1 Antibody Picoband®Sub-FS may increase TSP-1/TGF-β1, excitatory synapse and glutamate levels. A – C Gray bands and normalized gray values of TSP-1 and TGF-β1 relative to GAPDH at 3 days (n = 4/group). D – H Gray bands and normalized gray values of PSD-95, Synapsin I and VGLUT1 relative to GAPDH at 3 days ( n = 4/group). I , J Number of positive PSD-95 signals and representative immunohistochemical results of PSD-95 (green) in EC at 3 days (scale bar = 5 μm, n = 4/group). Blue, DAPI. K – N Immunohistochemical results of VGLUT1 (green) and CAMKII (red) in EC at 3 days (scale bar = 10 μm, n = 4/group). Blue, DAPI. O Content of glutamate ( n = 6/group) in EC and CA3 and ( P ) ratio of normalized power spectra intensity of beta waves ( n = 5/group) at 3 days. Mean ± SEMs were presented. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group (One-way ANOVA). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-024-01837-3'>38346981</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00667-1-41420_2024_1837_fig4_html.pngAnti-Thrombospondin/THBS1 Antibody Picoband®Reduced TSP-1 expression decreases susceptibility and neuronal injury induced by sub-FS stimuli and alleviates neuronal damage induced by subsequent FS stimuli. A Experimental design. B Threshold dosages of PTZ at P14 ( n = 6/group). C Threshold body temperature for induction of febrile seizures at P9 ( n = 8/group). D , E Analysis and representative images of FJB staining at 3 days after 41°C stimulus (scale bar = 50 μm). F – H Gray bands and normalized gray values of cleaved caspase-3 and caspase-3 relative to GAPDH at 3 days after 41°C stimulus. I , J Representative images (scale bar = 50 μm) and number of positive signals of FJB staining at 3 days after FS stimuli. K – M Gray bands and quantitative analysis of cleaved caspase-3 and caspase-3 at 3 days after FS stimuli. D – M n = 4/group. Mean ± SEMs were presented. * P < 0.05, ** P < 0.01, ***P < 0.001 vs siRNA-NC group (Unpaired T-test). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-024-01837-3'>38346981</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00667-1-41420_2024_1837_fig5_html.pngAnti-Thrombospondin/THBS1 Antibody Picoband®Reduced TSP-1 expression decreases excitatory synapse and glutamate levels. Gray bands and normalized gray values of TSP-1/TGF-β1 ( A – C ), PSD-95/synapsin I ( D – F ) and VGLUT1 ( G , H ) at 24 hours and 3 days ( n = 4/group). The immunohistochemistry results of PSD-95 (green, scale bar = 3 μm, I , J ), VGLUT1 (green, scale bar = 10 μm, K , L ) and CAMKII (red, scale bar = 10 μm, M , N ) in EC. I – N n = 4/group, Blue, DAPI. O Ratio of normalized power spectra intensity of beta waves ( n = 5/group) and ( P ) glutamate content ( n = 6/group). Mean ± SEMs were presented. * P < 0.05, ** P < 0.01, *** P < 0.001 vs siRNA-NC group (Unpaired T-test). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-024-01837-3'>38346981</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00667-1-41420_2024_1837_fig7_html.pngAnti-Thrombospondin/THBS1 Antibody Picoband®LSKL administration decreases excitatory synapse and glutamate levels. Gray bands and normalized gray values of TSP-1/TGF-β1 ( A – C ), PSD-95/synapsin I ( D – F ) and VGLUT1 ( G , H ) at 24 hours and 3 days ( n = 4/group). I , J Number of positive PSD-95 signals and representative immunohistochemical results of PSD-95 (green) in EC at 3 days (scale bar = 3 μm, n = 4/group). K , L Immunohistochemistry results of VGLUT1 (green) in EC at 3 days (scale bar = 10 μm, n = 4/group). M , N Representative immunohistochemical results of CAMKII (red) in EC at 3 days (scale bar = 10 μm, n = 4/group). Blue, DAPI. O Ratio of normalized power spectra intensity of beta waves ( n = 5/group) and ( P ) content of glutamate ( n = 6/group) at 3 days. Mean ± SEMs were presented. * P < 0.05, ** P < 0.01, *** P < 0.001 vs saline groups (Unpaired T-test). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-024-01837-3'>38346981</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-id2-picoband-trade-antibody-a00417-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00417-1-1_1.jpgAnti-ID2 Antibody Picoband® Western blot analysis of ID2 using anti-ID2 antibody (A00417-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ID2 antigen affinity purified polyclonal antibody (Catalog # A00417-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ID2 at approximately 15KD. The expected band size for ID2 is at 15KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ifngr1-picoband-trade-antibody-a01716-2-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01716-2-1-WB-anti-ifngr1-cd119-picoband-antibody.jpgAnti-IFNGR1 Antibody Picoband®<b> Western blot analysis of IFNGR1 using anti-IFNGR1 antibody (A01716-2). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HEPG2 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFNGR1 antigen affinity purified polyclonal antibody (Catalog # A01716-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFNGR1 at approximately 95KD. The expected band size for IFNGR1 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01716-2-2.pngAnti-IFNGR1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-IFNGR1 antibody (A01716-2). <br> Overlay histogram showing SiHa cells stained with A01716-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFNGR1 Antibody (A01716-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-thrombopoietin-picoband-trade-antibody-a03222-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03222-1-4-IHC-anti-thrombopoietin-picoband-antibody.jpgAnti-Thrombopoietin/Thpo Antibody Picoband®<b> IHC analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1).</b><br>
Thrombopoietin was detected in paraffin-embedded section of mouse kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Thrombopoietin Antibody (A03222-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03222-1-3-IHC-anti-thrombopoietin-picoband-antibody.jpgAnti-Thrombopoietin/Thpo Antibody Picoband®<b> IHC analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1).</b><br>
Thrombopoietin was detected in paraffin-embedded section of mouse spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Thrombopoietin Antibody (A03222-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03222-1-6-IHC-anti-thrombopoietin-picoband-antibody.jpgAnti-Thrombopoietin/Thpo Antibody Picoband®<b> IHC analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1).</b><br>
Thrombopoietin was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Thrombopoietin Antibody (A03222-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03222-1-2-IHC-anti-thrombopoietin-picoband-antibody.jpgAnti-Thrombopoietin/Thpo Antibody Picoband®<b> IHC analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1).</b><br>
Thrombopoietin was detected in paraffin-embedded section of mouse liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Thrombopoietin Antibody (A03222-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a03222-1-5-IHC-anti-thrombopoietin-picoband-antibody.jpgAnti-Thrombopoietin/Thpo Antibody Picoband®<b> IHC analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1).</b><br>
Thrombopoietin was detected in paraffin-embedded section of rat spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Thrombopoietin Antibody (A03222-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03222-1-1_1.jpgAnti-Thrombopoietin/Thpo Antibody Picoband® Western blot analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse liver tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Thrombopoietin antigen affinity purified polyclonal antibody (Catalog # A03222-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Thrombopoietin at approximately 38KD. The expected band size for Thrombopoietin is at 38KD.
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp1-picoband-trade-antibody-a00922-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00922-igfbp1-primary-antibodies-wb-testing-1.jpgAnti-IGFBP1 Antibody Picoband® Western blot analysis of IGFBP1 using anti-IGFBP1 antibody (A00922). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP1 antigen affinity purified polyclonal antibody (Catalog # A00922) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP1 at approximately 30 kDa. The expected band size for IGFBP1 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00922-igfbp1-primary-antibodies-ihc-testing-2.jpgAnti-IGFBP1 Antibody Picoband® IHC analysis of IGFBP1 using anti-IGFBP1 antibody (A00922). <br>
IGFBP1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGFBP1 Antibody (A00922) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd90-thy1-picoband-trade-antibody-a01818-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01818-thy1-primary-antibodies-wb-testing-1_1.jpgAnti-CD90/Thy1 Antibody Picoband® Western blot analysis of CD90/Thy1 using anti-CD90/Thy1 antibody (A01818). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: rai thymus tissue lysates, <br>
Lane 3: mouse brain tissue lysates, <br>
Lane 4: mouse thymus tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD90/Thy1 antigen affinity purified polyclonal antibody (Catalog # A01818) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD90/Thy1 at approximately 22 kDa. The expected band size for CD90/Thy1 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01818-thy1-primary-antibodies-ihc-testing-2_1.jpgAnti-CD90/Thy1 Antibody Picoband® IHC analysis of CD90/Thy1 using anti-CD90/Thy1 antibody (A01818). <br>
CD90/Thy1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD90/Thy1 Antibody (A01818) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01818-thy1-primary-antibodies-ihc-testing-3.jpgAnti-CD90/Thy1 Antibody Picoband® IHC analysis of CD90/Thy1 using anti-CD90/Thy1 antibody (A01818). <br>
CD90/Thy1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD90/Thy1 Antibody (A01818) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01818-thy1-primary-antibodies-ihc-testing-4.jpgAnti-CD90/Thy1 Antibody Picoband® IHC analysis of CD90/Thy1 using anti-CD90/Thy1 antibody (A01818). <br>
CD90/Thy1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD90/Thy1 Antibody (A01818) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01818-thy1-primary-antibodies-if-testing-5.jpgAnti-CD90/Thy1 Antibody Picoband® IF analysis of CD90/Thy1 using anti-CD90/Thy1 antibody (A01818). <br>
CD90/Thy1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-CD90/Thy1 Antibody (A01818) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-il-2-picoband-trade-antibody-a00387-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-1-il-2-primary-antibodies-wb-testing-1.jpgAnti-IL-2/IL2 Antibody Picoband® Western blot analysis of IL-2 using anti-IL-2 antibody (A00387-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. <br>
Lane 1: recombinant human IL-2 protein 25 ng,<br>
Lane 2: recombinant human IL-2 protein 10 ng,<br>
Lane 3: recombinant human IL-2 protein 5 ng,<br>
Lane 4: recombinant human IL-2 protein 1 ng.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL-2 antigen affinity purified polyclonal antibody (A00387-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL-2 at approximately 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-1-il-2-primary-antibodies-ihc-testing-2.jpgAnti-IL-2/IL2 Antibody Picoband® IHC analysis of IL-2 using anti-IL-2 antibody (A00387-1). <br>
IL-2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL-2 Antibody (A00387-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-1-il-2-primary-antibodies-ihc-testing-3.jpgAnti-IL-2/IL2 Antibody Picoband® IHC analysis of IL-2 using anti-IL-2 antibody (A00387-1). <br>
IL-2 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL-2 Antibody (A00387-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-timp3-picoband-trade-antibody-a00477-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00477-1_1.jpgAnti-TIMP3 Antibody Picoband® Western blot analysis of TIMP3 using anti-TIMP3 antibody (A00477). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysates, <br>Lane 2: NIH3T3 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMP3 antigen affinity purified polyclonal antibody (Catalog # A00477) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TIMP3 at approximately 24KD. The expected band size for TIMP3 is at 24KD.
https://www.bosterbio.com/products/primary-antibodies/anti-timp4-picoband-trade-antibody-a07131-boster.html2026-04-01T05:01:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a07131-2-IHC-anti-timp4-picoband-antibody.jpgAnti-TIMP4 Antibody Picoband®<b> IHC analysis of TIMP4 using anti-TIMP4 antibody (A07131).</b><br>
TIMP4 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TIMP4 Antibody (A07131) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07131-1_1.jpgAnti-TIMP4 Antibody Picoband® Western blot analysis of TIMP4 using anti-TIMP4 antibody (A07131). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates, <br>Lane 2: mouse heart tissue lysates, <br>Lane 3: HELA whole Cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMP4 antigen affinity purified polyclonal antibody (Catalog # A07131) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TIMP4 at approximately 25KD. The expected band size for TIMP4 is at 25KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a07131-3-IHC-anti-timp4-picoband-antibody.jpgAnti-TIMP4 Antibody Picoband®<b> IHC analysis of TIMP4 using anti-TIMP4 antibody (A07131).</b><br>
TIMP4 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TIMP4 Antibody (A07131) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a07131-4-IHC-anti-timp4-picoband-antibody.jpgAnti-TIMP4 Antibody Picoband®<b> IHC analysis of TIMP4 using anti-TIMP4 antibody (A07131).</b><br>
TIMP4 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TIMP4 Antibody (A07131) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07131-5.pngAnti-TIMP4 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-TIMP4 antibody (A07131). <br> Overlay histogram showing A549 cells stained with A07131 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TIMP4 Antibody (A07131,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07131-6.jpgAnti-TIMP4 Antibody Picoband® IF analysis of TIMP4 using anti-TIMP4 antibody (A07131). <br>
TIMP4 was detected in immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-TIMP4 Antibody (A07131) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-tlr2-picoband-trade-antibody-a00131-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00131-fncel-11-00099-g004.jpgAnti-TLR2 Antibody Picoband®Effect of Prdx6-iPLA2 on Toll-like receptor 2 (TLR2) and TLR4 expression in microglia in response to OGD/R. TLR2 and TLR4 were activated during OGD/R exposure. Prdx6-iPLA2 siRNA or MJ33 treatment could inhibit TLR2 and TLR4 mRNA (A,B) and protein expression (C–E) . Results are expressed as the mean ± SEM of three independent experiments. ** p < 0.01 vs. Control; # p < 0.05 vs. Scramble; ## p < 0.01 vs. Scramble.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2017.00099/full'>28424593</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00131-fncel-11-00099-g009.jpgAnti-TLR2 Antibody Picoband®Expression of TLR2 and TLR4 in response to Prdx6 siRNA and MJ33. Real-time PCR showed that TLR2 (A) and TLR4 (B) expression increased after MCAO or giving Prdx6-siRNA. Combined treatment with Prdx6-siRNA and MJ33 downregulated TLR2 and TLR4 levels. Representative Western blot (C) and semi-quantitative analyses of the levels of TLR2 (D) and TLR4 (E) in the cortex after MCAO. Results are expressed as the mean ± SEM of three independent experiments. & p < 0.01 vs. Sham; ** p < 0.01 vs. Scramble; # p < 0.05, vs. Prdx6 siRNA; ## p < 0.01 vs. Prdx6 siRNA.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2017.00099/full'>28424593</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00131-12985_2012_article_2038_fig5_html.jpgAnti-TLR2 Antibody Picoband®Expression of TLR2 in splenocytes of different vaccinated groups on day 2 after infection with S . aureus . (A) Western blot detection of TLR2 in splenocytes. Lane A: PBS group; lane B pEGFP-C2 group; lane C pEGFP /HA2 group; lane D pEGFP/Ag85A group; lane E pEGFP/Ag85A-HA2 group; lane F iPR group. (B) RT-PCR detection of TLR2 in splenocytes. Lanes 1, 8: pEGFP/Ag85A-HA2 group; lanes 2, 9: pEGFP-C2 group; lanes 3, 10: pEGFP /HA2 group; lanes 4, 11: pEGFP/Ag85A group; lanes 5, 12: PBS group; lanes 7, 13: iPR group. Lanes 1–5, 7: TLR2 (410 bp); lanes 8–13: GADPH (531 bp); lanes 6, 14: marker. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1743-422X-10-40'>23369570</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00131-tlr2-primary-antibodies-wb-testing-1.jpgAnti-TLR2 Antibody Picoband® Western blot analysis of TLR2 using anti-TLR2 antibody (A00131). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 (-LPS) whole cell lysates, <br>
Lane 2: human THP-1 (+LPS) whole cell lysates, <br>
Lane 3: human Hacat whole cell lysates, <br>
Lane 4: human PC-3 whole cell lysates, <br>
Lane 5: human Caco-2 whole cell lysates, <br>
Lane 6: human HepG2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TLR2 antigen affinity purified polyclonal antibody (A00131) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TLR2 at approximately 105 kDa. The expected band size for TLR2 is at 90 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-tmem107-picoband-trade-antibody-a04966-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04966-1_1.jpgAnti-TMEM107 Antibody Picoband® Western blot analysis of TMEM107 using anti-TMEM107 antibody (A04966). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: MCF-7 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMEM107 antigen affinity purified polyclonal antibody (Catalog # A04966) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TMEM107 at approximately 22KD. The expected band size for TMEM107 is at 16KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04966-2-IHC-anti-tmem107-picoband-antibody.jpgAnti-TMEM107 Antibody Picoband®<b> IHC analysis of TMEM107 using anti-TMEM107 antibody (A04966).</b><br>
TMEM107 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TMEM107 Antibody (A04966) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a04966-3-IHC-anti-tmem107-picoband-antibody.jpgAnti-TMEM107 Antibody Picoband®<b> IHC analysis of TMEM107 using anti-TMEM107 antibody (A04966).</b><br>
TMEM107 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TMEM107 Antibody (A04966) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04966-tmem107-primary-antibodies-fcm-testing-4_1.jpgAnti-TMEM107 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-TMEM107 antibody (A04966). <br>
Overlay histogram showing A431 cells stained with A04966 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TMEM107 Antibody (A04966, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-tnfrsf1a-picoband-trade-antibody-a00294-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00294-tnfrsf1a-primary-antibodies-wb-testing-1.jpgAnti-TNFRSF1A Antibody Picoband®Western blot analysis of TNFRSF1A using anti-TNFRSF1A antibody (A00294). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Raji whole cell lysates.<br>
Lane 4: rat brain tissue lysates.<br>
Lane 5: rat lung tissue lysates.<br>
Lane 6: mouse brain tissue lysates.<br>
Lane 7: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNFRSF1A antigen affinity purified polyclonal antibody (A00294) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TNFRSF1A at approximately 55-60 kDa. The expected band size for TNFRSF1A is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00294-tnfrsf1a-primary-antibodies-if-testing-1.jpgAnti-TNFRSF1A Antibody Picoband®IF analysis of TNFRSF1A using anti-TNFRSF1A antibody (A00294). <br>
TNFRSF1A was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TNFRSF1A Antibody (A00294) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00294-tnfrsf1a-primary-antibodies-fcm-testing-1.jpgAnti-TNFRSF1A Antibody Picoband®Flow Cytometry analysis of U937 cells using anti-TNFRSF1A antibody (A00294). <br>Overlay histogram showing CACO-2 cells stained with A00294 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TNFRSF1A Antibody (A00294, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-rank-picoband-trade-antibody-a01064-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01064-1-2-IHC-anti-rank-picoband-antibody.jpgAnti-RANK/TNFRSF11A Antibody Picoband®<b> IHC analysis of RANK using anti-RANK antibody (A01064-1).</b><br>
RANK was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RANK Antibody (A01064-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01064-1-3-IHC-anti-rank-picoband-antibody.jpgAnti-RANK/TNFRSF11A Antibody Picoband®<b> IHC analysis of RANK using anti-RANK antibody (A01064-1).</b><br>
RANK was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-RANK Antibody (A01064-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01064-1-1_1.jpgAnti-RANK/TNFRSF11A Antibody Picoband® Western blot analysis of RANK using anti-RANK antibody (A01064-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat thymus tissue lysates, <br>Lane 2: mouse thymus tissue lysates, <br>Lane 3: HEPG2 whole Cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RANK antigen affinity purified polyclonal antibody (Catalog # A01064-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RANK at approximately 80KD. The expected band size for RANK is at 66KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01064-1-tnfrsf11a-primary-antibodies-ihc-testing-4.jpgAnti-RANK/TNFRSF11A Antibody Picoband®IHC analysis of RANK/TNFRSF11A using anti-RANK/TNFRSF11A antibody (A01064-1). <br>RANK/TNFRSF11A was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RANK/TNFRSF11A Antibody (A01064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-trail-picoband-trade-antibody-a00466-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a00466-1-WB-anti-trail-picoband-antibody.jpgAnti-TRAIL/Tnfsf10 Antibody Picoband®<b> Western blot analysis of TRAIL using anti-TRAIL antibody (A00466). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: HEPA1-6 whole Cell lysates, <br>
Lane 2: NIH3T3 whole Cell lysates, <br>
Lane 3: PC12 whole Cell lysates, <br>
Lane 4: NRK whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAIL antigen affinity purified polyclonal antibody (Catalog # A00466) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRAIL at approximately 20KD. The expected band size for TRAIL is at 35KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cytokeratin-8-picoband-trade-antibody-a01421-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01421-1-WB-anti-cytokeratin-8-picoband-antibody.jpgAnti-Cytokeratin 8/KRT8 Antibody Picoband®<b> Western blot analysis of Cytokeratin 8 using anti-Cytokeratin 8 antibody (A01421). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates, <br>
Lane 2: mouse ovary tissue lysates, <br>
Lane 3: mouse liver tissue lysates, <br>
Lane 4: MCF-7 whole cell lysates,<br>
Lane 5: A549 whole cell lysates,<br>
Lane 6: HELA whole Cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 8 antigen affinity purified polyclonal antibody (Catalog # A01421) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytokeratin 8 at approximately 54KD, 56KD. The expected band size for Cytokeratin 8 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01421-2-IHC-anti-cytokeratin-8-picoband-antibody.jpgAnti-Cytokeratin 8/KRT8 Antibody Picoband®<b> IHC analysis of Cytokeratin 8 using anti-Cytokeratin 8 antibody (A01421).</b><br>
Cytokeratin 8 was detected in paraffin-embedded section of mouse liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 8 Antibody (A01421) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01421-3-IHC-anti-cytokeratin-8-picoband-antibody.jpgAnti-Cytokeratin 8/KRT8 Antibody Picoband®<b> IHC analysis of Cytokeratin 8 using anti-Cytokeratin 8 antibody (A01421).</b><br>
Cytokeratin 8 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 8 Antibody (A01421) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-5_1.jpgAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8 using anti-Cytokeratin 8 antibody (A01421). <br> Cytokeratin 8 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 8 Antibody (A01421) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-4_1.jpgAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8 using anti-Cytokeratin 8 antibody (A01421). <br> Cytokeratin 8 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytokeratin 8 Antibody (A01421) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-6_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-7_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-8_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-9_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-10_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-ihc-testing-11_1.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IHC analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human appendix cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) for 30 minutes at 37°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-if-testing-12.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IF analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-if-testing-13.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IF analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-if-testing-14.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IF analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of rat bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-if-testing-15.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IF analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01421-krt8-primary-antibodies-if-testing-16.pngAnti-Cytokeratin 8/KRT8 Antibody Picoband® IF analysis of Cytokeratin 8/KRT8 using anti-Cytokeratin 8/KRT8 antibody (A01421). <br>
Cytokeratin 8/KRT8 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin 8/KRT8 Antibody (A01421) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-trpc3-picoband-trade-antibody-a01472-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01472-trpc3-primary-antibodies-wb-testing-1.jpgAnti-TRPC3 Antibody Picoband®Western blot analysis of TRPC3 using anti-TRPC3 antibody (A01472). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRPC3 antigen affinity purified polyclonal antibody (A01472) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRPC3 at approximately 106 kDa. The expected band size for TRPC3 is at 106 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-brms1-picoband-trade-antibody-a03587-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03587-1-1_1.jpgAnti-BRMS1 Antibody Picoband® Western blot analysis of BRMS1 using anti-BRMS1 antibody (A03587-1).<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysates, <br>Lane 2: rat liver tissue lysates, <br>Lane 3: mouse liver tissue lysates, <br>Lane 4: HELA whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BRMS1 antigen affinity purified polyclonal antibody (Catalog # A03587-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BRMS1 at approximately 34KD. The expected band size for BRMS1 is at 28KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tsh-receptor-picoband-trade-antibody-a00576-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00576-1-tshr-primary-antibodies-wb-testing-1.jpgAnti-TSH Receptor/TSHR Antibody Picoband®Western blot analysis of TSH Receptor using anti-TSH Receptor antibody (A00576-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human REH whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human TT whole cell lysates,<br>
Lane 5: rat ovary tissue lysates,<br>
Lane 6: mouse ovary tissue lysates,<br>
Lane 7: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSH Receptor antigen affinity purified polyclonal antibody (A00576-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TSH Receptor at approximately 40, 70-80, 110 kDa. The expected band size for TSH Receptor is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00576-1-tshr-primary-antibodies-ihc-testing-1.jpgAnti-TSH Receptor/TSHR Antibody Picoband®IHC analysis of TSH Receptor using anti-TSH Receptor antibody (A00576-1). <br>TSH Receptor was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TSH Receptor Antibody (A00576-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-sca1-ly6a-e-picoband-trade-antibody-a30403-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30403-ly6a-primary-antibody-wb-testing-1.jpgAnti-Sca1/Ly6A/E Antibody Picoband® Western blot analysis of Sca1/Ly6A/E using anti-Sca1/Ly6A/E antibody (A30403). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: mouse HEPA1-6 whole cell lysates, <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Sca1/Ly6A/E antigen affinity purified polyclonal antibody (Catalog # A30403) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Sca1/Ly6A/E at approximately 14KD. The expected band size for Sca1/Ly6A/E is at 14KD.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30403-ly6a-primary-antibody-ihc-testing-2.jpgAnti-Sca1/Ly6A/E Antibody Picoband® IHC analysis of Sca1/Ly6A/E using anti-Sca1/Ly6A/Eantibody (A30403). <br>
Sca1/Ly6A/E was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Sca1/Ly6A/E Antibody (A30403) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30403-ly6a-primary-antibodies-fcm-testing-3.pngAnti-Sca1/Ly6A/E Antibody Picoband® Flow Cytometry analysis of HEPA1-6 cells using anti-Sca1/Ly6A/E antibody (A30403). <br>
Overlay histogram showing HEPA1-6 cells stained with A30403 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Sca1/Ly6A/E Antibody (A30403, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-musashi-1-msi1-picoband-trade-antibody-a05052-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-wb-testing-1.jpgAnti-Musashi 1/Msi1 Antibody Picoband® Western blot analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates, <br>
Lane 2: human T-47D whole cell lysates, <br>
Lane 3: human Colo320 whole cell lysates, <br>
Lane 4: rat brain tissue lysates, <br>
Lane 5: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Musashi 1/Msi1 antigen affinity purified polyclonal antibody (Catalog # A05052-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Musashi 1/Msi1 at approximately 39 kDa. The expected band size for Musashi 1/Msi1 is at 39 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05052-1-2-IHC-anti-musashi-1-msi1-picoband-antibody.jpgAnti-Musashi 1/Msi1 Antibody Picoband®<b> IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1).</b><br>
Musashi 1/Msi1 was detected in paraffin-embedded section of mouse intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05052-1-3-IHC-anti-musashi-1-msi1-picoband-antibody.jpgAnti-Musashi 1/Msi1 Antibody Picoband®<b> IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1).</b><br>
Musashi 1/Msi1 was detected in paraffin-embedded section of rat intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05052-1-4-IHC-anti-musashi-1-msi1-picoband-antibody.jpgAnti-Musashi 1/Msi1 Antibody Picoband®<b> IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1).</b><br>
Musashi 1/Msi1 was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05052-1-5-IHC-anti-musashi-1-msi1-picoband-antibody.jpgAnti-Musashi 1/Msi1 Antibody Picoband®<b> IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1).</b><br>
Musashi 1/Msi1 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a05052-1-6-IHC-anti-musashi-1-msi1-picoband-antibody.jpgAnti-Musashi 1/Msi1 Antibody Picoband®<b> IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1).</b><br>
Musashi 1/Msi1 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-7.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in an immunocytochemical section of MCF7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-8.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-9.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-10.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-11.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-12.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-13.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-14.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-15.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-16.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-17.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-18.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-19.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-ihc-testing-20.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IHC analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2.5 μg/ml rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-21.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-22.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-23.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-24.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-25.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05052-1-msi1-primary-antibodies-if-testing-26.jpgAnti-Musashi 1/Msi1 Antibody Picoband® IF analysis of Musashi 1/Msi1 using anti-Musashi 1/Msi1 antibody (A05052-1). <br>
Musashi 1/Msi1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Musashi 1/Msi1 Antibody (A05052-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/casestudy_a05052-1.jpgAnti-Musashi 1/Msi1 Antibody Picoband®
https://www.bosterbio.com/products/primary-antibodies/anti-nckap1-picoband-trade-antibody-a09238-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a09238-1-1-WB-anti-nckap1-picoband-antibody.jpgAnti-NCKAP1 Antibody Picoband®<b> Western blot analysis of NCKAP1 using anti-NCKAP1 antibody (A09238-1). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates, <br>
Lane 3: MCF-7 whole Cell lysates, <br>
Lane 4: 293T whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCKAP1 antigen affinity purified polyclonal antibody (Catalog # A09238-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NCKAP1 at approximately 129KD. The expected band size for NCKAP1 is at 129KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vinculin-picoband-trade-antibody-a01207-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01207-vinculin-primary-antibodies-wb-testing-1.jpgAnti-Vinculin/VCL Antibody Picoband® Western blot analysis of Vinculin using anti-Vinculin antibody (A01207). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human U87 whole cell lysates, <br>
Lane 3: rat RH35 whole cell lysates, <br>
Lane 4: rat PC-12 whole cell lysates, <br>
Lane 5: mouse RAW264.7 whole cell lysates, <br>
Lane 6: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vinculin antigen affinity purified polyclonal antibody (Catalog # A01207) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vinculin at approximately 124 kDa. The expected band size for Vinculin is at 124 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ca-iv-picoband-trade-antibody-a01523-1-boster.html2026-03-24T05:10:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01523-1_1.jpgAnti-Carbonic Anhydrase IV/CA4 Antibody Picoband® Western blot analysis of CA IV using anti-CA IV antibody (A01523-1).<br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat lung tissue lysates, <br>Lane 2: mouse lung tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CA IV antigen affinity purified polyclonal antibody (Catalog # A01523-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CA IV at approximately 35KD. The expected band size for CA IV is at 35KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ndrg3-picoband-trade-antibody-a10017-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10017-1-WB-anti-ndrg3-picoband-antibody.jpgAnti-NDRG3 Antibody Picoband®<b> Western blot analysis of NDRG3 using anti-NDRG3 antibody (A10017). </b><br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: COLO320 whole cell lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDRG3 antigen affinity purified polyclonal antibody (Catalog # A10017) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NDRG3 at approximately 41KD. The expected band size for NDRG3 is at 41KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10017-3-IHC-anti-ndrg3-picoband-antibody.jpgAnti-NDRG3 Antibody Picoband®<b> IHC analysis of NDRG3 using anti-NDRG3 antibody (A10017).</b><br>
NDRG3 was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NDRG3 Antibody (A10017) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10017-5-IHC-anti-ndrg3-picoband-antibody.jpgAnti-NDRG3 Antibody Picoband®<b> IHC analysis of NDRG3 using anti-NDRG3 antibody (A10017).</b><br>
NDRG3 was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NDRG3 Antibody (A10017) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10017-4-IHC-anti-ndrg3-picoband-antibody.jpgAnti-NDRG3 Antibody Picoband®<b> IHC analysis of NDRG3 using anti-NDRG3 antibody (A10017).</b><br>
NDRG3 was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NDRG3 Antibody (A10017) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a10017-2-IHC-anti-ndrg3-picoband-antibody.jpgAnti-NDRG3 Antibody Picoband®<b> IHC analysis of NDRG3 using anti-NDRG3 antibody (A10017).</b><br>
NDRG3 was detected in paraffin-embedded section of mouse brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NDRG3 Antibody (A10017) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd105-picoband-trade-antibody-a02997-1-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02997-1-cd105-primary-antibodies-wb-testing-1.jpgAnti-CD105/ENG Antibody Picoband® Western blot analysis of CD105/ENG using anti-CD105/ENG antibody (A02997-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates, <br>
Lane 2: human Hela whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD105/ENG antigen affinity purified polyclonal antibody (Catalog # A02997-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD105/ENG at approximately 95 kDa. The expected band size for CD105/ENG is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02997-1-cd105-primary-antibodies-fcm-testing-2.jpgAnti-CD105/ENG Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-CD105/ENG antibody (A02997-1). <br>Overlay histogram showing U87 cells stained with A02997-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit ant-iCD105/ENG Antibody (A02997-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-tmem240-picoband-trade-antibody-a14889-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14889-1_1.jpgAnti-TMEM240 Antibody Picoband® Western blot analysis of TMEM240 using anti-TMEM240 antibody (A14889). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates, <br>Lane 2: NIH3T3 whole Cell lysates, <br>Lane 3: COLO320 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMEM240 antigen affinity purified polyclonal antibody (Catalog # A14889) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TMEM240 at approximately 19KD. The expected band size for TMEM240 is at 19KD.
https://www.bosterbio.com/products/primary-antibodies/anti-chat-picoband-trade-antibody-a01192-3-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01192-3-2_2-IHC-anti-chat-choline-acetyltransferase-picoband-antibody.jpgAnti-Choline Acetyltransferase/CHAT Antibody Picoband®<b> IHC analysis of CHAT using anti-CHAT antibody (A01192-3).</b><br>
CHAT was detected in paraffin-embedded section of mouse brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHAT Antibody (A01192-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/a01192-3-3_2-IHC-anti-chat-choline-acetyltransferase-picoband-antibody.jpgAnti-Choline Acetyltransferase/CHAT Antibody Picoband®<b> IHC analysis of CHAT using anti-CHAT antibody (A01192-3).</b><br>
CHAT was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHAT Antibody (A01192-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01192-3-1_1.jpgAnti-Choline Acetyltransferase/CHAT Antibody Picoband®<b> Western blot analysis of CHAT using anti-CHAT antibody (A01192-3).</b><br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat testis tissue lysates, <br>Lane 2: mouse testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHAT antigen affinity purified polyclonal antibody (Catalog # A01192-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHAT at approximately 83KD. The expected band size for CHAT is at 83KD.
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-human-fgf2-protein-r00121-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Human FGF2 ProteinBoster Kit Box
https://www.bosterbio.com/products/primary-antibodies/anti-abcc1-picoband-trade-antibody-a00872-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00872-1_6-WB-anti-mrp1-picoband-antibody.jpgAnti-MRP1/ABCC1 Antibody Picoband®<strong> Western blot analysis of MRP1 using anti-MRP1 antibody (A00872). </strong><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>lane 1: HELA whole cell lysates,<br>lane 2: A549 whole cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MRP1 antigen affinity purified polyclonal antibody (Catalog # A00872) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MRP1 at approximately 220KD. The expected band size for MRP1 is at 220KD.<br>
https://www.bosterbio.com/products/primary-antibodies/anti-ikbkg-picoband-trade-antibody-a00874-boster.html2026-03-24T05:10:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00874-1_6-WB-anti-ikk-gamma-picoband-antibody.jpgAnti-IKK gamma/IKBKG Antibody Picoband®<strong> Western blot analysis of IKK gamma using anti-IKK gamma antibody (A00874). </strong><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>lane 1: rat cardiac muscle tissue lysates,<br>lane 2: HEPG2 whole cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKK gamma antigen affinity purified polyclonal antibody (Catalog # A00874) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IKK gamma at approximately 48KD. The expected band size for IKK gamma is at 48KD.<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00874-ikbkg-primary-antibody-if-testing-2.jpgAnti-IKK gamma/IKBKG Antibody Picoband® IF analysis of IKK gamma using anti- IKK gamma antibody (A00874). <br>
IKK gamma was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti- IKK gamma Antibody (A00874) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-pnp-picoband-trade-antibody-a00988-1-boster.html2026-04-01T05:01:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00988-1-pnp-primary-antibodies-wb-testing-1.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband® Western blot analysis of PNP using anti-PNP antibody (A00988-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates, <br>
Lane 3: rat liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PNP antigen affinity purified polyclonal antibody (Catalog # A00988-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PNP at approximately 32 kDa. The expected band size for PNP is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00988-1-2_1-IHC-anti-pnp-picoband-antibody.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband®<strong> IHC analysis of PNP using anti-PNP antibody (A00988-1).</strong><br>PNP was detected in paraffin-embedded section of mouse kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PNP Antibody (A00988-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00988-1-3_1-IHC-anti-pnp-picoband-antibody.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband®<strong> IHC analysis of PNP using anti-PNP antibody (A00988-1).</strong><br>PNP was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PNP Antibody (A00988-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00988-1-4_1-IHC-anti-pnp-picoband-antibody.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband®<strong> IHC analysis of PNP using anti-PNP antibody (A00988-1).</strong><br>PNP was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PNP Antibody (A00988-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A00988-1-5_1-IHC-anti-pnp-picoband-antibody.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband®<strong> IHC analysis of PNP using anti-PNP antibody (A00988-1).
</strong><br>PNP was detected in paraffin-embedded section of human renal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PNP Antibody (A00988-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00988-1-pnp-primary-antibodies-fc-testing-6.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-PNP antibody (A00988-1).<br>Overlay histogram showing U937 cells stained with A00988-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PNP Antibody (A00988-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00988-1-pnp-primary-antibodies-fc-testing-7.jpgAnti-Nucleoside phosphorylase/PNP Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PNP antibody (A00988-1).<br>Overlay histogram showing U251 cells stained with A00988-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PNP Antibody (A00988-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-apg3-picoband-trade-antibody-a01768-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01768-1-apg3-primary-antibodies-wb-testing-1.jpgAnti-Apg3/ATG3 Antibody Picoband® Western blot analysis of Apg3 using anti-Apg3 antibody (A01768-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: monkey COS-7 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Apg3 antigen affinity purified polyclonal antibody (Catalog # A01768-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Apg3 at approximately 36-40 kDa. The expected band size for Apg3 is at 36 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-math1-hath1-picoband-trade-antibody-a02207-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02207-1-atoh1-primary-antibodies-wb-testing-1.jpgAnti-MATH1/HATH1/ATOH1 Antibody Picoband® Western blot analysis of MATH1/HATH1/ATOH1 using anti-MATH1/HATH1/ATOH1 antibody (A02207-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates, <br>
Lane 2: rat PC-12 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MATH1/HATH1/ATOH1 antigen affinity purified polyclonal antibody (Catalog # A02207-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MATH1/HATH1/ATOH1 at approximately 38 kDa. The expected band size for MATH1/HATH1/ATOH1 is at 38 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bid-picoband-trade-antibody-a00730-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00730-bid-primary-antibodies-fcm-testing-3.pngAnti-Bid Antibody Picoband® Flow Cytometry analysis of Neuro-2a cells using anti-Bid antibody (A00730). <br>Overlay histogram showing Neuro-2a cells stained with A00730 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Bid Antibody (A00730, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00730-bid-primary-antibodies-wb-testing-1.jpgAnti-Bid Antibody Picoband® Western blot analysis of Bid using anti-Bid antibody (A00730). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse L929 whole cell lysates, <br>
Lane 2: mouse spleen tissue lysates, <br>
Lane 3: mouse RAW264.7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bid antigen affinity purified polyclonal antibody (Catalog # A00730) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bid at approximately 22 kDa. The expected band size for Bid is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00730-bid-primary-antibodies-ihc-testing-2.jpgAnti-Bid Antibody Picoband® IHC analysis of Bid using anti-Bid antibody (A00730). <br>
Bid was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Bid Antibody (A00730) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-c19orf80-picoband-trade-antibody-a02471-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02471-1-western-blotting.jpgAnti-C19orf80/ANGPTL8 Antibody Picoband®<b> Western blot analysis of C19orf80 using anti-C19orf80 antibody (A02471).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human HepG2 whole Cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C19orf80 antigen affinity purified polyclonal antibody (Catalog # A02471) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C19orf80 at approximately 22KD. The expected band size for C19orf80 is at 22KD.
https://www.bosterbio.com/products/primary-antibodies/anti-calpain-2-picoband-trade-antibody-a03492-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03492-capn2-primary-antibodies-wb-testing-1.jpgAnti-Calpain 2/CAPN2 Antibody Picoband® Western blot analysis of Calpain 2 using anti-Calpain 2 antibody (A03492). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human Hela whole cell lysates, <br>
Lane 4: rat kidney tissue lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: mouse kidney tissue lysates, <br>
Lane 7: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calpain 2 antigen affinity purified polyclonal antibody (Catalog # A03492) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calpain 2 at approximately 80 kDa. The expected band size for Calpain 2 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03492-2-immunohistochemistry.jpgAnti-Calpain 2/CAPN2 Antibody Picoband®<b> IHC analysis of Calpain 2 using anti-Calpain 2 antibody (A03492).
</b><br>Calpain 2 was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Calpain 2 Antibody (A03492) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03492-3-immunohistochemistry.jpgAnti-Calpain 2/CAPN2 Antibody Picoband®<b> IHC analysis of Calpain 2 using anti-Calpain 2 antibody (A03492).
</b><br>Calpain 2 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Calpain 2 Antibody (A03492) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03492-4-immunohistochemistry.jpgAnti-Calpain 2/CAPN2 Antibody Picoband®<b> IHC analysis of Calpain 2 using anti-Calpain 2 antibody (A03492).</b><br>Calpain 2 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Calpain 2 Antibody (A03492) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03492-capn2-primary-antibodies-if-testing-5.jpgAnti-Calpain 2/CAPN2 Antibody Picoband® IF analysis of Calpain 2 using anti-Calpain 2 antibody (A03492). <br>
Calpain 2 was detected in immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Calpain 2 Antibody (A03492) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01564-1-bub1b-primary-antibodies-fcm-testing-6.pngAnti-Calpain 2/CAPN2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-Calpain 2 antibody (A03492). <br>Overlay histogram showing U87 cells stained with A03492 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpain 2 Antibody (A03492, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-caspase-6-picoband-trade-antibody-a02631-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02631-1-western-blotting.jpgAnti-Caspase-6/CASP6 Antibody Picoband®<b> Western blot analysis of Caspase-6 using anti-Caspase-6 antibody (A02631).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat kidney tissue lysate,<br>Lane 2: mouse kidney tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase-6 antigen affinity purified polyclonal antibody (Catalog # A02631) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase-6 at approximately 33KD. The expected band size for Caspase-6 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ccl19-mip-3-beta-picoband-trade-antibody-a01605-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01605-1-1-western-blotting.jpgAnti-Macrophage Inflammatory Protein 3 beta/Ccl19 Antibody Picoband®<b> Western blot analysis of Ccl19/MIP-3 beta using anti-Ccl19/MIP-3 beta antibody (A01605-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat thymus tissue lysate,<br>Lane 2: rat lung tissue lysate,<br>Lane 3: rat spleen tissue lysate,<br>Lane 4: rat stomach tissue lysate,<br>Lane 5: rat PC-12 whole Cell lysate,<br>Lane 6: mouse thymus tissue lysate,<br>Lane 7: mouse NIH3T3 whole Cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ccl19/MIP-3 beta antigen affinity purified polyclonal antibody (Catalog # A01605-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ccl19/MIP-3 beta at approximately 20KD. The expected band size for Ccl19/MIP-3 beta is at 11KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ccr1-picoband-trade-antibody-a01896-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01896-1-1-western-blotting.jpgAnti-CCR1 Antibody Picoband®<b> Western blot analysis of CCR1 using anti-CCR1 antibody (A01896-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat PC-12 whole Cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR1 antigen affinity purified polyclonal antibody (Catalog # A01896-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCR1 at approximately 48KD. The expected band size for CCR1 is at 41KD.
https://www.bosterbio.com/products/primary-antibodies/anti-chd2-antibody-a04079-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04079-chd2-primary-antibodies-wb-testing-1.jpgAnti-CHD2 Antibody Picoband® Western blot analysis of CHD2 using anti-CHD2 antibody (A04079). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: monkey COS-7 whole cell lysates, <br>
Lane 2: human Siha whole cell lysates, <br>
Lane 3: rat brain tissue lysates, <br>
Lane 4: rat C6 whole cell lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHD2 antigen affinity purified polyclonal antibody (Catalog # A04079) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHD2 at approximately 250 kDa. The expected band size for CHD2 is at 211 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04079-chd2-primary-antibodies-ihc-testing-4.jpgAnti-CHD2 Antibody Picoband®IHC analysis of CHD2 using anti-CHD2 antibody (A04079). <br>CHD2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHD2 Antibody (A04079) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04079-2-immunohistochemistry.jpgAnti-CHD2 Antibody Picoband®<b> IHC analysis of CHD2 using anti-CHD2 antibody (A04079).</b><br>CHD2 was detected in paraffin-embedded section of rat brain tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHD2 Antibody (A04079) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04079-chd2-primary-antibodies-ihc-testing-3.jpgAnti-CHD2 Antibody Picoband® IHC analysis of CHD2 using anti-CHD2 antibody (A04079).<br>CHD2 was detected in paraffin-embedded section of mouse brain tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CHD2 Antibody (A04079) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cope-picoband-trade-antibody-a04544-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04544-cope-primary-antibodies-wb-testing-1.jpgAnti-COPE Antibody Picoband®Western blot analysis of COPE using anti-COPE antibody (A04544). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human 293T whole cell lysates, <br>
Lane 4: human PC-3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COPE antigen affinity purified polyclonal antibody (A04544) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for COPE at approximately 35 kDa. The expected band size for COPE is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04544-2-immunohistochemistry.jpgAnti-COPE Antibody Picoband®<b> IHC analysis of COPE using anti-COPE antibody (A04544).
</b><br>COPE was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-COPE Antibody (A04544) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04544-3-immunohistochemistry.jpgAnti-COPE Antibody Picoband®<b> IHC analysis of COPE using anti-COPE antibody (A04544).
</b><br>COPE was detected in paraffin-embedded section of mouse pancreas tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-COPE Antibody (A04544) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04544-4-immunohistochemistry.jpgAnti-COPE Antibody Picoband®<b> IHC analysis of COPE using anti-COPE antibody (A04544).</b><br>COPE was detected in paraffin-embedded section of rat pancreas tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-COPE Antibody (A04544) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04544-cope-primary-antibodies-fc-testing-6.pngAnti-COPE Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-COPE antibody (A04544). <br> Overlay histogram showing HepG2 cells stained with A04544 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-COPE Antibody (A04544,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04544-cope-primary-antibodies-if-testing-5.jpgAnti-COPE Antibody Picoband® IF analysis of COPE using anti-COPE antibody (A04544). <br> COPE was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-COPE Antibody (A04544) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04544-cope-primary-antibodies-if-testing-7.jpgAnti-COPE Antibody Picoband® IF analysis of COPE using anti-COPE antibody (A04544). <br> COPE was detected in immunocytochemical section of MCF-7 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-COPE Antibody (A04544) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04544-cope-primary-antibodies-ip-testing-1.jpgAnti-COPE Antibody Picoband®Immunoprecipitating (IP) COPE in 293T whole cell lysate.<br>
Western blot analysis of COPE using anti-COPE antibody (A04544); <br>
Lane 1: 293T whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-COPE antibody in 293T whole cell lysate;<br>
Lane 3: anti-COPE antibody (2μg) + 293T whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-COPE antigen affinity purified polyclonal antibody (A04544) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for COPE at approximately 34 kDa. The expected band size for COPE is at 34 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ctla4-picoband-trade-antibody-a00020-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00020-1-1-western-blotting_1.jpgAnti-CTLA4 Antibody Picoband® Western blot analysis of CTLA4 using anti-CTLA4 antibody (A00020-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse NIH3T3 whole Cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTLA4 antigen affinity purified polyclonal antibody (Catalog # A00020-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTLA4 at approximately 25KD. The expected band size for CTLA4 is at 25KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00020-1-41598_2025_88671_fig9_html.pngAnti-CTLA4 Antibody Picoband®Relative expression of genes expression in GBM tissues. Expression levels of WTAP and ZC3H13 genes were compared with those of the control group on GBM tissues, 10 GBM and adjacent tissues, respectively ( A ). The expression levels of siRNA WTAP and overexpression ZC3H13 genes ( B and C ). The expression levels of CD27, CD70, CD80, CD86, ICOS, CTLA4, and LAG3 in siRNA WTAP and overexpression ZC3H13 were demonstrated in Fig. D and F, respectively. The result were determined by qRT-PCR. The data are mean ± standard deviation of six replicate experiments. * P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00020-1-2-immunohistochemistry.jpgAnti-CTLA4 Antibody Picoband® IHC analysis of CTLA4 using anti-CTLA4 antibody (A00020-1).<br>CTLA4 was detected in paraffin-embedded section of mouse spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CTLA4 Antibody (A00020-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00020-1-3-immunohistochemistry.jpgAnti-CTLA4 Antibody Picoband® IHC analysis of CTLA4 using anti-CTLA4 antibody (A00020-1).<br>CTLA4 was detected in paraffin-embedded section of rat lymphaden tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CTLA4 Antibody (A00020-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00020-1-4-immunohistochemistry.jpgAnti-CTLA4 Antibody Picoband® IHC analysis of CTLA4 using anti-CTLA4 antibody (A00020-1).<br>CTLA4 was detected in paraffin-embedded section of rat spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CTLA4 Antibody (A00020-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cytochrome-c-picoband-trade-antibody-a03529-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-cycs-primary-antibodies-wb-testing-1.jpgAnti-Cytochrome C/Cycs Antibody Picoband® Western blot analysis of Cytochrome C using anti-Cytochrome C antibody (A03529). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human U-937 whole cell lysates,<br>
Lane 4: human U20S whole cell lysates,<br>
Lane 5: human T-47D whole cell lysates,<br>
Lane 6: human PC-3 whole cell lysates,<br>
Lane 7: human CACO-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytochrome C antigen affinity purified polyclonal antibody (Catalog # A03529) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytochrome C at approximately 14 kDa. The expected band size for Cytochrome C is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-cycs-primary-antibodies-wb-testing-2.jpgAnti-Cytochrome C/Cycs Antibody Picoband® Western blot analysis of Cytochrome C using anti-Cytochrome C antibody (A03529). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat heart tissue lysates,<br>
Lane 3: rat kidney tissue lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse kidney tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytochrome C antigen affinity purified polyclonal antibody (Catalog # A03529) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytochrome C at approximately 14 kDa. The expected band size for Cytochrome C is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-cycs-primary-antibodies-ihc-testing-6.jpgAnti-Cytochrome C/Cycs Antibody Picoband®IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (A03529). <br>Cytochrome c/CYCS was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Cytochrome c/CYCS Antibody (A03529) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529_12645_2025_336_fig9_html.pngAnti-Cytochrome C/Cycs Antibody Picoband®a Western blotting was used to examine mitochondrial apoptotic pathway-related proteins after treatment with control (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Key proteins involved in apoptosis such as Bax, Bcl-2, cytochrome c, and cleaved caspase-3 were examined to better understand how each treatment affects cell death at the mitochondrial level. b To further investigate the underlying molecular mechanisms, western blotting was used to investigate the PI3K/AKT/mTOR pathway (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Expression levels of PI3K, AKT (total and phosphorylated), and mTOR were evaluated to assess whether this survival pathway was activated or suppressed. Protein levels were quantified and compared to the control group to determine statistical significance. * p < 0.05, ** p < 0.01, *** p < 0.001 in comparison to the respective control <br><b>Index in Springer Nature under a CC BY license. DOI: <a href='https://link.springer.com/article/10.1186/s12645-025-00336-z'>10.1186/s12645-025-00336-z</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-3-immunohistochemistry.jpgAnti-Cytochrome C/Cycs Antibody Picoband®<b> IHC analysis of Cytochrome C using anti-Cytochrome C antibody (A03529).
</b><br>Cytochrome C was detected in paraffin-embedded section of mouse intestine tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome C Antibody (A03529) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-4-immunohistochemistry.jpgAnti-Cytochrome C/Cycs Antibody Picoband®<b> IHC analysis of Cytochrome C using anti-Cytochrome C antibody (A03529).
</b><br>Cytochrome C was detected in paraffin-embedded section of rat brain tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome C Antibody (A03529) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-5-immunohistochemistry.jpgAnti-Cytochrome C/Cycs Antibody Picoband®<b> IHC analysis of Cytochrome C using anti-Cytochrome C antibody (A03529).
</b><br>Cytochrome C was detected in paraffin-embedded section of rat intestine tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome C Antibody (A03529) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03529-6-immunohistochemistry.jpgAnti-Cytochrome C/Cycs Antibody Picoband®<b> IHC analysis of Cytochrome C using anti-Cytochrome C antibody (A03529).
</b><br>Cytochrome C was detected in paraffin-embedded section of mouse brain tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Cytochrome C Antibody (A03529) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ddx3-picoband-trade-antibody-a00751-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-1-ddx3-primary-antibodies-wb-testing-1.jpgAnti-DDX3/DDX3X Antibody Picoband® Western blot analysis of DDX3 using anti-DDX3 antibody (A00751-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human HT1080 whole cell lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: rat C6 whole cell lysates, <br>
Lane 6: mouse liver tissue lysates, <br>
Lane 7: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDX3 antigen affinity purified polyclonal antibody (Catalog # A00751-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DDX3 at approximately 73 kDa. The expected band size for DDX3 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-1-ddx3-primary-antibodies-if-testing-2.jpgAnti-DDX3/DDX3X Antibody Picoband® IF analysis of DDX3 using anti-DDX3 antibody (A00751-1). <br>
DDX3 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 4 μg/mL rabbit anti-DDX3 Antibody (A00751-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-1-ddx3-primary-antibodies-fcm-testing-3.jpgAnti-DDX3/DDX3X Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-DDX3 antibody (A00751-1). <br>Overlay histogram showing A549 cells stained with A00751-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DDX3 Antibody (A00751-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-1-ddx3-primary-antibodies-fcm-testing-4.jpgAnti-DDX3/DDX3X Antibody Picoband® Flow Cytometry analysis of ANA-1 cells using anti-DDX3 antibody (A00751-1). <br>Overlay histogram showing ANA-1 cells stained with A00751-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DDX3 Antibody (A00751-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00751-1-ddx3-primary-antibodies-fcm-testing-5.jpgAnti-DDX3/DDX3X Antibody Picoband® Flow Cytometry analysis of C6 cells using anti-DDX3 antibody (A00751-1). <br>Overlay histogram showing C6 cells stained with A00751-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DDX3 Antibody (A00751-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ddx58-picoband-trade-antibody-a00244-2-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-2-ddx58-primary-antibodies-wb-testing-1.jpgAnti-DDX58 Antibody Picoband® Western blot analysis of DDX58 using anti-DDX58 antibody (A00244-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: rat C6 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDX58 antigen affinity purified polyclonal antibody (Catalog # A00244-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DDX58 at approximately 107 kDa. The expected band size for DDX58 is at 107 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-2-ddx58-primary-antibodies-if-testing-2.jpgAnti-DDX58 Antibody Picoband® IF analysis of DDX58 using anti-DDX58 antibody (A00244-2). <br>
DDX58 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-DDX58 Antibody (A00244-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-2-ddx58-primary-antibodies-if-testing-3.jpgAnti-DDX58 Antibody Picoband® IF analysis of DDX58 using anti-DDX58 antibody (A00244-2). <br>
DDX58 was detected in a paraffin-embedded section of human intestine cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-DDX58 Antibody (A00244-2) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-2-4-flow-cytometry.pngAnti-DDX58 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-DDX58 antibody (A00244-2). <br> Overlay histogram showing A431 cells stained with A00244-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DDX58 Antibody (A00244-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-sap102-picoband-trade-antibody-a04152-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04152-1-dlg3-primary-antibodies-wb-testing-1.jpgAnti-SAP102/DLG3 Antibody Picoband®Western blot analysis of DLG3 using anti-DLG3 antibody (A04152-1). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DLG3 antigen affinity purified polyclonal antibody (A04152-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DLG3 at approximately 100 kDa. The expected band size for DLG3 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04152-1-dlg3-primary-antibodies-ihc-testing-1.jpgAnti-SAP102/DLG3 Antibody Picoband®IHC analysis of SAP102/DLG3 using anti-SAP102/DLG3 antibody (A04152-1). <br>SAP102/DLG3 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAP102/DLG3 Antibody (A04152-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04152-1-dlg3-primary-antibodies-ihc-testing-2.jpgAnti-SAP102/DLG3 Antibody Picoband®IHC analysis of SAP102/DLG3 using anti-SAP102/DLG3 antibody (A04152-1). <br>SAP102/DLG3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAP102/DLG3 Antibody (A04152-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04152-1-dlg3-primary-antibodies-ihc-testing-3.jpgAnti-SAP102/DLG3 Antibody Picoband®IHC analysis of SAP102/DLG3 using anti-SAP102/DLG3 antibody (A04152-1). <br>SAP102/DLG3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAP102/DLG3 Antibody (A04152-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-egf-picoband-trade-antibody-a00378-1-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00378-1-1-western-blotting.jpgAnti-EGF Antibody Picoband®<b> Western blot analysis of EGF using anti-EGF antibody (A00378-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.<br>Lane 1: recombinant rat EGF protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EGF antigen affinity purified polyclonal antibody (Catalog # A00378-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EGF at approximately 6KD. The expected band size for EGF is at 6KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00378-1-2-immunohistochemistry.jpgAnti-EGF Antibody Picoband®<b> IHC analysis of EGF using anti-EGF antibody (A00378-1).
</b><br>EGF was detected in paraffin-embedded section of rat kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EGF Antibody (A00378-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00378-1-3-immunohistochemistry.jpgAnti-EGF Antibody Picoband®<b> IHC analysis of EGF using anti-EGF antibody (A00378-1).
</b><br>EGF was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EGF Antibody (A00378-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00378-1-egf-primary-antibodies-elisa-testing-4.jpgAnti-EGF Antibody Picoband® Sandwich ELISA - Recombinant rat EGF protein standard curve.<br>
Use in combination with reagents from Rat EGF ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0954).
https://www.bosterbio.com/products/primary-antibodies/anti-egfr-picoband-trade-antibody-a00023-boster.html2026-03-24T05:10:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00023-egfr-primary-antibodies-wb-testing-1.jpgAnti-EGFR Antibody Picoband® Western blot analysis of EGFR using anti-EGFR antibody (A00023). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates, <br>
Lane 2: human A431 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EGFR antigen affinity purified polyclonal antibody (Catalog # A00023) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EGFR at approximately 175 kDa. The expected band size for EGFR is at 134 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00023-fnagi-17-1568337-g007.jpgAnti-EGFR Antibody Picoband®Validation of the pyroptosis-AD hub genes at the level of RNA and protein in AD mice. (A) A hierarchical clustering heatmap based on the normalized expression of the five pyroptosis-AD genes in the combined dataset. (B) A clustering heatmap was constructed based on the normalized expression of the five pyroptosis-AD genes in the 6- and 12-month-old APP/PS1 and control mice. The 6- and 12-month-old APP/PS1 or WT mice were abbreviated as A6 and A12 or W6 and W12, respectively. (C–G) qPCR validation of mRNA expression of the pyroptosis-AD hub genes (Chmp2a, Egfr, Pkn2, Hsp90b1, and Mdh1, respectively) between the 12 months APP/PS1 and wild-type (WT) mice. Data are mean ± SEM ( n = 6 for WT, and n = 5 for APP/PS1 mice group, * p < 0.05, ** p < 0.01, unpaired two-tailed t -test). (H–K) The cell lysates from the hippocampus of APP/PS1 and WT mice were prepared and blotted with anti-Egfr, Pkn2, Hsp90b1, and Mdh1, respectively (up). The relative protein expressions of Egfr, Pkn2, Hsp90b1, and Mdh1 were calculated using Gapdh as an internal reference (below). Data are mean ± SEM ( n = 6 per group, * p < 0.05, ** p < 0.01, unpaired two-tailed t -test).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2025.1568337/full'>40438507</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00023-fnagi-17-1568337-g009.jpgAnti-EGFR Antibody Picoband®Construction of lncRNA regulatory network of the pyroptosis-AD hub genes. (A) PCA of lncRNAs expression profiles of the APP/PS1 and WT mice at the age of 3, 6, and 12 months. (B) Visualization of the clustered volcano diagram for the DElncRs from six different comparisons, including APP/PS1 mice vs. WT mice at the age of 3, 6, and 12 months and comparison of APP/PS1 mice between different ages. (C) A hierarchical clustering heatmap based on the normalized expression in all samples of DElncRs. The 3-, 6-, and 12-month-old APP/PS1 or WT mice were abbreviated as A3, A6, and A12 or W3, W6, and W12, respectively. (D) The clustered heatmap was produced based on the membership scores of the six clusters obtained by time series analysis. All the DElncRs and five pyroptosis-AD hub genes were clustered into six groups. (E) Line charts showed the relative expression trend in each cluster. The five pyroptosis-AD hub genes were divided into cluster 2 (Champ2 and Mdh1), cluster 3 (Pkn2), and cluster (Egfr and Hsp90b1). The horizontal axis represents a total of nine samples in the age 3-, 6-, and 12-month groups in turn. (F) The heatmaps of correlation analysis of the five pyroptosis-AD hub genes and DElncRs. (G) Regulatory networks constructed by the five pyroptosis-AD hub genes and their top10 (show all if the numbers of lncRNA less than 10) correlated lncRNAs (the ID of lncRNAs could be queried in the NONCODE, NCBI, or Ensemble databases).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2025.1568337/full'>40438507</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00023-EGFR-primary-antibodies-FC-testing-2.jpgAnti-EGFR Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-EGFR antibody (A00023). <br>Overlay histogram showing A431 cells stained with A00023 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EGFR Antibody (A00023,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00023-EGFR-primary-antibodies-IHC-testing-3.jpgAnti-EGFR Antibody Picoband® IHC analysis of EGFR using anti-EGFR antibody (A00023). <br>EGFR was detected in paraffin-embedded section of human glioma tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EGFR Antibody (A00023) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00023-EGFR-primary-antibodies-IHC-testing-4.jpgAnti-EGFR Antibody Picoband® IHC analysis of EGFR using anti-EGFR antibody (A00023). <br>EGFR was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-EGFR Antibody (A00023) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-epigen-picoband-trade-antibody-a10011-1-boster.html2026-03-26T05:20:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-1-epigen-primary-antibodies-wb-testing-1.jpgAnti-Epigen/EPGN Antibody Picoband®Western blot analysis of Epigen using anti-Epigen antibody (A10011-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: rat testis tissue lysates,<br>
Lane 3: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Epigen antigen affinity purified polyclonal antibody (A10011-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Epigen at approximately 17 kDa. The expected band size for Epigen is at 17 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-epigen-picoband-trade-antibody-a10011-2-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-2-epigen-primary-antibodies-wb-testing-1.jpgAnti-Epigen/Epgn Antibody Picoband® Western blot analysis of Epigen using anti-Epigen antibody (A10011-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Epigen antigen affinity purified polyclonal antibody (Catalog # A10011-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Epigen at approximately 17 kDa. The expected band size for Epigen is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-2-epigen-primary-antibodies-ihc-testing-2.jpgAnti-Epigen/Epgn Antibody Picoband® IHC analysis of Epigen using anti-Epigen antibody (A10011-2). <br>
Epigen was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Epigen Antibody (A10011-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10011-2-epigen-primary-antibodies-ihc-testing-3.jpgAnti-Epigen/Epgn Antibody Picoband® IHC analysis of Epigen using anti-Epigen antibody (A10011-2). <br>
Epigen was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Epigen Antibody (A10011-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-esr2-picoband-trade-antibody-a00786-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00786-1-fphar-12-652989-g008.jpgAnti-Estrogen Receptor beta/ESR2 Antibody Picoband®The expression of ESR2 (A) and AR (B) in the renal tissues from the control group, oxalate group, oxalate + low-dose GS group, and oxalate + high-dose GS group detected using IHC staining.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.652989/full'>34248618</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00786-1-esr2-primary-antibodies-wb-testing-1.jpgAnti-Estrogen Receptor beta/ESR2 Antibody Picoband® Western blot analysis of ESR2 using anti-ESR2 antibody (A00786-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: rat brain tissue lysates, <br>
Lane 4: rat testis tissue lysates, <br>
Lane 5: mouse brain tissue lysates, <br>
Lane 6: mouse testis tissue lysates, <br>
Lane 7: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ESR2 antigen affinity purified polyclonal antibody (Catalog # A00786-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ESR2 at approximately 59 kDa. The expected band size for ESR2 is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-fabp4-picoband-trade-antibody-a01528-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01528-fabp4-primary-antibodies-wb-testing-1.jpgAnti-FABP4 Antibody Picoband® Western blot analysis of FABP4 using anti-FABP4 antibody (A01528). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat thymus tissue lysates, <br>
Lane 2: rat heart tissue lysates, <br>
Lane 3: mouse thymus tissue lysates, <br>
Lane 4: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FABP4 antigen affinity purified polyclonal antibody (Catalog # A01528) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FABP4 at approximately 15 kDa. The expected band size for FABP4 is at 15 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-fmn1-picoband-trade-antibody-a07520-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07520-2-immunohistochemistry.jpgAnti-FMN1 Antibody Picoband®<b> IHC analysis of FMN1 using anti-FMN1 antibody (A07520).</b><br>FMN1 was detected in paraffin-embedded section of mouse testis tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FMN1 Antibody (A07520) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07520-3-immunohistochemistry.jpgAnti-FMN1 Antibody Picoband®<b> IHC analysis of FMN1 using anti-FMN1 antibody (A07520).</b><br>FMN1 was detected in paraffin-embedded section of rat testis tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FMN1 Antibody (A07520) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07520-1-western-blotting.jpgAnti-FMN1 Antibody Picoband® Western blot analysis of FMN1 using anti-FMN1 antibody (A07520). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FMN1 antigen affinity purified polyclonal antibody (Catalog # A07520) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FMN1 at approximately 158KD. The expected band size for FMN1 is at 158KD.
https://www.bosterbio.com/products/primary-antibodies/anti-foxp2-picoband-trade-antibody-a01329-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01329-1-1-western-blotting.jpgAnti-FOXP2 Antibody Picoband®<b> Western blot analysis of FOXP2 using anti-FOXP2 antibody (A01329-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate,<br>Lane 3: human SK-OV-3 whole Cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXP2 antigen affinity purified polyclonal antibody (Catalog # A01329-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FOXP2 at approximately 90KD. The expected band size for FOXP2 is at 80KD.
https://www.bosterbio.com/products/primary-antibodies/anti-homer3-picoband-trade-antibody-a09145-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09145-1-homer3-primary-antibodies-wb-testing-1.jpgAnti-HOMER3 Antibody Picoband® Western blot analysis of HOMER3 using anti-HOMER3 antibody (A09145-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat lung tissue lysates.<br>
Lane 6: mouse brain tissue lysates.<br>
Lane 7: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HOMER3 antigen affinity purified polyclonal antibody (Catalog # A09145-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HOMER3 at approximately 45 kDa. The expected band size for HOMER3 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09145-1-4-immunohistochemistry.jpgAnti-HOMER3 Antibody Picoband®<b> IHC analysis of HOMER3 using anti-HOMER3 antibody (A09145-1).
</b><br>HOMER3 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HOMER3 Antibody (A09145-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09145-1-2-immunohistochemistry.jpgAnti-HOMER3 Antibody Picoband®<b> IHC analysis of HOMER3 using anti-HOMER3 antibody (A09145-1).
</b><br>HOMER3 was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HOMER3 Antibody (A09145-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09145-1-3-immunohistochemistry.jpgAnti-HOMER3 Antibody Picoband®<b> IHC analysis of HOMER3 using anti-HOMER3 antibody (A09145-1).
</b><br>HOMER3 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HOMER3 Antibody (A09145-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-hoxb1-picoband-trade-antibody-a04724-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04724-1-1-western-blotting.jpgAnti-HOXB1 Antibody Picoband®<b> Western blot analysis of HOXB1 using anti-HOXB1 antibody (A04724-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat testis tissue lysate,<br>Lane 2: mouse testis tissue lysate,<br>Lane 3: human MCF-7 whole Cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HOXB1 antigen affinity purified polyclonal antibody (Catalog # A04724-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HOXB1 at approximately 32KD. The expected band size for HOXB1 is at 32KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hsp20-picoband-trade-antibody-a07981-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07981-1-1-western-blotting.jpgAnti-Hsp20/HSPB6 Antibody Picoband®<b> Western blot analysis of Hsp20 using anti-Hsp20 antibody (A07981-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat cardiac muscle tissue lysate,<br>Lane 2: rat skeletal muscle tissue lysate,<br>Lane 3: rat testis tissue lysate,<br>Lane 4: mouse testis tissue lysate,<br>Lane 5: human A431 whole Cell lysate.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hsp20 antigen affinity purified polyclonal antibody (Catalog # A07981-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hsp20 at approximately 17KD. The expected band size for Hsp20 is at 17KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-2.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-3_1.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of rat cardiac muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-4.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-5.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-6.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of mouse cardiac muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-ihc-testing-7.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IHC analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07981-1-hsp20-primary-antibodies-if-testing-8.jpgAnti-Hsp20/HSPB6 Antibody Picoband® IF analysis of Hsp20 using anti-Hsp20 antibody (A07981-1). <br>
Hsp20 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Hsp20 Antibody (A07981-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp5-picoband-trade-antibody-a01952-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01952-1-1-western-blotting.jpgAnti-IGFBP5 Antibody Picoband® Western blot analysis of IGFBP5 using anti-IGFBP5 antibody (A01952-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human PC-3 whole cell lysates, <br> Lane 2: human Hela whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP5 antigen affinity purified polyclonal antibody (Catalog # A01952-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP5 at approximately 31KD. The expected band size for IGFBP5 is at 31KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il-1-beta-picoband-trade-antibody-a00101-boster.html2026-03-28T05:00:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-fphar-14-1184588-g004.jpgAnti-IL-1 beta/IL1B Antibody Picoband®Inhibition of GSDMD activation suppressed the expression of pyroptosis pathway-related proteins in ApoE −/− mice. After 4 weeks of treatment the ApoE −/− mice were killed at 18 weeks. (A) Western blotting analysis was conducted to detect protein levels of NLRP3, caspase-1, GSDMD, cleaved IL-1β, and HMGB1 in the aorta. (B–F) Quantitative analysis of expression of NLRP3, p10 (caspase-1), GSDMD-N, cleaved IL-1β, and HMGB1 ( n = 6). β-actin served as the loading control. Data represent means ± SEM.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427923/'>37593179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-fphar-14-1184588-g005.jpgAnti-IL-1 beta/IL1B Antibody Picoband®Z-LLSD-FMK or Z-YVAD-FMK inhibited GSDMD activation or pyroptosis induced by LPS + nigericin in BMDMs. BMDMs were primed with LPS for 4 h followed by nigericin for 30 min. Z-LLSD-FMK, Z-YVAD-FMK, and both combined were added 30 min before LPS + nigericin treatment. (A) Representative immunofluorescence images of cell death determination via PI (red) and Hoechst 33342 (blue) staining (scale bar = 75 μm). (B) The percentage of PI-positive BMDMs was calculated at five randomly selected image fields ( n = 5). (C) LDH release in supernatants ( n = 5). (D) IL-1β release in supernatants was analyzed by ELISA ( n = 5). (E) Western blotting analysis was performed to detect protein levels of NLRP3, caspase-1, GSDMD, cleaved IL-1β, and HMGB1 in supernatants and cell lysates. (F–J) Quantitative analysis of expression of NLRP3, p10 (caspase-1), GSDMD-N, cleaved IL-1β, and HMGB1 in cell lysates ( n = 5). β-actin served as the loading control. Data represent means ± SEM.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427923/'>37593179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-fphar-13-873090-g004.jpgAnti-IL-1 beta/IL1B Antibody Picoband®The effects of P2Y 14 shRNA and naringin on the expression of IL-1β in the SCG of type 2 diabetic rats. The expression level of IL-1β protein was determined by Western blotting (A) . The bar histogram displays the IOD ratio of IL-1β protein mass to β-actin protein mass in each group (B) , and the values are the mean ± SEM from three independent experiments. *** p < 0.001 vs. Ctrl; # p < 0.05 vs. DM; ## p < 0.01 vs. DM.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9068893/&orig_host=www.ncbi.nlm.nih.gov'>35529431</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-12906_2019_2539_fig2_html.pngAnti-IL-1 beta/IL1B Antibody Picoband®Effects of polysaccharide extract from XJEK on TNF-α, IL-1β and IL-10 of HUVECs induced by Ang II. ( a ) TNF-α level in supernatants of HUVECs; ( b ) IL-1β level in supernatants of HUVECs; ( c ) IL-10 level in supernatants of HUVECs. 1, blank control group; 2, Ang II (10 − 5 mol/L) group; 3, Ang II (10 − 5 mol/L) + AqE (0.15 mg/ml) group; 4, Ang II (10 − 5 mol/L) + AqE (0.3 mg/ml) group; 5, Ang II (10 − 5 mol/L) + AqE (0.6 mg/ml) group; 6, Ang II (10 − 5 mol/L) + AqE (1.2 mg/ml) group; 7, Ang II (10 − 5 mol/L) + XJEK (1.6 mg/ml) group. Data are expressed as mean ± SD, n = 6. ** P < 0.01 vs control group; ## P < 0.01 vs Ang II group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-019-2539-z'>31196042</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-12906_2019_2539_fig8_html.pngAnti-IL-1 beta/IL1B Antibody Picoband®Effects of polysaccharide extract from XJEK on TNF-α, IL-1β and IL-10 in L -NAME-induced hypertensive mice. ( a ) TNF-α expression level in plasma. ( b ) IL-1β expression level in plasma. ( c ) IL-10 expression level in plasma. ( d ) IL-1β expression level in cardiac tissues. ( e ) TNF-α expression level in cardiac tissues. ( f ) IL-10 expression level in cardiac tissues. ( g ) Representative image of IL-1β immunocytochemistry. ( h ) Representative image of TNF-α immunocytochemistry.( i ) Representative image of IL-10 immunocytochemistry.1,negative group; 2,control group; 3, model group; 4, L -NAME+AqE group; 5, L -NAME+XJEK group; 6, L -NAME+fosinopril group. Data are presented as the mean ± SD ( n = 10). ** P < 0.01 vs. control group; # P < 0.05, ## P < 0.01 vs, model group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-019-2539-z'>31196042</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-il1b-primary-antibodies-wb-testing-1.jpgAnti-IL-1 beta/IL1B Antibody Picoband®Western blot analysis of IL1B using anti-IL1B antibody (A00101). <br>
Electrophoresis was performed on a 13% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. <br>
Lane 1: recombinant rat IL1B protein 10 ng.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1B antigen affinity purified polyclonal antibody (Catalog # A00101) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL1B at approximately 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-il1b-primary-antibodies-wb-testing-2.jpgAnti-IL-1 beta/IL1B Antibody Picoband®Western blot analysis of IL1B using anti-IL1B antibody (A00101). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse RAW264.7(-LPS) whole cell lysates,<br>
Lane 2: mouse RAW264.7(+LPS) whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1B antigen affinity purified polyclonal antibody (Catalog # A00101) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL1B at approximately 31-35 kDa. The expected band size for IL1B is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-il1b-primary-antibodies-wb-review-1_1.pngAnti-IL-1 beta/IL1B Antibody Picoband®Western blot analysis of IL1B using anti-IL1B antibody (A00101). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: control group-normal mouse hippocampal tissue lysates,<br>
Lane 2: hippocampal tissue from Alzheimer’s disease model mouse,<br>
Lane 3: hippocampal tissue from Alzheimer’s disease model mouse treated with a self-developed drug.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1B antigen affinity purified polyclonal antibody (Catalog # A00101) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for IL1B at approximately 31-35 kDa. The expected band size for IL1B is at 31 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-il1ra-picoband-trade-antibody-a00651-2-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00651-2-il1ra-primary-antibodies-wb-testing-1.jpgAnti-IL1RA/IL1RN Antibody Picoband® Western blot analysis of IL1RA using anti-IL1RA antibody (A00651-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates, <br>
Lane 2: human Hacat whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1RA antigen affinity purified polyclonal antibody (Catalog # A00651-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL1RA at approximately 20 kDa. The expected band size for IL1RA is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00651-2-il1ra-primary-antibodies-ihc-testing-2.jpgAnti-IL1RA/IL1RN Antibody Picoband® IHC analysis of IL1RA using anti-IL1RA antibody (A00651-2). <br>
IL1RA was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL1RA Antibody (A00651-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00651-2-il1ra-primary-antibodies-fcm-testing-3.jpgAnti-IL1RA/IL1RN Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-IL1RA antibody (A00651-2). <br>
Overlay histogram showing U937 cells stained with A00651-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IL1RA Antibody (A00651-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-il6r-picoband-trade-antibody-a01425-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01425-1-1-western-blotting.jpgAnti-IL6R Antibody Picoband®<b> Western blot analysis of IL6R using anti-IL6R antibody (A01425-1). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL6R antigen affinity purified polyclonal antibody (Catalog # A01425-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL6R at approximately 52KD. The expected band size for IL6R is at 52KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il-16-antibody-a01635-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01635-il-16-primary-antibodies-wb-testing-1.jpgAnti-IL-16/Il16 Antibody Picoband® Western blot analysis of IL-16 using anti-IL-16 antibody (A01635). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant mouse IL-16 protein 1ng. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL-16 antigen affinity purified polyclonal antibody (Catalog # A01635) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL-16 at approximately 18KD. The expected band size for IL-16 is at 13KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01635-1-il-16-primary-antibodies-ihc-testing-2.jpgAnti-IL-16/Il16 Antibody Picoband® IHC analysis of IL-16 using anti-IL-16 antibody (A01635). IL-16 was detected in paraffin-embedded section of mouse brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL-16 Antibody (A01635) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01635-1-il-16-primary-antibodies-ihc-testing-3.jpgAnti-IL-16/Il16 Antibody Picoband® IHC analysis of IL-16 using anti-IL-16 antibody (A01635). IL-16 was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL-16 Antibody (A01635) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01635-1-il-16-primary-antibodies-ihc-testing-4.jpgAnti-IL-16/Il16 Antibody Picoband® IHC analysis of IL-16 using anti-IL-16 antibody (A01635). IL-16 was detected in paraffin-embedded section of rat spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL-16 Antibody (A01635) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-il17ra-antibody-a01311-2-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01311-2-il17ra-primary-antibodies-wb-testing-1.jpgAnti-L17A Receptor/IL17RA Antibody Picoband® Western blot analysis of IL17RA using anti-IL17RA antibody (A01311-2). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human MOLT-4 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17RA antigen affinity purified polyclonal antibody (A01311-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL17RA at approximately 120-150 kDa. The expected band size for IL17RA is at 96 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-il-22-picoband-trade-antibody-a00963-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-1-il22-primary-antibodies-wb-testing-1.jpgAnti-IL-22/IL22 Antibody Picoband® Western blot analysis of IL22 using anti-IL22 antibody (A00963-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: rat thymus tissue lysates,<br>
Lane 3: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL22 antigen affinity purified polyclonal antibody (Catalog # A00963-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL22 at approximately 24 kDa. The expected band size for IL22 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-1-il22-primary-antibodies-ihc-testing-2.jpgAnti-IL-22/IL22 Antibody Picoband® IHC analysis of IL22 using anti-IL22 antibody (A00963-1). <br>
IL22 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL22 Antibody (A00963-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-1-il22-primary-antibodies-ihc-testing-3.jpgAnti-IL-22/IL22 Antibody Picoband® IHC analysis of IL22 using anti-IL22 antibody (A00963-1). <br>
IL22 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL22 Antibody (A00963-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-1-il22-primary-antibodies-ihc-testing-4.jpgAnti-IL-22/IL22 Antibody Picoband® IHC analysis of IL22 using anti-IL22 antibody (A00963-1). <br>
IL22 was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL22 Antibody (A00963-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00963-1-il22-primary-antibodies-elisa-testing-5.jpgAnti-IL-22/IL22 Antibody Picoband® Sandwich ELISA - Recombinant human IL22 protein standard curve.<br>
Use in combination with reagents from Human IL22 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0933).
https://www.bosterbio.com/products/primary-antibodies/anti-kpna2-picoband-trade-antibody-a01776-1-boster.html2026-03-24T05:10:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01776-1-1-western-blotting.jpgAnti-KPNA2 Antibody Picoband®<b> Western blot analysis of KPNA2 using anti-KPNA2 antibody (A01776-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysate,<br>Lane 2: human HepG2 whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KPNA2 antigen affinity purified polyclonal antibody (Catalog # A01776-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KPNA2 at approximately 58KD. The expected band size for KPNA2 is at 58KD.
https://www.bosterbio.com/products/primary-antibodies/anti-laminin-picoband-trade-antibody-a03522-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-laminin-primary-antibodies-wb-testing-1.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband® Western blot analysis of Laminin using anti-Laminin antibody (A03522). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat NRK whole cell lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Laminin antigen affinity purified polyclonal antibody (Catalog # A03522) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Laminin at approximately 150, 220-250 kDa. The expected band size for Laminin is at 177 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-lamc3-primary-antibodies-ihc-testing-6.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®IHC analysis of LAMC1/LAMC2/LAMC3 using anti-LAMC1/LAMC2/LAMC3 antibody (A03522). <br>LAMC1/LAMC2/LAMC3 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LAMC1/LAMC2/LAMC3 Antibody (A03522) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-13287_2019_1151_fig5_html.pngAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®Transportation increased apoptosis and deceased cell viability, and BAM15 changed this trend adversely. a Immunofluorescence staining result showed transportation increased expression of Caspase-3 (green) in retinal cups of 30 days, but imposed little effects on expression of Laminin (red). The use of DMSO and BAM15 in transportation was able to alleviate the intensified expression of Caspase-3. b In retinal cups of 60 days, the addition of DMSO or BAM15 was able to reduce the elevated expression of Caspase-3 (green) in transportation. In addition, staining results indicated expression of Laminin (red) varied slightly in different groups. c Real-time PCR revealed dynamic expression changes of apoptotic-related genes NFκB, TNF-α and P53 in retinal tissue of 30 days. d Changes of NFκB, TNF-α, and P53 expression was assessed in retinal cups of 60 days by real-time PCR analysis. e Cell viability of retinal cups was assessed by CCK8 assay in transportation. Scale = 50 μm ( a ). Scale = 100 μm ( b ) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-019-1151-y'>30795805</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-ijcep0007-4827-f1.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®Identification of trabecular meshwork (TM) cells. (A-G) Representative images of TM cells from one of four cell lines established from the eyes of four donors. Cells from all four lines exhibited similar morphological and immunocytochemical features. The cells were observed by light microscopy (×40) (A) and transmission electron microscopy (×8,000) (B). Immunocytochemical staining of laminin (C) (×400), fibronectin (D) (×400), vimentin (E) (×400), neuron-specific enolase (F) (×400), and Factor VIII-associated antigen (G) (×400).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4152043/&orig_host=www.ncbi.nlm.nih.gov'>25197353</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03522-2-immunohistochemistry.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®<b> IHC analysis of Laminin using anti-Laminin antibody (A03522).
</b><br>Laminin was detected in paraffin-embedded section of mouse heart tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Laminin Antibody (A03522) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03522-3-immunohistochemistry.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®<b> IHC analysis of Laminin using anti-Laminin antibody (A03522).
</b><br>Laminin was detected in paraffin-embedded section of mouse kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Laminin Antibody (A03522) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03522-4-immunohistochemistry.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®<b> IHC analysis of Laminin using anti-Laminin antibody (A03522).
</b><br>Laminin was detected in paraffin-embedded section of rat cardiac muscle tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Laminin Antibody (A03522) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03522-5-immunohistochemistry.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband®<b> IHC analysis of Laminin using anti-Laminin antibody (A03522).
</b><br>Laminin was detected in paraffin-embedded section of rat kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Laminin Antibody (A03522) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-laminin-primary-antibodies-if-testing-6.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband® IF analysis of Laminin using anti-Laminin antibody (A03522). <br>
Laminin was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Laminin Antibody (A03522) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-laminin-primary-antibodies-if-testing-7.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband® IF analysis of Laminin using anti-Laminin antibody (A03522). <br>
Laminin was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Laminin Antibody (A03522) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-laminin-primary-antibodies-if-testing-8.jpgAnti-Laminin/Lamc1/Lamc2/Lamc3 Antibody Picoband® IF analysis of Laminin using anti-Laminin antibody (A03522). <br>
Laminin was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Laminin Antibody (A03522) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-leptin-picoband-trade-antibody-a00479-2-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00479-2-1-western-blotting.jpgAnti-Leptin Antibody Picoband®<b> Western blot analysis of Leptin using anti-Leptin antibody (A00479-2).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant rat Leptin protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Leptin antigen affinity purified polyclonal antibody (Catalog # A00479-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Leptin at approximately 16KD. The expected band size for Leptin is at 16KD.
https://www.bosterbio.com/products/primary-antibodies/anti-lyn-picoband-trade-antibody-a01424-2-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-1-western-blotting.jpgAnti-Lyn Antibody Picoband®<b> Western blot analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human 293T whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lyn antigen affinity purified polyclonal antibody (Catalog # A01424-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lyn at approximately 59KD. The expected band size for Lyn is at 59KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01424-2-ayn-primary-antibodies-wb-testing-2.jpg.pngAnti-Lyn Antibody Picoband®Western blot analysis of Lyn using anti-Lyn antibody (A01424-2).<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: Control group-mouse HT22 whole cell lysate,<br>
Lane 2: Low-dose drug treatment-mouse HT22 whole cell lysate,<br>
Lane 3: Medium-dose drug treatment-mouse HT22 whole cell lysate,<br>
Lane 4: High-dose drug treatment-mouse HT22 whole cell lysate.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lyn antigen affinity purified polyclonal antibody (Catalog # A01424-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:2000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for Lyn at approximately 59KD. The expected band size for Lyn is at 59KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-3-immunohistochemistry.jpgAnti-Lyn Antibody Picoband®<b> IHC analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br>Lyn was detected in paraffin-embedded section of rat lymphaden tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Lyn Antibody (A01424-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-2-immunohistochemistry.jpgAnti-Lyn Antibody Picoband®<b> IHC analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br>Lyn was detected in paraffin-embedded section of mouse spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Lyn Antibody (A01424-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-4-immunohistochemistry.jpgAnti-Lyn Antibody Picoband®<b> IHC analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br>Lyn was detected in paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Lyn Antibody (A01424-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-6-immunohistochemistry.jpgAnti-Lyn Antibody Picoband®<b> IHC analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br />Lyn was detected in paraffin-embedded section of rat spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Lyn Antibody (A01424-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01424-2-5-immunohistochemistry.jpgAnti-Lyn Antibody Picoband®<b> IHC analysis of Lyn using anti-Lyn antibody (A01424-2).
</b><br>Lyn was detected in paraffin-embedded section of mouse intestine tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Lyn Antibody (A01424-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-mak-picoband-trade-antibody-a00407-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00407-1-1-western-blotting.jpgAnti-MAK Antibody Picoband® Western blot analysis of MAK using anti-MAK antibody (A00407-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysate,<br>Lane 2: human MCF-7 whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAK antigen affinity purified polyclonal antibody (Catalog # A00407-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAK at approximately 70KD. The expected band size for MAK is at 70KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mek6-picoband-trade-antibody-a02011-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02011-map2k6-primary-antibodies-wb-testing-1.jpgAnti-MEK6/MAP2K6 Antibody Picoband® Western blot analysis of MKK6/MAP2K6 using anti-MKK6/MAP2K6 antibody (A02011). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human A549 whole cell lysates, <br>
Lane 3: rat C6 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MKK6/MAP2K6 antigen affinity purified polyclonal antibody (Catalog # A02011) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MKK6/MAP2K6 at approximately 38 kDa. The expected band size for MKK6/MAP2K6 is at 38 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-mavs-picoband-trade-antibody-a00169-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00169-1-5-immunohistochemistry.jpgAnti-MAVS Antibody Picoband®<b> IHC analysis of MAVS using anti-MAVS antibody (A00169-1).</b><br>MAVS was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MAVS Antibody (A00169-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00169-1-4-immunohistochemistry.jpgAnti-MAVS Antibody Picoband®<b> IHC analysis of MAVS using anti-MAVS antibody (A00169-1).</b><br>MAVS was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MAVS Antibody (A00169-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00169-1-2-immunohistochemistry.jpgAnti-MAVS Antibody Picoband®<b> IHC analysis of MAVS using anti-MAVS antibody (A00169-1).</b><br>MAVS was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MAVS Antibody (A00169-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00169-1-3-immunohistochemistry.jpgAnti-MAVS Antibody Picoband®<b> IHC analysis of MAVS using anti-MAVS antibody (A00169-1).</b><br>MAVS was detected in paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MAVS Antibody (A00169-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00169-1-1-western-blotting.jpgAnti-MAVS Antibody Picoband® Western blot analysis of MAVS using anti-MAVS antibody (A00169-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAVS antigen affinity purified polyclonal antibody (Catalog # A00169-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAVS at approximately 75KD. The expected band size for MAVS is at 57KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00169-1-6-flow-cytometry.pngAnti-MAVS Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-MAVS antibody (A00169-1). <br> Overlay histogram showing A431 cells stained with A00169-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAVS Antibody (A00169-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-myoglobin-picoband-trade-antibody-a04058-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04058-myoglobin-primary-antibodies-wb-testing-1.jpgAnti-Myoglobin/MB Antibody Picoband® Western blot analysis of Myoglobin using anti-Myoglobin antibody (A04058). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates,<br>
Lane 2: rat skeletal muscle tissue lysates,<br>
Lane 3: mouse heart tissue lysates,<br>
Lane 4: mouse skeletal muscle tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Myoglobin antigen affinity purified polyclonal antibody (Catalog # A04058) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Myoglobin at approximately 17 kDa. The expected band size for Myoglobin is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04058-mb-primary-antibodies-ihc-testing-4.jpgAnti-Myoglobin/MB Antibody Picoband®IHC analysis of Myoglobin/MB using anti-Myoglobin/MB antibody (A04058). <br>Myoglobin/MB was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Myoglobin/MB Antibody (A04058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04058-myoglobin-primary-antibodies-ihc-testing-2.jpgAnti-Myoglobin/MB Antibody Picoband® IHC analysis of Myoglobin using anti-Myoglobin antibody (A04058). <br>
Myoglobin was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Myoglobin Antibody (A04058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04058-myoglobin-primary-antibodies-ihc-testing-3.jpgAnti-Myoglobin/MB Antibody Picoband® IHC analysis of Myoglobin using anti-Myoglobin antibody (A04058). <br>
Myoglobin was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Myoglobin Antibody (A04058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-notch1-picoband-trade-antibody-a00033-2-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00033-2-1-western-blotting.jpgAnti-Notch1 Antibody Picoband®<b> Western blot analysis of Notch1 using anti-Notch1 antibody (A00033-2). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse skeletal muscle tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Notch1 antigen affinity purified polyclonal antibody (Catalog # A00033-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Notch1 at approximately 272KD. The expected band size for Notch1 is at 272KD.
https://www.bosterbio.com/products/primary-antibodies/anti-nov-ccn3-picoband-trade-antibody-a06319-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06319-1-2-immunohistochemistry.jpgAnti-NOV/CCN3 Antibody Picoband®<b> IHC analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1).</b><br>NOV/CCN3 was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NOV/CCN3 Antibody (A06319-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06319-1-1-western-blotting.jpgAnti-NOV/CCN3 Antibody Picoband® Western blot analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOV/CCN3 antigen affinity purified polyclonal antibody (Catalog # A06319-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOV/CCN3 at approximately 47KD. The expected band size for NOV/CCN3 is at 39KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06319-1-3-immunohistochemistry.jpgAnti-NOV/CCN3 Antibody Picoband®<b> IHC analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1).</b><br>NOV/CCN3 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NOV/CCN3 Antibody (A06319-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06319-1-4-immunohistochemistry.jpgAnti-NOV/CCN3 Antibody Picoband®<b> IHC analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1).</b><br>NOV/CCN3 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NOV/CCN3 Antibody (A06319-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06319-1-5-immunohistochemistry.jpgAnti-NOV/CCN3 Antibody Picoband®<b> IHC analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1).</b><br>NOV/CCN3 was detected in paraffin-embedded section of rat kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NOV/CCN3 Antibody (A06319-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06319-1-nov-ccn3-primary-antibodies-if-testing-6.jpgAnti-NOV/CCN3 Antibody Picoband® IF analysis of NOV/CCN3 using anti-NOV/CCN3 antibody (A06319-1). <br>
NOV/CCN3 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-NOV/CCN3 Antibody (A06319-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06319-1-nov-ccn3-primary-antibodies-fcm-testing-7.jpgAnti-NOV/CCN3 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-NOV/CCN3 antibody (A06319-1).<br>Overlay histogram showing U87 cells stained with A06319-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOV/CCN3 Antibody (A06319-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-npas2-picoband-trade-antibody-a02688-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02688-1-1-western-blotting.jpgAnti-NPAS2 Antibody Picoband®<b> Western blot analysis of NPAS2 using anti-NPAS2 antibody (A02688-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate,<br>Lane 3: human COLO-320 whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPAS2 antigen affinity purified polyclonal antibody (Catalog # A02688-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPAS2 at approximately 92KD. The expected band size for NPAS2 is at 92KD.
https://www.bosterbio.com/products/primary-antibodies/anti-nr1h4-picoband-trade-antibody-a00835-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00835-1-nr1h4-primary-antibodies-wb-testing-1.jpgAnti-Bile Acid Receptor NR1H4 Antibody Picoband® Western blot analysis of NR1H4 using anti-NR1H4 antibody (A00835-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HCCT tissue lysates, <br>
Lane 2: human HCCP tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR1H4 antigen affinity purified polyclonal antibody (Catalog # A00835-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NR1H4 at approximately 56 kDa. The expected band size for NR1H4 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00835-1-nr1h4-primary-antibodies-if-testing-2.jpgAnti-Bile Acid Receptor NR1H4 Antibody Picoband® IF analysis of NR1H4 using anti-NR1H4 antibody (A00835-1). <br>
NR1H4 was detected in immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-NR1H4 Antibody (A00835-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00835-1-nr1h4-primary-antibodies-fcm-testing-3.jpgAnti-Bile Acid Receptor NR1H4 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti- NR1H4 antibody (A00835-1). <br>Overlay histogram showing A549 cells stained with A00835-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti- NR1H4 Antibody (A00835-1, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-lox-1-olr1-picoband-trade-antibody-a00760-1-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00760-1-1-western-blotting.jpgAnti-LOX-1/OLR1 Antibody Picoband®<b> Western blot analysis of LOX-1/OLR1 using anti-LOX-1/OLR1 antibody (A00760-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX-1/OLR1 antigen affinity purified polyclonal antibody (Catalog # A00760-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX-1/OLR1 at approximately 38KD. The expected band size for LOX-1/OLR1 is at 31KD.
https://www.bosterbio.com/products/primary-antibodies/anti-pah-picoband-trade-antibody-a00761-1-boster.html2026-04-03T05:00:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-41598_2021_86663_fig1_html.pngAnti-PAH Antibody Picoband®Creation of a Pah -KO mouse model. ( A ) The mouse genomic locus on chromosome 10 and the murine targeted allele after CRISPR gene editing are shown. Exon 1 contains the translation initiation codon. NCBI GeneID: 18478; RefSeq transcript: NM_008777. Exon 1 sequence is shadowed gray, the start codon (ATG) is framed, gRNA is shown as white letters on a black background, the asterisks and arrow indicate the position of PAM and G>T transition. The donor oligo for CRISPR targeting is in bold and underlined. ( B ) Sequencing genomic DNA samples of the founder 5349. The point mutation of G to T is indicated in the black boxes. ( C ) Western blot analyses to detect PAH protein in liver or kidney of wildtype (wt) or Hom (ko) mice. Solubilized proteins (60 µg) from mouse liver or kidney were fractionated and immune-blotted with an anti-PAH antibody. The PAH protein (red; expected size 50 kDa) is evident in wildtype mice (lanes 1, 3, 5 and 7) but is absent in Hom mice (2, 4, 6 and 8); lanes 1, 2, 5, 6) are from kidney; lanes 3, 4, 7, 8 are from liver. Equal loading is indicated by probing with antibody to beta-actin (green). M, molecular weight marker lane (bands not visible in this image). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-021-86663-8'>33790381</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-41598_2021_86663_fig2_html.pngAnti-PAH Antibody Picoband®Characterization of Hom and Het Pah -KO mice for 6 months. ( A ) The Hom mice showed lower bodyweights than the Het mice throughout the study ( B ) Summary of blood Phe at various timepoints is shown (n = 7/group) ( C ) Summary of blood Tyr at various timepoints is shown (n = 7/group). The graphical data are represented as mean ± SD (Phe and Tyr levels in Hom vs Het mice p < 0.0001) (n = 7 mice/group). ( D ) Western blot analysis of liver homogenate using anti-PAH antibody is shown. Note the lack of PAH protein in the Hom mice whereas Het mice showed a corresponding band (~ 50 kDa) for mouse PAH protein. Each lane contained 135 µg protein. Beta actin was used as an internal control. Full-length blots/gels are presented in Supplementary Fig. 2. ( E ) Summary of % PAH positive hepatocytes in the Hom and Het mice are shown. The graphical data are represented as mean ± SD (** p = 0.0012). ( F ) Representative liver and kidney PAH-IHC images show lack of IHC signal in a Hom mouse whereas liver from a Het mouse exhibit strong IHC signal in hepatocytes, mostly in the centrilobular region. Renal cortical epithelial cells from a Hom mouse show no IHC signal as compared to Het mouse, where most proximal convoluted tubular epithelium exhibit strong signal. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-021-86663-8'>33790381</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-41598_2021_86663_fig4_html.pngAnti-PAH Antibody Picoband®Analysis of Phe, Tyr and neurotransmitters in brains of Hom and Het Pah -KO mice at 6 months. Scatter plot charts show brain Phe, Tyr, serotonin, dopamine, L-DOPA, DOPAC, NE, 5-HIAA, and HVA. n = 6 Hom, 7 Het. Bars indicate group mean and the error bars indicate standard deviation (* p = 0.01, ** p = 0.003—0.007, *** p = 0.0001, **** p < 0.0001). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-021-86663-8'>33790381</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-41598_2021_86663_fig7_html.pngAnti-PAH Antibody Picoband®Hair coat color in Hom- Pah KO mice. The difference in hair coat color is grossly visible ( A ). Hair coat of the Hom mouse is light brown whereas it is dark brown for the Het mouse. ( B ) Hair shafts from the Hom mouse contain less melanin pigment when compared to the Het mouse. H&E stain 20× ( C ) Summary of hair melanin scores is shown in the scatter plot graph. n = 7 Hom, 7 Het. Bars indicate group median score and the error bars indicate range (*** p = 0.0006). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-021-86663-8'>33790381</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-pah-primary-antibodies-wb-testing-1_1.jpgAnti-PAH Antibody Picoband® Western blot analysis of PAH using anti-PAH antibody (A00761-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: rat kidney tissue lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse kidney tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAH antigen affinity purified polyclonal antibody (Catalog # A00761-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAH at approximately 45 kDa. The expected band size for PAH is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-pah-primary-antibodies-ihc-testing-2.jpgAnti-PAH Antibody Picoband® IHC analysis of PAH using anti-PAH antibody (A00761-1). <br>
PAH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAH Antibody (A00761-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-pah-primary-antibodies-ihc-testing-3.jpgAnti-PAH Antibody Picoband® IHC analysis of PAH using anti-PAH antibody (A00761-1). <br>
PAH was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAH Antibody (A00761-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-pah-primary-antibodies-ihc-testing-4.jpgAnti-PAH Antibody Picoband® IHC analysis of PAH using anti-PAH antibody (A00761-1). <br>
PAH was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAH Antibody (A00761-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00761-1-pah-primary-antibodies-fcm-testing-5.jpgAnti-PAH Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PAH antibody (A00761-1). <br>
Overlay histogram showing HepG2 cells stained with A00761-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAH Antibody (A00761-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-pdcd4-antibody-a01105-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01105-pdcd4-primary-antibodies-wb-testing-1.jpgAnti-PDCD4 Antibody Picoband® Western blot analysis of PDCD4 using anti-PDCD4 antibody (A01105). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Daudi whole cell lysates, <br>
Lane 2: human Hela whole cell lysates, <br>
Lane 3: human 293T whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDCD4 antigen affinity purified polyclonal antibody (Catalog # A01105) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDCD4 at approximately 60 kDa. The expected band size for PDCD4 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01105-pdcd4-primary-antibodies-ihc-testing-2.jpgAnti-PDCD4 Antibody Picoband® IHC analysis of PDCD4 using anti-PDCD4 antibody (A01105). <br>
PDCD4 was detected in a paraffin-embedded section of human appendiceal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDCD4 Antibody (A01105) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01105-pdcd4-primary-antibodies-ihc-testing-3.jpgAnti-PDCD4 Antibody Picoband® IHC analysis of PDCD4 using anti-PDCD4 antibody (A01105). <br>
PDCD4 was detected in a paraffin-embedded section of human gall bladder adenosquamous carcinomaa tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDCD4 Antibody (A01105) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01105-pdcd4-primary-antibodies-ihc-testing-4.jpgAnti-PDCD4 Antibody Picoband® IHC analysis of PDCD4 using anti-PDCD4 antibody (A01105). <br>
PDCD4 was detected in a paraffin-embedded section of human gastric adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDCD4 Antibody (A01105) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01105-pdcd4-primary-antibodies-fcm-testing-5_1.jpgAnti-PDCD4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PDCD4 antibody (A01105). <br>Overlay histogram showing HepG2 cells stained with A01105 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDCD4 Antibody (A01105, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ppar-gamma-picoband-trade-antibody-a00449-2-boster.html2026-03-24T05:10:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00449-2-pparg-primary-antibodies-wb-testing-1.jpgAnti-PPAR gamma/PPARG Antibody Picoband® Western blot analysis of PPAR gamma using anti-PPAR gamma antibody (A00449-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPAR gamma antigen affinity purified polyclonal antibody (Catalog # A00449-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPAR gamma at approximately 58 kDa. The expected band size for PPAR gamma is at 58 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-preb-picoband-trade-antibody-a04946-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04946-1-western-blotting.jpgAnti-PREB Antibody Picoband®<b> Western blot analysis of PREB using anti-PREB antibody (A04946).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysate,<br>Lane 2: human placenta tissue lysate,<br>Lane 3: human A549 whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PREB antigen affinity purified polyclonal antibody (Catalog # A04946) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PREB at approximately 45KD. The expected band size for PREB is at 45KD.
https://www.bosterbio.com/products/primary-antibodies/anti-prom1-picoband-trade-antibody-a01767-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01767-1-western-blotting.jpgAnti-PROM1 Antibody Picoband®<b> Western blot analysis of PROM1 using anti-PROM1 antibody (A01767).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat liver tissue lysate,<br>Lane 2: mouse liver tissue lysate,<br>Lane 3: human MCF-7 whole cell lysate,<br>Lane 4: human COLO-320 whole cell lysate,<br>Lane 5: human Hela whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PROM1 antigen affinity purified polyclonal antibody (Catalog # A01767) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PROM1 at approximately 130KD. The expected band size for PROM1 is at 97KD.
https://www.bosterbio.com/products/primary-antibodies/anti-pten-antibody-a00006-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00006-1-1-western-blotting.jpgAnti-PTEN Antibody Picoband®<b> Western blot analysis of PTEN using anti-PTEN antibody (A00006-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse liver tissue lysate,<br>Lane 3: human A549 whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified polyclonal antibody (Catalog # A00006-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTEN at approximately 54KD. The expected band size for PTEN is at 47KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ptp1b-picoband-trade-antibody-a00613-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00613-1-ptp1b-primary-antibodies-wb-testing-1.jpgAnti-PTP1B/PTPN1 Antibody Picoband® Western blot analysis of PTP1B/PTPN1 using anti-PTP1B/PTPN1 antibody (A00613-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human CACO-2 whole cell lysates, <br>
Lane 3: human A431 whole cell lysates, <br>
Lane 4: human K562 whole cell lysates, <br>
Lane 5: rat testis tissue lysates, <br>
Lane 6: mouse testis tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTP1B/PTPN1 antigen affinity purified polyclonal antibody (A00613-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTP1B/PTPN1 at approximately 50 kDa. The expected band size for PTP1B/PTPN1 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00613-1-ptp1b-primary-antibodies-ihc-testing-2_1.jpgAnti-PTP1B/PTPN1 Antibody Picoband® IHC analysis of PTP1B/PTPN1 using anti-PTP1B/PTPN1 antibody (A00613-1). <br>PTP1B/PTPN1 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTP1B/PTPN1 Antibody (A00613-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00613-1-ptp1b-primary-antibodies-fcm-testing-3.jpgAnti-PTP1B/PTPN1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-PTP1B/PTPN1 antibody (A00613-1). <br>
Overlay histogram showing A549 cells stained with A00613-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTP1B/PTPN1 Antibody (A00613-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-raf1-picoband-trade-antibody-a00446-1-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00446-1-1-western-blotting_1.jpgAnti-Raf1 Antibody Picoband® Western blot analysis of Raf1 using anti-Raf1 antibody (A00446-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysate,<br>Lane 2: mouse kidney tissue lysate,<br>Lane 3: human MCF-7 whole cell lysate,<br>Lane 4: human 22RV1 whole cell lysate,<br>Lane 5: human Hela whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Raf1 antigen affinity purified polyclonal antibody (Catalog # A00446-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Raf1 at approximately 73KD. The expected band size for Raf1 is at 73KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00446-1-raf1-primary-antibodies-fc-testing-2.jpg.pngAnti-Raf1 Antibody Picoband® Flow Cytometry analysis of HeLa cells using anti-Raf1 antibody (A00446-1). <br> Overlay histogram showing HeLa cells stained with PB10089 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Raf1 Antibody (A00446-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ran-picoband-trade-antibody-a00204-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00204-1-ran-primary-antibodies-wb-testing-1.jpgAnti-Ran Antibody Picoband® Western blot analysis of Ran using anti-Ran antibody (A00204-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse thymus tissue lysates,<br>
Lane 8: mouse A20 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ran antigen affinity purified polyclonal antibody (Catalog # A00204-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ran at approximately 24 kDa. The expected band size for Ran is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00204-1-5-immunohistochemistry.jpgAnti-Ran Antibody Picoband®<b> IHC analysis of Ran using anti-Ran antibody (A00204-1).</b><br>Ran was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00204-1-6-immunohistochemistry.jpgAnti-Ran Antibody Picoband®<b> IHC analysis of Ran using anti-Ran antibody (A00204-1).</b><br>Ran was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00204-1-4-immunohistochemistry.jpgAnti-Ran Antibody Picoband®<b> IHC analysis of Ran using anti-Ran antibody (A00204-1).</b><br>Ran was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00204-1-2-immunohistochemistry.jpgAnti-Ran Antibody Picoband®<b> IHC analysis of Ran using anti-Ran antibody (A00204-1).</b><br>Ran was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00204-1-3-immunohistochemistry.jpgAnti-Ran Antibody Picoband®<b> IHC analysis of Ran using anti-Ran antibody (A00204-1).</b><br>Ran was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00204-1-7-immunofluorescence.jpg.jpgAnti-Ran Antibody Picoband® IF analysis of Ran using anti-Ran antibody (A00204-1) <br> Ran was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Ran Antibody (A00204-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00204-1-ran-primary-antibodies-fc-testing-8.pngAnti-Ran Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-Ran antibody (A00204-1). <br> Overlay histogram showing A431 cells stained with A00204-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Ran Antibody (A00204-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00204-1-ran-primary-antibodies-fc-testing-9.pngAnti-Ran Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-Ran antibody (A00204-1). <br> Overlay histogram showing U937 cells stained with A00204-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Ran Antibody (A00204-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00204-1-ran-primary-antibodies-ip-testing-10.jpgAnti-Ran Antibody Picoband® Immunoprecipitating Ran in HepG2 whole cell lysate.<br>Western blot analysis of Ran using anti-Ran antibody (A00204-1).<br>Lane 1: HepG2 whole cell lysates (30ug)<br>Lane 2: Rabbit control IgG instead of anti-Ran antibody in HepG2 whole cell lysate.<br>Lane 3: anti-Ran antibody (2μg) + HepG2 whole cell lysate (500μg)<br>After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Ran antigen affinity purified polyclonal antibody (A00204-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for Ran at approximately 24 kDa. The expected band size for Ran is at 24 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ranbp2-picoband-trade-antibody-a00981-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00981-1-western-blotting.jpgAnti-RanBP2 Antibody Picoband®<b> Western blot analysis of RanBP2 using anti-RanBP2 antibody (A00981).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RanBP2 antigen affinity purified polyclonal antibody (Catalog # A00981) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RanBP2 at approximately 270KD. The expected band size for RanBP2 is at 358KD.
https://www.bosterbio.com/products/primary-antibodies/anti-rnd1-picoband-trade-antibody-a06347-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06347-1-western-blotting.jpgAnti-RND1 Antibody Picoband®<b> Western blot analysis of RND1 using anti-RND1 antibody (A06347).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse liver tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RND1 antigen affinity purified polyclonal antibody (Catalog # A06347) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RND1 at approximately 26KD. The expected band size for RND1 is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-syndecan-1-sdc1-picoband-trade-antibody-a00991-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00991-1-1-western-blotting.jpgAnti-Syndecan-1/SDC1 Antibody Picoband®<b> Western blot analysis of Syndecan-1/SDC1 using anti-Syndecan-1/SDC1 antibody (A00991-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syndecan-1/SDC1 antigen affinity purified polyclonal antibody (Catalog # A00991-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Syndecan-1/SDC1 at approximately 60KD. The expected band size for Syndecan-1/SDC1 is at 32KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd62l-picoband-trade-antibody-a00652-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00652-1-western-blotting.jpgAnti-CD62L/SELL Antibody Picoband®<b> Western blot analysis of CD62L using anti-CD62L antibody (A00652).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human CD62L protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD62L antigen affinity purified polyclonal antibody (Catalog # A00652) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD62L at approximately 90KD. The expected band size for CD62L is at 60KD.
https://www.bosterbio.com/products/primary-antibodies/anti-six3-picoband-trade-antibody-a02604-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02604-1-western-blotting.jpgAnti-Six3 Antibody Picoband®<b> Western blot analysis of Six3 using anti-Six3 antibody (A02604).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Six3 antigen affinity purified polyclonal antibody (Catalog # A02604) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Six3 at approximately 35KD. The expected band size for Six3 is at 35KD.
https://www.bosterbio.com/products/primary-antibodies/anti-six6-picoband-trade-antibody-a06502-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06502-1-1-western-blotting.jpgAnti-Homeobox protein SIX6 Antibody Picoband®<b> Western blot analysis of SIX6 using anti-SIX6 antibody (A06502-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIX6 antigen affinity purified polyclonal antibody (Catalog # A06502-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIX6 at approximately 28KD. The expected band size for SIX6 is at 28KD.
https://www.bosterbio.com/products/primary-antibodies/anti-slc6a1-antibody-a05109-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-wb-testing-1.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®Western blot analysis of SLC6A1 using anti-SLC6A1 antibody (A05109). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC6A1 antigen affinity purified polyclonal antibody (Catalog # A05109) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC6A1 at approximately 67 kDa. The expected band size for SLC6A1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-ihc-testing-1.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®IHC analysis of SLC6A1 using anti-SLC6A1 antibody (A05109. <br>SLC6A1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A1 Antibody (A05109) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-ihc-testing-2.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®IHC analysis of SLC6A1 using anti-SLC6A1 antibody (A05109. <br>SLC6A1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A1 Antibody (A05109) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-ihc-testing-3.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®IHC analysis of SLC6A1 using anti-SLC6A1 antibody (A05109. <br>SLC6A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A1 Antibody (A05109) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-if-testing-1.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®IF analysis of SLC6A1 using anti-SLC6A1 antibody (A05109). <br>
SLC6A1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC6A1 Antibody (A05109) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-slc6a1-primary-antibodies-if-testing-2.jpgAnti-GABA Transporter 1/GAT 1/SLC6A1 Antibody Picoband®IF analysis of SLC6A1 using anti-SLC6A1 antibody (A05109). <br>
SLC6A1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC6A1 Antibody (A05109) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-slc7a3-picoband-trade-antibody-a09720-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09720-1-1-western-blotting.jpgAnti-SLC7A3 Antibody Picoband®<b> Western blot analysis of SLC7A3 using anti-SLC7A3 antibody (A09720-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human A431 whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC7A3 antigen affinity purified polyclonal antibody (Catalog # A09720-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC7A3 at approximately 67KD. The expected band size for SLC7A3 is at 67KD.
https://www.bosterbio.com/products/primary-antibodies/anti-sry-picoband-trade-antibody-a00614-1-boster.html2026-03-24T05:10:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00614-1-1-western-blotting.jpgAnti-SRY Antibody Picoband® Western blot analysis of SRY using anti-SRY antibody (A00614-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SRY antigen affinity purified polyclonal antibody (Catalog # A00614-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SRY at approximately 26KD. The expected band size for SRY is at 24KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tff1-picoband-trade-antibody-a01391-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01391-tff1-primary-antibodies-wb-testing-1.jpgAnti-Estrogen Inducible Protein pS2/Tff1 Antibody Picoband® Western blot analysis of Tff1 using anti-Tff1 antibody (A01391). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse stomach tissue lysates, <br>
Lane 2: mouse stomach tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tff1 antigen affinity purified polyclonal antibody (Catalog # A01391) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tff1 at approximately 17 kDa. The expected band size for Tff1 is at 9 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01391-tff1-primary-antibodies-ihc-testing-2.jpgAnti-Estrogen Inducible Protein pS2/Tff1 Antibody Picoband® IHC analysis of Tff1 using anti-Tff1 antibody (A01391). <br>
Tff1 was detected in a paraffin-embedded section of mouse gaster tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Tff1 Antibody (A01391) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tnfrsf18-picoband-trade-antibody-a03125-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03125-1-1-western-blotting.jpgAnti-TNFRSF18 Antibody Picoband® Western blot analysis of TNFRSF18 using anti-TNFRSF18 antibody (A03125-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysate,<br>Lane 2: mouse kidney tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNFRSF18 antigen affinity purified polyclonal antibody (Catalog # A03125-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNFRSF18 at approximately 28KD. The expected band size for TNFRSF18 is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-traf5-picoband-trade-antibody-a03076-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03076-1-1-western-blotting.jpgAnti-TRAF5 Antibody Picoband®<b> Western blot analysis of TRAF5 using anti-TRAF5 antibody (A03076-1).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat ovary tissue lysate,<br>Lane 2: mouse testis tissue lysate,<br>Lane 3: mouse thymus tissue lysate,<br>Lane 4: human MCF-7 whole cell lysate,<br>Lane 5: human A549 whole cell lysate,<br>Lane 6: human Hela whole cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAF5 antigen affinity purified polyclonal antibody (Catalog # A03076-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRAF5 at approximately 64KD. The expected band size for TRAF5 is at 64KD.
https://www.bosterbio.com/products/primary-antibodies/anti-trpc6-picoband-trade-antibody-a00625-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00625-1-western-blotting.jpgAnti-TRPC6 Antibody Picoband®<b> Western blot analysis of TRPC6 using anti-TRPC6 antibody (A00625).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat ovary tissue lysate,<br>Lane 2: mouse lung tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRPC6 antigen affinity purified polyclonal antibody (Catalog # A00625) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRPC6 at approximately 106KD. The expected band size for TRPC6 is at 106KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00625-trpc6-primary-antibodies-wb-testing-2.jpgAnti-TRPC6 Antibody Picoband® Western blot analysis of TRPC6 using anti-TRPC6 antibody (A00625). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRPC6 antibody (A00625) at 1:200 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using a fluorescent. A specific band was detected for TRPC6 at approximately 106 kDa. The expected band size for TRPC6 is at 106 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-ucp2-picoband-trade-antibody-a02256-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02256-1-1-western-blotting.jpgAnti-UCP2 Antibody Picoband®<b> Western blot analysis of UCP2 using anti-UCP2 antibody (A02256-1). </b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysate,<br>Lane 2: rat cardiac muscle tissue lysate,<br>Lane 3: rat brain tissue lysate,<br>Lane 4: mouse spleen tissue lysate,<br>Lane 5: mouse cardiac muscle tissue lysate,<br>Lane 6: mouse brain tissue lysate,<br>Lane 7: human Hela whole cell lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UCP2 antigen affinity purified polyclonal antibody (Catalog # A02256-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for UCP2 at approximately 33KD. The expected band size for UCP2 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-chx10-picoband-trade-antibody-a05180-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05180-1-western-blotting.jpgAnti-CHX10/VSX2 Antibody Picoband®<b> Western blot analysis of CHX10 using anti-CHX10 antibody (A05180).
</b><br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse eye ball tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHX10 antigen affinity purified polyclonal antibody (Catalog # A05180) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHX10 at approximately 43KD. The expected band size for CHX10 is at 39KD.
https://www.bosterbio.com/products/primary-antibodies/anti-xanthine-oxidase-picoband-trade-antibody-a01884-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01884-2-immunohistochemistry.jpgAnti-Xanthine Oxidase/XDH Antibody Picoband®<b> IHC analysis of Xanthine Oxidase using anti-Xanthine Oxidase antibody (A01884).</b><br>Xanthine Oxidase was detected in paraffin-embedded section of mouse intestine tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Xanthine Oxidase Antibody (A01884) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01884-3-immunohistochemistry.jpgAnti-Xanthine Oxidase/XDH Antibody Picoband®<b> IHC analysis of Xanthine Oxidase using anti-Xanthine Oxidase antibody (A01884).</b><br>Xanthine Oxidase was detected in paraffin-embedded section of rat intestine tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Xanthine Oxidase Antibody (A01884) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-1-western-blotting.jpgAnti-Xanthine Oxidase/XDH Antibody Picoband® Western blot analysis of Xanthine Oxidase using anti-Xanthine Oxidase antibody (A01884). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysate,<br>Lane 2: mouse liver tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Xanthine Oxidase antigen affinity purified polyclonal antibody (Catalog # A01884) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Xanthine Oxidase at approximately 146KD. The expected band size for Xanthine Oxidase is at 146KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-4-flow-cytometry.pngAnti-Xanthine Oxidase/XDH Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-Xanthine Oxidase antibody (A01884). <br> Overlay histogram showing A431 cells stained with A01884 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Xanthine Oxidase Antibody (A01884,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-exportin-5-picoband-trade-antibody-a02900-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02900-xpo5-primary-antibodies-wb-testing-1.jpgAnti-Exportin-5/XPO5 Antibody Picoband® Western blot analysis of Exportin-5/XPO5 using anti-Exportin-5/XPO5 antibody (A02900). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human K562 whole cell lysates, <br>
Lane 3: human HEL whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Exportin-5/XPO5 antigen affinity purified polyclonal antibody (Catalog # A02900) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Exportin-5/XPO5 at approximately 136 kDa. The expected band size for Exportin-5/XPO5 is at 136 kDa.
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-mouse-fgf2-protein-r00121-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Mouse FGF2 ProteinBoster Kit Box
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-human-osm-protein-r00804-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Human OSM ProteinBoster Kit Box
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-human-cntf-protein-r00609-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Human CNTF ProteinBoster Kit Box
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-mouse-fgf7-protein-r01931-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Mouse FGF7 ProteinBoster Kit Box
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-human-ifn-gamma-protein-r00393-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Human IFN gamma ProteinBoster Kit Box
https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/ez-set-accessory-kit-eza001-boster.html2026-03-24T05:10:07+00:00daily0.9
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-mouse-lif-protein-r01400-1-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Mouse LIF ProteinBoster Kit Box
https://www.bosterbio.com/products/all-recombinant-proteins/recombinant-human-tnf-alpha-protein-r00002-boster.html2026-03-24T05:10:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngRecombinant Human TNF alpha ProteinBoster Kit Box
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-polr2a-ser1619-antibody-p30431-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30431-polr2a-primary-antibodies-wb-testing-4.jpgAnti-Phospho POLR2A (Ser1619) AntibodyWestern blot analysis of VEC using p-Rpb1 (S1619) antibody. Antibody was diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30431-polr2a-primary-antibodies-elisa-testing-1.jpgAnti-Phospho POLR2A (Ser1619) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using POLR2A (Phospho-Ser1619) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30431-polr2a-primary-antibodies-if-testing-2.jpgAnti-Phospho POLR2A (Ser1619) AntibodyImmunofluorescence analysis of HeLa cells treated with PMA 125ng/ml 30', using POLR2A (Phospho-Ser1619) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30431-polr2a-primary-antibodies-ihc-testing-3.jpgAnti-Phospho POLR2A (Ser1619) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using POLR2A (Phospho-Ser1619) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30431-polr2a-primary-antibodies-wb-testing-5.jpgAnti-Phospho POLR2A (Ser1619) AntibodyWestern blot analysis of lysates from COS7 cells treated with EGF 200ng/ml 30', using POLR2A (Phospho-Ser1619) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-grf-1-tyr1105-antibody-p30433-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30433-arhgap35-primary-antibodies-ihc-testing-1.jpgAnti-Phospho GRF-1 (Tyr1105) AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30433-arhgap35-primary-antibodies-wb-testing-3.jpgAnti-Phospho GRF-1 (Tyr1105) AntibodyWestern Blot analysis of 3T3 cells using Phospho-GRF-1 (Y1105) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30433-arhgap35-primary-antibodies-ihc-testing-2.jpgAnti-Phospho GRF-1 (Tyr1105) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using GRF-1 (Phospho-Tyr1105) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30433-arhgap35-primary-antibodies-wb-testing-4.jpgAnti-Phospho GRF-1 (Tyr1105) AntibodyWestern blot analysis of lysates from 293 cells treated with EGF 200ng/ml 30', using GRF-1 (Phospho-Tyr1105) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-cd3-zeta-tyr142-antibody-p02421-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02421-cd247-primary-antibodies-elisa-testing-1.jpgAnti-Phospho CD3 zeta (Tyr142) CD247 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using CD3 zeta (Phospho-Tyr142) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02421-cd247-primary-antibodies-wb-testing-2.jpgAnti-Phospho CD3 zeta (Tyr142) CD247 AntibodyWestern blot analysis of lysates from Jurkat cells treated with UV 15', using CD3 zeta (Phospho-Tyr142) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-rhodopsin-ser334-antibody-p30435-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30435-rho-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Rhodopsin (Ser334) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Rhodopsin (Phospho-Ser334) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30435-rho-primary-antibodies-ihc-testing-2.jpgAnti-Phospho Rhodopsin (Ser334) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using Rhodopsin (Phospho-Ser334) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tk-ser13-antibody-p04850-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04850-tk1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho TK (Ser13) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using TK (Phospho-Ser13) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04850-tk1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho TK (Ser13) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using TK (Phospho-Ser13) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04850-tk1-primary-antibodies-wb-testing-3.jpgAnti-Phospho TK (Ser13) AntibodyWestern blot analysis of lysates from HeLa cells treated with paclitaxel 1uM 24h, using TK (Phospho-Ser13) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-p40-phox-thr154-antibody-p04208-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04208-ncf4-primary-antibodies-elisa-testing-1.jpgAnti-Phospho p40 phox (Thr154) NCF4 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using p40 phox (Phospho-Thr154) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04208-ncf4-primary-antibodies-ihc-testing-2.jpgAnti-Phospho p40 phox (Thr154) NCF4 AntibodyImmunohistochemistry analysis of paraffin-embedded human ovary, using p40 phox (Phospho-Thr154) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-pkd1-2-3-pkc-mu-ser738-ser742-antibody-p30439-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30439-prkd1-primary-antibodies-wb-testing-3.jpgAnti-Phospho PKD1/2/3/PKC mu (Ser738+Ser742) PRKD1 AntibodyWestern Blot analysis of A549 cells using Phospho-PKD1/2/3 (S738/S742) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30439-prkd1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho PKD1/2/3/PKC mu (Ser738+Ser742) PRKD1 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PKD1/2/3/PKC mu (Phospho-Ser738+Ser742) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30439-prkd1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho PKD1/2/3/PKC mu (Ser738+Ser742) PRKD1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart, using PKD1/2/3/PKC mu (Phospho-Ser738+Ser742) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30439-prkd1-primary-antibodies-wb-testing-4.jpgAnti-Phospho PKD1/2/3/PKC mu (Ser738+Ser742) PRKD1 AntibodyWestern blot analysis of lysates from A549 cells treated with PMA 125ng/ml 30' and HT29 cells treated with serum 20% 15', using PKD1/2/3/PKC mu (Phospho-Ser738+Ser742) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-pld1-ser561-antibody-p02031-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02031-pld1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho PLD1 (Ser561) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PLD1 (Phospho-Ser561) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02031-pld1-primary-antibodies-if-testing-2.jpgAnti-Phospho PLD1 (Ser561) AntibodyImmunofluorescence analysis of HepG2 cells, using PLD1 (Phospho-Ser561) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02031-pld1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho PLD1 (Ser561) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using PLD1 (Phospho-Ser561) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-ras-grf1-ser916-antibody-p03338-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03338-rasgrf1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Ras-GRF1 (Ser916) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Ras-GRF1 (Phospho-Ser916) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03338-rasgrf1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho Ras-GRF1 (Ser916) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using Ras-GRF1 (Phospho-Ser916) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-pfkfb2-ser483-antibody-p30440-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30440-pfkfb2-primary-antibodies-wb-testing-3.jpgAnti-Phospho PFKFB2 (Ser483) AntibodyWestern Blot analysis of Hela cells using Phospho-PFK-2 car (S483) Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30440-pfkfb2-primary-antibodies-wb-testing-4.jpgAnti-Phospho PFKFB2 (Ser483) AntibodyWestern Blot analysis of various cells using Phospho-PFK-2 car (S483) Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30440-pfkfb2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho PFKFB2 (Ser483) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PFKFB2 (Phospho-Ser483) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30440-pfkfb2-primary-antibodies-ihc-testing-2.jpgAnti-Phospho PFKFB2 (Ser483) AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using PFKFB2 (Phospho-Ser483) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-b-raf-thr599-antibody-p30441-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30441-braf-primary-antibodies-elisa-testing-1.jpgAnti-Phospho B-RAF (Thr599) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using B-RAF (Phospho-Thr599) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30441-braf-primary-antibodies-ihc-testing-2.jpgAnti-Phospho B-RAF (Thr599) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using B-RAF (Phospho-Thr599) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-histone-h3-3-ser31-antibody-p30442-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30442-h3f3a-primary-antibodies-ihc-testing-3.jpgAnti-Phospho Histone H3.3 (Ser31) H3F3A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30442-h3f3a-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Histone H3.3 (Ser31) H3F3A AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Histone H3.3 (Phospho-Ser31) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30442-h3f3a-primary-antibodies-if-testing-2.jpgAnti-Phospho Histone H3.3 (Ser31) H3F3A AntibodyImmunofluorescence analysis of HeLa cells, using Histone H3.3 (Phospho-Ser31) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-camk1-alpha-thr177-antibody-p02576-boster.html2026-03-24T05:10:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02576-camk1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho CaMK1-alpha (Thr177) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using CaMK1-alpha (Phospho-Thr177) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02576-camk1-primary-antibodies-if-testing-2.jpgAnti-Phospho CaMK1-alpha (Thr177) AntibodyImmunofluorescence analysis of HeLa cells, using CaMK1-alpha (Phospho-Thr177) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02576-camk1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho CaMK1-alpha (Thr177) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using CaMK1-alpha (Phospho-Thr177) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02576-camk1-primary-antibodies-wb-testing-4.jpgAnti-Phospho CaMK1-alpha (Thr177) AntibodyWestern blot analysis of lysates from K562 cells treated with insulin 0.01U/ml 15' and Jurkat cells treated with insulin 0.01U/ml 15', using CaMK1-alpha (Phospho-Thr177) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-hira-thr555-antibody-p03101-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03101-hira-primary-antibodies-ihc-testing-2.jpgAnti-Phospho HIRA (Thr555) AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03101-hira-primary-antibodies-if-testing-1.jpgAnti-Phospho HIRA (Thr555) AntibodyImmunofluorescence analysis of HeLa cells, using HIRA (Phospho-Thr555) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-il-7r-cd127-tyr449-antibody-p30449-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30449-il7r-primary-antibodies-if-testing-1.jpgAnti-Phospho IL-7R/CD127 (Tyr449) AntibodyImmunofluorescence analysis of HUVEC cells, using IL-7R/CD127 (Phospho-Tyr449) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30449-il7r-primary-antibodies-wb-testing-2.jpgAnti-Phospho IL-7R/CD127 (Tyr449) AntibodyWestern blot analysis of lysates from COLO205 cells, using IL-7R/CD127 (Phospho-Tyr449) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-ireb1-ser711-antibody-p30450-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30450-aco1-primary-antibodies-wb-testing-3.jpgAnti-Phospho IREB1 (Ser711) ACO1 AntibodyWestern Blot analysis of 293 cells using Phospho-IRP-1 (S711) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30450-aco1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho IREB1 (Ser711) ACO1 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using IREB1 (Phospho-Ser711) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30450-aco1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho IREB1 (Ser711) ACO1 AntibodyImmunohistochemistry analysis of paraffin-embedded human thyroid gland, using IREB1 (Phospho-Ser711) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30450-aco1-primary-antibodies-wb-testing-4.jpgAnti-Phospho IREB1 (Ser711) ACO1 AntibodyWestern blot analysis of lysates from 293 cells treated with insulin 0.01U/ml 30', using IREB1 (Phospho-Ser711) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-nifk-thr234-antibody-p30452-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30452-nifk-primary-antibodies-ihc-testing-3.jpgAnti-Phospho NIFK (Thr234) AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30452-nifk-primary-antibodies-elisa-testing-1.jpgAnti-Phospho NIFK (Thr234) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using NIFK (Phospho-Thr234) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30452-nifk-primary-antibodies-if-testing-2.jpgAnti-Phospho NIFK (Thr234) AntibodyImmunofluorescence analysis of HUVEC cells, using NIFK (Phospho-Thr234) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30452-nifk-primary-antibodies-ihc-testing-4.jpgAnti-Phospho NIFK (Thr234) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using NIFK (Phospho-Thr234) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-rapgef1-tyr504-antibody-p06527-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06527-rapgef1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho RapGEF1 (Tyr504) AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06527-rapgef1-primary-antibodies-elisa-testing-1.jpgAnti-Phospho RapGEF1 (Tyr504) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using RapGEF1 (Phospho-Tyr504) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06527-rapgef1-primary-antibodies-wb-testing-3.jpgAnti-Phospho RapGEF1 (Tyr504) AntibodyWestern blot analysis of lysates from HepG2 cells treated with Na3VO4 0.3nM 40', using RapGEF1 (Phospho-Tyr504) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-nek9-thr210-antibody-p04660-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04660-nek9-primary-antibodies-ihc-testing-3.jpgAnti-Phospho NEK9 (Thr210) AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04660-nek9-primary-antibodies-elisa-testing-1.jpgAnti-Phospho NEK9 (Thr210) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using NEK9 (Phospho-Thr210) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04660-nek9-primary-antibodies-if-testing-2.jpgAnti-Phospho NEK9 (Thr210) AntibodyImmunofluorescence analysis of HeLa cells, using NEK9 (Phospho-Thr210) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04660-nek9-primary-antibodies-wb-testing-4.jpgAnti-Phospho NEK9 (Thr210) AntibodyWestern blot analysis of lysates from HepG2 cells, using NEK9 (Phospho-Thr210) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-pip5k-ser307-antibody-p02638-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02638-pikfyve-primary-antibodies-elisa-testing-1.jpgAnti-Phospho PIP5K (Ser307) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PIP5K (Phospho-Ser307) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02638-pikfyve-primary-antibodies-if-testing-2.jpgAnti-Phospho PIP5K (Ser307) AntibodyImmunofluorescence analysis of HeLa cells, using PIP5K (Phospho-Ser307) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02638-pikfyve-primary-antibodies-ihc-testing-3.jpgAnti-Phospho PIP5K (Ser307) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using PIP5K (Phospho-Ser307) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-nfat5-ser1197-antibody-p01815-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01815-nfat5-primary-antibodies-ihc-testing-3.jpgAnti-Phospho NFAT5 (Ser1197) AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01815-nfat5-primary-antibodies-elisa-testing-1.jpgAnti-Phospho NFAT5 (Ser1197) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using NFAT5 (Phospho-Ser1197) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01815-nfat5-primary-antibodies-if-testing-2.jpgAnti-Phospho NFAT5 (Ser1197) AntibodyImmunofluorescence analysis of COS7 cells, using NFAT5 (Phospho-Ser1197) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-rgs16-tyr168-antibody-p04881-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04881-rgs16-primary-antibodies-ihc-testing-2.jpgAnti-Phospho RGS16 (Tyr168) AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04881-rgs16-primary-antibodies-elisa-testing-1.jpgAnti-Phospho RGS16 (Tyr168) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using RGS16 (Phospho-Tyr168) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04881-rgs16-primary-antibodies-wb-testing-3.jpgAnti-Phospho RGS16 (Tyr168) AntibodyWestern blot analysis of lysates from COS7 cells treated with heat shock, using RGS16 (Phospho-Tyr168) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-osr1-thr185-antibody-p05141-boster.html2026-03-24T05:10:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05141-oxsr1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho OSR1 (Thr185) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using OSR1 (Phospho-Thr185) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05141-oxsr1-primary-antibodies-wb-testing-2.jpgAnti-Phospho OSR1 (Thr185) AntibodyWestern blot analysis of lysates from HepG2 cells treated with serum 20% 15', using OSR1 (Phospho-Thr185) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-histone-h2a-thr121-antibody-p16777-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p16777-hist1h2ag-primary-antibodies-wb-testing-3.jpgAnti-Phospho Histone H2A (Thr121) HIST1H2AG AntibodyWestern Blot analysis of Hela+UV 5' cells using Phospho-Histone H2A (T121) Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p16777-hist1h2ag-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Histone H2A (Thr121) HIST1H2AG AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Histone H2A (Phospho-Thr121) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p16777-hist1h2ag-primary-antibodies-ihc-testing-2.jpgAnti-Phospho Histone H2A (Thr121) HIST1H2AG AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using Histone H2A (Phospho-Thr121) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-claudin-6-tyr219-antibody-p08182-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p08182-cldn6-primary-antibodies-ihc-testing-1.jpgAnti-Phospho Claudin 6 (Tyr219) AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p08182-cldn6-primary-antibodies-wb-testing-2.jpgAnti-Phospho Claudin 6 (Tyr219) AntibodyWestern blot analysis of lysates from RAW264.7 cells treated with UV 5', using Claudin 6 (Phospho-Tyr219) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-claudin-7-tyr210-antibody-p03851-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03851-cldn7-primary-antibodies-wb-testing-1.jpgAnti-Phospho Claudin 7 (Tyr210) CLDN7 AntibodyWestern blot analysis of lysates from rat liver, using Claudin 7 (Phospho-Tyr210) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-cyclin-c-ser275-antibody-p05832-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05832-ccnc-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Cyclin C (Ser275) CCNC AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Cyclin C (Phospho-Ser275) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05832-ccnc-primary-antibodies-ihc-testing-2.jpgAnti-Phospho Cyclin C (Ser275) CCNC AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using Cyclin C (Phospho-Ser275) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05832-ccnc-primary-antibodies-wb-testing-3.jpgAnti-Phospho Cyclin C (Ser275) CCNC AntibodyWestern blot analysis of lysates from NIH/3T3 cells treated with UV 15', using Cyclin C (Phospho-Ser275) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-girdin-ser1417-antibody-p03282-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03282-ccdc88a-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Girdin (Ser1417) CCDC88A AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Girdin (Phospho-Ser1417) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03282-ccdc88a-primary-antibodies-ihc-testing-2.jpgAnti-Phospho Girdin (Ser1417) CCDC88A AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using Girdin (Phospho-Ser1417) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-mkp-1-2-ser296-318-antibody-p30451-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30451-dusp1-primary-antibodies-wb-testing-2.jpgAnti-Phospho MKP-1/2 (Ser296/318) DUSP1 AntibodyWestern Blot analysis of JK cells using Phospho-MKP-1/2 (S296/318) Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30451-dusp1-primary-antibodies-wb-testing-3.jpgAnti-Phospho MKP-1/2 (Ser296/318) DUSP1 AntibodyWestern Blot analysis of various cells using Phospho-MKP-1/2 (S296/318) Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30451-dusp1-primary-antibodies-wb-testing-4.jpgAnti-Phospho MKP-1/2 (Ser296/318) DUSP1 AntibodyWestern blot analysis of lysates from K562 cells treated with heat shock , using MKP-1/2 (Phospho-Ser296/318) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-ncoa2-ser736-antibody-p01706-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01706-ncoa2-primary-antibodies-ihc-testing-1.jpgAnti-Phospho NCoA2 (Ser736) AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using NCoA2 (Phospho-Ser736) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01706-ncoa2-primary-antibodies-wb-testing-2.jpgAnti-Phospho NCoA2 (Ser736) AntibodyWestern blot analysis of lysates from HeLa cells treated with TSA 400nM 24H, using NCoA2 (Phospho-Ser736) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-cnot2-ser101-antibody-p06400-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06400-cnot2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho CNOT2 (Ser101) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using CNOT2 (Phospho-Ser101) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06400-cnot2-primary-antibodies-ihc-testing-2.jpgAnti-Phospho CNOT2 (Ser101) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using CNOT2 (Phospho-Ser101) Antibody. The picture on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-pld2-tyr169-antibody-p02586-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02586-pld2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho PLD2 (Tyr169) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using PLD2 (Phospho-Tyr169) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02586-pld2-primary-antibodies-ihc-testing-2.jpgAnti-Phospho PLD2 (Tyr169) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using PLD2 (Phospho-Tyr169) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02586-pld2-primary-antibodies-wb-testing-3.jpgAnti-Phospho PLD2 (Tyr169) AntibodyWestern blot analysis of lysates from Jurkat cells treated with TNF 20ng/ml 30', using PLD2 (Phospho-Tyr169) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tif-ia-ser649-antibody-p05439-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05439-rrn3-primary-antibodies-elisa-testing-1.jpgAnti-Phospho TIF-IA (Ser649) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using TIF-IA (Phospho-Ser649) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05439-rrn3-primary-antibodies-ihc-testing-2.jpgAnti-Phospho TIF-IA (Ser649) AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using TIF-IA (Phospho-Ser649) Antibody. The picture on the right is blocked with the phospho peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05439-rrn3-primary-antibodies-wb-testing-3.jpgAnti-Phospho TIF-IA (Ser649) AntibodyWestern blot analysis of lysates from Jurkat cells treated with starved 24h, using TIF-IA (Phospho-Ser649) Antibody. The lane on the right is blocked with the phospho peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ctip-antibody-a02076-boster.html2026-03-24T05:10:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-rbbp8-primary-antibodies-ihc-testing-1.jpgAnti-CTIP RBBP8 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using CTIP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-parkin-antibody-a30434-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30434-park2-primary-antibodies-wb-testing-2.jpgAnti-Parkin PARK2 AntibodyWestern Blot analysis of various cells using Parkin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30434-park2-primary-antibodies-ihc-testing-1.jpgAnti-Parkin PARK2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Parkin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30434-park2-primary-antibodies-wb-testing-3.jpgAnti-Parkin PARK2 AntibodyWestern blot analysis of lysates from HeLa and HUVEC cells, using Parkin Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rhodopsin-antibody-a30435-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30435-rho-primary-antibodies-wb-testing-2.jpgAnti-Rhodopsin AntibodyWestern Blot analysis of various cells using Rhodopsin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30435-rho-primary-antibodies-ihc-testing-1.jpgAnti-Rhodopsin AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Rhodopsin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30435-rho-primary-antibodies-wb-testing-3.jpgAnti-Rhodopsin AntibodyWestern blot analysis of lysates from COLO cells, using Rhodopsin Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tnni3-antibody-a01720-1-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01720-1-tnni3-primary-antibodies-wb-testing-3.jpgAnti-TNNI3/Troponin I AntibodyWestern Blot analysis of mouse cells using Troponin I-C Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01720-1-tnni3-primary-antibodies-if-testing-1.jpgAnti-TNNI3/Troponin I AntibodyImmunofluorescence analysis of HepG2 cells, using TNNI3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01720-1-tnni3-primary-antibodies-ihc-testing-2.jpgAnti-TNNI3/Troponin I AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using TNNI3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01720-1-tnni3-primary-antibodies-wb-testing-4.jpgAnti-TNNI3/Troponin I AntibodyWestern blot analysis of lysates from mouse heart cells, using TNNI3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vav1-antibody-a30436-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30436-vav1-primary-antibodies-wb-testing-2.jpgAnti-Proto-oncogene vav VAV1 AntibodyWestern Blot analysis of extracts from NIH-3T3 cells, using VAV1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30436-vav1-primary-antibodies-if-testing-1.jpgAnti-Proto-oncogene vav VAV1 AntibodyImmunofluorescence analysis of HeLa cells, using VAV1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pld1-antibody-a02031-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02031-pld1-primary-antibodies-ihc-testing-1.jpgAnti-PLD1/Phospholipase D1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using PLD1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ras-grf1-antibody-a03338-1-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03338-1-rasgrf1-primary-antibodies-ihc-testing-1.jpgAnti-Ras-GRF1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Ras-GRF1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03338-1-ijn-16-6441-g0002.jpgAnti-Ras-GRF1 AntibodyAN-FTS inhibited TGF-β1-induced activation of NRK-49F cells. NRK-49F cells were treated with free FTS and AN-FTS (20 μM of FTS) in the presence of 2 ng/mL TGF-β1 for 48 h. ( A ) Relative mRNA expression of α-SMA, collagen, Pai-1 and Fn in NRK-49F cells treated with free FTS and AN-FTS. ( B ) Protein expression of α-SMA, Col1a1 and Fn in NRK-49F cells treated with free FTS and AN-FTS. ( C ) Relative mRNA expression of H-Ras, K-Ras and N-Ras. Data are mean ± SEM (n = 3). ## P < 0.01 compared with control (ctrl) group, * P < 0.05 and ** P < 0.01 compared with AN-FTS group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8464329/&orig_host=www.ncbi.nlm.nih.gov'>34584410</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03338-1-ijn-16-6441-g0006.jpgAnti-Ras-GRF1 AntibodyAN-FTS inhibited UUO-induced Ras expression in kidney of mice. ( A ) The relative expression of H-Ras, K-Ras and N-Ras in kidney tissues of mice. ( B ) Immunohistochemistry staining of Ras in kidney sections. Data are mean ± SEM (n = 6–7). ## P < 0.01 compared with Sham group, * P < 0.05 and ** P < 0.01 compared with AN-FTS group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8464329/&orig_host=www.ncbi.nlm.nih.gov'>34584410</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-pfkfb2-antibody-a30440-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30440-pfkfb2-primary-antibodies-wb-testing-2.jpgAnti-PFKFB2/P Pfk 2 Car AntibodyWestern Blot analysis of various cells using PFK-2 car Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30440-pfkfb2-primary-antibodies-ihc-testing-1.jpgAnti-PFKFB2/P Pfk 2 Car AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using PFKFB2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30440-pfkfb2-primary-antibodies-wb-testing-3.jpgAnti-PFKFB2/P Pfk 2 Car AntibodyWestern blot analysis of lysates from 293 cells, treated with Heat shock, using PFKFB2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-histone-h3-3-antibody-a30442-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30442-h3f3a-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3.3 H3F3A AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30442-h3f3a-primary-antibodies-wb-testing-3.jpgAnti-Histone H3.3 H3F3A AntibodyWestern Blot analysis of Hela cells using Histone H3.3 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30442-h3f3a-primary-antibodies-if-testing-1.jpgAnti-Histone H3.3 H3F3A AntibodyImmunofluorescence analysis of HeLa cells, using Histone H3.3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dematin-antibody-a30444-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30444-dmtn-primary-antibodies-wb-testing-3.jpgAnti-Dematin DMTN AntibodyWestern Blot analysis of various cells using Dematin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30444-dmtn-primary-antibodies-if-testing-1.jpgAnti-Dematin DMTN AntibodyImmunofluorescence analysis of HUVEC cells, using Dematin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30444-dmtn-primary-antibodies-ihc-testing-2.jpgAnti-Dematin DMTN AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Dematin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30444-dmtn-primary-antibodies-wb-testing-4.jpgAnti-Dematin DMTN AntibodyWestern blot analysis of lysates from 293 cells, using Dematin Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pdgfr-alpha-antibody-a30446-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30446-pdgfra-primary-antibodies-wb-testing-3.jpgAnti-PDGFR alpha AntibodyWestern Blot analysis of SH-SY5Y cells using PDGFR-α Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30446-pdgfra-primary-antibodies-if-testing-1.jpgAnti-PDGFR alpha AntibodyImmunofluorescence analysis of HeLa cells, using PDGFR alpha Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30446-pdgfra-primary-antibodies-ihc-testing-2.jpgAnti-PDGFR alpha AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using PDGFR alpha Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rfa2-antibody-a30447-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30447-rpa2-primary-antibodies-if-testing-1.jpgAnti-RFA2 AntibodyImmunofluorescence analysis of HeLa cells, using RFA2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30447-rpa2-primary-antibodies-ihc-testing-2.jpgAnti-RFA2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using RFA2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30447-rpa2-primary-antibodies-wb-testing-3.jpgAnti-RFA2 AntibodyWestern blot analysis of lysates from K562 cells, using RFA2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vinculin-antibody-a30448-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30448-vcl-primary-antibodies-wb-testing-3.jpgAnti-Vinculin VCL AntibodyWestern Blot analysis of various cells using Vinculin Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30448-vcl-primary-antibodies-ihc-testing-2.jpgAnti-Vinculin VCL AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Vinculin Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30448-vcl-primary-antibodies-wb-testing-4.jpgAnti-Vinculin VCL AntibodyWestern blot analysis of lysates from HeLa cells, treated with forskolin 40nM 30', using Vinculin Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hand1-antibody-a06496-1-boster.html2026-03-24T05:10:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/H/A/HAND1-primary-antibodies-A06496-1-IHC-testing.jpgAnti-HAND1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using HAND1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nifk-antibody-a30452-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30452-nifk-primary-antibodies-wb-testing-3.jpgAnti-NIFK AntibodyWestern blot analysis of lysates from K562 cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30452-nifk-primary-antibodies-if-testing-1.jpgAnti-NIFK AntibodyImmunofluorescence analysis of HUVEC cells, using NIFK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30452-nifk-primary-antibodies-ihc-testing-2.jpgAnti-NIFK AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NIFK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rapgef1-antibody-a06527-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06527-rapgef1-primary-antibodies-ihc-testing-1.jpgAnti-RapGEF1/Grf2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using RapGEF1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-arhgdia-antibody-a03135-1-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03135-1-arhgdia-primary-antibodies-ihc-testing-1.jpgAnti-ARHGDIA/Rhogdi AntibodyImmunohistochemistry analysis of paraffin-embedded human cervix carcinoma tissue, using ARHGDIA Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vamp4-antibody-a05647-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05647-vamp4-primary-antibodies-if-testing-1.jpgAnti-VAMP4 AntibodyImmunofluorescence analysis of A549 cells, using VAMP4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rac1-cdc42-antibody-a03252-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03252-rac1-primary-antibodies-wb-testing-2.jpgAnti-Rac1/CDC42 AntibodyWestern Blot analysis of 3T3 cells using Rac1/2/3/CDC42 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03252-rac1-primary-antibodies-wb-testing-3.jpgAnti-Rac1/CDC42 AntibodyWestern Blot analysis of various cells using Rac1/2/3/CDC42 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03252-rac1-primary-antibodies-ihc-testing-1.jpgAnti-Rac1/CDC42 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Rac1/CDC42 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03252-rac1-primary-antibodies-wb-testing-4.jpgAnti-Rac1/CDC42 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, treated with EGF 200ng/ml 30', using Rac1/CDC42 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-girdin-antibody-a03282-1-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03282-1-ccdc88a-primary-antibodies-ihc-testing-1.jpgAnti-Girdin CCDC88A AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Girdin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-htra2-antibody-a01941-1-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/H/T/HTRA2-primary-antibodies-A01941-1-IHC-testing.jpgAnti-HtrA2/Omi AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using HtrA2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mkp-1-2-antibody-a30451-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-4.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern Blot analysis of Jurkat cells using MKP-1/2 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-5.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern Blot analysis of various cells using MKP-1/2 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-2.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern blot analysis of 293T lysis using MKP-1/2 antibody. Antibody was diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-3.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern blot analysis of Hela KB 293T SH-SY5Y lysis using MKP-1/2 antibody. Antibody was diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-7.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern blot analysis of the lysates from HepG2 cells using MKP-1/2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-ihc-testing-1.jpgAnti-MKP-1/2 DUSP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using MKP-1/2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30451-dusp1-primary-antibodies-wb-testing-6.jpgAnti-MKP-1/2 DUSP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using MKP-1/2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cnot2-antibody-a06400-1-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06400-1-cnot2-primary-antibodies-ihc-testing-1.jpgAnti-CNOT2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06400-1-cnot2-primary-antibodies-wb-testing-2.jpgAnti-CNOT2 AntibodyWestern blot analysis of lysates from HepG2 cells, treated with starved 24h, using CNOT2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mglur6-antibody-a06163-1-boster.html2026-03-24T05:10:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06163-1-grm6-primary-antibodies-ihc-testing-1.jpgAnti-mGluR6 GRM6 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using mGluR6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06163-1-grm6-primary-antibodies-wb-testing-2.jpgAnti-mGluR6 GRM6 AntibodyWestern blot analysis of lysates from mouse brain, using mGluR6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nkx3-1-antibody-a30460-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30460-nkx3-1-primary-antibodies-wb-testing-2.jpgAnti-NKX3.1 AntibodyWestern Blot analysis of various cells using Nkx-3.1 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30460-nkx3-1-primary-antibodies-ihc-testing-1.jpgAnti-NKX3.1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using NKX3.1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rcbtb1-antibody-a11528-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11528-rcbtb1-primary-antibodies-ihc-testing-1.jpgAnti-RCBTB1/Clld7 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RCBTB1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11528-rcbtb1-primary-antibodies-wb-testing-2.jpgAnti-RCBTB1/Clld7 AntibodyWestern blot analysis of lysates from LOVO cells, using RCBTB1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sodium-channel-pan-antibody-a01735-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01735-scn1a-primary-antibodies-wb-testing-2.jpgAnti-Sodium Channel-pan SCN1A AntibodyWestern Blot analysis of various cells using Na+ CP-pan Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01735-scn1a-primary-antibodies-ihc-testing-1.jpgAnti-Sodium Channel-pan SCN1A AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using Sodium Channel-pan Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01735-scn1a-primary-antibodies-wb-testing-3.jpgAnti-Sodium Channel-pan SCN1A AntibodyWestern blot analysis of lysates from HUVEC cells, using Sodium Channel-pan Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-top2b-antibody-a02750-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02750-top2b-primary-antibodies-ihc-testing-1.jpgAnti-TOP2B/Topoisomerase Ii Beta AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using TOP2B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02750-top2b-primary-antibodies-wb-testing-2.jpgAnti-TOP2B/Topoisomerase Ii Beta AntibodyWestern blot analysis of lysates from Jurkat cells, using TOP2B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-urocortin-antibody-a01807-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01807-1-ucn-primary-antibodies-ihc-testing-1.jpgAnti-Urocortin UCN AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using Urocortin Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nkx6-3-antibody-a30461-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30461-nkx6-3-primary-antibodies-wb-testing-2.jpgAnti-NKX6.3 AntibodyWestern Blot analysis of K562 cells using Nkx-6.3 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30461-nkx6-3-primary-antibodies-if-testing-1.jpgAnti-NKX6.3 AntibodyImmunofluorescence analysis of HUVEC cells, using NKX6.3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30461-nkx6-3-primary-antibodies-wb-testing-3.jpgAnti-NKX6.3 AntibodyWestern blot analysis of lysates from K562 and COS7 cells, using NKX6.3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pdzd2-antibody-a10309-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10309-1-pdzd2-primary-antibodies-if-testing-1.jpgAnti-PDZD2/Pdzk3 AntibodyImmunofluorescence analysis of HepG2 cells, using PDZD2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10309-1-pdzd2-primary-antibodies-ihc-testing-2.jpgAnti-PDZD2/Pdzk3 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using PDZD2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mast4-antibody-a11085-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11085-1-mast4-primary-antibodies-wb-testing-4.jpgAnti-MAST4 AntibodyWestern blot analysis of the lysates from HT-29 cells using MAST4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11085-1-mast4-primary-antibodies-if-testing-1.jpgAnti-MAST4 AntibodyImmunofluorescence analysis of COS7 cells, using MAST4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11085-1-mast4-primary-antibodies-ihc-testing-2.jpgAnti-MAST4 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using MAST4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11085-1-mast4-primary-antibodies-wb-testing-3.jpgAnti-MAST4 AntibodyWestern blot analysis of lysates from Jurkat, COLO, HUVEC, and MCF-7 cells, using MAST4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sox12-antibody-a11606-boster.html2026-04-01T05:01:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11606-sox12-primary-antibodies-ihc-testing-1.jpgAnti-SOX12/Sox22 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using SOX12 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-med14-antibody-a04799-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04799-1-med14-primary-antibodies-if-testing-1.jpgAnti-MED14/Crsp2 AntibodyImmunofluorescence analysis of COS7 cells, using MED14 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04799-1-med14-primary-antibodies-ihc-testing-2.jpgAnti-MED14/Crsp2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MED14 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sdcg1-antibody-a30462-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30462-nemf-primary-antibodies-ihc-testing-1.jpgAnti-SDCG1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30462-nemf-primary-antibodies-wb-testing-2.jpgAnti-SDCG1 AntibodyWestern Blot analysis of 3T3 cells using NY-CO-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30462-nemf-primary-antibodies-wb-testing-3.jpgAnti-SDCG1 AntibodyWestern Blot analysis of various cells using NY-CO-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30462-nemf-primary-antibodies-wb-testing-4.jpgAnti-SDCG1 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using SDCG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lat3-antibody-a10910-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10910-1-slc43a1-primary-antibodies-ihc-testing-1.jpgAnti-LAT3 SLC43A1 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10910-1-slc43a1-primary-antibodies-wb-testing-2.jpgAnti-LAT3 SLC43A1 AntibodyWestern Blot analysis of various cells using SLC43A1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10910-1-slc43a1-primary-antibodies-wb-testing-3.jpgAnti-LAT3 SLC43A1 AntibodyWestern blot analysis of lysates from A549 and Jurkat cells, using LAT3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dna-polymerase-thet-antibody-a02205-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02205-polq-primary-antibodies-ihc-testing-1.jpgAnti-DNA Polymerase thet POLQ AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using DNA Polymerase thet Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cib2-antibody-a08179-1-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08179-1-cib2-primary-antibodies-ihc-testing-1.jpgAnti-CIB2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using CIB2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-snapc5-antibody-a07260-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07260-snapc5-primary-antibodies-ihc-testing-1.jpgAnti-SNAPC5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using SNAPC5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-myst2-antibody-a30463-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30463-kat7-primary-antibodies-wb-testing-2.jpgAnti-MYST2 AntibodyWestern Blot analysis of Jurkat cells using HBO1 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30463-kat7-primary-antibodies-wb-testing-3.jpgAnti-MYST2 AntibodyWestern Blot analysis of various cells using HBO1 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30463-kat7-primary-antibodies-if-testing-1.jpgAnti-MYST2 AntibodyImmunofluorescence analysis of HUVEC cells, using MYST2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30463-kat7-primary-antibodies-wb-testing-4.jpgAnti-MYST2 AntibodyWestern blot analysis of lysates from Jurkat cells, using MYST2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nduc2-antibody-a09084-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09084-ndufc2-primary-antibodies-ihc-testing-1.jpgAnti-NDUC2 NDUFC2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NDUC2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-reck-antibody-a06439-boster.html2026-03-24T05:10:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-reck-primary-antibodies-if-testing-1.jpgAnti-RECK AntibodyImmunofluorescence analysis of HepG2 cells, using RECK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-reck-primary-antibodies-ihc-testing-2.jpgAnti-RECK AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RECK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lyl-1-antibody-a07491-1-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07491-1-lyl1-primary-antibodies-ihc-testing-1.jpgAnti-Lyl-1 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using Lyl-1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf7-antibody-a12285-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12285-znf7-primary-antibodies-if-testing-1.jpgAnti-Zinc finger protein 7 ZNF7 AntibodyImmunofluorescence analysis of HeLa cells, using ZNF7 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12285-znf7-primary-antibodies-ihc-testing-2.jpgAnti-Zinc finger protein 7 ZNF7 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ZNF7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atf1-antibody-a01600-1-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01600-1-atf1-primary-antibodies-ihc-testing-2.jpgAnti-ATF1 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01600-1-atf1-primary-antibodies-wb-testing-4.jpgAnti-ATF1 AntibodyWestern Blot analysis of various cells using ATF-1 Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01600-1-atf1-primary-antibodies-wb-testing-3.jpgAnti-ATF1 AntibodyWestern blot analysis of 293T 3T3 HELA KB SH-SY5Y lysis using ATF-1 antibody. Antibody was diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01600-1-atf1-primary-antibodies-wb-testing-5.jpgAnti-ATF1 AntibodyWestern blot analysis of lysates from HepG2, COLO205, and HeLa cells, using ATF1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nktr-antibody-a09881-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09881-nktr-primary-antibodies-if-testing-1.jpgAnti-NK-tumor recognition protein NKTR AntibodyImmunofluorescence analysis of HeLa cells, using NKTR Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09881-nktr-primary-antibodies-ihc-testing-2.jpgAnti-NK-tumor recognition protein NKTR AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NKTR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd153-antibody-a08216-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08216-tnfsf8-primary-antibodies-wb-testing-1.jpgAnti-CD153 TNFSF8 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using CD153 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08216-tnfsf8-primary-antibodies-wb-testing-2.jpgAnti-CD153 TNFSF8 AntibodyWestern blot analysis of the lysates from K562 cells using CD153 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cks2-antibody-a08202-1-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08202-1-cks2-primary-antibodies-ihc-testing-1.jpgAnti-CKS2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CKS2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sox6-antibody-a02877-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02877-sox6-primary-antibodies-ihc-testing-1.jpgAnti-Transcription factor SOX-6 SOX6 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02877-sox6-primary-antibodies-wb-testing-2.jpgAnti-Transcription factor SOX-6 SOX6 AntibodyWestern blot analysis of lysates from Jurkat cells, using SOX6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-g-antibody-a04738-1-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-1-rbmx-primary-antibodies-ihc-testing-2.jpgAnti-hnRNP G RBMX AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-1-rbmx-primary-antibodies-wb-testing-3.jpgAnti-hnRNP G RBMX AntibodyWestern Blot analysis of various cells using hnRNP G Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-1-rbmx-primary-antibodies-if-testing-1.jpgAnti-hnRNP G RBMX AntibodyImmunofluorescence analysis of HepG2 cells, using hnRNP G Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04738-1-rbmx-primary-antibodies-wb-testing-4.jpgAnti-hnRNP G RBMX AntibodyWestern blot analysis of lysates from HeLa cells, using hnRNP G Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-af4-antibody-a02590-1-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02590-1-aff1-primary-antibodies-ihc-testing-1.jpgAnti-AF4 AFF1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using AF4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnp-m-antibody-a06017-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06017-hnrnpm-primary-antibodies-if-testing-1.jpgAnti-hnRNP M AntibodyImmunofluorescence analysis of MCF7 cells, using hnRNP M Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06017-hnrnpm-primary-antibodies-ihc-testing-2.jpgAnti-hnRNP M AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using hnRNP M Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06017-hnrnpm-primary-antibodies-wb-testing-3.jpgAnti-hnRNP M AntibodyWestern blot analysis of lysates from HT-29 cells, using hnRNP M Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tf2a1-antibody-a09007-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09007-gtf2a1-primary-antibodies-ihc-testing-1.jpgAnti-TF2A1 GTF2A1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09007-gtf2a1-primary-antibodies-wb-testing-2.jpgAnti-TF2A1 GTF2A1 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using TF2A1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cks1-antibody-a30464-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30464-cks1b-primary-antibodies-wb-testing-2.jpgAnti-CKS1 CKS1B AntibodyWestern Blot analysis of various cells using Cks1 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30464-cks1b-primary-antibodies-if-testing-1.jpgAnti-CKS1 CKS1B AntibodyImmunofluorescence analysis of HeLa cells, using CKS1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30464-cks1b-primary-antibodies-wb-testing-3.jpgAnti-CKS1 CKS1B AntibodyWestern blot analysis of lysates from Jurkat cells, treated with serum 20% 15', using CKS1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ipka-antibody-a30465-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30465-pkia-primary-antibodies-if-testing-1.jpgAnti-IPKA PKIA AntibodyImmunofluorescence analysis of HeLa cells, using IPKA Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30465-pkia-primary-antibodies-ihc-testing-2.jpgAnti-IPKA PKIA AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using IPKA Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-blcap-antibody-a10808-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10808-blcap-primary-antibodies-if-testing-1.jpgAnti-BLCAP AntibodyImmunofluorescence analysis of NIH/3T3 cells, using BLCAP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cki-gamma2-antibody-a30466-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30466-csnk1g2-primary-antibodies-ihc-testing-1.jpgAnti-CKI-gamma2 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30466-csnk1g2-primary-antibodies-wb-testing-2.jpgAnti-CKI-gamma2 AntibodyWestern Blot analysis of HeLa cells using Casein Kinase Iγ2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30466-csnk1g2-primary-antibodies-wb-testing-3.jpgAnti-CKI-gamma2 AntibodyWestern blot analysis of lysates from HeLa and 293 cells, using CKI-gamma2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-crbp-iii-antibody-a30467-boster.html2026-03-24T05:10:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30467-rbp5-primary-antibodies-if-testing-1.jpgAnti-CRBP III AntibodyImmunofluorescence analysis of LOVO cells, using CRBP III Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30467-rbp5-primary-antibodies-ihc-testing-2.jpgAnti-CRBP III AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using CRBP III Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs3-antibody-a30468-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-ihc-testing-2.jpgAnti-SFRS3 SRSF3 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-wb-testing-4.jpgAnti-SFRS3 SRSF3 AntibodyWestern Blot analysis of Jurkat cells using SRp20 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-wb-testing-5.jpgAnti-SFRS3 SRSF3 AntibodyWestern Blot analysis of various cells using SRp20 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-wb-testing-3.jpgAnti-SFRS3 SRSF3 AntibodyWestern blot analysis of 293T lysis using SRp20 antibody. Antibody was diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-if-testing-1.jpgAnti-SFRS3 SRSF3 AntibodyImmunofluorescence analysis of MCF7 cells, using SFRS3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30468-srsf3-primary-antibodies-wb-testing-6.jpgAnti-SFRS3 SRSF3 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using SFRS3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tsg6-antibody-a30469-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30469-tnfaip6-primary-antibodies-ihc-testing-1.jpgAnti-TSG6 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30469-tnfaip6-primary-antibodies-wb-testing-2.jpgAnti-TSG6 AntibodyWestern blot analysis of lysates from Jurkat, HeLa, and HepG2 cells, using TSG6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-entk-antibody-a30470-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/E/N/ENTK-primary-antibodies-A30470-IHC-testing.jpgAnti-ENTK TMPRSS15 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ENTK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/E/N/ENTK-primary-antibodies-A30470-IF-testing.jpgAnti-ENTK TMPRSS15 AntibodyImmunofluorescence analysis of HepG2 cells, using ENTK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-k6pp-antibody-a30471-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30471-pfkp-primary-antibodies-ihc-testing-1.jpgAnti-K6PP AntibodyImmunohistochemical analysis of paraffin-embedded Human testis. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30471-pfkp-primary-antibodies-wb-testing-2.jpgAnti-K6PP AntibodyWestern Blot analysis of HuvEc cells using PFK-C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30471-pfkp-primary-antibodies-wb-testing-3.jpgAnti-K6PP AntibodyWestern Blot analysis of various cells using PFK-C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30471-pfkp-primary-antibodies-wb-testing-4.jpgAnti-K6PP AntibodyWestern blot analysis of lysates from A549 and COS7 cells, using K6PP Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sp2-antibody-a02284-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02284-sp2-primary-antibodies-ihc-testing-1.jpgAnti-Transcription factor Sp2 SP2 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02284-sp2-primary-antibodies-wb-testing-3.jpgAnti-Transcription factor Sp2 SP2 AntibodyWestern blot analysis of the lysates from 293 cells using SP2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02284-sp2-primary-antibodies-wb-testing-2.jpgAnti-Transcription factor Sp2 SP2 AntibodyWestern blot analysis of lysates from Jurkat cells, using SP2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hen1-2-antibody-a30472-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30472-nhlh1-primary-antibodies-ihc-testing-1.jpgAnti-HEN1/2 NHLH1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30472-nhlh1-primary-antibodies-wb-testing-2.jpgAnti-HEN1/2 NHLH1 AntibodyWestern Blot analysis of various cells using HEN1/2 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30472-nhlh1-primary-antibodies-wb-testing-3.jpgAnti-HEN1/2 NHLH1 AntibodyWestern blot analysis of lysates from Jurkat cells, using HEN1/2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-map3k10-antibody-a08285-1-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08285-1-map3k10-primary-antibodies-ihc-testing-1.jpgAnti-MAP3K10/Mlk2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MAP3K10 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mtssb-antibody-a30475-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30475-ssbp1-primary-antibodies-wb-testing-3.jpgAnti-MtSSB SSBP1 AntibodyWestern Blot analysis of various cells using SSBP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30475-ssbp1-primary-antibodies-if-testing-1.jpgAnti-MtSSB SSBP1 AntibodyImmunofluorescence analysis of A549 cells, using MtSSB Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30475-ssbp1-primary-antibodies-ihc-testing-2.jpgAnti-MtSSB SSBP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas tissue, using MtSSB Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30475-ssbp1-primary-antibodies-wb-testing-4.jpgAnti-MtSSB SSBP1 AntibodyWestern blot analysis of lysates from HUVEC and HeLa cells, using MtSSB Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tnfc-antibody-a30476-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30476-ltb-primary-antibodies-wb-testing-2.jpgAnti-TNFC LTB AntibodyWestern Blot analysis of various cells using LT-β Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30476-ltb-primary-antibodies-if-testing-1.jpgAnti-TNFC LTB AntibodyImmunofluorescence analysis of HeLa cells, using TNFC Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30476-ltb-primary-antibodies-wb-testing-3.jpgAnti-TNFC LTB AntibodyWestern blot analysis of lysates from HepG2 cells, using TNFC Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs4-antibody-a30477-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30477-srsf4-primary-antibodies-ihc-testing-1.jpgAnti-SFRS4 AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid gland. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30477-srsf4-primary-antibodies-wb-testing-2.jpgAnti-SFRS4 AntibodyWestern Blot analysis of various cells using SRp75 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30477-srsf4-primary-antibodies-wb-testing-3.jpgAnti-SFRS4 AntibodyWestern blot analysis of lysates from LOVO cells, using SFRS4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mtg16-antibody-a30478-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30478-cbfa2t3-primary-antibodies-ihc-testing-1.jpgAnti-MTG16 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MTG16 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-smf-antibody-a16486-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16486-hmgxb3-primary-antibodies-ihc-testing-1.jpgAnti-SMF HMGXB3 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using SMF Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-akap13-antibody-a03017-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03017-akap13-primary-antibodies-ihc-testing-1.jpgAnti-A-kinase anchor protein 13 AKAP13 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using AKAP13 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03017-akap13-primary-antibodies-wb-testing-2.jpgAnti-A-kinase anchor protein 13 AKAP13 AntibodyWestern blot analysis of lysates from Jurkat and A549 cells, using AKAP13 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-foxi1-antibody-a07512-1-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/F/O/FOXI1-primary-antibodies-A07512-1-IHC-testing.jpgAnti-Forkhead box protein I1 FOXI1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using FOXI1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-caf1b-antibody-a30479-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30479-chaf1b-primary-antibodies-ihc-testing-1.jpgAnti-CAF1B CHAF1B AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30479-chaf1b-primary-antibodies-wb-testing-2.jpgAnti-CAF1B CHAF1B AntibodyWestern blot analysis of lysates from Jurkat cells, using CAF1B Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30479-chaf1b-primary-antibodies-wb-testing-3.jpgAnti-CAF1B CHAF1B AntibodyWestern blot analysis of the lysates from RAW264.7cells using CAF1B antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dusp4-antibody-a30480-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30480-dusp4-primary-antibodies-wb-testing-3.jpgAnti-DUSP4 AntibodyWestern Blot analysis of HEPG2-UV cells using MKP-2 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30480-dusp4-primary-antibodies-ihc-testing-1.jpgAnti-DUSP4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using DUSP4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30480-dusp4-primary-antibodies-wb-testing-4.jpgAnti-DUSP4 AntibodyWestern blot analysis of lysates from RAW264.7, A549, COS7, and NIH/3T3 cells, using DUSP4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30480-dusp4-primary-antibodies-wb-testing-2.jpgAnti-DUSP4 AntibodyWestern blot analysis of A549 lysate, antibody was diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-cgk-2-antibody-a30481-boster.html2026-03-24T05:10:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30481-prkg2-primary-antibodies-ihc-testing-1.jpgAnti-CGK 2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30481-prkg2-primary-antibodies-wb-testing-2.jpgAnti-CGK 2 AntibodyWestern Blot analysis of HuvEc cells using cGKII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30481-prkg2-primary-antibodies-wb-testing-3.jpgAnti-CGK 2 AntibodyWestern Blot analysis of various cells using cGKII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30481-prkg2-primary-antibodies-wb-testing-4.jpgAnti-CGK 2 AntibodyWestern blot analysis of lysates from HUVEC cells, using CGK 2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-klf-antibody-a30483-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30483-klf1-primary-antibodies-wb-testing-2.jpgAnti-KLF AntibodyWestern Blot analysis of VEC cells using EKLF/CKLF/UKLF Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30483-klf1-primary-antibodies-wb-testing-1.jpgAnti-KLF AntibodyWestern Blot analysis of various cells using EKLF/CKLF/UKLF Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30483-klf1-primary-antibodies-wb-testing-4.jpgAnti-KLF AntibodyWestern blot analysis of the lysates from K562 cells using KLF antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30483-klf1-primary-antibodies-wb-testing-3.jpgAnti-KLF AntibodyWestern blot analysis of lysates from Jurkat cells, treated with serum 20% 15', using KLF Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-jip2-antibody-a30484-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30484-mapk8ip2-primary-antibodies-if-testing-1.jpgAnti-JIP2 MAPK8IP2 AntibodyImmunofluorescence analysis of HeLa cells, using JIP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30484-mapk8ip2-primary-antibodies-ihc-testing-2.jpgAnti-JIP2 MAPK8IP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using JIP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30484-mapk8ip2-primary-antibodies-wb-testing-3.jpgAnti-JIP2 MAPK8IP2 AntibodyWestern blot analysis of lysates from mouse brain, using JIP2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tcof1-antibody-a02653-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02653-tcof1-primary-antibodies-ihc-testing-1.jpgAnti-TCOF1/Treacle AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using TCOF1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02653-tcof1-primary-antibodies-wb-testing-2.jpgAnti-TCOF1/Treacle AntibodyWestern blot analysis of lysates from Jurkat, 293, HeLa cells, using TCOF1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-itpk1-antibody-a09106-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09106-itpk1-primary-antibodies-ihc-testing-1.jpgAnti-ITPK1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09106-itpk1-primary-antibodies-wb-testing-3.jpgAnti-ITPK1 AntibodyWestern blot analysis of the lysates from HepG2 cells using ITPK1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09106-itpk1-primary-antibodies-wb-testing-2.jpgAnti-ITPK1 AntibodyWestern blot analysis of lysates from HeLa, HepG2, and Jurkat cells, using ITPK1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dgkz-antibody-a06678-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06678-dgkz-primary-antibodies-ihc-testing-1.jpgAnti-DGKZ/Dgk Zeta AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using DGKZ Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tra-2-alpha-antibody-a30486-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30486-tra2a-primary-antibodies-wb-testing-3.jpgAnti-TRA-2 alpha AntibodyWestern Blot analysis of various cells using Tra-2α Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30486-tra2a-primary-antibodies-if-testing-1.jpgAnti-TRA-2 alpha AntibodyImmunofluorescence analysis of HeLa cells, using TRA-2 alpha Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30486-tra2a-primary-antibodies-ihc-testing-2.jpgAnti-TRA-2 alpha AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TRA-2 alpha Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30486-tra2a-primary-antibodies-wb-testing-4.jpgAnti-TRA-2 alpha AntibodyWestern blot analysis of lysates from HUVEC cells, using TRA-2 alpha Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dyr1a-antibody-a30487-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30487-dyrk1a-primary-antibodies-ihc-testing-2.jpgAnti-DYR1A DYRK1A AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30487-dyrk1a-primary-antibodies-wb-testing-3.jpgAnti-DYR1A DYRK1A AntibodyWestern Blot analysis of HepG2 cells using Dyrk1A Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30487-dyrk1a-primary-antibodies-wb-testing-4.jpgAnti-DYR1A DYRK1A AntibodyWestern Blot analysis of various cells using Dyrk1A Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30487-dyrk1a-primary-antibodies-if-testing-1.jpgAnti-DYR1A DYRK1A AntibodyImmunofluorescence analysis of HepG2 cells, using DYR1A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30487-dyrk1a-primary-antibodies-wb-testing-5.jpgAnti-DYR1A DYRK1A AntibodyWestern blot analysis of lysates from HepG2 cells, using DYR1A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf147-antibody-a30491-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30491-trim25-primary-antibodies-wb-testing-2.jpgAnti-ZNF147 TRIM25 AntibodyWestern Blot analysis of various cell lysis. Primary Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:10000
https://www.bosterbio.com/products/primary-antibodies/anti-gk3-antibody-a30492-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30492-gk3p-primary-antibodies-ihc-testing-1.jpgAnti-GK3 GK3P AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30492-gk3p-primary-antibodies-wb-testing-2.jpgAnti-GK3 GK3P AntibodyWestern Blot analysis of various cells using GK1/3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30492-gk3p-primary-antibodies-wb-testing-3.jpgAnti-GK3 GK3P AntibodyWestern blot analysis of lysates from 293 cells, using GK3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hlx1-antibody-a30494-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30494-hlx-primary-antibodies-ihc-testing-2.jpgAnti-HLX/Hlx11 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30494-hlx-primary-antibodies-wb-testing-3.jpgAnti-HLX/Hlx11 AntibodyWestern Blot analysis of various cells using HLX1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30494-hlx-primary-antibodies-if-testing-1.jpgAnti-HLX/Hlx11 AntibodyImmunofluorescence analysis of MCF7 cells, using HLX1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30494-hlx-primary-antibodies-wb-testing-4.jpgAnti-HLX/Hlx11 AntibodyWestern blot analysis of lysates from COLO205 cells, using HLX1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30494-hlx-primary-antibodies-wb-testing-5.jpgAnti-HLX/Hlx11 AntibodyWestern blot analysis of the lysates from HeLa cells using HLX1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-fakd3-antibody-a30495-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/F/A/FAKD3-primary-antibodies-A30495-WB-testing.jpgAnti-FAKD3 FASTKD3 AntibodyWestern blot analysis of lysates from HepG2 cells, using FAKD3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-zmy11-antibody-a30496-boster.html2026-03-24T05:10:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30496-zmynd11-primary-antibodies-ihc-testing-1.jpgAnti-ZMY11 ZMYND11 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ZMY11 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ssxt-antibody-a30497-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30497-ss18-primary-antibodies-ihc-testing-1.jpgAnti-SSXT SS18 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30497-ss18-primary-antibodies-wb-testing-2.jpgAnti-SSXT SS18 AntibodyWestern Blot analysis of COLO205 cells using SYT Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30497-ss18-primary-antibodies-wb-testing-3.jpgAnti-SSXT SS18 AntibodyWestern Blot analysis of various cells using SYT Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30497-ss18-primary-antibodies-wb-testing-4.jpgAnti-SSXT SS18 AntibodyWestern blot analysis of lysates from HepG2, Jurkat, and COLO205 cells, using SSXT Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-rhoh-antibody-a07101-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07101-rhoh-primary-antibodies-ihc-testing-2.jpgAnti-RhoH AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1,primary Antibody was diluted at 1:200(4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval(>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07101-rhoh-primary-antibodies-wb-testing-4.jpgAnti-RhoH AntibodyWestern blot analysis of the lysates from RAW264.7cells using RhoH antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07101-rhoh-primary-antibodies-if-testing-1.jpgAnti-RhoH AntibodyImmunofluorescence analysis of A549 cells, using RhoH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07101-rhoh-primary-antibodies-wb-testing-3.jpgAnti-RhoH AntibodyWestern blot analysis of lysates from HT-29 cells, using RhoH Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tsc22d1-antibody-a06397-1-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-1-tsc22d1-primary-antibodies-wb-testing-4.jpgAnti-TSC22 domain family protein 1 TSC22D1 AntibodyWestern blot analysis of the lysates from HepG2 cells using TSC22D1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-1-tsc22d1-primary-antibodies-if-testing-1.jpgAnti-TSC22 domain family protein 1 TSC22D1 AntibodyImmunofluorescence analysis of HepG2 cells, using TSC22D1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-1-tsc22d1-primary-antibodies-ihc-testing-2.jpgAnti-TSC22 domain family protein 1 TSC22D1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TSC22D1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-1-tsc22d1-primary-antibodies-wb-testing-3.jpgAnti-TSC22 domain family protein 1 TSC22D1 AntibodyWestern blot analysis of lysates from mouse liver and rat liver cells, using TSC22D1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ndf2-antibody-a30499-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30499-neurod2-primary-antibodies-ihc-testing-1.jpgAnti-NDF2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30499-neurod2-primary-antibodies-wb-testing-2.jpgAnti-NDF2 AntibodyWestern Blot analysis of various cells using Neuro D2 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30499-neurod2-primary-antibodies-wb-testing-4.jpgAnti-NDF2 AntibodyWestern blot analysis of the lysates from COLO205 cells using NDF2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30499-neurod2-primary-antibodies-wb-testing-3.jpgAnti-NDF2 AntibodyWestern blot analysis of lysates from 293, COLO, and Jurkat cells, using NDF2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf187-antibody-a30500-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30500-zscan26-primary-antibodies-ihc-testing-2.jpgAnti-ZNF187 ZSCAN26 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30500-zscan26-primary-antibodies-wb-testing-3.jpgAnti-ZNF187 ZSCAN26 AntibodyWestern Blot analysis of various cells using SRE-ZBP Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30500-zscan26-primary-antibodies-if-testing-1.jpgAnti-ZNF187 ZSCAN26 AntibodyImmunofluorescence analysis of A549 cells, using ZNF187 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30500-zscan26-primary-antibodies-wb-testing-4.jpgAnti-ZNF187 ZSCAN26 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using ZNF187 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pfkfb1-4-antibody-a30501-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30501-pfkfb1-primary-antibodies-ihc-testing-1.jpgAnti-PFKFB1/4 AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30501-pfkfb1-primary-antibodies-wb-testing-2.jpgAnti-PFKFB1/4 AntibodyWestern Blot analysis of various cells using PFK-2 liv/tes Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30501-pfkfb1-primary-antibodies-wb-testing-3.jpgAnti-PFKFB1/4 AntibodyWestern blot analysis of lysates from HeLa, HepG2, COLO205, and 293 cells, using PFKFB1/4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lrrk1-antibody-a06670-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06670-lrrk1-primary-antibodies-if-testing-1.jpgAnti-LRRK1 AntibodyImmunofluorescence analysis of HeLa cells, using LRRK1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06670-lrrk1-primary-antibodies-ihc-testing-2.jpgAnti-LRRK1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using LRRK1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-plch-antibody-a30503-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30503-gpat3-primary-antibodies-ihc-testing-2.jpgAnti-PLCH GPAT3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30503-gpat3-primary-antibodies-wb-testing-3.jpgAnti-PLCH GPAT3 AntibodyWestern Blot analysis of HEPG2 using LPAAT-θ Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30503-gpat3-primary-antibodies-wb-testing-4.jpgAnti-PLCH GPAT3 AntibodyWestern blot analysis of SH-SY5Y 3T3 lysis using LPAAT-θ antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30503-gpat3-primary-antibodies-if-testing-1.jpgAnti-PLCH GPAT3 AntibodyImmunofluorescence analysis of HepG2 cells, using PLCH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30503-gpat3-primary-antibodies-wb-testing-5.jpgAnti-PLCH GPAT3 AntibodyWestern blot analysis of lysates from Jurkat cells, COLO205 cells, HeLa cells, and HUVEC cells, using PLCH Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-qorx-antibody-a30504-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30504-tp53i3-primary-antibodies-ihc-testing-1.jpgAnti-QORX TP53I3 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30504-tp53i3-primary-antibodies-wb-testing-2.jpgAnti-QORX TP53I3 AntibodyWestern Blot analysis of various cells using PIG3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30504-tp53i3-primary-antibodies-wb-testing-3.jpgAnti-QORX TP53I3 AntibodyWestern blot analysis of lysates from 293 cells, using QORX Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-fakd1-antibody-a30505-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30505-fastkd1-primary-antibodies-wb-testing-2.jpgAnti-FAKD1 FASTKD1 AntibodyWestern blot analysis of lysates from COS7 cells, using FAKD1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ubxd5-antibody-a30506-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30506-ubxn11-primary-antibodies-ihc-testing-1.jpgAnti-UBXD5 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using UBXD5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30506-ubxn11-primary-antibodies-wb-testing-2.jpgAnti-UBXD5 AntibodyWestern blot analysis of lysates from HepG2 cells, using UBXD5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-map3kl4-antibody-a30507-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30507-map3k21-primary-antibodies-ihc-testing-1.jpgAnti-MAP3KL4 MAP3K21 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30507-map3k21-primary-antibodies-wb-testing-2.jpgAnti-MAP3KL4 MAP3K21 AntibodyWestern Blot analysis of various cells using MLK4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30507-map3k21-primary-antibodies-wb-testing-4.jpgAnti-MAP3KL4 MAP3K21 AntibodyWestern blot analysis of the lysates from HepG2 cells using MAP3KL4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30507-map3k21-primary-antibodies-wb-testing-3.jpgAnti-MAP3KL4 MAP3K21 AntibodyWestern blot analysis of lysates from HT-29 cells, using MAP3KL4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tm16a-antibody-a30508-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30508-ano1-primary-antibodies-if-testing-1.jpgAnti-TM16A ANO1 AntibodyImmunofluorescence analysis of HeLa cells, using TM16A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-stea3-antibody-a30509-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30509-steap3-primary-antibodies-ihc-testing-2.jpgAnti-STEA3 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30509-steap3-primary-antibodies-wb-testing-3.jpgAnti-STEA3 AntibodyWestern Blot analysis of various cells using pHyde Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30509-steap3-primary-antibodies-if-testing-1.jpgAnti-STEA3 AntibodyImmunofluorescence analysis of HeLa cells, using STEA3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30509-steap3-primary-antibodies-wb-testing-4.jpgAnti-STEA3 AntibodyWestern blot analysis of lysates from COLO205 cells, using STEA3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tens3-antibody-a30511-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30511-tns3-primary-antibodies-if-testing-1.jpgAnti-TENS3 AntibodyImmunofluorescence analysis of COS7 cells, using TENS3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30511-tns3-primary-antibodies-ihc-testing-2.jpgAnti-TENS3 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using TENS3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-camk1-beta-antibody-a11515-boster.html2026-03-24T05:10:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11515-pnck-primary-antibodies-ihc-testing-1.jpgAnti-CaMK1-beta PNCK AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CaMK1-beta Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11515-pnck-primary-antibodies-wb-testing-2.jpgAnti-CaMK1-beta PNCK AntibodyWestern blot analysis of lysates from LOVO cells, treated with H2O2 100uM 30', using CaMK1-beta Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tsh1-antibody-a30513-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30513-tshz1-primary-antibodies-ihc-testing-1.jpgAnti-TSH1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using TSH1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mol2c-antibody-a30514-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30514-mob3c-primary-antibodies-ihc-testing-1.jpgAnti-MOL2C MOB3C AntibodyImmunohistochemical analysis of paraffin-embedded Human pancreas. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30514-mob3c-primary-antibodies-wb-testing-2.jpgAnti-MOL2C MOB3C AntibodyWestern Blot analysis of RAW264.7 cells using Mob3C Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30514-mob3c-primary-antibodies-wb-testing-3.jpgAnti-MOL2C MOB3C AntibodyWestern blot analysis of lysates from RAW264.7 and K562 cells, using MOL2C Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ern2-antibody-a05659-1-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/E/R/ERN2-primary-antibodies-A05659-1-IHC-testing.jpgAnti-ERN2 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using ERN2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/E/R/ERN2-primary-antibodies-A05659-1-IF-testing.jpgAnti-ERN2 AntibodyImmunofluorescence analysis of A549 cells, using ERN2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-maea-antibody-a08766-1-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08766-1-maea-primary-antibodies-ihc-testing-1.jpgAnti-MAEA/Emp AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08766-1-maea-primary-antibodies-wb-testing-2.jpgAnti-MAEA/Emp AntibodyWestern Blot analysis of various cells using Emp Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08766-1-maea-primary-antibodies-wb-testing-3.jpgAnti-MAEA/Emp AntibodyWestern blot analysis of lysates from COLO205 cells, using MAEA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mol1a-antibody-a30515-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30515-mob1b-primary-antibodies-ihc-testing-1.jpgAnti-MOL1A MOB1B AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30515-mob1b-primary-antibodies-wb-testing-2.jpgAnti-MOL1A MOB1B AntibodyWestern Blot analysis of various cells using Mob1A Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30515-mob1b-primary-antibodies-wb-testing-3.jpgAnti-MOL1A MOB1B AntibodyWestern blot analysis of lysates from 293, COS7, and HUVEC cells, treated with IFN 2500U/ml 30', using MOL1A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-strad-antibody-a30516-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30516-strada-primary-antibodies-ihc-testing-1.jpgAnti-STRAD AntibodyImmunohistochemical analysis of paraffin-embedded human small intestinal carcinoma tissue. 1,primary Antibody was diluted at 1:200(4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval(>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30516-strada-primary-antibodies-wb-testing-2.jpgAnti-STRAD AntibodyWestern Blot analysis of various cells using Strad Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30516-strada-primary-antibodies-wb-testing-3.jpgAnti-STRAD AntibodyWestern blot analysis of lysates from HepG2 cells, using STRAD Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atpbd3-antibody-a30517-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30517-ctu1-primary-antibodies-wb-testing-1.jpgAnti-ATPBD3 CTU1 AntibodyWestern blot analysis of lysates from LOVO cells, using ATPBD3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30517-ctu1-primary-antibodies-wb-testing-2.jpgAnti-ATPBD3 CTU1 AntibodyWestern blot analysis of the lysates from 293 cells using ATPBD3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mobkl2b-antibody-a30518-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30518-mob3b-primary-antibodies-ihc-testing-1.jpgAnti-MOBKL2B MOB3B AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30518-mob3b-primary-antibodies-wb-testing-2.jpgAnti-MOBKL2B MOB3B AntibodyWestern Blot analysis of various cells using Mob3B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30518-mob3b-primary-antibodies-wb-testing-3.jpgAnti-MOBKL2B MOB3B AntibodyWestern blot analysis of lysates from COLO cells, using MOBKL2B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dgkh-antibody-a07077-1-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07077-1-dgkh-primary-antibodies-if-testing-1.jpgAnti-Diacylglycerol kinase eta DGKH AntibodyImmunofluorescence analysis of HeLa cells, using DGKH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07077-1-dgkh-primary-antibodies-ihc-testing-2.jpgAnti-Diacylglycerol kinase eta DGKH AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using DGKH Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lath-antibody-a30519-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30519-bpifa4p-primary-antibodies-if-testing-1.jpgAnti-LATH BPIFA4P AntibodyImmunofluorescence analysis of HeLa cells, using LATH Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30519-bpifa4p-primary-antibodies-ihc-testing-2.jpgAnti-LATH BPIFA4P AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using LATH Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-glctk-antibody-a30520-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30520-glyctk-primary-antibodies-if-testing-1.jpgAnti-GLCTK GLYCTK AntibodyImmunofluorescence analysis of A549 cells, using GLCTK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30520-glyctk-primary-antibodies-ihc-testing-2.jpgAnti-GLCTK GLYCTK AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GLCTK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30520-glyctk-primary-antibodies-wb-testing-3.jpgAnti-GLCTK GLYCTK AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using GLCTK Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30520-glyctk-primary-antibodies-wb-testing-4.jpgAnti-GLCTK GLYCTK AntibodyWestern blot analysis of the lysates from HUVECcells using GLCTK antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tp53inp2-antibody-a30521-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30521-tp53inp2-primary-antibodies-if-testing-1.jpgAnti-TP53INP2 AntibodyImmunofluorescence analysis of MCF7 cells, using TP53INP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30521-tp53inp2-primary-antibodies-ihc-testing-2.jpgAnti-TP53INP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using TP53INP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ccrk-antibody-a30522-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30522-cdk20-primary-antibodies-ihc-testing-2.jpgAnti-CCRK CDK20 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30522-cdk20-primary-antibodies-if-testing-1.jpgAnti-CCRK CDK20 AntibodyImmunofluorescence analysis of HUVEC cells, using CCRK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30522-cdk20-primary-antibodies-wb-testing-3.jpgAnti-CCRK CDK20 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using CCRK Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30522-cdk20-primary-antibodies-wb-testing-4.jpgAnti-CCRK CDK20 AntibodyWestern blot analysis of the lysates from RAW264.7cells using CCRK antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-kiaa1967-antibody-a30523-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30523-ccar2-primary-antibodies-ihc-testing-1.jpgAnti-KIAA1967 CCAR2 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30523-ccar2-primary-antibodies-wb-testing-2.jpgAnti-KIAA1967 CCAR2 AntibodyWestern blot analysis of lysates from Jurkat cells, using KIAA1967 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-map4k6-antibody-a30524-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30524-mink1-primary-antibodies-ihc-testing-1.jpgAnti-MAP4K6 MINK1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30524-mink1-primary-antibodies-wb-testing-2.jpgAnti-MAP4K6 MINK1 AntibodyWestern Blot analysis of various cells using MINK1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30524-mink1-primary-antibodies-wb-testing-3.jpgAnti-MAP4K6 MINK1 AntibodyWestern blot analysis of lysates from COLO cells, using MAP4K6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-camk5-antibody-a30525-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30525-camkv-primary-antibodies-wb-testing-3.jpgAnti-CAMK5 CAMKV AntibodyWestern Blot analysis of various cells using CaMKV Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30525-camkv-primary-antibodies-if-testing-1.jpgAnti-CAMK5 CAMKV AntibodyImmunofluorescence analysis of HeLa cells, using CAMK5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30525-camkv-primary-antibodies-ihc-testing-2.jpgAnti-CAMK5 CAMKV AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CAMK5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30525-camkv-primary-antibodies-wb-testing-4.jpgAnti-CAMK5 CAMKV AntibodyWestern blot analysis of lysates from HepG2 and HUVEC cells, using CAMK5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-actr-1c-antibody-a30526-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30526-acvr1c-primary-antibodies-if-testing-1.jpgAnti-ACTR-1C AntibodyImmunofluorescence analysis of COS7 cells, using ACTR-1C Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30526-acvr1c-primary-antibodies-ihc-testing-2.jpgAnti-ACTR-1C AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ACTR-1C Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-baf250b-antibody-a30528-boster.html2026-03-24T05:10:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30528-arid1b-primary-antibodies-ihc-testing-2.jpgAnti-BAF250B ARID1B AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30528-arid1b-primary-antibodies-wb-testing-3.jpgAnti-BAF250B ARID1B AntibodyWestern Blot analysis of 3T3 cells using BAF250b Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30528-arid1b-primary-antibodies-if-testing-1.jpgAnti-BAF250B ARID1B AntibodyImmunofluorescence analysis of HUVEC cells, using BAF250B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30528-arid1b-primary-antibodies-wb-testing-4.jpgAnti-BAF250B ARID1B AntibodyWestern blot analysis of lysates from LOVO cells, using BAF250B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-smrc2-antibody-a30530-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30530-smarcc2-primary-antibodies-wb-testing-1.jpgAnti-SMRC2 SMARCC2 AntibodyWestern Blot analysis of COLO205 cells using BAF170 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30530-smarcc2-primary-antibodies-wb-testing-2.jpgAnti-SMRC2 SMARCC2 AntibodyWestern Blot analysis of various cells using BAF170 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30530-smarcc2-primary-antibodies-wb-testing-3.jpgAnti-SMRC2 SMARCC2 AntibodyWestern blot analysis of lysates from HUVEC and COLO205 cells, using SMRC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-agr3-antibody-a05950-1-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05950-1-agr3-primary-antibodies-if-testing-1.jpgAnti-Anterior gradient protein 3 AGR3 AntibodyImmunofluorescence analysis of COS7 cells, using AGR3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05950-1-agr3-primary-antibodies-ihc-testing-2.jpgAnti-Anterior gradient protein 3 AGR3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using AGR3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dusp19-antibody-a30531-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30531-dusp19-primary-antibodies-wb-testing-2.jpgAnti-DUSP19/Skrp1 AntibodyWestern Blot analysis of various cells using DUSP19 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30531-dusp19-primary-antibodies-if-testing-1.jpgAnti-DUSP19/Skrp1 AntibodyImmunofluorescence analysis of HeLa cells, using DUSP19 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30531-dusp19-primary-antibodies-wb-testing-3.jpgAnti-DUSP19/Skrp1 AntibodyWestern blot analysis of lysates from COS7 cells, using DUSP19 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tf3c2-antibody-a30532-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30532-gtf3c2-primary-antibodies-ihc-testing-1.jpgAnti-TF3C2 AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30532-gtf3c2-primary-antibodies-wb-testing-2.jpgAnti-TF3C2 AntibodyWestern Blot analysis of various cells using TFIIIC110 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30532-gtf3c2-primary-antibodies-wb-testing-3.jpgAnti-TF3C2 AntibodyWestern blot analysis of lysates from HepG2, COLO205, and HUVEC cells, using TF3C2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-orav1-antibody-a30533-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30533-oraov1-primary-antibodies-ihc-testing-1.jpgAnti-ORAV1 ORAOV1 AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30533-oraov1-primary-antibodies-wb-testing-2.jpgAnti-ORAV1 ORAOV1 AntibodyWestern Blot analysis of various cells using ORAOV1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30533-oraov1-primary-antibodies-wb-testing-3.jpgAnti-ORAV1 ORAOV1 AntibodyWestern blot analysis of lysates from 293 and HeLa cells, using ORAV1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prp31-antibody-a30534-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30534-prpf31-primary-antibodies-ihc-testing-1.jpgAnti-PRP31 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30534-prpf31-primary-antibodies-wb-testing-2.jpgAnti-PRP31 AntibodyWestern blot analysis of lysates from HeLa cells, using PRP31 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cnkr2-antibody-a30535-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30535-cnksr2-primary-antibodies-wb-testing-1.jpgAnti-CNKR2 AntibodyWestern Blot analysis of 293T cells using CNK2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30535-cnksr2-primary-antibodies-wb-testing-2.jpgAnti-CNKR2 AntibodyWestern blot analysis of lysates from Jurkat cells, using CNKR2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-bri3b-antibody-a30536-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30536-bri3bp-primary-antibodies-ihc-testing-1.jpgAnti-BRI3B BRI3BP AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using BRI3B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30536-bri3bp-primary-antibodies-wb-testing-2.jpgAnti-BRI3B BRI3BP AntibodyWestern blot analysis of lysates from RAW264.7 cells, using BRI3B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sept1-antibody-a30537-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30537-sept1-primary-antibodies-ihc-testing-1.jpgAnti-SEPT1 SEPT1; AntibodyImmunohistochemical analysis of paraffin-embedded human spleen tissue. 1,primary Antibody was diluted at 1:200(4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval(>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30537-sept1-primary-antibodies-wb-testing-2.jpgAnti-SEPT1 SEPT1; AntibodyWestern Blot analysis of various cells using Septin 1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30537-sept1-primary-antibodies-wb-testing-3.jpgAnti-SEPT1 SEPT1; AntibodyWestern blot analysis of lysates from Jurkat cells, using SEPT1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-celf-1-antibody-a30541-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30541-celf1-primary-antibodies-ihc-testing-1.jpgAnti-CELF-1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30541-celf1-primary-antibodies-wb-testing-2.jpgAnti-CELF-1 AntibodyWestern Blot analysis of various cells using CUG-BP1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30541-celf1-primary-antibodies-wb-testing-3.jpgAnti-CELF-1 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using CELF-1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mekkk-1-antibody-a30542-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30542-map4k1-primary-antibodies-ihc-testing-1.jpgAnti-MEKKK 1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30542-map4k1-primary-antibodies-wb-testing-2.jpgAnti-MEKKK 1 AntibodyWestern Blot analysis of various cells using HPK1 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30542-map4k1-primary-antibodies-wb-testing-4.jpgAnti-MEKKK 1 AntibodyWestern blot analysis of the lysates from HUVECcells using MEKKK 1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30542-map4k1-primary-antibodies-wb-testing-3.jpgAnti-MEKKK 1 AntibodyWestern blot analysis of lysates from HepG2 cells, using MEKKK 1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tip60-antibody-a30543-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30543-kat5-primary-antibodies-ihc-testing-1.jpgAnti-TIP60 KAT5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TIP60 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tf3b-antibody-a30544-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30544-brf1-primary-antibodies-wb-testing-3.jpgAnti-TF3B BRF1 AntibodyWestern Blot analysis of various cells using TFIIIB90-1 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30544-brf1-primary-antibodies-if-testing-1.jpgAnti-TF3B BRF1 AntibodyImmunofluorescence analysis of MCF7 cells, using TF3B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30544-brf1-primary-antibodies-ihc-testing-2.jpgAnti-TF3B BRF1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TF3B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30544-brf1-primary-antibodies-wb-testing-4.jpgAnti-TF3B BRF1 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using TF3B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kpbb-antibody-a30545-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30545-phkb-primary-antibodies-ihc-testing-1.jpgAnti-KPBB PHKB AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30545-phkb-primary-antibodies-wb-testing-2.jpgAnti-KPBB PHKB AntibodyWestern blot analysis of lysates from K562 cells, using KPBB Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cnkr1-antibody-a30546-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30546-cnksr1-primary-antibodies-ihc-testing-1.jpgAnti-CNKR1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30546-cnksr1-primary-antibodies-wb-testing-2.jpgAnti-CNKR1 AntibodyWestern Blot analysis of COLO cells using CNK1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30546-cnksr1-primary-antibodies-wb-testing-3.jpgAnti-CNKR1 AntibodyWestern blot analysis of lysates from COLO205 cells, using CNKR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30546-cnksr1-primary-antibodies-wb-testing-4.jpgAnti-CNKR1 AntibodyWestern blot analysis of the lysates from HT-29 cells using CNKSR1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tmepa-antibody-a30547-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-wb-testing-3.jpgAnti-TMEPA PMEPA1 AntibodyWestern Blot analysis of HT29 cells using PMEPA1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-wb-testing-4.jpgAnti-TMEPA PMEPA1 AntibodyWestern Blot analysis of various cells using PMEPA1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-wb-testing-6.jpgAnti-TMEPA PMEPA1 AntibodyWestern blot analysis of the lysates from HeLa cells using PMEPA1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-if-testing-1.jpgAnti-TMEPA PMEPA1 AntibodyImmunofluorescence analysis of HUVEC cells, using TMEPA Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-ihc-testing-2.jpgAnti-TMEPA PMEPA1 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate tissue, using TMEPA Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30547-pmepa1-primary-antibodies-wb-testing-5.jpgAnti-TMEPA PMEPA1 AntibodyWestern blot analysis of lysates from HT-29 cells, using TMEPA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-orctl-2-antibody-a30548-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30548-slc22a18-primary-antibodies-wb-testing-1.jpgAnti-ORCTL-2 AntibodyWestern Blot analysis of various cells using ORCTL2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30548-slc22a18-primary-antibodies-wb-testing-2.jpgAnti-ORCTL-2 AntibodyWestern blot analysis of lysates from COLO205 cells, using ORCTL-2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ip3kc-antibody-a30549-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30549-itpkc-primary-antibodies-ihc-testing-1.jpgAnti-IP3KC ITPKC AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30549-itpkc-primary-antibodies-wb-testing-2.jpgAnti-IP3KC ITPKC AntibodyWestern Blot analysis of various cells using InsP 3-kinase C Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30549-itpkc-primary-antibodies-wb-testing-3.jpgAnti-IP3KC ITPKC AntibodyWestern blot analysis of lysates from HT-29 cells, using IP3KC Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mark4-antibody-a04672-1-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04672-1-mark4-primary-antibodies-if-testing-1.jpgAnti-MARK4 AntibodyImmunofluorescence analysis of A549 cells, using MARK4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tref1-antibody-a30550-boster.html2026-03-24T05:10:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30550-trerf1-primary-antibodies-ihc-testing-1.jpgAnti-TREF1 TRERF1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TREF1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rhg07-antibody-a30552-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30552-dlc1-primary-antibodies-if-testing-1.jpgAnti-RHG07 DLC1 AntibodyImmunofluorescence analysis of A549 cells, using RHG07 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30552-dlc1-primary-antibodies-ihc-testing-2.jpgAnti-RHG07 DLC1 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using RHG07 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-serc2-antibody-a30553-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30553-serinc2-primary-antibodies-ihc-testing-2.jpgAnti-SERC2 SERINC2 AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30553-serinc2-primary-antibodies-wb-testing-3.jpgAnti-SERC2 SERINC2 AntibodyWestern Blot analysis of various cells using TDE2L Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30553-serinc2-primary-antibodies-if-testing-1.jpgAnti-SERC2 SERINC2 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using SERC2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30553-serinc2-primary-antibodies-wb-testing-4.jpgAnti-SERC2 SERINC2 AntibodyWestern blot analysis of lysates from HeLa cells, using SERC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-begin-antibody-a30554-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30554-begain-primary-antibodies-if-testing-1.jpgAnti-BEGIN BEGAIN AntibodyImmunofluorescence analysis of HeLa cells, using BEGIN Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30554-begain-primary-antibodies-ihc-testing-2.jpgAnti-BEGIN BEGAIN AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using BEGIN Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nadap-antibody-a30555-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30555-slc4a1ap-primary-antibodies-ihc-testing-1.jpgAnti-NADAP SLC4A1AP AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-an30a-antibody-a30557-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30557-ankrd30a-primary-antibodies-ihc-testing-1.jpgAnti-AN30A AntibodyImmunohistochemical analysis of paraffin-embedded human Small intestinal stromal tumor. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30557-ankrd30a-primary-antibodies-wb-testing-2.jpgAnti-AN30A AntibodyWestern Blot analysis of various cells using ANKRD30A Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30557-ankrd30a-primary-antibodies-wb-testing-3.jpgAnti-AN30A AntibodyWestern blot analysis of lysates from 293 and COLO cells, using AN30A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pcdh-x-y-antibody-a07423-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07423-pcdh11y-primary-antibodies-if-testing-1.jpgAnti-PCDH-X/Y AntibodyImmunofluorescence analysis of HepG2 cells, using PCDH-X/Y Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07423-pcdh11y-primary-antibodies-ihc-testing-2.jpgAnti-PCDH-X/Y AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using PCDH-X/Y Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-bhlhb3-antibody-a04668-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04668-bhlhe41-primary-antibodies-ihc-testing-1.jpgAnti-BHLHB3 BHLHE41 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04668-bhlhe41-primary-antibodies-wb-testing-2.jpgAnti-BHLHB3 BHLHE41 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using BHLHB3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pbov1-antibody-a15695-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15695-pbov1-primary-antibodies-ihc-testing-1.jpgAnti-PBOV1 AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15695-pbov1-primary-antibodies-wb-testing-2.jpgAnti-PBOV1 AntibodyWestern blot analysis of lysates from K562 cells, using PBOV1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nt5c3-antibody-a30559-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30559-nt5c3a-primary-antibodies-wb-testing-3.jpgAnti-NT5C3 AntibodyWestern blot analysis of the lysates from 293 cells using NT5C3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30559-nt5c3a-primary-antibodies-ihc-testing-1.jpgAnti-NT5C3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NT5C3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30559-nt5c3a-primary-antibodies-wb-testing-2.jpgAnti-NT5C3 AntibodyWestern blot analysis of lysates from Jurkat and COLO205 cells, using NT5C3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ecrg4-antibody-a10864-1-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/C/2/C2orf40-primary-antibodies-A10864-1-IHC-testing.jpgAnti-ECRG4 C2orf40 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using ECRG4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/C/2/C2orf40-primary-antibodies-A10864-1-IF-testing.jpgAnti-ECRG4 C2orf40 AntibodyImmunofluorescence analysis of A549 cells, using ECRG4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-blzf1-antibody-a09997-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09997-blzf1-primary-antibodies-ihc-testing-1.jpgAnti-BLZF1/Golgin 45 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09997-blzf1-primary-antibodies-wb-testing-2.jpgAnti-BLZF1/Golgin 45 AntibodyWestern blot analysis of lysates from Jurkat cells, using BLZF1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09997-blzf1-primary-antibodies-wb-testing-3.jpgAnti-BLZF1/Golgin 45 AntibodyWestern blot analysis of the lysates from COLO205 cells using BLZF1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-myst1-antibody-a30560-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30560-kat8-primary-antibodies-ihc-testing-1.jpgAnti-MYST1 KAT8 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MYST1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ippk-antibody-a11126-1-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11126-1-ippk-primary-antibodies-if-testing-1.jpgAnti-IPPK AntibodyImmunofluorescence analysis of HepG2 cells, using IPPK Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11126-1-ippk-primary-antibodies-ihc-testing-2.jpgAnti-IPPK AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using IPPK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lass4-antibody-a30561-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30561-cers4-primary-antibodies-wb-testing-2.jpgAnti-LASS4 AntibodyWestern Blot analysis of various cells using LASS4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30561-cers4-primary-antibodies-ihc-testing-1.jpgAnti-LASS4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using LASS4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30561-cers4-primary-antibodies-wb-testing-3.jpgAnti-LASS4 AntibodyWestern blot analysis of lysates from HUVEC, COLO, and Jurkat cells, using LASS4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-bca3-antibody-a30562-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30562-akip1-primary-antibodies-wb-testing-2.jpgAnti-BCA3 AKIP1 AntibodyWestern Blot analysis of various cells using BCA3 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30562-akip1-primary-antibodies-ihc-testing-1.jpgAnti-BCA3 AKIP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using BCA3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30562-akip1-primary-antibodies-wb-testing-3.jpgAnti-BCA3 AKIP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using BCA3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30562-akip1-primary-antibodies-wb-testing-4.jpgAnti-BCA3 AKIP1 AntibodyWestern blot analysis of the lysates from HepG2 cells using BCA3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tsh2-antibody-a08863-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08863-tshz2-primary-antibodies-if-testing-1.jpgAnti-TSH2 TSHZ2 AntibodyImmunofluorescence analysis of MCF7 cells, using TSH2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08863-tshz2-primary-antibodies-ihc-testing-2.jpgAnti-TSH2 TSHZ2 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using TSH2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-chrc1-antibody-a12215-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12215-chrac1-primary-antibodies-ihc-testing-1.jpgAnti-CHRC1 CHRAC1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CHRC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-serc1-antibody-a10374-1-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-1-serinc1-primary-antibodies-ihc-testing-1.jpgAnti-SERC1 SERINC1 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-1-serinc1-primary-antibodies-wb-testing-2.jpgAnti-SERC1 SERINC1 AntibodyWestern Blot analysis of various cells using Serinc1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10374-1-serinc1-primary-antibodies-wb-testing-3.jpgAnti-SERC1 SERINC1 AntibodyWestern blot analysis of lysates from HepG2 cells, using SERC1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-asf1b-antibody-a05211-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05211-asf1b-primary-antibodies-ihc-testing-1.jpgAnti-Histone chaperone ASF1B ASF1B AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05211-asf1b-primary-antibodies-wb-testing-2.jpgAnti-Histone chaperone ASF1B ASF1B AntibodyWestern blot analysis of lysates from K562 cells, using ASF1B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dus2l-antibody-a30563-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30563-dus2-primary-antibodies-ihc-testing-1.jpgAnti-DUS2/Dus2LL AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using DUS2L Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30563-dus2-primary-antibodies-wb-testing-2.jpgAnti-DUS2/Dus2LL AntibodyWestern blot analysis of lysates from RAW264.7 cells, using DUS2L Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcip1-antibody-a05755-1-boster.html2026-03-24T05:10:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05755-1-kcnip1-primary-antibodies-if-testing-1.jpgAnti-KCIP1 KCNIP1 AntibodyImmunofluorescence analysis of HeLa cells, using KCIP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05755-1-kcnip1-primary-antibodies-ihc-testing-2.jpgAnti-KCIP1 KCNIP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using KCIP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-epha6-antibody-a08818-1-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08818-1-epha6-primary-antibodies-if-testing-1.jpgAnti-EPHA6/Eph Receptor A6 AntibodyImmunofluorescence analysis of COS7 cells, using EPHA6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08818-1-epha6-primary-antibodies-ihc-testing-2.jpgAnti-EPHA6/Eph Receptor A6 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using EPHA6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-armx3-antibody-a14662-1-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14662-1-armcx3-primary-antibodies-if-testing-1.jpgAnti-ARMX3 ARMCX3 AntibodyImmunofluorescence analysis of HepG2 cells, using ARMX3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14662-1-armcx3-primary-antibodies-ihc-testing-2.jpgAnti-ARMX3 ARMCX3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ARMX3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14662-1-armcx3-primary-antibodies-wb-testing-3.jpgAnti-ARMX3 ARMCX3 AntibodyWestern blot analysis of lysates from K562 cells, using ARMX3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14662-1-armcx3-primary-antibodies-wb-testing-4.jpgAnti-ARMX3 ARMCX3 AntibodyWestern blot analysis of the lysates from COLO205 cells using ARMX3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-akap11-antibody-a07963-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07963-akap11-primary-antibodies-if-testing-1.jpgAnti-A-kinase anchor protein 11 AKAP11 AntibodyImmunofluorescence analysis of HepG2 cells, using AKAP11 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07963-akap11-primary-antibodies-ihc-testing-2.jpgAnti-A-kinase anchor protein 11 AKAP11 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using AKAP11 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ergi3-antibody-a09260-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09260-ergic3-primary-antibodies-ihc-testing-2.jpgAnti-ERGI3 ERGIC3 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09260-ergic3-primary-antibodies-if-testing-1.jpgAnti-ERGI3 ERGIC3 AntibodyImmunofluorescence analysis of HepG2 cells, using ERGI3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09260-ergic3-primary-antibodies-wb-testing-3.jpgAnti-ERGI3 ERGIC3 AntibodyWestern blot analysis of lysates from LOVO and NIH/3T3 cells, using ERGI3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mobl3-antibody-a19781-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19781-mob4-primary-antibodies-ihc-testing-1.jpgAnti-MOBL3 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19781-mob4-primary-antibodies-wb-testing-3.jpgAnti-MOBL3 AntibodyWestern blot analysis of the lysates from HT-29 cells using MOBL3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19781-mob4-primary-antibodies-wb-testing-2.jpgAnti-MOBL3 AntibodyWestern blot analysis of lysates from rat brain cells, using MOBL3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sta13-antibody-a06178-1-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06178-1-stard13-primary-antibodies-ihc-testing-2.jpgAnti-STA13 STARD13 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06178-1-stard13-primary-antibodies-wb-testing-3.jpgAnti-STA13 STARD13 AntibodyWestern blot analysis of STA13 Antibody. The lane on the right is blocked with the STA13 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06178-1-stard13-primary-antibodies-if-testing-1.jpgAnti-STA13 STARD13 AntibodyImmunofluorescence analysis of A549 cells, using STA13 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-map3k4-antibody-a04842-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04842-map3k4-primary-antibodies-ihc-testing-1.jpgAnti-MAP3K4/Mekk4 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using MAP3K4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-14-3-3-eta-antibody-a04219-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-ywhah-primary-antibodies-if-testing-1.jpgAnti-14-3-3 eta YWHAH AntibodyImmunofluorescence analysis of HeLa cells, using 14-3-3 eta Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-ywhah-primary-antibodies-wb-testing-2.jpgAnti-14-3-3 eta YWHAH AntibodyWestern blot analysis of lysates from Jurkat cells, using 14-3-3 eta Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-14-3-3-gamma-antibody-a04148-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04148-ywhag-primary-antibodies-if-testing-1.jpgAnti-14-3-3 gamma YWHAG AntibodyImmunofluorescence analysis of COS7 cells, using 14-3-3 gamma Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04148-ywhag-primary-antibodies-ihc-testing-2.jpgAnti-14-3-3 gamma YWHAG AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using 14-3-3 gamma Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04148-ywhag-primary-antibodies-wb-testing-3.jpgAnti-14-3-3 gamma YWHAG AntibodyWestern blot analysis of lysates from K562 cells, treated with insulin 0.01U/ml 15', using 14-3-3 gamma Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-adra1d-antibody-a04571-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04571-adra1d-primary-antibodies-if-testing-1.jpgAnti-Alpha-1D adrenergic receptor ADRA1D AntibodyImmunofluorescence analysis of HeLa cells, using ADRA1D Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04571-adra1d-primary-antibodies-ihc-testing-2.jpgAnti-Alpha-1D adrenergic receptor ADRA1D AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ADRA1D Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-adcy8-antibody-a08061-1-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08061-1-adcy8-primary-antibodies-if-testing-1.jpgAnti-ADCY8/Adenylate Cyclase 8 AntibodyImmunofluorescence analysis of A549 cells, using ADCY8 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08061-1-adcy8-primary-antibodies-ihc-testing-2.jpgAnti-ADCY8/Adenylate Cyclase 8 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ADCY8 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-arrd4-antibody-a12500-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12500-arrdc4-primary-antibodies-ihc-testing-1.jpgAnti-ARRD4 ARRDC4 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12500-arrdc4-primary-antibodies-wb-testing-2.jpgAnti-ARRD4 ARRDC4 AntibodyWestern blot analysis of lysates from COLO cells, using ARRD4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-as250-antibody-a10416-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10416-ralgapa2-primary-antibodies-if-testing-1.jpgAnti-AS250 RALGAPA2 AntibodyImmunofluorescence analysis of HeLa cells, using AS250 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10416-ralgapa2-primary-antibodies-ihc-testing-2.jpgAnti-AS250 RALGAPA2 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using AS250 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10416-ralgapa2-primary-antibodies-wb-testing-3.jpgAnti-AS250 RALGAPA2 AntibodyWestern blot analysis of lysates from Jurkat cells, using AS250 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cytochrome-b561-d1-antibody-a16342-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16342-cyb561d1-primary-antibodies-if-testing-1.jpgAnti-Cytochrome b561 D1 CYB561D1 AntibodyImmunofluorescence analysis of MCF-7 cells, using Cytochrome b561 D1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16342-cyb561d1-primary-antibodies-wb-testing-2.jpgAnti-Cytochrome b561 D1 CYB561D1 AntibodyWestern blot analysis of lysates from HeLa cells and COLO205 cells, using Cytochrome b561 D1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh10-antibody-a10616-1-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/C/D/CDH10-primary-antibodies-A10616-1-IF-testing.jpgAnti-CDH10/T2-cadherin 10 AntibodyImmunofluorescence analysis of LOVO cells, using CDH10 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh20-antibody-a13390-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13390-cdh20-primary-antibodies-wb-testing-4.jpgAnti-Cadherin-20 CDH20 AntibodyWestern blot analysis of CDH20 Antibody. The lane on the right is blocked with the CDH20 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13390-cdh20-primary-antibodies-ihc-testing-3.jpgAnti-Cadherin-20 CDH20 AntibodyImmunohistochemistryt analysis of paraffin-embedded human brain, using CDH20 Antibody. The lane on the right is blocked with the CDH20 peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13390-cdh20-primary-antibodies-if-testing-1.jpgAnti-Cadherin-20 CDH20 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using CDH20 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13390-cdh20-primary-antibodies-ihc-testing-2.jpgAnti-Cadherin-20 CDH20 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CDH20 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh22-antibody-a14160-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14160-cdh22-primary-antibodies-if-testing-1.jpgAnti-Cadherin-22 CDH22 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using CDH22 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14160-cdh22-primary-antibodies-ihc-testing-2.jpgAnti-Cadherin-22 CDH22 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CDH22 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14160-cdh22-primary-antibodies-wb-testing-3.jpgAnti-Cadherin-22 CDH22 AntibodyWestern blot analysis of lysates from rat brain cells, using CDH22 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh23-antibody-a02149-2-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02149-2-cdh23-primary-antibodies-if-testing-1.jpgAnti-CDH23/OtoCadherin 23 AntibodyImmunofluorescence analysis of HeLa cells, using CDH23 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh24-antibody-a13245-boster.html2026-03-24T05:10:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13245-cdh24-primary-antibodies-if-testing-1.jpgAnti-CDH24/Cadherin 24 AntibodyImmunofluorescence analysis of HepG2 cells, using CDH24 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdh4-antibody-a07632-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07632-cdh4-primary-antibodies-if-testing-1.jpgAnti-R-Cadherin-4 CDH4-AntibodyImmunofluorescence analysis of A549 cells, using CDH4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07632-cdh4-primary-antibodies-ihc-testing-2.jpgAnti-R-Cadherin-4 CDH4-AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CDH4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07632-cdh4-primary-antibodies-wb-testing-3.jpgAnti-R-Cadherin-4 CDH4-AntibodyWestern blot analysis of the lysates from COLO205 cells using Cytochrome P450 2D6 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-tmem30c-antibody-a16756-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16756-tmem30c-primary-antibodies-if-testing-1.jpgAnti-Cell cycle control protein 50C TMEM30C AntibodyImmunofluorescence analysis of MCF7 cells, using TMEM30C Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ccrl1-antibody-a30564-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30564-ackr4-primary-antibodies-wb-testing-2.jpgAnti-CCRL1 AntibodyWestern Blot analysis of various cells using CCRL1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30564-ackr4-primary-antibodies-if-testing-1.jpgAnti-CCRL1 AntibodyImmunofluorescence analysis of MCF7 cells, using CCRL1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30564-ackr4-primary-antibodies-wb-testing-3.jpgAnti-CCRL1 AntibodyWestern blot analysis of lysates from HepG2 cells, using CCRL1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd99-antibody-a01724-1-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01724-1-cd99-primary-antibodies-if-testing-1.jpgAnti-CD99 antigen CD99 AntibodyImmunofluorescence analysis of COS7 cells, using CD99 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdca4-antibody-a13717-1-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13717-1-cdca4-primary-antibodies-wb-testing-3.jpgAnti-CDCA4 AntibodyWestern blot analysis of lysates from A431 cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13717-1-cdca4-primary-antibodies-if-testing-1.jpgAnti-CDCA4 AntibodyImmunofluorescence analysis of HepG2 cells, using CDCA4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13717-1-cdca4-primary-antibodies-ihc-testing-2.jpgAnti-CDCA4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CDCA4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-celsr1-antibody-a06056-1-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06056-1-celsr1-primary-antibodies-if-testing-1.jpgAnti-CELSR1 AntibodyImmunofluorescence analysis of HepG2 cells, using CELSR1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-celsr2-antibody-a06880-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06880-celsr2-primary-antibodies-if-testing-1.jpgAnti-CELSR2/Egfl2 AntibodyImmunofluorescence analysis of COS7 cells, using CELSR2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06880-celsr2-primary-antibodies-ihc-testing-2.jpgAnti-CELSR2/Egfl2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CELSR2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cdk5rap2-antibody-a03102-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03102-cdk5rap2-primary-antibodies-ihc-testing-1.jpgAnti-CDK5RAP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using CDK5RAP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-vi-alpha3-antibody-a02844-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02844-col6a3-primary-antibodies-if-testing-1.jpgAnti-Collagen VI alpha3 COL6A3 AntibodyImmunofluorescence analysis of HeLa cells, using Collagen VI alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02844-col6a3-primary-antibodies-ihc-testing-2.jpgAnti-Collagen VI alpha3 COL6A3 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Collagen VI alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-ix-alpha3-antibody-a05963-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05963-col9a3-primary-antibodies-if-testing-1.jpgAnti-Collagen IX alpha3 COL9A3 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using Collagen IX alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05963-col9a3-primary-antibodies-ihc-testing-2.jpgAnti-Collagen IX alpha3 COL9A3 AntibodyImmunohistochemistry analysis of paraffin-embedded human tonsil tissue, using Collagen IX alpha3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-xiii-alpha1-antibody-a06702-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06702-col13a1-primary-antibodies-if-testing-1.jpgAnti-Collagen XIII alpha1 COL13A1 AntibodyImmunofluorescence analysis of A549 cells, using Collagen XIII alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06702-col13a1-primary-antibodies-wb-testing-2.jpgAnti-Collagen XIII alpha1 COL13A1 AntibodyWestern blot analysis of the lysates from HT-29 cells using ADD3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-xvi-alpha1-antibody-a07515-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07515-col16a1-primary-antibodies-ihc-testing-1.jpgAnti-Collagen XVI alpha1 COL16A1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using Collagen XVI alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-xix-alpha1-antibody-a10551-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10551-col19a1-primary-antibodies-if-testing-1.jpgAnti-Collagen XIX alpha1 COL19A1 AntibodyImmunofluorescence analysis of A549 cells, using Collagen XIX alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10551-col19a1-primary-antibodies-ihc-testing-2.jpgAnti-Collagen XIX alpha1 COL19A1 AntibodyImmunohistochemistry analysis of paraffin-embedded human thymus gland tissue, using Collagen XIX alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-xx-alpha1-antibody-a14855-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14855-col20a1-primary-antibodies-if-testing-1.jpgAnti-Collagen XX alpha1 COL20A1 AntibodyImmunofluorescence analysis of NIH/3T3 cells, using Collagen XX alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14855-col20a1-primary-antibodies-ihc-testing-2.jpgAnti-Collagen XX alpha1 COL20A1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using Collagen XX alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14855-col20a1-primary-antibodies-wb-testing-3.jpgAnti-Collagen XX alpha1 COL20A1 AntibodyWestern blot analysis of lysates from LOVO and HT-19 cells, using Collagen XX alpha1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-collagen-xxiii-alpha1-antibody-a13263-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13263-col23a1-primary-antibodies-if-testing-1.jpgAnti-Collagen XXIII alpha1 COL23A1 AntibodyImmunofluorescence analysis of HepG2 cells, using Collagen XXIII alpha1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cox11-antibody-a09173-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09173-cox11-primary-antibodies-ihc-testing-1.jpgAnti-COX11 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09173-cox11-primary-antibodies-wb-testing-2.jpgAnti-COX11 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using COX11 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cox19-antibody-a13267-1-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13267-1-cox19-primary-antibodies-ihc-testing-1.jpgAnti-COX19 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using COX19 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cox7s-a2-antibody-a09993-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09993-cox7a2p2-primary-antibodies-ihc-testing-1.jpgAnti-COX7S/A2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using COX7S/A2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09993-cox7a2p2-primary-antibodies-wb-testing-3.jpgAnti-COX7S/A2 AntibodyWestern blot analysis of lysates from rat heart cells, using COX7S/A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cytl1-antibody-a12117-boster.html2026-03-24T05:10:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12117-cytl1-primary-antibodies-ihc-testing-1.jpgAnti-Cytokine-like protein 1 CYTL1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using CYTL1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12117-cytl1-primary-antibodies-wb-testing-2.jpgAnti-Cytokine-like protein 1 CYTL1 AntibodyWestern blot analysis of lysates from LOVO cells, using CYTL1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12117-cytl1-primary-antibodies-wb-testing-3.jpgAnti-Cytokine-like protein 1 CYTL1 AntibodyWestern blot analysis of the lysates from HT-29 cells using CYTL1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dap-antibody-a02756-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02756-dap-primary-antibodies-ihc-testing-1.jpgAnti-DAP/Dap1 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using DAP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ifit1-antibody-a02652-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02652-ifit1-primary-antibodies-ihc-testing-1.jpgAnti-IFIT1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02652-ifit1-primary-antibodies-wb-testing-2.jpgAnti-IFIT1 AntibodyWestern blot analysis of lysates from LOVO cells, using IFIT1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dmc1-antibody-a02978-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02978-dmc1-primary-antibodies-ihc-testing-1.jpgAnti-DMC1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using DMC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eloa2-antibody-a15837-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15837-tceb3b-primary-antibodies-if-testing-1.jpgAnti-ELOA2 TCEB3B AntibodyImmunofluorescence analysis of A549 cells, using ELOA2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-leg2-antibody-a04114-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04114-lgals2-primary-antibodies-if-testing-1.jpgAnti-LEG2 LGALS2 AntibodyImmunofluorescence analysis of COS7 cells, using LEG2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04114-lgals2-primary-antibodies-ihc-testing-2.jpgAnti-LEG2 LGALS2 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using LEG2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rad51l1-antibody-a20019-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/2/a20019-rad51b-primary-antibodies-ihc-testing-1.jpgAnti-RAD51L1 RAD51B AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas tissue, using RAD51L1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/2/a20019-rad51b-primary-antibodies-wb-testing-2.jpgAnti-RAD51L1 RAD51B AntibodyWestern blot analysis of lysates from COS7 cells, using RAD51L1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rad51l3-antibody-a20020-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/2/a20020-rad51d-primary-antibodies-ihc-testing-1.jpgAnti-RAD51L3 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/2/a20020-rad51d-primary-antibodies-wb-testing-3.jpgAnti-RAD51L3 AntibodyWestern blot analysis of the lysates from Jurkat cells using MLH3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/2/a20020-rad51d-primary-antibodies-wb-testing-2.jpgAnti-RAD51L3 AntibodyWestern blot analysis of lysates from Jurkat cells, using RAD51L3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rad54-antibody-a03328-1-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03328-1-rad54l-primary-antibodies-ihc-testing-1.jpgAnti-RAD54 RAD54L AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03328-1-rad54l-primary-antibodies-wb-testing-2.jpgAnti-RAD54 RAD54L AntibodyWestern blot analysis of lysates from HeLa cells, Jurkat cells, and 293 cells, using RAD54 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-agpat3-antibody-a09369-1-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09369-1-agpat3-primary-antibodies-ihc-testing-1.jpgAnti-AGPAT3 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09369-1-agpat3-primary-antibodies-wb-testing-2.jpgAnti-AGPAT3 AntibodyWestern blot analysis of lysates from K562 cells, using AGPAT3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09369-1-agpat3-primary-antibodies-wb-testing-3.jpgAnti-AGPAT3 AntibodyWestern blot analysis of the lysates from COLO205 cells using AGPAT3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps17-antibody-a14408-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14408-mrps17-primary-antibodies-ihc-testing-1.jpgAnti-MRPS17 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14408-mrps17-primary-antibodies-wb-testing-3.jpgAnti-MRPS17 AntibodyWestern blot analysis of the lysates from HeLa cells using MRPS17 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14408-mrps17-primary-antibodies-wb-testing-2.jpgAnti-MRPS17 AntibodyWestern blot analysis of lysates from NIH/3T3, RAW264.7, and A549 cells, using MRPS17 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps18a-antibody-a14515-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14515-mrps18a-primary-antibodies-ihc-testing-1.jpgAnti-MRPS18A AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using MRPS18A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps24-antibody-a15344-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15344-mrps24-primary-antibodies-ihc-testing-1.jpgAnti-MRPS24 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using MRPS24 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps7-antibody-a12749-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12749-mrps7-primary-antibodies-wb-testing-3.jpgAnti-MRPS7 AntibodyWestern blot analysis of the lysates from HeLa cells using MRPS7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12749-mrps7-primary-antibodies-ihc-testing-1.jpgAnti-MRPS7 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using MRPS7 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12749-mrps7-primary-antibodies-wb-testing-2.jpgAnti-MRPS7 AntibodyWestern blot analysis of lysates from rat tongue cells, using MRPS7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrpl22-antibody-a13598-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13598-mrpl22-primary-antibodies-ihc-testing-1.jpgAnti-MRPL22 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13598-mrpl22-primary-antibodies-wb-testing-3.jpgAnti-MRPL22 AntibodyWestern blot analysis of the lysates from Jurkat cells using MRPL22 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13598-mrpl22-primary-antibodies-wb-testing-2.jpgAnti-MRPL22 AntibodyWestern blot analysis of lysates from HepG2 cells, using MRPL22 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrpl34-antibody-a16116-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16116-mrpl34-primary-antibodies-ihc-testing-1.jpgAnti-MRPL34 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using MRPL34 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrpl47-antibody-a14516-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14516-mrpl47-primary-antibodies-ihc-testing-1.jpgAnti-MRPL47 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14516-mrpl47-primary-antibodies-wb-testing-3.jpgAnti-MRPL47 AntibodyWestern blot analysis of the lysates from 293 cells using MRPL47 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14516-mrpl47-primary-antibodies-wb-testing-2.jpgAnti-MRPL47 AntibodyWestern blot analysis of lysates from RAW264.7 and K562 cells, using MRPL47 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrpl52-antibody-a15101-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15101-mrpl52-primary-antibodies-if-testing-1.jpgAnti-MRPL52 AntibodyImmunofluorescence analysis of HUVEC cells, using MRPL52 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15101-mrpl52-primary-antibodies-ihc-testing-2.jpgAnti-MRPL52 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MRPL52 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hibadh-antibody-a08760-1-boster.html2026-03-24T05:10:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08760-1-hibadh-primary-antibodies-ihc-testing-1.jpgAnti-HIBADH AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using HIBADH Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-rps13-antibody-a06221-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06221-1-rps13-primary-antibodies-wb-testing-2.jpgAnti-RPS13/Ribosomal Protein S13 AntibodyWestern blot analysis of lysates from PC12 cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06221-1-rps13-primary-antibodies-ihc-testing-1.jpgAnti-RPS13/Ribosomal Protein S13 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RPS13 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rps21-antibody-a10068-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10068-rps21-primary-antibodies-ihc-testing-1.jpgAnti-RPS21/Ribosomal Protein S21 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RPS21 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rps25-antibody-a09150-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09150-1-rps25-primary-antibodies-ihc-testing-1.jpgAnti-RPS25/Ribosomal Protein S25 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RPS25 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-rps9-antibody-a05633-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05633-1-rps9-primary-antibodies-ihc-testing-2.jpgAnti-40S ribosomal protein S9 RPS9 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05633-1-rps9-primary-antibodies-wb-testing-3.jpgAnti-40S ribosomal protein S9 RPS9 AntibodyWestern Blot analysis of various cells using Ribosomal Protein S9 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05633-1-rps9-primary-antibodies-if-testing-1.jpgAnti-40S ribosomal protein S9 RPS9 AntibodyImmunofluorescence analysis of A549 cells, using RPS9 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05633-1-rps9-primary-antibodies-wb-testing-4.jpgAnti-40S ribosomal protein S9 RPS9 AntibodyWestern blot analysis of lysates from HepG2, COLO, HT-29, HeLa, and HUVEC cells, using RPS9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rplp2-antibody-a05244-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05244-1-rplp2-primary-antibodies-ihc-testing-1.jpgAnti-RPLP2/Ribosomal Protein Lp2 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using RPLP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpl31-antibody-a07002-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07002-1-rpl31-primary-antibodies-ihc-testing-1.jpgAnti-RPL31/Ribosomal Protein L31 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using RPL31 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpl37-antibody-a10535-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10535-rpl37-primary-antibodies-ihc-testing-1.jpgAnti-60S ribosomal protein L37 RPL37 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RPL37 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpl37a-antibody-a10125-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10125-rpl37a-primary-antibodies-ihc-testing-2.jpgAnti-RPL37A/Ribosomal Protein L37A AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10125-rpl37a-primary-antibodies-wb-testing-3.jpgAnti-RPL37A/Ribosomal Protein L37A AntibodyWestern blot analysis of lysates from K562 cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10125-rpl37a-primary-antibodies-ihc-testing-1.jpgAnti-RPL37A/Ribosomal Protein L37A AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using RPL37A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-abhd12b-antibody-a14869-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/B/ABHD12B-primary-antibodies-A14869-IHC-testing.jpgAnti-Protein ABHD12B ABHD12B AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using ABHD12B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-acot12-antibody-a11589-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11589-1-acot12-primary-antibodies-if-testing-1.jpgAnti-ACOT12 AntibodyImmunofluorescence analysis of A549 cells, using ACOT12 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11589-1-acot12-primary-antibodies-ihc-testing-2.jpgAnti-ACOT12 AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using ACOT12 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lpcat2-antibody-a07471-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-1-lpcat2-primary-antibodies-ihc-testing-1.jpgAnti-LPCAT2/Acyltransferase Like 1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-1-lpcat2-primary-antibodies-wb-testing-3.jpgAnti-LPCAT2/Acyltransferase Like 1 AntibodyWestern blot analysis of the lysates from HT-29 cells using LPCAT2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-1-lpcat2-primary-antibodies-wb-testing-2.jpgAnti-LPCAT2/Acyltransferase Like 1 AntibodyWestern blot analysis of lysates from K562 and HT-29 cells, using LPCAT2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-agxt2l2-antibody-a30567-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30567-phykpl-primary-antibodies-ihc-testing-1.jpgAnti-AGXT2L2 PHYKPL AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30567-phykpl-primary-antibodies-wb-testing-2.jpgAnti-AGXT2L2 PHYKPL AntibodyWestern blot analysis of lysates from K562 and HepG2 cells, using AGXT2L2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30567-phykpl-primary-antibodies-wb-testing-3.jpgAnti-AGXT2L2 PHYKPL AntibodyWestern blot analysis of the lysates from HUVECcells using AGXT2L2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-akr1cl1-antibody-a30568-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30568-akr1c8p-primary-antibodies-if-testing-1.jpgAnti-AKR1CL1 AKR1C8P AntibodyImmunofluorescence analysis of A549 cells, using AKR1CL1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-apba2-antibody-a06783-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06783-apba2-primary-antibodies-ihc-testing-1.jpgAnti-APBA2/X11Beta AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using APBA2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-apba3-antibody-a07396-1-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07396-1-apba3-primary-antibodies-ihc-testing-1.jpgAnti-APBA3/Mint3 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07396-1-apba3-primary-antibodies-wb-testing-2.jpgAnti-APBA3/Mint3 AntibodyWestern blot analysis of lysates from HUVEC cells, using APBA3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07396-1-apba3-primary-antibodies-wb-testing-3.jpgAnti-APBA3/Mint3 AntibodyWestern blot analysis of the lysates from COLO205 cells using APBA3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-als2cr4-antibody-a30569-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30569-tmem237-primary-antibodies-wb-testing-1.jpgAnti-ALS2CR4 TMEM237 AntibodyWestern blot analysis of lysates from Jurkat cells, using ALS2CR4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-als2cr8-antibody-a30570-boster.html2026-03-24T05:10:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30570-carf-primary-antibodies-wb-testing-2.jpgAnti-ALS2CR8 AntibodyWestern Blot analysis of various cells using ALS2CR8 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30570-carf-primary-antibodies-ihc-testing-1.jpgAnti-ALS2CR8 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ALS2CR8 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30570-carf-primary-antibodies-wb-testing-3.jpgAnti-ALS2CR8 AntibodyWestern blot analysis of lysates from HUVEC cells, using ALS2CR8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atxn7l1-antibody-a12910-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/T/ATXN7L1-primary-antibodies-A12910-IHC-testing.jpgAnti-ATXN7L1 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using ATXN7L1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atp5d-antibody-a10129-1-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10129-1-atp5d-primary-antibodies-if-testing-1.jpgAnti-ATP5D AntibodyImmunofluorescence analysis of A549 cells, using ATP5D Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10129-1-atp5d-primary-antibodies-ihc-testing-2.jpgAnti-ATP5D AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ATP5D Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atp5g3-antibody-a12221-1-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12221-1-atp5g3-primary-antibodies-if-testing-1.jpgAnti-ATP5G3 AntibodyImmunofluorescence analysis of A549 cells, using ATP5G3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12221-1-atp5g3-primary-antibodies-ihc-testing-2.jpgAnti-ATP5G3 AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas tissue, using ATP5G3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ddx3y-antibody-a06062-1-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06062-1-ddx3y-primary-antibodies-ihc-testing-1.jpgAnti-DDX3Y AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using DDX3Y Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-b3galt2-antibody-a14751-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14751-b3galt2-primary-antibodies-if-testing-1.jpgAnti-B3GALT2/Beta 1 3 Gal T2 AntibodyImmunofluorescence analysis of A549 cells, using B3GALT2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14751-b3galt2-primary-antibodies-ihc-testing-2.jpgAnti-B3GALT2/Beta 1 3 Gal T2 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using B3GALT2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-b3galtl-antibody-a30572-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30572-b3glct-primary-antibodies-wb-testing-2.jpgAnti-B3GALTL B3GLCT AntibodyWestern Blot analysis of various cells using β-1,3-Gal-TL Polyclonal Antibody diluted at 1:500. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30572-b3glct-primary-antibodies-ihc-testing-1.jpgAnti-B3GALTL B3GLCT AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using B3GALTL Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30572-b3glct-primary-antibodies-wb-testing-3.jpgAnti-B3GALTL B3GLCT AntibodyWestern blot analysis of lysates from HUVEC, MCF-7, Jurkat, and HepG2 cells, using B3GALTL Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-b4galt3-antibody-a30573-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30573-b4galt3-primary-antibodies-ihc-testing-1.jpgAnti-B4GALT3/Beta 1 4 Gal T3 AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using B4GALT3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30573-b4galt3-primary-antibodies-wb-testing-2.jpgAnti-B4GALT3/Beta 1 4 Gal T3 AntibodyWestern blot analysis of lysates from Jurkat, HeLa, and HepG2 cells, using B4GALT3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-glb1l3-antibody-a30574-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30574-glb1l3-primary-antibodies-ihc-testing-1.jpgAnti-GLB1L3 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using GLB1L3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc27a5-antibody-a30575-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30575-slc27a5-primary-antibodies-wb-testing-3.jpgAnti-SLC27A5/Fatp5 AntibodyWestern Blot analysis of Hela cells using ACSVL6 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30575-slc27a5-primary-antibodies-if-testing-1.jpgAnti-SLC27A5/Fatp5 AntibodyImmunofluorescence analysis of A549 cells, using SLC27A5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30575-slc27a5-primary-antibodies-ihc-testing-2.jpgAnti-SLC27A5/Fatp5 AntibodyImmunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue, using SLC27A5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30575-slc27a5-primary-antibodies-wb-testing-4.jpgAnti-SLC27A5/Fatp5 AntibodyWestern blot analysis of lysates from HepG2 cells, using SLC27A5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-brp16-antibody-a30576-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30576-hgh1-primary-antibodies-wb-testing-2.jpgAnti-BRP16 AntibodyWestern Blot analysis of various cells using Brp16 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30576-hgh1-primary-antibodies-ihc-testing-1.jpgAnti-BRP16 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using BRP16 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30576-hgh1-primary-antibodies-wb-testing-3.jpgAnti-BRP16 AntibodyWestern blot analysis of lysates from COLO cells, using BRP16 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-brp44-antibody-a30577-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30577-mpc2-primary-antibodies-ihc-testing-1.jpgAnti-BRP44 MPC2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using BRP44 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-brp44l-antibody-a30578-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30578-mpc1-primary-antibodies-if-testing-1.jpgAnti-BRP44L AntibodyImmunofluorescence analysis of Hela cell. 1,Brp44L Polyclonal Antibody(green) was diluted at 1:200(4° overnight). (red) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000(room temperature, 50min). Goat Anti Mouse Alexa Fluor 594 was diluted at 1:1000(room temperature, 50min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30578-mpc1-primary-antibodies-wb-testing-3.jpgAnti-BRP44L AntibodyWestern Blot analysis of various cells using Brp44L Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30578-mpc1-primary-antibodies-ihc-testing-2.jpgAnti-BRP44L AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using BRP44L Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30578-mpc1-primary-antibodies-wb-testing-4.jpgAnti-BRP44L AntibodyWestern blot analysis of lysates from COLO and HeLa cells, using BRP44L Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-baiap2l1-antibody-a30579-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30579-baiap2l1-primary-antibodies-ihc-testing-1.jpgAnti-BAIAP2L1 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-baiap2l2-antibody-a30580-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30580-baiap2l2-primary-antibodies-ihc-testing-1.jpgAnti-BAIAP2L2 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30580-baiap2l2-primary-antibodies-wb-testing-2.jpgAnti-BAIAP2L2 AntibodyWestern blot analysis of the lysates from HT-29 cells using BAIAP2L2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-arfgef2-antibody-a30581-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30581-arfgef2-primary-antibodies-ihc-testing-3.jpgAnti-ARFGEF2 AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30581-arfgef2-primary-antibodies-ihc-testing-2.jpgAnti-ARFGEF2 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30581-arfgef2-primary-antibodies-wb-testing-4.jpgAnti-ARFGEF2 AntibodyWestern Blot analysis of various cells using BIG2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30581-arfgef2-primary-antibodies-if-testing-1.jpgAnti-ARFGEF2 AntibodyImmunofluorescence analysis of A549 cells, using ARFGEF2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30581-arfgef2-primary-antibodies-wb-testing-5.jpgAnti-ARFGEF2 AntibodyWestern blot analysis of lysates from A549 cells, using ARFGEF2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-brwd3-antibody-a08515-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08515-brwd3-primary-antibodies-ihc-testing-1.jpgAnti-BRWD3 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using BRWD3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08515-brwd3-primary-antibodies-wb-testing-2.jpgAnti-BRWD3 AntibodyWestern blot analysis of lysates from COLO cells, using BRWD3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnmb2-antibody-a30582-boster.html2026-03-24T05:10:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30582-kcnmb2-primary-antibodies-wb-testing-1.jpgAnti-KCNMB2 AntibodyWestern Blot analysis of various cells using MaxiKβ2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30582-kcnmb2-primary-antibodies-wb-testing-3.jpgAnti-KCNMB2 AntibodyWestern blot analysis of the lysates from HepG2 cells using KCNMB2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30582-kcnmb2-primary-antibodies-wb-testing-2.jpgAnti-KCNMB2 AntibodyWestern blot analysis of lysates from Jurkat, COLO, and HepG2 cells, using KCNMB2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pnpla8-antibody-a30583-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30583-pnpla8-primary-antibodies-ihc-testing-1.jpgAnti-PNPLA8/Ipla2 Gamma AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-arpp21-antibody-a30584-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30584-arpp21-primary-antibodies-wb-testing-2.jpgAnti-ARPP21 AntibodyWestern Blot analysis of HeLa cells using ARPP-21 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30584-arpp21-primary-antibodies-ihc-testing-1.jpgAnti-ARPP21 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using ARPP21 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30584-arpp21-primary-antibodies-wb-testing-3.jpgAnti-ARPP21 AntibodyWestern blot analysis of lysates from HeLa cells, using ARPP21 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-chst10-antibody-a30586-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30586-chst10-primary-antibodies-wb-testing-2.jpgAnti-CHST10/Hnk 1St AntibodyWestern Blot analysis of various cells using HNK-1ST Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30586-chst10-primary-antibodies-ihc-testing-1.jpgAnti-CHST10/Hnk 1St AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using CHST10 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30586-chst10-primary-antibodies-wb-testing-3.jpgAnti-CHST10/Hnk 1St AntibodyWestern blot analysis of lysates from HUVEC cells, using CHST10 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-chst8-antibody-a10989-1-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10989-1-chst8-primary-antibodies-wb-testing-1.jpgAnti-CHST8/Galnac4St 1 AntibodyWestern blot analysis of lysates from K562 cells, using CHST8 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10989-1-chst8-primary-antibodies-wb-testing-2.jpgAnti-CHST8/Galnac4St 1 AntibodyWestern blot analysis of the lysates from HT-29 cells using CHST8 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-chst9-antibody-a11901-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11901-chst9-primary-antibodies-if-testing-1.jpgAnti-CHST9 AntibodyImmunofluorescence analysis of HUVEC cells, using CHST9 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11901-chst9-primary-antibodies-ihc-testing-2.jpgAnti-CHST9 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CHST9 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ca12-antibody-a30588-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30588-ca12-primary-antibodies-ihc-testing-1.jpgAnti-CA12/Ca Xii AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30588-ca12-primary-antibodies-wb-testing-2.jpgAnti-CA12/Ca Xii AntibodyWestern Blot analysis of NIH-3T3 293T cells using CA XII Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30588-ca12-primary-antibodies-wb-testing-3.jpgAnti-CA12/Ca Xii AntibodyWestern blot analysis of lysates from MCF-7 cells, using CA12 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30588-ca12-primary-antibodies-wb-testing-4.jpgAnti-CA12/Ca Xii AntibodyWestern blot analysis of the lysates from COLO205 cells using CA12 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ca13-antibody-a30589-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30589-ca13-primary-antibodies-wb-testing-1.jpgAnti-CA13/Ca Xiii AntibodyWestern Blot analysis of various cells using CA XIII Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30589-ca13-primary-antibodies-wb-testing-2.jpgAnti-CA13/Ca Xiii AntibodyWestern blot analysis of lysates from HepG2 cells, using CA13 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30589-ca13-primary-antibodies-wb-testing-3.jpgAnti-CA13/Ca Xiii AntibodyWestern blot analysis of the lysates from K562 cells using CA13 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ca14-antibody-a30590-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30590-ca14-primary-antibodies-wb-testing-1.jpgAnti-CA14/Ca Xiv AntibodyWestern Blot analysis of various cells using CA XIV Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30590-ca14-primary-antibodies-wb-testing-2.jpgAnti-CA14/Ca Xiv AntibodyWestern blot analysis of lysates from Jurkat, COLO, and 293 cells, using CA14 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ca5a-antibody-a30592-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30592-ca5a-primary-antibodies-wb-testing-1.jpgAnti-CA5A/Carbonic Anhydrase Va AntibodyWestern Blot analysis of various cells using CA VA Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30592-ca5a-primary-antibodies-wb-testing-2.jpgAnti-CA5A/Carbonic Anhydrase Va AntibodyWestern blot analysis of lysates from A549, LOVO, and K562 cells, using CA5A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30592-ca5a-primary-antibodies-wb-testing-3.jpgAnti-CA5A/Carbonic Anhydrase Va AntibodyWestern blot analysis of the lysates from K562 cells using CA5A antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ca5b-antibody-a30593-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30593-ca5b-primary-antibodies-ihc-testing-2.jpgAnti-CA5B/Ca Vb AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30593-ca5b-primary-antibodies-wb-testing-3.jpgAnti-CA5B/Ca Vb AntibodyWestern Blot analysis of 3T3 cells using CA VB Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30593-ca5b-primary-antibodies-if-testing-1.jpgAnti-CA5B/Ca Vb AntibodyImmunofluorescence analysis of MCF7 cells, using CA5B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30593-ca5b-primary-antibodies-wb-testing-4.jpgAnti-CA5B/Ca Vb AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using CA5B Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30593-ca5b-primary-antibodies-wb-testing-5.jpgAnti-CA5B/Ca Vb AntibodyWestern blot analysis of the lysates from HT-29 cells using CA5B antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ca6-antibody-a30037-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30037-ca6-primary-antibodies-wb-testing-1.jpgAnti-CA6/Carbonic Anhydrase Vi AntibodyWestern Blot analysis of various cells using CA VI Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30037-ca6-primary-antibodies-wb-testing-2.jpgAnti-CA6/Carbonic Anhydrase Vi AntibodyWestern blot analysis of lysates from HepG2, and LOVO cells, using CA6 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30037-ca6-primary-antibodies-wb-testing-3.jpgAnti-CA6/Carbonic Anhydrase Vi AntibodyWestern blot analysis of the lysates from HepG2 cells using CA6 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cpe-antibody-a30595-boster.html2026-03-24T05:10:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30595-cpe-primary-antibodies-wb-testing-1.jpgAnti-CPE/Carboxypeptidase E AntibodyWestern Blot analysis of K562 cells using CPE Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30595-cpe-primary-antibodies-wb-testing-2.jpgAnti-CPE/Carboxypeptidase E AntibodyWestern Blot analysis of various cells using CPE Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30595-cpe-primary-antibodies-wb-testing-3.jpgAnti-CPE/Carboxypeptidase E AntibodyWestern blot analysis of lysates from RAW264.7 and NIH/3T3 cells, using CPE Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30595-cpe-primary-antibodies-wb-testing-4.jpgAnti-CPE/Carboxypeptidase E AntibodyWestern blot analysis of the lysates from HeLa cells using CPE antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ctdsp1-antibody-a30598-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30598-ctdsp1-primary-antibodies-wb-testing-3.jpgAnti-CTDSP1 AntibodyWestern Blot analysis of various cells using CTDSP1 Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30598-ctdsp1-primary-antibodies-wb-testing-2.jpgAnti-CTDSP1 AntibodyWestern blot analysis of mouse-brain HELA KB SH-SY5Y 293T 3T3 lysis using CTDSP1 antibody. Antibody was diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30598-ctdsp1-primary-antibodies-ihc-testing-1.jpgAnti-CTDSP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using CTDSP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30598-ctdsp1-primary-antibodies-wb-testing-4.jpgAnti-CTDSP1 AntibodyWestern blot analysis of lysates from HeLa and HUVEC cells, using CTDSP1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30598-ctdsp1-primary-antibodies-wb-testing-5.jpgAnti-CTDSP1 AntibodyWestern blot analysis of the lysates from HepG2 cells using CTDSP1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cnot4-antibody-a08405-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08405-cnot4-primary-antibodies-ihc-testing-1.jpgAnti-CNOT4 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CNOT4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08405-cnot4-primary-antibodies-wb-testing-2.jpgAnti-CNOT4 AntibodyWestern blot analysis of lysates from Jurkat and K562 cells, using CNOT4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-borg1-antibody-a30599-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30599-cdc42ep2-primary-antibodies-ihc-testing-1.jpgAnti-BORG1 CDC42EP2 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30599-cdc42ep2-primary-antibodies-wb-testing-2.jpgAnti-BORG1 CDC42EP2 AntibodyWestern Blot analysis of K562 cells using Cdc42EP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30599-cdc42ep2-primary-antibodies-wb-testing-3.jpgAnti-BORG1 CDC42EP2 AntibodyWestern blot analysis of lysates from K562 cells, using BORG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-borg4-antibody-a30600-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30600-cdc42ep4-primary-antibodies-ihc-testing-1.jpgAnti-BORG4 CDC42EP4 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30600-cdc42ep4-primary-antibodies-wb-testing-2.jpgAnti-BORG4 CDC42EP4 AntibodyWestern blot analysis of lysates from Jurkat cells, using BORG4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-borg3-antibody-a30601-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30601-cdc42ep5-primary-antibodies-ihc-testing-1.jpgAnti-BORG3 CDC42EP5 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30601-cdc42ep5-primary-antibodies-wb-testing-2.jpgAnti-BORG3 CDC42EP5 AntibodyWestern Blot analysis of various cells using Cdc42EP5 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30601-cdc42ep5-primary-antibodies-wb-testing-3.jpgAnti-BORG3 CDC42EP5 AntibodyWestern blot analysis of lysates from Jurkat cells, using BORG3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-crabp2-antibody-a30602-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30602-crabp2-primary-antibodies-ihc-testing-1.jpgAnti-CRABP2 AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30602-crabp2-primary-antibodies-wb-testing-2.jpgAnti-CRABP2 AntibodyWestern Blot analysis of various cells using CRABP-II Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30602-crabp2-primary-antibodies-wb-testing-3.jpgAnti-CRABP2 AntibodyWestern blot analysis of lysates from HT-29 cells, using CRABP2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep290-antibody-a30603-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30603-cep290-primary-antibodies-wb-testing-1.jpgAnti-Centrosomal protein of 290 kDa CEP290 AntibodyWestern Blot analysis of various cells using CEP290 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30603-cep290-primary-antibodies-wb-testing-2.jpgAnti-Centrosomal protein of 290 kDa CEP290 AntibodyWestern blot analysis of lysates from K562 cells, using CEP290 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep135-antibody-a30604-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30604-cep135-primary-antibodies-ihc-testing-1.jpgAnti-CEP135 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30604-cep135-primary-antibodies-wb-testing-2.jpgAnti-CEP135 AntibodyWestern Blot analysis of COLO cells using CEP135 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30604-cep135-primary-antibodies-wb-testing-3.jpgAnti-CEP135 AntibodyWestern blot analysis of mouse-lung mouse-heart 293T lysis using CEP135 antibody. Antibody was diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30604-cep135-primary-antibodies-wb-testing-4.jpgAnti-CEP135 AntibodyWestern blot analysis of lysates from COLO cells, using CEP135 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep152-antibody-a30605-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30605-cep152-primary-antibodies-wb-testing-2.jpgAnti-CEP152 AntibodyWestern Blot analysis of HuvEc cells using CEP152 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30605-cep152-primary-antibodies-ihc-testing-1.jpgAnti-CEP152 AntibodyImmunohistochemistry analysis of paraffin-embedded human lymph node tissue, using CEP152 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep170-antibody-a30606-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30606-cep170-primary-antibodies-wb-testing-2.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern Blot analysis of AD293 cells using CEP170 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30606-cep170-primary-antibodies-wb-testing-3.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern Blot analysis of various cells using CEP170 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30606-cep170-primary-antibodies-ihc-testing-1.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CEP170 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30606-cep170-primary-antibodies-wb-testing-4.jpgAnti-Centrosomal protein of 170 kDa CEP170 AntibodyWestern blot analysis of lysates from HepG2 and Jurkat cells, using CEP170 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep350-antibody-a30607-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30607-cep350-primary-antibodies-ihc-testing-1.jpgAnti-CEP350 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using CEP350 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-huce1-antibody-a30608-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30608-rrp8-primary-antibodies-ihc-testing-1.jpgAnti-HUCE1 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30608-rrp8-primary-antibodies-wb-testing-2.jpgAnti-HUCE1 AntibodyWestern Blot analysis of MCF-7 cells using Cerebral 1 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30608-rrp8-primary-antibodies-wb-testing-3.jpgAnti-HUCE1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using HUCE1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-csglcat-antibody-a30609-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30609-chpf2-primary-antibodies-ihc-testing-1.jpgAnti-CSGLCAT CHPF2 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30609-chpf2-primary-antibodies-wb-testing-2.jpgAnti-CSGLCAT CHPF2 AntibodyWestern blot analysis of lysates from Jurkat cells, using CSGLCAT Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-chsy2-antibody-a30610-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30610-chpf-primary-antibodies-if-testing-1.jpgAnti-CHSY2 CHPF AntibodyImmunofluorescence analysis of MCF7 cells, using CHSY2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30610-chpf-primary-antibodies-ihc-testing-2.jpgAnti-CHSY2 CHPF AntibodyImmunohistochemistry analysis of paraffin-embedded human cervix carcinoma tissue, using CHSY2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30610-chpf-primary-antibodies-wb-testing-3.jpgAnti-CHSY2 CHPF AntibodyWestern blot analysis of lysates from LOVO and K562 cells, using CHSY2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cklf1-antibody-a30611-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30611-cmtm1-primary-antibodies-if-testing-1.jpgAnti-CKLF1 CMTM1 AntibodyImmunofluorescence analysis of MCF7 cells, using CKLF1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cklf2-antibody-a30612-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30612-cmtm2-primary-antibodies-wb-testing-1.jpgAnti-CKLF2 AntibodyWestern Blot analysis of K562 cells using CMTM2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30612-cmtm2-primary-antibodies-wb-testing-2.jpgAnti-CKLF2 AntibodyWestern blot analysis of lysates from K562 cells, using CKLF2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30612-cmtm2-primary-antibodies-wb-testing-3.jpgAnti-CKLF2 AntibodyWestern blot analysis of the lysates from COLO205 cells using CKLF2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cklf3-antibody-a30613-boster.html2026-03-24T05:10:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30613-cmtm3-primary-antibodies-wb-testing-1.jpgAnti-CKLF3 CMTM3 AntibodyWestern Blot analysis of various cells using CMTM3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30613-cmtm3-primary-antibodies-wb-testing-2.jpgAnti-CKLF3 CMTM3 AntibodyWestern blot analysis of lysates from Jurkat and COS cells, using CKLF3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cldn19-antibody-a30615-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30615-cldn19-primary-antibodies-wb-testing-1.jpgAnti-CLDN19/Claudin 19 AntibodyWestern Blot analysis of various cells using Claudin-19 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30615-cldn19-primary-antibodies-wb-testing-2.jpgAnti-CLDN19/Claudin 19 AntibodyWestern blot analysis of lysates from Jurkat and HepG2 cells, using CLDN19 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cldn6-antibody-a30616-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30616-cldn6-primary-antibodies-wb-testing-3.jpgAnti-CLDN6/Claudin 6 AntibodyWestern Blot analysis of various cells using Claudin-6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30616-cldn6-primary-antibodies-if-testing-1.jpgAnti-CLDN6/Claudin 6 AntibodyImmunofluorescence analysis of HUVEC cells, using CLDN6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30616-cldn6-primary-antibodies-ihc-testing-2.jpgAnti-CLDN6/Claudin 6 AntibodyImmunohistochemistry analysis of paraffin-embedded human ovary tissue, using CLDN6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30616-cldn6-primary-antibodies-wb-testing-4.jpgAnti-CLDN6/Claudin 6 AntibodyWestern blot analysis of lysates from Jurkat cells, using CLDN6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-clasp1-antibody-a30619-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30619-clasp1-primary-antibodies-wb-testing-2.jpgAnti-CLIP-associating protein 1 CLASP1 AntibodyWestern Blot analysis of SH-SY5Y cells using CLASP1 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30619-clasp1-primary-antibodies-ihc-testing-1.jpgAnti-CLIP-associating protein 1 CLASP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CLASP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30619-clasp1-primary-antibodies-wb-testing-3.jpgAnti-CLIP-associating protein 1 CLASP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using CLASP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-st6gal1-antibody-a30620-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30620-st6gal1-primary-antibodies-ihc-testing-2.jpgAnti-ST6GAL1/Cd75 AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach. 1, Antibody was diluted at 1:200(4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30620-st6gal1-primary-antibodies-wb-testing-3.jpgAnti-ST6GAL1/Cd75 AntibodyWestern Blot analysis of COLO cells using CD75 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30620-st6gal1-primary-antibodies-ihc-testing-1.jpgAnti-ST6GAL1/Cd75 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using ST6GAL1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30620-st6gal1-primary-antibodies-wb-testing-4.jpgAnti-ST6GAL1/Cd75 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using ST6GAL1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rcl-antibody-a30621-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30621-dnph1-primary-antibodies-ihc-testing-1.jpgAnti-RCL AntibodyImmunohistochemical analysis of paraffin-embedded human uterus. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30621-dnph1-primary-antibodies-wb-testing-2.jpgAnti-RCL AntibodyWestern Blot analysis of various cells using RCL Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30621-dnph1-primary-antibodies-wb-testing-4.jpgAnti-RCL AntibodyWestern blot analysis of the lysates from 293 cells using RCL antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30621-dnph1-primary-antibodies-wb-testing-3.jpgAnti-RCL AntibodyWestern blot analysis of lysates from Jurkat and K562 cells, using RCL Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ccdc102a-antibody-a30622-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30622-ccdc102a-primary-antibodies-wb-testing-1.jpgAnti-CCDC102A AntibodyWestern blot analysis of lysates from LOVO cells, using CCDC102A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30622-ccdc102a-primary-antibodies-wb-testing-2.jpgAnti-CCDC102A AntibodyWestern blot analysis of the lysates from HepG2 cells using CCDC102A antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-c1qc-antibody-a05666-1-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05666-1-c1qc-primary-antibodies-ihc-testing-1.jpgAnti-C1QC/Complement Component C1Qc AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using C1QC Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05666-1-c1qc-primary-antibodies-wb-testing-2.jpgAnti-C1QC/Complement Component C1Qc AntibodyWestern blot analysis of lysates from rat lung, using C1QC Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ncaph-antibody-a30627-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30627-ncaph-primary-antibodies-wb-testing-1.jpgAnti-Condensin complex subunit 2 NCAPH AntibodyWestern Blot analysis of COLO cells using hCAP-H Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30627-ncaph-primary-antibodies-wb-testing-3.jpgAnti-Condensin complex subunit 2 NCAPH AntibodyWestern blot analysis of the lysates from COLO205 cells using NCAPH antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30627-ncaph-primary-antibodies-wb-testing-2.jpgAnti-Condensin complex subunit 2 NCAPH AntibodyWestern blot analysis of lysates from COLO cells, using NCAPH Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cnga2-antibody-a07901-1-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-1-cnga2-primary-antibodies-wb-testing-2.jpgAnti-CNGA2 AntibodyWestern Blot analysis of K562 cells using CNG-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-1-cnga2-primary-antibodies-wb-testing-3.jpgAnti-CNGA2 AntibodyWestern Blot analysis of various cells using CNG-2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07901-1-cnga2-primary-antibodies-if-testing-1.jpgAnti-CNGA2 AntibodyImmunofluorescence analysis of A549 cells, using CNGA2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cst8-antibody-a11538-1-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11538-1-cst8-primary-antibodies-ihc-testing-1.jpgAnti-CST8/Cystatin 8 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using CST8 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cstl1-antibody-a30629-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30629-cstl1-primary-antibodies-if-testing-1.jpgAnti-Cystatin-like 1 CSTL1 AntibodyImmunofluorescence analysis of A549 cells, using CSTL1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cst1-antibody-a30630-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30630-cst1-primary-antibodies-wb-testing-3.jpgAnti-CST1/Cystatin Sn AntibodyWestern Blot analysis of Jurkat cells using Cystatin SN Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30630-cst1-primary-antibodies-if-testing-1.jpgAnti-CST1/Cystatin Sn AntibodyImmunofluorescence analysis of MCF7 cells, using CST1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30630-cst1-primary-antibodies-ihc-testing-2.jpgAnti-CST1/Cystatin Sn AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using CST1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nt5c1a-antibody-a30631-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30631-nt5c1a-primary-antibodies-if-testing-1.jpgAnti-Cytosolic 5'-nucleotidase 1A NT5C1A AntibodyImmunofluorescence analysis of A549 cells, using NT5C1A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30631-nt5c1a-primary-antibodies-wb-testing-2.jpgAnti-Cytosolic 5'-nucleotidase 1A NT5C1A AntibodyWestern blot analysis of lysates from MCF-7 and HepG2 cells, using NT5C1A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nt5c1b-antibody-a30632-boster.html2026-03-24T05:10:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30632-nt5c1b-primary-antibodies-ihc-testing-2.jpgAnti-Cytosolic 5'-nucleotidase 1B NT5C1B AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30632-nt5c1b-primary-antibodies-if-testing-1.jpgAnti-Cytosolic 5'-nucleotidase 1B NT5C1B AntibodyImmunofluorescence analysis of A549 cells, using NT5C1B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cbcp2-antibody-a30633-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30633-agbl2-primary-antibodies-wb-testing-2.jpgAnti-CBCP2 AGBL2 AntibodyWestern Blot analysis of various cells using CCP2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30633-agbl2-primary-antibodies-ihc-testing-1.jpgAnti-CBCP2 AGBL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using CBCP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30633-agbl2-primary-antibodies-wb-testing-3.jpgAnti-CBCP2 AGBL2 AntibodyWestern blot analysis of lysates from HUVEC cells, using CBCP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30633-agbl2-primary-antibodies-wb-testing-4.jpgAnti-CBCP2 AGBL2 AntibodyWestern blot analysis of the lysates from Jurkat cells using CBCP2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cbcp3-antibody-a13582-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13582-agbl3-primary-antibodies-ihc-testing-1.jpgAnti-CBCP3 AGBL3 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma, using CBCP3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pla2g4d-antibody-a12553-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12553-pla2g4d-primary-antibodies-ihc-testing-1.jpgAnti-PLA2G4D AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using PLA2G4D Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pla2g4c-antibody-a30634-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30634-pla2g4c-primary-antibodies-wb-testing-2.jpgAnti-PLA2G4C AntibodyWestern blot analysis of the lysates from HeLa cells using PLA2G4C antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30634-pla2g4c-primary-antibodies-wb-testing-1.jpgAnti-PLA2G4C AntibodyWestern blot analysis of lysates from Jurkat cells, using PLA2G4C Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dhrs11-antibody-a30635-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30635-dhrs11-primary-antibodies-ihc-testing-1.jpgAnti-DHRS11 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using DHRS11 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dhps-antibody-a30637-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30637-dhps-primary-antibodies-wb-testing-1.jpgAnti-DHPS/Dhs AntibodyWestern Blot analysis of K562 cells using DHS Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30637-dhps-primary-antibodies-wb-testing-2.jpgAnti-DHPS/Dhs AntibodyWestern Blot analysis of various cells using DHS Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30637-dhps-primary-antibodies-wb-testing-3.jpgAnti-DHPS/Dhs AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using DHPS Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30637-dhps-primary-antibodies-wb-testing-4.jpgAnti-DHPS/Dhs AntibodyWestern blot analysis of the lysates from HUVECcells using DHPS antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dgat2l6-antibody-a30638-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30638-dgat2l6-primary-antibodies-wb-testing-1.jpgAnti-DGAT2L6 AntibodyWestern blot analysis of lysates from Jurkat cells, using DGAT2L6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dpysl4-antibody-a30640-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30640-dpysl4-primary-antibodies-wb-testing-1.jpgAnti-DPYSL4/Crmp3 AntibodyWestern Blot analysis of LOVO cells using CRMP-3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30640-dpysl4-primary-antibodies-wb-testing-2.jpgAnti-DPYSL4/Crmp3 AntibodyWestern blot analysis of lysates from LOVO and HT-29 cells, using DPYSL4 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30640-dpysl4-primary-antibodies-wb-testing-3.jpgAnti-DPYSL4/Crmp3 AntibodyWestern blot analysis of the lysates from RAW264.7cells using DPYSL4 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dmgdh-antibody-a30641-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30641-dmgdh-primary-antibodies-ihc-testing-1.jpgAnti-DMGDH AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30641-dmgdh-primary-antibodies-wb-testing-2.jpgAnti-DMGDH AntibodyWestern Blot analysis of various cells using DMGDH Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30641-dmgdh-primary-antibodies-wb-testing-3.jpgAnti-DMGDH AntibodyWestern blot analysis of lysates from HT-29 and A549 cells, using DMGDH Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30641-dmgdh-primary-antibodies-wb-testing-4.jpgAnti-DMGDH AntibodyWestern blot analysis of the lysates from HeLa cells using DMGDH antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-dlgap5-antibody-a30642-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30642-dlgap5-primary-antibodies-wb-testing-1.jpgAnti-DLGAP5/Hurp AntibodyWestern Blot analysis of A549 cells using HURP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30642-dlgap5-primary-antibodies-wb-testing-2.jpgAnti-DLGAP5/Hurp AntibodyWestern Blot analysis of various cells using HURP Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30642-dlgap5-primary-antibodies-wb-testing-3.jpgAnti-DLGAP5/Hurp AntibodyWestern blot analysis of lysates from A549, 293, and HUVEC cells, using DLGAP5 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30642-dlgap5-primary-antibodies-wb-testing-4.jpgAnti-DLGAP5/Hurp AntibodyWestern blot analysis of the lysates from HT-29 cells using DLGAP5 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-pold1-antibody-a30643-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30643-pold1-primary-antibodies-wb-testing-1.jpgAnti-POLD1 AntibodyWestern blot analysis of lysates from K562 cells, using POLD1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pole1-antibody-a30644-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30644-pole-primary-antibodies-ihc-testing-1.jpgAnti-POLE1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using POLE1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pole4-antibody-a30645-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30645-pole4-primary-antibodies-ihc-testing-1.jpgAnti-POLE4 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using POLE4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pold3-antibody-a30646-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30646-pold3-primary-antibodies-wb-testing-1.jpgAnti-POLD3 AntibodyWestern Blot analysis of hela cells using DNA pol δ3 Polyclonal Antibody diluted at 1:500.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30646-pold3-primary-antibodies-wb-testing-2.jpgAnti-POLD3 AntibodyWestern blot analysis of lysates from LOVO, HepG2, and mouse brain cells, using POLD3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prim1-antibody-a30648-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30648-prim1-primary-antibodies-ihc-testing-1.jpgAnti-DNA primase small subunit PRIM1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30648-prim1-primary-antibodies-wb-testing-2.jpgAnti-DNA primase small subunit PRIM1 AntibodyWestern Blot analysis of various cells using PRIM1 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30648-prim1-primary-antibodies-wb-testing-4.jpgAnti-DNA primase small subunit PRIM1 AntibodyWestern blot analysis of the lysates from K562 cells using PRIM1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30648-prim1-primary-antibodies-wb-testing-3.jpgAnti-DNA primase small subunit PRIM1 AntibodyWestern blot analysis of lysates from COLO and HeLa cells, using PRIM1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cd3eap-antibody-a30649-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30649-cd3eap-primary-antibodies-ihc-testing-1.jpgAnti-CD3EAP/Paf49 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30649-cd3eap-primary-antibodies-wb-testing-2.jpgAnti-CD3EAP/Paf49 AntibodyWestern Blot analysis of A549 cells using CD3EAP Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30649-cd3eap-primary-antibodies-wb-testing-3.jpgAnti-CD3EAP/Paf49 AntibodyWestern blot analysis of lysates from A549 cells, using CD3EAP Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30649-cd3eap-primary-antibodies-wb-testing-4.jpgAnti-CD3EAP/Paf49 AntibodyWestern blot analysis of the lysates from HUVECcells using CD3EAP antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rpb11-antibody-a30650-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30650-polr2j-primary-antibodies-ihc-testing-1.jpgAnti-RPB11 POLR2J AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30650-polr2j-primary-antibodies-wb-testing-3.jpgAnti-RPB11 POLR2J AntibodyWestern blot analysis of the lysates from HeLa cells using RPB11 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30650-polr2j-primary-antibodies-wb-testing-2.jpgAnti-RPB11 POLR2J AntibodyWestern blot analysis of lysates from RAW264.7 cells, using RPB11 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpc1-antibody-a30651-boster.html2026-03-24T05:10:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30651-polr3a-primary-antibodies-ihc-testing-1.jpgAnti-RPC1 POLR3A AntibodyImmunohistochemical analysis of paraffin-embedded human spleen. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30651-polr3a-primary-antibodies-wb-testing-2.jpgAnti-RPC1 POLR3A AntibodyWestern Blot analysis of various cells using POLR3A Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30651-polr3a-primary-antibodies-wb-testing-4.jpgAnti-RPC1 POLR3A AntibodyWestern blot analysis of the lysates from 293 cells using RPC1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30651-polr3a-primary-antibodies-wb-testing-3.jpgAnti-RPC1 POLR3A AntibodyWestern blot analysis of lysates from COS and HUVEC cells, using RPC1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpc2-antibody-a06213-1-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06213-1-polr3b-primary-antibodies-ihc-testing-1.jpgAnti-RPC2 POLR3B AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06213-1-polr3b-primary-antibodies-wb-testing-2.jpgAnti-RPC2 POLR3B AntibodyWestern blot analysis of lysates from LOVO cells, using RPC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpc4-antibody-a30652-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30652-polr3d-primary-antibodies-ihc-testing-1.jpgAnti-RPC4 POLR3D AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30652-polr3d-primary-antibodies-wb-testing-3.jpgAnti-RPC4 POLR3D AntibodyWestern blot analysis of the lysates from HepG2 cells using RPC4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30652-polr3d-primary-antibodies-wb-testing-2.jpgAnti-RPC4 POLR3D AntibodyWestern blot analysis of lysates from MCF-7 cells, using RPC4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpc5-antibody-a30653-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30653-polr3e-primary-antibodies-ihc-testing-3.jpgAnti-RPC5 POLR3E AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30653-polr3e-primary-antibodies-wb-testing-4.jpgAnti-RPC5 POLR3E AntibodyWestern Blot analysis of JK cells using POLR3E Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30653-polr3e-primary-antibodies-wb-testing-5.jpgAnti-RPC5 POLR3E AntibodyWestern Blot analysis of various cells using POLR3E Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30653-polr3e-primary-antibodies-if-testing-1.jpgAnti-RPC5 POLR3E AntibodyImmunofluorescence analysis of LOVO cells, using RPC5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30653-polr3e-primary-antibodies-ihc-testing-2.jpgAnti-RPC5 POLR3E AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RPC5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpc8-antibody-a30654-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30654-polr3h-primary-antibodies-ihc-testing-1.jpgAnti-RPC8 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30654-polr3h-primary-antibodies-wb-testing-2.jpgAnti-RPC8 AntibodyWestern Blot analysis of K562 cells using POLR3H Polyclonal Antibody diluted at 1:1000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30654-polr3h-primary-antibodies-wb-testing-3.jpgAnti-RPC8 AntibodyWestern blot analysis of lysates from K562 cells, using RPC8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpab1-antibody-a30655-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30655-polr2e-primary-antibodies-ihc-testing-1.jpgAnti-RPAB1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30655-polr2e-primary-antibodies-wb-testing-2.jpgAnti-RPAB1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using RPAB1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tesk1-antibody-a09099-1-boster.html2026-03-25T05:22:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09099-1-tesk1-primary-antibodies-wb-testing-1.jpgAnti-TESK1 AntibodyWestern blot analysis of lysates from rat heart, rat kidney, and rat liver cells, using TESK1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dynll2-antibody-a30657-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30657-dynll2-primary-antibodies-ihc-testing-2.jpgAnti-DYNLL2 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30657-dynll2-primary-antibodies-ihc-testing-3.jpgAnti-DYNLL2 AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30657-dynll2-primary-antibodies-ihc-testing-1.jpgAnti-DYNLL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using DYNLL2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dnal4-antibody-a13115-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13115-dnal4-primary-antibodies-ihc-testing-1.jpgAnti-Dynein light chain 4, axonemal DNAL4 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using DNAL4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-dynlrb2-antibody-a30658-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30658-dynlrb2-primary-antibodies-ihc-testing-1.jpgAnti-DYNLRB2/Dnlc2B AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using DYNLRB2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ccnb1ip1-antibody-a30659-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30659-ccnb1ip1-primary-antibodies-ihc-testing-1.jpgAnti-CCNB1IP1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30659-ccnb1ip1-primary-antibodies-wb-testing-2.jpgAnti-CCNB1IP1 AntibodyWestern Blot analysis of various cells using HEI10 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30659-ccnb1ip1-primary-antibodies-wb-testing-3.jpgAnti-CCNB1IP1 AntibodyWestern blot analysis of lysates from Jurkat and COLO cells, using CCNB1IP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-march2-antibody-a30660-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30660-march2-primary-antibodies-if-testing-1.jpgAnti-MARCH2 MARCH2; AntibodyImmunofluorescence analysis of A549 cells, using MARCH2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30660-march2-primary-antibodies-ihc-testing-2.jpgAnti-MARCH2 MARCH2; AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MARCH2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-march3-antibody-a30661-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30661-march3-primary-antibodies-wb-testing-2.jpgAnti-MARCH3 MARCH3; AntibodyWestern Blot analysis of K562 cells using MARCH3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30661-march3-primary-antibodies-wb-testing-4.jpgAnti-MARCH3 MARCH3; AntibodyWestern blot analysis of the lysates from RAW264.7cells using MARCH3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30661-march3-primary-antibodies-ihc-testing-1.jpgAnti-MARCH3 MARCH3; AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using MARCH3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30661-march3-primary-antibodies-wb-testing-3.jpgAnti-MARCH3 MARCH3; AntibodyWestern blot analysis of lysates from K562 and COS7 cells, using MARCH3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-march4-antibody-a30662-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30662-march4-primary-antibodies-ihc-testing-1.jpgAnti-MARCH4 MARCH4; AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MARCH4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-march5-antibody-a30663-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30663-march5-primary-antibodies-if-testing-2.jpgAnti-MARCH5 MARCH5; AntibodyImmunofluorescence analysis of Hela cell. 1,MARCH5 Polyclonal Antibody(green) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000(room temperature, 50min). 3 DAPI(blue) 10min.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30663-march5-primary-antibodies-wb-testing-3.jpgAnti-MARCH5 MARCH5; AntibodyWestern blot analysis of lysates from U2OS cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30663-march5-primary-antibodies-if-testing-1.jpgAnti-MARCH5 MARCH5; AntibodyImmunofluorescence analysis of A549 cells, using MARCH5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf125-antibody-a30664-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30664-rnf125-primary-antibodies-ihc-testing-1.jpgAnti-RNF125 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30664-rnf125-primary-antibodies-wb-testing-2.jpgAnti-RNF125 AntibodyWestern blot analysis of lysates from K562 and HT-29 cells, using RNF125 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf138-antibody-a30665-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30665-rnf138-primary-antibodies-ihc-testing-1.jpgAnti-RNF138/Ring Finger Protein 138 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30665-rnf138-primary-antibodies-wb-testing-2.jpgAnti-RNF138/Ring Finger Protein 138 AntibodyWestern blot analysis of lysates from MCF-7 cells, using RNF138 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf14-antibody-a08956-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08956-rnf14-primary-antibodies-wb-testing-1.jpgAnti-RNF14/Ara54 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using RNF14 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf144a-antibody-a30666-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30666-rnf144a-primary-antibodies-wb-testing-1.jpgAnti-RNF144A/Rnf144 AntibodyWestern Blot analysis of various cells using UBCE7IP4 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30666-rnf144a-primary-antibodies-wb-testing-2.jpgAnti-RNF144A/Rnf144 AntibodyWestern blot analysis of lysates from COLO cells, using RNF144A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf149-antibody-a30667-boster.html2026-03-24T05:10:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30667-rnf149-primary-antibodies-ihc-testing-1.jpgAnti-RNF149 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RNF149 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znrf2-antibody-a11505-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11505-znrf2-primary-antibodies-ihc-testing-2.jpgAnti-ZNRF2 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11505-znrf2-primary-antibodies-if-testing-1.jpgAnti-ZNRF2 AntibodyImmunofluorescence analysis of A549 cells, using ZNRF2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tufm-antibody-a30672-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30672-tufm-primary-antibodies-wb-testing-2.jpgAnti-TUFM AntibodyWestern Blot analysis of various cell lysis. Primary Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:10000
https://www.bosterbio.com/products/primary-antibodies/anti-elovl4-antibody-a30673-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30673-elovl4-primary-antibodies-wb-testing-1.jpgAnti-ELOVL4 AntibodyWestern Blot analysis of various cells using ELOVL4 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30673-elovl4-primary-antibodies-wb-testing-2.jpgAnti-ELOVL4 AntibodyWestern blot analysis of lysates from HeLa cells, using ELOVL4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-elovl5-antibody-a30674-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30674-elovl5-primary-antibodies-ihc-testing-1.jpgAnti-ELOVL5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using ELOVL5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30674-elovl5-primary-antibodies-wb-testing-2.jpgAnti-ELOVL5 AntibodyWestern blot analysis of lysates from MCF-7 cells, using ELOVL5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-erd22-antibody-a30676-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30676-kdelr2-primary-antibodies-ihc-testing-2.jpgAnti-ERD22 KDELR2 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30676-kdelr2-primary-antibodies-wb-testing-3.jpgAnti-ERD22 KDELR2 AntibodyWestern Blot analysis of various cells using KDEL Receptor 2 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30676-kdelr2-primary-antibodies-if-testing-1.jpgAnti-ERD22 KDELR2 AntibodyImmunofluorescence analysis of A549 cells, using ERD22 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30676-kdelr2-primary-antibodies-wb-testing-4.jpgAnti-ERD22 KDELR2 AntibodyWestern blot analysis of lysates from HUVEC and COLO cells, using ERD22 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-erd23-antibody-a30677-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30677-kdelr3-primary-antibodies-wb-testing-1.jpgAnti-ERD23 KDELR3 AntibodyWestern Blot analysis of 3T3 cells using KDEL Receptor 3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30677-kdelr3-primary-antibodies-wb-testing-2.jpgAnti-ERD23 KDELR3 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using ERD23 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eif1ay-antibody-a30678-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30678-eif1ay-primary-antibodies-ihc-testing-2.jpgAnti-EIF1AY AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eif3f-antibody-a30682-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30682-eif3f-primary-antibodies-wb-testing-2.jpgAnti-EIF3F/Eif3 Epsilon AntibodyWestern Blot analysis of various cells using eIF3ε Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30682-eif3f-primary-antibodies-ihc-testing-1.jpgAnti-EIF3F/Eif3 Epsilon AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using EIF3F Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30682-eif3f-primary-antibodies-wb-testing-3.jpgAnti-EIF3F/Eif3 Epsilon AntibodyWestern blot analysis of lysates from HeLa cells, using EIF3F Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eif3d-antibody-a30683-boster.html2026-03-24T05:10:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30683-eif3d-primary-antibodies-ihc-testing-1.jpgAnti-EIF3D AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using EIF3D Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30683-eif3d-primary-antibodies-wb-testing-2.jpgAnti-EIF3D AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using EIF3D Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eif4e3-antibody-a30684-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30684-eif4e3-primary-antibodies-wb-testing-1.jpgAnti-EIF4E3 AntibodyWestern Blot analysis of 3T3 cells using eIF4E3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30684-eif4e3-primary-antibodies-wb-testing-2.jpgAnti-EIF4E3 AntibodyWestern blot analysis of lysates from LOVO cells, using EIF4E3 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30684-eif4e3-primary-antibodies-wb-testing-3.jpgAnti-EIF4E3 AntibodyWestern blot analysis of the lysates from HepG2 cells using EIF4E3 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-foxd4-l2-l3-l4-l5-l6-antibody-a30686-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30686-foxd4l6-primary-antibodies-wb-testing-1.jpgAnti-FOXD4/L2/L3/L4/L5/L6 AntibodyWestern blot analysis of lysates from Jurkat cells, using FOXD4/L2/L3/L4/L5/L6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnj9-antibody-a30687-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30687-kcnj9-primary-antibodies-wb-testing-1.jpgAnti-KCNJ9/Kir3.3 AntibodyWestern blot analysis of lysates from LOVO cells, using KCNJ9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gabra6-antibody-a30101-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30101-gabra6-primary-antibodies-wb-testing-1.jpgAnti-GABRA6/Gaba A Receptor Alpha 6 AntibodyWestern Blot analysis of MOUSE-BRAIN cells using GABAA Rα6 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30101-gabra6-primary-antibodies-wb-testing-2.jpgAnti-GABRA6/Gaba A Receptor Alpha 6 AntibodyWestern Blot analysis of various cells using GABAA Rα6 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30101-gabra6-primary-antibodies-wb-testing-3.jpgAnti-GABRA6/Gaba A Receptor Alpha 6 AntibodyWestern blot analysis of lysates from HeLa and Jurkat cells, using GABRA6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gabrd-antibody-a30688-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30688-gabrd-primary-antibodies-ihc-testing-1.jpgAnti-GABRD/Gaba A Receptor Delta AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30688-gabrd-primary-antibodies-wb-testing-2.jpgAnti-GABRD/Gaba A Receptor Delta AntibodyWestern blot analysis of lysates from LOVO and HT-29 cells, using GABRD Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gabrg1-antibody-a30689-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30689-gabrg1-primary-antibodies-ihc-testing-1.jpgAnti-GABRG1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30689-gabrg1-primary-antibodies-wb-testing-2.jpgAnti-GABRG1 AntibodyWestern blot analysis of lysates from LOVO and RAW264.7 cells, using GABRG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ifi16-antibody-a30690-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30690-ifi16-primary-antibodies-wb-testing-2.jpgAnti-IFI16 AntibodyWestern blot analysis of the lysates from HepG2 cells using IFI16 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30690-ifi16-primary-antibodies-wb-testing-1.jpgAnti-IFI16 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using IFI16 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tubgcp3-antibody-a30691-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30691-tubgcp3-primary-antibodies-wb-testing-2.jpgAnti-TUBGCP3 AntibodyWestern Blot analysis of K562 cells using GCP3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30691-tubgcp3-primary-antibodies-wb-testing-3.jpgAnti-TUBGCP3 AntibodyWestern Blot analysis of various cells using GCP3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30691-tubgcp3-primary-antibodies-ihc-testing-1.jpgAnti-TUBGCP3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TUBGCP3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tubgcp4-antibody-a30692-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30692-tubgcp4-primary-antibodies-ihc-testing-1.jpgAnti-TUBGCP4/Gcp4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30692-tubgcp4-primary-antibodies-wb-testing-2.jpgAnti-TUBGCP4/Gcp4 AntibodyWestern Blot analysis of various cells using GCP4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30692-tubgcp4-primary-antibodies-wb-testing-3.jpgAnti-TUBGCP4/Gcp4 AntibodyWestern blot analysis of lysates from COLO and HT-29 cells, using TUBGCP4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tubgcp5-antibody-a30693-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30693-tubgcp5-primary-antibodies-ihc-testing-1.jpgAnti-TUBGCP5/Gcp5 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30693-tubgcp5-primary-antibodies-wb-testing-2.jpgAnti-TUBGCP5/Gcp5 AntibodyWestern Blot analysis of 293 cells using GCP5 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30693-tubgcp5-primary-antibodies-wb-testing-4.jpgAnti-TUBGCP5/Gcp5 AntibodyWestern Blot analysis of various cells using GCP5 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30693-tubgcp5-primary-antibodies-wb-testing-3.jpgAnti-TUBGCP5/Gcp5 AntibodyWestern blot analysis of Mouse-kidney mouse-brain HELA KB SH-SY5Y 293T lysis using GCP5 antibody. Antibody was diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30693-tubgcp5-primary-antibodies-wb-testing-5.jpgAnti-TUBGCP5/Gcp5 AntibodyWestern blot analysis of lysates from HT-29, Jurkat, and 293 cells, using TUBGCP5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tubgcp6-antibody-a30694-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30694-tubgcp6-primary-antibodies-ihc-testing-2.jpgAnti-TUBGCP6/Gcp6 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30694-tubgcp6-primary-antibodies-wb-testing-3.jpgAnti-TUBGCP6/Gcp6 AntibodyWestern Blot analysis of various cells using GCP6 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30694-tubgcp6-primary-antibodies-wb-testing-5.jpgAnti-TUBGCP6/Gcp6 AntibodyWestern blot analysis of the lysates from HeLa cells using TUBGCP6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30694-tubgcp6-primary-antibodies-ihc-testing-1.jpgAnti-TUBGCP6/Gcp6 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using TUBGCP6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30694-tubgcp6-primary-antibodies-wb-testing-4.jpgAnti-TUBGCP6/Gcp6 AntibodyWestern blot analysis of lysates from COLO cells, using TUBGCP6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cxg2-antibody-a30695-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30695-gjc2-primary-antibodies-wb-testing-2.jpgAnti-CXG2 AntibodyWestern Blot analysis of A549 cells using Connexin 47 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30695-gjc2-primary-antibodies-if-testing-1.jpgAnti-CXG2 AntibodyImmunofluorescence analysis of A549 cells, using CXG2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30695-gjc2-primary-antibodies-wb-testing-3.jpgAnti-CXG2 AntibodyWestern blot analysis of lysates from A549 cells, using CXG2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gja3-antibody-a30696-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30696-gja3-primary-antibodies-ihc-testing-1.jpgAnti-GJA3/Connexin 46 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using GJA3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gjb7-antibody-a30698-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30698-gjb7-primary-antibodies-wb-testing-1.jpgAnti-Gap junction beta-7 protein GJB7 AntibodyWestern Blot analysis of various cells using Connexin 25 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30698-gjb7-primary-antibodies-wb-testing-2.jpgAnti-Gap junction beta-7 protein GJB7 AntibodyWestern blot analysis of lysates from HT-29 cells, using GJB7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30698-gjb7-primary-antibodies-wb-testing-3.jpgAnti-Gap junction beta-7 protein GJB7 AntibodyWestern blot analysis of the lysates from HeLa cells using GJB7 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-pofut1-antibody-a30700-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30700-pofut1-primary-antibodies-ihc-testing-1.jpgAnti-POFUT1 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using POFUT1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30700-pofut1-primary-antibodies-wb-testing-2.jpgAnti-POFUT1 AntibodyWestern blot analysis of lysates from Jurkat, HeLa, and HepG2 cells, using POFUT1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pofut2-antibody-a30701-boster.html2026-03-24T05:10:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30701-pofut2-primary-antibodies-ihc-testing-1.jpgAnti-POFUT2 AntibodyImmunohistochemistry analysis of paraffin-embedded human placenta tissue, using POFUT2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-uso1-antibody-a30703-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30703-uso1-primary-antibodies-wb-testing-1.jpgAnti-USO1/P115 AntibodyWestern Blot analysis of K562 cells using p115 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30703-uso1-primary-antibodies-wb-testing-2.jpgAnti-USO1/P115 AntibodyWestern Blot analysis of various cells using p115 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30703-uso1-primary-antibodies-wb-testing-3.jpgAnti-USO1/P115 AntibodyWestern blot analysis of lysates from MCF-7, HeLa, and Jurkat cells, using USO1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gorasp2-antibody-a30705-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30705-gorasp2-primary-antibodies-ihc-testing-1.jpgAnti-GORASP2/Grasp55 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30705-gorasp2-primary-antibodies-wb-testing-2.jpgAnti-GORASP2/Grasp55 AntibodyWestern Blot analysis of various cells using GRASP55 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30705-gorasp2-primary-antibodies-wb-testing-3.jpgAnti-GORASP2/Grasp55 AntibodyWestern blot analysis of lysates from HeLa, HepG2, Jurkat, and LOVO cells, using GORASP2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gosr1-antibody-a09064-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09064-gosr1-primary-antibodies-wb-testing-1.jpgAnti-GOSR1/Gs28 AntibodyWestern blot analysis of lysates from COLO and K562 cells, using GOSR1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gasp1-antibody-a30706-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30706-gprasp1-primary-antibodies-if-testing-1.jpgAnti-GASP1 GPRASP1 AntibodyImmunofluorescence analysis of A549 cells, using GASP1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30706-gprasp1-primary-antibodies-ihc-testing-2.jpgAnti-GASP1 GPRASP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GASP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gidrp88-antibody-a30707-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30707-r3hcc1l-primary-antibodies-ihc-testing-1.jpgAnti-GIDRP88 R3HCC1L AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using GIDRP88 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30707-r3hcc1l-primary-antibodies-wb-testing-2.jpgAnti-GIDRP88 R3HCC1L AntibodyWestern blot analysis of lysates from Jurkat and COS cells, using GIDRP88 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gas1-antibody-a06815-1-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06815-1-gas1-primary-antibodies-wb-testing-1.jpgAnti-GAS1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using GAS1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06815-1-gas1-primary-antibodies-wb-testing-2.jpgAnti-GAS1 AntibodyWestern blot analysis of the lysates from HeLa cells using GAS1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gchfr-antibody-a30708-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30708-gchfr-primary-antibodies-ihc-testing-1.jpgAnti-GCHFR AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using GCHFR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eras-antibody-a30709-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30709-eras-primary-antibodies-if-testing-1.jpgAnti-GTPase ERas ERAS AntibodyImmunofluorescence analysis of A549 cells, using ERAS Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30709-eras-primary-antibodies-wb-testing-2.jpgAnti-GTPase ERas ERAS AntibodyWestern blot analysis of lysates from Jurkat cells, using ERAS Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30709-eras-primary-antibodies-wb-testing-3.jpgAnti-GTPase ERas ERAS AntibodyWestern blot analysis of the lysates from HeLa cells using ERAS antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gimap2-antibody-a30710-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30710-gimap2-primary-antibodies-wb-testing-2.jpgAnti-GTPase IMAP family member 2 GIMAP2 AntibodyWestern Blot analysis of various cells using GIMAP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30710-gimap2-primary-antibodies-if-testing-1.jpgAnti-GTPase IMAP family member 2 GIMAP2 AntibodyImmunofluorescence analysis of A549 cells, using GIMAP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30710-gimap2-primary-antibodies-wb-testing-3.jpgAnti-GTPase IMAP family member 2 GIMAP2 AntibodyWestern blot analysis of lysates from HT-29 cells, using GIMAP2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gimap5-antibody-a30712-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30712-gimap5-primary-antibodies-wb-testing-2.jpgAnti-GIMAP5 AntibodyWestern Blot analysis of various cells using GIMAP5 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30712-gimap5-primary-antibodies-ihc-testing-1.jpgAnti-GIMAP5 AntibodyImmunohistochemistry analysis of paraffin-embedded human placenta tissue, using GIMAP5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30712-gimap5-primary-antibodies-wb-testing-3.jpgAnti-GIMAP5 AntibodyWestern blot analysis of lysates from HeLa and HT-29 cells, using GIMAP5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gtpbp2-antibody-a30713-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30713-gtpbp2-primary-antibodies-ihc-testing-1.jpgAnti-GTPBP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using GTPBP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gtpbp5-antibody-a30714-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30714-mtg2-primary-antibodies-ihc-testing-1.jpgAnti-GTPBP5 AntibodyImmunohistochemistry analysis of paraffin-embedded human cervix carcinoma tissue, using GTPBP5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rad-antibody-a30715-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30715-rrad-primary-antibodies-wb-testing-3.jpgAnti-RAD RRAD AntibodyWestern Blot analysis of various cells using Rad GTPase Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30715-rrad-primary-antibodies-if-testing-1.jpgAnti-RAD RRAD AntibodyImmunofluorescence analysis of A549 cells, using RAD Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30715-rrad-primary-antibodies-ihc-testing-2.jpgAnti-RAD RRAD AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using RAD Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30715-rrad-primary-antibodies-wb-testing-4.jpgAnti-RAD RRAD AntibodyWestern blot analysis of lysates from HeLa and HepG2/MCF-7 cells, using RAD Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gng5-antibody-a30716-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30716-gng5-primary-antibodies-if-testing-1.jpgAnti-GNG5 AntibodyImmunofluorescence analysis of A549 cells, using GNG5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hnrnpul2-antibody-a30718-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30718-hnrnpul2-primary-antibodies-wb-testing-2.jpgAnti-HNRNPUL2 AntibodyWestern Blot analysis of K562 cells using SAF-A2 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30718-hnrnpul2-primary-antibodies-ihc-testing-1.jpgAnti-HNRNPUL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using HNRNPUL2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hla-doa-antibody-a30721-boster.html2026-03-24T05:10:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30721-hla-doa-primary-antibodies-ihc-testing-1.jpgAnti-HLA-DOA/Hla Doa AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30721-hla-doa-primary-antibodies-wb-testing-2.jpgAnti-HLA-DOA/Hla Doa AntibodyWestern Blot analysis of various cells using HLA-DOα Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30721-hla-doa-primary-antibodies-wb-testing-3.jpgAnti-HLA-DOA/Hla Doa AntibodyWestern blot analysis of lysates from COLO cells, using HLA-DOA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hoxb2-antibody-a30723-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30723-hoxb2-primary-antibodies-wb-testing-1.jpgAnti-HOXB2 AntibodyWestern blot analysis of lysates from MCF-7, HUVEC, A549, and LOVO cells, using HOXB2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30723-hoxb2-primary-antibodies-wb-testing-2.jpgAnti-HOXB2 AntibodyWestern blot analysis of the lysates from HUVECcells using HOXB2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-hoxd10-antibody-a30724-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30724-hoxd10-primary-antibodies-wb-testing-1.jpgAnti-Homeobox protein Hox-D10 HOXD10 AntibodyWestern blot analysis of lysates from K562 and RAW264.7 cells, using HOXD10 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nanogp8-antibody-a30725-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30725-nanogp8-primary-antibodies-ihc-testing-1.jpgAnti-NANOGP8 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30725-nanogp8-primary-antibodies-wb-testing-2.jpgAnti-NANOGP8 AntibodyWestern Blot analysis of various cells using Nanog P8 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30725-nanogp8-primary-antibodies-wb-testing-3.jpgAnti-NANOGP8 AntibodyWestern blot analysis of lysates from HUVEC, HT-29, HepG2, and Jurkat cells, using NANOGP8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nkx26-antibody-a30727-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30727-nkx2-6-primary-antibodies-wb-testing-1.jpgAnti-NKX26 AntibodyWestern Blot analysis of various cells using Nkx-2.6 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30727-nkx2-6-primary-antibodies-wb-testing-3.jpgAnti-NKX26 AntibodyWestern blot analysis of the lysates from Jurkat cells using NKX26 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30727-nkx2-6-primary-antibodies-wb-testing-2.jpgAnti-NKX26 AntibodyWestern blot analysis of lysates from HeLa and COLO cells, using NKX26 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-usp53-antibody-a15639-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15639-usp53-primary-antibodies-ihc-testing-1.jpgAnti-USP53 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using USP53 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ints2-antibody-a30729-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30729-ints2-primary-antibodies-ihc-testing-1.jpgAnti-Integrator complex subunit 2 INTS2 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30729-ints2-primary-antibodies-wb-testing-2.jpgAnti-Integrator complex subunit 2 INTS2 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using INTS2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnj2-antibody-a30730-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30730-kcnj2-primary-antibodies-wb-testing-2.jpgAnti-KCNJ2/Kir2.1 AntibodyWestern Blot analysis of various cells using KIR2.1 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30730-kcnj2-primary-antibodies-ihc-testing-1.jpgAnti-KCNJ2/Kir2.1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using KCNJ2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-klhl29-antibody-a30731-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30731-klhl29-primary-antibodies-ihc-testing-1.jpgAnti-Kelch-like protein 29 KLHL29 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using KLHL29 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kir2dl5b-antibody-a30732-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30732-kir2dl5b-primary-antibodies-wb-testing-2.jpgAnti-KIR2DL5B AntibodyWestern blot analysis of lysates from KB cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30732-kir2dl5b-primary-antibodies-if-testing-1.jpgAnti-KIR2DL5B AntibodyImmunofluorescence analysis of A549 cells, using KIR2DL5B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kif13b-antibody-a06122-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06122-kif13b-primary-antibodies-ihc-testing-1.jpgAnti-Kinesin-like protein KIF13B KIF13B AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using KIF13B Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-aasdhppt-antibody-a30733-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30733-aasdhppt-primary-antibodies-ihc-testing-1.jpgAnti-AASDHPPT/Aasd Ppt AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30733-aasdhppt-primary-antibodies-wb-testing-2.jpgAnti-AASDHPPT/Aasd Ppt AntibodyWestern Blot analysis of various cells using AASD-PPT Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30733-aasdhppt-primary-antibodies-wb-testing-3.jpgAnti-AASDHPPT/Aasd Ppt AntibodyWestern blot analysis of lysates from COLO cells, using AASDHPPT Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cep97-antibody-a30735-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30735-cep97-primary-antibodies-ihc-testing-1.jpgAnti-CEP97 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30735-cep97-primary-antibodies-wb-testing-2.jpgAnti-CEP97 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using CEP97 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30735-cep97-primary-antibodies-wb-testing-3.jpgAnti-CEP97 AntibodyWestern blot analysis of the lysates from COLO205 cells using CEP97 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-lrrc41-antibody-a30736-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30736-lrrc41-primary-antibodies-ihc-testing-1.jpgAnti-LRRC41 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30736-lrrc41-primary-antibodies-wb-testing-2.jpgAnti-LRRC41 AntibodyWestern Blot analysis of K562 cells using LRRC41 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30736-lrrc41-primary-antibodies-wb-testing-3.jpgAnti-LRRC41 AntibodyWestern Blot analysis of various cells using LRRC41 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30736-lrrc41-primary-antibodies-wb-testing-4.jpgAnti-LRRC41 AntibodyWestern blot analysis of lysates from rat kidney and rat heart cells, using LRRC41 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-med13l-antibody-a05593-1-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05593-1-med13l-primary-antibodies-ihc-testing-1.jpgAnti-MED13L/Thrap2 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05593-1-med13l-primary-antibodies-wb-testing-2.jpgAnti-MED13L/Thrap2 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using POLDIP3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mia-antibody-a01570-2-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01570-2-mia-primary-antibodies-ihc-testing-1.jpgAnti-MIA AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using MIA Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mbtps2-antibody-a07369-1-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07369-1-mbtps2-primary-antibodies-if-testing-1.jpgAnti-MBTPS2/S2P AntibodyImmunofluorescence analysis of A549 cells, using MBTPS2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps32-antibody-a30737-boster.html2026-03-24T05:10:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30737-mrpl42-primary-antibodies-ihc-testing-1.jpgAnti-MRPS32 MRPL42 AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30737-mrpl42-primary-antibodies-ihc-testing-2.jpgAnti-MRPS32 MRPL42 AntibodyImmunohistochemistry analysis of paraffin-embedded human placenta, using MRPS32 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrps33-antibody-a15211-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15211-mrps33-primary-antibodies-ihc-testing-1.jpgAnti-MRPS33/Rt33 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using MRPS33 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mot12-antibody-a11725-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11725-slc16a12-primary-antibodies-ihc-testing-1.jpgAnti-MOT12 SLC16A12 AntibodyImmunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue, using MOT12 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-myo1d-antibody-a09126-1-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09126-1-myo1d-primary-antibodies-ihc-testing-1.jpgAnti-MYO1D/Myosin Id AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MYO1D Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ndufa4l2-antibody-a30738-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30738-ndufa4l2-primary-antibodies-wb-testing-1.jpgAnti-NDUFA4L2 AntibodyWestern Blot analysis of various cells using NDUFA4L2 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30738-ndufa4l2-primary-antibodies-wb-testing-2.jpgAnti-NDUFA4L2 AntibodyWestern blot analysis of lysates from HepG2, HUVEC, COLO, and Jurkat cells, using NDUFA4L2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mt-nd5-antibody-a30739-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30739-mt-nd5-primary-antibodies-wb-testing-1.jpgAnti-MT-ND5 AntibodyWestern Blot analysis of various cells using ND5 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30739-mt-nd5-primary-antibodies-wb-testing-3.jpgAnti-MT-ND5 AntibodyWestern blot analysis of the lysates from Jurkat cells using MT-ND5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30739-mt-nd5-primary-antibodies-wb-testing-2.jpgAnti-MT-ND5 AntibodyWestern blot analysis of lysates from HT-29 cells, using MT-ND5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-neurl1-antibody-a30740-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30740-neurl1-primary-antibodies-ihc-testing-1.jpgAnti-NEURL1 AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30740-neurl1-primary-antibodies-wb-testing-2.jpgAnti-NEURL1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using NEURL1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nxph1-antibody-a12696-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12696-nxph1-primary-antibodies-ihc-testing-1.jpgAnti-NXPH1/Neurexophilin 1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using NXPH1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12696-nxph1-primary-antibodies-wb-testing-2.jpgAnti-NXPH1/Neurexophilin 1 AntibodyWestern blot analysis of lysates from rat heart cells, using NXPH1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nbeal1-antibody-a15493-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15493-nbeal1-primary-antibodies-ihc-testing-1.jpgAnti-NBEAL1/Neurobeachin Like 1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15493-nbeal1-primary-antibodies-wb-testing-3.jpgAnti-NBEAL1/Neurobeachin Like 1 AntibodyWestern blot analysis of the lysates from HeLa cells using NBEAL1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15493-nbeal1-primary-antibodies-wb-testing-2.jpgAnti-NBEAL1/Neurobeachin Like 1 AntibodyWestern blot analysis of lysates from HepG2 cells, using NBEAL1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nbpf5-antibody-a30741-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30741-nbpf5p-primary-antibodies-ihc-testing-1.jpgAnti-NBPF5 NBPF5P AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30741-nbpf5p-primary-antibodies-wb-testing-3.jpgAnti-NBPF5 NBPF5P AntibodyWestern blot analysis of the lysates from K562 cells using NBPF5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30741-nbpf5p-primary-antibodies-wb-testing-2.jpgAnti-NBPF5 NBPF5P AntibodyWestern blot analysis of lysates from Jurkat cells, using NBPF5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-c5orf13-antibody-a09054-1-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09054-1-nrep-primary-antibodies-ihc-testing-1.jpgAnti-C5orf13 NREP AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using C5orf13 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sept3-antibody-a30742-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30742-sept3-primary-antibodies-ihc-testing-1.jpgAnti-SEPT3 SEPT3; AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30742-sept3-primary-antibodies-wb-testing-2.jpgAnti-SEPT3 SEPT3; AntibodyWestern Blot analysis of various cells using Septin 3 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30742-sept3-primary-antibodies-wb-testing-3.jpgAnti-SEPT3 SEPT3; AntibodyWestern blot analysis of various lysis using Septin 3 Polyclonal Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30742-sept3-primary-antibodies-wb-testing-4.jpgAnti-SEPT3 SEPT3; AntibodyWestern blot analysis of lysates from 293 cells, using SEPT3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ncln-antibody-a12284-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-ncln-primary-antibodies-ihc-testing-1.jpgAnti-NCLN/Nicalin AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-ncln-primary-antibodies-wb-testing-2.jpgAnti-NCLN/Nicalin AntibodyWestern blot analysis of lysates from HepG2 and HUVEC cells, using NCLN Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nid1-antibody-a05621-1-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05621-1-nid1-primary-antibodies-wb-testing-1.jpgAnti-NID1/Entactin AntibodyWestern blot analysis of lysates from K562 cells, using NID1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nup93-antibody-a07090-boster.html2026-03-24T05:10:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07090-nup93-primary-antibodies-wb-testing-1.jpgAnti-NUP93 AntibodyWestern blot analysis of lysates from rat liver cells, using NUP93 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-hcc1-antibody-a11119-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11119-sarnp-primary-antibodies-ihc-testing-1.jpgAnti-HCC1 SARNP AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using HCC1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11119-sarnp-primary-antibodies-wb-testing-2.jpgAnti-HCC1 SARNP AntibodyWestern blot analysis of lysates from mouse liver, using HCC1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ncoa5-antibody-a07810-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-ncoa5-primary-antibodies-ihc-testing-1.jpgAnti-Nuclear receptor coactivator 5 NCOA5 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using NCOA5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-noc2l-antibody-a11194-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11194-noc2l-primary-antibodies-wb-testing-1.jpgAnti-NOC2L AntibodyWestern blot analysis of lysates from MCF-7 cells, using NOC2L Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nom1-antibody-a09439-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09439-nom1-primary-antibodies-ihc-testing-1.jpgAnti-NOM1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using NOM1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-zcchc17-antibody-a12008-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12008-zcchc17-primary-antibodies-ihc-testing-1.jpgAnti-Nucleolar protein of 40 kDa ZCCHC17 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ZCCHC17 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-oaz1-antibody-a06486-2-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06486-2-oaz1-primary-antibodies-ihc-testing-1.jpgAnti-OAZ1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using OAZ1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nr4a3-antibody-a02578-1-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02578-1-nr4a3-primary-antibodies-wb-testing-1.jpgAnti-NR4A3/Nor1 AntibodyWestern blot analysis of lysates from COLO cells, using NR4A3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc6a16-antibody-a14901-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14901-slc6a16-primary-antibodies-ihc-testing-1.jpgAnti-SLC6A16 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using SLC6A16 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc6a15-antibody-a07589-1-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07589-1-slc6a15-primary-antibodies-ihc-testing-1.jpgAnti-SLC6A15 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07589-1-slc6a15-primary-antibodies-wb-testing-2.jpgAnti-SLC6A15 AntibodyWestern blot analysis of lysates from Jurkat cells, using SLC6A15 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-decr2-antibody-a11948-1-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11948-1-decr2-primary-antibodies-wb-testing-1.jpgAnti-DECR2 AntibodyWestern blot analysis of lysates from LOVO cells, using DECR2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11948-1-decr2-primary-antibodies-wb-testing-2.jpgAnti-DECR2 AntibodyWestern blot analysis of the lysates from HepG2 cells using DECR2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-peci-antibody-a30744-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30744-eci2-primary-antibodies-wb-testing-2.jpgAnti-PECI ECI2 AntibodyWestern Blot analysis of 293 cells using DRS-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30744-eci2-primary-antibodies-wb-testing-3.jpgAnti-PECI ECI2 AntibodyWestern Blot analysis of various cells using DRS-1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30744-eci2-primary-antibodies-wb-testing-5.jpgAnti-PECI ECI2 AntibodyWestern blot analysis of the lysates from COLO205 cells using PECI antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30744-eci2-primary-antibodies-ihc-testing-1.jpgAnti-PECI ECI2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PECI Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30744-eci2-primary-antibodies-wb-testing-4.jpgAnti-PECI ECI2 AntibodyWestern blot analysis of lysates from 293 cells, using PECI Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pex19-antibody-a03186-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03186-pex19-primary-antibodies-ihc-testing-1.jpgAnti-PEX19/Peroxin 19 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03186-pex19-primary-antibodies-wb-testing-3.jpgAnti-PEX19/Peroxin 19 AntibodyWestern blot analysis of the lysates from HT-29 cells using PEX19 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03186-pex19-primary-antibodies-wb-testing-2.jpgAnti-PEX19/Peroxin 19 AntibodyWestern blot analysis of lysates from MCF-7 cells, using PEX19 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lonp2-antibody-a11643-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11643-lonp2-primary-antibodies-ihc-testing-1.jpgAnti-LONP2 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using LONP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pex11c-antibody-a12566-boster.html2026-03-24T05:10:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12566-pex11g-primary-antibodies-ihc-testing-1.jpgAnti-PEX11C PEX11G AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas, using PEX11C Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pprc1-antibody-a08308-1-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08308-1-pprc1-primary-antibodies-ihc-testing-1.jpgAnti-PPRC1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using PPRC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pigy-antibody-a14537-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14537-pigy-primary-antibodies-ihc-testing-1.jpgAnti-PIGY AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PIGY Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-plcxd1-antibody-a16218-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16218-plcxd1-primary-antibodies-ihc-testing-1.jpgAnti-PLCXD1 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16218-plcxd1-primary-antibodies-ihc-testing-2.jpgAnti-PLCXD1 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma, using PLCXD1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pabpc5-antibody-a14533-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14533-pabpc5-primary-antibodies-ihc-testing-1.jpgAnti-PABPC5 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14533-pabpc5-primary-antibodies-wb-testing-3.jpgAnti-PABPC5 AntibodyWestern blot analysis of the lysates from HeLa cells using PABPC5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14533-pabpc5-primary-antibodies-wb-testing-2.jpgAnti-PABPC5 AntibodyWestern blot analysis of lysates from K562 cells, using PABPC5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnk17-antibody-a10170-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10170-kcnk17-primary-antibodies-if-testing-1.jpgAnti-KCNK17 AntibodyImmunofluorescence analysis of Caco2 cell. 1,primary Antibody was diluted at 1:100(4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500(room temperature, 50min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10170-kcnk17-primary-antibodies-wb-testing-2.jpgAnti-KCNK17 AntibodyWestern blot analysis of lysates from Jurkat cells, using KCNK17 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnt1-antibody-a05367-1-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05367-1-kcnt1-primary-antibodies-ihc-testing-1.jpgAnti-KCNT1 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using KCNT1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prpf39-antibody-a15727-1-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15727-1-prpf39-primary-antibodies-ihc-testing-1.jpgAnti-Pre-mRNA-processing factor 39 PRPF39 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15727-1-prpf39-primary-antibodies-wb-testing-3.jpgAnti-Pre-mRNA-processing factor 39 PRPF39 AntibodyWestern blot analysis of the lysates from COLO205 cells using PRPF39 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15727-1-prpf39-primary-antibodies-wb-testing-2.jpgAnti-Pre-mRNA-processing factor 39 PRPF39 AntibodyWestern blot analysis of lysates from K562 cells, using PRPF39 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prpf38a-antibody-a13639-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13639-prpf38a-primary-antibodies-ihc-testing-1.jpgAnti-PRPF38A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13639-prpf38a-primary-antibodies-wb-testing-3.jpgAnti-PRPF38A AntibodyWestern blot analysis of the lysates from HUVECcells using PRPF38A antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13639-prpf38a-primary-antibodies-wb-testing-2.jpgAnti-PRPF38A AntibodyWestern blot analysis of lysates from COLO cells, using PRPF38A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pote8-antibody-a18602-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18602-potea-primary-antibodies-ihc-testing-1.jpgAnti-POTE8 POTEA AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma, using POTE8 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-fntb-antibody-a07620-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07620-fntb-primary-antibodies-wb-testing-1.jpgAnti-FNTB AntibodyWestern blot analysis of lysates from RAW264.7 abd NIH/3T3 cells, using FNTB Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ppp1r11-antibody-a10474-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10474-ppp1r11-primary-antibodies-ihc-testing-1.jpgAnti-PPP1R11/Tctex5 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PPP1R11 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ppp1r1c-antibody-a11702-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11702-ppp1r1c-primary-antibodies-ihc-testing-1.jpgAnti-PPP1R1C AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using PPP1R1C Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ppp1r3a-antibody-a07755-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07755-ppp1r3a-primary-antibodies-ihc-testing-1.jpgAnti-PPP1R3A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07755-ppp1r3a-primary-antibodies-wb-testing-3.jpgAnti-PPP1R3A AntibodyWestern blot analysis of the lysates from HT-29 cells using PPP1R3A antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07755-ppp1r3a-primary-antibodies-wb-testing-2.jpgAnti-PPP1R3A AntibodyWestern blot analysis of lysates from MCF-7 and COLO cells, using PPP1R3A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ppm1k-antibody-a04319-1-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-1-ppm1k-primary-antibodies-wb-testing-2.jpgAnti-PPM1K/Pp2C Kappa AntibodyWestern Blot analysis of various cells using PP2Cκ Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-1-ppm1k-primary-antibodies-wb-testing-3.jpgAnti-PPM1K/Pp2C Kappa AntibodyWestern blot analysis of the lysates from HeLa cells using PPM1K antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04319-1-ppm1k-primary-antibodies-ihc-testing-1.jpgAnti-PPM1K/Pp2C Kappa AntibodyImmunohistochemistry analysis of paraffin-embedded human pancreas tissue, using PPM1K Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pms2-pms2cl-antibody-a12407-boster.html2026-03-24T05:10:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12407-pms2cl-primary-antibodies-ihc-testing-1.jpgAnti-PMS2/PMS2CL AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using PMS2/PMS2CL Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-plekhg4-antibody-a10252-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10252-plekhg4-primary-antibodies-ihc-testing-1.jpgAnti-Puratrophin-1 PLEKHG4 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10252-plekhg4-primary-antibodies-wb-testing-3.jpgAnti-Puratrophin-1 PLEKHG4 AntibodyWestern blot analysis of the lysates from HUVECcells using PLEKHG4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10252-plekhg4-primary-antibodies-wb-testing-2.jpgAnti-Puratrophin-1 PLEKHG4 AntibodyWestern blot analysis of lysates from COS7 and K562 cells, using PLEKHG4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rabep1-antibody-a04172-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04172-rabep1-primary-antibodies-ihc-testing-1.jpgAnti-RABEP1/Rabaptin 5 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RABEP1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab11fip3-antibody-a09469-1-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09469-1-rab11fip3-primary-antibodies-ihc-testing-1.jpgAnti-RAB11FIP3 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using RAB11FIP3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rapgef5-antibody-a12923-1-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12923-1-rapgef5-primary-antibodies-ihc-testing-1.jpgAnti-RAPGEF5 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12923-1-rapgef5-primary-antibodies-wb-testing-3.jpgAnti-RAPGEF5 AntibodyWestern blot analysis of the lysates from COLO205 cells using RAPGEF5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12923-1-rapgef5-primary-antibodies-wb-testing-2.jpgAnti-RAPGEF5 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using RAPGEF5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-g3bp2-antibody-a05742-1-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05742-1-g3bp2-primary-antibodies-wb-testing-1.jpgAnti-G3BP2 AntibodyWestern Blot analysis of various cells using G3BP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05742-1-g3bp2-primary-antibodies-wb-testing-2.jpgAnti-G3BP2 AntibodyWestern blot analysis of lysates from HeLa, HUVEC, and A549 cells, using G3BP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05742-1-g3bp2-primary-antibodies-wb-testing-3.jpgAnti-G3BP2 AntibodyWestern blot analysis of the lysates from HeLa cells using G3BP2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rab37-antibody-a10452-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10452-rab37-primary-antibodies-wb-testing-3.jpgAnti-Ras-related protein Rab-37 RAB37 AntibodyWestern blot analysis of the lysates from HepG2 cells using RAB37 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10452-rab37-primary-antibodies-ihc-testing-1.jpgAnti-Ras-related protein Rab-37 RAB37 AntibodyImmunohistochemistry analysis of paraffin-embedded human prostate carcinoma tissue, using RAB37 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10452-rab37-primary-antibodies-wb-testing-2.jpgAnti-Ras-related protein Rab-37 RAB37 AntibodyWestern blot analysis of lysates from HUVEC cells, using RAB37 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab38-antibody-a05500-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05500-rab38-primary-antibodies-ihc-testing-1.jpgAnti-Ras-related protein Rab-38 RAB38 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05500-rab38-primary-antibodies-wb-testing-2.jpgAnti-Ras-related protein Rab-38 RAB38 AntibodyWestern blot analysis of lysates from Jurkat cells, using RAB38 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab40b-antibody-a30752-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30752-rab40b-primary-antibodies-ihc-testing-1.jpgAnti-Ras-related protein Rab-40B RAB40B AntibodyImmunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30752-rab40b-primary-antibodies-wb-testing-2.jpgAnti-Ras-related protein Rab-40B RAB40B AntibodyWestern Blot analysis of Jurkat cells using Rab 40B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30752-rab40b-primary-antibodies-wb-testing-3.jpgAnti-Ras-related protein Rab-40B RAB40B AntibodyWestern blot analysis of lysates from Jurkat cells, using RAB40B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab5c-antibody-a05148-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05148-rab5c-primary-antibodies-ihc-testing-1.jpgAnti-Ras-related protein Rab-5C RAB5C AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05148-rab5c-primary-antibodies-wb-testing-3.jpgAnti-Ras-related protein Rab-5C RAB5C AntibodyWestern blot analysis of the lysates from 293 cells using RAB5C antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05148-rab5c-primary-antibodies-wb-testing-2.jpgAnti-Ras-related protein Rab-5C RAB5C AntibodyWestern blot analysis of lysates from LOVO, HeLa, and Jurkat cells, using RAB5C Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rab7l1-antibody-a30753-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30753-rab29-primary-antibodies-ihc-testing-1.jpgAnti-RAB7L1 RAB29 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30753-rab29-primary-antibodies-wb-testing-2.jpgAnti-RAB7L1 RAB29 AntibodyWestern Blot analysis of various cells using Rab 7L1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30753-rab29-primary-antibodies-wb-testing-4.jpgAnti-RAB7L1 RAB29 AntibodyWestern blot analysis of the lysates from HepG2 cells using RAB7L1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30753-rab29-primary-antibodies-wb-testing-3.jpgAnti-RAB7L1 RAB29 AntibodyWestern blot analysis of lysates from HT-29 cells, using RAB7L1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rgs7-antibody-a04305-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04305-rgs7-primary-antibodies-ihc-testing-1.jpgAnti-RGS7 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04305-rgs7-primary-antibodies-wb-testing-2.jpgAnti-RGS7 AntibodyWestern blot analysis of lysates from Jurkat cells, using RGS7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rhg1-antibody-a06116-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06116-arhgap1-primary-antibodies-ihc-testing-1.jpgAnti-RHG1 ARHGAP1 AntibodyImmunohistochemistry analysis of paraffin-embedded human heart tissue, using RHG1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06116-arhgap1-primary-antibodies-wb-testing-2.jpgAnti-RHG1 ARHGAP1 AntibodyWestern blot analysis of lysates from HeLa and HUVEC cells, using RHG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-arhgef7-antibody-a02764-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-arhgef7-primary-antibodies-ihc-testing-1.jpgAnti-ARHGEF7/Beta Pix AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-arhgef7-primary-antibodies-wb-testing-2.jpgAnti-ARHGEF7/Beta Pix AntibodyWestern blot analysis of lysates from rat muscle and rat heart cells, using ARHGEF7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-arhgef9-antibody-a06931-1-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06931-1-arhgef9-primary-antibodies-ihc-testing-1.jpgAnti-ARHGEF9/Collybistin AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using ARHGEF9 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rpl7l1-antibody-a15655-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15655-rpl7l1-primary-antibodies-ihc-testing-1.jpgAnti-RPL7L1 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15655-rpl7l1-primary-antibodies-wb-testing-2.jpgAnti-RPL7L1 AntibodyWestern blot analysis of lysates from HepG2 cells, using RPL7L1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rtcd1-antibody-a30754-boster.html2026-03-24T05:10:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30754-rtca-primary-antibodies-ihc-testing-1.jpgAnti-RTCD1 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using RTCD1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30754-rtca-primary-antibodies-wb-testing-2.jpgAnti-RTCD1 AntibodyWestern blot analysis of lysates from Jurkat cells, using RTCD1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ell2-antibody-a06309-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06309-ell2-primary-antibodies-ihc-testing-1.jpgAnti-ELL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ELL2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sec16a-antibody-a05622-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05622-sec16a-primary-antibodies-ihc-testing-1.jpgAnti-SEC16A AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using SEC16A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-scamp1-antibody-a08692-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08692-scamp1-primary-antibodies-ihc-testing-1.jpgAnti-SCAMP1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08692-scamp1-primary-antibodies-wb-testing-3.jpgAnti-SCAMP1 AntibodyWestern blot analysis of the lysates from HeLa cells using SCAMP1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08692-scamp1-primary-antibodies-wb-testing-2.jpgAnti-SCAMP1 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using SCAMP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sept2-antibody-a30757-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30757-sept2-primary-antibodies-ihc-testing-1.jpgAnti-SEPT2 SEPT2; AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30757-sept2-primary-antibodies-wb-testing-3.jpgAnti-SEPT2 SEPT2; AntibodyWestern blot analysis of the lysates from HepG2 cells using SEPT2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30757-sept2-primary-antibodies-wb-testing-2.jpgAnti-SEPT2 SEPT2; AntibodyWestern blot analysis of lysates from Jurkat and MCF-7 cells, using SEPT2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sept7-antibody-a30759-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30759-sept7-primary-antibodies-ihc-testing-1.jpgAnti-SEPT7 SEPT7; AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30759-sept7-primary-antibodies-wb-testing-2.jpgAnti-SEPT7 SEPT7; AntibodyWestern Blot analysis of various cells using Septin 7 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30759-sept7-primary-antibodies-wb-testing-3.jpgAnti-SEPT7 SEPT7; AntibodyWestern blot analysis of lysates from HeLa, HUVEC, and MCF-7 cells, using SEPT7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sept8-antibody-a30760-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30760-sept8-primary-antibodies-ihc-testing-1.jpgAnti-SEPT8 SEPT8; AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30760-sept8-primary-antibodies-wb-testing-2.jpgAnti-SEPT8 SEPT8; AntibodyWestern Blot analysis of various cells using Septin 8 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30760-sept8-primary-antibodies-wb-testing-3.jpgAnti-SEPT8 SEPT8; AntibodyWestern blot analysis of lysates from HeLa cells, using SEPT8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-stk36-antibody-a09526-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09526-1-stk36-primary-antibodies-wb-testing-3.jpgAnti-STK36 AntibodyWestern blot analysis of the lysates from HepG2 cells using STK36 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09526-1-stk36-primary-antibodies-ihc-testing-1.jpgAnti-STK36 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using STK36 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09526-1-stk36-primary-antibodies-wb-testing-2.jpgAnti-STK36 AntibodyWestern blot analysis of lysates from K562 cells, using STK36 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-prkx-antibody-a06585-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06585-1-prkx-primary-antibodies-wb-testing-3.jpgAnti-PRKX AntibodyWestern blot analysis of the lysates from HepG2 cells using PRKX antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06585-1-prkx-primary-antibodies-ihc-testing-1.jpgAnti-PRKX AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using PRKX Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06585-1-prkx-primary-antibodies-wb-testing-2.jpgAnti-PRKX AntibodyWestern blot analysis of lysates from MCF-7 cells, using PRKX Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-qsk-antibody-a30762-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30762-sik3-primary-antibodies-wb-testing-2.jpgAnti-QSK AntibodyWestern Blot analysis of LOVO cells using QSK Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30762-sik3-primary-antibodies-ihc-testing-1.jpgAnti-QSK AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using QSK Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-riok3-antibody-a09262-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09262-1-riok3-primary-antibodies-ihc-testing-1.jpgAnti-RIOK3/Sudd AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09262-1-riok3-primary-antibodies-wb-testing-3.jpgAnti-RIOK3/Sudd AntibodyWestern blot analysis of the lysates from HeLa cells using RIOK3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09262-1-riok3-primary-antibodies-wb-testing-2.jpgAnti-RIOK3/Sudd AntibodyWestern blot analysis of lysates from HepG2 cells, using RIOK3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-srpk1-antibody-a01937-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01937-srpk1-primary-antibodies-wb-testing-2.jpgAnti-SRSF protein kinase 1 SRPK1 AntibodyWestern blot analysis of the lysates from HUVECcells using SRPK1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01937-srpk1-primary-antibodies-wb-testing-1.jpgAnti-SRSF protein kinase 1 SRPK1 AntibodyWestern blot analysis of lysates from K562 and RAW264.7 cells, using SRPK1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-taok1-antibody-a07063-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07063-taok1-primary-antibodies-ihc-testing-1.jpgAnti-TAOK1/Psk2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using TAOK1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07063-taok1-primary-antibodies-wb-testing-2.jpgAnti-TAOK1/Psk2 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using TAOK1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vrk2-antibody-a04821-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04821-1-vrk2-primary-antibodies-wb-testing-1.jpgAnti-VRK2 AntibodyWestern blot analysis of lysates from Jurkat cells, using VRK2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-serpina11-antibody-a17849-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17849-serpina11-primary-antibodies-ihc-testing-1.jpgAnti-Serpin A11 SERPINA11 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17849-serpina11-primary-antibodies-wb-testing-2.jpgAnti-Serpin A11 SERPINA11 AntibodyWestern blot analysis of lysates from HT-29 cells, using SERPINA11 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-saa4-antibody-a07115-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07115-saa4-primary-antibodies-ihc-testing-1.jpgAnti-SAA4/Serum Amyloid A4 AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma, using SAA4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sesn1-antibody-a05559-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05559-1-sesn1-primary-antibodies-ihc-testing-1.jpgAnti-SESN1/Pa26 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using SESN1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05559-1-sesn1-primary-antibodies-wb-testing-2.jpgAnti-SESN1/Pa26 AntibodyWestern blot analysis of lysates from rat muscle cells, using SESN1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-shd-antibody-a08238-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08238-shd-primary-antibodies-wb-testing-2.jpgAnti-SHD AntibodyWestern blot analysis of the lysates from HepG2 cells using SHD antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08238-shd-primary-antibodies-wb-testing-1.jpgAnti-SHD AntibodyWestern blot analysis of lysates from HepG2 cells, using SHD Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-stac2-antibody-a16187-1-boster.html2026-03-24T05:10:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16187-1-stac2-primary-antibodies-wb-testing-1.jpgAnti-STAC2 AntibodyWestern blot analysis of lysates from K562 cells, using STAC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sh3bgr-antibody-a13419-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13419-sh3bgr-primary-antibodies-ihc-testing-1.jpgAnti-SH3BGR AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13419-sh3bgr-primary-antibodies-wb-testing-2.jpgAnti-SH3BGR AntibodyWestern blot analysis of lysates from Jurkat cells, using SH3BGR Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-shc2-antibody-a09660-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09660-shc2-primary-antibodies-ihc-testing-1.jpgAnti-SHC2/Sck AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09660-shc2-primary-antibodies-wb-testing-2.jpgAnti-SHC2/Sck AntibodyWestern blot analysis of lysates from Jurkat cells, using SHC2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sgol2-antibody-a30763-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30763-sgo2-primary-antibodies-ihc-testing-1.jpgAnti-SGOL2 SGO2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using SGOL2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc6a6-antibody-a06936-1-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06936-1-slc6a6-primary-antibodies-ihc-testing-1.jpgAnti-SLC6A6/Taut AntibodyImmunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using SLC6A6 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc10a7-antibody-a07374-1-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07374-1-slc10a7-primary-antibodies-ihc-testing-1.jpgAnti-SLC10A7 AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07374-1-slc10a7-primary-antibodies-wb-testing-3.jpgAnti-SLC10A7 AntibodyWestern blot analysis of the lysates from 293 cells using SLC10A7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07374-1-slc10a7-primary-antibodies-wb-testing-2.jpgAnti-SLC10A7 AntibodyWestern blot analysis of lysates from mouse liver, using SLC10A7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc5a2-antibody-a03748-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03748-slc5a2-primary-antibodies-ihc-testing-1.jpgAnti-SLC5A2/Sglt2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03748-slc5a2-primary-antibodies-wb-testing-3.jpgAnti-SLC5A2/Sglt2 AntibodyWestern blot analysis of the lysates from Jurkat cells using SLC5A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03748-slc5a2-primary-antibodies-wb-testing-2.jpgAnti-SLC5A2/Sglt2 AntibodyWestern blot analysis of lysates from 293 cells, using SLC5A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-atp1a2-antibody-a02064-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-atp1a2-primary-antibodies-ihc-testing-1.jpgAnti-ATP1A2 AntibodyImmunohistochemical analysis of paraffin-embedded human meningioma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-atp1a2-primary-antibodies-wb-testing-2.jpgAnti-ATP1A2 AntibodyWestern blot analysis of lysates from COS7 cells, HepG2 cells, and Jurkat cells, using ATP1A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sptbn1-antibody-a03164-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03164-sptbn1-primary-antibodies-ihc-testing-1.jpgAnti-SPTBN1 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03164-sptbn1-primary-antibodies-wb-testing-3.jpgAnti-SPTBN1 AntibodyWestern blot analysis of the lysates from Jurkat cells using SPTBN1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03164-sptbn1-primary-antibodies-wb-testing-2.jpgAnti-SPTBN1 AntibodyWestern blot analysis of lysates from COLO cells, using SPTBN1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs11-antibody-a30765-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30765-srsf11-primary-antibodies-ihc-testing-1.jpgAnti-SFRS11 SRSF11 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30765-srsf11-primary-antibodies-wb-testing-2.jpgAnti-SFRS11 SRSF11 AntibodyWestern blot analysis of lysates from LOVO and RAW264.7 cells, using SFRS11 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs15-antibody-a30766-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30766-scaf4-primary-antibodies-ihc-testing-1.jpgAnti-SFRS15 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30766-scaf4-primary-antibodies-wb-testing-2.jpgAnti-SFRS15 AntibodyWestern Blot analysis of COLO cells using SFRS15 Polyclonal Antibody diluted at 1:2000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30766-scaf4-primary-antibodies-wb-testing-3.jpgAnti-SFRS15 AntibodyWestern blot analysis of lysates from COLO cells, using SFRS15 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sfrs7-antibody-a30768-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30768-srsf7-primary-antibodies-ihc-testing-1.jpgAnti-SFRS7 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4° overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30768-srsf7-primary-antibodies-wb-testing-2.jpgAnti-SFRS7 AntibodyWestern Blot analysis of HuvEc cells using 9G8 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30768-srsf7-primary-antibodies-wb-testing-3.jpgAnti-SFRS7 AntibodyWestern Blot analysis of various cells using 9G8 Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30768-srsf7-primary-antibodies-wb-testing-5.jpgAnti-SFRS7 AntibodyWestern blot analysis of the lysates from HT-29 cells using SFRS7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30768-srsf7-primary-antibodies-wb-testing-4.jpgAnti-SFRS7 AntibodyWestern blot analysis of lysates from HT-29 cells, using SFRS7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-stmn4-antibody-a13020-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13020-stmn4-primary-antibodies-ihc-testing-1.jpgAnti-STMN4/Rb3 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13020-stmn4-primary-antibodies-wb-testing-2.jpgAnti-STMN4/Rb3 AntibodyWestern blot analysis of lysates from K562 cells, using STMN4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf280c-antibody-a14715-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14715-znf280c-primary-antibodies-ihc-testing-1.jpgAnti-ZNF280C/Suhw3 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14715-znf280c-primary-antibodies-wb-testing-3.jpgAnti-ZNF280C/Suhw3 AntibodyWestern blot analysis of the lysates from HeLa cells using ZNF280C antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14715-znf280c-primary-antibodies-wb-testing-2.jpgAnti-ZNF280C/Suhw3 AntibodyWestern blot analysis of lysates from HepG2 cells, using ZNF280C Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-svop-antibody-a15475-1-boster.html2026-03-24T05:10:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15475-1-svop-primary-antibodies-ihc-testing-1.jpgAnti-SVOP AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15475-1-svop-primary-antibodies-wb-testing-3.jpgAnti-SVOP AntibodyWestern blot analysis of the lysates from Jurkat cells using SVOP antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15475-1-svop-primary-antibodies-wb-testing-2.jpgAnti-SVOP AntibodyWestern blot analysis of lysates from K562 cells, using SVOP Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sytl4-antibody-a07875-1-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07875-1-sytl4-primary-antibodies-wb-testing-1.jpgAnti-SYTL4/Granuphilin AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using SYTL4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tagap-antibody-a09403-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09403-tagap-primary-antibodies-ihc-testing-1.jpgAnti-TAGAP AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma, using TAGAP Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-trappc1-antibody-a14697-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14697-trappc1-primary-antibodies-ihc-testing-1.jpgAnti-TRAPPC1/Bet5 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using TRAPPC1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-trappc6a-antibody-a13195-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13195-trappc6a-primary-antibodies-ihc-testing-1.jpgAnti-TRAPPC6A AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma, using TRAPPC6A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-btf3l4-antibody-a15784-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15784-btf3l4-primary-antibodies-ihc-testing-1.jpgAnti-BTF3L4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using BTF3L4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mterf-antibody-a30769-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30769-mterf1-primary-antibodies-wb-testing-3.jpgAnti-MTERF AntibodyWestern blot analysis of the lysates from HUVECcells using MTERF antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30769-mterf1-primary-antibodies-ihc-testing-1.jpgAnti-MTERF AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using MTERF Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30769-mterf1-primary-antibodies-wb-testing-2.jpgAnti-MTERF AntibodyWestern blot analysis of lysates from Jurkat cells, using MTERF Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tbl2-antibody-a07879-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07879-tbl2-primary-antibodies-ihc-testing-1.jpgAnti-Transducin beta-like protein 2 TBL2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07879-tbl2-primary-antibodies-wb-testing-2.jpgAnti-Transducin beta-like protein 2 TBL2 AntibodyWestern blot analysis of lysates from MCF-7 cells, using TBL2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tmbim4-antibody-a09304-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09304-tmbim4-primary-antibodies-ihc-testing-1.jpgAnti-TMBIM4/Gaap AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09304-tmbim4-primary-antibodies-wb-testing-2.jpgAnti-TMBIM4/Gaap AntibodyWestern blot analysis of lysates from HepG2 cells, using TMBIM4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ubqln3-antibody-a15748-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15748-ubqln3-primary-antibodies-wb-testing-2.jpgAnti-Ubiquilin-3 UBQLN3 AntibodyWestern blot analysis of the lysates from Jurkat cells using UBQLN3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15748-ubqln3-primary-antibodies-ihc-testing-1.jpgAnti-Ubiquilin-3 UBQLN3 AntibodyImmunohistochemistry analysis of paraffin-embedded human testis tissue, using UBQLN3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ubqln4-antibody-a08887-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08887-ubqln4-primary-antibodies-ihc-testing-1.jpgAnti-UBQLN4/A1Up AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using UBQLN4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08887-ubqln4-primary-antibodies-wb-testing-2.jpgAnti-UBQLN4/A1Up AntibodyWestern blot analysis of lysates from mouse brain, using UBQLN4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-usp24-antibody-a08241-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08241-usp24-primary-antibodies-ihc-testing-1.jpgAnti-USP24 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using USP24 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-usp32-antibody-a10571-1-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10571-1-usp32-primary-antibodies-ihc-testing-1.jpgAnti-USP32 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using USP32 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-usp48-antibody-a09214-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09214-usp48-primary-antibodies-ihc-testing-1.jpgAnti-USP48 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using USP48 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ubtd1-antibody-a16697-1-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16697-1-ubtd1-primary-antibodies-ihc-testing-1.jpgAnti-UBTD1 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using UBTD1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ube3b-antibody-a10679-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10679-ube3b-primary-antibodies-ihc-testing-1.jpgAnti-Ubiquitin-protein ligase E3B UBE3B AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10679-ube3b-primary-antibodies-wb-testing-2.jpgAnti-Ubiquitin-protein ligase E3B UBE3B AntibodyWestern blot analysis of lysates from Jurkat cells, using UBE3B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-thoc5-antibody-a04619-1-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04619-1-thoc5-primary-antibodies-ihc-testing-1.jpgAnti-THOC5/Fmip AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using THOC5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-golt1a-antibody-a15330-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15330-golt1a-primary-antibodies-ihc-testing-1.jpgAnti-GOLT1A AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using GOLT1A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sft2b-antibody-a30770-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30770-sft2d2-primary-antibodies-ihc-testing-1.jpgAnti-SFT2B SFT2D2 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30770-sft2d2-primary-antibodies-wb-testing-2.jpgAnti-SFT2B SFT2D2 AntibodyWestern blot analysis of lysates from LOVO cells, using SFT2B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-wee2-antibody-a10843-boster.html2026-03-24T05:10:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10843-wee2-primary-antibodies-wb-testing-2.jpgAnti-Wee1-like protein kinase 2 WEE2 AntibodyWestern blot analysis of the lysates from K562 cells using WEE2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10843-wee2-primary-antibodies-wb-testing-1.jpgAnti-Wee1-like protein kinase 2 WEE2 AntibodyWestern blot analysis of lysates from HUVEC cells, using WEE2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-wasf4-antibody-a30771-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30771-wasf4-primary-antibodies-ihc-testing-1.jpgAnti-WASF4 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain, using WASF4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-zmym4-antibody-a11190-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11190-zmym4-primary-antibodies-wb-testing-2.jpgAnti-ZMYM4/Znf262 AntibodyWestern Blot analysis of HEK293 lysis, using primary antibody at 1:1000 dilution. Secondary antibody was diluted at 1:10000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11190-zmym4-primary-antibodies-ihc-testing-1.jpgAnti-ZMYM4/Znf262 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ZMYM4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf295-antibody-a30772-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30772-zbtb21-primary-antibodies-ihc-testing-1.jpgAnti-ZNF295 ZBTB21 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using ZNF295 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-znf592-antibody-a12580-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12580-znf592-primary-antibodies-ihc-testing-1.jpgAnti-Zinc finger protein 592 ZNF592 AntibodyImmunohistochemistry analysis of paraffin-embedded human colon carcinoma tissue, using ZNF592 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12580-znf592-primary-antibodies-wb-testing-2.jpgAnti-Zinc finger protein 592 ZNF592 AntibodyWestern blot analysis of lysates from K562 cells, using ZNF592 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc39a2-antibody-a09140-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09140-slc39a2-primary-antibodies-wb-testing-1.jpgAnti-SLC39A2/Zip2 AntibodyWestern blot analysis of lysates from Jurkat cells, using SLC39A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-slc38a2-antibody-a03242-1-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03242-1-slc38a2-primary-antibodies-ihc-testing-1.jpgAnti-SLC38A2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03242-1-slc38a2-primary-antibodies-wb-testing-3.jpgAnti-SLC38A2 AntibodyWestern blot analysis of the lysates from HeLa cells using SLC38A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03242-1-slc38a2-primary-antibodies-wb-testing-2.jpgAnti-SLC38A2 AntibodyWestern blot analysis of lysates from HeLa cells, using SLC38A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mox2r-antibody-a30776-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30776-cd200r1-primary-antibodies-wb-testing-1.jpgAnti-MOX2R CD200R1 AntibodyWestern Blot analysis of HepG2 cells using OX2R Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30776-cd200r1-primary-antibodies-wb-testing-2.jpgAnti-MOX2R CD200R1 AntibodyWestern Blot analysis of K562 cells using OX2R Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30776-cd200r1-primary-antibodies-wb-testing-3.jpgAnti-MOX2R CD200R1 AntibodyWestern blot analysis of lysates from K562 cells, using MOX2R Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-noxin-antibody-a30777-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30777-ddias-primary-antibodies-wb-testing-1.jpgAnti-NOXIN DDIAS AntibodyWestern Blot analysis of 823, 293T, AD293, Hela, HepG2 cells using NOXIN Polyclonal Antibody. Antibody was diluted at 1:2000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-pvrl1-antibody-a30778-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30778-nectin1-primary-antibodies-wb-testing-1.jpgAnti-PVRL1 AntibodyWestern Blot analysis of KB cells using Nectin 1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30778-nectin1-primary-antibodies-wb-testing-2.jpgAnti-PVRL1 AntibodyWestern Blot analysis of KB cells using Nectin 1 Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-pvrl3-antibody-a30746-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30746-nectin3-primary-antibodies-wb-testing-1.jpgAnti-PVRL3 NECTIN3 AntibodyWestern Blot analysis of HeLa cells using Nectin 3 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30746-nectin3-primary-antibodies-wb-testing-2.jpgAnti-PVRL3 NECTIN3 AntibodyWestern blot analysis of lysate from HeLa cells, using PVRL3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ptprj-antibody-a02319-1-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02319-1-ptprj-primary-antibodies-wb-testing-2.jpgAnti-PTPRJ/Dep1 AntibodyWestern Blot analysis of HeLa, 293 cells using CD148 Polyclonal Antibody. Secondary antibody was diluted at 1:20000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02319-1-ptprj-primary-antibodies-ihc-testing-1.jpgAnti-PTPRJ/Dep1 AntibodyImmunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02319-1-ptprj-primary-antibodies-wb-testing-3.jpgAnti-PTPRJ/Dep1 AntibodyWestern blot analysis of lysate from 293, HeLa cells, using PTPRJ Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-il29-antibody-a30780-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30780-ifnl1-primary-antibodies-wb-testing-1.jpgAnti-IL29 AntibodyWestern Blot analysis of L929 cells using IL-29 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30780-ifnl1-primary-antibodies-wb-testing-2.jpgAnti-IL29 AntibodyWestern blot analysis of lysate from L929 cells, using IL29 Antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-il28a-antibody-a30781-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30781-ifnl2-primary-antibodies-wb-testing-3.jpgAnti-IL28A AntibodyWestern Blot analysis of MCF7 cells using IL-28 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30781-ifnl2-primary-antibodies-ihc-testing-1.jpgAnti-IL28A AntibodyImmunohistochemical analysis of paraffin-embedded human-spleen, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30781-ifnl2-primary-antibodies-ihc-testing-2.jpgAnti-IL28A AntibodyImmunohistochemical analysis of paraffin-embedded human-tonsil, antibody was diluted at 1:100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30781-ifnl2-primary-antibodies-wb-testing-4.jpgAnti-IL28A AntibodyWestern blot analysis of lysate from MCF7 cells, using IL28A Antibody.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-acetylated-histone-h1-lys25-antibody-p12111-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12111-h1foo-primary-antibodies-ihc-testing-1.jpgAnti-Acetylated Histone H1 (Lys25) H1FOO AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Histone H1 (Acetyl-Lys25) Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12111-h1foo-primary-antibodies-wb-testing-2.jpgAnti-Acetylated Histone H1 (Lys25) H1FOO AntibodyWestern blot analysis of lysates from COS7 cells, treated with TSA 400nM 24h, using Histone H1 (Acetyl-Lys25) Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-acetylated-eif5a-lys47-antibody-p01727-boster.html2026-03-24T05:10:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01727-eif5a-primary-antibodies-if-testing-1.jpgAnti-Acetylated eIF5A (Lys47) AntibodyImmunofluorescence analysis of MCF7 cell. 1,primary Antibody was diluted at 1:100(4°C overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500(room temperature, 50min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01727-eif5a-primary-antibodies-wb-testing-2.jpgAnti-Acetylated eIF5A (Lys47) AntibodyWestern blot analysis of L929 lysis using antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01727-eif5a-primary-antibodies-wb-testing-3.jpgAnti-Acetylated eIF5A (Lys47) AntibodyWestern blot analysis of lysate from L929 cells, using eIF5A (Acetyl-Lys47) Antibody.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-acetylated-h2b-lys126-antibody-p16595-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p16595-hist1h2ba-primary-antibodies-wb-testing-1.jpgAnti-Acetylated H2B (Lys126) HIST1H2BA AntibodyWestern Blot analysis of A549 cells using Acetyl-Histone H2B (K126) Polyclonal Antibody. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-htr5b-antibody-a30783-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30783-htr5b-primary-antibodies-wb-testing-2.jpgAnti-HTR5B AntibodyWestern Blot analysis of COLO cells using SR-5B Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30783-htr5b-primary-antibodies-wb-testing-4.jpgAnti-HTR5B AntibodyWestern blot analysis of the lysates from HepG2 cells using HTR5B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30783-htr5b-primary-antibodies-if-testing-1.jpgAnti-HTR5B AntibodyImmunofluorescence analysis of HUVEC cells, using HTR5B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30783-htr5b-primary-antibodies-wb-testing-3.jpgAnti-HTR5B AntibodyWestern blot analysis of lysates from COLO cells, using HTR5B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-c3ar1-antibody-a06350-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06350-c3ar1-primary-antibodies-if-testing-1.jpgAnti-C3AR1/C3Ar AntibodyImmunofluorescence analysis of COS7 cells, using C3AR1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06350-c3ar1-primary-antibodies-ihc-testing-2.jpgAnti-C3AR1/C3Ar AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using C3AR1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-celsr3-antibody-a07204-1-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07204-1-celsr3-primary-antibodies-if-testing-1.jpgAnti-CELSR3/Flamingo Homolog 1 AntibodyImmunofluorescence analysis of A549 cells, using CELSR3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-cxcr7-antibody-a30784-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30784-ackr3-primary-antibodies-wb-testing-2.jpgAnti-CXCR7 ACKR3 AntibodyWestern Blot analysis of various cells using CXCR-7 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30784-ackr3-primary-antibodies-if-testing-1.jpgAnti-CXCR7 ACKR3 AntibodyImmunofluorescence analysis of COS7 cells, using CXCR7 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30784-ackr3-primary-antibodies-wb-testing-3.jpgAnti-CXCR7 ACKR3 AntibodyWestern blot analysis of the lysates from RAW264.7cells using CXCR7 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ccbp2-antibody-a30785-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30785-ackr2-primary-antibodies-ihc-testing-2.jpgAnti-CCBP2 ACKR2 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30785-ackr2-primary-antibodies-wb-testing-3.jpgAnti-CCBP2 ACKR2 AntibodyWestern Blot analysis of various cells using Chemokine Receptor D6 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30785-ackr2-primary-antibodies-if-testing-1.jpgAnti-CCBP2 ACKR2 AntibodyImmunofluorescence analysis of COS7 cells, using CCBP2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30785-ackr2-primary-antibodies-wb-testing-4.jpgAnti-CCBP2 ACKR2 AntibodyWestern blot analysis of lysates from HepG2 cells, using CCBP2 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30785-ackr2-primary-antibodies-wb-testing-5.jpgAnti-CCBP2 ACKR2 AntibodyWestern blot analysis of the lysates from HT-29 cells using CCBP2 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-cd234-antibody-a30786-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30786-ackr1-primary-antibodies-if-testing-1.jpgAnti-CD234 ACKR1 AntibodyImmunofluorescence analysis of A549 cells, using CD234 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-edg7-antibody-a06597-1-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/L/P/LPAR3-primary-antibodies-A06597-1-WB-testing.jpgAnti-EDG7 LPAR3 AntibodyWestern blot analysis of lysates from Jurkat cells, using EDG7 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/L/P/LPAR3-primary-antibodies-A06597-1-IF-testing.jpgAnti-EDG7 LPAR3 AntibodyImmunofluorescence analysis of LOVO cells, using EDG7 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-emr1-antibody-a30787-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30787-adgre1-primary-antibodies-wb-testing-1.jpgAnti-EMR1 AntibodyWestern Blot analysis of Jurkat cells using EMR1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30787-adgre1-primary-antibodies-wb-testing-2.jpgAnti-EMR1 AntibodyWestern blot analysis of lysates from Jurkat cells, using EMR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30787-adgre1-primary-antibodies-wb-testing-3.jpgAnti-EMR1 AntibodyWestern blot analysis of the lysates from HUVECcells using EMR1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-emr3-antibody-a30788-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30788-adgre3-primary-antibodies-wb-testing-1.jpgAnti-EMR3 ADGRE3 AntibodyWestern blot analysis of lysates from Jurkat cells, using EMR3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-eltd1-antibody-a30789-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30789-adgrl4-primary-antibodies-if-testing-1.jpgAnti-ELTD1 AntibodyImmunofluorescence analysis of LOVO cells, using ELTD1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-fpr1-antibody-a02509-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02509-fpr1-primary-antibodies-ihc-testing-2.jpgAnti-FPR1/Fpr AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02509-fpr1-primary-antibodies-if-testing-1.jpgAnti-FPR1/Fpr AntibodyImmunofluorescence analysis of MCF7 cells, using FPR1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02509-fpr1-primary-antibodies-wb-testing-3.jpgAnti-FPR1/Fpr AntibodyWestern blot analysis of lysates from K562 cells, using FPR1 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02509-fpr1-primary-antibodies-wb-testing-4.jpgAnti-FPR1/Fpr AntibodyWestern blot analysis of the lysates from COLO205 cells using FPR1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr109-antibody-a30790-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30790-hcar3-primary-antibodies-if-testing-1.jpgAnti-GPR109 HCAR3 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR109 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30790-hcar3-primary-antibodies-wb-testing-2.jpgAnti-GPR109 HCAR3 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using GPR109 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30790-hcar3-primary-antibodies-wb-testing-3.jpgAnti-GPR109 HCAR3 AntibodyWestern blot analysis of the lysates from HepG2 cells using GPR109 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr110-antibody-a30791-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30791-adgrf1-primary-antibodies-wb-testing-2.jpgAnti-GPR110 AntibodyWestern Blot analysis of 3T3 cells using GPR110 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30791-adgrf1-primary-antibodies-wb-testing-3.jpgAnti-GPR110 AntibodyWestern Blot analysis of various cells using GPR110 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30791-adgrf1-primary-antibodies-if-testing-1.jpgAnti-GPR110 AntibodyImmunofluorescence analysis of A549 cells, using GPR110 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30791-adgrf1-primary-antibodies-wb-testing-4.jpgAnti-GPR110 AntibodyWestern blot analysis of lysates from Jurkat, HUVEC, and COLO cells, using GPR110 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr115-antibody-a30792-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30792-adgrf4-primary-antibodies-wb-testing-2.jpgAnti-GPR115 ADGRF4 AntibodyWestern Blot analysis of RAW264.7 cells using GPR115 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30792-adgrf4-primary-antibodies-if-testing-1.jpgAnti-GPR115 ADGRF4 AntibodyImmunofluorescence analysis of LOVO cells, using GPR115 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30792-adgrf4-primary-antibodies-wb-testing-3.jpgAnti-GPR115 ADGRF4 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using GPR115 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr116-antibody-a30793-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR116-primary-antibodies-A30793-IHC-testing.jpgAnti-GPR116 ADGRF5 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using GPR116 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR116-primary-antibodies-A30793-IF-testing.jpgAnti-GPR116 ADGRF5 AntibodyImmunofluorescence analysis of A549 cells, using GPR116 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr120-antibody-a19859-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19859-ffar4-primary-antibodies-wb-testing-3.jpgAnti-GPR120 FFAR4 AntibodyWestern blot analysis of lysates from 1) HEPG2-UV,2) HEK-293T, 3) LOVO cells, (Green) primary antibody was diluted at 1:1000, 4°over night, secondary antibody(cat:SA33333)was diluted at 1:10000, 37° 1hour. (Red) Tubulin β Monoclonal Antibody(5G3) (cat:N1294) antibody was diluted at 1:5000 as loading control, 4° over night,secondary antibody(cat:SA0436)was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19859-ffar4-primary-antibodies-wb-testing-2.jpgAnti-GPR120 FFAR4 AntibodyWestern Blot analysis of HEPG2-UV cells using GPR120 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19859-ffar4-primary-antibodies-wb-testing-4.jpgAnti-GPR120 FFAR4 AntibodyWestern Blot analysis of various cells using GPR120 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19859-ffar4-primary-antibodies-if-testing-1.jpgAnti-GPR120 FFAR4 AntibodyImmunofluorescence analysis of LOVO cells, using GPR120 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19859-ffar4-primary-antibodies-wb-testing-5.jpgAnti-GPR120 FFAR4 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR120 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr150-antibody-a17320-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17320-gpr150-primary-antibodies-if-testing-1.jpgAnti-GPR150 AntibodyImmunofluorescence analysis of HepG2 cells, using GPR150 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17320-gpr150-primary-antibodies-wb-testing-2.jpgAnti-GPR150 AntibodyWestern blot analysis of lysates from HUVEC cells, using GPR150 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr160-antibody-a14818-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14818-gpr160-primary-antibodies-wb-testing-1.jpgAnti-GPR160/Gpcr150 AntibodyWestern blot analysis of lysates from COLO205 cells, using GPR160 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr171-antibody-a14498-1-boster.html2026-03-24T05:10:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR171-primary-antibodies-A14498-1-WB-testing.jpgAnti-GPR171 AntibodyWestern blot analysis of lysates from K562 cells, using GPR171 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR171-primary-antibodies-A14498-1-IF-testing.jpgAnti-GPR171 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR171 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr174-antibody-a13035-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR174-primary-antibodies-A13035-WB-testing.jpgAnti-GPR174 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR174 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GPR174-primary-antibodies-A13035-IF-testing.jpgAnti-GPR174 AntibodyImmunofluorescence analysis of HeLa cells, using GPR174 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-bai2-antibody-a30794-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30794-adgrb2-primary-antibodies-if-testing-1.jpgAnti-BAI2 ADGRB2 AntibodyImmunofluorescence analysis of HUVEC cells, using BAI2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30794-adgrb2-primary-antibodies-ihc-testing-2.jpgAnti-BAI2 ADGRB2 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using BAI2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-bai3-antibody-a30795-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30795-adgrb3-primary-antibodies-if-testing-1.jpgAnti-BAI3 AntibodyImmunofluorescence analysis of HUVEC cells, using BAI3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30795-adgrb3-primary-antibodies-ihc-testing-2.jpgAnti-BAI3 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using BAI3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-csrl1-antibody-a30796-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30796-csrl1-primary-antibodies-if-testing-1.jpgAnti-CSRL1 AntibodyImmunofluorescence analysis of A549 cells, using CSRL1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30796-csrl1-primary-antibodies-wb-testing-2.jpgAnti-CSRL1 AntibodyWestern blot analysis of lysates from K562 cells and A549 cells, using CSRL1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-emr4-antibody-a30797-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30797-adgre4p-primary-antibodies-wb-testing-3.jpgAnti-EMR4 ADGRE4P AntibodyWestern blot analysis of lysates from HUVEC cells, COS7 cells, HeLa cells, and COLO205 cells, using EMR4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-etbr2-antibody-a11679-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11679-gpr37l1-primary-antibodies-if-testing-1.jpgAnti-ETBR2 GPR37L1 AntibodyImmunofluorescence analysis of LOVO cells, using ETBR2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11679-gpr37l1-primary-antibodies-wb-testing-3.jpgAnti-ETBR2 GPR37L1 AntibodyWestern blot analysis of lysates from HepG2 cells, using ETBR2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ffar3-antibody-a02437-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02437-ffar3-primary-antibodies-wb-testing-2.jpgAnti-FFAR3/Gpr41 AntibodyWestern blot analysis of lysates from U2OS cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02437-ffar3-primary-antibodies-if-testing-1.jpgAnti-FFAR3/Gpr41 AntibodyImmunofluorescence analysis of LOVO cells, using FFAR3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-kcnj5-antibody-a02160-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02160-kcnj5-primary-antibodies-ihc-testing-2.jpgAnti-KCNJ5/Kir3.4 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02160-kcnj5-primary-antibodies-if-testing-1.jpgAnti-KCNJ5/Kir3.4 AntibodyImmunofluorescence analysis of A549 cells, using KCNJ5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02160-kcnj5-primary-antibodies-wb-testing-3.jpgAnti-KCNJ5/Kir3.4 AntibodyWestern blot analysis of lysates from HeLa cells, using KCNJ5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr113-antibody-a30798-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30798-adgrf3-primary-antibodies-wb-testing-1.jpgAnti-GPR113 ADGRF3 AntibodyWestern Blot analysis of Hela cells using GPR113 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30798-adgrf3-primary-antibodies-wb-testing-2.jpgAnti-GPR113 ADGRF3 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR113 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr114-antibody-a30799-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30799-adgrg5-primary-antibodies-wb-testing-1.jpgAnti-GPR114 AntibodyWestern Blot analysis of COLO205 cells using GPR114 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30799-adgrg5-primary-antibodies-wb-testing-2.jpgAnti-GPR114 AntibodyWestern blot analysis of lysates from COLO205 cells, using GPR114 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30799-adgrg5-primary-antibodies-wb-testing-3.jpgAnti-GPR114 AntibodyWestern blot analysis of the lysates from 293 cells using GPR114 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr116-antibody-a30800-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30800-adgrf5-primary-antibodies-ihc-testing-2.jpgAnti-GPR116 ADGRF5 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30800-adgrf5-primary-antibodies-wb-testing-3.jpgAnti-GPR116 ADGRF5 AntibodyWestern Blot analysis of various cells using GPR116 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30800-adgrf5-primary-antibodies-if-testing-1.jpgAnti-GPR116 ADGRF5 AntibodyImmunofluorescence analysis of HeLa cells, using GPR116 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30800-adgrf5-primary-antibodies-wb-testing-4.jpgAnti-GPR116 ADGRF5 AntibodyWestern blot analysis of lysates from A549 cells, using GPR116 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30800-adgrf5-primary-antibodies-wb-testing-5.jpgAnti-GPR116 ADGRF5 AntibodyWestern blot analysis of the lysates from HeLa cells using GPR116 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr123-antibody-a30801-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30801-adgra1-primary-antibodies-if-testing-1.jpgAnti-GPR123 ADGRA1 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR123 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr124-antibody-a30802-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30802-adgra2-primary-antibodies-if-testing-1.jpgAnti-GPR124 ADGRA2 AntibodyImmunofluorescence analysis of HeLa cells, using GPR124 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr126-antibody-a30803-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30803-adgrg6-primary-antibodies-ihc-testing-1.jpgAnti-GPR126 ADGRG6 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30803-adgrg6-primary-antibodies-wb-testing-2.jpgAnti-GPR126 ADGRG6 AntibodyWestern Blot analysis of various cells using GPR126 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30803-adgrg6-primary-antibodies-wb-testing-3.jpgAnti-GPR126 ADGRG6 AntibodyWestern blot analysis of lysates from HUVEC cells, using GPR126 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr132-antibody-a30804-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30804-gpr132-primary-antibodies-ihc-testing-1.jpgAnti-GPR132/G2A AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30804-gpr132-primary-antibodies-wb-testing-2.jpgAnti-GPR132/G2A AntibodyWestern blot analysis of lysates from Jurkat cells, using GPR132 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30804-gpr132-primary-antibodies-wb-testing-3.jpgAnti-GPR132/G2A AntibodyWestern blot analysis of the lysates from HT-29 cells using GPR132 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr133-antibody-a30805-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30805-adgrd1-primary-antibodies-if-testing-1.jpgAnti-GPR133 AntibodyImmunofluorescence analysis of HeLa cells, using GPR133 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30805-adgrd1-primary-antibodies-wb-testing-2.jpgAnti-GPR133 AntibodyWestern blot analysis of lysates from COS7 cells, using GPR133 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30805-adgrd1-primary-antibodies-wb-testing-3.jpgAnti-GPR133 AntibodyWestern blot analysis of the lysates from K562 cells using GPR133 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr135-antibody-a30806-boster.html2026-03-24T05:10:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30806-gpr135-primary-antibodies-ihc-testing-1.jpgAnti-GPR135 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30806-gpr135-primary-antibodies-wb-testing-2.jpgAnti-GPR135 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using GPR135 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr139-antibody-a30807-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30807-gpr139-primary-antibodies-wb-testing-2.jpgAnti-GPR139 AntibodyWestern Blot analysis of K562 cells using GPR139 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30807-gpr139-primary-antibodies-if-testing-1.jpgAnti-GPR139 AntibodyImmunofluorescence analysis of LOVO cells, using GPR139 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr142-antibody-a30808-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30808-gpr142-primary-antibodies-if-testing-1.jpgAnti-GPR142 AntibodyImmunofluorescence analysis of A549 cells, using GPR142 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30808-gpr142-primary-antibodies-wb-testing-2.jpgAnti-GPR142 AntibodyWestern blot analysis of lysates from Jurkat cells, using GPR142 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30808-gpr142-primary-antibodies-wb-testing-3.jpgAnti-GPR142 AntibodyWestern blot analysis of the lysates from HeLa cells using GPR142 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr143-antibody-a30809-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30809-gpr143-primary-antibodies-if-testing-1.jpgAnti-GPR143/Oa1 AntibodyImmunofluorescence analysis of LOVO cells, using GPR143 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr144-antibody-a30810-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30810-adgrd2-primary-antibodies-wb-testing-1.jpgAnti-GPR144 AntibodyWestern blot analysis of lysates from K562 cells, using GPR144 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr146-antibody-a30811-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30811-gpr146-primary-antibodies-wb-testing-1.jpgAnti-GPR146 AntibodyWestern Blot analysis of LOVO cells using GPR146 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30811-gpr146-primary-antibodies-wb-testing-2.jpgAnti-GPR146 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR146 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr149-antibody-a30812-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30812-gpr149-primary-antibodies-if-testing-1.jpgAnti-GPR149 AntibodyImmunofluorescence analysis of HeLa cells, using GPR149 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30812-gpr149-primary-antibodies-wb-testing-2.jpgAnti-GPR149 AntibodyWestern blot analysis of lysates from HeLa and COLO205 cells, using GPR149 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30812-gpr149-primary-antibodies-wb-testing-3.jpgAnti-GPR149 AntibodyWestern blot analysis of the lysates from 293 cells using GPR149 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr151-antibody-a30814-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30814-gpr151-primary-antibodies-if-testing-1.jpgAnti-GPR151/Gpcr 2037 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR151 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30814-gpr151-primary-antibodies-wb-testing-2.jpgAnti-GPR151/Gpcr 2037 AntibodyWestern blot analysis of lysates from K562 cells, using GPR151 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30814-gpr151-primary-antibodies-wb-testing-3.jpgAnti-GPR151/Gpcr 2037 AntibodyWestern blot analysis of the lysates from HeLa cells using GPR151 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr153-antibody-a30816-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GP153-primary-antibodies-A30816-WB-testing.jpgAnti-GPR153 AntibodyWestern blot analysis of lysates from K562 cells, using GPR153 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GP153-primary-antibodies-A30816-IF-testing.jpgAnti-GPR153 AntibodyImmunofluorescence analysis of A549 cells, using GPR153 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr156-antibody-a30817-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30817-gpr156-primary-antibodies-wb-testing-2.jpgAnti-GPR156 AntibodyWestern Blot analysis of various cells using GPR156 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30817-gpr156-primary-antibodies-if-testing-1.jpgAnti-GPR156 AntibodyImmunofluorescence analysis of HeLa cells, using GPR156 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30817-gpr156-primary-antibodies-wb-testing-3.jpgAnti-GPR156 AntibodyWestern blot analysis of lysates from 293 cells, using GPR156 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr157-antibody-a30818-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30818-gpr157-primary-antibodies-if-testing-1.jpgAnti-G-protein coupled receptor 157 GPR157 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR157 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30818-gpr157-primary-antibodies-wb-testing-2.jpgAnti-G-protein coupled receptor 157 GPR157 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using GPR157 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30818-gpr157-primary-antibodies-wb-testing-3.jpgAnti-G-protein coupled receptor 157 GPR157 AntibodyWestern blot analysis of the lysates from RAW264.7cells using GPR157 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr158-antibody-a30819-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30819-gpr158-primary-antibodies-wb-testing-3.jpgAnti-GPR158 AntibodyWestern Blot analysis of COLO 293T HELA cells using GPR158 Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30819-gpr158-primary-antibodies-if-testing-1.jpgAnti-GPR158 AntibodyImmunofluorescence analysis of HUVEC cells, using GPR158 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30819-gpr158-primary-antibodies-ihc-testing-2.jpgAnti-GPR158 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR158 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30819-gpr158-primary-antibodies-wb-testing-4.jpgAnti-GPR158 AntibodyWestern blot analysis of lysates from K562 cells, using GPR158 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30819-gpr158-primary-antibodies-wb-testing-5.jpgAnti-GPR158 AntibodyWestern blot analysis of the lysates from HeLa cells using GPR158 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr180-antibody-a30824-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GP180-primary-antibodies-A30824-IHC-testing.jpgAnti-GPR180 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR180 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/G/P/GP180-primary-antibodies-A30824-IF-testing.jpgAnti-GPR180 AntibodyImmunofluorescence analysis of A549 cells, using GPR180 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpbar-antibody-a30825-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30825-gpbar1-primary-antibodies-ihc-testing-2.jpgAnti-GPBAR AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30825-gpbar1-primary-antibodies-if-testing-1.jpgAnti-GPBAR AntibodyImmunofluorescence analysis of LOVO cells, using GPBAR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gprc5b-antibody-a30826-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30826-gprc5b-primary-antibodies-if-testing-1.jpgAnti-GPRC5B AntibodyImmunofluorescence analysis of MCF7 cells, using GPRC5B Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30826-gprc5b-primary-antibodies-wb-testing-2.jpgAnti-GPRC5B AntibodyWestern blot analysis of lysates from Jurkat, HUVEC, and 293 cells, using GPRC5B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gprc5c-antibody-a30827-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30827-gprc5c-primary-antibodies-wb-testing-1.jpgAnti-GPRC5C AntibodyWestern blot analysis of lysates from RAW264.7 and COS7 cells, using GPRC5C Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gprc5d-antibody-a30828-boster.html2026-03-24T05:10:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30828-gprc5d-primary-antibodies-if-testing-1.jpgAnti-GPRC5D AntibodyImmunofluorescence analysis of MCF7 cells, using GPRC5D Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30828-gprc5d-primary-antibodies-wb-testing-2.jpgAnti-GPRC5D AntibodyWestern blot analysis of lysates from Jurkat cells, using GPRC5D Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30828-gprc5d-primary-antibodies-wb-testing-3.jpgAnti-GPRC5D AntibodyWestern blot analysis of the lysates from HUVECcells using GPRC5D antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gprc6a-antibody-a30829-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30829-gprc6a-primary-antibodies-wb-testing-2.jpgAnti-GPRC6A AntibodyWestern Blot analysis of Jurkat cells using GPRC6A Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30829-gprc6a-primary-antibodies-wb-testing-3.jpgAnti-GPRC6A AntibodyWestern Blot analysis of various cells using Antibody diluted at 1:1000. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30829-gprc6a-primary-antibodies-if-testing-1.jpgAnti-GPRC6A AntibodyImmunofluorescence analysis of MCF7 cells, using GPRC6A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30829-gprc6a-primary-antibodies-wb-testing-4.jpgAnti-GPRC6A AntibodyWestern blot analysis of lysates from Jurkat cells, using GPRC6A Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30829-gprc6a-primary-antibodies-wb-testing-5.jpgAnti-GPRC6A AntibodyWestern blot analysis of the lysates from HeLa cells using GPRC6A antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr1-antibody-a07199-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07199-gpr1-primary-antibodies-if-testing-1.jpgAnti-G-protein coupled receptor 1 GPR1 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr12-antibody-a10818-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10818-gpr12-primary-antibodies-wb-testing-2.jpgAnti-GPR12/Gpcr12 AntibodyWestern blot analysis of lysates from PC12 cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10818-gpr12-primary-antibodies-if-testing-1.jpgAnti-GPR12/Gpcr12 AntibodyImmunofluorescence analysis of A549 cells, using GPR12 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr20-antibody-a14205-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14205-gpr20-primary-antibodies-ihc-testing-2.jpgAnti-GPR20 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR20 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14205-gpr20-primary-antibodies-wb-testing-3.jpgAnti-GPR20 AntibodyWestern blot analysis of lysates from LOVO cells, using GPR20 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr22-antibody-a14444-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14444-gpr22-primary-antibodies-if-testing-1.jpgAnti-G-protein coupled receptor 22 GPR22 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR22 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr27-antibody-a15225-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15225-gpr27-primary-antibodies-if-testing-1.jpgAnti-GPR27/Sreb1 AntibodyImmunofluorescence analysis of A549 cells, using GPR27 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15225-gpr27-primary-antibodies-wb-testing-2.jpgAnti-GPR27/Sreb1 AntibodyWestern blot analysis of lysates from HUVEC cells, using GPR27 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15225-gpr27-primary-antibodies-wb-testing-3.jpgAnti-GPR27/Sreb1 AntibodyWestern blot analysis of the lysates from HeLa cells using GPR27 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr32-antibody-a13621-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13621-gpr32-primary-antibodies-if-testing-1.jpgAnti-GPR32 AntibodyImmunofluorescence analysis of A549 cells, using GPR32 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13621-gpr32-primary-antibodies-wb-testing-2.jpgAnti-GPR32 AntibodyWestern blot analysis of lysates from A549 cells, using GPR32 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr56-antibody-a30830-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30830-adgrg1-primary-antibodies-wb-testing-2.jpgAnti-GPR56 ADGRG1 AntibodyWestern Blot analysis of NIH-3T3 cells using GPR56 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30830-adgrg1-primary-antibodies-if-testing-1.jpgAnti-GPR56 ADGRG1 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR56 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30830-adgrg1-primary-antibodies-wb-testing-3.jpgAnti-GPR56 ADGRG1 AntibodyWestern blot analysis of lysates from K562 cells, using GPR56 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr63-antibody-a14960-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14960-gpr63-primary-antibodies-if-testing-1.jpgAnti-GPR63 AntibodyImmunofluorescence analysis of MCF7 cells, using GPR63 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr85-antibody-a10636-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10636-gpr85-primary-antibodies-if-testing-1.jpgAnti-GPR85 AntibodyImmunofluorescence analysis of LOVO cells, using GPR85 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10636-gpr85-primary-antibodies-ihc-testing-2.jpgAnti-GPR85 AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using GPR85 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr92-antibody-a30831-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30831-lpar5-primary-antibodies-wb-testing-1.jpgAnti-GPR92 AntibodyWestern Blot analysis of various cells using GPR92 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30831-lpar5-primary-antibodies-wb-testing-2.jpgAnti-GPR92 AntibodyWestern blot analysis of lysates from HT-29 and K562 cells, using GPR92 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lphn1-antibody-a30832-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30832-adgrl1-primary-antibodies-ihc-testing-2.jpgAnti-LPHN1 ADGRL1 AntibodyImmunohistochemical analysis of paraffin-embedded human meningioma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30832-adgrl1-primary-antibodies-if-testing-1.jpgAnti-LPHN1 ADGRL1 AntibodyImmunofluorescence analysis of LOVO cells, using LPHN1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lphn2-antibody-a30833-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30833-adgrl2-primary-antibodies-if-testing-1.jpgAnti-LPHN2 ADGRL2 AntibodyImmunofluorescence analysis of COS7 cells, using LPHN2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30833-adgrl2-primary-antibodies-ihc-testing-2.jpgAnti-LPHN2 ADGRL2 AntibodyImmunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using LPHN2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-lshr-antibody-a30834-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30834-lhcgr-primary-antibodies-ihc-testing-2.jpgAnti-LSHR AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30834-lhcgr-primary-antibodies-wb-testing-3.jpgAnti-LSHR AntibodyWestern Blot analysis of A549 cells using LHR Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30834-lhcgr-primary-antibodies-if-testing-1.jpgAnti-LSHR AntibodyImmunofluorescence analysis of A549 cells, using LSHR Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30834-lhcgr-primary-antibodies-wb-testing-4.jpgAnti-LSHR AntibodyWestern blot analysis of various lysate, antibody was diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-mchr2-antibody-a09361-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09361-mchr2-primary-antibodies-ihc-testing-1.jpgAnti-MCHR2 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09361-mchr2-primary-antibodies-wb-testing-3.jpgAnti-MCHR2 AntibodyWestern blot analysis of the lysates from HeLa cells using MCHR2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09361-mchr2-primary-antibodies-wb-testing-2.jpgAnti-MCHR2 AntibodyWestern blot analysis of lysates from HUVEC cells, using MCHR2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mpra-antibody-a30835-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30835-paqr7-primary-antibodies-ihc-testing-1.jpgAnti-MPRA AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30835-paqr7-primary-antibodies-wb-testing-2.jpgAnti-MPRA AntibodyWestern Blot analysis of 293 cells using mPRα Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30835-paqr7-primary-antibodies-wb-testing-3.jpgAnti-MPRA AntibodyWestern blot analysis of lysates from 293 and COLO cells, using MPRA Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mprg-antibody-a30836-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30836-paqr5-primary-antibodies-ihc-testing-1.jpgAnti-MPRG PAQR5 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30836-paqr5-primary-antibodies-wb-testing-2.jpgAnti-MPRG PAQR5 AntibodyWestern blot analysis of lysates from HUVEC cells, using MPRG Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgre-antibody-a30837-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30837-mrgpre-primary-antibodies-ihc-testing-1.jpgAnti-MRGRE MRGPRE AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30837-mrgpre-primary-antibodies-wb-testing-2.jpgAnti-MRGRE MRGPRE AntibodyWestern Blot analysis of various cells using MRGE Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30837-mrgpre-primary-antibodies-wb-testing-3.jpgAnti-MRGRE MRGPRE AntibodyWestern blot analysis of lysates from HeLa cells, using MRGRE Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgrf-antibody-a30838-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30838-mrgprf-primary-antibodies-ihc-testing-1.jpgAnti-MRGRF MRGPRF AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30838-mrgprf-primary-antibodies-wb-testing-2.jpgAnti-MRGRF MRGPRF AntibodyWestern Blot analysis of various cells using MRGF Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30838-mrgprf-primary-antibodies-wb-testing-3.jpgAnti-MRGRF MRGPRF AntibodyWestern blot analysis of lysates from HUVEC cells, using MRGRF Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgrg-antibody-a30839-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30839-mrgprg-primary-antibodies-ihc-testing-2.jpgAnti-MRGRG MRGPRG AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30839-mrgprg-primary-antibodies-wb-testing-3.jpgAnti-MRGRG MRGPRG AntibodyWestern Blot analysis of various cells using MRGG Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30839-mrgprg-primary-antibodies-wb-testing-5.jpgAnti-MRGRG MRGPRG AntibodyWestern blot analysis of the lysates from HepG2 cells using MRGRG antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30839-mrgprg-primary-antibodies-if-testing-1.jpgAnti-MRGRG MRGPRG AntibodyImmunofluorescence analysis of A549 cells, using MRGRG Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30839-mrgprg-primary-antibodies-wb-testing-4.jpgAnti-MRGRG MRGPRG AntibodyWestern blot analysis of lysates from HUVEC cells, using MRGRG Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgx1-antibody-a30840-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30840-mrgprx1-primary-antibodies-ihc-testing-2.jpgAnti-MRGX1 MRGPRX1 AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30840-mrgprx1-primary-antibodies-if-testing-1.jpgAnti-MRGX1 MRGPRX1 AntibodyImmunofluorescence analysis of HepG2 cells, using MRGX1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30840-mrgprx1-primary-antibodies-wb-testing-3.jpgAnti-MRGX1 MRGPRX1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using MRGX1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mrgx4-antibody-a30841-boster.html2026-03-24T05:10:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30841-mrgprx4-primary-antibodies-ihc-testing-2.jpgAnti-MRGX4 MRGPRX4 AntibodyImmunohistochemical analysis of paraffin-embedded human cervical carcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30841-mrgprx4-primary-antibodies-wb-testing-3.jpgAnti-MRGX4 MRGPRX4 AntibodyWestern Blot analysis of HUVEC cells using MRGX4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30841-mrgprx4-primary-antibodies-wb-testing-5.jpgAnti-MRGX4 MRGPRX4 AntibodyWestern blot analysis of the lysates from HUVECcells using MRGX4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30841-mrgprx4-primary-antibodies-if-testing-1.jpgAnti-MRGX4 MRGPRX4 AntibodyImmunofluorescence analysis of A549 cells, using MRGX4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30841-mrgprx4-primary-antibodies-wb-testing-4.jpgAnti-MRGX4 MRGPRX4 AntibodyWestern blot analysis of lysates from HUVEC and COLO cells, using MRGX4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mshr-antibody-a30842-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30842-mc1r-primary-antibodies-ihc-testing-2.jpgAnti-MSHR MC1R AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30842-mc1r-primary-antibodies-wb-testing-3.jpgAnti-MSHR MC1R AntibodyWestern Blot analysis of COLO205 cells using MC1-R Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30842-mc1r-primary-antibodies-wb-testing-5.jpgAnti-MSHR MC1R AntibodyWestern blot analysis of the lysates from HepG2 cells using MSHR antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30842-mc1r-primary-antibodies-if-testing-1.jpgAnti-MSHR MC1R AntibodyImmunofluorescence analysis of LOVO cells, using MSHR Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30842-mc1r-primary-antibodies-wb-testing-4.jpgAnti-MSHR MC1R AntibodyWestern blot analysis of lysates from COLO205 cells, using MSHR Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mtr1a-antibody-a30843-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30843-mtnr1a-primary-antibodies-ihc-testing-2.jpgAnti-MTR1A AntibodyImmunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30843-mtnr1a-primary-antibodies-if-testing-1.jpgAnti-MTR1A AntibodyImmunofluorescence analysis of HepG2 cells, using MTR1A Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mtr1b-antibody-a30844-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30844-mtnr1b-primary-antibodies-ihc-testing-1.jpgAnti-MTR1B MTNR1B AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30844-mtnr1b-primary-antibodies-wb-testing-2.jpgAnti-MTR1B MTNR1B AntibodyWestern Blot analysis of HepG2 cells using MEL-1B-R Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30844-mtnr1b-primary-antibodies-wb-testing-3.jpgAnti-MTR1B MTNR1B AntibodyWestern Blot analysis of various cells using MEL-1B-R Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30844-mtnr1b-primary-antibodies-wb-testing-5.jpgAnti-MTR1B MTNR1B AntibodyWestern blot analysis of the lysates from HeLa cells using MTR1B antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30844-mtnr1b-primary-antibodies-wb-testing-4.jpgAnti-MTR1B MTNR1B AntibodyWestern blot analysis of lysates from 293, Jurkat, and HepG2 cells, using MTR1B Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-mtr1l-antibody-a30845-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30845-gpr50-primary-antibodies-wb-testing-2.jpgAnti-MTR1L AntibodyWestern Blot analysis of various cells using GPR50 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30845-gpr50-primary-antibodies-if-testing-1.jpgAnti-MTR1L AntibodyImmunofluorescence analysis of LOVO cells, using MTR1L Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nk2r-antibody-a30847-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30847-tacr2-primary-antibodies-wb-testing-1.jpgAnti-NK2R TACR2 AntibodyWestern blot analysis of lysates from NIH/3T3 and HT-29 cells, using NK2R Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-nk3r-antibody-a30848-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30848-tacr3-primary-antibodies-wb-testing-2.jpgAnti-NK3R AntibodyWestern Blot analysis of COLO205 cells using NK-3R Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30848-tacr3-primary-antibodies-wb-testing-3.jpgAnti-NK3R AntibodyWestern Blot analysis of various cells using NK-3R Polyclonal Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30848-tacr3-primary-antibodies-wb-testing-5.jpgAnti-NK3R AntibodyWestern blot analysis of the lysates from HepG2 cells using NK3R antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30848-tacr3-primary-antibodies-if-testing-1.jpgAnti-NK3R AntibodyImmunofluorescence analysis of A549 cells, using NK3R Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30848-tacr3-primary-antibodies-wb-testing-4.jpgAnti-NK3R AntibodyWestern blot analysis of lysates from COLO205 cells, using NK3R Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-ntr2-antibody-a30850-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30850-ntsr2-primary-antibodies-wb-testing-3.jpgAnti-NTR2 AntibodyWestern blot analysis of the lysates from HeLa cells using NTR2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30850-ntsr2-primary-antibodies-if-testing-1.jpgAnti-NTR2 AntibodyImmunofluorescence analysis of A549 cells, using NTR2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30850-ntsr2-primary-antibodies-wb-testing-2.jpgAnti-NTR2 AntibodyWestern blot analysis of lysates from Jurkat cells, using NTR2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10a4-antibody-a30851-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30851-or10a4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10A4 OR10A4 AntibodyWestern blot analysis of the lysates from HUVECcells using OR10A4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30851-or10a4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10A4 OR10A4 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10A4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30851-or10a4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10A4 OR10A4 AntibodyWestern blot analysis of lysates from COLO cells, using OR10A4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10ad1-antibody-a30852-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30852-or10ad1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10AD1 OR10AD1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10AD1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30852-or10ad1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 10AD1 OR10AD1 AntibodyWestern blot analysis of the lysates from 293 cells using OR10AD1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30852-or10ad1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10AD1 OR10AD1 AntibodyImmunofluorescence analysis of A549 cells, using OR10AD1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30852-or10ad1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10AD1 OR10AD1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR10AD1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10ag1-antibody-a30853-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30853-or10ag1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10AG1 OR10AG1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 10AG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30853-or10ag1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10AG1 OR10AG1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10AG1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30853-or10ag1-primary-antibodies-wb-testing-5.jpgAnti-Olfactory receptor 10AG1 OR10AG1 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR10AG1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30853-or10ag1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10AG1 OR10AG1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10AG1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30853-or10ag1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 10AG1 OR10AG1 AntibodyWestern blot analysis of lysates from HUVEC, MCF-7, and Jurkat cells, using OR10AG1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10c1-antibody-a30854-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30854-or10c1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10C1 OR10C1 AntibodyWestern blot analysis of the lysates from HeLa cells using OR10C1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30854-or10c1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10C1 OR10C1 AntibodyWestern blot analysis of lysates from LOVO cells, using OR10C1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10g2-antibody-a30855-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30855-or10g2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10G2 OR10G2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 10G2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30855-or10g2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 10G2 OR10G2 AntibodyWestern blot analysis of the lysates from HUVECcells using OR10G2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30855-or10g2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10G2 OR10G2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10G2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30855-or10g2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 10G2 OR10G2 AntibodyWestern blot analysis of lysates from HUVEC, HeLa, MCF-7, Jurkat, and COLO cells, using OR10G2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10g9-antibody-a30856-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30856-or10g9-primary-antibodies-if-testing-1.jpgAnti-OR10G9 AntibodyImmunofluorescence analysis of A549 cells, using OR10G9 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10j6-antibody-a30857-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30857-or10j6p-primary-antibodies-wb-testing-3.jpgAnti-OR10J6 OR10J6P AntibodyWestern blot analysis of the lysates from COLO205 cells using OR10J6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30857-or10j6p-primary-antibodies-if-testing-1.jpgAnti-OR10J6 OR10J6P AntibodyImmunofluorescence analysis of A549 cells, using OR10J6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30857-or10j6p-primary-antibodies-wb-testing-2.jpgAnti-OR10J6 OR10J6P AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using OR10J6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or11g2-antibody-a30858-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30858-or11g2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 11G2 OR11G2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 11G2 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30858-or11g2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 11G2 OR11G2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR11G2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30858-or11g2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 11G2 OR11G2 AntibodyImmunofluorescence analysis of A549 cells, using OR11G2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30858-or11g2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 11G2 OR11G2 AntibodyWestern blot analysis of lysates from HUVEC, Jurkat, and MCF-7 cells, using OR11G2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or11l1-antibody-a30859-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30859-or11l1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 11L1 OR11L1 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR11L1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30859-or11l1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 11L1 OR11L1 AntibodyImmunofluorescence analysis of A549 cells, using OR11L1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30859-or11l1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 11L1 OR11L1 AntibodyWestern blot analysis of lysates from LOVO cells, using OR11L1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13c3-antibody-a30860-boster.html2026-03-24T05:10:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30860-or13c3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 13C3 OR13C3 AntibodyWestern blot analysis of the lysates from HeLa cells using OR13C3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30860-or13c3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 13C3 OR13C3 AntibodyImmunofluorescence analysis of A549 cells, using OR13C3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30860-or13c3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 13C3 OR13C3 AntibodyWestern blot analysis of lysates from LOVO cells, using OR13C3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13c4-antibody-a30861-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30861-or13c4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 13C4 OR13C4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 13C4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30861-or13c4-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 13C4 OR13C4 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR13C4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30861-or13c4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 13C4 OR13C4 AntibodyImmunofluorescence analysis of LOVO cells, using OR13C4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30861-or13c4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 13C4 OR13C4 AntibodyWestern blot analysis of lysates from COS7 cells, using OR13C4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2a5-2a14-antibody-a30862-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30862-or2a14-primary-antibodies-wb-testing-2.jpgAnti-OR2A5/2A14 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR2A5/2A14 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30862-or2a14-primary-antibodies-wb-testing-1.jpgAnti-OR2A5/2A14 AntibodyWestern blot analysis of lysates from K562 cells, using OR2A5/2A14 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2a25-antibody-a30863-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30863-or2a25-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2A25 OR2A25 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2A25 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30863-or2a25-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 2A25 OR2A25 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR2A25 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30863-or2a25-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2A25 OR2A25 AntibodyImmunofluorescence analysis of A549 cells, using OR2A25 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30863-or2a25-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2A25 OR2A25 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR2A25 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2a42-antibody-a30864-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30864-or2a1-primary-antibodies-wb-testing-2.jpgAnti-OR2A42 OR2A1 AntibodyWestern Blot analysis of COLO cells using Olfactory receptor 2A42 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30864-or2a1-primary-antibodies-if-testing-1.jpgAnti-OR2A42 OR2A1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2A42 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2ag1-2ag2-antibody-a30865-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30865-or2ag2-primary-antibodies-wb-testing-2.jpgAnti-OR2AG1 OR2AG2 AntibodyWestern Blot analysis of 293 cells using Olfactory receptor 2AG1/2 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30865-or2ag2-primary-antibodies-wb-testing-4.jpgAnti-OR2AG1 OR2AG2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR2AG1/2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30865-or2ag2-primary-antibodies-if-testing-1.jpgAnti-OR2AG1 OR2AG2 AntibodyImmunofluorescence analysis of LOVO cells, using OR2AG1/2AG2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30865-or2ag2-primary-antibodies-wb-testing-3.jpgAnti-OR2AG1 OR2AG2 AntibodyWestern blot analysis of lysates from LOVO cells, using OR2AG1/2AG2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2aj1-antibody-a30866-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30866-or2aj1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2AJ1 OR2AJ1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 2AJ1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30866-or2aj1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2AJ1 OR2AJ1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR2AJ1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30866-or2aj1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2AJ1 OR2AJ1 AntibodyWestern blot analysis of lysates from Jurkat and HUVEC cells, using OR2AJ1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2ak2-antibody-a30867-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30867-or2ak2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2AK2 OR2AK2 AntibodyImmunofluorescence analysis of COS7 cells, using OR2AK2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2ap1-antibody-a30868-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30868-or2ap1-primary-antibodies-wb-testing-1.jpgAnti-OR2AP1 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 2AP1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30868-or2ap1-primary-antibodies-wb-testing-3.jpgAnti-OR2AP1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR2AP1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30868-or2ap1-primary-antibodies-wb-testing-2.jpgAnti-OR2AP1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR2AP1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2t10-antibody-a30869-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30869-or2t10-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2T10 OR2T10 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2T10 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2t11-antibody-a30870-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30870-or2t11-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2T11 OR2T11 AntibodyWestern Blot analysis of MCF-7 cells using Olfactory receptor 2T11 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30870-or2t11-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 2T11 OR2T11 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR2T11 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30870-or2t11-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2T11 OR2T11 AntibodyImmunofluorescence analysis of LOVO cells, using OR2T11 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30870-or2t11-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2T11 OR2T11 AntibodyWestern blot analysis of lysates from MCF-7 and HeLa cells, using OR2T11 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2t2-2t35-antibody-a30872-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30872-or2t35-primary-antibodies-wb-testing-1.jpgAnti-OR2T2/2T35 AntibodyWestern Blot analysis of various cells using Olfactory receptor 2T2/35 Polyclonal Antibody diluted at 1:500https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30872-or2t35-primary-antibodies-wb-testing-3.jpgAnti-OR2T2/2T35 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR2T2/2T35 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30872-or2t35-primary-antibodies-wb-testing-2.jpgAnti-OR2T2/2T35 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR2T2/2T35 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4f4-4f5-4f17-antibody-a30873-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30873-or4f17-primary-antibodies-wb-testing-1.jpgAnti-OR4F4/4F5/4F17 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR4F4/4F5/4F17 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51e1-antibody-a30874-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30874-or51e1-primary-antibodies-wb-testing-2.jpgAnti-OR51E1/Gpr164 AntibodyWestern Blot analysis of various cells using D-GPCR Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30874-or51e1-primary-antibodies-wb-testing-4.jpgAnti-OR51E1/Gpr164 AntibodyWestern blot analysis of the lysates from K562 cells using OR51E1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30874-or51e1-primary-antibodies-if-testing-1.jpgAnti-OR51E1/Gpr164 AntibodyImmunofluorescence analysis of A549 cells, using OR51E1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30874-or51e1-primary-antibodies-wb-testing-3.jpgAnti-OR51E1/Gpr164 AntibodyWestern blot analysis of lysates from HeLa cells, using OR51E1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51e2-antibody-a30875-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30875-or51e2-primary-antibodies-ihc-testing-2.jpgAnti-OR51E2/Psgr AntibodyImmunohistochemical analysis of paraffin-embedded human oophoroma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30875-or51e2-primary-antibodies-wb-testing-4.jpgAnti-OR51E2/Psgr AntibodyWestern blot analysis of the lysates from HepG2 cells using OR51E2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30875-or51e2-primary-antibodies-if-testing-1.jpgAnti-OR51E2/Psgr AntibodyImmunofluorescence analysis of A549 cells, using OR51E2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30875-or51e2-primary-antibodies-wb-testing-3.jpgAnti-OR51E2/Psgr AntibodyWestern blot analysis of lysates from Jurkat cells, using OR51E2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51g2-antibody-a30876-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30876-or51g2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51G2 OR51G2 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR51G2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30876-or51g2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 51G2 OR51G2 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using OR51G2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51i1-antibody-a30877-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30877-or51i1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51I1 OR51I1 AntibodyWestern blot analysis of lysates from KB cells, primary antibody was diluted at 1:1000, 4°over nighthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30877-or51i1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51I1 OR51I1 AntibodyImmunofluorescence analysis of COS7 cells, using OR51I1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51i2-antibody-a30878-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30878-or51i2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51I2 OR51I2 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR51I2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30878-or51i2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 51I2 OR51I2 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR51I2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51q1-antibody-a30879-boster.html2026-03-24T05:10:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30879-or51q1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51Q1 OR51Q1 AntibodyImmunofluorescence analysis of LOVO cells, using OR51Q1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51s1-antibody-a30880-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30880-or51s1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51S1 OR51S1 AntibodyImmunofluorescence analysis of A549 cells, using OR51S1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51t1-antibody-a30881-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30881-or51t1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51T1 OR51T1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 51T1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30881-or51t1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 51T1 OR51T1 AntibodyWestern blot analysis of the lysates from K562 cells using OR51T1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30881-or51t1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51T1 OR51T1 AntibodyImmunofluorescence analysis of A549 cells, using OR51T1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30881-or51t1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 51T1 OR51T1 AntibodyWestern blot analysis of lysates from HT-29 and A549 cells, using OR51T1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52a4-antibody-a30882-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30882-or52a4p-primary-antibodies-wb-testing-2.jpgAnti-OR52A4 OR52A4P AntibodyWestern blot analysis of the lysates from K562 cells using OR52A4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30882-or52a4p-primary-antibodies-wb-testing-1.jpgAnti-OR52A4 OR52A4P AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR52A4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52b2-antibody-a30883-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30883-or52b2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52B2 OR52B2 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52B2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30883-or52b2-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 52B2 OR52B2 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR52B2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30883-or52b2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 52B2 OR52B2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR52B2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30883-or52b2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52B2 OR52B2 AntibodyWestern blot analysis of lysates from COLO, HUVEC, and HepG2 cells, using OR52B2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52d1-antibody-a30884-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30884-or52d1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52D1 OR52D1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52D1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30884-or52d1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 52D1 OR52D1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR52D1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30884-or52d1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 52D1 OR52D1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR52D1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30884-or52d1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52D1 OR52D1 AntibodyWestern blot analysis of lysates from COLO and COS7 cells, using OR52D1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52e1-antibody-a30885-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30885-or52e1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E1 OR52E1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52E1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30885-or52e1-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 52E1 OR52E1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR52E1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30885-or52e1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 52E1 OR52E1 AntibodyImmunofluorescence analysis of HeLa cells, using OR52E1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30885-or52e1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E1 OR52E1 AntibodyWestern blot analysis of lysates from COS7 and HepG2 cells, using OR52E1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52e2-antibody-a30886-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30886-or52e2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52E2 OR52E2 AntibodyWestern Blot analysis of Jurkat cells using Olfactory receptor 52E2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30886-or52e2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E2 OR52E2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR52E2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30886-or52e2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E2 OR52E2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR52E2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52e6-antibody-a30887-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30887-or52e6-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52E6 OR52E6 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52E6 Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30887-or52e6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52E6 OR52E6 AntibodyWestern blot analysis of the lysates from HeLa cells using OR52E6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30887-or52e6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52E6 OR52E6 AntibodyWestern blot analysis of lysates from HeLa, HepG2, COLO, and MCF-7 cells, using OR52E6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52n4-antibody-a30888-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30888-or52n4-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52N4 OR52N4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52N4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30888-or52n4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52N4 OR52N4 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR52N4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30888-or52n4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52N4 OR52N4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR52N4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52w1-antibody-a30889-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30889-or52w1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52W1 OR52W1 AntibodyWestern Blot analysis of various cells using Olfactory receptor 52W1 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30889-or52w1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52W1 OR52W1 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR52W1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30889-or52w1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52W1 OR52W1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR52W1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or56a1-antibody-a30890-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30890-or56a1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 56A1 OR56A1 AntibodyImmunofluorescence analysis of HeLa cells, using OR56A1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or56b1-antibody-a30891-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30891-or56b1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 56B1 OR56B1 AntibodyImmunofluorescence analysis of HUVEC cells, using OR56B1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or56b4-antibody-a30892-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30892-or56b4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 56B4 OR56B4 AntibodyWestern Blot analysis of various cells using Olfactory receptor 56B4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30892-or56b4-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 56B4 OR56B4 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR56B4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30892-or56b4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 56B4 OR56B4 AntibodyImmunofluorescence analysis of MCF7 cells, using OR56B4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30892-or56b4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 56B4 OR56B4 AntibodyWestern blot analysis of lysates from COLO cells, using OR56B4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5ak3p-antibody-a30893-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30893-or5ak3p-primary-antibodies-wb-testing-1.jpgAnti-OR5AK3P AntibodyWestern Blot analysis of various cells using Olfactory receptor 5AK3 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30893-or5ak3p-primary-antibodies-wb-testing-3.jpgAnti-OR5AK3P AntibodyWestern blot analysis of the lysates from HepG2 cells using OR5AK3P antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30893-or5ak3p-primary-antibodies-wb-testing-2.jpgAnti-OR5AK3P AntibodyWestern blot analysis of lysates from HUVEC and COS7 cells, using OR5AK3P Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5ap2-antibody-a30894-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30894-or5ap2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5AP2 OR5AP2 AntibodyWestern Blot analysis of 3T3 cells using Olfactory receptor 5AP2 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30894-or5ap2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5AP2 OR5AP2 AntibodyImmunofluorescence analysis of HeLa cells, using OR5AP2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5as1-antibody-a30895-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30895-or5as1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5AS1 OR5AS1 AntibodyImmunofluorescence analysis of LOVO cells, using OR5AS1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5au1-antibody-a30896-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30896-or5au1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5AU1 OR5AU1 AntibodyWestern blot analysis of the lysates from K562 cells using OR5AU1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30896-or5au1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5AU1 OR5AU1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR5AU1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5h15-antibody-a30897-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30897-or5h15-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5H15 OR5H15 AntibodyWestern Blot analysis of COLO cells using Olfactory receptor 5H15 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30897-or5h15-primary-antibodies-wb-testing-4.jpgAnti-Olfactory receptor 5H15 OR5H15 AntibodyWestern blot analysis of the lysates from HeLa cells using OR5H15 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30897-or5h15-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5H15 OR5H15 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5H15 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30897-or5h15-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5H15 OR5H15 AntibodyWestern blot analysis of lysates from COLO cells, using OR5H15 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6c68-antibody-a30898-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30898-or6c68-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6C68 OR6C68 AntibodyWestern Blot analysis of various cells using Olfactory receptor 6C68 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30898-or6c68-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 6C68 OR6C68 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR6C68 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30898-or6c68-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6C68 OR6C68 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR6C68 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6c70-antibody-a30899-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30899-or6c70-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6C70 OR6C70 AntibodyWestern blot analysis of the lysates from HeLa cells using OR6C70 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30899-or6c70-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6C70 OR6C70 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR6C70 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or89-antibody-a30900-boster.html2026-03-24T05:10:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30900-olfr89-primary-antibodies-wb-testing-2.jpgAnti-OR89 AntibodyWestern blot analysis of the lysates from RAW264.7cells using OR89 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30900-olfr89-primary-antibodies-wb-testing-1.jpgAnti-OR89 AntibodyWestern blot analysis of lysates from HepG2 and HUVEC cells, using OR89 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rrh-antibody-a30904-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30904-rrh-primary-antibodies-wb-testing-1.jpgAnti-RRH/Peropsin AntibodyWestern Blot analysis of Jurkat cells using Peropsin Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30904-rrh-primary-antibodies-wb-testing-2.jpgAnti-RRH/Peropsin AntibodyWestern blot analysis of lysates from Jurkat and COLO cells, using RRH Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10d4-antibody-a30905-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30905-or10d4p-primary-antibodies-wb-testing-2.jpgAnti-OR10D4 OR10D4P AntibodyWestern Blot analysis of various cells using Olfactory receptor 10D4 Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30905-or10d4p-primary-antibodies-wb-testing-4.jpgAnti-OR10D4 OR10D4P AntibodyWestern blot analysis of the lysates from K562 cells using OR10D4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30905-or10d4p-primary-antibodies-if-testing-1.jpgAnti-OR10D4 OR10D4P AntibodyImmunofluorescence analysis of LOVO cells, using OR10D4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30905-or10d4p-primary-antibodies-wb-testing-3.jpgAnti-OR10D4 OR10D4P AntibodyWestern blot analysis of lysates from COLO cells, using OR10D4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10h2-antibody-a16363-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16363-or10h2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10H2 OR10H2 AntibodyWestern blot analysis of lysates from A549 cells, using OR10H2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13d1-antibody-a15810-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15810-or13d1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 13D1 OR13D1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR13D1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13f1-antibody-a16512-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16512-or13f1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 13F1 OR13F1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR13F1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or1d2-antibody-a10241-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10241-or1d2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 1D2 OR1D2 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR1D2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10241-or1d2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 1D2 OR1D2 AntibodyImmunofluorescence analysis of HUVEC cells, using OR1D2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10241-or1d2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 1D2 OR1D2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR1D2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or1n1-antibody-a15016-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15016-or1n1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 1N1 OR1N1 AntibodyImmunofluorescence analysis of HUVEC cells, using OR1N1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2ae1-antibody-a18761-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18761-or2ae1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2AE1 OR2AE1 AntibodyImmunofluorescence analysis of A549 cells, using OR2AE1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2b2-antibody-a16517-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16517-or2b2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2B2 OR2B2 AntibodyWestern blot analysis of the lysates from Jurkat cells using OR2B2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16517-or2b2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2B2 OR2B2 AntibodyImmunofluorescence analysis of A549 cells, using OR2B2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16517-or2b2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2B2 OR2B2 AntibodyWestern blot analysis of lysates from HeLa and HT-29 cells, using OR2B2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2b8-antibody-a30906-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30906-or2b8p-primary-antibodies-wb-testing-2.jpgAnti-OR2B8 OR2B8P AntibodyWestern blot analysis of the lysates from HT-29 cells using OR2B8 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30906-or2b8p-primary-antibodies-wb-testing-1.jpgAnti-OR2B8 OR2B8P AntibodyWestern blot analysis of lysates from HeLa cells, using OR2B8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2c1-antibody-a15367-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15367-or2c1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2C1 OR2C1 AntibodyImmunofluorescence analysis of A549 cells, using OR2C1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15367-or2c1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2C1 OR2C1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR2C1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2c3-antibody-a15814-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15814-or2c3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2C3 OR2C3 AntibodyWestern blot analysis of lysates from COLO cells, using OR2C3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2d2-antibody-a15018-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15018-or2d2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2D2 OR2D2 AntibodyImmunofluorescence analysis of A549 cells, using OR2D2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2g2-antibody-a16518-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16518-or2g2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2G2 OR2G2 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR2G2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16518-or2g2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2G2 OR2G2 AntibodyImmunofluorescence analysis of A549 cells, using OR2G2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16518-or2g2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2G2 OR2G2 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR2G2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2g3-antibody-a16877-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16877-or2g3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2G3 OR2G3 AntibodyImmunofluorescence analysis of A549 cells, using OR2G3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16877-or2g3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2G3 OR2G3 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR2G3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2i1-antibody-a30907-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30907-or2i1p-primary-antibodies-wb-testing-3.jpgAnti-OR2I1 OR2I1P AntibodyWestern blot analysis of the lysates from HUVECcells using OR2I1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30907-or2i1p-primary-antibodies-if-testing-1.jpgAnti-OR2I1 OR2I1P AntibodyImmunofluorescence analysis of LOVO cells, using OR2I1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30907-or2i1p-primary-antibodies-wb-testing-2.jpgAnti-OR2I1 OR2I1P AntibodyWestern blot analysis of lysates from HUVEC cells, using OR2I1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2j3-antibody-a14086-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14086-or2j3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2J3 OR2J3 AntibodyImmunofluorescence analysis of A549 cells, using OR2J3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2m2-antibody-a17539-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17539-or2m2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2M2 OR2M2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2M2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17539-or2m2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2M2 OR2M2 AntibodyWestern blot analysis of lysates from LOVO and A549 cells, using OR2M2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2m3-antibody-a17071-boster.html2026-03-24T05:10:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17071-or2m3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2M3 OR2M3 AntibodyImmunofluorescence analysis of LOVO cells, using OR2M3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2t3-2t34-antibody-a17737-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17737-or2t3-primary-antibodies-wb-testing-3.jpgAnti-OR2T3/2T34 AntibodyWestern blot analysis of the lysates from 293 cells using OR2T3/34 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17737-or2t3-primary-antibodies-if-testing-1.jpgAnti-OR2T3/2T34 AntibodyImmunofluorescence analysis of A549 cells, using OR2T3/2T34 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17737-or2t3-primary-antibodies-wb-testing-2.jpgAnti-OR2T3/2T34 AntibodyWestern blot analysis of lysates from MCF-7, HUVEC, HeLa, and HepG2 cells, using OR2T3/2T34 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2y1-antibody-a16880-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16880-or2y1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 2Y1 OR2Y1 AntibodyWestern blot analysis of the lysates from K562 cells using OR2Y1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16880-or2y1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2Y1 OR2Y1 AntibodyImmunofluorescence analysis of A549 cells, using OR2Y1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16880-or2y1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 2Y1 OR2Y1 AntibodyWestern blot analysis of lysates from RAW264.7 and HT-29 cells, using OR2Y1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2z1-antibody-a13370-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13370-or2z1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2Z1 OR2Z1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2Z1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or3a2-antibody-a15019-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15019-or3a2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 3A2 OR3A2 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR3A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15019-or3a2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 3A2 OR3A2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR3A2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15019-or3a2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 3A2 OR3A2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR3A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4a4-4a47-antibody-a30908-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30908-or4a4p-primary-antibodies-wb-testing-3.jpgAnti-OR4A4/4A47 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR4A4/47 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30908-or4a4p-primary-antibodies-if-testing-1.jpgAnti-OR4A4/4A47 AntibodyImmunofluorescence analysis of A549 cells, using OR4A4/4A47 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30908-or4a4p-primary-antibodies-wb-testing-2.jpgAnti-OR4A4/4A47 AntibodyWestern blot analysis of lysates from LOVO cells and HT29 cells, using OR4A4/4A47 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4b1-antibody-a17689-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17689-or4b1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4B1 OR4B1 AntibodyImmunofluorescence analysis of A549 cells, using OR4B1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4c3-antibody-a12738-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12738-or4c3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4C3 OR4C3 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR4C3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12738-or4c3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4C3 OR4C3 AntibodyImmunofluorescence analysis of A549 cells, using OR4C3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12738-or4c3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4C3 OR4C3 AntibodyWestern blot analysis of lysates from K562 cells, using OR4C3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4e2-antibody-a17549-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17549-or4e2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4E2 OR4E2 AntibodyImmunofluorescence analysis of A549 cells, using OR4E2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4f4-antibody-a16373-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16373-or4f4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4F4 OR4F4 AntibodyWestern blot analysis of the lysates from HeLa cells using OR4F4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16373-or4f4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4F4 OR4F4 AntibodyImmunofluorescence analysis of A549 cells, using OR4F4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16373-or4f4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4F4 OR4F4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR4F4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4f6-antibody-a17550-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17550-or4f6-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4F6 OR4F6 AntibodyImmunofluorescence analysis of A549 cells, using OR4F6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17550-or4f6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4F6 OR4F6 AntibodyWestern blot analysis of lysates from HeLa, Jurkat, HepG2, and MCF-7 cells, using OR4F6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4k2-antibody-a17553-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17553-or4k2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4K2 OR4K2 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR4K2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17553-or4k2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 4K2 OR4K2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR4K2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4k3-antibody-a15372-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15372-or4k3-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 4K3 OR4K3 AntibodyWestern blot analysis of the lysates from HeLa cells using OR4K3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15372-or4k3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4K3 OR4K3 AntibodyImmunofluorescence analysis of A549 cells, using OR4K3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15372-or4k3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 4K3 OR4K3 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR4K3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4k17-antibody-a17552-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17552-or4k17-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 4K17 OR4K17 AntibodyImmunofluorescence analysis of A549 cells, using OR4K17 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or4n4-antibody-a15973-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15973-or4n4-primary-antibodies-wb-testing-1.jpgAnti-OR4N4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR4N4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51a2-antibody-a18865-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18865-or51a2-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 51A2 OR51A2 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR51A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18865-or51a2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51A2 OR51A2 AntibodyImmunofluorescence analysis of A549 cells, using OR51A2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18865-or51a2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51A2 OR51A2 AntibodyWestern blot analysis of lysates from K562 cells, using OR51A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5b3-antibody-a17769-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17769-or5b3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5B3 OR5B3 AntibodyImmunofluorescence analysis of COS7 cells, using OR5B3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5d13-antibody-a18796-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18796-or5d13-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5D13 OR5D13 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR5D13 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18796-or5d13-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5D13 OR5D13 AntibodyWestern blot analysis of lysates from COS7 cells, using OR5D13 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5h1-antibody-a16530-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16530-or5h1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5H1 OR5H1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR5H1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16530-or5h1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5H1 OR5H1 AntibodyImmunofluorescence analysis of A549 cells, using OR5H1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16530-or5h1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5H1 OR5H1 AntibodyWestern blot analysis of lysates from HeLa cells, using OR5H1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5h6-antibody-a16532-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16532-or5h6-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5H6 OR5H6 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR5H6 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16532-or5h6-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5H6 OR5H6 AntibodyImmunofluorescence analysis of A549 cells, using OR5H6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16532-or5h6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5H6 OR5H6 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using OR5H6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5k3-antibody-a18799-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18799-or5k3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5K3 OR5K3 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR5K3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18799-or5k3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5K3 OR5K3 AntibodyWestern blot analysis of lysates from K562 cells, using OR5K3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5l1-2-antibody-a16897-boster.html2026-03-24T05:10:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16897-or5l1-primary-antibodies-if-testing-1.jpgAnti-OR5L1/2 AntibodyImmunofluorescence analysis of HUVEC cells, using OR5L1/2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5m9-antibody-a17571-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17571-or5m9-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 5M9 OR5M9 AntibodyWestern blot analysis of the lysates from HUVECcells using OR5M9 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17571-or5m9-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5M9 OR5M9 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5M9 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17571-or5m9-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5M9 OR5M9 AntibodyWestern blot analysis of lysates from Jurkat, HepG2, and HeLa cells, using OR5M9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5t3-antibody-a17573-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17573-or5t3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5T3 OR5T3 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5T3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5u1-antibody-a15874-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15874-or14j1-primary-antibodies-if-testing-1.jpgAnti-OR5U1 OR14J1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5U1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5v1-antibody-a16114-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16114-or5v1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 5V1 OR5V1 AntibodyWestern blot analysis of the lysates from HUVECcells using OR5V1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16114-or5v1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5V1 OR5V1 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR5V1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6a2-antibody-a15376-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15376-or6a2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6A2 OR6A2 AntibodyWestern blot analysis of the lysates from HeLa cells using OR6A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15376-or6a2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6A2 OR6A2 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR6A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6c2-antibody-a17575-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17575-or6c2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6C2 OR6C2 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR6C2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17575-or6c2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6C2 OR6C2 AntibodyWestern blot analysis of lysates from HT-29 cells, using OR6C2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6s1-antibody-a18809-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18809-or6s1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6S1 OR6S1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR6S1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18809-or6s1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 6S1 OR6S1 AntibodyWestern blot analysis of lysates from HeLa, HepG2, HUVEC, and HT-29 cells, using OR6S1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8b2-8b3-antibody-a17683-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17683-or8b2-primary-antibodies-wb-testing-2.jpgAnti-OR8B2/8B3 AntibodyWestern blot analysis of the lysates from K562 cells using OR8B2/B3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17683-or8b2-primary-antibodies-wb-testing-1.jpgAnti-OR8B2/8B3 AntibodyWestern blot analysis of lysates from Jurkat and HT-29 cells, using OR8B2/8B3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8g1-antibody-a15379-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15379-or8g1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8G1 OR8G1 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR8G1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15379-or8g1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 8G1 OR8G1 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using OR8G1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8h2-antibody-a18810-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18810-or8h2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8H2 OR8H2 AntibodyImmunofluorescence analysis of A549 cells, using OR8H2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8h3-antibody-a18811-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18811-or8h3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8H3 OR8H3 AntibodyImmunofluorescence analysis of HUVEC cells, using OR8H3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8k1-antibody-a16911-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16911-or8k1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8K1 OR8K1 AntibodyImmunofluorescence analysis of A549 cells, using OR8K1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8u1-8-9-antibody-a18813-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18813-or8u1-primary-antibodies-if-testing-1.jpgAnti-OR8U1/8/9 AntibodyImmunofluorescence analysis of MCF7 cells, using OR8U1/8/9 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or9a2-antibody-a17589-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17589-or9a2-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 9A2 OR9A2 AntibodyWestern blot analysis of the lysates from HT-29 cells using OR9A2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17589-or9a2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 9A2 OR9A2 AntibodyWestern blot analysis of lysates from HUVEC cells, using OR9A2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or9g1-antibody-a16586-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16586-or9g1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 9G1 OR9G1 AntibodyWestern blot analysis of the lysates from HeLa cells using OR9G1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16586-or9g1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 9G1 OR9G1 AntibodyWestern blot analysis of lysates from HeLa and COLO cells, using OR9G1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or9g4-antibody-a15830-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15830-or9g4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 9G4 OR9G4 AntibodyWestern blot analysis of the lysates from HeLa cells using OR9G4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15830-or9g4-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 9G4 OR9G4 AntibodyWestern blot analysis of lysates from HeLa cells, using OR9G4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-p2ry13-antibody-a08207-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08207-p2ry13-primary-antibodies-wb-testing-1.jpgAnti-P2RY13/P2Y13 AntibodyWestern blot analysis of lysates from HeLa, COLO, HT-29, HepG2, and HUVEC cells, using P2RY13 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pevr1-antibody-a30909-boster.html2026-03-24T05:10:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30909-slc52a2-primary-antibodies-wb-testing-2.jpgAnti-PEVR1 AntibodyWestern Blot analysis of A549 cells using GPR172A Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30909-slc52a2-primary-antibodies-wb-testing-4.jpgAnti-PEVR1 AntibodyWestern blot analysis of the lysates from HepG2 cells using PEVR1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30909-slc52a2-primary-antibodies-if-testing-1.jpgAnti-PEVR1 AntibodyImmunofluorescence analysis of MCF7 cells, using PEVR1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30909-slc52a2-primary-antibodies-wb-testing-3.jpgAnti-PEVR1 AntibodyWestern blot analysis of lysates from A549 cells, using PEVR1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-pevr2-antibody-a30910-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30910-slc52a1-primary-antibodies-wb-testing-2.jpgAnti-PEVR2 AntibodyWestern Blot analysis of 293T cells using GPR172B Polyclonal Antibody diluted at 1:1000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30910-slc52a1-primary-antibodies-if-testing-1.jpgAnti-PEVR2 AntibodyImmunofluorescence analysis of MCF7 cells, using PEVR2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or7e5p-antibody-a30911-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30911-or7e5p-primary-antibodies-wb-testing-2.jpgAnti-OR7E5P AntibodyWestern Blot analysis of 3T3 cells using Olfactory receptor 7E5P Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30911-or7e5p-primary-antibodies-wb-testing-4.jpgAnti-OR7E5P AntibodyWestern blot analysis of the lysates from COLO205 cells using OR7E5P antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30911-or7e5p-primary-antibodies-if-testing-1.jpgAnti-OR7E5P AntibodyImmunofluorescence analysis of MCF-7 cells, using OR7E5P Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30911-or7e5p-primary-antibodies-wb-testing-3.jpgAnti-OR7E5P AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using OR7E5P Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr103-antibody-a09519-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09519-qrfpr-primary-antibodies-if-testing-1.jpgAnti-GPR103 QRFPR AntibodyImmunofluorescence analysis of MCF7 cells, using GPR103 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09519-qrfpr-primary-antibodies-wb-testing-2.jpgAnti-GPR103 QRFPR AntibodyWestern blot analysis of lysates from LOVO cells, using GPR103 Antibody. The lane on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09519-qrfpr-primary-antibodies-wb-testing-3.jpgAnti-GPR103 QRFPR AntibodyWestern blot analysis of the lysates from Jurkat cells using GPR103 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rgr-antibody-a04759-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04759-rgr-primary-antibodies-if-testing-1.jpgAnti-RGR AntibodyImmunofluorescence analysis of MCF7 cells, using RGR Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04759-rgr-primary-antibodies-ihc-testing-2.jpgAnti-RGR AntibodyImmunohistochemistry analysis of paraffin-embedded human brain tissue, using RGR Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-rxfp3-antibody-a06438-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06438-rxfp3-primary-antibodies-ihc-testing-1.jpgAnti-RXFP3/Salpr AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06438-rxfp3-primary-antibodies-wb-testing-3.jpgAnti-RXFP3/Salpr AntibodyWestern blot analysis of the lysates from Jurkat cells using RXFP3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06438-rxfp3-primary-antibodies-wb-testing-2.jpgAnti-RXFP3/Salpr AntibodyWestern blot analysis of lysates from K562 cells, using RXFP3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sstr4-antibody-a05232-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05232-sstr4-primary-antibodies-wb-testing-2.jpgAnti-SSTR4/Somatostatin Receptor 4 AntibodyWestern blot analysis of the lysates from HepG2 cells using SSTR4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05232-sstr4-primary-antibodies-wb-testing-1.jpgAnti-SSTR4/Somatostatin Receptor 4 AntibodyWestern blot analysis of lysates from LOVO cells, using SSTR4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-sucnr1-antibody-a08485-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08485-sucnr1-primary-antibodies-wb-testing-1.jpgAnti-SUCNR1/Gpr91 AntibodyWestern blot analysis of lysates from HUVEC and MCF-7 cells, using SUCNR1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tmem185a-antibody-a14846-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14846-tmem185a-primary-antibodies-ihc-testing-2.jpgAnti-Transmembrane protein 185A TMEM185A AntibodyImmunohistochemical analysis of paraffin-embedded human spleen tissue. 1,primary Antibody was diluted at 1:200(4° overnight). 2, Sodium citrate pH 6.0 was used for antigen retrieval(>98°C,20min). 3,Secondary antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14846-tmem185a-primary-antibodies-wb-testing-4.jpgAnti-Transmembrane protein 185A TMEM185A AntibodyWestern blot analysis of the lysates from HT-29 cells using TMEM185A antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14846-tmem185a-primary-antibodies-if-testing-1.jpgAnti-Transmembrane protein 185A TMEM185A AntibodyImmunofluorescence analysis of MCF7 cells, using TMEM185A Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14846-tmem185a-primary-antibodies-wb-testing-3.jpgAnti-Transmembrane protein 185A TMEM185A AntibodyWestern blot analysis of lysates from K562 cells, using TMEM185A Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r10-antibody-a10959-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-tas2r10-primary-antibodies-ihc-testing-2.jpgAnti-TAS2R10 AntibodyImmunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-tas2r10-primary-antibodies-wb-testing-4.jpgAnti-TAS2R10 AntibodyWestern blot analysis of the lysates from HepG2 cells using TAS2R10 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-tas2r10-primary-antibodies-if-testing-1.jpgAnti-TAS2R10 AntibodyImmunofluorescence analysis of MCF7 cells, using TAS2R10 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-tas2r10-primary-antibodies-wb-testing-3.jpgAnti-TAS2R10 AntibodyWestern blot analysis of lysates from LOVO cells, using TAS2R10 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r13-antibody-a12309-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12309-tas2r13-primary-antibodies-ihc-testing-2.jpgAnti-TAS2R13 AntibodyImmunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12309-tas2r13-primary-antibodies-wb-testing-4.jpgAnti-TAS2R13 AntibodyWestern blot analysis of the lysates from COLO205 cells using TAS2R13 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12309-tas2r13-primary-antibodies-if-testing-1.jpgAnti-TAS2R13 AntibodyImmunofluorescence analysis of MCF7 cells, using TAS2R13 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12309-tas2r13-primary-antibodies-wb-testing-3.jpgAnti-TAS2R13 AntibodyWestern blot analysis of lysates from Jurkat cells, using TAS2R13 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r14-antibody-a10520-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10520-tas2r14-primary-antibodies-ihc-testing-2.jpgAnti-TAS2R14/T2R14 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10520-tas2r14-primary-antibodies-wb-testing-4.jpgAnti-TAS2R14/T2R14 AntibodyWestern blot analysis of the lysates from COLO205 cells using TAS2R14 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10520-tas2r14-primary-antibodies-if-testing-1.jpgAnti-TAS2R14/T2R14 AntibodyImmunofluorescence analysis of MCF7 cells, using TAS2R14 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10520-tas2r14-primary-antibodies-wb-testing-3.jpgAnti-TAS2R14/T2R14 AntibodyWestern blot analysis of lysates from MCF-7 cells, using TAS2R14 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r16-antibody-a09669-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09669-tas2r16-primary-antibodies-wb-testing-1.jpgAnti-TAS2R16 AntibodyWestern blot analysis of lysates from MCF-7 cells, using TAS2R16 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r49-antibody-a14508-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14508-tas2r20-primary-antibodies-wb-testing-2.jpgAnti-TAS2R49 TAS2R20 AntibodyWestern blot analysis of the lysates from COLO205 cells using TAS2R49 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14508-tas2r20-primary-antibodies-wb-testing-1.jpgAnti-TAS2R49 TAS2R20 AntibodyWestern blot analysis of lysates from COLO and HepG2 cells, using TAS2R49 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r1-antibody-a08714-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08714-tas2r1-primary-antibodies-ihc-testing-1.jpgAnti-Taste receptor type 2 member 1 TAS2R1 AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08714-tas2r1-primary-antibodies-wb-testing-3.jpgAnti-Taste receptor type 2 member 1 TAS2R1 AntibodyWestern blot analysis of the lysates from K562 cells using TAS2R1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08714-tas2r1-primary-antibodies-wb-testing-2.jpgAnti-Taste receptor type 2 member 1 TAS2R1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using TAS2R1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r3-antibody-a12110-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12110-tas2r3-primary-antibodies-if-testing-1.jpgAnti-TAS2R3/T2R3 AntibodyImmunofluorescence analysis of A549 cells, using TAS2R3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-tas2r7-antibody-a12764-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12764-tas2r7-primary-antibodies-wb-testing-3.jpgAnti-Taste receptor type 2 member 7 TAS2R7 AntibodyWestern blot analysis of the lysates from HepG2 cells using TAS2R7 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12764-tas2r7-primary-antibodies-if-testing-1.jpgAnti-Taste receptor type 2 member 7 TAS2R7 AntibodyImmunofluorescence analysis of MCF7 cells, using TAS2R7 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12764-tas2r7-primary-antibodies-wb-testing-2.jpgAnti-Taste receptor type 2 member 7 TAS2R7 AntibodyWestern blot analysis of lysates from K562, LOVO, and A549 cells, using TAS2R7 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vn1r3-antibody-a17618-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17618-vn1r3-primary-antibodies-wb-testing-1.jpgAnti-Vomeronasal type-1 receptor 3 VN1R3 AntibodyWestern blot analysis of lysates from HUVEC, HeLa, and COLO cells, using VN1R3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-vn1r4-antibody-a15094-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15094-vn1r4-primary-antibodies-wb-testing-3.jpgAnti-Vomeronasal type-1 receptor 4 VN1R4 AntibodyWestern blot analysis of the lysates from COLO205 cells using VN1R4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15094-vn1r4-primary-antibodies-if-testing-1.jpgAnti-Vomeronasal type-1 receptor 4 VN1R4 AntibodyImmunofluorescence analysis of MCF7 cells, using VN1R4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15094-vn1r4-primary-antibodies-wb-testing-2.jpgAnti-Vomeronasal type-1 receptor 4 VN1R4 AntibodyWestern blot analysis of lysates from COS7 cells, using VN1R4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-gpr42-antibody-a13013-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13013-gpr42-primary-antibodies-if-testing-1.jpgAnti-G-protein coupled receptor 42 GPR42 AntibodyImmunofluorescence analysis of MCF-7 cells, using GPR42 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10a5-antibody-a15012-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15012-or10a5-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10A5 OR10A5 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10A5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10j3-antibody-a18868-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18868-or10j3-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 10J3 OR10J3 AntibodyWestern blot analysis of the lysates from HUVECcells using OR10J3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18868-or10j3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 10J3 OR10J3 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR10J3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or11h1-11h2-11h12-antibody-a18756-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18756-or11h1-primary-antibodies-wb-testing-2.jpgAnti-OR11H1/11H2/11H12 AntibodyWestern blot analysis of the lysates from HeLa cells using OR11H1/11H2/11H12 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18756-or11h1-primary-antibodies-wb-testing-1.jpgAnti-OR11H1/11H2/11H12 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR11H1/11H2/11H12 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13c2-13c9-antibody-a17534-boster.html2026-03-24T05:10:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17534-or13c2-primary-antibodies-wb-testing-2.jpgAnti-OR13C2/13C9 AntibodyWestern blot analysis of the lysates from K562 cells using OR13C2/13C9 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17534-or13c2-primary-antibodies-wb-testing-1.jpgAnti-OR13C2/13C9 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR13C2/13C9 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or13c8-antibody-a16723-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16723-or13c8-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 13C8 OR13C8 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using OR13C8 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2at4-antibody-a15631-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15631-or2at4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 2AT4 OR2AT4 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2AT4 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2t5-2t29-antibody-a17736-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17736-or2t29-primary-antibodies-wb-testing-3.jpgAnti-OR2T5/2T29 AntibodyWestern blot analysis of the lysates from HeLa cells using OR2T5/2T29 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17736-or2t29-primary-antibodies-if-testing-1.jpgAnti-OR2T5/2T29 AntibodyImmunofluorescence analysis of MCF7 cells, using OR2T5/2T29 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17736-or2t29-primary-antibodies-wb-testing-2.jpgAnti-OR2T5/2T29 AntibodyWestern blot analysis of lysates from K562 cells, using OR2T5/2T29 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51b5-antibody-a13766-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13766-or51b5-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 51B5 OR51B5 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR51B5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13766-or51b5-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51B5 OR51B5 AntibodyImmunofluorescence analysis of LOVO cells, using OR51B5 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13766-or51b5-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51B5 OR51B5 AntibodyWestern blot analysis of lysates from LOVO cells, using OR51B5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51b6-antibody-a16555-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16555-or51b6-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51B6 OR51B6 AntibodyImmunofluorescence analysis of MCF7 cells, using OR51B6 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16555-or51b6-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51B6 OR51B6 AntibodyWestern blot analysis of lysates from K562 cells, using OR51B6 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51f1-antibody-a16574-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16574-or51f1-primary-antibodies-wb-testing-3.jpgAnti-OR51F1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR51F1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16574-or51f1-primary-antibodies-if-testing-1.jpgAnti-OR51F1 AntibodyImmunofluorescence analysis of COS7 cells, using OR51F1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16574-or51f1-primary-antibodies-wb-testing-2.jpgAnti-OR51F1 AntibodyWestern blot analysis of lysates from K562 cells, using OR51F1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51g1-antibody-a16524-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16524-or51g1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51G1 OR51G1 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR51G1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16524-or51g1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 51G1 OR51G1 AntibodyWestern blot analysis of lysates from COLO and MCF-7 cells, using OR51G1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51h1-antibody-a30912-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30912-or51h1-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 51H1 OR51H1 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR51H1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52a5-antibody-a17138-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17138-or52a5-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52A5 OR52A5 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR52A5 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17138-or52a5-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 52A5 OR52A5 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR52A5 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or52n1-antibody-a18786-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18786-or52n1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 52N1 OR52N1 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR52N1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18786-or52n1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 52N1 OR52N1 AntibodyImmunofluorescence analysis of LOVO cells, using OR52N1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18786-or52n1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 52N1 OR52N1 AntibodyWestern blot analysis of lysates from Jurkat cells, using OR52N1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or56a3-antibody-a17562-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17562-or56a3-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 56A3 OR56A3 AntibodyImmunofluorescence analysis of LOVO cells, using OR56A3 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10j5-antibody-a17073-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17073-or10j5-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 10J5 OR10J5 AntibodyImmunofluorescence analysis of MCF7 cells, using OR10J5 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or10k1-10k2-antibody-a17529-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17529-or10k1-primary-antibodies-wb-testing-3.jpgAnti-OR10K1/10K2 AntibodyWestern blot analysis of the lysates from HUVECcells using OR10K1/10K2 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17529-or10k1-primary-antibodies-if-testing-1.jpgAnti-OR10K1/10K2 AntibodyImmunofluorescence analysis of LOVO cells, using OR10K1/10K2 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17529-or10k1-primary-antibodies-wb-testing-2.jpgAnti-OR10K1/10K2 AntibodyWestern blot analysis of lysates from HepG2 cells, using OR10K1/10K2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or12d3-antibody-a15038-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15038-or12d3-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 12D3 OR12D3 AntibodyWestern blot analysis of lysates from RAW264.7 cells, using OR12D3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or2f2-antibody-a16370-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16370-or2f2-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 2F2 OR2F2 AntibodyWestern blot analysis of lysates from NIH/3T3 cells, using OR2F2 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or3a2-3-antibody-a14729-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14729-or3a3-primary-antibodies-wb-testing-3.jpgAnti-OR3A2/3 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR3A2/3 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14729-or3a3-primary-antibodies-if-testing-1.jpgAnti-OR3A2/3 AntibodyImmunofluorescence analysis of MCF7 cells, using OR3A2/3 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14729-or3a3-primary-antibodies-wb-testing-2.jpgAnti-OR3A2/3 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR3A2/3 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or51a4-antibody-a18864-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18864-or51a4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 51A4 OR51A4 AntibodyWestern blot analysis of the lysates from HepG2 cells using OR51A4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18864-or51a4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 51A4 OR51A4 AntibodyImmunofluorescence analysis of LOVO cells, using OR51A4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18864-or51a4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 51A4 OR51A4 AntibodyWestern blot analysis of lysates from Jurkat, HepG2, and MCF-7 cells, using OR51A4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5d16-antibody-a17569-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17569-or5d16-primary-antibodies-wb-testing-1.jpgAnti-Olfactory receptor 5D16 OR5D16 AntibodyWestern blot analysis of lysates from MCF-7 cells, using OR5D16 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5m1-antibody-a17570-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17570-or5m1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 5M1 OR5M1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5M1 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or5m1-5m10-antibody-a16898-boster.html2026-03-24T05:10:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16898-or5m1-primary-antibodies-wb-testing-3.jpgAnti-OR5M1/5M10 AntibodyWestern blot analysis of the lysates from Jurkat cells using OR5M1/5M10 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16898-or5m1-primary-antibodies-if-testing-1.jpgAnti-OR5M1/5M10 AntibodyImmunofluorescence analysis of MCF7 cells, using OR5M1/5M10 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16898-or5m1-primary-antibodies-wb-testing-2.jpgAnti-OR5M1/5M10 AntibodyWestern blot analysis of lysates from HeLa and HepG2 cells, using OR5M1/5M10 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6b2-antibody-a17574-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17574-or6b2-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 6B2 OR6B2 AntibodyImmunofluorescence analysis of MCF7 cells, using OR6B2 Antibody. The picture on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or6j1-antibody-a18808-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18808-or6j1-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 6J1 OR6J1 AntibodyWestern blot analysis of the lysates from COLO205 cells using OR6J1 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18808-or6j1-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 6J1 OR6J1 AntibodyImmunofluorescence analysis of MCF7 cells, using OR6J1 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18808-or6j1-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 6J1 OR6J1 AntibodyWestern blot analysis of lysates from HUVEC and MCF-7 cells, using OR6J1 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/anti-or8b4-antibody-a16908-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16908-or8b4-primary-antibodies-wb-testing-3.jpgAnti-Olfactory receptor 8B4 OR8B4 AntibodyWestern blot analysis of the lysates from Jurkat cells using OR8B4 antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16908-or8b4-primary-antibodies-if-testing-1.jpgAnti-Olfactory receptor 8B4 OR8B4 AntibodyImmunofluorescence analysis of MCF7 cells, using OR8B4 Antibody. The picture on the right is blocked with the synthesized peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16908-or8b4-primary-antibodies-wb-testing-2.jpgAnti-Olfactory receptor 8B4 OR8B4 AntibodyWestern blot analysis of lysates from MCF-7 and HeLa cells, using OR8B4 Antibody. The lane on the right is blocked with the synthesized peptide.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-erbin-tyr1104-antibody-p30915-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30915-erbin-primary-antibodies-wb-testing-2.jpgAnti-Phospho Erbin (Tyr1104) AntibodyWestern Blot analysis of various cells using Phospho-Erbin (Y1104) Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30915-erbin-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Erbin (Tyr1104) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Erbin (Phospho-Tyr1104) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30915-erbin-primary-antibodies-wb-testing-3.jpgAnti-Phospho Erbin (Tyr1104) AntibodyWestern blot analysis of lysates from HeLa cells, using phospho-Erbin (Phospho-Tyr1104) antibody.
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-tensin-2-tyr483-antibody-p30917-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30917-tns2-primary-antibodies-wb-testing-2.jpgAnti-Phospho Tensin-2 (Tyr483) AntibodyWestern Blot analysis of 3T3 cells using Phospho-Tensin-2 (Y483) Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30917-tns2-primary-antibodies-wb-testing-3.jpgAnti-Phospho Tensin-2 (Tyr483) AntibodyWestern Blot analysis of A549 NIH-3T3 SH-SY5Y K562 HELA cells using Phospho-Tensin-2 (Y483) Polyclonal Antibody diluted at 1:2000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30917-tns2-primary-antibodies-elisa-testing-1.jpgAnti-Phospho Tensin-2 (Tyr483) AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Tensin-2 (Phospho-Tyr483) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30917-tns2-primary-antibodies-wb-testing-4.jpgAnti-Phospho Tensin-2 (Tyr483) AntibodyWestern blot analysis of lysate from K562 cells, using phospho-Thrensin-2 (Phospho-Tyr483) antibody .
https://www.bosterbio.com/products/primary-antibodies/phospho-specific-antibodies/anti-phospho-zfp598-tyr306-antibody-p15343-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p15343-znf598-primary-antibodies-ihc-testing-2.jpgAnti-Phospho ZFP598 (Tyr306) ZNF598 AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p15343-znf598-primary-antibodies-elisa-testing-1.jpgAnti-Phospho ZFP598 (Tyr306) ZNF598 AntibodyEnzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using ZFP598 (Phospho-Tyr306) Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p15343-znf598-primary-antibodies-wb-testing-3.jpgAnti-Phospho ZFP598 (Tyr306) ZNF598 AntibodyWestern blot analysis of lysate from Jurkat cells, uisng phospho-ZFP598 (Phospho-Tyr306) antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ameloblastin-antibody-a05093-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05093-ambn-primary-antibodies-wb-testing-1.jpgAnti-Ameloblastin AMBN AntibodyWestern blot analysis of lysates from HeLa cells, using Ameloblastin antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-atp5j2-antibody-a12564-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12564-atp5j2-primary-antibodies-ihc-testing-1.jpgAnti-ATP5J2 AntibodyImmunohistochemistry analysis of ATP5J2 antibody in paraffin-embedded human lung carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-cacna2d1-antibody-a04282-2-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04282-2-cacna2d1-primary-antibodies-wb-testing-1.jpgAnti-Cacna2d1 AntibodyWestern blot analysis of lysate from NIH/3T3 cells, using Cacna2d1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-caspase-4-antibody-a02941-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-casp4-primary-antibodies-wb-testing-2.jpgAnti-Caspase-4 CASP4 AntibodyWestern blot analysis of lysates from 1) Hela ,2)THP-1, (Green) primary antibody was diluted at 1:1000, 4°over night, secondary antibody(cat:SA33333)was diluted at 1:10000, 37° 1hour.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-casp4-primary-antibodies-ihc-testing-1.jpgAnti-Caspase-4 CASP4 AntibodyImmunohistochemistry analysis of Caspase-4 antibody in paraffin-embedded human lung carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-colq-antibody-a03301-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03301-colq-primary-antibodies-ihc-testing-1.jpgAnti-COLQ AntibodyImmunohistochemical analysis of paraffin-embedded human Breast cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
https://www.bosterbio.com/products/primary-antibodies/anti-defensin-alpha4-antibody-a06846-boster.html2026-03-24T05:10:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06846-defa4-primary-antibodies-ihc-testing-1.jpgAnti-Defensin alpha4 DEFA4 AntibodyImmunohistochemistry analysis of Defensin α4 antibody in paraffin-embedded human heart tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-ef-1beta-antibody-a07669-1-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07669-1-eef1b2-primary-antibodies-wb-testing-1.jpgAnti-EF-1beta EEF1B2 AntibodyWestern Blot analysis of extracts from K562 cells, using EF-1β Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07669-1-eef1b2-primary-antibodies-wb-testing-2.jpgAnti-EF-1beta EEF1B2 AntibodyWestern blot analysis of lysates from K562 cells , using EF-1β antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gata-5-antibody-a03284-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03284-gata5-primary-antibodies-ihc-testing-2.jpgAnti-GATA-5 AntibodyImmunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03284-gata5-primary-antibodies-ihc-testing-1.jpgAnti-GATA-5 AntibodyImmunohistochemistry analysis of GATA-5 antibody in paraffin-embedded human lung carcinoma tissue.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03284-gata5-primary-antibodies-wb-testing-3.jpgAnti-GATA-5 AntibodyWestern blot analysis of lysate from NIH/3T3 cells, using GATA-5 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-gcs-beta-2-antibody-a13667-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13667-gucy1b2-primary-antibodies-ihc-testing-1.jpgAnti-GCS-beta-2 AntibodyImmunohistochemistry analysis of GCS-β-2 antibody in paraffin-embedded human lung carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-gnrh-i-antibody-a02307-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02307-gnrh1-primary-antibodies-ihc-testing-1.jpgAnti-GnRH I GNRH1 AntibodyImmunohistochemistry analysis of GnRH I antibody in paraffin-embedded human heart tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-nt-4-antibody-a06935-2-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06935-2-ntf4-primary-antibodies-ihc-testing-2.jpgAnti-NT-4 NTF4 AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06935-2-ntf4-primary-antibodies-ihc-testing-1.jpgAnti-NT-4 NTF4 AntibodyImmunohistochemistry analysis of NT-4 antibody in paraffin-embedded human prostate carcinoma tissue.
https://www.bosterbio.com/products/primary-antibodies/anti-oat1-antibody-a02456-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02456-slc22a6-primary-antibodies-wb-testing-1.jpgAnti-OAT1 SLC22A6 AntibodyWestern blot analysis of HEPG2 lysate, antibody was diluted at 1000. Secondary antibody was diluted at 1:20000
https://www.bosterbio.com/products/primary-antibodies/anti-pepsin-a-antibody-a09465-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09465-pga4-primary-antibodies-wb-testing-2.jpgAnti-Pepsin A PGA4 AntibodyWestern Blot analysis of K562 cells using Pepsin A Polyclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09465-pga4-primary-antibodies-ihc-testing-1.jpgAnti-Pepsin A PGA4 AntibodyImmunohistochemistry analysis of Pepsin A antibody in paraffin-embedded human lung carcinoma tissue.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09465-pga4-primary-antibodies-wb-testing-3.jpgAnti-Pepsin A PGA4 AntibodyWestern blot analysis of lysate from K562 cells, using Pepsin A antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-rnase-iii-drosha-antibody-a19835-boster.html2026-03-24T05:10:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19835-drosha-primary-antibodies-ihc-testing-1.jpgAnti-RNase III Drosha AntibodyImmunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:200https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19835-drosha-primary-antibodies-wb-testing-3.jpgAnti-RNase III Drosha AntibodyWestern blot analysis of SH-SY5Y K562 HELA using RNase III Drosha antibody. Antibody was diluted at 1:1000. Secondary antibody was diluted at 1:20000.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19835-drosha-primary-antibodies-wb-testing-2.jpgAnti-RNase III Drosha AntibodyWestern blot analysis of lysates from brain tissue, using RNase III Drosha antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-ttf-1-antibody-a30726-boster.html2026-03-24T05:10:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30726-nkx2-1-primary-antibodies-wb-testing-1.jpgAnti-TTF-1 NKX2-1 AntibodyWestern blot analysis of lysate from NIH/3T3 cells, using TTF-1 antibody.
https://www.bosterbio.com/products/primary-antibodies/anti-zfp106-antibody-a30921-boster.html2026-03-24T05:10:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30921-znf106-primary-antibodies-wb-testing-1.jpgAnti-ZFP106 ZNF106 AntibodyWestern Blot analysis of COS7 cells using ZFP106 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30921-znf106-primary-antibodies-wb-testing-2.jpgAnti-ZFP106 ZNF106 AntibodyWestern Blot analysis of various cells using ZFP106 Polyclonal Antibody. Secondary antibody was diluted at 1:20000https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30921-znf106-primary-antibodies-wb-testing-3.jpgAnti-ZFP106 ZNF106 AntibodyWestern blot analysis of lysate from COS7 cells, using ZFP106 antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-cd68-macrophage-marker-antibody-m00602-boster.html2026-03-24T05:11:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00602-fphar-09-00618-g002.jpgAnti-CD68 (Macrophage Marker) Monoclonal Antibody(A) Representative photomicrographs showing infiltrating CD68-positive macrophages or Gr-1 positive neutrophils (indicated by arrowheads) in the liver and kidney tissues of mice from three different groups: Ctrl, saline operated; AGNH, An-Gong-Niu-Huang Wan 2.5 g/kg/d treatment for consecutive 28 days; C+R, cinnabar and reaglar 0.14 + 0.14 g/kg/d combinational treatment for consecutive 28 days. Scale bar: 50 μm. (B) Quantification of the number of CD68-positive macrophages or Gr-1 positive neutrophils per high-power field in different groups. Each bar represents mean ± SD for 6 mice. ∗ P < 0.05 saline control versus cinnabar and reaglar co-administration; # P < 0.05, An-Gong-Niu-Huang Wan versus cinnabar and reaglar co-administration.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fphar.2018.00618/full'>29950994</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/d/cd68-primary-antibodies-m00602-ihc-testing-1.jpgAnti-CD68 (Macrophage Marker) Monoclonal AntibodyFormalin-fixed, paraffin-embedded human Tonsil stained with Anti-CD68 Mouse Monoclonal Antibody (SPM130).
https://www.bosterbio.com/products/primary-antibodies/anti-adam17-picoband-trade-antibody-a00604-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00604-ADAM17-primary-antibodies-WB-testing-1.jpgAnti-ADAM17 Antibody Picoband® Western blot analysis of ADAM17 using anti-ADAM17 antibody (A00604). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse thymus tissue lysates,<br>Lane 2: human Hela whole cell lysates,<br>Lane 3: human placenta tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM17 antigen affinity purified polyclonal antibody (Catalog # A00604) at 0.5 ug/mL overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM17 at approximately 78KD. The expected band size for ADAM17 is at 97KD.
https://www.bosterbio.com/products/primary-antibodies/anti-amd1-antibody-a06146-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06146-amd1-primary-antibodies-wb-testing-1_1.jpgAnti-AMD1 Antibody Picoband®Western blot analysis of AMD1 using anti-AMD1 antibody (A06146). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AMD1 antigen affinity purified polyclonal antibody (A06146) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AMD1 at approximately 40-42 kDa. The expected band size for AMD1 is at 38 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bmp4-picoband-trade-antibody-a00321-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00321-bmp4-primary-antibodies-wb-testing-1.jpgAnti-BMP4 Antibody Picoband®Western blot analysis of BMP4 using anti-BMP4 antibody (A00321). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: rat lung tissue lysates,<br>
Lane 5: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMP4 antigen affinity purified polyclonal antibody (A00321) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BMP4 at approximately 47 kDa. The expected band size for BMP4 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-mip-3-alpha-ccl20-picoband-trade-antibody-a00748-2-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00748-2-CCL20-primary-antibodies-WB-testing-1.jpgAnti-MIP-3 Alpha/CCL20 Antibody Picoband® Western blot analysis of MIP-3 Alpha/CCL20 using anti-MIP-3 Alpha/CCL20 antibody (A00748-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat testis tissue lysates,<br>Lane 2: mouse testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIP-3 Alpha/CCL20 antigen affinity purified polyclonal antibody (Catalog # A00748-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIP-3 Alpha/CCL20 at approximately 14KD. The expected band size for MIP-3 Alpha/CCL20 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00748-2-ccl20-primary-antibodies-elisa-testing-2.jpgAnti-MIP-3 Alpha/CCL20 Antibody Picoband® Sandwich ELISA - Recombinant mouse MIP-3 Alpha/CCL20 protein standard curve.<br>
Use in combination with reagents from Mouse MIP-3 Alpha/CCL20 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0454).
https://www.bosterbio.com/products/primary-antibodies/anti-cd14-picoband-trade-antibody-a00137-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00137-cd14-primary-antibodies-wb-testing-1.jpgAnti-CD14 Antibody Picoband® Western blot analysis of CD14 using anti-CD14 antibody (A00137). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse thymus tissue lysates,<br>Lane 2: mouse spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD14 antigen affinity purified polyclonal antibody (Catalog # A00137) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD14 at approximately 50KD. The expected band size for CD14 is at 40KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00137-CD14-primary-antibodies-IHC-testing-2.jpgAnti-CD14 Antibody Picoband® IHC analysis of CD14 using anti-CD14 antibody (A00137).<br>CD14 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD14 Antibody (A00137) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00137-CD14-primary-antibodies-IHC-testing-3.jpgAnti-CD14 Antibody Picoband® IHC analysis of CD14 using anti-CD14 antibody (A00137).<br>CD14 was detected in paraffin-embedded section of rat lymphaden tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD14 Antibody (A00137) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00137-CD14-primary-antibodies-IHC-testing-4.jpgAnti-CD14 Antibody Picoband® IHC analysis of CD14 using anti-CD14 antibody (A00137).<br>CD14 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD14 Antibody (A00137) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00137-cd14-primary-antibodies-fc-testing-5.pngAnti-CD14 Antibody Picoband® Flow Cytometry analysis of mouse PBMC cells using anti-CD14 antibody (A00137). <br> Overlay histogram showing mouse PBMC cells stained with A00137 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD14 Antibody (A00137,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd47-picoband-trade-antibody-a00360-1-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00360-1-cd47-primary-antibodies-wb-testing-1_1.jpgAnti-CD47 Antibody Picoband®Western blot analysis of CD47 using anti-CD47 antibody (A00360-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HT1080 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD47 antigen affinity purified polyclonal antibody (A00360-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD47 at approximately 50 kDa. The expected band size for CD47 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00360-1-cd47-primary-antibodies-ihc-testing-1.jpgAnti-CD47 Antibody Picoband®IHC analysis of CD47 using anti-CD47 antibody (A00360-1). <br>CD47 was detected in a paraffin-embedded section of human ovarican cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD47 Antibody (A00360-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00360-1-cd47-primary-antibodies-fcm-testing-1.jpgAnti-CD47 Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-CD47 antibody (A00360-1). <br>
Overlay histogram showing A549 cells stained with A00360-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD47 Antibody (A00360-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cdc20-picoband-trade-antibody-a00382-1-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-WB-testing-1.jpgAnti-Cdc20 Antibody Picoband® Western blot analysis of Cdc20 using anti-Cdc20 antibody (A00382-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cdc20 antigen affinity purified polyclonal antibody (Catalog # A00382-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cdc20 at approximately 55KD. The expected band size for Cdc20 is at 55KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-IHC-testing-2.jpgAnti-Cdc20 Antibody Picoband® IHC analysis of Cdc20 using anti-Cdc20 antibody (A00382-1).<br>Cdc20 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-IHC-testing-3.jpgAnti-Cdc20 Antibody Picoband® IHC analysis of Cdc20 using anti-Cdc20 antibody (A00382-1).<br>Cdc20 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-IHC-testing-4.jpgAnti-Cdc20 Antibody Picoband® IHC analysis of Cdc20 using anti-Cdc20 antibody (A00382-1).<br>Cdc20 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-IHC-testing-5.jpgAnti-Cdc20 Antibody Picoband® IHC analysis of Cdc20 using anti-Cdc20 antibody (A00382-1).<br>Cdc20 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00382-1-Cdc20-primary-antibodies-IHC-testing-6.jpgAnti-Cdc20 Antibody Picoband® IHC analysis of Cdc20 using anti-Cdc20 antibody (A00382-1).<br>Cdc20 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00382-1-cdc20-primary-antibodies-if-testing-7.jpgAnti-Cdc20 Antibody Picoband® IF analysis of Cdc20 using anti-Cdc20 antibody (A00382-1). <br> Cdc20 was detected in immunocytochemical section of NIH3T3 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Cdc20 Antibody (A00382-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00382-1-cdc20-primary-antibodies-fc-testing-8.pngAnti-Cdc20 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Cdc20 antibody (A00382-1). <br> Overlay histogram showing SiHa cells stained with A00382-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cdc20 Antibody (A00382-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00382-1-cdc20-primary-antibodies-fc-testing-9.pngAnti-Cdc20 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Cdc20 antibody (A00382-1). <br> Overlay histogram showing U20S cells stained with A00382-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cdc20 Antibody (A00382-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-chi3l1-picoband-trade-antibody-a01283-1-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01283-1-chi3l1-primary-antibodies-wb-testing-1.jpgAnti-CHI3L1 Antibody Picoband® Western blot analysis of CHI3L1 using anti-CHI3L1 antibody (A01283-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse RAW264.7 whole cell lysates,<br>Lane 2: mouse HEPA1-6 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHI3L1 antigen affinity purified polyclonal antibody (Catalog # A01283-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHI3L1 at approximately 43KD. The expected band size for CHI3L1 is at 43KD.
https://www.bosterbio.com/products/primary-antibodies/anti-beta-catenin-picoband-trade-antibody-a00004-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-fig-6-1x.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband®CTHRC1 knockdown inhibited the Wnt/β-catenin pathway. Western blotting was used to analyze the β-catenin, Cyclin D1, and c-myc expression in CTHRC1 knockdown and control group. ***P < 0.001 . Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/15458/'>37273536</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-wb-testing-1.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® Western blot analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human RT4 whole cell lysates, <br>
Lane 4: human T47D whole cell lysates, <br>
Lane 5: human A549 whole cell lysates, <br>
Lane 6: human PC-3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTNNB1 antigen affinity purified polyclonal antibody (Catalog # A00004) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTNNB1 at approximately 95 kDa. The expected band size for CTNNB1 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-wb-testing-2.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® Western blot analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: rat C6 whole cell lysates, <br>
Lane 3: rat RH35 whole cell lysates, <br>
Lane 4: mouse brain tissue lysates, <br>
Lane 5: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTNNB1 antigen affinity purified polyclonal antibody (Catalog # A00004) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTNNB1 at approximately 95 kDa. The expected band size for CTNNB1 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-ihc-testing-3.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IHC analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-ihc-testing-4.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IHC analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-ihc-testing-5.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IHC analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-ihc-testing-6.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IHC analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-ihc-testing-7.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IHC analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-if-testing-8.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IF analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-if-testing-9.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® IF analysis of CTNNB1 using anti-CTNNB1 antibody (A00004). <br>
CTNNB1 was detected in a paraffin-embedded section of human intestine cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-CTNNB1 Antibody (A00004) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00004-ctnnb1-primary-antibodies-fcm-testing-10_1.jpgAnti-beta Catenin/CTNNB1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-CTNNB1 antibody (A00004). <br>
Overlay histogram showing Hela cells stained with A00004 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CTNNB1 Antibody (A00004, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cxcl12-picoband-trade-antibody-a00053-1-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00053-1-cxcl12-primary-antibodies-wb-testing-1.jpgAnti-CXCL12 Antibody Picoband® Western blot analysis of CXCL12 using anti-CXCL12 antibody (A00053-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat stomach tissue lysates. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CXCL12 antigen affinity purified polyclonal antibody (Catalog # A00053-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CXCL12 at approximately 11 kDa. The expected band size for CXCL12 is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00053-1-cxcl12-primary-antibodies-ihc-testing-2.jpgAnti-CXCL12 Antibody Picoband® IHC analysis of CXCL12 using anti-CXCL12 antibody (A00053-1). <br>
CXCL12 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CXCL12 Antibody (A00053-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd105-picoband-trade-antibody-a02997-2-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02997-2-cd105-primary-antibodies-wb-testing-1.jpgAnti-CD105/Eng Antibody Picoband® Western blot analysis of CD105 using anti-CD105 antibody (A02997-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse lung tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD105 antigen affinity purified polyclonal antibody (Catalog # A02997-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD105 at approximately 95-105KD. The expected band size for CD105 is at 71KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-2.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-3.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-4.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-5.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-6.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02997-2-CD105-primary-antibodies-IHC-testing-7.jpgAnti-CD105/Eng Antibody Picoband® IHC analysis of CD105 using anti-CD105 antibody (A02997-2).<br>CD105 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD105 Antibody (A02997-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-cardiac-fabp-picoband-trade-antibody-a01734-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01734-fabp3-primary-antibodies-wb-testing-1.jpgAnti-Cardiac FABP/Fabp3 Antibody Picoband® Western blot analysis of Cardiac FABP/Fabp3 using anti-Cardiac FABP/Fabp3 antibody (A01734). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates,<br>
Lane 2: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cardiac FABP/Fabp3 antigen affinity purified polyclonal antibody (Catalog # A01734) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cardiac FABP/Fabp3 at approximately 15 kDa. The expected band size for Cardiac FABP/Fabp3 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01734-cardiac-fabp-primary-antibodies-elisa-testing-2_1.jpgAnti-Cardiac FABP/Fabp3 Antibody Picoband® Sandwich ELISA - Recombinant rat Cardiac FABP/Fabp3 protein standard curve.<br>
Use in combination with reagents from Rat Cardiac FABP/Fabp3 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1623).
https://www.bosterbio.com/products/primary-antibodies/anti-kgf-picoband-trade-antibody-a01931-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01931-KGF-primary-antibodies-WB-testing-1.jpgAnti-KGF/Fgf7 Antibody Picoband® Western blot analysis of KGF using anti-KGF antibody (A01931). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse brain tissue lysates,<br>Lane 2: rat RH35 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KGF antigen affinity purified polyclonal antibody (Catalog # A01931) at 0.5 ug/mL overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KGF at approximately 22KD. The expected band size for KGF is at 22KD.
https://www.bosterbio.com/products/primary-antibodies/anti-fgf8-picoband-trade-antibody-a00841-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00841-fgf8-primary-antibodies-wb-testing-1.jpgAnti-FGF8 Antibody Picoband® Western blot analysis of FGF8 using anti-FGF8 antibody (A00841). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat ovary tissue lysates,<br>Lane 2: human Hela whole cell lysates,<br>Lane 3: human placenta tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGF8 antigen affinity purified polyclonal antibody (Catalog # A00841) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGF8 at approximately 26KD. The expected band size for FGF8 is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-fh-picoband-trade-antibody-a02097-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02097-fh-primary-antibodies-wb-testing-1.jpgAnti-FH Antibody Picoband® Western blot analysis of FH using anti-FH antibody (A02097). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat lymphaden tissue lysates, <br>Lane 2: rat small intestine tissue lysates,<br>Lane 3: rat gaster tissue lysates,<br>Lane 4: mouse kidney tissue lysates,<br>Lane 5: mouse testis tissue lysates,<br>Lane 6: mouse gaster tissue lysates,<br>Lane 7: human K562 whole cell lysates,<br>Lane 8: human U937 whole cell lysates,<br>Lane 9:human HL-60 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FH antigen affinity purified polyclonal antibody (Catalog # A02097) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FH at approximately 49KD. The expected band size for FH is at 55KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02097-FH-primary-antibodies-IHC-testing-2.jpgAnti-FH Antibody Picoband® IHC analysis of FH using anti-FH antibody (A02097).<br>FH was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-FH Antibody (A02097) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02097-FH-primary-antibodies-IHC-testing-3.jpgAnti-FH Antibody Picoband® IHC analysis of FH using anti-FH antibody (A02097).<br>FH was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-FH Antibody (A02097) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02097-FH-primary-antibodies-IHC-testing-4.jpgAnti-FH Antibody Picoband® IHC analysis of FH using anti-FH antibody (A02097).<br>FH was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-FH Antibody (A02097) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02097-FH-primary-antibodies-IHC-testing-5.jpgAnti-FH Antibody Picoband® IHC analysis of FH using anti-FH antibody (A02097).<br>FH was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-FH Antibody (A02097) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02097-FH-primary-antibodies-IHC-testing-6.jpgAnti-FH Antibody Picoband® IHC analysis of FH using anti-FH antibody (A02097).<br>FH was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-FH Antibody (A02097) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02097-fh-primary-antibodies-fc-testing-7.pngAnti-FH Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-FH antibody (A02097). <br> Overlay histogram showing A431 cells stained with A02097 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FH Antibody (A02097,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02097-fh-primary-antibodies-fc-testing-8.pngAnti-FH Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-FH antibody (A02097). <br> Overlay histogram showing PC-3 cells stained with A02097 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FH Antibody (A02097,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02097-fh-primary-antibodies-if-testing-9.jpgAnti-FH Antibody Picoband® IF analysis of FH using anti-FH antibody (A02097). <br> FH was detected in immunocytochemical section of PC-3 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-FH Antibody (A02097) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-flt3-cd135-picoband-trade-antibody-a00188-4-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00188-4-cd135-primary-antibodies-wb-testing-1_1.jpgAnti-Flt3/CD135 Antibody Picoband®Western blot analysis of Flt3/CD135 using anti-Flt3/CD135 antibody (A00188-4). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Flt3/CD135 antigen affinity purified polyclonal antibody (A00188-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Flt3/CD135 at approximately 150 kDa. The expected band size for Flt3/CD135 is at 130 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00188-4-cd135-primary-antibodies-fcm-testing-1.jpgAnti-Flt3/CD135 Antibody Picoband®Flow Cytometry analysis of RAW264.7 cells using anti-Flt3/CD135 antibody (A00188-4). <br>
Overlay histogram showing RAW264.7 cells stained with A00188-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Flt3/CD135 Antibody (A00188-4, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-flt3-ligand-picoband-trade-antibody-a04987-boster.html2026-03-24T05:11:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04987-Flt3-ligand-primary-antibodies-WB-testing-1.jpgAnti-Flt3 ligand/Flt3lg Antibody Picoband® Western blot analysis of Flt3 ligand using anti-Flt3 ligand antibody (A04987). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Flt3 ligand antigen affinity purified polyclonal antibody (Catalog # A04987) at 0.5 ug/mL overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Flt3 ligand at approximately 26KD. The expected band size for Flt3 ligand is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-flt3-ligand-picoband-trade-antibody-a04987-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04987-1-flt3lg-primary-antibodies-wb-testing-1.jpgAnti-Flt3 ligand/Flt3lg Antibody Picoband®Western blot analysis of Flt3 ligand using anti-Flt3 ligand antibody (A04987-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat thymus tissue lysates,<br>
Lane 2: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Flt3 ligand antigen affinity purified polyclonal antibody (A04987-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Flt3 ligand at approximately 26 kDa. The expected band size for Flt3 ligand is at 26 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-3-picoband-trade-antibody-a01276-2-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-WB-testing-1.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® Western blot analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human MCF-7 whole cell lysates,<br>Lane 3: human HepG2 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF Receptor 3 antigen affinity purified polyclonal antibody (Catalog # A01276-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF Receptor 3 at approximately 153KD. The expected band size for VEGF Receptor 3 is at 153KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-2.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-3.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-4.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-5.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-6.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-7.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-2-VEGF-Receptor-3-primary-antibodies-IHC-testing-8.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br>VEGF Receptor 3 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-2-vegf-receptor_3-primary-antibodies-if-testing-9.jpg.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IF analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-2).<br> VEGF Receptor 3 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-VEGF Receptor 3 Antibody (A01276-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-2-vegf-receptor_3-primary-antibodies-fc-testing-10.png.pngAnti-VEGF Receptor 3/FLT4 Antibody Picoband®10. Flow Cytometry analysis of U20S cells using anti-VEGF Receptor 3 antibody (A01276-2). <br> Overlay histogram showing U20S cells stained with A01276-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VEGF Receptor 3 Antibody (A01276-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-follistatin-picoband-trade-antibody-a00972-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00972-1-FSTL1-primary-antibodies-WB-testing-1.jpgAnti-Follistatin/FST Antibody Picoband® Western blot analysis of Follistatin using anti-Follistatin antibody (A00972-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse kidney tissue lysates,<br>Lane 2: human MCF-7 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Follistatin antigen affinity purified polyclonal antibody (Catalog # A00972-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Follistatin at approximately 40KD. The expected band size for Follistatin is at 38KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tls-fus-picoband-trade-antibody-a00771-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00771-1-tls-primary-antibodies-wb-testing-1.jpgAnti-TLS/FUS Antibody Picoband® Western blot analysis of TLS / FUS using anti-TLS / FUS antibody (A00771-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>Lane 2: human K562 whole cell lysates,<br>Lane 3: mouse NIH3T3 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TLS / FUS antigen affinity purified polyclonal antibody (Catalog # A00771-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TLS / FUS at approximately 75KD. The expected band size for TLS / FUS is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vitamin-d-binding-protein-picoband-trade-antibody-a03364-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03364-1-vitamin_d_binding_protein-primary-antibodies-wb-testing-1.jpgAnti-Vitamin D Binding protein/GC Antibody Picoband® Western blot analysis of Vitamin D Binding protein using anti-Vitamin D Binding protein antibody (A03364-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: human A431 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vitamin D Binding protein antigen affinity purified polyclonal antibody (Catalog # A03364-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vitamin D Binding protein at approximately 53KD. The expected band size for Vitamin D Binding protein is at 53KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03364-1-Vitamin-D-Binding-protein-primary-antibodies-IHC-testing-2.jpgAnti-Vitamin D Binding protein/GC Antibody Picoband® IHC analysis of Vitamin D Binding protein using anti-Vitamin D Binding protein antibody (A03364-1).<br>Vitamin D Binding protein was detected in paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Vitamin D Binding protein Antibody (A03364-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03364-1-Vitamin-D-Binding-protein-primary-antibodies-IHC-testing-3.jpgAnti-Vitamin D Binding protein/GC Antibody Picoband® IHC analysis of Vitamin D Binding protein using anti-Vitamin D Binding protein antibody (A03364-1).<br>Vitamin D Binding protein was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Vitamin D Binding protein Antibody (A03364-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03364-1-Vitamin-D-Binding-protein-primary-antibodies-IHC-testing-4.jpgAnti-Vitamin D Binding protein/GC Antibody Picoband® IHC analysis of Vitamin D Binding protein using anti-Vitamin D Binding protein antibody (A03364-1).<br>Vitamin D Binding protein was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Vitamin D Binding protein Antibody (A03364-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03364-1-Vitamin-D-Binding-protein-primary-antibodies-IHC-testing-5.jpgAnti-Vitamin D Binding protein/GC Antibody Picoband® IHC analysis of Vitamin D Binding protein using anti-Vitamin D Binding protein antibody (A03364-1).<br>Vitamin D Binding protein was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Vitamin D Binding protein Antibody (A03364-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-gsta1-a2-a3-a4-a5-picoband-trade-antibody-a01462-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-1-gsta1-5-primary-antibodies-wb-testing-1.jpgAnti-GSTA1/A2/A3/A4/A5 Antibody Picoband® Western blot analysis of GSTA1/A2/A3/A4/A5 using anti-GSTA1/A2/A3/A4/A5 antibody (A01462-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human HCCT tissue lysates,<br>
Lane 3: human HCCP tissue lysates,<br>
Lane 4: human HUH-7 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTA1/A2/A3/A4/A5 antigen affinity purified polyclonal antibody (Catalog # A01462-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GSTA1/A2/A3/A4/A5 at approximately 26 kDa. The expected band size for GSTA1/A2/A3/A4/A5 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-1-gsta1-5-primary-antibodies-ihc-testing-2.jpgAnti-GSTA1/A2/A3/A4/A5 Antibody Picoband® IHC analysis of GSTA1/A2/A3/A4/A5 using anti-GSTA1/A2/A3/A4/A5 antibody (A01462-1).<br> GSTA1/A2/A3/A4/A5 was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GSTA1/A2/A3/A4/A5 Antibody (A01462-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-1-gsta1-5-primary-antibodies-ihc-testing-3.jpgAnti-GSTA1/A2/A3/A4/A5 Antibody Picoband® IHC analysis of GSTA1/A2/A3/A4/A5 using anti-GSTA1/A2/A3/A4/A5 antibody (A01462-1).<br> GSTA1/A2/A3/A4/A5 was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GSTA1/A2/A3/A4/A5 Antibody (A01462-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-1-gsta1-5-primary-antibodies-ihc-testing-5.jpgAnti-GSTA1/A2/A3/A4/A5 Antibody Picoband® IHC analysis of GSTA1/A2/A3/A4/A5 using anti-GSTA1/A2/A3/A4/A5 antibody (A01462-1).<br> GSTA1/A2/A3/A4/A5 was detected in paraffin-embedded section of human liver cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GSTA1/A2/A3/A4/A5 Antibody (A01462-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-gst3-gst-pi-picoband-trade-antibody-a00394-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00394-gst3-primary-antibodies-wb-testing-1.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® Western blot analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse lung tissue lysates, <br>Lane 2: mouse testis tissue lysates,<br>Lane 3: rat spleen tissue lysates,<br>Lane 4: human A549 whole cell lysates,<br>Lane 5: human placenta tissue lysates,<br>Lane 6: human Hela whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GST3 / GST pi antigen affinity purified polyclonal antibody (Catalog # A00394) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GST3 / GST pi at approximately 23KD. The expected band size for GST3 / GST pi is at 23KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-GST3-primary-antibodies-IHC-testing-2.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394).<br>GST3 / GST pi was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-GST3-primary-antibodies-IHC-testing-3.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394).<br>GST3 / GST pi was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-GST3-primary-antibodies-IHC-testing-4.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394).<br>GST3 / GST pi was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-GST3-primary-antibodies-IHC-testing-5.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394).<br>GST3 / GST pi was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-gst3-gst-pi-picoband-trade-antibody-a00394-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00394-1-gst3-primary-antibodies-wb-testing-1_1.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® Western blot analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat stomach tissue lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse stomach tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GST3 / GST pi antigen affinity purified polyclonal antibody (Catalog # A00394-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GST3 / GST pi at approximately 25 kDa. The expected band size for GST3 / GST pi is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00394-1-gstp1-primary-antibodies-ihc-testing-4.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband®IHC analysis of GSTP1 using anti-GSTP1 antibody (A00394-1). <br>GSTP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GSTP1 Antibody (A00394-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-1-GST3-primary-antibodies-IHC-testing-2.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394-1).<br>GST3 / GST pi was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00394-1-GST3-primary-antibodies-IHC-testing-3.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IHC analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394-1).<br>GST3 / GST pi was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-GST3 / GST pi Antibody (A00394-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00394-1-gst3-primary-antibodies-if-testing-4.jpgAnti-GST3/GST pi/Gstp1 Antibody Picoband® IF analysis of GST3 / GST pi using anti-GST3 / GST pi antibody (A00394-1). <br>
GST3 / GST pi was detected in an immunocytochemical section of NRK cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GST3 / GST pi Antibody (A00394-1) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-gstt1-picoband-trade-antibody-a01084-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01084-gstt1-primary-antibodies-wb-testing-1.jpgAnti-GSTT1 Antibody Picoband® Western blot analysis of GSTT1 using anti-GSTT1 antibody (A01084). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat lung tissue lysates,<br>Lane 3: mouse liver tissue lysates,<br>Lane 4: mouse lung tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTT1 antigen affinity purified polyclonal antibody (Catalog # A01084) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GSTT1 at approximately 27KD. The expected band size for GSTT1 is at 27KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hbd-picoband-trade-antibody-a01076-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01076-hbd-primary-antibodies-wb-testing-1.jpgAnti-HBD Antibody Picoband® Western blot analysis of HBD using anti-HBD antibody (A01076). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: rat spleen tissue lysates,<br>Lane 3: mouse spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBD antigen affinity purified polyclonal antibody (Catalog # A01076) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HBD at approximately 16KD. The expected band size for HBD is at 16KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01076-hbd-primary-antibodies-wb-testing-2.jpgAnti-HBD Antibody Picoband® Western blot analysis of HBD using anti-HBD antibody (A01076). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBD antigen affinity purified polyclonal antibody (Catalog # A01076) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HBD at approximately 16KD. The expected band size for HBD is at 16KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-3.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-4.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-5.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-6.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-7.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01076-HBD-primary-antibodies-IHC-testing-8.jpgAnti-HBD Antibody Picoband® IHC analysis of HBD using anti-HBD antibody (A01076).<br>HBD was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HBD Antibody (A01076) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-ibsp-picoband-trade-antibody-a03183-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03183-ibsp-primary-antibodies-wb-testing-1.jpgAnti-IBSP Antibody Picoband® Western blot analysis of IBSP using anti-IBSP antibody (A03183). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IBSP antigen affinity purified polyclonal antibody (Catalog # A03183) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IBSP at approximately 65 kDa. The expected band size for IBSP is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-igf1-receptor-picoband-trade-antibody-a00070-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00070-igf1_receptor-primary-antibodies-wb-testing-1.jpgAnti-IGF1 Receptor/Igf1r Antibody Picoband® Western blot analysis of IGF1 Receptor using anti-IGF1 Receptor antibody (A00070). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse liver tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGF1 Receptor antigen affinity purified polyclonal antibody (Catalog # A00070) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGF1 Receptor at approximately 155KD. The expected band size for IGF1 Receptor is at 155KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00070-41598_2017_article_bfsrep44473_fig4_html.jpgAnti-IGF1 Receptor/Igf1r Antibody Picoband®Overexpression of decorin activated the IGF1R-AKT-AP-1 pathway. ( A , B ) The phosphorylation of AKT was decreased by HG treatment in a time-dependent manner. ( C – E ) The expression of IGF1R, Bcl2, and Bax and the phosphorylation of AKT. ( F , G ) The phosphorylation of AP-1. All data are presented as the mean ± SEM. *p < 0.05; **p < 0.01. # p < 0.05, compared to Con. & p < 0.05, && p < 0.01, compared to HG + GFP. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fsrep44473'>28290552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00070-41598_2017_article_bfsrep44473_fig6_html.jpgAnti-IGF1 Receptor/Igf1r Antibody Picoband®The IGF1R antibody (αIGF1R) blocked the effects induced by overexpression of decorin. ( A , B ) The tube formation test; the photographs were taken at a magnification of 100×. ( C , D ) The cell wound healing test; the photographs were taken at a magnification of 100×. ( E , F ) The apoptosis assay. ( G ) CCK8 assessment. ( H , I ) The expression of VEGF, Bcl2, and Bax and the phosphorylation of AKT and AP 1. All data are presented as the mean ± SEM. *p < 0.05; **p < 0.01. # p < 0.05, ## p < 0.01, compared to Con. & p < 0.05, && p < 0.01, compared to HG + GFP. $ p < 0.05, $$ p < 0.01, compared to HG + DCN. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fsrep44473'>28290552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00070-IGF1-Receptor-primary-antibodies-IHC-testing-2.jpgAnti-IGF1 Receptor/Igf1r Antibody Picoband® IHC analysis of IGF1 Receptor using anti-IGF1 Receptor antibody (A00070).<br>IGF1 Receptor was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGF1 Receptor Antibody (A00070) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00070-IGF1-Receptor-primary-antibodies-IHC-testing-3.jpgAnti-IGF1 Receptor/Igf1r Antibody Picoband® IHC analysis of IGF1 Receptor using anti-IGF1 Receptor antibody (A00070).<br>IGF1 Receptor was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGF1 Receptor Antibody (A00070) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp1-picoband-trade-antibody-a00922-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/i/g/igfbp1-primary-antibodies-a00922-1-wb-testing-1.jpgAnti-IGFBP1 Antibody Picoband® Western blot analysis of IGFBP1 using anti-IGFBP1 antibody (A00922-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: rat liver tissue lysates, <br> Lane 2: mouse liver tissue lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP1 antigen affinity purified polyclonal antibody (Catalog # A00922-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP1 at approximately 30KD. The expected band size for IGFBP1 is at 28KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00922-1-IGFBP1-primary-antibodies-IHC-testing-2.jpgAnti-IGFBP1 Antibody Picoband® IHC analysis of IGFBP1 using anti-IGFBP1 antibody (A00922-1).<br>IGFBP1 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP1 Antibody (A00922-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00922-1-IGFBP1-primary-antibodies-IHC-testing-3.jpgAnti-IGFBP1 Antibody Picoband® IHC analysis of IGFBP1 using anti-IGFBP1 antibody (A00922-1).<br>IGFBP1 was detected in paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP1 Antibody (A00922-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00922-1-IGFBP1-primary-antibodies-IHC-testing-4.jpgAnti-IGFBP1 Antibody Picoband® IHC analysis of IGFBP1 using anti-IGFBP1 antibody (A00922-1).<br>IGFBP1 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP1 Antibody (A00922-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00922-1-IGFBP1-primary-antibodies-IHC-testing-5.jpgAnti-IGFBP1 Antibody Picoband® IHC analysis of IGFBP1 using anti-IGFBP1 antibody (A00922-1).<br>IGFBP1 was detected in paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP1 Antibody (A00922-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp2-picoband-trade-antibody-a01373-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01373-1-igfbp2-primary-antibodies-wb-testing-1_1.jpgAnti-IGFBP2 Antibody Picoband® Western blot analysis of IGFBP2 using anti-IGFBP2 antibody (A01373-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human T-47D whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP2 antigen affinity purified polyclonal antibody (Catalog # A01373-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP2 at approximately 35 kDa. The expected band size for IGFBP2 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01373-1-IGFBP2-primary-antibodies-IHC-testing-2.jpgAnti-IGFBP2 Antibody Picoband® IHC analysis of IGFBP2 using anti-IGFBP2 antibody (A01373-1).<br>IGFBP2 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP2 Antibody (A01373-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01373-1-IGFBP2-primary-antibodies-IHC-testing-3.jpgAnti-IGFBP2 Antibody Picoband® IHC analysis of IGFBP2 using anti-IGFBP2 antibody (A01373-1).<br>IGFBP2 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IGFBP2 Antibody (A01373-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01373-1-igfbp2-primary-antibodies-elisa-testing-4.jpgAnti-IGFBP2 Antibody Picoband® Sandwich ELISA - Recombinant human IGFBP2 protein standard curve.<br>
Use in combination with reagents from Human IGFBP2 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0384).
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp3-picoband-trade-antibody-a00435-2-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00435-2-IGFBP3-primary-antibodies-WB-testing-1.jpgAnti-IGFBP3 Antibody Picoband® Western blot analysis of IGFBP3 using anti-IGFBP3 antibody (A00435-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human IGFBP3 protein 1ng. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP3 antigen affinity purified polyclonal antibody (Catalog # A00435-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP3 at approximately 37KD. The expected band size for IGFBP3 is at 29KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00435-2-igfbp3-primary-antibodies-elisa-testing-2_1.jpgAnti-IGFBP3 Antibody Picoband® Sandwich ELISA - Recombinant human IGFBP3 protein standard curve.<br>
Use in combination with reagents from Human IGFBP3 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0386).
https://www.bosterbio.com/products/primary-antibodies/anti-igfbp3-picoband-trade-antibody-a00435-3-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00435-3-igfbp3-primary-antibodies-wb-testing-1.jpgAnti-IGFBP3 Antibody Picoband® Western blot analysis of IGFBP3 using anti-IGFBP3 antibody (A00435-3). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFBP3 antigen affinity purified polyclonal antibody (Catalog # A00435-3) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFBP3 at approximately 40KD. The expected band size for IGFBP3 is at 32KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il1-beta-picoband-trade-antibody-a00101-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00101-1-il1-beta-primary-antibodies-wb-testing-1.jpgAnti-IL1 beta/Il1b Antibody Picoband® Western blot analysis of IL1 beta using anti-IL1 beta antibody (A00101-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse RAW264.7(-LPS) whole cell lysates, <br>
Lane 2: mouse RAW264.7(+LPS) whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1 beta antigen affinity purified polyclonal antibody (Catalog # A00101-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL1 beta at approximately 36 kDa. The expected band size for IL1 beta is at 31 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-il1f10-picoband-trade-antibody-a09268-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09268-1-il1f10-primary-antibodies-wb-testing-1.jpgAnti-IL1F10 Antibody Picoband® Western blot analysis of IL1F10 using anti-IL1F10 antibody (A09268-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human U87MG whole cell lysates,<br>Lane 2: human placenta tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1F10 antigen affinity purified polyclonal antibody (Catalog # A09268-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL1F10 at approximately 17KD. The expected band size for IL1F10 is at 17KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09268-1-il1f10-primary-antibodies-ihc-testing-2.jpgAnti-IL1F10 Antibody Picoband® IHC analysis of IL1F10 using anti-IL1F10 antibody (A09268-1).<br> IL1F10 was detected in paraffin-embedded section of human tonsil tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL1F10 Antibody (A09268-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-il11-picoband-trade-antibody-a01160-1-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01160-1-il11-primary-antibodies-wb-testing-1.jpgAnti-IL11 Antibody Picoband® Western blot analysis of IL11 using anti-IL11 antibody (A01160-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL11 antigen affinity purified polyclonal antibody (Catalog # A01160-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL11 at approximately 21KD. The expected band size for IL11 is at 21KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il12b-picoband-trade-antibody-a01152-2-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01152-2-il12b-primary-antibodies-wb-testing-1.jpgAnti-IL12B Antibody Picoband® Western blot analysis of IL12B using anti-IL12B antibody (A01152-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL12B antigen affinity purified polyclonal antibody (Catalog # A01152-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL12B at approximately 37-45KD. The expected band size for IL12B is at 37KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il12b-picoband-trade-antibody-a01152-3-boster.html2026-03-24T05:11:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01152-3-il12b-primary-antibodies-wb-testing-1.jpgAnti-IL12B Antibody Picoband® Western blot analysis of IL12B using anti-IL12B antibody (A01152-3). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL12B antigen affinity purified polyclonal antibody (Catalog # A01152-3) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL12B at approximately 37-45KD. The expected band size for IL12B is at 37KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01152-3-12931_2023_2557_fig3_html.pngAnti-IL12B Antibody Picoband®IL-25 inhibited the production of IL-12, IL-23 in amouse model of of neutrophilia-dominant airway inflammation. ( A - D ) Measurement of Il12a , Il12b , Il23a and Il25 mRNA levels in mouse lung tissue using RT-PCR. ( E ) Representative images of IL-12B and CD80 immunofluorescence staining in mouse lung sections. Scale bar, 50 μm. ( F ) The proportion of CD80 staining-positive cells in mouse lung sections in different groups. ( G ) The proportion of IL-12B staining-positive cells in mouse lung sections in different groups. ( H ) The proportion of CD80 and IL-12B staining-positive cells in mouse lung sections in different groups. There were 4–6 mice in each group. One-way ANOVA was used for statistical analysis (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01152-3-12931_2023_2557_fig4_html.pngAnti-IL12B Antibody Picoband®Exogenous IL-25 inhibited LPS-induced M1 polarization and the expression of IL-12 and IL-23 in mouse pulmonary cells. ( A ) Representative Western blots showing IL-12 A and β-Tubulin protein in primary culture of mouse pulmonary macrophages. ( B ) Quantitative analysis of IL-12 A in mouse pulmonary macrophages using ImageJ. Values are expressed in arbitrary units (a.u.). ( C ) Representative Western blots showing IL-12B, IL-23 A, and β-Tubulin protein in mouse pulmonary macrophages. ( D - E ) Quantitative analysis IL-12B, and IL-23A in mouse pulmonary macrophages using ImageJ. ( F - J ) Detection of Il12a, Il12b, Il23a, Cd80 , and Il-1β mRNA level in mouse pulmonary macrophages using RT-PCR. The experiment was repeated 3 times independently, and a similar trend was obtained. One-way ANOVA was used for statistical analysis (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01152-3-12931_2023_2557_fig6_html.pngAnti-IL12B Antibody Picoband®The expression of IL-25 was decreased whereas IL-12, IL-23, and M1 macrophage markers were increased in severe of non-eosinophilic asthmatics. ( A ) IL-25 protein levels were decreased in sputum from a cohort of non-smoker severe asthma in the U-BIOPRED study. Based on the analysis of the data provided by Takahashi et al. [ ], 158 downregulated and 187 upregulated proteins were identified in the supernatant of induced sputum from non-smoker severe asthma patients (n = 37) compared to controls (n = 18) by proteomic assay and were shown in the volcano plot. The protein level of IL-25 (indicated by the red arrow) was decreased in the supernatant of induced sputum from non-smoker severe asthma patients compared to controls (log2 of fold change = -0.274, P = 0.019). ( B ) Detection of IL-25 mRNA level in airway brushings of eosinophilic asthma (n = 20) and non-eosinophilic asthma (n = 14) by RT-PCR. ( C - E ) Detection of IL-12 A, IL-12B and IL-23 A mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. ( F - J ) Detection of I L-1β, IFN-γ, CD80, iNOS , and CD206 mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. ( K ) Representative images of IL-12B and CD80 immunofluorescence staining in BALF cells of control, eosinophilic asthma, and non-eosinophilic asthma. Scale bar, 5 μm. ( L ) Detection of IL-25 mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. One way ANOVA was used for statistical analysis. (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01152-3-IL12B-primary-antibodies-IHC-testing-2.jpgAnti-IL12B Antibody Picoband® IHC analysis of IL12B using anti-IL12B antibody (A01152-3).<br>IL12B was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IL12B Antibody (A01152-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-il15ra-picoband-trade-antibody-a03016-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-1-il15ra-primary-antibodies-wb-testing-1.jpgAnti-IL15RA Antibody Picoband® Western blot analysis of IL15RA using anti-IL15RA antibody (A03016-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL15RA antigen affinity purified polyclonal antibody (Catalog # A03016-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL15RA at approximately 28KD. The expected band size for IL15RA is at 28KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03016-1-IL15RA-primary-antibodies-IHC-testing-2.jpgAnti-IL15RA Antibody Picoband® IHC analysis of IL15RA using anti-IL15RA antibody (A03016-1).<br>IL15RA was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IL15RA Antibody (A03016-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03016-1-IL15RA-primary-antibodies-IHC-testing-3.jpgAnti-IL15RA Antibody Picoband® IHC analysis of IL15RA using anti-IL15RA antibody (A03016-1).<br>IL15RA was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IL15RA Antibody (A03016-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-1-il15ra-primary-antibodies-if-testing-4.jpgAnti-IL15RA Antibody Picoband® IF analysis of IL15RA using anti-IL15RA antibody (A03016-1). <br>
IL15RA was detected in immunocytochemical section of K562 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-IL15RA Antibody (A03016-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-1-il15ra-primary-antibodies-fcm-testing-5_1.jpgAnti-IL15RA Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-IL15RA antibody (A03016-1).<br>Overlay histogram showing K562 cells stained with A03016-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IL15RA Antibody (A03016-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03016-1-il15ra-primary-antibodies-elisa-testing-6.jpgAnti-IL15RA Antibody Picoband® Sandwich ELISA - Recombinant human IL15RA protein standard curve.<br>
Use in combination with reagents from Human IL15RA ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1663).
https://www.bosterbio.com/products/primary-antibodies/anti-il17b-picoband-trade-antibody-a10846-2-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10846-2-il17b-primary-antibodies-wb-testing-1.jpgAnti-IL17B Antibody Picoband® Western blot analysis of IL17B using anti-IL17B antibody (A10846-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates,<br>Lane 2: human COLO-320 whole cell lysates,<br>Lane 3: human Hela whole cell lysates,<br>Lane 4: human SGC-7901 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17B antigen affinity purified polyclonal antibody (Catalog # A10846-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17B at approximately 17KD. The expected band size for IL17B is at 20KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il17f-picoband-trade-antibody-a02062-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02062-1-il17f-primary-antibodies-wb-testing-1.jpgAnti-IL17F Antibody Picoband®Western blot analysis of IL17F using anti-IL17F antibody (A02062-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: rat small intestine lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: mouse small intestine lysates,<br>
Lane 7: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17F antigen affinity purified polyclonal antibody (A02062-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL17F at approximately 27-30 kDa. The expected band size for IL17F is at 18 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-il17f-picoband-trade-antibody-a02062-2-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02062-2-IL17F-primary-antibodies-WB-testing-1.jpgAnti-IL17F Antibody Picoband® Western blot analysis of IL17F using anti-IL17F antibody (A02062-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse thymus tissue lysates,<br>Lane 3: mouse NIH3T3 whole cell lysates,<br>Lane 4: mouse SP20 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17F antigen affinity purified polyclonal antibody (Catalog # A02062-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17F at approximately 30KD. The expected band size for IL17F is at 18KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02062-2-il17f-primary-antibodies-elisa-testing-2.jpgAnti-IL17F Antibody Picoband® Sandwich ELISA - Recombinant mouse IL17F protein standard curve.<br>
Use in combination with reagents from Mouse IL17F ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0796).
https://www.bosterbio.com/products/primary-antibodies/anti-il17f-picoband-trade-antibody-a02062-3-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02062-3-il17f-primary-antibodies-wb-testing-1.jpgAnti-IL17F Antibody Picoband® Western blot analysis of IL17F using anti-IL17F antibody (A02062-3). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17F antigen affinity purified polyclonal antibody (Catalog # A02062-3) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17F at approximately 30KD. The expected band size for IL17F is at 18KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il22-picoband-trade-antibody-a00963-2-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00963-2-IL22-primary-antibodies-WB-testing-1.jpgAnti-IL22 Antibody Picoband® Western blot analysis of IL22 using anti-IL22 antibody (A00963-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human placenta tissue lysates,<br>Lane 3: rat thymus tissue lysates,<br>Lane 4: mouse thymus tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL22 antigen affinity purified polyclonal antibody (Catalog # A00963-2) at 0.5 ug/mL overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL22 at approximately 20KD. The expected band size for IL22 is at 20KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il23-receptor-picoband-trade-antibody-a00607-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00607-1-il23_receptor-primary-antibodies-wb-testing-1.jpgAnti-IL23 Receptor/Il23r Antibody Picoband® Western blot analysis of IL23 Receptor using anti-IL23 Receptor antibody (A00607-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse brain tissue lysates,<br>Lane 2: mouse liver tissue lysates,<br>Lane 3: mouse kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL23 Receptor antigen affinity purified polyclonal antibody (Catalog # A00607-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL23 Receptor at approximately 58KD. The expected band size for IL23 Receptor is at 72KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00607-1-il23r-primary-antibodies-elisa-testing-2.jpgAnti-IL23 Receptor/Il23r Antibody Picoband® Sandwich ELISA - Recombinant mouse IL23 Receptor/Il23r protein standard curve.<br>
Use in combination with reagents from Mouse IL23 Receptor/Il23r ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1613)
https://www.bosterbio.com/products/primary-antibodies/anti-il33-picoband-trade-antibody-a00113-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-il33-primary-antibodies-wb-testing-1.jpgAnti-IL33 Antibody Picoband® Western blot analysis of IL33 using anti-IL33 antibody (A00113). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.<br>
Lane 1: recombinant human IL33 protein 1ng. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL33 antigen affinity purified polyclonal antibody (Catalog # A00113) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL33 at approximately 18KD. The expected band size for IL33 is at 18KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-fmed-10-1168359-g004.jpgAnti-IL33 Antibody Picoband®Immunohistochemistry analysis of TNF-α, PPAR-γ, IL-6, and IL-33 in lesional and non-lesional skin samples of patients with dermatomyositis. (A) TNF-α: Left panel: Expression of TNF-α in lesional and non-lesional dermatomyositis skin samples. The cytoplasmic expression is similar in the keratinocytes, dendritic cells (black arrow), and endothelial cells (empty arrow). Top right and left corners: Negative controls were obtained by omitting the primary antibody. Right panel: Statistical analysis of semi-quantitative measurements; (independent sample t -test; p > 0.1). (B) PPAR-γ: Left panel: Expression of PPAR-γ in lesional and non-lesional dermatomyositis skin samples. There is no difference between the lesional and non-lesional DM skin samples in the expression of the PPAR-γ. Empty arrow: endothelial cells. Black arrow: dendritic cells. Top right and left corners: Negative controls were obtained by omitting the primary antibody. Right panel: Statistical analysis of semi-quantitative measurements; (independent sample t -test; p > 0.1). (C) IL-6: Left panel: Expression of IL-6 in lesional and non-lesional dermatomyositis skin samples. Strong cytoplasmic/nuclear reaction with IL-6 in the epidermal endothelial (empty arrow) and dendritic cells (black arrow). Top right and left corners: Negative controls were obtained by omitting the primary antibody. Right panel: Statistical analysis of semi-quantitative measurements; (independent sample t -test; p > 0.1). (D) IL-33: Expression of IL-33 in lesional and non-lesional dermatomyositis skin samples. Positive reaction was detected in the nucleus of endothelial cells with IL-33, but there was no significant difference between lesional and non-lesional DM skin samples. Top right and left corners: Negative controls were obtained by omitting the primary antibody. Right panel: Statistical analysis of semi-quantitative measurements; (independent sample t -test; p > 0.1).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2023.1168359/full'>37250649</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00113-IL33-primary-antibodies-IHC-testing-2.jpgAnti-IL33 Antibody Picoband® IHC analysis of IL33 using anti-IL33 antibody (A00113).<br>IL33 was detected in paraffin-embedded section of human tonsil . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-IL33 Antibody (A00113) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-il33-primary-antibodies-elisa-testing-3_1.jpgAnti-IL33 Antibody Picoband® Sandwich ELISA - Recombinant human IL33 protein standard curve.<br>
Use in combination with reagents from Human IL33 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0929).
https://www.bosterbio.com/products/primary-antibodies/anti-il33-picoband-trade-antibody-a00113-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-1-il33-primary-antibodies-wb-testing-1_1.jpgAnti-IL33 Antibody Picoband®Western blot analysis of IL33 using anti-IL33 antibody (A00113-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat lung tissue lysates,<br>
Lane 2: mouse lung tissue lysates,<br>
Lane 3: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL33 antigen affinity purified polyclonal antibody (A00113-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL33 at approximately 35 kDa. The expected band size for IL33 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-1-il33-primary-antibodies-ihc-testing-1.jpgAnti-IL33 Antibody Picoband®IHC analysis of IL33 using anti-IL33 antibody (A00113-1). <br>IL33 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL33 Antibody (A00113-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-1-il33-primary-antibodies-ihc-testing-2_1.jpgAnti-IL33 Antibody Picoband®IHC analysis of IL33 using anti-IL33 antibody (A00113-1). <br>IL33 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL33 Antibody (A00113-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-il36-alpha-picoband-trade-antibody-a09802-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09802-1-IL36-alpha-primary-antibodies-WB-testing-1.jpgAnti-IL36 alpha/IL36A Antibody Picoband® Western blot analysis of IL36 alpha using anti-IL36 alpha antibody (A09802-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates, <br>Lane 2: human K562 whole cell lysates,<br>Lane 3: human Raji whole cell lysates,<br>Lane 4: rat thymus tissue lysates,<br>Lane 5: mouse thymus tissue lysates.<br> <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL36 alpha antigen affinity purified polyclonal antibody (Catalog # A09802-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL36 alpha at approximately 25KD. The expected band size for IL36 alpha is at 17KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-2-picoband-trade-antibody-a00901-2-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-2-vegfr2-primary-antibodies-wb-testing-1.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband® Western blot analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: human PC-3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF Receptor 2 antigen affinity purified polyclonal antibody (Catalog # A00901-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF Receptor 2 at approximately 180-250 kDa. The expected band size for VEGF Receptor 2 is at 156 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-2-ijbsv16p0272g001.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband®Tumor necrosis factor-α induced protein 8 (TIPE) and vascular endothelial growth factor receptor 2 (VEGFR2) are highly expressed in CRC and act as oncogenes. (a) TIPE expression in five pairs of fresh human CRC tumor tissues and matched adjacent tissues analyzed by immunohistochemistry staining. (b) Representative results of TIPE expression in five pairs of fresh CRC tumor tissues and adjacent tissues as detected by Western blot; T indicates tumor tissue, and N indicates normal tissue. (c) Comparison of TIPE mRNA expression levels in human CRC tissues and matched adjacent tissues. TIPE mRNA expression was quantified by qRT-PCR and normalized to that in the matched adjacent normal tissues. (d) Through immunohistochemical staining, VEGFR2 expression was analyzed in five randomly selected pairs of CRC tumor tissues and matched adjacent tissues. (e) Comparison of VEGFR2 mRNA expression levels in human CRC tissues and matched adjacent tissues. VEGFR2 mRNA expression was quantified by qRT-PCR and normalized to that in the matched adjacent normal tissues.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6949158/&orig_host=www.ncbi.nlm.nih.gov'>31929755</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-2-ijbsv16p0272g002.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband®Knockdown of TIPE downregulates VEGFR2 expression and inhibits cell proliferation, cell migration and angiogenesis. (a) qRT-PCR of TIPE expression in HCT116 cells infected with lentiviral shTIPE or control shRNA. TIPE mRNA expression was quantified by qRT-PCR and normalized to that in the shRNA control cells. (b) TIPE expression in HCT116 cells infected with lentiviral shTIPE or control shRNA according to Western blot analysis. (c) Expression of VEGFR2 in shTIPE and shRNA control HCT116 cells based on qRT-PCR assays. (d) Tumor cell culture conditioned medium (TCM) from HCT116 cells stably transduced with shTIPE or control shRNA inhibited the proliferation of HUVECs as determined by CCK-8 assays. (e) Representative immunofluorescence (IF) images demonstrated that the level of TIPE has an effect on the expression of microfilaments and initial pseudopod extension in the stably transduced HCT116 cell lines. Scale bar, 50 µm. (f) Representative images (left panel) and quantification (right panel) of tube formation of HUVECs treated with TCM derived from control HCT116 cells or HCT116 cells with stable TIPE knockdown. The data were collected from four independent experiments using different batches of cells. Scale bar, 500 μm. **p <0.01, ***p<0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6949158/&orig_host=www.ncbi.nlm.nih.gov'>31929755</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-2-ijbsv16p0272g004.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband®TIPE promotes VEGFR2-mediated angiogenesis by upregulating PDK1 expression and phosphorylation. (a) TIPE knockdown in HCT116 cells inhibits PDK1 phosphorylation according to Western blot analysis. (b) After cells were treated with a PDK1 inhibitor (GSK2334470), the expression levels of TIPE and PDK1 and their corresponding phosphorylation levels were detected by Western blot analysis. (c) After cells were treated with GSK2334470 and DMSO, the expression levels of VEGFR2 were tested and verified by Western blot analysis. (d) The proliferation of HUVECs cultured with TCM in the presence of GSK2334470 was determined by CCK-8 assays. (e) Tube formation by HUVECs treated with GSK2334470 was measured, and the results are expressed as the tubule length. Representative statistical results are shown. (f) Representative morphological images are shown. Scale bar, 500 µm. ns: no significance, **p <0.01, ***p<0.001. (g) Schematic diagram representing the role of TIPE and VEGFR2 in tumor angiogenesis in CRC.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6949158/&orig_host=www.ncbi.nlm.nih.gov'>31929755</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-2-VEGF-Receptor-2--primary-antibodies-IHC-testing-2.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-2).<br>VEGF Receptor 2 was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-2-VEGF-Receptor-2--primary-antibodies-IHC-testing-3.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-2).<br>VEGF Receptor 2 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-2-VEGF-Receptor-2--primary-antibodies-IHC-testing-4.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-2).<br>VEGF Receptor 2 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-2-VEGF-Receptor-2--primary-antibodies-IHC-testing-5.jpgAnti-VEGF Receptor 2/KDR Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-2).<br>VEGF Receptor 2 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-scf-picoband-trade-antibody-a01254-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01254-1-scf-primary-antibodies-wb-testing-1.jpgAnti-SCF/KITLG Antibody Picoband®Western blot analysis of SCF/KITLG using anti-SCF/KITLG antibody (A01254-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human CACO-2 whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCF/KITLG antigen affinity purified polyclonal antibody (Catalog # A01254-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SCF/KITLG at approximately 45 kDa. The expected band size for SCF/KITLG is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01254-1-scf-primary-antibodies-ihc-testing-1.jpgAnti-SCF/KITLG Antibody Picoband®IHC analysis of SCF/KITLG using anti-SCF/KITLG antibody (A01254-1. <br>SCF/KITLG was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCF/KITLG Antibody (A01254-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01254-1-scf-primary-antibodies-if-testing-1.jpgAnti-SCF/KITLG Antibody Picoband®IF analysis of SCF/KITLG using anti-SCF/KITLG antibody (A01254-1). <br>
SCF/KITLG was detected in an immunocytochemical section of CACO-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SCF/KITLG Antibody (A01254-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-lbp-picoband-trade-antibody-a00809-2-boster.html2026-04-01T05:01:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00809-2-LBP-primary-antibodies-WB-testing-1.jpgAnti-LBP Antibody Picoband® Western blot analysis of LBP using anti-LBP antibody (A00809-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human LBP protein 1ng. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LBP antigen affinity purified polyclonal antibody (Catalog # A00809-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LBP at approximately 65KD. The expected band size for LBP is at 51KD.
https://www.bosterbio.com/products/primary-antibodies/anti-lbp-picoband-trade-antibody-a00809-3-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/l/b/lbp-primary-antibodies-a00809-3-wb-testing-1.jpgAnti-LBP Antibody Picoband® Western blot analysis of LBP using anti-LBP antibody (A00809-3). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human Hela whole cell lysates, <br> Lane 2: human Jurkat whole cell lysates, <br> Lane 3: human A549 whole cell lysates, <br> Lane 4: human Raji whole cell lysates, <br> Lane 5: rat liver tissue lysates, <br> Lane 6: mouse liver tissue lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LBP antigen affinity purified polyclonal antibody (Catalog # A00809-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LBP at approximately 65KD. The expected band size for LBP is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-galectin-1-picoband-trade-antibody-a00470-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-wb-testing-1.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®Western blot analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Electrophoresis was performed on a 13% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human A549 whole cell lysates, <br>
Lane 3: human A375 whole cell lysates, <br>
Lane 4: human MCF-7 whole cell lysates, <br>
Lane 5: rat kidney tissue lysates, <br>
Lane 6: rat PC-12 whole cell lysates, <br>
Lane 7: mouse kidney tissue lysates, <br>
Lane 8: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Galectin 1 antigen affinity purified polyclonal antibody (A00470) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Galectin 1 at approximately 15 kDa. The expected band size for Galectin 1 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-ihc-testing-1.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Galectin 1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Galectin 1 Antibody (A00470) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-ihc-testing-2.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Galectin 1 was detected in a paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Galectin 1 Antibody (A00470) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-ihc-testing-3.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Galectin 1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Galectin 1 Antibody (A00470) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-ihc-testing-4.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Galectin 1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Galectin 1 Antibody (A00470) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-if-testing-1.jpgAnti-Galectin 1/Lgals1 Antibody Picoband®IF analysis of Galectin 1 using anti-Galectin 1 antibody (A00470). <br>Galectin 1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Galectin 1 Antibody (A00470) overnight at 4°C. Fluoro594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-galectin-1-primary-antibodies-elisa-testing-5.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® Sandwich ELISA - Recombinant mouse Galectin 1/Lgals1 protein standard curve.<br>
Use in combination with reagents from Mouse Galectin 1/Lgals1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0763).
https://www.bosterbio.com/products/primary-antibodies/anti-galectin-1-picoband-trade-antibody-a00470-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00470-1-Galectin-1-primary-antibodies-WB-testing-1.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® Western blot analysis of Galectin 1 using anti-Galectin 1 antibody (A00470-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates, <br>Lane 2: rat ovary tissue lysates,<br>Lane 3: rat testis tissue lysates,<br>Lane 4: mouse kidney tissue lysates,<br>Lane 5: human Hela whole cell lysates.<br> <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Galectin 1 antigen affinity purified polyclonal antibody (Catalog # A00470-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Galectin 1 at approximately 15KD. The expected band size for Galectin 1 is at 15KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00470-1-Galectin-1-primary-antibodies-IHC-testing-2.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470-1).<br>Galectin 1 was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Galectin 1 Antibody (A00470-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00470-1-Galectin-1-primary-antibodies-IHC-testing-3.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470-1).<br>Galectin 1 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Galectin 1 Antibody (A00470-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00470-1-Galectin-1-primary-antibodies-IHC-testing-4.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470-1).<br>Galectin 1 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Galectin 1 Antibody (A00470-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00470-1-Galectin-1-primary-antibodies-IHC-testing-5.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® IHC analysis of Galectin 1 using anti-Galectin 1 antibody (A00470-1).<br>Galectin 1 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Galectin 1 Antibody (A00470-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-1-galectin-1-primary-antibodies-elisa-testing-6.jpgAnti-Galectin 1/Lgals1 Antibody Picoband® Sandwich ELISA - Recombinant rat Galectin 1/Lgals1 protein standard curve.<br>
Use in combination with reagents from Rat Galectin 1/Lgals1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1589).
https://www.bosterbio.com/products/primary-antibodies/anti-mbl2-picoband-trade-antibody-a01000-2-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-2-mbl2-primary-antibodies-wb-testing-1_1.jpgAnti-MBL2 Antibody Picoband®Western blot analysis of MBL2 using anti-MBL2 antibody (A01000-2). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MBL2 antigen affinity purified polyclonal antibody (A01000-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MBL2 at approximately 26 kDa. The expected band size for MBL2 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01000-2-mbl2-primary-antibodies-ihc-testing-2.jpgAnti-MBL2 Antibody Picoband® IHC analysis of MBL2 using anti-MBL2 antibody (A01000-2). <br> MBL2 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MBL2 Antibody (A01000-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-med8-picoband-trade-antibody-a08094-1-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08094-1-med8-primary-antibodies-wb-testing-1_1.jpgAnti-MED8 Antibody Picoband® Western blot analysis of MED8 using anti-MED8 antibody (A08094-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human U251 whole cell lysates, <br>
Lane 4: human Caco-2 whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat liver tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED8 antigen affinity purified polyclonal antibody (Catalog # A08094-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED8 at approximately 29 kDa. The expected band size for MED8 is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A08094-1-MED8-primary-antibodies-IHC-testing-2.jpgAnti-MED8 Antibody Picoband® IHC analysis of MED8 using anti-MED8 antibody (A08094-1).<br>MED8 was detected in paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED8 Antibody (A08094-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A08094-1-MED8-primary-antibodies-IHC-testing-3.jpgAnti-MED8 Antibody Picoband® IHC analysis of MED8 using anti-MED8 antibody (A08094-1).<br>MED8 was detected in paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED8 Antibody (A08094-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08094-1-med8-primary-antibodies-if-testing-4.jpgAnti-MED8 Antibody Picoband® IF analysis of MED8 and Tubulin beta using anti-MED8 antibody (A08094-1) and anti-Tubulin beta antibody (M03989-3).
MED8 and Tubulin beta were detected in immunocytochemical section of U87 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-MED8 antibody (A08094-1) and mouse anti-Tubulin beta Antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08094-1-med8-primary-antibodies-fcm-testing-5.pngAnti-MED8 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MED8 antibody (A08094-1). <br>
Overlay histogram showing 293T cells stained with A08094-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED8 Antibody (A08094-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-med9-picoband-trade-antibody-a12781-boster.html2026-03-24T05:11:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-WB-testing-1.jpgAnti-MED9 Antibody Picoband® Western blot analysis of MED9 using anti-MED9 antibody (A12781). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates, <br>Lane 2: rat heart tissue lysates,<br>Lane 3: rat kidney tissue lysates,<br>Lane 4: mouse brain tissue lysates,<br>Lane 5: mouse heart tissue lysates,<br>Lane 6: mouse kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED9 antigen affinity purified polyclonal antibody (Catalog # A12781) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED9 at approximately 19KD. The expected band size for MED9 is at 16KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-IHC-testing-2.jpgAnti-MED9 Antibody Picoband® IHC analysis of MED9 using anti-MED9 antibody (A12781).<br>MED9 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED9 Antibody (A12781) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-IHC-testing-3.jpgAnti-MED9 Antibody Picoband® IHC analysis of MED9 using anti-MED9 antibody (A12781).<br>MED9 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED9 Antibody (A12781) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-IHC-testing-4.jpgAnti-MED9 Antibody Picoband® IHC analysis of MED9 using anti-MED9 antibody (A12781).<br>MED9 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED9 Antibody (A12781) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-IHC-testing-5.jpgAnti-MED9 Antibody Picoband® IHC analysis of MED9 using anti-MED9 antibody (A12781).<br>MED9 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED9 Antibody (A12781) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A12781-MED9-primary-antibodies-IHC-testing-6.jpgAnti-MED9 Antibody Picoband® IHC analysis of MED9 using anti-MED9 antibody (A12781).<br>MED9 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED9 Antibody (A12781) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12781-med9-primary-antibodies-if-testing-7.jpgAnti-MED9 Antibody Picoband® IF analysis of MED9 using anti-MED9 antibody (A12781). <br>
MED9 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MED9 Antibody (A12781) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12781-med9-primary-antibodies-fcm-testing-8.pngAnti-MED9 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MED9 antibody (A12781).<br>Overlay histogram showing MCF-7 cells stained with A12781 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED9 Antibody (A12781,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-med13-picoband-trade-antibody-a04545-1-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04545-1-med13-primary-antibodies-wb-testing-1.jpgAnti-MED13 Antibody Picoband® Western blot analysis of MED13 using anti-MED13 antibody (A04545-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human U2OS whole cell lysates,<br>Lane 2: human MCF-7 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED13 antigen affinity purified polyclonal antibody (Catalog # A04545-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED13 at approximately 300KD. The expected band size for MED13 is at 239KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04545-1-med13-primary-antibodies-if-testing-2.jpgAnti-MED13 Antibody Picoband® IF analysis of MED13 using anti-MED13 antibody (A04545-1). <br>
MED13 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-MED13 Antibody (A04545-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04545-1-med13-primary-antibodies-fcm-testing-3.pngAnti-MED13 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-MED13 antibody (A04545-1). <br>Overlay histogram showing A431 cells stained with A04545-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED13 Antibody (A04545-1, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-med14-picoband-trade-antibody-a04799-2-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04799-2-med14-primary-antibodies-wb-testing-1.jpgAnti-MED14 Antibody Picoband® Western blot analysis of MED14 using anti-MED14 antibody (A04799-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: mouse liver tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED14 antigen affinity purified polyclonal antibody (Catalog # A04799-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED14 at approximately 160KD. The expected band size for MED14 is at 160KD.
https://www.bosterbio.com/products/primary-antibodies/anti-med15-picoband-trade-antibody-a03568-1-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03568-1-med15-primary-antibodies-wb-testing-1.jpgAnti-MED15 Antibody Picoband® Western blot analysis of MED15 using anti-MED15 antibody (A03568-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates, <br>
Lane 2: huamn K562 whole cell lysates, <br>
Lane 3: human Hela whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED15 antigen affinity purified polyclonal antibody (Catalog # A03568-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED15 at approximately 97 kDa. The expected band size for MED15 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-IHC-testing-2.jpgAnti-MED15 Antibody Picoband® IHC analysis of MED15 using anti-MED15 antibody (A03568-1).<br>MED15 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED15 Antibody (A03568-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-IHC-testing-3.jpgAnti-MED15 Antibody Picoband® IHC analysis of MED15 using anti-MED15 antibody (A03568-1).<br>MED15 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED15 Antibody (A03568-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-IHC-testing-4.jpgAnti-MED15 Antibody Picoband® IHC analysis of MED15 using anti-MED15 antibody (A03568-1).<br>MED15 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED15 Antibody (A03568-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-IHC-testing-5.jpgAnti-MED15 Antibody Picoband® IHC analysis of MED15 using anti-MED15 antibody (A03568-1).<br>MED15 was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED15 Antibody (A03568-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-IHC-testing-6.jpgAnti-MED15 Antibody Picoband® IHC analysis of MED15 using anti-MED15 antibody (A03568-1).<br>MED15 was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED15 Antibody (A03568-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03568-1-MED15-primary-antibodies-FC-testing-7.jpgAnti-MED15 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-MED15 antibody (A03568-1). <br>Overlay histogram showing U20S cells stained with A03568-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED15 Antibody (A03568-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03568-1-med15-primary-antibodies-if-testing-8.jpgAnti-MED15 Antibody Picoband® IF analysis of MED15 using anti-MED15 antibody (A03568-1). <br>
MED15 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MED15 Antibody (A03568-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-med18-picoband-trade-antibody-a10600-2-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10600-2-med18-primary-antibodies-wb-testing-1.jpgAnti-MED18 Antibody Picoband® Western blot analysis of MED18 using anti-MED18 antibody (A10600-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates, <br>
Lane 2: human HEL whole cell lysates, <br>
Lane 3: human K562 whole cell lysates, <br>
Lane 4: human U251 whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat stomach tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse stomach tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED18 antigen affinity purified polyclonal antibody (Catalog # A10600-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED18 at approximately 24 kDa. The expected band size for MED18 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-2.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-3.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-4.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-5.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-6.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-7.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10600-2-MED18-primary-antibodies-IHC-testing-8.jpgAnti-MED18 Antibody Picoband® IHC analysis of MED18 using anti-MED18 antibody (A10600-2).<br>MED18 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED18 Antibody (A10600-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/e/med18-primary-antibodies-a10600-2-fc-testing-9.pngAnti-MED18 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-MED18 antibody (A10600-2). <br> Overlay histogram showing A431 cells stained with A10600-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED18 Antibody (A10600-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10600-2-med18-primary-antibodies-if-testing-10.jpgAnti-MED18 Antibody Picoband® IF analysis of MED18 using anti-MED18 antibody (A10600-2). <br>
MED18 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MED18 Antibody (A10600-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp10-picoband-trade-antibody-a03759-1-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03759-1-mmp10-primary-antibodies-wb-testing-1.jpgAnti-MMP10 Antibody Picoband® Western blot analysis of MMP10 using anti-MMP10 antibody (A03759-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: rat cardiac muscle tissue lysates,<br> Lane 2: mouse cardiac muscle tissue lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP10 antigen affinity purified polyclonal antibody (Catalog # A03759-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP10 at approximately 54KD. The expected band size for MMP10 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A03759-10-primary-antibodies-ihc-testing-2.jpgAnti-MMP10 Antibody Picoband® IHC analysis of MMP10 using anti-MMP10 antibody (A03759-1). <br> MMP10 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP10 Antibody (A03759-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/antibody/A03759-10-primary-antibodies-ihc-testing-3.jpgAnti-MMP10 Antibody Picoband® IHC analysis of MMP10 using anti-MMP10 antibody (A03759-1). <br> MMP10 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP10 Antibody (A03759-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03759-1-mmp10-primary-antibodies-wb-testing-4.jpgAnti-MMP10 Antibody Picoband® Western blot analysis of MMP10 using anti-MMP10 antibody (A03759-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human placenta tissue lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP10 antigen affinity purified polyclonal antibody (Catalog # A03759-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP10 at approximately 54KD. The expected band size for MMP10 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03759-1-mmp10-primary-antibodies-if-testing-5.jpgAnti-MMP10 Antibody Picoband® IF analysis of MMP10 using anti-MMP10 antibody (A03759-1).<br> MMP10 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MMP10 Antibody (A03759-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. isualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp16-picoband-trade-antibody-a05065-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05065-MMP16-primary-antibodies-WB-testing-1.jpgAnti-MMP16 Antibody Picoband® Western blot analysis of MMP16 using anti-MMP16 antibody (A05065). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse intestine tissue lysates,<br>Lane 2: human SMMC-7721 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP16 antigen affinity purified polyclonal antibody (Catalog # A05065) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP16 at approximately 53KD. The expected band size for MMP16 is at 53KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05065-MMP16-primary-antibodies-IHC-testing-2.jpgAnti-MMP16 Antibody Picoband® IHC analysis of MMP16 using anti-MMP16 antibody (A05065).<br>MMP16 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MMP16 Antibody (A05065) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05065-MMP16-primary-antibodies-IHC-testing-3.jpgAnti-MMP16 Antibody Picoband® IHC analysis of MMP16 using anti-MMP16 antibody (A05065).<br>MMP16 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MMP16 Antibody (A05065) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05065-MMP16-primary-antibodies-IHC-testing-4.jpgAnti-MMP16 Antibody Picoband® IHC analysis of MMP16 using anti-MMP16 antibody (A05065).<br>MMP16 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MMP16 Antibody (A05065) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A05065-MMP16-primary-antibodies-IHC-testing-5.jpgAnti-MMP16 Antibody Picoband® IHC analysis of MMP16 using anti-MMP16 antibody (A05065).<br>MMP16 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MMP16 Antibody (A05065) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05065-mmp16-primary-antibodies-if-testing-6.jpgAnti-MMP16 Antibody Picoband® IF analysis of MMP16 using anti-MMP16 antibody (A05065). <br>
MMP16 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MMP16 Antibody (A05065) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05065-mmp16-primary-antibodies-fcm-testing-7.jpgAnti-MMP16 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-MMP16 antibody (A05065).<br>Overlay histogram showing CACO-2 cells stained with A05065 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MMP16 Antibody (A05065,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-myd88-picoband-trade-antibody-a00025-1-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00025-1-MyD88-primary-antibodies-WB-testing-1.jpgAnti-MyD88 Antibody Picoband® Western blot analysis of MyD88 using anti-MyD88 antibody (A00025-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse testis tissue lysates,<br>Lane 3: rat spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MyD88 antigen affinity purified polyclonal antibody (Catalog # A00025-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MyD88 at approximately 33KD. The expected band size for MyD88 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-myd88-picoband-trade-antibody-a00025-2-boster.html2026-03-24T05:11:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00025-2-MyD88-primary-antibodies-WB-testing-1.jpgAnti-MyD88 Antibody Picoband® Western blot analysis of MyD88 using anti-MyD88 antibody (A00025-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat ovary tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MyD88 antigen affinity purified polyclonal antibody (Catalog # A00025-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MyD88 at approximately 33KD. The expected band size for MyD88 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-neurocan-picoband-trade-antibody-a06700-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06700-1-neurocan-primary-antibodies-wb-testing-1.jpgAnti-Neurocan/NCAN Antibody Picoband® Western blot analysis of Neurocan using anti-Neurocan antibody (A06700-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Neurocan antigen affinity purified polyclonal antibody (Catalog # A06700-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Neurocan at approximately 200KD. The expected band size for Neurocan is at 143KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06700-1-Neurocan-primary-antibodies-IHC-testing-2.jpgAnti-Neurocan/NCAN Antibody Picoband® IHC analysis of Neurocan using anti-Neurocan antibody (A06700-1).<br>Neurocan was detected in paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Neurocan Antibody (A06700-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06700-1-Neurocan-primary-antibodies-IHC-testing-3.jpgAnti-Neurocan/NCAN Antibody Picoband® IHC analysis of Neurocan using anti-Neurocan antibody (A06700-1).<br>Neurocan was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Neurocan Antibody (A06700-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-nfat2-picoband-trade-antibody-a00340-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00340-1-nfat2-primary-antibodies-wb-testing-1.jpgAnti-NFAT2/NFATC1 Antibody Picoband® Western blot analysis of NFAT2/NFATC1 using anti-NFAT2/NFATC1 antibody (A00340-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human Daudi whole cell lysates, <br>
Lane 3: human Ramos whole cell lysates, <br>
Lane 4: human Raji whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFAT2/NFATC1 antigen affinity purified polyclonal antibody (A00340-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NFAT2/NFATC1 at approximately 101 kDa. The expected band size for NFAT2/NFATC1 is at 101 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00340-1-nfat2-primary-antibodies-fcm-testing-2.jpgAnti-NFAT2/NFATC1 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-NFAT2/NFATC1 antibody (A00340-1). <br>
Overlay histogram showing Jurkat cells stained with A00340-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT2/NFATC1 Antibody (A00340-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-nfat1-picoband-trade-antibody-a00969-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00969-nfat1-primary-antibodies-wb-testing-1_1.jpgAnti-NFAT1/NFATC2 Antibody Picoband®Western blot analysis of NFAT1/NFATC2 using anti-NFAT1/NFATC2 antibody (A00969). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Ramos whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human MOLT-4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFAT1/NFATC2 antigen affinity purified polyclonal antibody (A00969) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NFAT1/NFATC2 at approximately 135 kDa. The expected band size for NFAT1/NFATC2 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00969-nfat1-primary-antibodies-if-testing-1.jpgAnti-NFAT1/NFATC2 Antibody Picoband®IF analysis of NFAT1/NFATC2 using anti-NFAT1/NFATC2 antibody (A06945-1) and anti-Tubulin Alpha antibody (M03989-3).<br>
NFAT1/NFATC2 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NFAT1/NFATC2 Antibody (A06945-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00969-nfat1-primary-antibodies-fcm-testing-1.jpgAnti-NFAT1/NFATC2 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-NFAT1/NFATC2 antibody (A00969). <br>
Overlay histogram showing Jurkat cells stained with A00969 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT1/NFATC2 Antibody (A00969, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-nfat4-picoband-trade-antibody-a02727-2-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02727-2-NFAT4-primary-antibodies-WB-testing-1.jpgAnti-NFAT4/NFATC3 Antibody Picoband® Western blot analysis of NFAT4 using anti-NFAT4 antibody (A02727-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human 22RV1 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFAT4 antigen affinity purified polyclonal antibody (Catalog # A02727-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFAT4 at approximately 115KD. The expected band size for NFAT4 is at 115KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-2-nfat4-primary-antibodies-fc-testing-2.jpgAnti-NFAT4/NFATC3 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-NFAT4 antibody (A02727-2). <br>Overlay histogram showing A431 cells stained with A02727-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT4 Antibody (A02727-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-2-nfat4-primary-antibodies-fc-testing-3.jpgAnti-NFAT4/NFATC3 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-NFAT4 antibody (A02727-2). <br>Overlay histogram showing U20S cells stained with A02727-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT4 Antibody (A02727-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-2-nfat4-primary-antibodies-fc-testing-4.jpgAnti-NFAT4/NFATC3 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NFAT4 antibody (A02727-2). <br>Overlay histogram showing K562 cells stained with A02727-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT4 Antibody (A02727-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02727-2-nfat4-primary-antibodies-fc-testing-5.jpgAnti-NFAT4/NFATC3 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-NFAT4 antibody (A02727-2). <br>Overlay histogram showing SiHa cells stained with A02727-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFAT4 Antibody (A02727-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-nfatc4-picoband-trade-antibody-a02599-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02599-1-NFATC4-primary-antibodies-WB-testing-1.jpgAnti-NFATC4 Antibody Picoband® Western blot analysis of NFATC4 using anti-NFATC4 antibody (A02599-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat testis tissue lysates, <br>Lane 2: mouse testis tissue lysates,<br>Lane 3: human Hela whole cell lysates,<br>Lane 4: human placenta tissue lysates,<br>Lane 5: human A549 whole cell lysates,<br>Lane 6: human SK-OV-3 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFATC4 antigen affinity purified polyclonal antibody (Catalog # A02599-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFATC4 at approximately 95120KD. The expected band size for NFATC4 is at 95KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02599-1-nfatc4-primary-antibodies-fc-testing-2.jpgAnti-NFATC4 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-NFATC4 antibody (A02599-1). <br>Overlay histogram showing U20S cells stained with A02599-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFATC4 Antibody (A02599-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02599-1-nfatc4-primary-antibodies-fc-testing-3.jpgAnti-NFATC4 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-NFATC4 antibody (A02599-1). <br>Overlay histogram showing A431 cells stained with A02599-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFATC4 Antibody (A02599-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02599-1-nfatc4-primary-antibodies-fc-testing-4.jpgAnti-NFATC4 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-NFATC4 antibody (A02599-1). <br>Overlay histogram showing SiHa cells stained with A02599-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFATC4 Antibody (A02599-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-noggin-picoband-trade-antibody-a04448-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04448-1-Noggin-primary-antibodies-WB-testing-1.jpgAnti-Noggin Antibody Picoband® Western blot analysis of Noggin using anti-Noggin antibody (A04448-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates, <br>Lane 2: human MCF-7 whole cell lysates,<br>Lane 3: human HepG2 whole cell lysates,<br>Lane 4: human A375 whole cell lysates,<br>Lane 5: human 22RV1 whole cell lysates.<br> <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Noggin antigen affinity purified polyclonal antibody (Catalog # A04448-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Noggin at approximately 26KD. The expected band size for Noggin is at 26KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04448-1-noggin-primary-antibodies-ihc-testing-2.jpgAnti-Noggin Antibody Picoband® IHC analysis of Noggin using anti-Noggin antibody (A04448-1). <br>
Noggin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Noggin Antibody (A04448-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-oncostatin-m-picoband-trade-antibody-a00804-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00804-Oncostatin-M-primary-antibodies-WB-testing-1.jpgAnti-Oncostatin M/Osm Antibody Picoband® Western blot analysis of Oncostatin M using anti-Oncostatin M antibody (A00804). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse HEPA1-6 whole cell lysates,<br>Lane 2: rat kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Oncostatin M antigen affinity purified polyclonal antibody (Catalog # A00804) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Oncostatin M at approximately 28KD. The expected band size for Oncostatin M is at 28KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00804-oncostatin-m-primary-antibodies-elisa-testing-2.jpgAnti-Oncostatin M/Osm Antibody Picoband® Sandwich ELISA - Recombinant mouse Oncostatin M/Osm protein standard curve.<br>
Use in combination with reagents from Mouse Oncostatin M/Osm ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0479).
https://www.bosterbio.com/products/primary-antibodies/anti-park7-dj1-picoband-trade-antibody-a00757-2-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00757-2-park7-primary-antibodies-wb-testing-1.jpgAnti-PARK7/DJ1 Antibody Picoband® Western blot analysis of PARK7/DJ1 using anti-PARK7/DJ1 antibody (A00757-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat RH35 whole cell lysates,<br>
Lane 3: mouse kidney tissue lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse Hepa1/6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARK7/DJ1 antigen affinity purified polyclonal antibody (Catalog # A00757-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARK7/DJ1 at approximately 20 kDa. The expected band size for PARK7/DJ1 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-2.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-3.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-4.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-5.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-6.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00757-2-PARK7-primary-antibodies-IHC-testing-7.jpgAnti-PARK7/DJ1 Antibody Picoband® IHC analysis of PARK7 / DJ1 using anti-PARK7 / DJ1 antibody (A00757-2).<br>PARK7 / DJ1 was detected in paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PARK7 / DJ1 Antibody (A00757-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-pgf-picoband-trade-antibody-a01164-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01164-1-pgf-primary-antibodies-wb-testing-1.jpgAnti-PGF Antibody Picoband® Western blot analysis of PGF using anti-PGF antibody (A01164-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates, <br>Lane 2: rat liver tissue lysates,<br>Lane 3: mouse gaster tissue lysates,<br>Lane 4: mouse liver tissue lysates,<br>Lane 5: mouse HEPA1-6 whole cell lysates.<br> <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGF antigen affinity purified polyclonal antibody (Catalog # A01164-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGF at approximately 25KD. The expected band size for PGF is at 25KD.
https://www.bosterbio.com/products/primary-antibodies/anti-perilipin-a-picoband-trade-antibody-a03918-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03918-1-perilipin-a-primary-antibodies-wb-testing-1.jpgAnti-Perilipin A/PLIN1 Antibody Picoband® Western blot analysis of Perilipin A using anti-Perilipin A antibody (A03918-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Perilipin A antigen affinity purified polyclonal antibody (Catalog # A03918-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Perilipin A at approximately 56 kDa. The expected band size for Perilipin A is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03918-1-13287_2019_1404_fig4_html.pngAnti-Perilipin A/PLIN1 Antibody Picoband®Antioxidants preserve ADSC cell stemness and multidirectional differentiation potential during long-term in vitro expansion. After treatment with 10 μM GSH or melatonin, the ADSCs cultured for passage 3 (P3), passage 6 (P6), and passage 9 (P9) were used in the following analysis. a Osteogenesis differentiation of passaged ADSCs (Alizarin Red S staining; scale bar, 50 μm). b Adipogenesis differentiation of passaged ADSCs (Oil Red O staining; scale bar, 50 μm). c Western blot analysis for RUNX-2 in osteogenic cells. d Western blot analysis for perilipin A in adipogenic cells. e Chondrogenesis differentiation of passaged ADSCs (Alcian blue staining; scale bar, 50 μm). f Western blot analysis for SOX-9 in chondrogenic cells. g Western blot analysis for SOX-2, OCT-4, and β-actin in ADSCs. ADSCs, adipose tissue-derived stem cells; GSH, reduced glutathione <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-019-1404-9'>31623678</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-pon1-picoband-trade-antibody-a00516-1-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00516-1-pon1-primary-antibodies-elisa-testing-1_1.jpgAnti-PON1 Antibody Sandwich ELISA - Recombinant mouse PON1 protein standard curve.<br>
Use in combination with reagents from Mouse PON1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1621).
https://www.bosterbio.com/products/primary-antibodies/anti-periostin-picoband-trade-antibody-a01378-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01378-periostin-primary-antibodies-wb-testing-1.jpgAnti-Periostin/Postn Antibody Picoband® Western blot analysis of Periostin using anti-Periostin antibody (A01378). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates, <br>Lane 2: rat lung tissue lysates,<br>Lane 3: rat NRK whole cell lysates,<br>Lane 4: mouse gaster tissue lysates,<br>Lane 5: mouse intestine tissue lysates,<br>Lane 6: mouse lung tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Periostin antigen affinity purified polyclonal antibody (Catalog # A01378) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Periostin at approximately 93KD. The expected band size for Periostin is at 93KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-2.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of mouse gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-3.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-4.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-5.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of rat gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-6.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01378-Periostin-primary-antibodies-IHC-testing-7.jpgAnti-Periostin/Postn Antibody Picoband® IHC analysis of Periostin using anti-Periostin antibody (A01378).<br>Periostin was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Periostin Antibody (A01378) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/loading-control-antibodies/anti-cyclophilin-b-picoband-trade-antibody-a03229-boster.html2026-03-24T05:11:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03229-cyclophilin_b-primary-antibodies-wb-testing-1.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® Western blot analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: mouse HEPA1-6 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse SP2/0 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclophilin B antigen affinity purified polyclonal antibody (Catalog # A03229) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclophilin B at approximately 19 kDa. The expected band size for Cyclophilin B is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03229-Cyclophilin-B-primary-antibodies-IHC-testing-2.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IHC analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229).<br>Cyclophilin B was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03229-Cyclophilin-B-primary-antibodies-IHC-testing-3.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IHC analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229).<br>Cyclophilin B was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03229-Cyclophilin-B-primary-antibodies-IHC-testing-4.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IHC analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229).<br>Cyclophilin B was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03229-Cyclophilin-B-primary-antibodies-IHC-testing-5.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IHC analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229).<br>Cyclophilin B was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03229-Cyclophilin-B-primary-antibodies-IHC-testing-6.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IHC analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229).<br>Cyclophilin B was detected in paraffin-embedded section of rat thyroid gland tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03229-cyclophilin_b-primary-antibodies-if-testing-7.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® IF analysis of Cyclophilin B using anti-Cyclophilin B antibody (A03229). <br>
Cyclophilin B was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Cyclophilin B Antibody (A03229) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03229-cyclophilin_b-primary-antibodies-fcm-testing-8.jpgAnti-Cyclophilin B/PPIB Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-Cyclophilin B antibody (A03229).<br>Overlay histogram showing U937 cells stained with A03229 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cyclophilin B Antibody (A03229,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-rbp4-picoband-trade-antibody-a01089-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01089-rbp4-primary-antibodies-wb-testing-1_1.jpgAnti-RBP4 Antibody Picoband® Western blot analysis of RBP4 using anti-RBP4 antibody (A01089). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: rat lung tissue lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBP4 antigen affinity purified polyclonal antibody (Catalog # A01089) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBP4 at approximately 21 kDa. The expected band size for RBP4 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01089-rbp4-primary-antibodies-ihc-testing-6.jpgAnti-RBP4 Antibody Picoband®IHC analysis of RBP4 using anti-RBP4 antibody (A01089). <br>RBP4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01089-rbp4-primary-antibodies-ihc-testing-7.jpgAnti-RBP4 Antibody Picoband®IHC analysis of RBP4 using anti-RBP4 antibody (A01089). <br>RBP4 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01089-RBP4-primary-antibodies-IHC-testing-2.jpgAnti-RBP4 Antibody Picoband® IHC analysis of RBP4 using anti-RBP4 antibody (A01089).<br>RBP4 was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01089-RBP4-primary-antibodies-IHC-testing-3.jpgAnti-RBP4 Antibody Picoband® IHC analysis of RBP4 using anti-RBP4 antibody (A01089).<br>RBP4 was detected in paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01089-RBP4-primary-antibodies-IHC-testing-4.jpgAnti-RBP4 Antibody Picoband® IHC analysis of RBP4 using anti-RBP4 antibody (A01089).<br>RBP4 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01089-RBP4-primary-antibodies-IHC-testing-5.jpgAnti-RBP4 Antibody Picoband® IHC analysis of RBP4 using anti-RBP4 antibody (A01089).<br>RBP4 was detected in paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-RBP4 Antibody (A01089) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01089-rbp4-primary-antibodies-ihc-testing-7_1.jpgAnti-RBP4 Antibody Picoband®IHC analysis of RBP4 using anti-RBP4 antibody (A01089).<br>
RBP4 was detected in a paraffin-embedded section of mouse knee joint. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 5% BSA . The tissue section was then incubated with rabbit anti-RBP4 antibody (A01089) at 5 μg/ml overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-retinal-s-antigen-picoband-trade-antibody-a03775-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03775-retinal_s_antigen-primary-antibodies-wb-testing-1.jpgAnti-Retinal S antigen/SAG Antibody Picoband® Western blot analysis of Retinal S antigen using anti-Retinal S antigen antibody (A03775). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat eye ball tissue lysates,<br>Lane 2: mouse eye ball tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Retinal S antigen antigen affinity purified polyclonal antibody (Catalog # A03775) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Retinal S antigen at approximately 45-55KD. The expected band size for Retinal S antigen is at 45KD.
https://www.bosterbio.com/products/primary-antibodies/anti-semaphorin-3a-picoband-trade-antibody-a01761-1-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01761-1-Semaphorin-3A-primary-antibodies-WB-testing-1.jpgAnti-Semaphorin 3A/SEMA3A Antibody Picoband® Western blot analysis of Semaphorin 3A using anti-Semaphorin 3A antibody (A01761-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: mouse brain tissue lysates,<br>Lane 3: human U-87MG whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Semaphorin 3A antigen affinity purified polyclonal antibody (Catalog # A01761-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Semaphorin 3A at approximately 95KD. The expected band size for Semaphorin 3A is at 89KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tff2-picoband-trade-antibody-a07013-1-boster.html2026-04-01T05:01:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07013-1-tff2-primary-antibodies-wb-testing-1.jpgAnti-TFF2 Antibody Picoband® Western blot analysis of TFF2 using anti-TFF2 antibody (A07013-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFF2 antigen affinity purified polyclonal antibody (Catalog # A07013-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFF2 at approximately 14KD. The expected band size for TFF2 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07013-1-TFF2-primary-antibodies-IHC-testing-2.jpgAnti-TFF2 Antibody Picoband® IHC analysis of TFF2 using anti-TFF2 antibody (A07013-1).<br>TFF2 was detected in paraffin-embedded section of mouse gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF2 Antibody (A07013-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07013-1-TFF2-primary-antibodies-IHC-testing-3.jpgAnti-TFF2 Antibody Picoband® IHC analysis of TFF2 using anti-TFF2 antibody (A07013-1).<br>TFF2 was detected in paraffin-embedded section of rat gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF2 Antibody (A07013-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-tff2-picoband-trade-antibody-a07013-2-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07013-2-tff2-primary-antibodies-wb-testing-1.jpgAnti-TFF2 Antibody Picoband® Western blot analysis of TFF2 using anti-TFF2 antibody (A07013-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates,<br>Lane 2: mouse gaster tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFF2 antigen affinity purified polyclonal antibody (Catalog # A07013-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFF2 at approximately 14KD. The expected band size for TFF2 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07013-2-tff2-primary-antibodies-wb-testing-2.pngAnti-TFF2 Antibody Picoband® Western blot analysis of TFF2 using anti-TFF2 antibody (A07013-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates,<br>
Lane 2: Model group-rat colon tissue lysates,<br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates,<br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates,<br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates,<br>
Lane 6: Western medicine treatment-rat colon tissue lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFF2 antigen affinity purified polyclonal antibody (Catalog # A07013-2) at 1:1000 overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for TFF2 at approximately 14KD. The expected band size for TFF2 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A07013-2-TFF2-primary-antibodies-IHC-testing-2.jpgAnti-TFF2 Antibody Picoband® IHC analysis of TFF2 using anti-TFF2 antibody (A07013-2).<br>TFF2 was detected in paraffin-embedded section of rat gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF2 Antibody (A07013-2) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-tff3-picoband-trade-antibody-a01738-2-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-2-TFF3-primary-antibodies-WB-testing-1.jpgAnti-TFF3 Antibody Picoband® Western blot analysis of TFF3 using anti-TFF3 antibody (A01738-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat gaster tissue lysates,<br>Lane 2: rat small intestine tissue lysates,<br>Lane 3: mouse small intestine tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFF3 antigen affinity purified polyclonal antibody (Catalog # A01738-2) at 0.5 ug/mL overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFF3 at approximately 12KD. The expected band size for TFF3 is at 9KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-2-TFF3-primary-antibodies-IHC-testing-2.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-2).<br>TFF3 was detected in paraffin-embedded section of mouse gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF3 Antibody (A01738-2) overnight at 4℃. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37℃. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-2-TFF3-primary-antibodies-IHC-testing-3.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-2).<br>TFF3 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF3 Antibody (A01738-2) overnight at 4℃. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37℃. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-2-TFF3-primary-antibodies-IHC-testing-4.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-2).<br>TFF3 was detected in paraffin-embedded section of rat gaster tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF3 Antibody (A01738-2) overnight at 4℃. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37℃. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-2-TFF3-primary-antibodies-IHC-testing-5.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-2).<br>TFF3 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TFF3 Antibody (A01738-2) overnight at 4℃. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37℃. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-timp1-picoband-trade-antibody-a00561-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00561-timp1-primary-antibodies-wb-testing-1_1.jpgAnti-TIMP1 Antibody Picoband®Western blot analysis of TIMP1 using anti-TIMP1 antibody (A00561). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates, <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human HT29 whole cell lysates,<br>
Lane 3: human SKOV3 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: human U2OS whole cell lysates,<br>
Lane 6: human PC-3 whole cell lysates,<br>
Lane 7: human THP-1 whole cell lysates. <br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMP1 antigen affinity purified polyclonal antibody (A00561) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIMP1 at approximately 23 kDa. The expected band size for TIMP1 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00561-ijo-16-09-1441-g004.jpgAnti-TIMP1 Antibody Picoband®17β-estradiol inhibits the production of TIMPs and MMPs in HTFs. Representative graphs showing the production of MMP-1, MMP-3, proMMP-2, active MMP-2, TIMP-1, and TIMP-2 in the supernatants of HTFs after the treatment of indicated concentration of 17β-estradiol based on immunoblot and gelatin zymography. MMP-1 and MMP-3 in the supernatants but not proMMP-2 and active MMP-2 were decreased following the pre-incubation with 17β-estradiol. In addition, 17β-estradiol induced a concentration-dependent reduction in the level of TIMP-2 but not TIMP-1 in the supernatants of HTFs exposed to TGF-β (5 ng/mL). HTF: Human Tenon fibroblasts; TGF: Transforming growth factor; MMP: Matrix metalloproteinases; TIMPs: Tissue inhibitors of metalloproteinases.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10475634/&orig_host=www.ncbi.nlm.nih.gov'>37724268</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-trail-picoband-trade-antibody-a00466-1-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00466-1-trail-primary-antibodies-wb-testing-1.jpgAnti-TRAIL/TNFSF10 Antibody Picoband® Western blot analysis of TRAIL using anti-TRAIL antibody (A00466-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human HL-60 whole cell lysates, <br> Lane 2: human THP-1 whole cell lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAIL antigen affinity purified polyclonal antibody (Catalog # A00466-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRAIL at approximately 35KD. The expected band size for TRAIL is at 33KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00466-1-trail-primary-antibodies-ihc-testing-2.jpgAnti-TRAIL/TNFSF10 Antibody Picoband® IHC analysis of TRAIL using anti-TRAIL antibody (A00466-1). <br> TRAIL was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TRAIL Antibody (A00466-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00466-1-trail-primary-antibodies-ihc-testing-3.jpgAnti-TRAIL/TNFSF10 Antibody Picoband® IHC analysis of TRAIL using anti-TRAIL antibody (A00466-1). <br> TRAIL was detected in paraffin-embedded section of mouse spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TRAIL Antibody (A00466-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00466-1-trail-primary-antibodies-ihc-testing-4.jpgAnti-TRAIL/TNFSF10 Antibody Picoband® IHC analysis of TRAIL using anti-TRAIL antibody (A00466-1). <br> TRAIL was detected in paraffin-embedded section of rat liver tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TRAIL Antibody (A00466-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-light-picoband-trade-antibody-a03516-1-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03516-1-light_-primary-antibodies-wb-testing-1.jpgAnti-LIGHT/Tnfsf14 Antibody Picoband® Western blot analysis of LIGHT using anti-LIGHT antibody (A03516-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse cardiac muscle tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIGHT antigen affinity purified polyclonal antibody (Catalog # A03516-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIGHT at approximately 26KD. The expected band size for LIGHT is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tnfsf18-picoband-trade-antibody-a04408-1-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04408-1-TNFSF18-primary-antibodies-WB-testing-1.jpgAnti-TNFSF18 Antibody Picoband® Western blot analysis of TNFSF18 using anti-TNFSF18 antibody (A04408-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human TNFSF18 protein 1ng. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNFSF18 antigen affinity purified polyclonal antibody (Catalog # A04408-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNFSF18 at approximately 15KD. The expected band size for TNFSF18 is at 15KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04408-1-TNFSF18-primary-antibodies-IHC-testing-2.jpgAnti-TNFSF18 Antibody Picoband® IHC analysis of TNFSF18 using anti-TNFSF18 antibody (A04408-1).<br>TNFSF18 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TNFSF18 Antibody (A04408-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04408-1-TNFSF18-primary-antibodies-IHC-testing-3.jpgAnti-TNFSF18 Antibody Picoband® IHC analysis of TNFSF18 using anti-TNFSF18 antibody (A04408-1).<br>TNFSF18 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TNFSF18 Antibody (A04408-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04408-1-TNFSF18-primary-antibodies-IHC-testing-4.jpgAnti-TNFSF18 Antibody Picoband® IHC analysis of TNFSF18 using anti-TNFSF18 antibody (A04408-1).<br>TNFSF18 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TNFSF18 Antibody (A04408-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-trem1-picoband-trade-antibody-a02135-1-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02135-1-trem1-primary-antibodies-wb-testing-1.jpgAnti-TREM1 Antibody Picoband® Western blot analysis of TREM1 using anti-TREM1 antibody (A02135-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human TREM1 protein 1ng. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TREM1 antigen affinity purified polyclonal antibody (Catalog # A02135-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TREM1 at approximately 26KD. The expected band size for TREM1 is at 26KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02135-1-trem1-primary-antibodies-fc-testing-2.pngAnti-TREM1 Antibody Picoband®2. Flow Cytometry analysis of H-PBMC cells using anti-TREM1 antibody (A02135-1).<br> Overlay histogram showing H-PBMC cells stained with A02135-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TREM1 Antibody (A02135-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-trem1-picoband-trade-antibody-a02135-2-boster.html2026-03-24T05:11:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02135-2-trem1-primary-antibodies-wb-testing-1.jpgAnti-TREM1 Antibody Picoband® Western blot analysis of TREM1 using anti-TREM1 antibody (A02135-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse lung tissue lysates,<br>Lane 2: mouse spleen tissue lysates,<br>Lane 3: rat spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TREM1 antigen affinity purified polyclonal antibody (Catalog # A02135-2) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TREM1 at approximately 26KD. The expected band size for TREM1 is at 26KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tslp-picoband-trade-antibody-a01096-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01096-TSLP-primary-antibodies-WB-testing-1.jpgAnti-TSLP Antibody Picoband® Western blot analysis of TSLP using anti-TSLP antibody (A01096). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>Lane 2: mouse spleen tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSLP antigen affinity purified polyclonal antibody (Catalog # A01096) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSLP at approximately 18KD. The expected band size for TSLP is at 18KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tslp-picoband-trade-antibody-a01096-1-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01096-1-tslp-primary-antibodies-wb-testing-1.jpgAnti-TSLP Antibody Picoband® Western blot analysis of TSLP using anti-TSLP antibody (A01096-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse liver tissue lysates, <br>Lane 2: mouse kidney tissue lysates,<br>Lane 3: mouse testis tissue lysates,<br>Lane 4: rat heart tissue lysates,<br>Lane 5: rat liver tissue lysates,<br>Lane 6: rat kidney tissue lysates,<br>Lane 7: rat testis tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSLP antigen affinity purified polyclonal antibody (Catalog # A01096-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSLP at approximately 18KD. The expected band size for TSLP is at 18KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vcam1-picoband-trade-antibody-a01199-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01199-vcam1-primary-antibodies-wb-testing-1.jpgAnti-VCAM1 Antibody Picoband® Western blot analysis of VCAM1 using anti-VCAM1 antibody (A01199). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse lung tissue lysates,<br>Lane 3: rat spleen tissue lysates,<br>Lane 4: rat lung tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VCAM1 antigen affinity purified polyclonal antibody (Catalog # A01199) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VCAM1 at approximately 110KD. The expected band size for VCAM1 is at 81KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01199-VCAM1-primary-antibodies-IHC-testing-2.jpgAnti-VCAM1 Antibody Picoband® IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).<br>VCAM1 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VCAM1 Antibody (A01199) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01199-VCAM1-primary-antibodies-IHC-testing-3.jpgAnti-VCAM1 Antibody Picoband® IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).<br>VCAM1 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-VCAM1 Antibody (A01199) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01199-vcam1-primary-antibodies-elisa-testing-4.jpgAnti-VCAM1 Antibody Picoband® Sandwich ELISA - Recombinant mouse VCAM1 protein standard curve.<br>
Use in combination with reagents from Mouse VCAM1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0538).https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01199-vcam1-primary-antibodies-ihc-testing-3.jpgAnti-VCAM1 Antibody Picoband®IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).<br>
VCAM1 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 9.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-VCAM1 Antibody (A01199) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-vegfb-picoband-trade-antibody-a04494-1-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04494-1-VEGFB-primary-antibodies-WB-testing-1.jpgAnti-VEGFB Antibody Picoband® Western blot analysis of VEGFB using anti-VEGFB antibody (A04494-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: rat pancreas tissue lysates,<br>Lane 3: mouse cardiac muscle tissue lysates,<br>Lane 4: mouse skeletal muscle tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGFB antigen affinity purified polyclonal antibody (Catalog # A04494-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGFB at approximately 29KD. The expected band size for VEGFB is at 22KD.
https://www.bosterbio.com/products/primary-antibodies/anti-he4-picoband-trade-antibody-a02685-3-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02685-3-he4-primary-antibodies-wb-testing-1.jpgAnti-HE4/Wfdc2 Antibody Picoband® Western blot analysis of HE4 using anti-HE4 antibody (A02685-3). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat testis tissue lysates, <br>Lane 2: rat brain tissue lysates,<br>Lane 3: rat thymus tissue lysates,<br>Lane 4: mouse testis tissue lysates,<br>Lane 5: mouse brain tissue lysates,<br>Lane 6: mouse thymus tissue lysates,<br>Lane 7: mouse HEPA1-6 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HE4 antigen affinity purified polyclonal antibody (Catalog # A02685-3) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HE4 at approximately 19KD. The expected band size for HE4 is at 13KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02685-3-HE4-primary-antibodies-IHC-testing-2.jpgAnti-HE4/Wfdc2 Antibody Picoband® IHC analysis of HE4 using anti-HE4 antibody (A02685-3).<br>HE4 was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HE4 Antibody (A02685-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02685-3-HE4-primary-antibodies-IHC-testing-3.jpgAnti-HE4/Wfdc2 Antibody Picoband® IHC analysis of HE4 using anti-HE4 antibody (A02685-3).<br>HE4 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HE4 Antibody (A02685-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02685-3-HE4-primary-antibodies-IHC-testing-4.jpgAnti-HE4/Wfdc2 Antibody Picoband® IHC analysis of HE4 using anti-HE4 antibody (A02685-3).<br>HE4 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HE4 Antibody (A02685-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02685-3-HE4-primary-antibodies-IHC-testing-5.jpgAnti-HE4/Wfdc2 Antibody Picoband® IHC analysis of HE4 using anti-HE4 antibody (A02685-3).<br>HE4 was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HE4 Antibody (A02685-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02685-3-HE4-primary-antibodies-IHC-testing-6.jpgAnti-HE4/Wfdc2 Antibody Picoband® IHC analysis of HE4 using anti-HE4 antibody (A02685-3).<br>HE4 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HE4 Antibody (A02685-3) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02685-3-he4-primary-antibodies-elisa-testing-7.jpgAnti-HE4/Wfdc2 Antibody Picoband® Sandwich ELISA - Recombinant rat HE4/Wfdc2 protein standard curve.<br>
Use in combination with reagents from Rat HE4/Wfdc2 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1624).
https://www.bosterbio.com/picokine-elisa-kits/human-mmp-10-picokine-elisa-kit-ek0467-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0467.jpgHuman MMP-10/Stromelysin-2 ELISA Kit PicoKine®Human MMP-10 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-bmp-6-picokine-elisa-kit-ek1608-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1608.pngMouse BMP-6 ELISA Kit PicoKine®Mouse BMP-6 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/rat-bmp-6-picokine-elisa-kit-ek1609-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1609.pngRat BMP-6 ELISA Kit PicoKine®Rat BMP-6 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-bmp-9-picokine-elisa-kit-ek1610-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1610.pngMouse BMP-9 ELISA Kit PicoKine®Mouse BMP-9 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/rat-bmp-9-picokine-elisa-kit-ek1611-boster.html2026-04-06T05:04:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1611.pngRat BMP-9 ELISA Kit PicoKine®Rat BMP-9 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-dystroglycan-picokine-elisa-kit-ek1614-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1614.pngHuman Dystroglycan ELISA Kit PicoKine®Human Dystroglycan PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-il-23r-picokine-elisa-kit-ek1612-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1612.pngHuman IL-23R/Interleukin-23 receptor ELISA Kit PicoKine®Human IL-23R PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-il-23r-picokine-elisa-kit-ek1613-boster.html2026-03-24T05:11:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1613.jpgMouse IL-23R/Interleukin-23 receptor ELISA Kit PicoKine®Mouse IL-23R PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-bmp-9-picokine-elisa-kit-ek1560-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1560.pngHuman BMP-9 ELISA Kit PicoKine®Human BMP-9 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-trailr3-tnfrsf10c-picokine-elisa-kit-ek0533-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0533.pngHuman TRAILR3/TNFRSF10C ELISA Kit PicoKine®Human TRAILR3/ TNFRSF10C PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-cardiotrophin-1-picokine-elisa-kit-ek0564-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0564.pngMouse Cardiotrophin-1 / CT-1 ELISA Kit PicoKine®Mouse Cardiotrophin-1 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/rat-clusterin-picokine-elisa-kit-ek1615-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1615.jpgRat Clusterin ELISA Kit PicoKine®Rat Clusterin PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-pon1-picokine-elisa-kit-ek1621-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1621_2.pngMouse PON1/Paraoxonase 1 ELISA Kit PicoKine®Mouse PON1 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-pd-l2-b7-dc-picokine-elisa-kit-ek1447-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1447.pngHuman PD-L2/B7-DC ELISA Kit PicoKine®Human PD-L2/B7-DC PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/rat-ccl7-mcp-3-picokine-elisa-kit-ek1300-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1300.pngRat CCL7/MCP-3 ELISA Kit PicoKine®Rat CCL7/MCP-3 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-mimecan-picokine-elisa-kit-ek1617-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1617.pngMouse Mimecan ELISA Kit PicoKine®Mouse Mimecan PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/mouse-pglyrp1-picokine-elisa-kit-ek1618-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1618.pngMouse PGLYRP1/Pgrps ELISA Kit PicoKine®Mouse PGLYRP1 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/picokine-elisa-kits/human-notch1-picokine-elisa-kit-ek1619-boster.html2026-03-24T05:11:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1619.pngHuman NOTCH1 / TAN 1 ELISA Kit PicoKine®Human NOTCH1 PicoKine ELISA Kit standard curve
https://www.bosterbio.com/products/primary-antibodies/anti-znf507-antibody-a15510-boster.html2026-03-24T05:13:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A15510-ZNF507-primary-antibodies-WB-testing-1.jpgAnti-Zinc finger protein 507 ZNF507 AntibodyWestern blot analysis of ZNF507 expression in Human Muscle. ZNF507 at 106KD was detected using rabbit anti-ZNF507 Antigen Affinity purified polyclonal antibody (Catalog # A15510) at Dilution:0.2-1ug/ml. The blot was developed using chemiluminescence (ECL) method (Catalog # EK1002).
https://www.bosterbio.com/products/primary-antibodies/anti-argininosuccinate-lyase-asl-picoband-trade-antibody-a00742-1-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00742-1-adenylosuccinate_lyase-primary-antibodies-wb-testing-1.jpgAnti-Argininosuccinate Lyase/ASL Antibody Picoband® Western blot analysis of Argininosuccinate Lyase/ASL using anti-Argininosuccinate Lyase/ASL antibody (A00742-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: rat lung tissue lysates,<br>Lane 4: mouse liver tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Argininosuccinate Lyase/ASL antigen affinity purified polyclonal antibody (Catalog # A00742-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Argininosuccinate Lyase/ASL at approximately 52KD. The expected band size for Argininosuccinate Lyase/ASL is at 52KD.
https://www.bosterbio.com/products/primary-antibodies/anti-med4-picoband-trade-antibody-a06467-1-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-1-med4-primary-antibodies-wb-testing-1_1.jpgAnti-MED4 Antibody Picoband® Western blot analysis of MED4 using anti-MED4 antibody (A06467-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Ana-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED4 antigen affinity purified polyclonal antibody (Catalog # A06467-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED4 at approximately 36 kDa. The expected band size for MED4 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-2.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-3.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-4.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-5.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-6.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A06467-1-MED4-primary-antibodies-IHC-testing-7.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-1).<br>MED4 was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-MED4 Antibody (A06467-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/anti-trfp-med20-picoband-trade-antibody-a09407-1-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09407-1-TRFP-primary-antibodies-WB-testing-1.jpgAnti-TRFP/MED20 Antibody Picoband® Western blot analysis of TRFP / MED20 using anti-TRFP / MED20 antibody (A09407-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: human PANC-1 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRFP / MED20 antigen affinity purified polyclonal antibody (Catalog # A09407-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRFP / MED20 at approximately 23KD. The expected band size for TRFP / MED20 is at 23KD.
https://www.bosterbio.com/products/primary-antibodies/anti-relaxin-1-picoband-trade-antibody-a08367-1-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08367-1-relaxin_1-primary-antibodies-wb-testing-1.jpgAnti-Relaxin 1/RLN1 Antibody Picoband® Western blot analysis of Relaxin 1 using anti-Relaxin 1 antibody (A08367-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat PC-12 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Relaxin 1 antigen affinity purified polyclonal antibody (Catalog # A08367-1) at 0.5 ug/mL overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Relaxin 1 at approximately 21KD. The expected band size for Relaxin 1 is at 21KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08367-1-relaxin_1-primary-antibodies-ihc-testing-2.jpgAnti-Relaxin 1/RLN1 Antibody Picoband® IHC analysis of Relaxin 1 using anti-Relaxin 1 antibody (A08367-1).<br>Relaxin 1 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Relaxin 1 Antibody (A08367-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08367-1-relaxin_1-primary-antibodies-wb-testing-3.jpgAnti-Relaxin 1/RLN1 Antibody Picoband® IHC analysis of Relaxin 1 using anti-Relaxin 1 antibody (A08367-1).<br>Relaxin 1 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Relaxin 1 Antibody (A08367-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08367-1-relaxin_1-primary-antibodies-ihc-testing-4.jpgAnti-Relaxin 1/RLN1 Antibody Picoband® IHC analysis of Relaxin 1 using anti-Relaxin 1 antibody (A08367-1).<br>Relaxin 1 was detected in paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Relaxin 1 Antibody (A08367-1) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfp-rabbit-monoclonal-antibody-hrp-conjugated-h30939-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/h/3/h30939-gfp-primary-antibodies-wb-testing-1.jpgAnti-GFP Rabbit Monoclonal Antibody, HRP Conjugated Western blot analysis of GFP fusion protein expression in (1) 293T cell lysate; (2) 293T cell transfected GFP fusion protein with GFP Antibody(HRP conjugated).
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gapdh-rabbit-monoclonal-antibody-hrp-conjugated-h00227-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/H/0/H00227-GAPDH-primary-antibodies-WB-testing-1.jpgAnti-GAPDH Rabbit Monoclonal Antibody, HRP ConjugatedWestern blot analysis of GAPDH expression in (1) Jurkat cell lysate; (2) A375 cell lysate; (3) Human hippocampus lysate; (4) Human fetal liver lysate; (5) COS-1 cell lysate; (6) Raw264.7 cell lysate; (7) Mouse kidney lysate; (8) PC-12 cell lysate; (9) Rat brain lysatehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/h/0/h00227-gr7_lrg.jpgAnti-GAPDH Rabbit Monoclonal Antibody, HRP Conjugated(A) The eluted products obtained from co-immunoprecipitation (coIP) were subjected to western blot detection for GAPDH and galectin-3. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(24)01793-0'>39188985</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gst-tag-rabbit-monoclonal-antibody-hrp-conjugated-ht0015-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/h/t/ht0015-gst-tag-primary-antibodies-wb-testing-1.jpgAnti-GST-Tag Rabbit Monoclonal Antibody, HRP ConjugatedWestern blot analysis of GST expression in GST recombinant protein, using GST tag Antibody(HRP conjugated)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-tubulin-rabbit-monoclonal-antibody-hrp-conjugated-h01857-boster.html2026-03-24T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/H/0/H01857-TUBB3-primary-antibodies-WB-testing-1.jpgAnti-beta Tubulin Rabbit Monoclonal Antibody, HRP ConjugatedWestern blot analysis of beta Tubulin expression in (1) Jurkat cell lysate, (2) Human kidney lysate, (3) 3T3 cell lysate, (4) Mouse brain lysate, (5) C6 cell lysate, (6) Rat heart lysate (H01857). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBB3 monoclonal antibody (Catalog # H01857) overnight at 4℃, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TUBB3
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p53-s9-rabbit-monoclonal-antibody-p00001-3-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-3-wb.jpgAnti-Phospho-p53 (S9) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-p53 (Ser9) expression in (1)HepG2 cell lysates treated with etoposide; (2)HeLa cell lysates treated with etoposide.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tyrosine-rabbit-monoclonal-antibody-pt0005-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/t/pt0005-wb.jpgAnti-Phospho-Tyrosine Rabbit Monoclonal AntibodyWestern blot analysis of Phosphotyrosine expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/t/pt0005-if.jpgAnti-Phospho-Tyrosine Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells treated with pervanadate, using Phosphotyrosine Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p53-s33-rabbit-monoclonal-antibody-p00001-4-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-4-wb.jpgAnti-Phospho-p53 (S33) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-p53 (Ser33) in T47D cell lysates treated with etoposide.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p53-t55-rabbit-monoclonal-antibody-p00001-5-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-5-wb.jpgAnti-Phospho-p53 (T55) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-p53 (T55) in HEK293 cell lysates treated with Calyculin A and Okadaic Acid.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rb-s807-rabbit-monoclonal-antibody-p00039-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00039-1-rb1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Rb (S807) RB1 Rabbit Monoclonal Antibody Western blot analysis of Retinoblastoma using anti-Retinoblastoma antibody (P00039-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Retinoblastoma antigen affinity purified monoclonal antibody (Catalog # P00039-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Retinoblastoma at approximately 106 kDa. The expected band size for Retinoblastoma is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00039-1-rb1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Rb (S807) RB1 Rabbit Monoclonal Antibody IHC analysis of Retinoblastoma using anti-Retinoblastoma antibody (P00039-1). <br>
Retinoblastoma was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Retinoblastoma Antibody (P00039-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00039-1-rb1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Rb (S807) RB1 Rabbit Monoclonal Antibody IHC analysis of Retinoblastoma using anti-Retinoblastoma antibody (P00039-1). <br>
Retinoblastoma was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Retinoblastoma Antibody (P00039-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/P/0/P00039-1-RB1-primary-antibodies-IHC-testing-1.jpgAnti-Phospho-Rb (S807) RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse spleen, using Phospho-Retinoblastoma (S807) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-lat-y191-rabbit-monoclonal-antibody-p01654-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01654-p-lat-primary-antibodies-wb-testing-1.jpgAnti-Phospho-LAT (Y191) Rabbit Monoclonal AntibodyWestern blot analysis of P-LAT using anti-P-LAT antibody (P01654). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat thymus tissue lysates,<br>
Lane 4: rat RH35 whole cell lysates,<br>
Lane 5: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-LAT antigen affinity purified monoclonal antibody (P01654) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-LAT at approximately 38 kDa. The expected band size for P-LAT is at 28 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p53-s392-rabbit-monoclonal-antibody-p00001-6-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-6-p53-primary-antibodies-wb-testing-1.jpgAnti-Phospho-p53 (S392) TP53 Rabbit Monoclonal Antibody Western blot analysis of p53 using anti-p53 antibody (P00001-6). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates,<br>
Lane 4: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p53 antigen affinity purified monoclonal antibody (Catalog # P00001-6) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for p53 at approximately 53 kDa. The expected band size for p53 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-6-ihc.jpgAnti-Phospho-p53 (S392) TP53 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using Phospho-p53 (S392) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-6-icc1.jpgAnti-Phospho-p53 (S392) TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkr-t446-rabbit-monoclonal-antibody-p01384-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01384-wb7.jpgAnti-Phospho-PKR (T446) EIF2AK2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01384-wb.jpgAnti-Phospho-PKR (T446) EIF2AK2 Rabbit Monoclonal AntibodyWestern blot analysis of PKR phosphorylation expression in HeLa cell lysate treated with Calyculin A and TNF-alpha.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01384-ihc.jpgAnti-Phospho-PKR (T446) EIF2AK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Phospho-PKR (T446) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p53-s376-rabbit-monoclonal-antibody-p00001-7-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-7-wb7.jpgAnti-Phospho-p53 (S376) TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-7-wb.jpgAnti-Phospho-p53 (S376) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-p53 (S376) in HEK293 cell lysates treated with Calyculin A and Okadaic Acid.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-btk-y223-rabbit-monoclonal-antibody-p00245-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00245-1-wb.jpgAnti-Phospho-BTK (Y223) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-BTK (Y223) expression in Raji cell lysate treated with pervanadate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-fak-y397-rabbit-monoclonal-antibody-p00151-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00151-wb.jpgAnti-Phospho-FAK (Y397) PTK2 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-FAK (Y397) expression in EGF treated 293 whole cell lysates,The lane on the left is treated with the antigen-specific peptide.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-t231-rabbit-monoclonal-antibody-p00097-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-1-tau-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Tau (T231) MAPT Rabbit Monoclonal Antibody Western blot analysis of Tau using anti-Tau antibody (P00097-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tau antigen affinity purified monoclonal antibody (Catalog # P00097-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tau at approximately 50-70 kDa. The expected band size for Tau is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-1-tau-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Tau (T231) MAPT Rabbit Monoclonal Antibody IHC analysis of Tau using anti-Tau antibody (P00097-1). <br>
Tau was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Tau Antibody (P00097-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-1-tau-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Tau (T231) MAPT Rabbit Monoclonal Antibody IHC analysis of Tau using anti-Tau antibody (P00097-1). <br>
Tau was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Tau Antibody (P00097-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-1-wb8.jpgAnti-Phospho-Tau (T231) MAPT Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-1-wb.jpgAnti-Phospho-Tau (T231) MAPT Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (T231) expression in (1) SH-SY5Y cell lysate; (2) SH-SY5Y cell lysate, treated with sorbitol.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-atf2-t71-rabbit-monoclonal-antibody-p00916-3-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/P/0/P00916-3-ATF2-primary-antibodies-WB-testing-1.jpgAnti-Phospho-ATF2 (T71) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-ATF2 (T71) expression in (1) HeLa cell lysate; (2) HeLa cell lysate treated with Anisomycin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00916-3-atf2-primary-antibodies-if-testing-2.jpg.jpgAnti-Phospho-ATF2 (T71) Rabbit Monoclonal AntibodyICC staining of Phospho-ATF2 (T71) in SH-SY5Y cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (1/50) for 1 hour at room temperature, washed with PBS.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s396-rabbit-monoclonal-antibody-p00097-2-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-2-phospho-tau-s396-mapt-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Tau (S396) MAPT Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (S396) MAPT using anti-Phospho-Tau (S396) MAPT antibody (P00097-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin V antigen affinity purified monoclonal antibody (P00097-2) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Annexin V at approximately 54 kDa. The expected band size for Annexin V is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00097-2-ihc.jpgAnti-Phospho-Tau (S396) MAPT Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Phospho-Tau (S396) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rpa2-t21-rabbit-monoclonal-antibody-p02067-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02067-1-rpa2-primary-antibodies-wb-testing-1.jpgAnti-Phospho-RPA2 (T21) Rabbit Monoclonal Antibody Western blot analysis of RPA2 using anti-RPA2 antibody (P02067-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPA2 antigen affinity purified monoclonal antibody (Catalog # P02067-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPA2 at approximately 29 kDa. The expected band size for RPA2 is at 29 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-hsl-s853-rabbit-monoclonal-antibody-p06762-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06762-1-p-lipe-primary-antibodies-wb-testing-1.jpgAnti-Phospho-HSL (S853) LIPE Rabbit Monoclonal AntibodyWestern blot analysis of P-LIPE using anti-P-LIPE antibody (P06762-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat skeletal muscle tissue lysates,<br>
Lane 2: mouse skeletal muscle tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-LIPE antigen affinity purified monoclonal antibody (P06762-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-LIPE at approximately 83 kDa. The expected band size for P-LIPE is at 117 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06762-1-p-lipe-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-HSL (S853) LIPE Rabbit Monoclonal AntibodyIHC analysis of P-LIPE using anti-P-LIPE antibody (P06762-1). <br>P-LIPE was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-LIPE Antibody (P06762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06762-1-12576_2024_902_fig5_html.pngAnti-Phospho-HSL (S853) LIPE Rabbit Monoclonal AntibodyLevels of proteins related to lipolysis after 6 weeks of 3-OBA and ET intervention. A , G Western blot (WB) analysis of P-HSL and HSL. B , H WB analysis of P-ATGL and ATGL. ( C , I ) WB analysis of CPT1b. D , J Ratio of P-HSL/HSL. E , K P-ATGL/ATGL ratio. F , L Fold protein of CPT1b. Three bands per group of rats are used. Relative levels were standardized to GAPDH. Measurement data were presented as the mean ± SD. The significance of the difference between the two groups C and H was calculated with the independent samples t test, and the four groups (S, 3, SH, and 3H) were analyzed with the two-way ANOVA. * p < 0.05 and ** p < 0.01. The number of biological repeats ( n = 10) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12576-024-00902-x'>38331728</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-btk-y551-rabbit-monoclonal-antibody-p00245-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00245-wb.jpgAnti-Phospho-BTK (Y551) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-BTK (Y551) expression in Ramos cell lysate treated with Pervanadate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-cdc6-s54-rabbit-monoclonal-antibody-p01355-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01355-wb.jpgAnti-Phospho-Cdc6 (S54) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Cdc6 (S54) expression in (1) Raji cell lysate; (2) Raji + FBS cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-raf1-s43-rabbit-monoclonal-antibody-p00446-3-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00446-3-p-raf1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Raf1 (S43) Rabbit Monoclonal AntibodyWestern blot analysis of P-RAF1 using anti-P-RAF1 antibody (P00446-3). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: rat PC-12 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-RAF1 antigen affinity purified monoclonal antibody (P00446-3) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-RAF1 at approximately 73 kDa. The expected band size for P-RAF1 is at 73 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-nrf2-s40-rabbit-monoclonal-antibody-p00078-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-nrf2-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal Antibody Western blot analysis of Nrf2 using anti-Nrf2 antibody (P00078). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human SiHa whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Nrf2 antigen affinity purified monoclonal antibody (Catalog # P00078) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Nrf2 at approximately 100 kDa. The expected band size for Nrf2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-nrf2-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal Antibody IHC analysis of Nrf2 using anti-Nrf2 antibody (P00078). <br>
Nrf2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nrf2 Antibody (P00078) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-nrf2-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal Antibody IHC analysis of Nrf2 using anti-Nrf2 antibody (P00078). <br>
Nrf2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nrf2 Antibody (P00078) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-nrf2-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal Antibody IHC analysis of Nrf2 using anti-Nrf2 antibody (P00078). <br>
Nrf2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nrf2 Antibody (P00078) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-if.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using Phospho-Nrf2 (S40) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-icc1.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-icc2.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00078-icc3.jpgAnti-Phospho-Nrf2 (S40) NFE2L2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-lyn-y396-rabbit-monoclonal-antibody-p01424-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01424-1-wb.jpgAnti-Phospho-Lyn (Y396) Rabbit Monoclonal AntibodyWestern blot analysis of Lyn phosphorylation expression in Jurkat cell lysate treated with Pervanadate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01424-1-phospho-lyn_y396_-custom-antibodies-fc-testing-1.pngAnti-Phospho-Lyn (Y396) Rabbit Monoclonal Antibody Flow Cytometry analysis of B cells using anti-Phospho-Lyn (Y396) rabbit monoclonal antibody (P01424-1). <br>
Overlay histogram showing B cells stained with P01424-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 5% FBS. And then incubated with rabbit anti-Phospho-Lyn (Y396) rabbit monoclonal antibody (P01424-1) at 0.25 µl/1x10<sup>6</sup> cells 50min RT. F(ab')2-Donkey anti-Rabbit IgG (H+L), PE 0.1 µl/1x10<sup>6</sup> was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-creb-s133-rabbit-monoclonal-antibody-p00577-1-boster.html2026-03-24T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00577-1-wb7.jpgAnti-Phospho-Creb (S133) CREB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00577-1-wb.jpgAnti-Phospho-Creb (S133) CREB1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Creb(Ser133) expression in HeLa cell lysates treated with Calyculin A.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00577-1-ihc.jpgAnti-Phospho-Creb (S133) CREB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human gastric carcinoma, using Phospho-Creb (S133) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-gcn2-t899-rabbit-monoclonal-antibody-p01172-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01172-wb.jpgAnti-Phospho-GCN2 (T899) EIF2AK4 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-GCN2 (Thr899) in (1) HeLa cell lysate; (2) HeLa cell lysate treated with Calyculin.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-atm-s1981-rabbit-monoclonal-antibody-p00014-1-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00014-1-wb.jpgAnti-Phospho-ATM (S1981) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-ATM (Ser1981) in (1) HEK293 cell lysate; (2) HEK293 cell lysate treated with Doxorubicin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00014-1-ihc.jpgAnti-Phospho-ATM (S1981) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Phospho-ATM (S1981) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-hsf1-s326-rabbit-monoclonal-antibody-p00250-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00250-hsf1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-HSF1 (S326) Rabbit Monoclonal Antibody Western blot analysis of HSF1 using anti-HSF1 antibody (P00250). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSF1 antigen affinity purified monoclonal antibody (Catalog # P00250) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSF1 at approximately 80 kDa. The expected band size for HSF1 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00250-hsf1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-HSF1 (S326) Rabbit Monoclonal Antibody IHC analysis of HSF1 using anti-HSF1 antibody (P00250). <br>
HSF1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSF1 Antibody (P00250) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00250-hsf1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-HSF1 (S326) Rabbit Monoclonal Antibody IHC analysis of HSF1 using anti-HSF1 antibody (P00250). <br>
HSF1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSF1 Antibody (P00250) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00250-icc1.jpgAnti-Phospho-HSF1 (S326) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00250-icc2.jpgAnti-Phospho-HSF1 (S326) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-c-myc-s62-rabbit-monoclonal-antibody-p00026-2-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-2-p-myc-primary-antibodies-wb-testing-1.jpgAnti-Phospho-c-Myc (S62) Rabbit Monoclonal AntibodyWestern blot analysis of P-MYC using anti-P-MYC antibody (P00026-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-MYC antigen affinity purified monoclonal antibody (P00026-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-MYC at approximately 57 kDa. The expected band size for P-MYC is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-2-ihc.jpgAnti-Phospho-c-Myc (S62) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung carcinoma, using Phospho-c-Myc (S62) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rsk1-s380-rabbit-monoclonal-antibody-p01058-1-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01058-1-p-rps6ka1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-RSK1 (S380) RPS6KA1 Rabbit Monoclonal AntibodyWestern blot analysis of P-RPS6KA1 using anti-P-RPS6KA1 antibody (P01058-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A4361 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-RPS6KA1 antigen affinity purified monoclonal antibody (P01058-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-RPS6KA1 at approximately 83 kDa. The expected band size for P-RPS6KA1 is at 83 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-trkb-y817-rabbit-monoclonal-antibody-p01388-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-trkb-primary-antibodies-wb-testing-1.jpgAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal Antibody Western blot analysis of TrkB using anti-TrkB antibody (P01388). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TrkB antigen affinity purified monoclonal antibody (Catalog # P01388) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TrkB at approximately 130 kDa. The expected band size for TrkB is at 92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-wb.jpgAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-TrkB (Y817) expression in SH-SY5Y cell lysate treated with BDNF.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41398_2023_2429_fig4_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyDecreased hippocampal dentate gyrus (DG) neurogenesis in CPE flox/flox mice. a – e Western blot analysis of p -TrkB, BDNF, p -mTOR, mTOR, p -AKT, and AKT levels in the hippocampus. f Immunofluorescence of CPE, MAP2, DCX, and GFAP; and the relative fluorescent intensities of g CPE in Sub, h MAP2 in Sub, i MAP2 in hilius, j DCX in DG, k GFAP in DG of WT, CPE flox/− , and CPE flox/flox mice at 100× and 400× (square in the panel). n = 6; * P < 0.05 and ** P < 0.01 compared with WT; values are mean ± SEM. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41398-023-02429-y'>37100779</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-gr7.jpgAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyResults of western blotting (n = 3). (A) Relative expressions of GR, SERT, BDNF, Trk B, and p-Trk B in hippocampal tissues of GS + MS and PS + MS groups; Relative gray values of (B) GR, (C) SERT, and (D) BDNF and (E) the ratio of p-Trk B to Trk B in hippocampal tissues of female mice. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/heliyon/fulltext/S2405-8440(24)11394-1'>39166014</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41419_2025_7990_fig1_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyMTFL 457 preserves pY816-TrkB-FL at the cell surface, protecting it from proteolytic machinery activated secondarily by excitotoxicity. A – D Kinetics of TrkB-FL downregulation. Primary cortical cultures were treated with 100 μM NMDA and its co-agonist 10 μM glycine (hereafter referred to as ‘NMDA’). Immunofluorescence ( A ) and immunoblotting ( B ) used a C-terminal (C-ter) isoform-specific antibody (TrkB-FL Ct) recognizing both the full-length protein (FL) and the intracellular fragment (f32). A Shows TrkB-FL (green) and nuclei (blue, DAPI stain). Arrowheads indicate varicosities in neuronal projections. Scale bar: 20 μm. Insets show cell body details for untreated cells and cells treated with NMDA for 120 min. B Compares the decrease in TrkB-FL and formation of f32 with PSD-95 downregulation, detected using a C-terminal antibody (PSD-95 Ct). Calpain activation was confirmed by the accumulation of characteristic spectrin breakdown products (BDPs; 150 and 145 kDa). Neuron-specific enolase (NSE) served as a loading control for protein normalization. C , D Quantification of normalized TrkB-FL and PSD-95 levels, shown relative to levels in the absence of NMDA (control). Data are represented as means ± SD. Statistical analysis: one-way analysis of variance (ANOVA) followed by Bonferroni post hoc test (** P < 0.01, *** P < 0.001, **** P < 0.0001; 0-90 min, n = 5; 120 min, n = 3). E , F Effect of dynasore preincubation (80 μM, 30 min) on TrkB-FL levels after 2 h NMDA treatment. Data are means ± SD ( n = 4); statistical analysis as above (* P < 0.05). G Sequences of the cell-penetrating neuroprotective peptide (MTFL 457 ) and control peptide (MTMyc). Both contain Tat amino acids (aa) 47–57 (italic), followed by rat TrkB-FL aa 457-471 (light blue) or c-Myc aa 408-421 (dark blue), respectively. H , I Effect of peptide preincubation (25 μM, 30 min) on TrkB-FL shedding and processing during NMDA treatment. Culture media were analyzed using an antibody against the TrkB-FL extracellular domain (panTrkB), which recognizes the ectodomains (ECDs) of all isoforms (TrkB-ECD), to assess receptor shedding by metalloproteinase (MP) activation. Total lysates were analyzed with the TrkB-FL Ct antibody to evaluate TrkB-FL calpain processing via f32 production. Relative TrkB-ECD levels are shown as means ± SD (0-4 h, n = 7; 6 h, n = 4). Statistical analysis: two-way ANOVA followed by Bonferroni post hoc test (** P < 0.01, **** P < 0.0001, comparing each peptide + NMDA vs. peptide alone; # P < 0.05, #### P < 0.0001, comparing MTMyc vs. MTFL 457 at each time point). J , K Effect of NMDA on total and cell-surface pY816-TrkB-FL levels. Cultures were preincubated with peptides as above, then treated briefly with NMDA (1 h) to minimize receptor degradation. Cell-surface proteins were biotin-labeled and precipitated, then compared to corresponding total lysates. Data are represented as means ± SD ( n = 4). Statistical analysis: two-way ANOVA followed by Bonferroni post hoc test ( n.s . = n ot significant; ** P < 0.01, comparing NMDA vs. no NMDA; ## P < 0.01, comparing MTMyc + NMDA vs. MTFL 457 + NMDA). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07990-6'>40883288</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41419_2025_7990_fig3_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyEffect of excitotoxicity on TrkB-FL interaction with endosomal protein Hrs. A – C Analysis by immunofluorescence of TrkB-FL/Hrs colocalization. A Cortical neurons were treated with NMDA for the indicated times and analyzed with antibodies specific for Hrs (green) and TrkB-FL Ct (red); nuclear staining was performed with DAPI (blue). Representative images obtained by confocal microscopy correspond to single sections and show the fused channels. Scale bar: 20 μm. B Mean values ± SD of Pearson correlation coefficient (PCC; n = 3). For each independent experiment, a minimum of 80 different neurons were analyzed. Statistical analysis was performed using a generalized linear model followed by a post-hoc Fisher’s LSD test (* P < 0.05, compared to untreated cultures). C Percentage of cells showing at different times of NMDA treatment a PCC ≥ 0.50, generally considered as a threshold for protein colocalization. Statistical analysis was performed as before ( * P < 0.05, compared to untreated cultures; n = 3). D , E Analysis by immunoprecipitation of TrkB-FL/Hrs interaction. Neuronal cultures were treated with NMDA (100 μM) or BDNF (100 ng/ml) for 30 min and compared to untreated cultures. Immunoprecipitation was performed with the Hrs antibody, and the immunoprecipitated proteins (IP) were analyzed by immunoblot using the same antibody ( D ) or TrkB-FL Ct ( E ). Total protein lysates were analyzed in parallel with the immunoprecipitated proteins. Mean values ± SD ( n = 5, except for BDNF-treated cells where n = 4) of Hrs and TrkB-FL levels in NMDA- or BDNF-treated cultures relative to untreated cells are represented for both total lysates and Hrs-immunoprecipitated proteins. Statistical analysis was performed as above ( *P < 0.05, compared to the respective untreated cultures; # P < 0.05 and ## P < 0.01, as indicated). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07990-6'>40883288</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41419_2025_7990_fig4_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyRegulation by MTFL 457 of the TrkB-FL/Hrs interaction induced by excitotoxicity. A Cortical neurons were preincubated with MTMyc and MTFL 457 (25 μM, 30 min) and treated with NMDA for the indicated times. Cells were analyzed by immunofluorescence with antibodies for Hrs (green) and TrkB-FL Ct (red), together with DAPI staining (blue). Representative confocal microscopy images correspond to single sections and show the fused channels. Scale bar: 10 μm. B Mean values ± SD of Pearson correlation coefficient (PCC; n = 3). For each independent experiment, a minimum of 80 different neurons were analyzed. Statistical analysis was performed using a generalized linear model followed by a post-hoc Fisher’s LSD test ( P = 0.06, 0 vs. 60 min of NMDA treatment in MTMyc-cultures). C , D Analysis by immunoprecipitation of TrkB-FL/Hrs interaction. Cultures preincubated with cell-penetrating peptides (CPPs) as above were treated with NMDA for 30 min and compared to untreated cultures. Immunoprecipitation (IP) was performed with the Hrs antibody, and the immunoprecipitated proteins were analyzed by immunoblot using the same antibody ( C ) or TrkB-FL Ct ( D ). Total protein lysates and immunoprecipitated proteins were analyzed in parallel. Mean values ± SD ( n = 4) of Hrs and TrkB-FL levels relative to those found in cells preincubated with MTMyc and without NMDA are represented. Statistical analysis was performed using two-way ANOVA followed by a Bonferroni test (* P < 0.05, ** P < 0.01). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07990-6'>40883288</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41419_2025_7990_fig5_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyEffect of excitotoxicity on TrkB-FL transport to the Golgi complex and regulation by MTFL 457 action. Cortical neurons were treated with NMDA for the indicated times and analyzed by immunofluorescence with antibodies specific for the Golgi matrix protein GM130 (green) and TrkB-FL Ct (red); nuclear staining was performed with DAPI (blue). Excitotoxicity was induced in the absence of peptides ( A – C ) or after preincubation with MTMyc and MTFL 457 (25 μM, 30 min) ( D – F ). A , D Representative images obtained by confocal microscopy corresponding to single sections, showing channels fused. Scale bar: 20 μm. B , E Mean PCC values ± SD (0-30 min, n = 4; 60 min, n = 3) for TrkB-FL and GM130 colocalization. Statistical analysis was performed using a generalized linear model followed by a post-hoc Fisher’s LSD test (* P < 0.05, ** P < 0.01, compared to basal conditions without peptide or with MTMyc, respectively). C , F Percentage of cells showing, at different treatment times, a PCC ≥ 0.52 ( C ), the value obtained for TrkB-FL/GM130 colocalization in basal conditions in the absence of peptide, or ≥ 0.50 ( F ). Statistical analysis was performed by one-way ANOVA followed by a Bonferroni post hoc test (* P < 0.05, compared to basal conditions without peptide or with MTMyc, respectively; 0–30 min, n = 4; 60 min, n = 3). For each independent experiment, a minimum of 80 different neurons were analyzed. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07990-6'>40883288</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-41419_2025_7990_fig8_html.pngAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyEffect of brain ischemia on GA stability, MTFL 457 regulation, and proposed model. A Strong association between neuronal degeneration and serum protein leakage after ischemic damage. Immunohistochemistry of brain coronal sections from animals sacrificed 5 h after insult was performed with an antibody recognizing a calpain-generated neoepitope in spectrin N-terminal fragment (SNTF, magenta), labeling cells where this protease is overactive, and a mouse antibody recognizing GM130 (red). Neurodegeneration was also detected by Fluoro-Jade C (FJC) staining (green). Three different tissue areas were compared: the ischemic core, an area peripheral to the infarct core, and the equivalent area of the contralateral hemisphere. Leakage of mouse immunoglobulins due to early blood-brain barrier (BBB) breakage after the ischemic insult, detected by the secondary anti-mouse antibody (see Fig. S ), was observed in the neurodegenerating tissue and strongly interfered with GM130 detection. B , C GM130 staining after preincubation of coronal sections with an anti-mouse IgG (Fab specific) antibody to improve detection. Animals were retro-orbitally injected with peptides MTMyc or MTFL 457 (10 nmol/g) 10 min after damage initiation and sacrificed 5 h later. Comparison of the contralateral ( B ) and the ischemic peripheral areas ( C ). Representative images correspond to single sections. Scale bar: 10 µm. D Model of TrkB-FL regulation in excitotoxicity and MTFL 457 action. Endocytosis of neurotrophin receptor TrkB-FL is promoted by excitotoxicity in neurons treated with control peptide MTMyc or without treatment (left panel). In endosomes, TrkB-FL interacts with the protein Hrs and is retrogradely transported to the Golgi apparatus (GA), where activation of organelle-associated proteinases would be responsible for receptor processing by calpain and regulated intramembrane proteolysis (RIP). Although partial recycling back to the membrane might occur via mechanisms similar to those found after BDNF activation, there is a strong decrease in BDNF/TrkB-FL signaling and CREB/MEF2 promoter activities, causing transcriptional changes that favor neuronal death. In parallel, the GA is disrupted, a hallmark common to many neurodegenerative diseases (NDDs). The neuroprotective peptide MTFL 457 interferes with the TrkB-FL/Hrs interaction induced by excitotoxicity, receptor retrograde transport and processing, as well as GA fragmentation (right panel). We propose that interference by MTFL 457 with the TrkB-FL/Hrs interaction might favor rapid recycling back to the membrane, similar to that of isoform TrkB-T1, sustained BDNF/TrkB-FL/PLCγ signaling, and promotion of neuronal survival. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07990-6'>40883288</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-ihc.jpgAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain cancer, using Phospho-TrkB (Y817) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01388-icc1.jpgAnti-Phospho-TrkB (Y817) NTRK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ire1-s724-rabbit-monoclonal-antibody-p00683-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00683-p-ire1-primary-antibodies-wb-testing-1.pngAnti-Phospho-IRE1 (S724) ERN1 Rabbit Monoclonal AntibodyWestern blot analysis of P-IRE1 using anti-P-IRE1 antibody (P00683). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1-6:Different intestinal tissues from pigs infected with classical swine fever.<br>
electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-IRE1 antigen affinity purified monoclonal antibody (P00683) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for P-IRE1 at approximately 100-110 kDa. The expected band size for P-IRE1 is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00683-p-ire1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-IRE1 (S724) ERN1 Rabbit Monoclonal AntibodyWestern blot analysis of P-IRE1 using anti-P-IRE1 antibody (P00683). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-IRE1 antigen affinity purified monoclonal antibody (P00683) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-IRE1 at approximately 100 kDa. The expected band size for P-IRE1 is at 110 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-c-myc-t58-rabbit-monoclonal-antibody-p00026-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-p-myc-primary-antibodies-wb-testing-1.jpgAnti-Phospho-c-Myc (T58) Rabbit Monoclonal AntibodyWestern blot analysis of P-Myc using anti-P-Myc antibody (P00026). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-Myc antigen affinity purified monoclonal antibody (P00026) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-Myc at approximately 57 kDa. The expected band size for P-Myc is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-p-myc-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-c-Myc (T58) Rabbit Monoclonal AntibodyIHC analysis of P-Myc using anti-P-Myc antibody (P00026). <br>P-Myc was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-Myc Antibody (P00026) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-p-myc-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-c-Myc (T58) Rabbit Monoclonal AntibodyIHC analysis of P-Myc using anti-P-Myc antibody (P00026). <br>P-Myc was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-Myc Antibody (P00026) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-shp2-y542-rabbit-monoclonal-antibody-p00150-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00150-ptpn11-primary-antibodies-wb-testing-1.jpgAnti-Phospho-SHP2 (Y542) PTPN11 Rabbit Monoclonal AntibodyWestern blot analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (P00150). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHP2/PTPN11 antigen affinity purified monoclonal antibody (P00150) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHP2/PTPN11 at approximately 70 kDa. The expected band size for SHP2/PTPN11 is at 68 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-sirt1-s47-rabbit-monoclonal-antibody-p00018-1-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-wb.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-SIRT1 (S47) expression in (1) HEK293 cell lysate; (2) HEK293 cell lysate treated with LP.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-1-s2.0-s014765132501142x-gr4.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyProteins expressions of SIRT1-AMPK-FOXO3 pathway and autophagy markers in C28/I2 chondrocytes after 4-hour T-2 toxin treatment. T5: 5 ng/mL T-2 toxin; T20: 20 ng/mL T-2 toxin. n = 3. *P < 0.05, **P < 0.01, ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S014765132501142X'>40763514</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-1-s2.0-s014765132501142x-gr7.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyProteins expressions of SIRT1-AMPK-FOXO3 pathway and autophagy markers of C28/I2 chondrocytes treated with 20 ng/mL T-2 toxin and 100 ng/mL CSA-SeNP for 12 h. ST: Treatment separately with T-2 toxin; SC: Treatment separately with CSA-SeNP; TC: Treatment with T-2 toxin and CSA-SeNP. n = 3. *P < 0.05, **P < 0.01, ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S014765132501142X'>40763514</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-p-sirt1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyIHC analysis of P-SIRT1 using anti-P-SIRT1 antibody (P00018-1). <br>P-SIRT1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-SIRT1 Antibody (P00018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-p-sirt1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyIHC analysis of P-SIRT1 using anti-P-SIRT1 antibody (P00018-1). <br>P-SIRT1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-SIRT1 Antibody (P00018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-p-sirt1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyIHC analysis of P-SIRT1 using anti-P-SIRT1 antibody (P00018-1). <br>P-SIRT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-SIRT1 Antibody (P00018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-1-p-sirt1-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-SIRT1 (S47) Rabbit Monoclonal AntibodyIHC analysis of P-SIRT1 using anti-P-SIRT1 antibody (P00018-1). <br>P-SIRT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-SIRT1 Antibody (P00018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-chk1-s296-rabbit-monoclonal-antibody-p01060-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01060-wb.jpgAnti-Phospho-Chk1 (S296) CHEK1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Chk1 (S296) expression in HEK293 cell lysate Treated with Calyculin.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-hsp27-s82-rabbit-monoclonal-antibody-p00676-1-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00676-1-p-hsp27-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Hsp27 (S82) HSPB1 Rabbit Monoclonal AntibodyWestern blot analysis of P-HSP27 using anti-P-HSP27 antibody (P00676-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse HEPA1-6 whole cell lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-HSP27 antigen affinity purified monoclonal antibody (P00676-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-HSP27 at approximately 27 kDa. The expected band size for P-HSP27 is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-yap1-s127-rabbit-monoclonal-antibody-p00116-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00116-yap1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-YAP1 (S127) Rabbit Monoclonal Antibody Western blot analysis of YAP1 using anti-YAP1 antibody (P00116). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat RH35 whole cell lysates,<br>
Lane 4: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YAP1 antigen affinity purified monoclonal antibody (Catalog # P00116) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YAP1 at approximately 70, 75 kDa. The expected band size for YAP1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00116-yap1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-YAP1 (S127) Rabbit Monoclonal Antibody Immunohistochemical analysis of paraffin-embedded human stomach, using Phospho-YAP1 (S127) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-s695-rabbit-monoclonal-antibody-p00023-4-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-4-wb.jpgAnti-Phospho-EGFR (S695) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-EGFR (S695) expression in A431 cell lysate treated with EGF.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pten-s380-rabbit-monoclonal-antibody-p00006-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00006-wb7.jpgAnti-Phospho-PTEN (S380) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00006-wb.jpgAnti-Phospho-PTEN (S380) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PTEN (S380) expression in (1) MCF-7 cell treated with alkaline phosphatase lysate; (2) MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-mek1-s298-rabbit-monoclonal-antibody-p00292-3-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00292-3-map2k1-primary-antibodies-wb-testing-1_1.jpgAnti-Phospho-MEK1 (S298) MAP2K1 Rabbit Monoclonal Antibody Western blot analysis of Phospho-MEK1 (S298) using anti-Phospho-MEK1 (S298) antibody (P00292-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human U251 whole cell lysates, <br>
Lane 4: human SIHA whole cell lysates, <br>
Lane 5: rat lung tissue lysates, <br>
Lane 6: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-MEK1 (S298) antigen affinity purified monoclonal antibody (P00292-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Phospho-MEK1 (S298) at approximately 54 kDa. The expected band size for Phospho-MEK1 (S298) is at 43 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-mek1-t292-rabbit-monoclonal-antibody-p00292-4-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00292-4-wb.jpgAnti-Phospho-MEK1 (T292) MAP2K1 Rabbit Monoclonal AntibodyWestern blot analysis of MEK5 expression in (1) HeLa cell lysate; (2) HeLa cell treated with Nocodazole.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-c-jun-t91-rabbit-monoclonal-antibody-p02038-1-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-1-p-jun-primary-antibodies-wb-testing-1.jpgAnti-Phospho-c-Jun (T91) Rabbit Monoclonal AntibodyWestern blot analysis of P-JUN using anti-P-JUN antibody (P02038-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-JUN antigen affinity purified monoclonal antibody (P02038-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-JUN at approximately 45 kDa. The expected band size for P-JUN is at 36 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-akt1-t450-rabbit-monoclonal-antibody-p00024-2-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2_fonc-15-1582040-g005.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal AntibodyAMP treatment regulates the PI3K/AKT and MAPK signaling pathways. Lung cells (A549, NCI-H1299, and NCI-H520) with stable CHRM3 overexpression (A) or knockdown (B) were treated with or without 100 μg/mL AMPs for 48 h. The expression levels of PI3K/AKT pathway proteins and MAPK pathway proteins were detected using western blot.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12289679/'>40718823</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2_12645_2025_336_fig9_html.pngAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibodya Western blotting was used to examine mitochondrial apoptotic pathway-related proteins after treatment with control (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Key proteins involved in apoptosis such as Bax, Bcl-2, cytochrome c, and cleaved caspase-3 were examined to better understand how each treatment affects cell death at the mitochondrial level. b To further investigate the underlying molecular mechanisms, western blotting was used to investigate the PI3K/AKT/mTOR pathway (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Expression levels of PI3K, AKT (total and phosphorylated), and mTOR were evaluated to assess whether this survival pathway was activated or suppressed. Protein levels were quantified and compared to the control group to determine statistical significance. * p < 0.05, ** p < 0.01, *** p < 0.001 in comparison to the respective control <br><b>Index in Springer Nature under a CC BY license. DOI: <a href='https://link.springer.com/article/10.1186/s12645-025-00336-z'>10.1186/s12645-025-00336-z</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody Western blot analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AKT1 antigen affinity purified monoclonal antibody (Catalog # P00024-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AKT1 at approximately 65 kDa. The expected band size for AKT1 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-fphar-12-683613-g009.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal AntibodyEffect of Lactucin on the activation of signaling pathways. (A) The whole-cell lysates were extracted for immunoblotting to determine the level of iNOS, COX-2. (B, C) The whole-cell lysates were extracted for immunoblotting to determine the levels of phospho- or total MAPKs (ERK, p38, and JNK) and AKT identified based on their antibodies. Data are shown as mean ± SD for each group (* p < 0.05 with the LPS Group, n = 3. Normal Group: RAW264.7 cells without LPS activation).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.683613/full'>33995112</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody IHC analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
AKT1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AKT1 Antibody (P00024-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody IHC analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
AKT1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AKT1 Antibody (P00024-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody IHC analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
AKT1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AKT1 Antibody (P00024-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-wb-testing-2_1.pngAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody Western blot analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates,<br>
Lane 2: Control group-rat colon tissue lysates,<br>
Lane 3: Low-dose drug treatment-rat colon tissue lysates,<br>
Lane 4: Medium-dose drug treatment-rat colon tissue lysates,<br>
Lane 5: Positive drug treatment-rat colon tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AKT1 antigen affinity purified monoclonal antibody (Catalog # P00024-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for AKT1 at approximately 70 kDa. The expected band size for AKT1 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-ihc-testing-5.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody IHC analysis of AKT1 using anti-AKT1 antibody (P00024-2). <br>
AKT1 was detected in a paraffin-embedded section of intestinal diffuse large B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AKT1 Antibody (P00024-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-2-akt1-primary-antibodies-if-testing-6.jpgAnti-Phospho-AKT1 (T450) Rabbit Monoclonal Antibody IF analysis of AKT1 using anti-AKT1 antibody (P00024-2) and anti-Beta Tubulin antibody (M01857-3).<br>
AKT1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-AKT1 Antibody (P00024-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-jund-s255-rabbit-monoclonal-antibody-p05609-boster.html2026-03-24T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p05609-wb.jpgAnti-Phospho-JunD (S255) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-JunD (S255) expression in (1) HeLa cell lysate treated with Alkaline Phosphatase; (2) HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-akt1-s129-rabbit-monoclonal-antibody-p00024-3-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-wb7.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fphar-10-01459-g006.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyEffects of magnolol on mice alcohol-induced liver damage in the AKT/PI3K signaling pathway. Liver tissues were extracted for protein analysis by western blotting. AKT and PI3K, proteins expression were detected. The levels of AKT and PI3K were compared with GAPDH. The data were demonstrated as means ± SD. (*P < 0.05, **P < 0.01, ***P < 0.001).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.01459/full'>31920652</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fphar-09-00674-g002.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyEpigallocatechin-3-gallate activates the Shh and AKT signaling pathways in hair follicles. After treatment with 0.5 and 1 μM EGCG, the mRNA levels of Shh (A) , PTCH (B) , Smo (C) , and Gli1 (D) in hair follicles were detected by qRT-PCR. The relative mRNA levels were calculated using 2 -ΔΔC t method. Western blot was also performed to detect the protein levels of Shh (E) , PTCH (F) , Smo (G) , and Gli1 (H) in hair follicles. β-actin served as the internal reference. (I) Level of Shh in hair follicles was assessed by immunofluorescence. Red fluorescence: Shh; blue fluorescence: DAPI. (J) The phosphorylation level of AKT was assessed by western blot. (K) Level of p-AKT in hair follicles was assessed by immunofluorescence. Red fluorescence: p-AKT; blue fluorescence: DAPI. Each experiment was repeated three times and the results are presented as mean ± SD. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 compared with the control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00674/full'>29997505</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fphar-09-00674-g003.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyEpigallocatechin-3-gallate activates the Shh and AKT signaling pathways in DPCS and ORSCs. Upon treatment with EGCG, the protein levels of Shh (A) , PTCH (B) , Smo (C) , and Gli1 (D) in DPCs and ORSCs were detected by western blot with β-actin as the internal reference. (E) Western blot was performed to assess the levels of AKT and p-AKT in each group with β-actin as the internal reference. (F) Chemical structure of EGCG. Each experiment was repeated three times.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00674/full'>29997505</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fphar-09-00674-g004.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyShh and AKT signaling pathway inhibitors abolish the effect of EGCG on the growth of DPCs and ORSCs. (A,B) After treatment with EGCG and/or cyclopamine, GANT61 or LY294002, the cell viability of DPCs and ORSCs was assessed by MTT assay. (C,D) Protein levels of cyclinB1 and cyclinD1 in DPCs and ORSCs were assessed by western blot with β-actin as the internal reference. All experiments were repeated three times. The results are presented as mean ± SD. ### p < 0.001 compared with the control group; ∗∗∗ p < 0.001 compared with the EGCG group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00674/full'>29997505</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fig-4-1x.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyPTEN/PI3K/Akt pathway’s contribution in miR-21 induced proliferation in c-kit + CSCs. Cultured c-kit + CSCs were treated with miR-21 mimics for 48 h before subjected to EdU immunofluorescence (A–B), flow cytometry (C) or Western blot (D). To test the contribution of PTEN/PI3K/Akt signaling, PTEN and PI3K were inhibited with Phen or LY294002 respectively. (A) c-kit + CSCs were double stained by EdU (green) and DAPI (blue), and observed under a fluorescence microscope (Olympus). Bar = 50 µm. DAPI = propidium iodide. (B) The statistics of EdU positive CSCs from immunofluorescence in (A). n = 6 in each group. (C) Flow cytometry was employed to detect cell cycle profiles in CSCs underwent different treatments miR-21 mimics or Phen increased the proportion of S phase CSCs compared with Control or scramble treated groups. n = 3. (D) PTEN/PI3K/Akt pathway’s influences on BrdU expression, which was detected with immune blotting. Just like miR-21 mimics’ effect on BrdU, when PTEN was inhibited by Phen, there was notably increase of BrdU compared with Normal or Scramble group. When PI3K was inhibited by LY294002, there was notably decrease of BrdU in mimics+LY294002 group compared with mimics group in CSCs. n = 3 in each group. a, P < 0.05 compared with Control; b, P < 0.05 compared with Scramble; c, P < 0.05 compared with miR-21 mimics group; d, P < 0.05 compared with Phen group. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/2859/'>28168101</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-fig-5-1x.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyExpression change of PTEN/PI3K/Akt pathway in the process of miR-21 mimics induced proliferation in c-kit + CSCs. Cultured CSCs were treated with miR-21 mimics for 48 h before the subsequent procedures. To test the contribution of PTEN/PI3K/Akt signaling to miR-21 mimics’s pro-proliferation effects in c-kit + CSCs, PTEN and PI3K were inhibited with Phen or LY294002 respectively. (A) RT-PCR was carried out to detect miR-21 mimics’s effects on PTEN expression at the mRNA level, which showed no change between Control, miR-21 scramble, miR-21 mimics and miR-21 mimics+ LY294002 group, while Phen resulted in a significant down-regulation of PTEN compared with the other groups. (B–C) Western blot was carried out to detect miR-21 mimics’s effects on PTEN protein expression, which showed that miR-21 mimics significantly down-regulated PTEN protein in miR-21 mimics group compared with the scramble group. In addition, both Phen treatment and miR-21 mimics incubation increased p-Akt level, while PI3K inhibitor LY294002 decreased p-Akt level dramatically ( P < 0.05). a, P < 0.05 compared with Control; b, P < 0.05 compared with miR-21 scramble group; c, P < 0.05 compared with miR-21 mimics group; d, P < 0.05 compared with Phen group. n = 3 in each group. p-Akt = phosphor-Akt. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/2859/'>28168101</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-pm-12-139-g007.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyEffect of treadmill exercise and epicatechin on brain-derived neurotrophic factor levels and Akt/GSK-3/cAMP response element binding protein signaling pathway in the hippocampus. (a) Representative Western blot of protein expressions normalized to β-actin protein in the hippocampus. (b) Protein expressions were semi-quantified by densitometry analysis. Values are expressed as mean ± standard error. * P < 0.05 compared with wild-type littermates; # P < 0.05 compared with transgenic; and P < 0.05 compared with COMA<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4883070/&orig_host=www.ncbi.nlm.nih.gov'>27279698</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-wb8.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-3-wb.jpgAnti-Phospho-AKT1 (S129) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AKT1 (S129) expression in (1) MCF-7 cell lysate treated with Alkaline Phosphatase; (2) MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-akt1-s124-rabbit-monoclonal-antibody-p00024-4-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-4-wb7.jpgAnti-Phospho-AKT1 (S124) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-4-wb8.jpgAnti-Phospho-AKT1 (S124) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-4-wb.jpgAnti-Phospho-AKT1 (S124) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AKT1 (S124) expression in (1) MCF-7 cell treated with Alkaline Phosphatase lysate; (2) MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-4-phospho-akt1-s124-primary-antibodies-wb-testing-1.pngAnti-Phospho-AKT1 (S124) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AKT1 (S124) using anti-Phospho-AKT1 (S124) antibody (P00024-4).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: mouse 4T1 whole cell lysates,<br>
Lane 2: LPS-stimulated mouse 4T1 whole cell lysates,<br>
Lane 3: Low-dose drug mouse 4T1 whole cell lysates,<br>
Lane 4: Medium-dose drug mouse 4T1 whole cell lysates,<br>
Lane 5: High-dose drug mouse 4T1 whole cell lysates,<br>
Lane 6: Positive control drug mouse 4T1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-AKT1 (S124) antigen affinity purified monoclonal antibody (Catalog # P00024-4) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with ChemiDoc MP system. A specific band was detected for Phospho-AKT1 (S124) at approximately 60 kDa. The expected band size for Phospho-AKT1 (S124) is at 60 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-cdc37-s13-rabbit-monoclonal-antibody-p02169-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02169-wb7.jpgAnti-Phospho-CDC37 (S13) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02169-wb.jpgAnti-Phospho-CDC37 (S13) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-CDC37 (S13) expression in (1) Jurkat cell lysate treated with Alkaline Phosphatase; (2) Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-raf1-s621-rabbit-monoclonal-antibody-p00446-4-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00446-4-wb.jpgAnti-Phospho-Raf1 (S621) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Raf1 (S621) expression in (1) HeLa cell lysate treated with LP; (2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00446-4-wb7.jpgAnti-Phospho-Raf1 (S621) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00446-4-wb8.jpgAnti-Phospho-Raf1 (S621) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-raf1-s259-rabbit-monoclonal-antibody-p00446-5-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00446-5-raf1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Raf1 (S259) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Raf1 using anti-Phospho-Raf1 antibody (P00446-5). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Raf1 antigen affinity purified monoclonal antibody (P00446-5) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Phospho-Raf1 at approximately 73 kDa. The expected band size for Phospho-Raf1 is at 73 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-hsp27-s78-rabbit-monoclonal-antibody-p00676-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00676-wb.jpgAnti-Phospho-Hsp27 (S78) HSPB1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Hsp27 (S78) expression in (1) A431 cell lysate; (2) A431 cell lysate treated with Anisomycin.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-irf3-s386-rabbit-monoclonal-antibody-p00165-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00165-p-irf3-primary-antibodies-wb-testing-1.jpgAnti-Phospho-IRF3 (S386) Rabbit Monoclonal AntibodyWestern blot analysis of P-IRF3 using anti-P-IRF3 antibody (P00165). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SIHA whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-IRF3 antigen affinity purified monoclonal antibody (P00165) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-IRF3 at approximately 55 kDa. The expected band size for P-IRF3 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-c-jun-s63-rabbit-monoclonal-antibody-p02038-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-wb.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyWestern blot analysis of c-Jun phosphorylation expression in NIH/3T3 cell lysate treated with Anisomycin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-wb7.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-wb9.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-wb8.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-ihc.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Phospho-c-Jun (S63) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-if.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells treated with anisomycin, using Phospho-c-Jun (S63) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02038-icc1.jpgAnti-Phospho-c-Jun (S63) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-polr2a-s2-rabbit-monoclonal-antibody-p01029-1-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-p-polr2a-primary-antibodies-wb-testing-1.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyWestern blot analysis of P-POLR2A using anti-P-POLR2A antibody (P01029-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-POLR2A antigen affinity purified monoclonal antibody (P01029-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-POLR2A at approximately 270 kDa. The expected band size for P-POLR2A is at 217 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-p-polr2a-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyIHC analysis of P-POLR2A using anti-P-POLR2A antibody (P01029-1). <br>P-POLR2A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-POLR2A Antibody (P01029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-p-polr2a-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyIHC analysis of P-POLR2A using anti-P-POLR2A antibody (P01029-1). <br>P-POLR2A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-POLR2A Antibody (P01029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-if.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using Phospho-POLR2A (S2) Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-p-polr2a-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyIHC analysis of P-POLR2A using anti-P-POLR2A antibody (P01029-1). <br>P-POLR2A was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-POLR2A Antibody (P01029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-1-p-polr2a-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-POLR2A (S2) Rabbit Monoclonal AntibodyIHC analysis of P-POLR2A using anti-P-POLR2A antibody (P01029-1). <br>P-POLR2A was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-POLR2A Antibody (P01029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-polr2a-s5-rabbit-monoclonal-antibody-p01029-2-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-2-wb.jpgAnti-Phospho-POLR2A (S5) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-POLR2A (S5) expression in (1) HeLa cell lysate treated with Lambda Phosphatase; (2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-2-ihc.jpgAnti-Phospho-POLR2A (S5) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using Phospho-POLR2A (S5) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01029-2-if.jpgAnti-Phospho-POLR2A (S5) Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Phospho-POLR2A (S5) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-eif2s1-s51-rabbit-monoclonal-antibody-p04387-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04387-eif2s1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-EIF2S1 (S51) Rabbit Monoclonal Antibody Western blot analysis of EIF2S1 using anti-EIF2S1 antibody (P04387). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF2S1 antigen affinity purified monoclonal antibody (Catalog # P04387) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EIF2S1 at approximately 36 kDa. The expected band size for EIF2S1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04387-ihc.jpgAnti-Phospho-EIF2S1 (S51) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using Phospho-eIF2 alpha (Ser51) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04387-eif2s1-primary-antibodies-wb-testing-2.pngAnti-Phospho-EIF2S1 (S51) Rabbit Monoclonal Antibody Western blot analysis of EIF2S1 using anti-EIF2S1 antibody (P04387). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-6: Different segments of the porcine large intestine and small intestine lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF2S1 antigen affinity purified monoclonal antibody (Catalog # P04387) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for EIF2S1 at approximately 36 kDa. The expected band size for EIF2S1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p04387-icc1.jpgAnti-Phospho-EIF2S1 (S51) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pka-r2-s99-rabbit-monoclonal-antibody-p03911-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03911-wb7.jpgAnti-Phospho-PKA R2 (S99) PRKAR2A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03911-wb.jpgAnti-Phospho-PKA R2 (S99) PRKAR2A Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PKA R2 (Ser99) in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03911-wb8.jpgAnti-Phospho-PKA R2 (S99) PRKAR2A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03911-wb9.jpgAnti-Phospho-PKA R2 (S99) PRKAR2A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-y1092-rabbit-monoclonal-antibody-p00023-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-wb.jpgAnti-Phospho-EGFR (Y1092) Rabbit Monoclonal AntibodyWestern blot analysis of EGFR phosphorylation expression in A431 cell treated with EGF.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-ihc.jpgAnti-Phospho-EGFR (Y1092) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Phospho-EGFR (Y1092) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-lrrk2-s935-rabbit-monoclonal-antibody-p00221-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00221-wb.jpgAnti-Phospho-LRRK2 (S935) Rabbit Monoclonal AntibodyWestern blot analysis of Filamin A phosphorylation expression in WT-LRRK2 cell lysate treated LRRK2.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-stat3-s727-rabbit-monoclonal-antibody-p00007-1-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-1-p-stat3-primary-antibodies-wb-testing-1.jpgAnti-Phospho-STAT3 (S727) Rabbit Monoclonal Antibody Western blot analysis of STAT3 using anti-STAT3 antibody (P00007-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT3 antigen affinity purified monoclonal antibody (Catalog # P00007-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT3 at approximately 88 kDa. The expected band size for STAT3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-1-stat3-primary-antibodies-if-testing-2.jpgAnti-Phospho-STAT3 (S727) Rabbit Monoclonal Antibody IF analysis of STAT3 using anti-STAT3 antibody (P00007-1).<br>
STAT3 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-STAT3 Antibody (P00007-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-1-wb8.jpgAnti-Phospho-STAT3 (S727) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-1-ihc.jpgAnti-Phospho-STAT3 (S727) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat brain, using Phospho-STAT3 (S727) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-eif4e-s209-rabbit-monoclonal-antibody-p00135-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00135-p-eif4e-primary-antibodies-wb-testing-1.jpgAnti-Phospho-eIF4E (S209) Rabbit Monoclonal AntibodyWestern blot analysis of P-EIF4E using anti-P-EIF4E antibody (P00135). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-EIF4E antigen affinity purified monoclonal antibody (P00135) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-EIF4E at approximately 25 kDa. The expected band size for P-EIF4E is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00135-p-eif4e-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-eIF4E (S209) Rabbit Monoclonal AntibodyIHC analysis of P-EIF4E using anti-P-EIF4E antibody (P00135). <br>P-EIF4E was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-EIF4E Antibody (P00135) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00135-p-eif4e-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-eIF4E (S209) Rabbit Monoclonal AntibodyIHC analysis of P-EIF4E using anti-P-EIF4E antibody (P00135). <br>P-EIF4E was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-EIF4E Antibody (P00135) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-cdk1-2-t14-rabbit-monoclonal-antibody-p00209-1-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00209-1-cdk1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Cdk1/2 (T14) Rabbit Monoclonal Antibody Western blot analysis of Phospho-Cdk1/2 (T14) using anti-Phospho-Cdk1/2 (T14) antibody (P00209-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human Hacat whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Cdk1/2 (T14) antigen affinity purified monoclonal antibody (Catalog # P00209-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Phospho-Cdk1/2 (T14) at approximately 34 kDa. The expected band size for Phospho-Cdk1/2 (T14) is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00209-1-ihc.jpgAnti-Phospho-Cdk1/2 (T14) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat spleen, using Phospho-Cdk1/2 (T14) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-gata3-s308-rabbit-monoclonal-antibody-p00593-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00593-wb.jpgAnti-Phospho-GATA3 (S308) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-GATA3 (S308) Jurkat cell lysate treated with Bromo-cAMP.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00593-ihc.jpgAnti-Phospho-GATA3 (S308) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder cancer, using Phospho-GATA3 (S308) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-stat5-y694-rabbit-monoclonal-antibody-p01087-1-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01087-1-stat5a-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Stat5 (Y694) STAT5A Rabbit Monoclonal Antibody Western blot analysis of STAT5A using anti-STAT5A antibody (P01087-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5A antigen affinity purified monoclonal antibody (Catalog # P01087-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT5A at approximately 95 kDa. The expected band size for STAT5A is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01087-1-wb7.jpgAnti-Phospho-Stat5 (Y694) STAT5A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01087-1-ihc.jpgAnti-Phospho-Stat5 (Y694) STAT5A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid, using Phospho-Stat5 (Y694) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-y1086-rabbit-monoclonal-antibody-p00023-1-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-1-wb.jpgAnti-Phospho-EGFR (Y1086) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-EGFR (Y1110) expression in (1) A431 cell lysate; (2) A431 cell lysate treated with EGF.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-y1173-rabbit-monoclonal-antibody-p00023-2-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-2-icc1.jpgAnti-Phospho-EGFR (Y1197) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-2-wb.jpgAnti-Phospho-EGFR (Y1197) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-EGFR (Y1197) expression in A431 cell lysate treated with EGF.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-2-ihc.jpgAnti-Phospho-EGFR (Y1197) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat stomach, using Phospho-EGFR (Y1197) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-y1092-rabbit-monoclonal-antibody-p00023-3-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-3-wb.jpgAnti-Phospho-EGFR (Y1092) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-EGFR (Y1092) expression in (1) A431 cell lysate; (2) A431 cell treated with EGF lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00023-3-12935_2021_2277_fig9_html.pngAnti-Phospho-EGFR (Y1092) Rabbit Monoclonal AntibodyRHBDF2 related functions were mediated by EGFR signaling pathway. a , b Phosphorylation of EGFR and PD-L1 protein level in 786-O and 769-P cells were detected by western blot. Significance testing of gray statistics was analyzed by two-way ANOVA. c Growth rate of the transplanted tumor in the control group and RHBDF2 knockdown group (data were presented as the mean ± SEM and subjected to two-way ANOVA for significance test). d Representative images of xenografts in nude mice. e Immunofluorescent staining of phosphorylation of EGFR in the graft sections (The horizontal line at the bottom right represents 50 microns). f The mean fluorescence intensity of the phosphorylation staining of EGFR in the graft sections (t-test). g The migratory ability testing of 786-O cells and 769-P cells after Gefitinib treatment. h Statistics of the cell migratory ability after Gefitinib treatment (two-way ANOVA). i The detection of pEGFR and PD-L1 level in 786-O and 769-P cells after Gefitinib treatment. j Gray statistics of pEGFR and PD-L1 level in 786-O and 769-P cells (two-way ANOVA, * p < 0.05, ** p < 0.01, *** p < 0.005, **** p < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-021-02277-0'>34736454</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-sirt1-t530-rabbit-monoclonal-antibody-p00018-boster.html2026-03-24T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00018-wb.jpgAnti-Phospho-SIRT1 (T530) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-SIRT1 (T530) expression in (1) 293T cell lysate; (2) 293T cell treated with Calyculin A.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-smad2-s250-rabbit-monoclonal-antibody-p00090-1-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-1-13659_2024_446_fig3_html.pngAnti-Phospho-Smad2 (S250) Rabbit Monoclonal AntibodyScutellarin Inhibits TGF-β1 and Its Downstream Signalling Pathway. a Representative images of Western blotting samples for TGF-β1, p-SMAD2, p-SMAD3, SMAD2/3, SMAD4, p-p38, p38 and p-Erk and Erk1/2 of the mice treated with vehicle, scutellarin or empagliflozin. b – g Quantifications of the protein as indicated. All data are normalized to the STZ group and presented as the mean ± S.D.; n = 4–6 for each group, “n” stands for the number of animals; p vs. the model group (STZ) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1007/s13659-024-00446-y'>38656633</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-1-12931_2022_2040_fig5_html.pngAnti-Phospho-Smad2 (S250) Rabbit Monoclonal AntibodyRecombinant HE4 promoted fibroblast-myofibroblast transition and fibroblastic proliferation. A, B Different concentrations of rHE4 facilitated fibronectin, collagen I and α-SMA expression both in mRNA level (n = 3) and protein level (n = 4). The representative western blot images were shown and the band intensity was quantified by ImageJ. C Treatment with rHE4 in HPF cells enhanced phosphorylation of Smad2 (n = 4). D Typical images of EdU-staining HPFs followed by rHE4 treatment for 48 h and the quantitative graph were shown (n = 3). magnification = × 200. E CCK8 proliferation curve signified the pro-proliferative effect of rHE4 (n = 4). HPF was stimulated by rHE4 for 0 h, 24 h, 48 h and 72 h. F Representative western blot images of PCNA and Survivin were displayed and quantified by ImageJ (n = 3). Data are presented as mean ± SEM. P-values were calculated using one-way ANOVA followed by Newman–Keuls test. *P < 0.05, **P < 0.01, and ***P < 0.001 represent significant differences. rHE4, recombinant human epididymis protein 4; EdU, 5-ethynyl-2′-deoxyuridine; CCK8, Cell Counting Kit-8; PCNA, proliferating cell nuclear antigen; HPF, human pulmonary fibroblast <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-022-02040-7'>35550579</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-1-smad2-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Smad2 (S250) Rabbit Monoclonal Antibody Western blot analysis of Phospho-Smad2 (S250) using anti-Phospho-Smad2 (S250) antibody (P00090-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human HT-1080 whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat skeletal muscle tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse skeletal muscle tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Smad2 (S250) antigen affinity purified monoclonal antibody (Catalog # P00090-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Phospho-Smad2 (S250) at approximately 58 kDa. The expected band size for Phospho-Smad2 (S250) is at 52 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-smad2-s255-rabbit-monoclonal-antibody-p00090-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-wb.jpgAnti-Phospho-Smad2 (S255) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Smad2 (S255) expression in Hela cell treated with Okadaic acid and Calyculin A lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-thnov11p7110g003.jpgAnti-Phospho-Smad2 (S255) Rabbit Monoclonal AntibodySRPX2 is elevated in fibroblasts in a TGF-β/SMADs manner. A : Western blot analysis of SRPX2 expression in HPFs following different dose of TGF-β1 induction for 24 h. B : Results for time-course Western blot analysis of SRPX2 expression in HPFs following TGF-β1 (10 ng/ml). C : Results for co-immunostaining of SRPX2 and p-SMAD2/3 in HPFs following TGF-β1 induction for 1h (up), lung sections of pulmonary fibrosis mice (middle), and lung sections from IPF patients (down). The nuclei were stained blue by DAPI, and the images were taken under original magnification ×400. D-E : Western blot (D) and RT-PCR (E) analysis of SRPX2 expression in HPFs pre-treated with SB431542 treatment following TGF-β1 induction. F-G : Western blot (F) and RT-PCR (G) analysis of SRPX2 expression in HPFs pre-treated with SIS3-HCL following TGF-β1 induction. The data are represented as the mean ± SEM of three independent experiments. ***, p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8171094/&orig_host=www.ncbi.nlm.nih.gov'>34093874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-thnov11p7110g004.jpgAnti-Phospho-Smad2 (S255) Rabbit Monoclonal AntibodySRPX2 regulated TGF-β/SMADs signaling pathways by AP1 and SMAD7. A: Results for Western blot analysis of p-SMAD2, SMAD2, p-SMAD3 and SMAD3 expression in HPFs following TGF-β1 stimulation. B-C : Western blot (B) and RT-PCR (C) analysis of SMAD7 expression in HPFs following TGF-β1 induction. D : Expression of AP1 in HPFs after TGF-β1 stimulation. E : Western blot results for analysis of the levels of P-SMAD2, P-SMAD3 and SMAD7 in HPFs pre-treated with T-5224 (an inhibitor for AP-1) treatment following TGF-β1 induction. The data are represented as the mean ± SEM of three independent experiments. *, p < 0.05; **, p < 0.01; ***, p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8171094/&orig_host=www.ncbi.nlm.nih.gov'>34093874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-thnov11p7110g007.jpgAnti-Phospho-Smad2 (S255) Rabbit Monoclonal AntibodySrpx2 promoted FMT in BLM-induced pulmonary fibrosis. A : Western blot analysis of Fibronectin, Col1a1, α-SMA and Srpx2 expression in mice after BLM induction with Scrambled or Srpx2 siRNA-loaded liposomes. B : Representative images of immunostaining of Fibronectin, Col1a1 and α-SMA in the mice lung sections. The nuclei were stained blue by DAPI, and the images were taken under original magnification ×400. C : Western blot analysis of p-Smad2, p-Smad3 and Smad7 expression in mice after BLM induction. D : RT-PCR analysis of AP-1 expression in mice in each group. Six mice were included in each study group. The data are represented as the mean ± SEM. *, p < 0.05; **, p < 0.01; ***, p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8171094/&orig_host=www.ncbi.nlm.nih.gov'>34093874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00090-ihc.jpgAnti-Phospho-Smad2 (S255) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human transitional cell carcinoma of bladder, using Phospho-Smad2 (S255) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ship-y1020-rabbit-monoclonal-antibody-p03358-1-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03358-1-wb.jpgAnti-Phospho-SHIP (Y1020) INPP5D Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-SHIP (Y1020) expression in (1) Raji cell lysate; (2) Raji cell treated with pervanadate lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-stat1-y701-rabbit-monoclonal-antibody-p00036-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00036-wb7.jpgAnti-Phospho-STAT1 (Y701) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00036-wb.jpgAnti-Phospho-STAT1 (Y701) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-STAT1 (Y701) expression in (1) A431 cell lysate; (2) A431 lysate cell treated with EGF.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-b-raf-t401-rabbit-monoclonal-antibody-p00075-boster.html2026-04-06T05:04:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00075-p-braf-primary-antibodies-wb-testing-1.jpgAnti-Phospho-B Raf (T401) Rabbit Monoclonal AntibodyWestern blot analysis of P-BRAF using anti-P-BRAF antibody (P00075). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-BRAF antigen affinity purified monoclonal antibody (P00075) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-BRAF at approximately 84 kDa. The expected band size for P-BRAF is at 84 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-mtor-s2481-rabbit-monoclonal-antibody-p00003-1-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-1-wb.jpgAnti-Phospho-mTOR (S2481) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-mTOR (S2481) expression in (1)293 cell lysate treated with LP; (2)293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-stat3-y705-rabbit-monoclonal-antibody-p00007-2-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-stat3-primary-antibodies-wb-testing-1.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal Antibody Western blot analysis of STAT3 using anti-STAT3 antibody (P00007-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: mouse NIH/3T3 whole cell lysates,<br>
Lane 3: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT3 antigen affinity purified monoclonal antibody (Catalog # P00007-2) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT3 at approximately 88 kDa. The expected band size for STAT3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-stat3-primary-antibodies-wb-testing-2_1.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal Antibody Western blot analysis of Phospho-STAT3 (Y705) using anti-Phospho-STAT3 (Y705) antibody (P00007-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates, <br>
Lane 2: Model group-rat colon tissue lysates, <br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates, <br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates, <br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates, <br>
Lane 6: Western medicine treatment-rat colon tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-STAT3 (Y705) antigen affinity purified monoclonal antibody (Catalog # P00007-2) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a HRP Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for Phospho-STAT3 (Y705) at approximately 88 kDa. The expected band size for Phospho-STAT3 (Y705) is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-stat3-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyIHC analysis of STAT3 using anti-STAT3 antibody (P00007-2). <br>STAT3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAT3 Antibody (P00007-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-if.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells treated with IFN-alpha, using Phospho-STAT3 (Y705) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2_12951_2025_3576_fig9_html.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyTranscriptomic analysis elucidated the mechanism of action of FA-PPI-Ms in the treatment of RA. ( A ) Volcano plot of significantly differentially expressed genes between the model group and the FA-PPI-Ms group, where blue circles represent downregulated genes and red circles represent upregulated genes; ( B ) Heatmap of significantly differentially expressed genes in cells of the model group and the FA-PPI-Ms group, where deeper blue indicates lower expression levels and deeper red indicates higher expression levels; ( C ) Histogram of GO functional annotation of significantly differentially expressed genes between the model group and the FA-PPI-Ms group; ( D ) Histogram of GO functional enrichment of significantly different genes between the model group and the FA-PPI-Ms group; ( E ) Bubble plot of GO functional enrichment of significantly differentially expressed genes between the model group and the FA-PPI-Ms group; ( F ) Histogram of KEGG pathway enrichment of genes with significant differences between the model group and the FA-PPI-Ms group; ( G-H ) To validate the transcriptomics results, qRT-PCR was employed to measure the mRNA expression levels of JAK ( G ) and STAT3 ( H ) in RAW264.7 cells; ( I ) Western blot was utilized to assess the expression levels of proteins associated with the JAK2-STAT3 signaling pathway; ( J-K ) Statistical analysis of the ratios of p-JAK2/JAK2 ( J ) and p-STAT3/STAT3 ( K ) was conducted. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03576-8'>40660236</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2_12951_2025_3576_fig10_html.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyValidation of the mechanism by which FA-PPI-Ms reverse M1/M2 imbalance. ( A-B ) qRT-PCR analysis of CD86 and CD206 mRNA expression on activated RAW264.7 cells treated with different formulations; ( C-D ) Flow cytometric histograms of proportion of M1and M2 macrophages in different formulations; ( E-F ) Quantitative analysis of proportion of M1 and M2 macrophages in different formulations; ( G-H ) Representative fluorescence images of CD86 and CD206 staining of values with varying formulations, scale bar = 50 μm; ( I-J ) Analysis of relative fluorescence intensity in ( G-H ); ( K-L ) qRT-PCR analysis of JAK2 and STAT3 mRNA expression on activated RAW264.7 cells treated with different formulations; ( M ) Western blot analysis of JAK2-STAT3 signalling axis-related protein expression. ( N-O ) Semi-quantitative analysis of p-JAK2/ JAK2 and p-STAT3/ STAT3 levels by Image J, Data are presented as mean ± SD ( n = 3). One-way ANOVA followed by Bonferroni’s test was used. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03576-8'>40660236</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-12929_2024_1040_fig5_html.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyRuxolitinib effectively reverse the PDGFRB Y562D -induced phenotypic modulation in HBVSMCs. Western blotting illustrates the alterations in p-JAK2 and p-STAT (p-STAT1 and p-STAT3) expression across different treatment groups ( A ). After normalization to the control group, the relative density of immunoblot bands in ( A ) is presented in scatter bar graph ( B ). Immunoblots ( C ) and relative density of bands ( D ) of markers associated with phenotypic modulation in HBVSMCs under different treatments are shown. A bar graph is used to present the rt-qPCR results for smooth muscle cell (SMC) markers and inflammatory markers in HBVSMCs under different treatment conditions ( E ). The results of RT-qPCR are analyzed using Tukey's multiple comparisons test. EDU assay demonstrate the proliferative capacity of HBVSMCs receiving different treatments ( F ) and statistical analysis of the proportion of Edu-positive cells in the different groups from 5 different fields of each group at × 200 magnification. Statistical differences are detected using Tukey's multiple comparisons test ( G ). Scratch assay shows the proliferative capacity of HBVSMCs underwent different treatment ( H ) and statistical analysis of the rate of wound healing (reduced area at 4H /area at 0H) in the different groups from 5 different fields of each group at × 200 magnification. Statistical differences are detected using Tukey's multiple comparisons test ( I ). ns, no significant; * p < 0.05; ** p < 0.01. The above experiments are all repeated three times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-12885_2022_10001_fig6_html.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyGO term, KEGG pathway, and GSEA enrichment analyses of HK2-related genes. A - B Heatmap of the top 50 positively and negatively related genes with HK2. C KEGG pathway enrichment analysis using the GSEA database. D - I Gene set enrichment plots of the NF-κB ( D ), complement and coagulation cascades ( E ), Toll-like receptor ( F ), NOD-like receptor ( G ), Th17 cell differentiation ( H ), and JAK-STAT ( I ) signalling pathways. J - M GO and KEGG enrichment analyses of HK2 positively or negatively related genes (Pearson’s rho ≥0.5, P < 0.05). N Expression levels of p-STAT3, STAT3, p-Akt, Akt in HK2-knockdown and control groups in T98 and GBM1 cell lines . Data shown as mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-022-10001-y'>35982398</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-12929_2024_1040_fig4_html.pngAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyThe JAK2-STAT pathway serves as the major downstream signaling pathway of the mutated PDGFB. mIF demonstrate the important downstream signaling pathway markers of PDGFRβ (p-JAK, p-Src, p-Erk1/2 and p-PLCγ) in FIA sections and NCA sections ( A ). Scale bar, 100 μm. Statistical analysis is performed to compare the mean fluorescence intensity of different signal markers between NCAs ( n = 4) and FIAs ( n = 5) ( C ). The expression of p-STAT1 and p-STAT3, which are downstream of p-JAK2, is detected by mIF in FIAs and NCAs. Scale bar, 50 μm ( B ). Statistical analysis of mean fluorescence intensity of these marks between NCAs ( n = 4) and FIAs ( n = 5) ( D ). Western blotting displays the expression of the important downstream signal pathway markers of PDGFRβ (p-JAK2, p-Src, p-Erk1/2 and p-PLCγ) in the HBVSMCs underwent different treatment in vitro ( E ). Relative density (normalized to Control) of immunoblot bands from ( E ) corresponding to pPLCγ, p-JAK2, p-Src, and p-ERK1/2 ( n = 3) ( F ). 'n' represented the number of samples. Three random fields were selected for statistical analysis in each sample, and the average value represented the detection value of this marker in this sample. Tukey's multiple comparisons test is conducted to evaluate the statistical differences. ns, no significant; ***padj < 0.001, ****padj < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-fphar-16-1514997-g008.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyCurcumol combined with sorafenib inhibited the tumor growth of Huh7-R cell xenografts in vivo . (A) The gross appearance of the tumors in xenografted mice. (B) The tumor weight of xenografted mice after 14 days of intervention. (C) Tumor volumes in xenograft mice after 7 and 14 days of intervention. (D) Body weight of xenografted mice before and after 14 days of intervention. (E) HE staining of tumors. Scar bar = 100 μm. (F) Ki67 staining of tumors. Scar bar = 100 μm. (G) TUNEL staining of tumors. Scar bar = 50 μm. (H, I) Tumor tissues were stained for p-AKT (H) , and p-STAT3 (I) . Scar bar = 100 μm *p < 0.05, **p < 0.01, ***p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1514997/full'>40242448</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-fphar-16-1514997-g007.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyExperimental verification of the function of Curcumol in Sorafenib-resistant HCC cells. (A) Effect of Sorafenib (5, 10, 15, 20, 30, 40, and 50 μM) on Huh7-R and HepG2-R cells viability. (B) Effect of Curcumol (31.25, 62.5, 125, 250, 500, and 1000 μM) on Huh7-R and HepG2-R cells viability. (C) Effect of Curcumol combined with Sorafenib (5, 10, 15, 20, 30, 40, and 50 μM) on Huh7-R and HepG2-R cells viability. (D) Colony formation assay of Huh7-R and HepG2-R cells treated with Curcumol, Sorafenib, and Curcumol combined with Sorafenib, respectively. (E) Flow cytometry detection of apoptosis analysis of Huh7-R and HepG2-R cells treated with Curcumol, Sorafenib, and Curcumol combined with Sorafenib, respectively. (F) Transwell assay was performed to detect the effect of Curcumol on the migratory ability of Huh7-R cells. (G) Transwell assay to detect the effect of Curcumol on the invasive ability of Huh7-R cells. (H) Cell scratch assay of Huh7-R cells treated with Curcumol, Sorafenib, and Curcumol combined with Sorafenib, respectively. (I) The protein expression levels of PI3K\AKT pathway and JAK/STAT3 pathway following intervention with Curcumol combined with Sorafenib. *p < 0.05, **p < 0.01, ***p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1514997/full'>40242448</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-fphar-16-1514997-g006.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyRelationship between differentially expressed core targets and immune cell infiltration. (A) ALB (B) STAT3 (C) HSP90AA1 (D) HSP90AB1 (E) SRC.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1514997/full'>40242448</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00007-2-fphar-16-1514997-g004.jpgAnti-Phospho-STAT3 (Y705) Rabbit Monoclonal AntibodyMolecular docking pattern of Curcumol with target proteins. (A) ALB (B) STAT3 (C) HSP90AA1 (D) HSP90AB1 (E) SRC.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1514997/full'>40242448</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-akt-ser473-rabbit-monoclonal-antibody-p00024-5-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-wb7.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-wb.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyWestern blot analysis on 2 NIH/3T3 cell lysate treated with PDGF using Phospho-Akt(Ser473) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-wb8.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-ihc.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Phospho-Akt(Ser473) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-icc2.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-icc1.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00024-5-if.jpgAnti-Phospho-Akt (Ser473) AKT1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of NIH/3T3 cells treated with PDGF, using Phospho-Akt(Ser473) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-mtor-s2448-rabbit-monoclonal-antibody-p00003-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-wb.jpgAnti-Phospho-mTOR (S2448) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-mTOR (S2448) expression in HEK293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-jcav11p5802g003.jpgAnti-Phospho-mTOR (S2448) Rabbit Monoclonal AntibodyAKT/mTOR pathway is involved in MOX-induced autophagy of glioma cells. ( A, B ) U251 and C6 cells were incubated with MOX at different concentrations (0, 10, 15, 20 µM) for 48 h, the effects of MOX on the levels of AKT, p-AKT (Ser473), mTOR, p-mTOR (S2448), P70S6K, p-P70S6K (Ser417), GSK3β, p-GSK3β were examined by western blot. Data were presented as the means ± SD of three independent tests. * P < 0.05, ** P < 0.01, *** P < 0.001 as compared with control group. β-actin was used as an internal standard.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7477456/&orig_host=www.ncbi.nlm.nih.gov'>32913473</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-fcell-08-00383-g003.jpgAnti-Phospho-mTOR (S2448) Rabbit Monoclonal AntibodyRelationship between ciRNA13761/novel-miR-3880/ ELF2 axis and PI3K/AKT/mTOR/S6K1 pathway. (A) Schematic diagram of animal treatment. C57BL/6 mice were injected with novel-miR-3880 or si ELF2 in an interval of three days and four days alternatively. Samples were harvested at day 22. (B) Immunohistochemistry of mammary gland for p-PI3K, p-AKT, p-mTOR and p-S6K1 in Normal Saline, novel-miR-3880 and si ELF2 groups. (C) Protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in mammary gland. (D,E) Effects of novel-miR-3880 and ELF2 on Bcl2/Bax pathway and protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in MEC. (F) PI3K, AKT, mTOR and S6K1 inhibitors suppressed the phosphorylation of PI3K, AKT, mTOR and S6K1 in MEC. (G–J) The role of novel-miR-3880 and si ELF2 in Bcl2/Bax and protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in MEC with PI3K, AKT, mTOR or S6K1 inhibited. (K) Regulation of ciRNA13761 on Bcl2/Bax and PI3K, AKT, mTOR and S6K1 phosphorylation, and the balance effects of novel-miR-3880. (L) Effects of si DOCK1 on Bcl2/Bax and PI3K, AKT, mTOR and S6K1 phosphorylation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.00383/full'>32656203</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003_12645_2025_336_fig9_html.pngAnti-Phospho-mTOR (S2448) Rabbit Monoclonal Antibodya Western blotting was used to examine mitochondrial apoptotic pathway-related proteins after treatment with control (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Key proteins involved in apoptosis such as Bax, Bcl-2, cytochrome c, and cleaved caspase-3 were examined to better understand how each treatment affects cell death at the mitochondrial level. b To further investigate the underlying molecular mechanisms, western blotting was used to investigate the PI3K/AKT/mTOR pathway (i), PANI-PEG-CS (ii), Ir(III) complex (iii), and Ir(III)@PANI-PEG-CS (iv). Expression levels of PI3K, AKT (total and phosphorylated), and mTOR were evaluated to assess whether this survival pathway was activated or suppressed. Protein levels were quantified and compared to the control group to determine statistical significance. * p < 0.05, ** p < 0.01, *** p < 0.001 in comparison to the respective control <br><b>Index in Springer Nature under a CC BY license. DOI: <a href='https://link.springer.com/article/10.1186/s12645-025-00336-z'>10.1186/s12645-025-00336-z</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-ihc.jpgAnti-Phospho-mTOR (S2448) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Phospho-mTOR (S2448) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00003-phospho-mtor-s2448--primary-antibodies-wb-testing-1.pngAnti-Phospho-mTOR (S2448) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-mTOR (S2448) using anti-Phospho-mTOR (S2448) antibody (P00003). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse 4T1 whole cell lysates,<br>
Lane 2: LPS-stimulated mouse 4T1 whole cell lysates,<br>
Lane 3: Low-dose drug mouse 4T1 whole cell lysates,<br>
Lane 4: Medium-dose drug mouse 4T1 whole cell lysates,<br>
Lane 5: High-dose drug mouse 4T1 whole cell lysates,<br>
Lane 6: Positive control drug mouse 4T1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-mTOR (S2448) antigen affinity purified monoclonal antibody (Catalog # P00003) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with ChemiDoc MP system. A specific band was detected for Phospho-mTOR (S2448) at approximately 289 kDa. The expected band size for Phospho-mTOR (S2448) is at 289 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-foxo3a-s253-rabbit-monoclonal-antibody-p00252-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00252-foxo3a-primary-antibodies-wb-testing-1.jpgAnti-Phospho-FoxO3a (S253) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-FoxO3a (S253) using anti-Phospho-FoxO3a (S253) antibody (P00252). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human T47D whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-FoxO3a (S253) antigen affinity purified monoclonal antibody (P00252) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Phospho-FoxO3a (S253) at approximately 80-100 kDa. The expected band size for Phospho-FoxO3a (S253) is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00252-ihc.jpgAnti-Phospho-FoxO3a (S253) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus cancer, using Phospho-FoxO3a (S253) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-crkii-tyr221-rabbit-monoclonal-antibody-p02533-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p02533-wb.jpgAnti-Phospho-CrkII (Tyr221) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-CrkII (Tyr221) expression in (1) K562 cell lysate treated with AP; (2) K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p95-nbs1-s343-rabbit-monoclonal-antibody-p00732-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00732-wb.jpgAnti-Phospho-p95/NBS1 (S343) NBN Rabbit Monoclonal AntibodyWestern blot analysis of p95/NBS1 phosphorylation expression in Jurkat cell lysate treated with Etopside.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ikb-alpha-s32-rabbit-monoclonal-antibody-p01139-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01139-p-nfkbia-primary-antibodies-wb-testing-1.jpgAnti-Phospho-IKB alpha (S32) NFKBIA Rabbit Monoclonal AntibodyWestern blot analysis of P-NFKBIA using anti-P-NFKBIA antibody (P01139). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-NFKBIA antigen affinity purified monoclonal antibody (P01139) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-NFKBIA at approximately 39 kDa. The expected band size for P-NFKBIA is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01139-41420_2025_2756_fig5_html.pngAnti-Phospho-IKB alpha (S32) NFKBIA Rabbit Monoclonal AntibodyDuvelisib and chidamide stabilize IκBα via PI3Kδ and HDAC2 targeting, respectively. A Western blotting analysis was performed to determine the expression levels of drug-targeted proteins corresponding to chidamide (HDAC1, HDAC2, HDAC3, HDAC10) and duvelisib (AKT, p-AKT Ser473) in TMD8, Toledo, and DB cells following gradient concentration treatment with chidamide, duvelisib, or their combination. B Western blotting was utilized to assess the protein expression levels of IKKα/β, p-IKKα/β (Ser176/180), IκBα and p-IκBα (Ser32) in DB cells after treatment with specified drug concentrations. C The effects of duvelisib, PI3Kδ inhibitor (PI3Kδ-IN-15), and PI3Kγ inhibitor (AZ2) on IKK and IκBα protein expression in DB cells were evaluated by western blotting. D Following histone H1.5 protein recruitment, the acetylation status of histone H1.5 and its interaction with IκBα were examined. E A co-immunoprecipitation (co-IP) assay was employed to directly detect the acetylation level of IκBα. In western blotting, DMSO served as the vehicle control, diluted in culture medium to a final concentration of 0.05% (v/v). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-025-02756-7'>41053160</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01139-41420_2025_2756_fig6_html.pngAnti-Phospho-IKB alpha (S32) NFKBIA Rabbit Monoclonal AntibodyChidamide treatment inhibits HDAC2 activity and leads to histone H1.5 acetylation. A , B Knockdown of HDAC1, HDAC2, HDAC3, and HDAC10 was performed using siRNA. Following histone H1.5 enrichment, western blotting analysis was conducted to detect histone H1.5 acetylation levels and its interaction with IκBα. ( C ) Mass spectrometry identified five histone H1.5 acetylation sites (A-score >13) after chidamide treatment. D – H Acetylation-deficient mutants were generated by replacing these lysine residues with arginine. Following histone H1.5 enrichment, co-immunoprecipitation (Co-IP) assays were performed to evaluate histone H1.5 acetylation, NF-κB p65 protein levels, and histone H1.5-IκBα interaction. The K67 and K93 mutations significantly reduced acetylation and weakened the histone H1.5-IκBα interaction. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-025-02756-7'>41053160</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-er-alpha-s118-rabbit-monoclonal-antibody-p00057-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-p-esr1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal Antibody Western blot analysis of ER/ESR1 (Phospho-S118) using anti-ER/ESR1 (Phospho-S118) antibody (P00057). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat C6 whole cell lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ER/ESR1 (Phospho-S118) antigen affinity purified monoclonal antibody (P00057) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ER/ESR1 (Phospho-S118) at approximately 66 kDa. The expected band size for ER/ESR1 (Phospho-S118) is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-wb8.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-if.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells treated with EGF, using Phospho-ER alpha (S118) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-wb.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-ER alpha (S118) expression in (1) MCF7 cell lysate; (2) MCF7 cell lysate treated with b-Estradiol and EGF.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-p-esr-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal Antibody IHC analysis of p-ESR using anti-p-ESR antibody (P00057). <br>p-ESR was detected in a paraffin-embedded section of rat uterus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p-ESR Antibody (P00057) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-p-esr-primary-antibodies-ihc-testing-5.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal Antibody IHC analysis of p-ESR using anti-p-ESR antibody (P00057). <br>p-ESR was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p-ESR Antibody (P00057) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00057-p-esr-primary-antibodies-ihc-testing-6.jpgAnti-Phospho-ER alpha (S118) ESR1 Rabbit Monoclonal Antibody IHC analysis of p-ESR using anti-p-ESR antibody (P00057). <br>p-ESR was detected in a paraffin-embedded section of human prostatic hyperplasia tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p-ESR Antibody (P00057) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-zeta-t560-rabbit-monoclonal-antibody-p01796-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01796-wb.jpgAnti-Phospho-PKC zeta (T560) PRKCZ Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PKC zeta (T560) expression in HeLa cell treated with Calyculin A lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01796-wb7.jpgAnti-Phospho-PKC zeta (T560) PRKCZ Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01796-wb8.jpgAnti-Phospho-PKC zeta (T560) PRKCZ Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-cyclin-e1-t77-rabbit-monoclonal-antibody-p00543-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00543-wb.jpgAnti-Phospho-Cyclin E1 (T77) CCNE1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Cyclin E1 (T77) expression in (1) JAR cell treated with Lambda Phosphatase lysate; (2) JAR cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-paxillin-y118-rabbit-monoclonal-antibody-p01033-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01033-wb.jpgAnti-Phospho-Paxillin (Y118) PXN Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Paxillin (Y118) expression in (1) HeLa cell lysate; (2) HeLa cell treated with pervanadate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-smad5-s463-465-rabbit-monoclonal-antibody-p01423-1-boster.html2026-03-24T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01423-1-ihc.jpgAnti-Phospho-Smad5 (S463/465) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human pancreas, using Phospho-Smad5 (S463/465) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01423-1-phospho-smad5-s463-465-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Smad5 (S463/465) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Smad5 (S463/465) using anti-Phospho-Smad5 (S463/465) antibody (P01423-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Smad5 (S463/465) antigen affinity purified monoclonal antibody (P01423-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Phospho-Smad5 (S463/465) at approximately 52 kDa. The expected band size for Phospho-Smad5 (S463/465) is at 52 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-dna-pkcs-s2056-rabbit-monoclonal-antibody-p00645-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/P/0/P00645-PRKDC-primary-antibodies-WB-testing-1.jpgAnti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-DNA PKcs (Ser2056) expression in alkaline treated Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00645-prkdc-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon tissue using anti-Phospho-DNA PKcs (S2056) antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00645-prkdc-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma tissue using anti-Phospho-DNA PKcs (S2056) antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-gsk3-beta-ser9-rabbit-monoclonal-antibody-p00791-1-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-wb7.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-if.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells treated with Calyculin A, using Phospho-GSK3 beta (Ser9) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-fphar-14-1038039-g004.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyWECP activated Akt/GSK3β/β-Catenin signaling pathway in DPCs. DPCs were incubated with WECP (40, 80 and 160 μg/mL) in culture medium for 24 h. (A) Akt and GSK3β phosphorylation levels were detected in DPCs after WECP treatment. (B) Effects of WECP treatment on β-Catenin and Wnt10b protein expression levels in DPCs. (C) Transcriptional expression of LEF1, IGF1, and VEGF in DPCs detected using RT-PCR. Data are presented as means ± SD of three independent replicates. * p < 0.05, ** p < 0.01 vs. control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9986263/&orig_host=www.ncbi.nlm.nih.gov'>36891275</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-fphar-14-1038039-g005.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyWECP activated Akt/GSK3β/β-Catenin signaling pathway in denuded mouse skin. (A) Effects of WECP and finasteride treatments on Akt and GSK3β protein phosphorylation in mouse skin. (B) Effects of WECP and finasteride treatments on β-Catenin and Wnt10 translational expression in mouse skin. (C) Effects of WECP and finasteride treatments on transcriptional expression of β-Catenin, Wnt10b, Wnt5a, LEF1, VEGF, and IGF1 in mouse skin. Data are means ± SD of three independent replicates. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control group. WECPL, WECPH, and Fin represent low-dose WECP, high-dose WECP, and finasteride treatment, respectively.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9986263/&orig_host=www.ncbi.nlm.nih.gov'>36891275</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-wb.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyWestern blot analysis of GSK3 beta (phospho S9) expression in 293T cell lysates, treated with Calyculin A.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00791-1-ihc.jpgAnti-Phospho-GSK3 beta (Ser9) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Phospho-GSK3 beta (Ser9) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-alpha-t638-rabbit-monoclonal-antibody-p00743-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00743-p-prkca-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-PKC alpha (T638) PRKCA Rabbit Monoclonal AntibodyIHC analysis of P-PRKCA using anti-P-PRKCA antibody (P00743). <br>P-PRKCA was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-PRKCA Antibody (P00743) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00743-p-prkca-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-PKC alpha (T638) PRKCA Rabbit Monoclonal AntibodyIHC analysis of P-PRKCA using anti-P-PRKCA antibody (P00743). <br>P-PRKCA was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-PRKCA Antibody (P00743) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00743-prkca-primary-antibodies-wb-testing-1.jpgAnti-Phospho-PKC alpha (T638) PRKCA Rabbit Monoclonal Antibody Western blot analysis of PRKCA using anti-PRKCA antibody (P00743). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat kidney tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKCA antigen affinity purified monoclonal antibody (Catalog # P00743) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRKCA at approximately 77 kDa. The expected band size for PRKCA is at 77 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-c-myc-t58-s62-rabbit-monoclonal-antibody-p00026-1-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00026-1-p-myc-primary-antibodies-wb-testing-1.jpgAnti-Phospho-c-Myc (T58 + S62) Rabbit Monoclonal AntibodyWestern blot analysis of P-MYC using anti-P-MYC antibody (P00026-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-MYC antigen affinity purified monoclonal antibody (P00026-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-MYC at approximately 57 kDa. The expected band size for P-MYC is at 49 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pp2a-alpha-y307-rabbit-monoclonal-antibody-p01893-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01893-p-ppp2ca-primary-antibodies-wb-testing-1.jpgAnti-Phospho-PP2A alpha (Y307) PPP2CA Rabbit Monoclonal AntibodyWestern blot analysis of P-PPP2CA using anti-P-PPP2CA antibody (P01893). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse kidney tissue lysates,<br>
Lane 7: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-PPP2CA antigen affinity purified monoclonal antibody (P01893) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-PPP2CA at approximately 36 kDa. The expected band size for P-PPP2CA is at 36 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ampk-alpha-t172-rabbit-monoclonal-antibody-p01420-2-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-2-wb7.jpgAnti-Phospho-AMPK alpha (T172) PRKAA2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-2-wb.jpgAnti-Phospho-AMPK alpha (T172) PRKAA2 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AMPK alpha (T172) expression in Mouse heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-smad5-s463-s465-rabbit-monoclonal-antibody-p01423-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01423-p-smad159-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Smad1/5/9 (S463/S465/S467) Rabbit Monoclonal AntibodyWestern blot analysis of P-SMAD1/5/9 using anti-P-SMAD1/5/9 antibody (P01423). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-SMAD1/5/9 antigen affinity purified monoclonal antibody (P01423) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-SMAD1/5/9 at approximately 52 kDa. The expected band size for P-SMAD1/5/9 is at 52 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-s6k1-t421-s424-rabbit-monoclonal-antibody-p01475-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01475-wb.jpgAnti-Phospho-S6K1 (T421 + S424) RPS6KB1 Rabbit Monoclonal AntibodyWestern blot analysis of SK61 phosphorylation expression in HEK293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01475-ajtr0011-5134-f3.jpgAnti-Phospho-S6K1 (T421 + S424) RPS6KB1 Rabbit Monoclonal AntibodyPKI-587 enhances the oxaliplatin-induced cytotoxicity by blocking the PI3K/mTOR/S6K1/4EBP1 signaling pathway in HCC cells. A. Effect of PKI-587 on oxaliplatin-induced cytotoxicity by MTT assay. Data are presented as mean ± SD, n=3. * P <0.05, ** P <0.01; *** P <0.001 all versus PKI-587 or oxaliplatin single agent group. OXA: oxaliplatin. B and C. Representative images of the colony formation assay in HCC cells. The percentage of colony formation was calculated. Data are presented as mean ± SD, n=3. *** P <0.001 versus PKI-587 or oxaliplatin single agent group. OXA: oxaliplatin. D-H. Response of PI3K/mTOR pathway downstream direct effectors (S6K1 and elF4EBP1) after treatment of PKI-587, oxaliplatin or PKI-587 combined with oxaliplatin for 24 h in HepG2 and SK-Hep1 cells. The cell lysates were gathered and the designated proteins were detected by Western blotting. Data are presented as mean ± SD, n=3. *** P <0.001 versus oxaliplatin single agent. OXA: Oxaliplatin.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731445/'>31497229</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-histone-h2a-s129-rabbit-monoclonal-antibody-p30931-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30931-wb.jpgAnti-Phospho-Histone H2A (S129) HIST1H2AB Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Histone H2A (S129) expression in Saccharomyces cerevisiae treated with Methyl methanesulfonate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-histone-h2b-t129-rabbit-monoclonal-antibody-p30930-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/3/p30930-wb.jpgAnti-Phospho-Histone H2B (T129) HIST1H2BC Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B expression in Saccharomyces cerevisiae cell lysate treated with Methyl methanesulfonate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-histone-h1-4-t17-rabbit-monoclonal-antibody-p06652-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-hist1h1e-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Histone H1.4 (T17) using anti-Phospho-Histone H1.4 (T17) antibody (P06652). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U20S whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Histone H1.4 (T17) antigen affinity purified monoclonal antibody (P06652) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Phospho-Histone H1.4 (T17) at approximately 32 kDa. The expected band size for Phospho-Histone H1.4 (T17) is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-wb-testing-2.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyWestern blot analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human U20S whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-H1-4 antigen affinity purified monoclonal antibody (P06652) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-H1-4 at approximately 32 kDa. The expected band size for P-H1-4 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-13.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-11.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-12.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-9.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-10.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-7.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-8.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-5.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-6.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p06652-p-h1-4-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Histone H1.4 (T17) HIST1H1E Rabbit Monoclonal AntibodyIHC analysis of P-H1-4 using anti-P-H1-4 antibody (P06652). <br>P-H1-4 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-H1-4 Antibody (P06652) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rac1-cdc42-ser71-rabbit-monoclonal-antibody-p00119-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00119-wb.jpgAnti-Phospho-Rac1/Cdc42 (Ser71) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Rac1/Cdc42 (Ser71) expression in (1) A431 cell lysate treated with LP; (2) A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-smad3-s423-s425-rabbit-monoclonal-antibody-p00059-1-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-wb10.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-wb7.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-thnov11p7110g004.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodySRPX2 regulated TGF-β/SMADs signaling pathways by AP1 and SMAD7. A: Results for Western blot analysis of p-SMAD2, SMAD2, p-SMAD3 and SMAD3 expression in HPFs following TGF-β1 stimulation. B-C : Western blot (B) and RT-PCR (C) analysis of SMAD7 expression in HPFs following TGF-β1 induction. D : Expression of AP1 in HPFs after TGF-β1 stimulation. E : Western blot results for analysis of the levels of P-SMAD2, P-SMAD3 and SMAD7 in HPFs pre-treated with T-5224 (an inhibitor for AP-1) treatment following TGF-β1 induction. The data are represented as the mean ± SEM of three independent experiments. *, p < 0.05; **, p < 0.01; ***, p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8171094/&orig_host=www.ncbi.nlm.nih.gov'>34093874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-thnov11p7110g007.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodySrpx2 promoted FMT in BLM-induced pulmonary fibrosis. A : Western blot analysis of Fibronectin, Col1a1, α-SMA and Srpx2 expression in mice after BLM induction with Scrambled or Srpx2 siRNA-loaded liposomes. B : Representative images of immunostaining of Fibronectin, Col1a1 and α-SMA in the mice lung sections. The nuclei were stained blue by DAPI, and the images were taken under original magnification ×400. C : Western blot analysis of p-Smad2, p-Smad3 and Smad7 expression in mice after BLM induction. D : RT-PCR analysis of AP-1 expression in mice in each group. Six mice were included in each study group. The data are represented as the mean ± SEM. *, p < 0.05; **, p < 0.01; ***, p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC8171094/&orig_host=www.ncbi.nlm.nih.gov'>34093874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-41419_2020_2818_fig2_html.pngAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyTGF-β2 gene expression and TGF-Smad signaling are augmented in Sema7A-HUVECs. a The top 30 upregulated genes in Sema7A-HUVECs compared with Con335-HVUECs. b TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, *** p < 0.001. c The concentration of TGF-β2 in cell supernatant was detected by ELISA. N = 10. Unpaired two-tailed Student’s t tests was used to analysis the data. Data are mean ± SEM, ** p < 0.01. d GSEA based on gene ontology (GO) pathway database showed TGF-β signaling pathway was enrich in Sema7A-HUVECs. e , f Cells were treated with Oxymatrine (Oxy) (20 μmol/l) or T4442 (1 μg/ml) and the lysates were analyzed by western blotting for Smad3 phosphorylation, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. g , h CD31 and α-SMA mRNA in cells treated with inhibitors were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. i – k CD31 and α-SMA proteins in cells treated with inhibitors were analysis by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. T4442: TGF-β2 blocking antibody; Oxymatrine (Oxy): TGF/Smad signaling pathway inhibitor. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-41419_2020_2818_fig3_html.pngAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyInhibition of ATF3 reduced TGF-β2 expression and Sema7A-induced EndMT. a ATF3 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, *** p < 0.001 b ATF3 protein expression were analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, *** p < 0.001. c TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. d The concentration of TGF-β2 in cell supernatant was detected by ELISA among Con335-HUVECs, Sema7A-HUVECs, and Sema7A-HUVECs + ATF3-siRNA. N = 10. Data are mean ± SEM, * p < 0.05; *** p < 0.001. e Chip-qPCR product in agarose gel electrophoresis. f Chip-qPCR TGF-β2 percentage of input in con335-HUVECs and Sema7A - HUVECs were analyzed by qPCR normalized to IgG. Data are mean ± SEM, N = 3, ** p < 0.01. g Schematic graph of the constructed reporter plasmid. TGF-β2 mut indicates the TGF-β2 mutation promoter region in ATF3 binding site. The mutated nucleotides in TGF-β2 fragments are in red letters. h Luciferase reporter assays were performed on HEK 293 T cells. Data are mean ± SEM, N = 3, ** p < 0.01 vs negative control. i , j ATF3-overexpression plasmid was transfected to HUVECs, and the mRNA levels of TGF - β2 and TGF-β1 were performed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, ** p < 0.01. k , l P-Smad3 protein in cells treated with siRNA was analyzed by Western blotting, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. m – q CD31 and α-SMA RNA and proteins in cells treated with siRNA or control was analyzed by qPCR and western blotting. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-41419_2020_2818_fig4_html.pngAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyΒ1 integrin mediates Sema7A signal to TGF-β2 via ATF3. a Cells were treated with β1 integrin antibody (P5D2), and ATF3 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.0.1. b ATF3 protein expression was analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. c TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.0.1. d The concentration of TGF-β2 in cell supernatant was detected by ELISA for Con335-HUVECs, Sema7A-HUVECs, and Sema7A-HUVECs + P5D2. Data are mean ± SEM, N = 10, * p < 0.05; *** p < 0.001. e , f Smad3 phosphorylation were analyzed by western blotting, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05. g , h CD31 and α-SMA mRNA level were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. i – k CD31 and α-SMA proteins were analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. l ATF3 overexpression plasmid was transfected into P5D2 incubated Sema7A-HUVECs, and TGF-β2 mRNA expression in Sema7A-HUVECs + P5D2 and Sema7A-HUVECs + P5D2 + ATF3 were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, ** p < 0.01. m – o CD31 and α-SMA protein expressions were analyzed by western blotting, normalized to GAPDH. Data are mean ± SEM, N = 3, ** p < 0.01 (Sema7A-HUVECs + P5D2 vs Sema7A-HUVECs + P5D2 + ATF3). P5D2 β1 integrin antibody. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-wb.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Smad3 (S423/S425) expression in A549 cell lysate treated with TGF-?1.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-wb8.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-wb9.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-ihc.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human gastric adenocarcinoma, using Phospho-Smad3 (S423 + S425) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00059-1-if.jpgAnti-Phospho-Smad3 (S423 + S425) Rabbit Monoclonal AntibodyImmunofluorescent analysis of A549 cells treated with TGFβ , using Phospho-Smad3 (S423 + S425) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-v-myb-c-myb-s11-rabbit-monoclonal-antibody-p00157-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00157-wb.jpgAnti-Phospho-v-Myb + c-Myb (S11) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-v-Myb + c-Myb (S11) Antibody expression in Ramos cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00157-wb7.jpgAnti-Phospho-v-Myb + c-Myb (S11) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ampk-alpha-1-s496-rabbit-monoclonal-antibody-p00994-1-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00994-1-wb.jpgAnti-Phospho-AMPK alpha 1 (S496) PRKAA1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AMPK alpha 1 (S496) expression in (1) 293T cell lysate treated with LP; (2) 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ampk-alpha-2-s345-rabbit-monoclonal-antibody-p01420-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-wb7.jpgAnti-Phospho-AMPK alpha 2 (S345) PRKAA2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-wb8.jpgAnti-Phospho-AMPK alpha 2 (S345) PRKAA2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-wb.jpgAnti-Phospho-AMPK alpha 2 (S345) PRKAA2 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AMPK alpha 2 (S345) expression in (1) 293T cell lysate treated with Lambda Phosphatase; (2) 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ampk-alpha-2-s491-rabbit-monoclonal-antibody-p01420-1-boster.html2026-03-24T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-1-wb7.jpgAnti-Phospho-AMPK alpha 2 (S491) PRKAA2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-1-wb8.jpgAnti-Phospho-AMPK alpha 2 (S491) PRKAA2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p01420-1-wb.jpgAnti-Phospho-AMPK alpha 2 (S491) PRKAA2 Rabbit Monoclonal AntibodyWestern blot analysis of AMPK beta 1 expression in (1) 293T cell lysate treated with Lambda lysate; (2) 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-nf-kappa-b-p65-s529-rabbit-monoclonal-antibody-p00284-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00284-wb.jpgAnti-Phospho-NF-Kappa B p65 (S529) RELA Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-NF-κB p65 (S529) expression in HeLa cell lysates treated with Calyculin A and TNF-alpha.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-alpha-synuclein-s129-rabbit-monoclonal-antibody-p00215-1-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00215-1-wb.jpgAnti-Phospho-alpha Synuclein (S129) SNCA Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-alpha Synuclein (Ser129) expression in (1) 293T cell lysate; (2) 293T cell lysate transfected with Polo-Like Kinase 2 and alpha Synuclein.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-alpha-synuclein-s129-rabbit-monoclonal-antibody-p00215-2-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00215-2-wb.jpgAnti-Phospho-alpha Synuclein (S129) SNCA Rabbit Monoclonal AntibodyWestern blot analysis of Synuclein phosphorylation expression in Human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-beta-catenin-s33-s37-rabbit-monoclonal-antibody-p00004-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00004-wb.jpgAnti-Phospho-beta Catenin (S33/S37) CTNNB1 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-beta Catenin (S33/S37) expression in (1) 293T cell lysate; (2) 293T cell lysate treated with calyculin A.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pak1-2-3-s144-s141-s139-rabbit-monoclonal-antibody-p03124-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-wb7.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-wb10.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-wb8.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-wb.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PAK1/2/3 expression in HeLa Cell lysate treated with lambda phosphatase.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-wb9.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03124-ihc.jpgAnti-Phospho-PAK1/2/3 (S144+S141+S139) PAK3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using Phospho-PAK1/2/3 (S144+S141+S139) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pdgf-receptor-beta-y740-rabbit-monoclonal-antibody-p00096-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00096-wb.jpgAnti-Phospho-PDGF Receptor beta (Y740) PDGFRB Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PDGF Receptor beta (Y740) expression in NIH 3T3 treated with PDGF.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-glycogen-synthase-1-s641-rabbit-monoclonal-antibody-p03512-2-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03512-2-gys1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Glycogen synthase 1 (S641) GYS1 Rabbit Monoclonal Antibody Western blot analysis of Phospho-Glycogen synthase 1 (S641) using anti-Phospho-Glycogen synthase 1 (S641) antibody (P03512-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human RT4 whole cell lysates, <br>
Lane 3: human SIHA whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-Glycogen synthase 1 (S641) antigen affinity purified monoclonal antibody (P03512-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Phospho-Glycogen synthase 1 (S641) at approximately 84 kDa. The expected band size for Phospho-Glycogen synthase 1 (S641) is at 84 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-gsk3-alpha-beta-y216-y279-rabbit-monoclonal-antibody-p03152-1-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03152-1-gsk3a-b-primary-antibodies-wb-testing-1.jpgAnti-Phospho-GSK3 (alpha + beta) (Y216 + Y279) GSK3A Rabbit Monoclonal AntibodyWestern blot analysis of GSK3 Alpha/Beta (Phospho-Y216+Y279) using anti-GSK3 Alpha/Beta (Phospho-Y216+Y279) antibody (P03152-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse thymus tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSK3 Alpha/Beta (Phospho-Y216+Y279) antigen affinity purified monoclonal antibody (P03152-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSK3 Alpha/Beta (Phospho-Y216+Y279) at approximately 47,51 kDa. The expected band size for GSK3 Alpha/Beta (Phospho-Y216+Y279) is at 47,51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p03152-1-gsk3a-b-primary-antibodies-wb-testing-2.jpgAnti-Phospho-GSK3 (alpha + beta) (Y216 + Y279) GSK3A Rabbit Monoclonal AntibodyWestern blot analysis of GSK3 Alpha/Beta (Phospho-Y216+Y279) using anti-GSK3 Alpha/Beta (Phospho-Y216+Y279) antibody (P03152-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U2OS whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: rat heart tissue lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse heart tissue lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSK3 Alpha/Beta (Phospho-Y216+Y279) antigen affinity purified monoclonal antibody (P03152-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSK3 Alpha/Beta (Phospho-Y216+Y279) at approximately 47,51 kDa. The expected band size for GSK3 Alpha/Beta (Phospho-Y216+Y279) is at 47,51 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-erk1-t202-y204-erk2-t185-y187-rabbit-monoclonal-antibody-p00104-1-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-1-wb.jpgAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal AntibodyWestern blot analysis of Phospho- Erk1 (T202/Y204) + Erk2 (T185/Y187) expression in A431 cell lysate treated with EGF.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-erk1-t202-y204-erk2-t185-y187-rabbit-monoclonal-antibody-p00104-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-12951_2025_3154_fig4_html.pngAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal AntibodyGenome-wide RNA-sequencing of KPC cells treated with Cel in vitro. (A) Volcano plots of the total differentially expressed genes (DEGs) between Cel-treated group and PBS group. (B) Heat map of the specific DEGs. (C) Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. (D) The expression levels of p-AKT, p-ERK, p-JNK, and p-P38 were detected in KPC cells treated with Cel at the 0 h, 0.5 h, 2 h, and 4 h by western blotting <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03154-y'>40050985</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-41398_2023_2624_fig4_html.pngAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal AntibodyEffects of knocking-down ADRB1 CaMKII on mPFC activity and subsequent signals in METH-sired male F1. a Levels of c-Fos protein. b The c-Fos immunostaining. Scale bar, 500 μm /100 μm. c Density of dendritic spine. Scale bar, 50 μm /10 μm. d Levels of β-arestin2 and PKA protein. e Levels of ERK1/2, p-ERK1/2, ERK1/2/p-ERK1/2, CREB, p-CREB, p-CREB/ CREB and ΔFosB protein. F1-METH-Ctrl, METH-sired male F1 mice injected with Ctrl virus. F1-METH-KD, METH-sired male F1 mice injected with KD virus. The data are presented as the Mean ± SD. N.S., P > 0.05. * P < 0.05, ** P < 0.01 vs F1-METH-Ctrl. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41398-023-02624-x'>37857642</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-m_rsob.230427.f005.pngAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal AntibodyEffect of MYH7 R453C mutation on TGF-β/Smad2/3, ERK1/2, NF-κB and PI3K/AKT pathways. (a) The protein expression of TGF-β/Smad2/3 and ERK1/2 cascades were detected by western blotting. (b–d) The protein expression of TGF-β1/2, p-Smad2/3/Smad2/3 and p-ERK1/2/ERK1/2 were quantitated using densitometry. (e) The protein expression of NF-κB signalling was detected by western blotting. (f) Quantitative analysis of the protein expression of p-NF-κB p65 and NF-κB p65. **p < 0.01, ****p < 0.0001. n = 3 biologically independent samples. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://royalsocietypublishing.org/doi/abs/10.1098/rsob.230427'>38862020</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-feb413914-fig-0010-m.jpgAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal AntibodyEffects of OPN and OVE on activation of MAPK signaling pathways in LPS-stimulated RAW264.7 cells. Expression levels of p-ERK, ERK, p-p38, p-38, p-JNK, and JNK were detected in the same samples for COX-2 detection after 24 h of LPS stimulation. (A) OVE treatment. (B) OPN treatment. All experiments were carried out in triplicates and data are presented as means ± SDs; one-way ANOVA analysis was adopted for multiple comparisons; ###P < 0.001, ####P < 0.0001, compared to the untreated control group; ***P < 0.001 and ****P < 0.0001, compared to the LPS control group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://febs.onlinelibrary.wiley.com/doi/abs/10.1002/2211-5463.13914'>39455284</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00104-mapk3-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Erk1 (T202/Y204) + Erk2 (T185/Y187) MAPK3 Rabbit Monoclonal Antibody Western blot analysis of MAPK3 using anti-MAPK3 antibody (P00104). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat skin tissue lysates,<br>
Lane 7: mouse skiin tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAPK3 antigen affinity purified monoclonal antibody (Catalog # P00104) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAPK3 at approximately 39 kDa. The expected band size for MAPK3 is at 42 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c9-rabbit-monoclonal-antibody-m01010-boster.html2026-04-03T05:00:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01010-c9-primary-antibodies-wb-testing-1.jpgAnti-C9/Complement Component C9 Rabbit Monoclonal Antibody Western blot analysis of C9 using anti-C9 antibody (M01010). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C9 antigen affinity purified monoclonal antibody (Catalog # M01010) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C9 at approximately 70 kDa. The expected band size for C9 is at 63,70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01010-ihc.jpgAnti-C9/Complement Component C9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using C9 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-retinoblastoma-s780rabbit-monoclonal-antibody-m00039-1-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-1-wb.jpgAnti-Phospho-Retinoblastoma (S780) RB1 Rabbit Monoclonal AntibodyWestern blot analysis of Retinoblastoma phosphorylation expression in Jurkat cell lysate treated with Alkaline Phosphatase.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rb-rabbit-monoclonal-antibody-m00039-2-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-wb7.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-rb1-primary-antibodies-wb-testing-1.jpgAnti-Rb RB1 Rabbit Monoclonal Antibody Western blot analysis of Rb using anti-Rb antibody (M00039-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human 293T whole cell lysates, <br>
Lane 4: human K562 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rb antigen affinity purified monoclonal antibody (M00039-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Rb at approximately 106 kDa. The expected band size for Rb is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ijbsv19p4511g004.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyChanges in chromatin accessibility are consistent with global transcriptome changes. A. Genome tracks showing a comparison of ATAC-seq profiles of RB1 in apatinib-resistant and non-resistant HepG2 cells. B. The mRNA expression levels of RB1 in apatinib-resistant versus untreated HepG2 cells, statistical analysis was performed by Student t-test. C. Boxplots of chromatin accessibility values for high expression genes and low expression genes in apatinib-resistant cells.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535702/'>37781033</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ijbsv19p4511g006.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyExpression status of RB1 pathway targets in HCC cells and in clinical samples; CDK2-IN-73 and Palbociclib can relieve apatinib resistance. A. qPCR analysis showed that the expression levels of RB1, PCNA, KIAA0101 and MCM7 in HepG2-resistant cells were significantly reduced, and the expression levels of CDKN2B andCDKN2AIP were increased. B. Western blot detection of the above proteins is consistent with qPCR detection results. C. Analysis of mRNA expression of five PD patients showed high expression of CDKN2B and low expression of RB1, PCNA, and MCM7. D. Western blot analysis showed that PD patients had high expression of CDKN2B but low expression of RB1, PCNA, and MCM7. E. Representative photographs of staining of RB1 protein in a pair of HCC patients tissues in PD and PR (20X). F. Representative photographs of staining of CDKN2B protein in a pair of HCC patients tissues in PD and PR (20X). G. The proliferation inhibition curves of resistant HepG2 cells and HepG2 cells treated with CDK2-IN-73. H. Western blot analysis showed that the expression of CDKN2B in HepG2resistant cells was not significantly different, and the expression levels of RB1, PCNA and MCM7 were upregulated. I. Proliferation inhibition curves of HepG2 resistant cells and HepG2 cells treated with Palbociclib. J. Western blot analysis results showed that the expression levels of RB1, PCNA, and MCM7 were upregulated. The bars represent mean ± standard deviation; ∗ P < 0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535702/'>37781033</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc7.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat lung, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc8.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tongue cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc9.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human renal cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc10.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human kidney, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc11.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse spleen, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-ihc.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer, using Retinoblastoma Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-icc1.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039-2-if.jpgAnti-Rb RB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of SH-SY5Y cells, using Retinoblastoma Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gr-rabbit-monoclonal-antibody-m00503-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00503-wb7.jpgAnti-GR NR3C1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00503-wb8.jpgAnti-GR NR3C1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00503-wb.jpgAnti-GR NR3C1 Rabbit Monoclonal AntibodyWestern blot analysis of GR expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c3-rabbit-monoclonal-antibody-m00168-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00168-wb7.jpgAnti-C3/Complement C3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00168-wb.jpgAnti-C3/Complement C3 Rabbit Monoclonal AntibodyWestern blot analysis of C3 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mbp-rabbit-monoclonal-antibody-m30934-2-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30934-2-malE-primary-antibodies-WB-testing-1.jpgAnti-MBP Rabbit Monoclonal AntibodyWestern blot analysis of MBP expression in Ecoli lysate (M30934-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-malE monoclonal antibody (Catalog # M30934-2) overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for malE
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfp-rabbit-monoclonal-antibody-m30939-2-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30939-2-gfp-primary-antibodies-wb-testing-1_1.jpgAnti-GFP Rabbit Monoclonal AntibodyWestern blot analysis of GFP expression in 293 cell lysate transfected with GFP.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30939-2-GFP-primary-antibodies-IHC-testing-1.jpgAnti-GFP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded GFP transgenic mouse liver, using GFP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30939-2-3.jpgAnti-GFP Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using GFP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfp-rabbit-monoclonal-antibody-m30939-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30939-fimmu-14-1169869-g004.jpgAnti-GFP Rabbit Monoclonal AntibodyMCMV infection influence the lipid metabolism pathway in infant mice hepatocytes. (A) The hepatocytes cell cluster in Figure 1A were selected. Enriched GO terms for significantly down-regulated genes in hepatocytes cluster, compared with other clusters, were shown as bubble diagram. (B) Hepatocytes from three uninfected and three MCMV infected 2 weeks old WT mice were isolated and proteomic mass spectrometry analysis were performed individually. PCA analysis showed that the difference between infection group and control group. Each point represents an individual mice. (C) Enriched KEGG terms for significantly down-regulated genes of hepatocytes between uninfected and infected group in proteomic mass spectrometry analysis. (D) Proteomic gene regulation network of down-regulated PPAR-γ pathway analyzed by STRING. (E) WT mice were infected by MCMV at 14 days post birth. Immunoblotting with antibodies target ACOX1, ACSL1, FABP1, SLC27A2 and GFP in hepatocytes from mice infected with MCMV at three dpi or treated with PBS. Experiments were repeated three times. Each lane represents an individual mice. (F) Quantitative analysis of (E) (mean ± SD). Statistical significance was determined by non-parametric Mann Whitney test between groups (*P < 0.05, ***P < 0.001). (G) AML12 mice hepatocyte cell were transfected with siRNA that does not match any known genes or regulatory regions(siControl) or target Pparg mRNA(si Pparg ). qPCR analysis of indicated genes in different cells at 24 hours post MCMV infection (n=4, mean ± SD). Statistical significance was determined by non-parametric Mann Whitney test between groups (*P < 0.05, ***P < 0.001). Experiments were repeated three times. Each point represents an individual cell sample.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10449610/&orig_host=www.ncbi.nlm.nih.gov'>37638012</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30939-GFP-primary-antibodies-IHC-testing-1.jpgAnti-GFP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded GFP transgenic human colon, using GFP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30939-gfp-primary-antibodies-if-testing-3.jpgAnti-GFP Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using GFP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30939-gfp-primary-antibodies-wb-testing-1_1.jpgAnti-GFP Rabbit Monoclonal AntibodyWestern blot analysis of GFP expression in 293 cell lysate transfected with GFP.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfp-rabbit-monoclonal-antibody-m30939-1-boster.html2026-03-24T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30939-1-GFP-primary-antibodies-WB-testing-1.jpgAnti-GFP Rabbit Monoclonal AntibodyWestern blot analysis of GFP expression in 293 cell lysate transfected with GFP.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gst-rabbit-monoclonal-antibody-m00394-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00394-GSTP1-primary-antibodies-WB-testing-1.jpgAnti-GST GSTP1 Rabbit Monoclonal AntibodyWestern blot analysis of GST expression in GST recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00394-gstp1-primary-antibodies-if-testing-2.jpgAnti-GST GSTP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using GST Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rfp-rabbit-monoclonal-antibody-m30958-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30958-RFP-primary-antibodies-WB-testing-1.jpgAnti-RFP rfp1 Rabbit Monoclonal AntibodyWestern blot analysis of RFP expression in (1) 293T cell lysate; (2) 293T cell lysate transfected with RFP.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30958-rfp-primary-antibodies-if-testing-2.jpgAnti-RFP rfp1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using RFP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tau-rabbit-monoclonal-antibody-m00097-1-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-1-wb7.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-1-wb.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyWestern blot analysis of Tau expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aif-rabbit-monoclonal-antibody-m01571-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01571-aif-primary-antibodies-wb-testing-1.jpgAnti-AIF AIFM1 Rabbit Monoclonal AntibodyWestern blot analysis of AIF using anti-AIF antibody (M01571). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AIF antigen affinity purified monoclonal antibody (M01571) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AIF at approximately 70 kDa. The expected band size for AIF is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01571-icc1.jpgAnti-AIF AIFM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01571-if.jpgAnti-AIF AIFM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using AIF Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bax-rabbit-monoclonal-antibody-m00183-1-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-43556_2024_203_fig7_html.pngAnti-Bax Rabbit Monoclonal AntibodyMice reconstituted with FGF2 KO macrophages and subjected to CLP exhibit increased proinflammatory gene expression and apoptosis. a - c The expression of the inflammatory factors CXCL1, IL1β, and IL6 in lung tissue was detected by real-time PCR ( n = 3 per group). d TUNEL staining was used to evaluate apoptosis in the lung tissue. e - f The apoptosis-associated genes BCL2 and Bax were identified by western blot analysis. Bar is 20 μm. * p < 0.05, vs. WT; Δ p < 0.05, vs. WT + LPS; # p < 0.05 vs. FGF2 KO <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s43556-024-00203-0'>39436561</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-fphar-16-1650534-g004.jpgAnti-Bax Rabbit Monoclonal AntibodyRegulatory effects of KSG on the expression of cytokines and apoptosis-related factors in Aβ-induced PC12 cells. (A) Expression of IL-1β (n = 3). (B) Expression of IL-18 (n = 3). (C) Expression of TNF-α (n = 3). (D) Protein expression of apoptosis-related factors in PC12 cells of each group (n = 3). (E) Expression of Caspase-3 (n = 3). (F) Expression of Bax (n = 3). Data were expressed as mean ± SD. * P < 0.05, ** P < 0.01, and *** P < 0.001 vs. Con. # P < 0.05, ## P < 0.01, and ### P < 0.001 vs. AD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1650534/full'>41050397</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-bax-primary-antibodies-wb-testing-1.jpgAnti-Bax Rabbit Monoclonal Antibody Western blot analysis of Bax using anti-Bax antibody (M00183-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bax antigen affinity purified polyclonal antibody (Catalog # M00183-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bax at approximately 21 kDa. The expected band size for Bax is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-ihc7.jpgAnti-Bax Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-ihc8.jpgAnti-Bax Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-1-ihc.jpgAnti-Bax Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human adenocarcinoma of colon, using Bax Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-id1-rabbit-monoclonal-antibody-m00945-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00945-id1-primary-antibodies-wb-testing-1.jpgAnti-Id1 Rabbit Monoclonal AntibodyWestern blot analysis of ID1 using anti-ID1 antibody (M00945). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ID1 antigen affinity purified monoclonal antibody (M00945) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ID1 at approximately 25 kDa. The expected band size for ID1 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00945-ihc.jpgAnti-Id1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Id1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00945-if.jpgAnti-Id1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Id1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p21-rabbit-monoclonal-antibody-m00145-3-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-wb7.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-ihc.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using p21 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-12935_2021_1934_fig6_html.pngAnti-p21 CDKN1A Rabbit Monoclonal AntibodyExploration of mechanism underlying PSMC2-induced regulation of prostate cancer. a The expression levels of Akt, p-Akt, CDK6, Cyclin D1 and P21 detected by western blotting in PC-3 cells of shCtrl and shPSMC2 groups. b The expression levels of Akt, p-Akt, CDK6, Cyclin D1 and P21 detected by western blotting in PC-3 cells of Control and PSMC2 overexpression groups with or without treatment of MK-2206 (500 nM). c MTT assay was performed to assess the cell proliferation rate of PC-3 cells of Control and PSMC2 overexpression groups with or without treatment of MK-2206 (500 nM). Results were presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-021-01934-8'>33902600</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-13287_2025_4422_fig1_html.pngAnti-p21 CDKN1A Rabbit Monoclonal AntibodyShort-term DMOG treatment reduces MSC senescence by activating HIF-1α and decreasing apoptosis. ( A , B ) Representative images of SA-β-gal staining showing the proportion of senescent cells in H₂O₂-treated MSCs before and after DMOG treatment. Scale bar = 500 μm. ( C ) Western blot analysis of p53 and p21 protein expression during oxidative stress-induced senescence. ( D , E ) SA-β-gal staining in replicative senescence (P15) MSCs, demonstrating the effect of DMOG in reducing senescence markers. Scale bar = 500 μm. ( F ) Western blot analysis of p53 and p21 protein levels in P5 (young) and P15 (senescent) MSCs. ( G ) Expression levels of senescence-associated genes (IL6, CXCL1, and MMP3) in both senescence models as assessed by qRT-PCR. ( H ) Western blotting and qPCR analysis showing increased HIF-1α protein and mRNA levels in both senescence models after DMOG treatment. ( I ) Calcein/PI live-dead staining revealed an increase in the proportion of live cells following DMOG treatment in both senescence models. ( J , K ) Flow cytometric analysis of apoptosis. Error bars represent the mean ± SD of three independent experiments. Statistical significance was set as p < 0.05. Full-length blots are presented in Supplementary Materials - WB Raw Data Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04422-2'>40457488</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-icc1.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-if.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using p21 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-3-wb.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyWestern blot analysis of p21 in (1) MCF-7 cell lysate; (2) LnCaP cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erg-rabbit-monoclonal-antibody-m00793-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00793-erg-primary-antibodies-wb-testing-1.jpgAnti-ERG Rabbit Monoclonal AntibodyWestern blot analysis of ERG using anti-ERG antibody (M00793). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human COLO-320 whole cell lysates,<br>
Lane 3: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERG antigen affinity purified monoclonal antibody (M00793) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ERG at approximately 55 kDa. The expected band size for ERG is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00793-ihc.jpgAnti-ERG Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using ERG Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p53-rabbit-monoclonal-antibody-m00001-1-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-1-p35-primary-antibodies-wb-testing-1.jpgAnti-p53 TP53 Rabbit Monoclonal Antibody Western blot analysis of p53 using anti-p53 antibody (M00001-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-9 (WT) whole cell lysates, <br>
Lane 2: human PC-9 (KO) whole cell lysates, <br>
Lane 3: human A431 whole cell lysates, <br>
Lane 4: human 293T whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p53 antigen affinity purified monoclonal antibody (M00001-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for p53 at approximately 53 kDa. The expected band size for p53 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-1-ihc.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using p53 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-1-12935_2025_3993_fig4_html.pngAnti-p53 TP53 Rabbit Monoclonal AntibodyIndirect co-culture of MSCs regulates the CRC cell cycle. (A) CRC cell cycle distribution as assessed using flow cytometry. (B) Immunoblotting assessment of P16, P21 and P53 levels, with GAPDH as the loading control. * P < 0.05 compared with the control and ** P < 0.01 compared with the. control <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-025-03993-7'>41063156</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-1-if.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using p53 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-yy1-rabbit-monoclonal-antibody-m00833-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-yy1-primary-antibodies-wb-testing-1.jpgAnti-YY1 Rabbit Monoclonal Antibody Western blot analysis of YY1 using anti-YY1 antibody (M00833). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates,<br>
Lane 7: mouse ANA-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YY1 antigen affinity purified monoclonal antibody (Catalog # M00833) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YY1 at approximately 68 kDa. The expected band size for YY1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-ihc.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder using YY1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc3.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc4.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc5.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc1.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc6.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-if.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using YY1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00833-icc2.jpgAnti-YY1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ngf-rabbit-monoclonal-antibody-m00341-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-ngf-primary-antibodies-wb-testing-1.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal Antibody Western blot analysis of NGF using anti-NGF antibody (M00341). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NGF antigen affinity purified monoclonal antibody (Catalog # M00341) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NGF at approximately 35 kDa. The expected band size for NGF is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-wb.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyWestern blot analysis of NGF expression in (1)Mouse thyroid lysate;(2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-41598_2025_17274_fig1_html.pngAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyGel electrophoresis analysis of the RT-PCR products for the CDS region. ( a ) NGF (To obtain clearer band images, only the edges of the membrane were trimmed, original image in Supplementary Fig. a); ( b ) S100β (original image in Supplementary Fig. b). M, DL2000 DNA marker. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-17274-w'>41006582</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-41598_2025_17274_fig10_html.pngAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyNGF mRNA expression levels in the various intestinal segments of broilers at various ages. ( a ) The duodenal NGF mRNA expression at the age of 20 days was highly significant higher than at other ages ( n = 3, *** P < 0.001). ( b ) The jejunal NGF mRNA expression at the age of 20 days was significantly higher than at the ages of 40, 55, and 70 days ( n = 3, *** P < 0.001). ( c ) The ileal NGF mRNA expression at the age of 20 days was highly significantly higher than at the ages of 7, 40, 55, and 70 days ( n = 3, *** P < 0.001). ( d ) Observations among different intestinal segments of the small intestine at the same day of age revealed that the relative expression level of NGF mRNA was highly significantly higher in the duodenum than in the jejunum and ileum ( n = 3, *** P < 0.001). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-17274-w'>41006582</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-41598_2025_17274_fig5_html.pngAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyImmunohistochemistry staining of NGF in the small intestine of broilers of various ages. (g) NGF protein expression was strongest at the age of 40 days, and was strongly positive in the duodenal mucosal epithelium, intestinal glands, and submucosal plexus, and positive in the lamina propria and interosseous plexus; (h) it was strongly positive in the jejunal mucosal epithelium, positive in the lamina propria, intestinal glands, and submucosal plexus, and weakly positive in the interosseous plexus; (i) it was strongly positive in the ileal mucosal epithelium, intestinal glands, submucosal plexus, lamina propria, and intermuscular plexus. Day 7 (a, b, c); Day 20 (d, e, f); Day 40 (g, h, i); Day 55 (j, k, l); Day 70 (m, n, o); Duodenum (a, d, g, j, m); Jejunum (b, e, h, k, n); Ileum (c, f, i, l, o); Scale bar: 200 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-17274-w'>41006582</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-41598_2025_17274_fig7_html.pngAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyExpression levels of NGF in the small intestine of yellow-feathered broiler chickens of different days of age. ( a ) Western blot to detect NGF protein and β-actin internal reference bands. 7 days duodenum, jejunum, ileum (1–3)(To better visualize the grayscale value comparison of WB bands for proteins across different intestinal segments at various postnatal ages, only the relevant bands are displayed, original images in Supplementary Fig. S7a, f); 20 days duodenum, jejunum, ileum (4–6)(original images in Supplementary Fig. S7b, g); 40 days duodenum, jejunum, ileum (7–9)(original images in Supplementary Fig. S7c, h); 55 days duodenum, jejunum, ileum (10–12)(original iamges in Supplementary Fig. S7d, i); 70 days duodenum, jejunum, ileum (13–15)(original images in Supplementary Fig. S7e, j); The samples were from the same experiment and the gels were processed in parallel; ( b - c ) Western blot to detect the relative expression level of NGF protein, and Image J to measure the gray value. n = 3, *** P < 0.001; ** P < 0.01; * P < 0.05. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-17274-w'>41006582</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-41598_2025_17274_fig9_html.pngAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyRT-PCR electropherograms. (M) DL1000 DNA Marker; (1–2) NGF protein migration band; (3–6) S100β protein migration band; (To obtain clearer band images, only the edges of the membrane were trimmed, original image in Supplementary Fig. S9) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-17274-w'>41006582</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-wb8.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-ihc.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using NGF Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-if.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyImmunofluorescent analysis of SH-SY5Y cells, using NGF Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-icc1.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-icc2.jpgAnti-NGF/Beta Ngf Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fyn-rabbit-monoclonal-antibody-m00684-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00684-fyn-primary-antibodies-wb-testing-1.jpgAnti-Fyn Rabbit Monoclonal AntibodyWestern blot analysis of FYN using anti-FYN antibody (M00684). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FYN antigen affinity purified monoclonal antibody (M00684) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FYN at approximately 61 kDa. The expected band size for FYN is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00684-icc1.jpgAnti-Fyn Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pd1-rabbit-monoclonal-antibody-m00178-1-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-1-ihc.jpgAnti-PD1 PDCD1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using PD1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bim-rabbit-monoclonal-antibody-m01552-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-wb7.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-wb.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyWestern blot analysis of Bim expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-12885_2023_10974_fig2_html.pngAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyCYD0281 promotes HUVECs cell apoptosis by the exposure of the Bcl-2 BH3 domain. A Cell viability of HUVECs at 48 h. The exposure of the BH3 domain of Bcl-2 detected by immunofluorescence (IF) staining using anti-Bcl-2/BH3 domain antibody ( B ), and flow cytometry analysis of cell apoptosis ( C ) in HUVECs treated with BDA-366 and CYD0281 at the IC 50 concentration. HUVECs were treated with CYD0281 at the IC 50 concentration for 48 h, mitochondrial dysfunction was analyzed by Mito-Tracker Red CMXRos staining ( D ), Cyt c release ( E ) and PARP cleavage ( F ) were analyzed by western blotting assay, and Bcl-2 associated Bax or Bim was analyzed by co-IP using Bcl-2 antibody ( G ). H The expression of Bcl-2 in HUVECs was inhibited using siRNAs (1, 2, and 3) and analyzed by western blotting assay. I Flow cytometry analysis of cell apoptosis in Bcl-2-silenced HUVECs that were treated with CYD0281 ( n = 3). Significant effect compared to the DMSO group: * P < 0.05 and *** P < 0.001. ns: no significant differences. Scale bars: 50 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-023-10974-4'>37237269</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-ihc7.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-ihc.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix cancer, using Bim Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-bim-primary-antibodies-wb-testing-1.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyWestern blot analysis of Bim using anti-Bim antibody (M01552).<br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: huamn OE19 whole cell lysates,<br>
Lane 2: human OE19 whole cell lysates,<br>
Lane 3: human OE33 whole cell lysates,<br>
Lane 4: human OE33 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bim antigen affinity purified monoclonal antibody (M01552) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Bim-L at approximately ~22 kDa. The expected band size for Bim is at ~22 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-ihc8.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-if.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Raji cells, using Bim Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01552-icc1.jpgAnti-Bim BCL2L11 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-5t4-rabbit-monoclonal-antibody-m07442-1-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-1-wb.jpgAnti-5T4 TPBG Rabbit Monoclonal AntibodyWestern blot analysis of 5T4 expression in MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd9-rabbit-monoclonal-antibody-m01202-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-wb-testing-1_1.jpgAnti-CD9 Rabbit Monoclonal Antibody Western blot analysis of CD9 using anti-CD9 antibody (M01202). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD9 antigen affinity purified monoclonal antibody (M01202) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD9 at approximately 23 kDa. The expected band size for CD9 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-1_1.jpgAnti-CD9 Rabbit Monoclonal AntibodyIHC analysis of CD9 using anti-CD9 antibody (M01202). <br>
CD9 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-13287_2025_4205_fig2_html.pngAnti-CD9 Rabbit Monoclonal AntibodyIllustrates the characterization of DFATs and exosomes. DFATs exhibited a spindle-shaped morphology ( A-B ). Flow cytometry analysis showed that DFATs were positive for markers CD90, CD105, and CD73, and negative for CD34, CD11b, CD19, CD45, and HLA-DR ( C ). NTA showed that the average diameter of the exosomes was 136.3 nm ( D ). TEM showed that DFATs-Exos exhibited a typical bilayer membrane structure ( E ). Western blot analysis revealed that DFATs exosomes were enriched in markers such as CD63, CD9, and TSG101, while lacking the marker Calnexin ( F ). Full-length blots are presented in Supplementary Digital Material 1 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04205-9'>40022232</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-41598_2024_56036_fig1_html.pngAnti-CD9 Rabbit Monoclonal AntibodyCharacterization of EVs (extracellular vesicles) from HC (healthy control) and BTI (biliary tract infection) samples. ( A ) Representative images of EVs, which were captured by TEM (Transmission Electron Microscope), from HC or BTI samples (bar = 100 nm). ( B , C , D ) Plot showing the sizes ( B ) or concentrations (Conc.; C ) and cell surface expression of CD9/CD81/IgG ( D ) of EVs which were measured by the NFCM (Nano-Flow Cytometry Measurement). ( E ) CD9, CD81, CD63 and TSG101 were detectable by Western blot (WB) analysis. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-56036-y'>38459197</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-2.jpgAnti-CD9 Rabbit Monoclonal Antibody IHC analysis of CD9 using anti-CD9 antibody (M01202). <br>CD9 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-3.jpgAnti-CD9 Rabbit Monoclonal Antibody IHC analysis of CD9 using anti-CD9 antibody (M01202). <br>CD9 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-4.jpgAnti-CD9 Rabbit Monoclonal Antibody IHC analysis of CD9 using anti-CD9 antibody (M01202). <br>CD9 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-5.jpgAnti-CD9 Rabbit Monoclonal Antibody IHC analysis of CD9 using anti-CD9 antibody (M01202). <br>CD9 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-6.jpgAnti-CD9 Rabbit Monoclonal AntibodyIHC analysis of CD9 using anti-CD9 antibody (M01202). <br>
CD9 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-7.jpgAnti-CD9 Rabbit Monoclonal AntibodyIHC analysis of CD9 using anti-CD9 antibody (M01202). <br>
CD9 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-cd9-primary-antibodies-ihc-testing-8.jpgAnti-CD9 Rabbit Monoclonal AntibodyIHC analysis of CD9 using anti-CD9 antibody (M01202). <br>
CD9 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD9 Antibody (M01202) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-if.jpgAnti-CD9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CD9 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bad-rabbit-monoclonal-antibody-m03520-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-bad-primary-antibodies-wb-testing-1.jpgAnti-Bad Rabbit Monoclonal Antibody Western blot analysis of BAD using anti-BAD antibody (M03520). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BAD antigen affinity purified monoclonal antibody (Catalog # M03520) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BAD at approximately 23 kDa. The expected band size for BAD is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-if.jpgAnti-Bad Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Bad Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-bad-primary-antibodies-ihc-testing-1.jpgAnti-Bad Rabbit Monoclonal AntibodyIHC analysis of BAD using anti-BAD antibody (M03520). <br>BAD was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BAD Antibody (M03520) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-bad-primary-antibodies-ihc-testing-2.jpgAnti-Bad Rabbit Monoclonal AntibodyIHC analysis of BAD using anti-BAD antibody (M03520). <br>BAD was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BAD Antibody (M03520) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-bad-primary-antibodies-ihc-testing-3.jpgAnti-Bad Rabbit Monoclonal AntibodyIHC analysis of BAD using anti-BAD antibody (M03520). <br>BAD was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BAD Antibody (M03520) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03520-bad-primary-antibodies-ihc-testing-4.jpgAnti-Bad Rabbit Monoclonal AntibodyIHC analysis of BAD using anti-BAD antibody (M03520). <br>BAD was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BAD Antibody (M03520) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bak-rabbit-monoclonal-antibody-m01163-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01163-bak-primary-antibodies-wb-testing-1.jpgAnti-Bak BAK1 Rabbit Monoclonal Antibody Western blot analysis of Bak using anti-Bak antibody (M01163). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Daudi whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bak antigen affinity purified monoclonal antibody (Catalog # M01163) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bak at approximately 23-25 kDa. The expected band size for Bak is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01163-wb7.jpgAnti-Bak BAK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01163-BAK1-primary-antibodies-IHC-testing-1.jpgAnti-Bak BAK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse liver, using Bak Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01163-if.jpgAnti-Bak BAK1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Bak Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tbp-rabbit-monoclonal-antibody-m00302-boster.html2026-03-24T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00302-wb.jpgAnti-TBP/Tata Binding Protein Tbp Rabbit Monoclonal AntibodyWestern blot analysis of TBP expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pbr-rabbit-monoclonal-antibody-m01153-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01153-wb7.jpgAnti-PBR TSPO Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01153-ihc.jpgAnti-PBR TSPO Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PBR Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01153-wb8.jpgAnti-PBR TSPO Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01153-ip7.jpgAnti-PBR TSPO Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01153-wb.jpgAnti-PBR TSPO Rabbit Monoclonal AntibodyWestern blot analysis of Calreticulin expression in (1) U87-MG cell lysate; (2) A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ras-rabbit-monoclonal-antibody-m00099-2-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00099-2-wb.jpgAnti-Ras NRAS Rabbit Monoclonal AntibodyWestern blot analysis of Ras expression in (1) C6 cell lysate; (2) Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-src-rabbit-monoclonal-antibody-m00107-1-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-1-wb.jpgAnti-Src Rabbit Monoclonal AntibodyWestern blot analysis of Src expression in U87-MG cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-1-wb7.jpgAnti-Src Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-1-wb8.jpgAnti-Src Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-yb1-rabbit-monoclonal-antibody-m01054-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01054-yb1-primary-antibodies-wb-testing-1.jpgAnti-YB1 YBX1 Rabbit Monoclonal Antibody Western blot analysis of YB1 using anti-YB1 antibody (M01054). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human T-47D whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YB1 antigen affinity purified monoclonal antibody (Catalog # M01054) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YB1 at approximately 48 kDa. The expected band size for YB1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01054-YBX1-primary-antibodies-IHC-testing-1.jpgAnti-YB1 YBX1 Rabbit Monoclonal Antibody<br>
<br>
Immunohistochemical analysis of paraffin-embedded human kidney, using YB1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01054-ybx1-primary-antibodies-if-testing-3.jpgAnti-YB1 YBX1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using YB1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fak-rabbit-monoclonal-antibody-m00151-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-ptk2-primary-antibodies-wb-testing-1.jpgAnti-FAK PTK2 Rabbit Monoclonal Antibody Western blot analysis of FAK using anti-FAK antibody (M00151). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAK antigen affinity purified monoclonal antibody (Catalog # M00151) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAK at approximately 119 kDa. The expected band size for FAK is at 119 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-13048_2025_1679_fig5_html.pngAnti-FAK PTK2 Rabbit Monoclonal AntibodyYJD affected the VEGF/VEGFR-2/FAK pathway in vivo. ( A – B ) Germ cell markers MVH and Oct4 were detected by IF. ( C ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( D ) VEGF, VEGFR-2, FAK expression in the ovaries was examined by IHC; Black arrows point to areas of positive staining. ( E - F ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ** P < 0.01, *** P < 0.001 vs. Control; # P < 0.05, ## P < 0.01, ### P < 0.001 vs. TP; & P < 0.05, && P < 0.01 vs. TP + M-YJD <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-13048_2025_1679_fig6_html.pngAnti-FAK PTK2 Rabbit Monoclonal AntibodyYJD affected the VEGF/VEGFR-2/FAK pathway and KGN cell injury in vitro. ( A ) Screening of YJD for medicated serum concentrations utilized the CCK-8 assay. ( B ) The cell viability of each group was measured by CCK-8. ( C – G ) Serum levels of the hormones P, E2, FSH, LH, and AMH were examined by ELISA. ( H ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( I - J ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ( K ) Apoptosis index was detected by Annexin V-FITC flow cytometry. ( L ) The expression of Bcl-2, pro-Caspase-3, Caspase-3 and AIF were assessed by WB. ** P < 0.01, *** P < 0.001 vs. Control; # P < 0.05, ## P < 0.01, ### P < 0.001 vs. TP <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-13048_2025_1679_fig7_html.pngAnti-FAK PTK2 Rabbit Monoclonal AntibodyYJD affected POF by regulating the VEGF/VEGFR-2/FAK signaling pathway. ( A – E ) Serum levels of the hormones P, E2, FSH, LH, and AMH were examined by ELISA. Control and TP groups were set up, and the remaining groups were co-treated with TP and 15% medicated serum, along with VEGF inhibitor (Avastin), VEGFR-2 inhibitor (SU5408), or FAK inhibitor (Y15). ( F - G ) Serum levels of indicators of oxidative stress, MDA and SOD were assessed by ELISA. ( H - J ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( K - L ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ( M ) Apoptosis rate was detected by Annexin V-FITC flow cytometry. ( N ) The expression of Bcl-2, pro-Caspase-3, Caspase-3 and AIF were assessed by western blotting. ** P < 0.01, *** P < 0.001 vs. Control; ## P < 0.01, ### P < 0.001 vs. TP; & P < 0.05, && P < 0.01, &&& P < 0.001 vs. TP + 15% medicated serum <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-ihc.jpgAnti-FAK PTK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse spleen, using FAK Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151-if.jpgAnti-FAK PTK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using FAK Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p53-rabbit-monoclonal-antibody-m00001-2-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-wb7.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-wb8.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-wb.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyWestern blot analysis of p53 expression in (1) Raji cell lysate; (2) HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-wb9.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-if.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using p53 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-icc2.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-2-icc1.jpgAnti-p53 TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p38-rabbit-monoclonal-antibody-m00176-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-wb10.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-wb7.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-wb.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyWestern blot analysis of p38 MAPK expression in (1) HeLa cell lysate; (2) Jurkat cell lysate; (3) NIH/3T3 cell lysate; (4) Mouse heart lysate; (5) Mouse kidney lysate; (6) Rat heart lysate; (7) Rat kidney lysate; (8) C6 cell lysate; (9) PC12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-wb8.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-wb9.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-if.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using p38 MAPK Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-ip7.jpgAnti-p38 MAPK14 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd8-rabbit-monoclonal-antibody-m02236-1-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-wb7.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-cd8a-primary-antibodies-wb-testing-1.jpgAnti-CD8 CD8A Rabbit Monoclonal Antibody Western blot analysis of CD8A using anti-CD8A antibody (M02236-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD8A antigen affinity purified monoclonal antibody (Catalog # M02236-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD8A at approximately 36 kDa. The expected band size for CD8A is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-wb8.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-fonc-15-1525635-g006.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyESRRG is positively correlated with PD-L1. (A-B) The positive correlation between ESRRG and PD-L1 in GBC cells was investigated using Real-time PCR (A) and Western Blot (B) . (C-D) The expressions of ESRRG, PD-L1 and CD8 were detected by immunofluorescence assay in GBC tissues. **p < 0.01; ***p < 0.001; p < 0.05 was considered statistically significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12066295/'>40356747</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-ihc8.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:600 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-ihc9.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human kidney, using the Antibody at 1:600 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-ihc10.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-ihc7.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat kidney, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-ihc.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using CD8 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-icc1.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-icc2.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-1-if.jpgAnti-CD8 CD8A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using CD8 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p21-rabbit-monoclonal-antibody-m00145-2-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-icc1.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-13287_2020_2112_fig6_html.pngAnti-p21 CDKN1A Rabbit Monoclonal AntibodyExpression changes of stemness/senescence-associated genes in BMSCs from rats with and without Desferal® treatment. mRNA levels of Nanog ( a ), Oct-4 ( b ), P16 ( c ), P21 ( d ), and P53 ( e ) were analyzed by real-time PCR. These data were drawn from three independent experiments and the results were expressed as mean ± SD. * p < 0.05, ** p < 0.01. f Western blot results of HIF-1α, P16, P21, and P53. GAPDH was used to as an internal reference <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-020-02112-9'>33413663</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-41419_2019_1742_fig6_html.pngAnti-p21 CDKN1A Rabbit Monoclonal AntibodyNeat1 inhibits P21 expression throngh Ezh2. a Western blotting analysis showing that Neat1 knockdown enhanced P21 protein expression but decreased Cdk4 protein expression in C2C12 cells. The relative protein levels of P21 and Cdk4 were quantified using ImageJ software. b , c ChIP-qPCR results revealed that the enrichments of Ezh2 ( b ) and H3k27me3 ( c ) at the P21 promoter were significantly decreased after Neat1 knockdown. d , e ChIP-qPCR results revealed that the enrichments of Ezh2 ( d ) and H3k27me3 ( e ) at the P21 promoter were significantly increased after Neat1 overexpression. f Co-transfection of Ezh2 siRNA fragment and Neat1 expression vector in C2C12 cells for 2 days. Immunofluorescence staining of P21 was performed, and P21 expression was quantified by ImageJ. The quantification of P21 immunofluorescence staining results showed that the overexpression of Neat1 inhibited P21 protein expression, but had no significant effect on P21 expression after co-transfection with Ezh2 siRNA fragment. g Neat1 siRNA fragment and Ezh2 expression vector were co-transfected into C2C12 cells and the cells were performed with EdU staining at 2 days after transfection. The percentage of EdU + cells was quantified. The quantification of EdU staining results showed that Neat1 knockdown inhibited myoblast proliferation. After co-transfected with Ezh2 expression vector, Neat1 knockdown can not inhibit myoblast proliferation. h Neat1 and P21 siRNA fragments were co-transfected into C2C12 cells and the cells were performed with EdU staining at 2 days after transfection. The quantification of EdU staining results showed that Neat1 knockdown significantly reduced the percentage of EdU + cells, but did not reduce the number of EdU + cells after co-transfection with P21 siRNA fragment. Protein levels were normalized to those of β-actin. All values represent the mean ± s.d. of three independent experiments. * p < 0.05, ** p < 0.01, N.S. indicates not significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-019-1742-7'>31243262</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-41419_2019_1742_fig8_html.pngAnti-p21 CDKN1A Rabbit Monoclonal AntibodySchematic model of Neat1 regulation in myogenesis. In proliferating myoblasts, Neat1 guides Ezh2 to the P21 promoter and inhibits P21 expression, leading to the promotion of myoblast proliferation. Upon differentiation, Neat1 recruits Ezh2 to inhibit the expression of muscle-specific genes, such as Myog , Myh4 , and Tnni2 , and suppresses myogenic differentiation <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-019-1742-7'>31243262</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-fphys-09-00941-g006.jpgAnti-p21 CDKN1A Rabbit Monoclonal Antibody(A–F) Cisatracurium inhibits metastatic ability of CRC in vivo . (A) Line graph of subcutaneous tumor volume. (B) Weight of subcutaneous tumors in grams. Data are expressed as mean tumor volume or weight ± SE. ∗ p < 0.05. (C–F) Representative densities of tumor viability and migration regulatory proteins (p53, p21 and CD1, SNAI-1, CALD1, E-Cadherin) in tumor tissue samples. β-Actin was used as internal control. The cluster bar chats in (D , F) indicates the levels of viability and migration regulatory proteins in the treatment group. Data are expressed as Mean ± SEM ( n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 versus control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2018.00941/full'>30108509</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-wb.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyWestern blot analysis of p21 in (1) MCF-7 cell lysate; (2) HeLa cell lysate. (3) LnCap cell lysate; (4) U87 MG cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00145-2-if.jpgAnti-p21 CDKN1A Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using p21 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ca9-rabbit-monoclonal-antibody-m01083-1-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-1-wb.jpgAnti-CA9/Ca Ix Rabbit Monoclonal AntibodyWestern blot analysis of CA9 expression in Human stomach lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-1-ihc.jpgAnti-CA9/Ca Ix Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kindey cancer, using CA9 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-5t4-rabbit-monoclonal-antibody-m07442-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-wb.jpgAnti-5T4 TPBG Rabbit Monoclonal AntibodyWestern blot analysis of 5T4 expression in Caco-2 cell lysates.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-ihc.jpgAnti-5T4 TPBG Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uters cancer, using 5T4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p73-rabbit-monoclonal-antibody-m00688-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-p73-primary-antibodies-wb-testing-1_1.jpgAnti-p73 Rabbit Monoclonal Antibody Western blot analysis of p73 using anti-p73 antibody (M00688). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p73 antigen affinity purified monoclonal antibody (M00688) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for p73 at approximately 73 kDa. The expected band size for p73 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-6.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-7.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-5.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-4.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-3.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-2.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00688-tp73-primary-antibodies-ihc-testing-1.jpgAnti-p73 Rabbit Monoclonal AntibodyIHC analysis of TP73 using anti-TP73 antibody (M00688). <br>TP73 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TP73 Antibody (M00688) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-scf-rabbit-monoclonal-antibody-m01254-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01254-wb.jpgAnti-SCF Rabbit Monoclonal AntibodyWestern blot analysis of SCF expression in recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01254-ihc.jpgAnti-SCF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using SCF Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nse-rabbit-monoclonal-antibody-m02930-1-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02930-1-wb.jpgAnti-NSE ENO2 Rabbit Monoclonal AntibodyWestern blot analysis of NSE expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02930-1-ihc.jpgAnti-NSE ENO2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus cancer, using NSE Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02930-1-if.jpgAnti-NSE ENO2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using NSE Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p63-rabbit-monoclonal-antibody-m00167-1-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-tp63-primary-antibodies-wb-testing-1.jpgAnti-p63 TP63 Rabbit Monoclonal Antibody Western blot analysis of P63 using anti-P63 antibody (M00167-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates, <br>
Lane 2: human Hacat whole cell lysates, <br>
Lane 3: human A431 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P63 antigen affinity purified monoclonal antibody (M00167-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for P63 at approximately 77 kDa. The expected band size for P63 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-wb10.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-wb8.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-wb12.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-wb9.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-ihc7.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-ihc8.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-ihc9.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human small cell lung cancer , using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-ihc.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using p63 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00167-1-if.jpgAnti-p63 TP63 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using p63 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkr-rabbit-monoclonal-antibody-m01384-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01384-wb.jpgAnti-PKR EIF2AK2 Rabbit Monoclonal AntibodyWestern blot analysis of PKR expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01384-ihc.jpgAnti-PKR EIF2AK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using PKR Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01384-if.jpgAnti-PKR EIF2AK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PKR Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bpi-rabbit-monoclonal-antibody-m01444-boster.html2026-03-24T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01444-wb.jpgAnti-BPI Rabbit Monoclonal AntibodyWestern blot analysis of BPI expression in THP1 lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ilk-rabbit-monoclonal-antibody-m02932-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02932-ilk-primary-antibodies-wb-testing-1.jpgAnti-ILK/Integrin Linked Ilk Rabbit Monoclonal AntibodyWestern blot analysis of ILK/Integrin Linked using anti-ILK/Integrin Linked antibody (M02932). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: Rat spleen tissue lysates,<br>
Lane 6: Rat PC-12 whole cell lysates,<br>
Lane 7: Mouse spleen tissue lysates,<br>
Lane 8: Mouse heart tissue lysates,<br>
Lane 9: Rabbit-IgG lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ILK/Integrin Linked antigen affinity purified monoclonal antibody (M02932) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ILK/Integrin Linked at approximately 51 kDa. The expected band size for ILK/Integrin Linked is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02932-ilk-primary-antibodies-wb-testing-2.jpgAnti-ILK/Integrin Linked Ilk Rabbit Monoclonal AntibodyWestern blot analysis of ILK using anti-ILK antibody (M02932). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U2OS whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat Kidney tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ILK antigen affinity purified monoclonal antibody (M02932) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ILK at approximately 51 kDa. The expected band size for ILK is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02932-ihc.jpgAnti-ILK/Integrin Linked Ilk Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using ILK Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02932-if.jpgAnti-ILK/Integrin Linked Ilk Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using ILK Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ret-rabbit-monoclonal-antibody-m00293-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00293-wb.jpgAnti-Ret Rabbit Monoclonal AntibodyWestern blot analysis of Ret expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-btk-rabbit-monoclonal-antibody-m00245-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00245-wb.jpgAnti-BTK Rabbit Monoclonal AntibodyWestern blot analysis of BTK expression in (1) Daudi cell lysate; (2) Ramos cell lysate; (3) K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00245-ihc.jpgAnti-BTK Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human gastric cancer, using BTK Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00245-wb7.jpgAnti-BTK Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rho-rabbit-monoclonal-antibody-m00207-2-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-2-wb7.jpgAnti-Rho RHOA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-2-ihc.jpgAnti-Rho RHOA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid cancer, using Rho Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-2-wb8.jpgAnti-Rho RHOA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-2-wb.jpgAnti-Rho RHOA Rabbit Monoclonal AntibodyWestern blot analysis of Rho expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ron-rabbit-monoclonal-antibody-m01532-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-wb.jpgAnti-RON Rabbit Monoclonal AntibodyWestern blot analysis of RON expression in SKBR3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tau-rabbit-monoclonal-antibody-m00097-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-wb.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyWestern blot analysis of Tau expression in Mouse brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-wb7.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-wb8.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-icc3.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-icc2.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-icc1.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-icc4.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-icc6.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-if.jpgAnti-Tau MAPT Rabbit Monoclonal AntibodyImmunofluorescent analysis of T-47D cells, using Tau Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rip-rabbit-monoclonal-antibody-m00141-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00141-ripk1-primary-antibodies-wb-testing-1.jpgAnti-RIP RIPK1 Rabbit Monoclonal Antibody Western blot analysis of RIPK1 using anti-RIPK1 antibody (M00141). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RIPK1 antigen affinity purified monoclonal antibody (Catalog # M00141) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RIPK1 at approximately 76 kDa. The expected band size for RIPK1 is at 76 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vwf-rabbit-monoclonal-antibody-m00270-1-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00270-1-wb.jpgAnti-VWF/Von Willebrand Factor Rabbit Monoclonal AntibodyWestern blot analysis of VWF expression in human serum lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fas-rabbit-monoclonal-antibody-m00055-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-fas-primary-antibodies-wb-testing-1.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyWestern blot analysis of FAS using anti-FAS antibody (M00055). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human Ramos whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: human A549 whole cell lysates,<br>
Lane 6: human SIHA whole cell lysates,<br>
Lane 7: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAS antigen affinity purified monoclonal antibody (M00055) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FAS at approximately 38-45 kDa. The expected band size for FAS is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-icc3.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-fas-primary-antibodies-ihc-testing-4.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyIHC analysis of FAS using anti-FAS antibody (M00055). <br>FAS was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FAS Antibody (M00055) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-icc1.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-fas-primary-antibodies-ihc-testing-3.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyIHC analysis of FAS using anti-FAS antibody (M00055). <br>FAS was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FAS Antibody (M00055) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-icc2.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00055-fas-primary-antibodies-ihc-testing-2.jpgAnti-Fas/Cd95 Rabbit Monoclonal AntibodyIHC analysis of FAS using anti-FAS antibody (M00055). <br>FAS was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FAS Antibody (M00055) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-src-rabbit-monoclonal-antibody-m00107-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-wb-testing-1.jpgAnti-Src Rabbit Monoclonal Antibody Western blot analysis of Src using anti-Src antibody (M00107). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Src antigen affinity purified monoclonal antibody (Catalog # M00107) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Src at approximately 60 kDa. The expected band size for Src is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-ihc-testing-2.jpgAnti-Src Rabbit Monoclonal Antibody IHC analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Src Antibody (M00107) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-ihc-testing-3.jpgAnti-Src Rabbit Monoclonal Antibody IHC analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Src Antibody (M00107) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-icc1.jpgAnti-Src Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-ihc-testing-4.jpgAnti-Src Rabbit Monoclonal Antibody IHC analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Src Antibody (M00107) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-ihc-testing-5.jpgAnti-Src Rabbit Monoclonal Antibody IHC analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Src Antibody (M00107) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-ihc-testing-6.jpgAnti-Src Rabbit Monoclonal Antibody IHC analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Src Antibody (M00107) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-if-testing-7.jpgAnti-Src Rabbit Monoclonal Antibody IF analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Src Antibody (M00107) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107-src-primary-antibodies-if-testing-8.jpgAnti-Src Rabbit Monoclonal Antibody IF analysis of Src using anti-Src antibody (M00107). <br>
Src was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Src Antibody (M00107) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/casestudy_m00107.jpgAnti-Src Rabbit Monoclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ide-rabbit-monoclonal-antibody-m01358-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01358-ide-primary-antibodies-wb-testing-1.jpgAnti-IDE/Insulysin Rabbit Monoclonal Antibody Western blot analysis of IDE using anti-IDE antibody (M01358). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human U251 whole cell lysates, <br>
Lane 3: human U2OS whole cell lysates, <br>
Lane 4: human SH-SY5Y whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat C6 whole cell lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse Neuro-2a whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDE antigen affinity purified monoclonal antibody (M01358) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDE at approximately 118 kDa. The expected band size for IDE is at 118 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sp1-rabbit-monoclonal-antibody-m00110-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00110-wb7.jpgAnti-SP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00110-wb.jpgAnti-SP1 Rabbit Monoclonal AntibodyWestern blot analysis of SP1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dcx-rabbit-monoclonal-antibody-m01053-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01053-wb.jpgAnti-DCX/Doublecortin Rabbit Monoclonal AntibodyWestern blot analysis of DCX expression in C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-he4-rabbit-monoclonal-antibody-m02685-1-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02685-1-wb7.jpgAnti-HE4 WFDC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02685-1-if.jpgAnti-HE4 WFDC2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of SK-OV-3 cells, using HE4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02685-1-wb8.jpgAnti-HE4 WFDC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02685-1-wb.jpgAnti-HE4 WFDC2 Rabbit Monoclonal AntibodyWestern blot analysis of HE4 expression in SW480 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdi-rabbit-monoclonal-antibody-m03275-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03275-wb.jpgAnti-PDI PDIA2 Rabbit Monoclonal AntibodyWestern blot analysis of PDI expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-he4-rabbit-monoclonal-antibody-m02685-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02685-wb.jpgAnti-HE4 WFDC2 Rabbit Monoclonal AntibodyWestern blot analysis of HE4 expression in human ovary cancer whole cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ras-rabbit-monoclonal-antibody-m00099-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00099-nras-primary-antibodies-wb-testing-1.jpgAnti-Ras NRAS Rabbit Monoclonal AntibodyWestern blot analysis of NRAS using anti-NRAS antibody (M00099). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human HUVEC whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: mouse lung tissue lysates,<br>
Lane 7: mouse small intestine tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRAS antigen affinity purified monoclonal antibody (M00099) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NRAS at approximately 21 kDa. The expected band size for NRAS is at 21 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ng2-rabbit-monoclonal-antibody-m03394-boster.html2026-03-24T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03394-wb.jpgAnti-NG2 CSPG4 Rabbit Monoclonal AntibodyWestern blot analysis of NG2 expression in A375 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ahr-rabbit-monoclonal-antibody-m00225-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00225-ahr-primary-antibodies-wb-testing-1.jpgAnti-AhR Rabbit Monoclonal Antibody Western blot analysis of AhR using anti-AhR antibody (M00225). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human U-87MG whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AhR antigen affinity purified monoclonal antibody (Catalog # M00225) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AhR at approximately 96,105 kDa. The expected band size for AhR is at 96 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-iga-rabbit-monoclonal-antibody-m07514-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07514-wb.jpgAnti-IgA Rabbit Monoclonal AntibodyWestern blot analysis of IgA expression in human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-afp-rabbit-monoclonal-antibody-m00522-1-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00522-1-wb8.jpgAnti-AFP/Alpha 1 Fetoprotein Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00522-1-wb.jpgAnti-AFP/Alpha 1 Fetoprotein Rabbit Monoclonal AntibodyWestern blot analysis of AFP expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gba-rabbit-monoclonal-antibody-m01162-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01162-wb7.jpgAnti-GBA/Glucosylceramidase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01162-wb8.jpgAnti-GBA/Glucosylceramidase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01162-wb.jpgAnti-GBA/Glucosylceramidase Rabbit Monoclonal AntibodyWestern blot analysis of GBA expression in U87-MG cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il4-rabbit-monoclonal-antibody-m00230-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00230-il-4-primary-antibodies-wb-testing-1.jpgAnti-IL4 Rabbit Monoclonal AntibodyWestern blot analysis of IL-4 using anti-IL-4 antibody (M00230). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL-4 antigen affinity purified monoclonal antibody (M00230) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL-4 at approximately 15 kDa. The expected band size for IL-4 is at 17 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bid-rabbit-monoclonal-antibody-m00730-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00730-wb.jpgAnti-Bid Rabbit Monoclonal AntibodyWestern blot analysis of Bid expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00730-ihc.jpgAnti-Bid Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung, using Bid Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00730-if.jpgAnti-Bid Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Bid Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vcp-rabbit-monoclonal-antibody-m00610-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00610-wb.jpgAnti-VCP Rabbit Monoclonal AntibodyWestern blot analysis of VCP expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ttr-rabbit-monoclonal-antibody-m00290-1-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00290-1-wb.jpgAnti-TTR/Prealbumin Rabbit Monoclonal AntibodyWestern blot analysis of TTR expression in human serum lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-egf-rabbit-monoclonal-antibody-m00378-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00378-wb.jpgAnti-EGF Rabbit Monoclonal AntibodyWestern blot analysis of EGF expression in human urine sample lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-a2m-rabbit-monoclonal-antibody-m01498-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01498-a2m-primary-antibodies-wb-testing-1.jpgAnti-A2M/Alpha 2 Macroglobulin Rabbit Monoclonal AntibodyWestern blot analysis of A2M using anti-A2M antibody (M01498). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-A2M antigen affinity purified monoclonal antibody (M01498) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for A2M at approximately 163 kDa. The expected band size for A2M is at 163 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01498-a2m-primary-antibodies-ihc-testing-1.jpgAnti-A2M/Alpha 2 Macroglobulin Rabbit Monoclonal AntibodyIHC analysis of A2M using anti-A2M antibody (M01498). <br>A2M was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-A2M Antibody (M01498) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01498-a2m-primary-antibodies-ihc-testing-2.jpgAnti-A2M/Alpha 2 Macroglobulin Rabbit Monoclonal AntibodyIHC analysis of A2M using anti-A2M antibody (M01498). <br>A2M was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-A2M Antibody (M01498) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pml-rabbit-monoclonal-antibody-m00093-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00093-wb7.jpgAnti-PML Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00093-wb.jpgAnti-PML Rabbit Monoclonal AntibodyWestern blot analysis of PML expression in 293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mif-rabbit-monoclonal-antibody-m00411-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00411-mif-primary-antibodies-wb-testing-1.jpgAnti-MIF Rabbit Monoclonal Antibody Western blot analysis of MIF using anti-MIF antibody (M00411). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human U2OS whole cell lysates, <br>
Lane 4: human HepG2 whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat liver tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIF antigen affinity purified monoclonal antibody (M00411) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIF at approximately 12 kDa. The expected band size for MIF is at 12 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lox-rabbit-monoclonal-antibody-m00575-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00575-lox-primary-antibodies-wb-testing-1.jpgAnti-LOX Rabbit Monoclonal Antibody Western blot analysis of LOX using anti-LOX antibody (M00575). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX antigen affinity purified monoclonal antibody (Catalog # M00575) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX at approximately 47 kDa. The expected band size for LOX is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00575-lox-primary-antibodies-ihc-testing-2.jpgAnti-LOX Rabbit Monoclonal Antibody IHC analysis of LOX using anti-LOX antibody (M00575). <br>
LOX was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LOX Antibody (M00575) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00575-lox-primary-antibodies-ihc-testing-3.jpgAnti-LOX Rabbit Monoclonal Antibody IHC analysis of LOX using anti-LOX antibody (M00575). <br>
LOX was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LOX Antibody (M00575) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00575-if.jpgAnti-LOX Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using LOX Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00575-lox-primary-antibodies-ihc-testing-4.jpgAnti-LOX Rabbit Monoclonal Antibody IHC analysis of LOX using anti-LOX antibody (M00575). <br>
LOX was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LOX Antibody (M00575) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dr5-rabbit-monoclonal-antibody-m00410-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-wb7.jpgAnti-DR5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-wb.jpgAnti-DR5 Rabbit Monoclonal AntibodyWestern blot analysis of DR5 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pcna-rabbit-monoclonal-antibody-m00125-1-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-pcna-primary-antibodies-wb-testing-1.jpgAnti-PCNA Rabbit Monoclonal Antibody Western blot analysis of PCNA using anti-PCNA antibody (M00125-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U-937 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: mouse spleen tissue lysates,<br>
Lane 6: rat RAW264.7 tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCNA antigen affinity purified monoclonal antibody (Catalog # M00125-1) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCNA at approximately 36 kDa. The expected band size for PCNA is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00125-1-PCNA-primary-antibodies-IHC-testing-1.jpgAnti-PCNA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PCNA Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-13046_2021_2201_fig2_html.pngAnti-PCNA Rabbit Monoclonal AntibodyBMS-1 induces intestinal barrier injury in mice with melanoma. In the B16F10 melanoma model, the mice were intraperitoneally administered with the PD-1/PD-L1 inhibitor BMS-1 (0, 5 and 10 mg/kg) every 2 days for 6 times ( n = 10). A Representative images of hematoxylin and eosin (HE) staining of colonic tissues and corresponding quantification analysis. Scale bars, 100 μm. B Representative images of Alcian blue-periodic acid-Schiff (ABPAS) of colonic tissues and corresponding quantification analysis. Scale bars, 100 μm. C Representative images of proliferating cell nuclear antigen (PCNA) and corresponding quantification analysis. Scale bars, 100 μm. D Representative western blot images of Claudin-1, Occludin and ZO-1 in colonic tissues and corresponding quantification analysis. E Representative images of laser Doppler analysis and corresponding quantification analysis. Scale bar, 2 mm. The values are presented as the mean ± standard error of the mean. * P < 0.05, ** P < 0.01 vs. control <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-021-02201-4'>34980222</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-ott-13-6229-g0002.jpgAnti-PCNA Rabbit Monoclonal AntibodyOverexpression of the CCDC7 gene promoted HeLa cell proliferation in vitro. ( A ) EdU-positive cells. Each bar represents the mean ± SD of three independent experiments. *** p < 0.0001, compared with control group cells. ( B ) HeLa cells were transfected with CCDC7, and cell viability was measured 24 h later using EdU assays. Newly grown HeLa cells were marked by combined Edu and Hoechst 33258 staining. EdU stained cells (red) were observed under a fluorescence microscope (200×), and cells stained with Hoechst 33258 (blue) were counted as a proliferation control (%)( C ) MTT assays were used to determine cell proliferation in HeLa cells transfected with CCDC7. Left, starting cell count of 3000 ( D ) HeLa cells were transfected with CCDC7 for 48 h, and Western blotting was then used to determine the levels of PCNA. Equal amounts of total cellular protein (50 μg) were resolved by 12% SDS-PAGE. β-Actin was used as loading control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7335771/&orig_host=www.ncbi.nlm.nih.gov'>32669853</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-ott-13-6229-g0003.jpgAnti-PCNA Rabbit Monoclonal AntibodyKnockdown of CCDC7 suppressed HeLa cell proliferation in vitro. ( A ) EdU-positive cells. Each bar represents the mean ± SD of three independent experiments. *** p < 0.0001, compared with control group cells. ( B ) At 24 h after transfection with siCCDC7, cell viability was estimated by EdU assay. Newly grown HeLa cells were stained by combined EdU and Hoechst 33258 staining. EdU stained cells (red) were observed under a fluorescence microscope (200×), and cells stained with Hoechst 33258 (blue) were counted as a proliferation control (%) ( C ) MTT assays were used to determine cell proliferation at 24 h after transfection with CCDC7. Left, starting cell count of 3000. ( D ) HeLa cells were transfected with CCDC7 for 48 h, and Western blotting was then used to determine the levels of PCNA. Equal amounts of total cellular protein (50 μg) were resolved by 12% SDS-PAGE. β-Actin was used as loading control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7335771/&orig_host=www.ncbi.nlm.nih.gov'>32669853</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-ott-13-6229-g0007.jpgAnti-PCNA Rabbit Monoclonal Antibody(A) The expression levels of CCDC7, IL-6, and VEGF exhibited similar patterns in tumors from nude mice and in human cervical cancer samples. Immunohistochemical staining of CCDC7, IL-6, and VEGF (brown) in paraffin-embedded sections of nude mice’s tumors. Typical images were taken under a light microscope (magnification 400×). ( B ) Western blotting was used to analyze the expression of CCDC7, IL-6, VEGF, and PCNA in nude mice with HeLa cell-derived tumors. ( C ) Western blotting was used to analyze the expression of CCDC7, IL-6, and VEGF in human clinical cervical cancer samples,left: stage 1; right: stage 3. β-Actin was used as a loading control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7335771/&orig_host=www.ncbi.nlm.nih.gov'>32669853</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-pcna-primary-antibodies-if-testing-3.jpgAnti-PCNA Rabbit Monoclonal Antibody IF analysis of PCNA using anti-PCNA antibody (M00125-1) and anti-Beta Tubulin antibody (M01857-3).<br>
PCNA was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:100 with rabbit anti-PCNA Antibody (M00125-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Dylight550-conjugated Anti- mouse IgG Secondary Antibody (red)(Catalog#BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00125-1-ip7.jpgAnti-PCNA Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dsg1-rabbit-monoclonal-antibody-m02655-1-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02655-1-wb.jpgAnti-DSG1/Desmoglein 1 Rabbit Monoclonal AntibodyWestern blot analysis of DSG1 expression in human skin lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02655-1-dsg1-primary-antibodies-ihc-testing-1.jpgAnti-DSG1/Desmoglein 1 Rabbit Monoclonal AntibodyIHC analysis of DSG1 using anti-DSG1 antibody (M02655-1). <br>DSG1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DSG1 Antibody (M02655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02655-1-dsg1-primary-antibodies-ihc-testing-2.jpgAnti-DSG1/Desmoglein 1 Rabbit Monoclonal AntibodyIHC analysis of DSG1 using anti-DSG1 antibody (M02655-1). <br>DSG1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DSG1 Antibody (M02655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prc1-rabbit-monoclonal-antibody-m00160-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00160-prc1-primary-antibodies-wb-testing-1.jpgAnti-PRC1 Rabbit Monoclonal Antibody Western blot analysis of PRC1 using anti-PRC1 antibody (M00160). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRC1 antigen affinity purified monoclonal antibody (Catalog # M00160) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRC1 at approximately 72 kDa. The expected band size for PRC1 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00160-prc1-primary-antibodies-ihc-testing-2.jpgAnti-PRC1 Rabbit Monoclonal Antibody IHC analysis of PRC1 using anti-PRC1 antibody (M00160). <br>
PRC1 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRC1 Antibody (M00160) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00160-prc1-primary-antibodies-ihc-testing-3.jpgAnti-PRC1 Rabbit Monoclonal Antibody IHC analysis of PRC1 using anti-PRC1 antibody (M00160). <br>
PRC1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRC1 Antibody (M00160) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk2-rabbit-monoclonal-antibody-m00166-boster.html2026-03-24T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-cdk2-primary-antibodies-wb-testing-1.jpg.jpgAnti-CDK2 Rabbit Monoclonal Antibody Western blot analysis of CDK2 using anti-CDK2 antibody (M00166). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat L6 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse C2C12 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK2 antigen affinity purified monoclonal antibody (Catalog # M00166) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDK2 at approximately 30 kDa. The expected band size for CDK2 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00166-CDK2-primary-antibodies-IHC-testing-1.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human beast carcinoma, using CDK2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-ihc7.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-ihc8.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat pancreas, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-ihc9.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human non-Hodgkin's lymphoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-ihc10.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-ihc11.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse testis, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-if.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CDK2 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00166-icc1.jpgAnti-CDK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atf2-rabbit-monoclonal-antibody-m00916-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-atf2-primary-antibodies-wb-testing-1.jpgAnti-ATF2 Rabbit Monoclonal Antibody Western blot analysis of ATF2 using anti-ATF2 antibody (M00916). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human HUVEC whole cell lysates, <br>
Lane 4: human K562 whole cell lysates, <br>
Lane 5: human HEL whole cell lysates, <br>
Lane 6: human SiHa whole cell lysates, <br>
Lane 7: human SH-SY5Y whole cell lysates, <br>
Lane 8: human Caco-2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF2 antigen affinity purified monoclonal antibody (M00916) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF2 at approximately 70 kDa. The expected band size for ATF2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-if.jpgAnti-ATF2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using ATF2 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-atf2-primary-antibodies-ihc-testing-2.jpgAnti-ATF2 Rabbit Monoclonal Antibody IHC analysis of ATF2 using anti-ATF2 antibody (M00916) . <br> ATF2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATF2 Antibody (M00916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-atf2-primary-antibodies-ihc-testing-3.jpgAnti-ATF2 Rabbit Monoclonal Antibody IHC analysis of ATF2 using anti-ATF2 antibody (M00916) . <br> ATF2 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATF2 Antibody (M00916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-atf2-primary-antibodies-ihc-testing-4.jpgAnti-ATF2 Rabbit Monoclonal Antibody IHC analysis of ATF2 using anti-ATF2 antibody (M00916) . <br> ATF2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATF2 Antibody (M00916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00916-atf2-primary-antibodies-ihc-testing-5.jpgAnti-ATF2 Rabbit Monoclonal Antibody IHC analysis of ATF2 using anti-ATF2 antibody (M00916) . <br> ATF2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATF2 Antibody (M00916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek1-rabbit-monoclonal-antibody-m00292-2-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-wb7.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-wb8.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-wb9.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-wb.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyWestern blot analysis of MEK1 expression in (1) A431 cell lysate;(2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-icc1.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-icc2.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-icc3.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-2-icc4.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ccr9-rabbit-monoclonal-antibody-m02348-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02348-ccr9-primary-antibodies-wb-testing-1.jpgAnti-CCR9 Rabbit Monoclonal Antibody Western blot analysis of CCR9 using anti-CCR9 antibody (M02348). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MOLT-4 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR9 antigen affinity purified monoclonal antibody (Catalog # M02348) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCR9 at approximately 42 kDa. The expected band size for CCR9 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02348-icc1.jpgAnti-CCR9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02348-ccr9-primary-antibodies-wb-testing-2.jpgAnti-CCR9 Rabbit Monoclonal AntibodyWestern blot analysis of CCR9 using anti-CCR9 antibody (M02348). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: human PANC-1 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human MOLT-4 whole cell lysates,<br>
Lane 4: human A2780 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR9 antigen affinity purified monoclonal antibody (M02348) at 0.5 ug/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CCR9 at approximately 42 kDa. The expected band size for CCR9 is at 42 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02348-ccr9-primary-antibodies-ihc-testing-1.jpgAnti-CCR9 Rabbit Monoclonal AntibodyIHC analysis of CCR9 using anti-CCR9 antibody (M02348).<br>
CCR9 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with rabbit anti-CCR9 Antibody (M02348) at a dilution of 1:100 overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk1-rabbit-monoclonal-antibody-m00209-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-1-wb.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal AntibodyWestern blot analysis of CDK1 in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chk1-rabbit-monoclonal-antibody-m01060-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01060-1-chk1-primary-antibodies-wb-testing-1.jpgAnti-Chk1 CHEK1 Rabbit Monoclonal Antibody Western blot analysis of Chk1 using anti-Chk1 antibody (M01060-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: mouse thymus tissue lysates,<br>
Lane 7: mouse SP2/0 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Chk1 antigen affinity purified monoclonal antibody (Catalog # M01060-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Chk1 at approximately 54 kDa. The expected band size for Chk1 is at 54 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkn2-rabbit-monoclonal-antibody-m04066-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04066-wb.jpgAnti-PKN2/Prk2 Rabbit Monoclonal AntibodyWestern blot analysis of PKN2 in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erk1-rabbit-monoclonal-antibody-m00104-2-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-2-wb7.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-2-ihc.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using ERK1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-2-wb8.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-2-wb.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyWestern blot analysis of ERK1 in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vegf-rabbit-monoclonal-antibody-m00045-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-1.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-2.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-3.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-4.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-5.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-6.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-7.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-8.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of rat thyroid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-ihc-testing-9.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IHC analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/ml rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-10.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-11.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-12.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-13.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-14.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-1-vegfa-primary-antibodies-if-testing-15.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody IF analysis of VEGFA using anti-VEGFA antibody (M00045-1). <br>
VEGFA was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-VEGFA Antibody (M00045-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/case_study--an_excellent_anti-vegfa_antibody_for_ihc_and_if_00.jpgAnti-VEGF VEGFA Rabbit Monoclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erk1-rabbit-monoclonal-antibody-m00104-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-erk1-primary-antibodies-wb-testing-1.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyWestern blot analysis of ERK1 using anti-ERK1 antibody (M00104). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERK1 antigen affinity purified monoclonal antibody (M00104) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ERK1 at approximately 40 kDa. The expected band size for ERK1 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-erk1-primary-antibodies-ihc-testing-1.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyIHC analysis of ERK1 using anti-ERK1 antibody (M00104). <br>ERK1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ERK1 Antibody (M00104) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-erk1-primary-antibodies-ihc-testing-2.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyIHC analysis of ERK1 using anti-ERK1 antibody (M00104). <br>ERK1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ERK1 Antibody (M00104) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-erk1-primary-antibodies-ihc-testing-3.jpgAnti-ERK1 MAPK3 Rabbit Monoclonal AntibodyIHC analysis of ERK1 using anti-ERK1 antibody (M00104). <br>ERK1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ERK1 Antibody (M00104) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-arg1-rabbit-monoclonal-antibody-m01106-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01106-1-arg1-primary-antibodies-wb-testing-1.jpgAnti-ARG1/Arginase 1 Rabbit Monoclonal Antibody Western blot analysis of ARG1 using anti-ARG1 antibody (M01106-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARG1 antigen affinity purified monoclonal antibody (Catalog # M01106-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARG1 at approximately 36, 38 kDa. The expected band size for ARG1 is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tlr2-rabbit-monoclonal-antibody-m00131-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-tlr2-primary-antibodies-wb-testing-1.jpgAnti-TLR2 Rabbit Monoclonal Antibody Western blot analysis of TLR2 using anti-TLR2 antibody (M00131). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human CACO-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TLR2 antigen affinity purified monoclonal antibody (Catalog # M00131) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TLR2 at approximately 90 kDa. The expected band size for TLR2 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-wb7.jpgAnti-TLR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-jvs-21-e50-g007.jpgAnti-TLR2 Rabbit Monoclonal AntibodyPPV NS1 protein induced the expression of TLR2 during infection. The expression of TLR2 mRNA (A) in 293T cells were tested following pEGFP-N1-NS1 transfection at different time points. Mock- and 4 μg pEGFP-N1-transfected 293T cells were used as the controls. The level of TLR2 protein expression was confirmed following transfection with 4 μg pEGFP-N1-NS1 by western blot (B) and an empty vector control test at the protein level was used to detect the level of TLR2 expression (C). The expression of TLR2 (D) and NF-κB (E) were both inhibited following TLR2 interference. Compared with the control group at the same time, there was a highly significant difference between groups ( ** p < 0.01), or significant difference between groups ( * p < 0.05, Student's t -test). PPV, porcine parvovirus; TLR, toll-like receptor; NF-κB, nuclear factor kappa B.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263913/'>32476323</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-12974_2013_article_936_fig5_html.jpgAnti-TLR2 Rabbit Monoclonal AntibodyThe effect of ischemic postconditioning on TLR2 between 2 hour and 4.5 hour ischemia groups. (A) Representative images of cells with positive immunochemical staining to TLR2, scale bar = 50 μm. (B) Statistics of the number of cells stained with TLR2. (C) Statistics of the transcriptional levels of TLR2. (D) Representative Western blotting images of TLR2. (E) Statistics of the expressional level of TLR2. (F) Representative images under confocal microscope in the sham group. (G) Representative images under confocal microscope in the ischemia group; (n = 4 in each group). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://jneuroinflammation.biomedcentral.com/articles/10.1186/1742-2094-11-15'>24460643</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-wb8.jpgAnti-TLR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eno1-rabbit-monoclonal-antibody-m01250-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01250-eno1-primary-antibodies-wb-testing-1.jpgAnti-ENO1/Alpha Enolase Rabbit Monoclonal Antibody Western blot analysis of ENO1 using anti-ENO1 antibody (M01250). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human Hela whole cell lysates, <br>
Lane 3: human U251 whole cell lysates, <br>
Lane 4: human A549 whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat testis tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse testis tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ENO1 antigen affinity purified monoclonal antibody (M01250) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ENO1 at approximately 47 kDa. The expected band size for ENO1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01250-ihc.jpgAnti-ENO1/Alpha Enolase Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using ENO1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-msh6-rabbit-monoclonal-antibody-m00553-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-wb-testing-1.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyWestern blot analysis of MSH6 using anti-MSH6 antibody (M00553). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat RH35 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSH6 antigen affinity purified monoclonal antibody (M00553) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MSH6 at approximately 160 kDa. The expected band size for MSH6 is at 153 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-1.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-2.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-3.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-4.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-5.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-6.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-7.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-8.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00553-msh6-primary-antibodies-ihc-testing-9.jpgAnti-MSH6/Gtbp Rabbit Monoclonal AntibodyIHC analysis of MSH6 using anti-MSH6 antibody (M00553). <br>MSH6 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MSH6 Antibody (M00553) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdx1-rabbit-monoclonal-antibody-m00491-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00491-pdx1-primary-antibodies-wb-testing-1_1.jpgAnti-PDX1/Ipf1 Rabbit Monoclonal Antibody Western blot analysis of PDX1 using anti-PDX1 antibody (M00491). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates, <br>
Lane 2: human U251 whole cell lysates, <br>
Lane 3: human RT4 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDX1 antigen affinity purified monoclonal antibody (M00491) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDX1 at approximately 42 kDa. The expected band size for PDX1 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00491-ipf1-primary-antibodies-ihc-testing-1.jpgAnti-PDX1/Ipf1 Rabbit Monoclonal AntibodyIHC analysis of PDX1/Ipf1 using anti-PDX1/Ipf1 antibody (M00491). <br>
PDX1/Ipf1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PDX1/Ipf1 Antibody (M00491) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00491-ipf1-primary-antibodies-ihc-testing-2.jpgAnti-PDX1/Ipf1 Rabbit Monoclonal AntibodyIHC analysis of PDX1/Ipf1 using anti-PDX1/Ipf1 antibody (M00491). <br>
PDX1/Ipf1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PDX1/Ipf1 Antibody (M00491) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mlh1-rabbit-monoclonal-antibody-m00126-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00126-mlh1-primary-antibodies-wb-testing-1_1.jpgAnti-MLH1 Rabbit Monoclonal AntibodyWestern blot analysis of MLH1 using anti-MLH1 antibody (M00126). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MLH1 antigen affinity purified monoclonal antibody (M00126) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MLH1 at approximately 85 kDa. The expected band size for MLH1 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00126-mlh1-primary-antibodies-ihc-testing-1.jpgAnti-MLH1 Rabbit Monoclonal AntibodyIHC analysis of MLH1 using anti-MLH1 antibody (M00126). <br>
MLH1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MLH1 Antibody (M00126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00126-mlh1-primary-antibodies-ihc-testing-2.jpgAnti-MLH1 Rabbit Monoclonal AntibodyIHC analysis of MLH1 using anti-MLH1 antibody (M00126). <br>MLH1 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-MLH1 Antibody (M00126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00126-mlh1-primary-antibodies-ihc-testing-3.jpgAnti-MLH1 Rabbit Monoclonal AntibodyIHC analysis of MLH1 using anti-MLH1 antibody (M00126). <br>MLH1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-MLH1 Antibody (M00126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00126-mlh1-primary-antibodies-ihc-testing-4.jpgAnti-MLH1 Rabbit Monoclonal AntibodyIHC analysis of MLH1 using anti-MLH1 antibody (M00126). <br>MLH1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-MLH1 Antibody (M00126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pms2-rabbit-monoclonal-antibody-m01028-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01028-1-pms2-primary-antibodies-wb-testing-1.jpg.jpgAnti-PMS2 Rabbit Monoclonal Antibody Western blot analysis of PMS2 using anti-PMS2 antibody (M01028-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U20S whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-PMS2 antigen affinity purified monoclonal antibody (Catalog # M01028-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PMS2 at approximately 120 kDa. The expected band size for PMS2 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01028-1-pms2-primary-antibodies-wb-testing-2.jpgAnti-PMS2 Rabbit Monoclonal AntibodyWestern blot analysis of PMS2 using anti-PMS2 antibody (M01028-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PMS2 antigen affinity purified monoclonal antibody (M01028-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PMS2 at approximately 120 kDa. The expected band size for PMS2 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01028-1-PMS2-primary-antibodies-IHC-testing-1.jpgAnti-PMS2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using PMS2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01028-1-icc1.jpgAnti-PMS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01028-1-ip7.jpgAnti-PMS2 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd46-rabbit-monoclonal-antibody-m00377-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-1-cd46-primary-antibodies-wb-testing-1.jpgAnti-CD46 Rabbit Monoclonal AntibodyWestern blot analysis of CD46 using anti-CD46 antibody (M00377-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD46 antigen affinity purified monoclonal antibody (M00377-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD46 at approximately 70 kDa. The expected band size for CD46 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-1-cd46-primary-antibodies-ihc-testing-4.jpgAnti-CD46 Rabbit Monoclonal AntibodyIHC analysis of CD46 using anti-CD46 antibody (M00377-1). <br>CD46 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD46 Antibody (M00377-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-1-cd46-primary-antibodies-ihc-testing-5.jpgAnti-CD46 Rabbit Monoclonal AntibodyIHC analysis of CD46 using anti-CD46 antibody (M00377-1). <br>CD46 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD46 Antibody (M00377-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-1-cd46-primary-antibodies-ihc-testing-3.jpgAnti-CD46 Rabbit Monoclonal AntibodyIHC analysis of CD46 using anti-CD46 antibody (M00377-1). <br>CD46 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD46 Antibody (M00377-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-1-cd46-primary-antibodies-ihc-testing-2.jpgAnti-CD46 Rabbit Monoclonal AntibodyIHC analysis of CD46 using anti-CD46 antibody (M00377-1). <br>CD46 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD46 Antibody (M00377-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-snf5-rabbit-monoclonal-antibody-m00500-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00500-wb.jpgAnti-SNF5 SMARCB1 Rabbit Monoclonal AntibodyWestern blot analysis of SNF5 in (1) HeLa cell lysate; (2) K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdx2-rabbit-monoclonal-antibody-m00877-1-boster.html2026-03-24T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-cdx2-primary-antibodies-wb-testing-1.jpgAnti-CDX2 Rabbit Monoclonal Antibody Western blot analysis of CDX2 using anti-CDX2 antibody (M00877-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDX2 antigen affinity purified monoclonal antibody (Catalog # M00877-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDX2 at approximately 37 kDa. The expected band size for CDX2 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-wb10.jpgAnti-CDX2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-cdx2-primary-antibodies-ihc-testing-2.jpgAnti-CDX2 Rabbit Monoclonal Antibody IHC analysis of CDX2 using anti-CDX2 antibody (M00877-1). <br>
CDX2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDX2 Antibody (M00877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-fmicb-11-622354-g003.jpgAnti-CDX2 Rabbit Monoclonal AntibodyThe distribution of Lgr5 + ISCs in the intestinalmucosa and the subcellular localization and relative expression level detection of epithelial function proteins CDX2 and villin in the intestinal mucosa of IBD at 7 days after termination of DSS administration. (A) The Lgr5 + ISCs (brown) in the small intestinal mucosa: (A1) the normal group, the villi and the crypts were arranged compactly, and Lgr5 + ISCs were observed in the crypts; (A2) the DSS group, the villi and the crypts were scattered, with few Lgr5 + ISCs; (A3) the DSS + B. subtilis -fermented milk group, there were more Lgr5 + ISCs in villi and crypts compared with those in the DSS group. (B) The Lgr5 + ISCs (brown) in the colonic mucosa: (B1) the normal group, the glands were arranged compactly, and there were large amounts of Lgr5 + ISCs at the bottom of the glands; (B2) the DSS group: the ulcers were replaced by scars. No Lgr5 + ISCs were observed in the scars; (B3) the DSS + B. subtilis -fermented milk group: the colonic epithelium was integrated, with some regenerated glands. A number of Lgr5 + ISCs were observed at the bottom of the regenerated glands. (C) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the small intestinal mucosa: (C1) the normal group: the villi and the crypts were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the villi and the crypts; (C2) the DSS group: the villi and the crypts were scattered, and few CDX2 + epithelial cells were observed on the surface of the crypt and the villi; (C3) the DSS + B. subtilis -fermented milk group: more villi and crypts were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells covering the villi and crypts. (D) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the colonic mucosa: (D1) the normal group: the colonic glands were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the glands; (D2) the DSS group: the glands were scattered, and few CDX2 + epithelial cells were observed in the scar; (D3) the DSS + B. subtilis -fermented milk group: more colonic glands were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells in the glands. (E) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the small intestinal mucosa: (E1) the normal group, a number of Mucin2 + goblet cells observed in the epithelium; (E2) the DSS group: only few Mucin2 + goblet cells were observed in the remaining villi and crypts; (E3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered mucosa. (F) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the colonic mucosa: (F1) the normal group, large amounts of Mucin2 + goblet cells were observed in the mucosa; (F2) the DSS group: only few Mucin2 + goblet cells were observed in the scars; (F3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered colonic mucosa. (G,H) Western blotting was applied for detection of the relative expression level of Lgr5, CDX2, and Mucin2 in the samples containing equivalent ileum and colon. The expression level of Lgr5, CDX2, and Mucin2 in the DSS group was significantly lower than that of the normal (control) group. The expression level of Lgr5, CDX2, and Mucin2 in the DSS + B. subtilis -fermented milk (FM) group was significantly higher than that of the DSS group ( n = 5, ** represents p < 0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2020.622354/full'>33519783</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-cdx2-primary-antibodies-ihc-testing-3.jpgAnti-CDX2 Rabbit Monoclonal Antibody IHC analysis of CDX2 using anti-CDX2 antibody (M00877-1). <br>
CDX2 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDX2 Antibody (M00877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00877-1-ihc.jpgAnti-CDX2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using CDX2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nrf2-rabbit-monoclonal-antibody-m00078-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00078-wb.jpgAnti-Nrf2 NFE2L2 Rabbit Monoclonal AntibodyWestern blot analysis of Nrf2 expression in 293T cell treated with arsenite.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00078-ihc.jpgAnti-Nrf2 NFE2L2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Nrf2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00078-if.jpgAnti-Nrf2 NFE2L2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Nrf2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd44-rabbit-monoclonal-antibody-m00052-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-1-wb7.jpgAnti-CD44 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-1-wb.jpgAnti-CD44 Rabbit Monoclonal AntibodyWestern blot analysis of CD44 expression in TF-1 cells lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-1-wb8.jpgAnti-CD44 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-1-ihc.jpgAnti-CD44 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human skin, using CD44 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-1-wb9.jpgAnti-CD44 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ship-rabbit-monoclonal-antibody-m03358-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03358-wb.jpgAnti-SHIP INPP5D Rabbit Monoclonal AntibodyWestern blot analysis of SHIP1 expression in Daudi cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03358-ihc.jpgAnti-SHIP INPP5D Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat spleen, using SHIP Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kdel-rabbit-monoclonal-antibody-m07617-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07617-1-wb.jpgAnti-KDEL Rabbit Monoclonal AntibodyWestern blot analysis of KDEL expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07617-1-ihc.jpgAnti-KDEL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using KDEL Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd20-rabbit-monoclonal-antibody-m03780-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-1-wb7.jpgAnti-CD20 MS4A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-1-ihc.jpgAnti-CD20 MS4A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using CD20 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-1-wb8.jpgAnti-CD20 MS4A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-1-wb.jpgAnti-CD20 MS4A1 Rabbit Monoclonal AntibodyWestern blot analysis of CD20 expression in Raji cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-iap2-rabbit-monoclonal-antibody-m01562-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01562-wb.jpgAnti-IAP2 BIRC3 Rabbit Monoclonal AntibodyWestern blot analysis of IAP2 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kap1-rabbit-monoclonal-antibody-m00409-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00409-wb.jpgAnti-KAP1 TRIM28 Rabbit Monoclonal AntibodyWestern blot analysis of KAP1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk1-rabbit-monoclonal-antibody-m00209-2-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-wb-testing-1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody Western blot analysis of CDK1 using anti-CDK1 antibody (M00209-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK1 antigen affinity purified monoclonal antibody (Catalog # M00209-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDK1 at approximately 30 kDa. The expected band size for CDK1 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-ihc-testing-2_1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IHC analysis of CDK1 using anti-CDK1 antibody (M00209-2). <br>
CDK1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDK1 Antibody (M00209-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-ihc-testing-3_1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IHC analysis of CDK1 using anti-CDK1 antibody (M00209-2). <br>
CDK1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDK1 Antibody (M00209-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-ihc-testing-4_1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IHC analysis of CDK1 using anti-CDK1 antibody (M00209-2). <br>
CDK1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDK1 Antibody (M00209-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-ihc-testing-5_1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IHC analysis of CDK1 using anti-CDK1 antibody (M00209-2). <br>
CDK1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDK1 Antibody (M00209-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-2-cdk1-primary-antibodies-if-testing-6.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IF analysis of CDK1 using anti-CDK1 antibody (M00209-2) and anti-Beta Tubulin antibody (M01857-3).<br>
CDK1 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-CDK1 Antibody (M00209-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk1-rabbit-monoclonal-antibody-m00209-3-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-3-wb7.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-3-wb.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal AntibodyWestern blot analysis of CDK1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp3-rabbit-monoclonal-antibody-m00775-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-mmp3-primary-antibodies-wb-testing-1.jpgAnti-MMP3 Rabbit Monoclonal AntibodyWestern blot analysis of MMP3 using anti-MMP3 antibody (M00775). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat PC-12 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP3 antigen affinity purified monoclonal antibody (M00775) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MMP3 at approximately 50 kDa. The expected band size for MMP3 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-if.jpgAnti-MMP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using MMP3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-fphar-15-1435274-g003.jpgAnti-MMP3 Rabbit Monoclonal AntibodyEffects of MOIG on adhesion, migration, invasion and the expression of associated proteins of TNF-α-stimulated FLSs cells. (A) Adhesion of FLSs cells. (B) and (C) The wound healing of FLSs at 24 and 48 h; (D) and (F) The migration of FLSs at 6 h; (E) and (G) The invasion of FLSs at 24 h; ( H–M ) the expression of ICAM-1, VCAM-1, cadherin 11, MMP2 and MMP3 of FLSs. The data were expressed as mean ± SD (n = 3). # p < 0.05, ## p < 0.01, ### p < 0.001 vs. normal ctrl group; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. TNF-α model group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1435274/full'>39444614</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12964_2024_1744_fig2_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyZBP1 is essential for chondrocyte damage. Chondrocytes were transfected with siNC or ZBP1 siRNA for 24 h following TNF-α induction for 24 h. (A, B) Western blots and quantitative analysis of ZBP1, MMP13, and MMP3 expression levels ( n = 3). (C, D) Western blots and quantitative analysis of SOX9 expression levels. (E, F) Western blot and quantitative analysis of iNOS expression levels ( n = 3). (G) qPCR results showing the relative expression levels of Zbp1 and Inos ( n = 3). (H-K) Immunofluorescence staining and fluorescence intensity analysis of the relative expression levels of COL2A1 and MMP13 ( n = 3; scale bar: 50 μm). Chondrocytes were transfected with siNC or ZBP1 siRNA following TSZ (20 ng/ml TNF-α, 100 nM Smac mimetic, and 20 mM Z-VAD) induction for 12 h. (L, M) Western blots and quantitative analysis of ZBP1, P-RIPK3, and P-MLKL expression levels ( n = 3). The data are shown as the means ± SDs. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01744-1'>39026271</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12964_2024_1744_fig5_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyZBP1 overexpression depends on IRF1. Chondrocytes were transfected with siNC or IRF1 siRNA for 24 h following TNF-α induction for 12 h. (A) Prediction of transcription factors using the UCSC Genome Browser database, SPP-ominer database, and Cistrome Data Browser. (B) qPCR results showing the relative mRNA expression levels of Irf1 and Zbp1 ( n = 3). (C, D) Western blots and quantitative analysis of the relative protein expression level of IRF1 ( n = 3). (E, F) Immunofluorescence staining and fluorescence intensity analysis of ZBP1 expression in chondrocytes transfected with siNC or IRF1 siRNA following TNF-α induction for 12 h ( n = 3; scale bar: 50 μm). (G-L) Western blots and quantitative analysis of the relative protein expression levels of iNOS, COX2, MMP3, MMP13, AGGRECAN, COL2A1, and SOX9 ( n = 3). (M-P) Immunofluorescence staining and fluorescence intensity analysis of COL2A1 and MMP13 expression in chondrocytes transfected with siNC or IRF1 siRNA following TNF-α induction for 12 h ( n = 3; scale bar: 50 μm). Chondrocytes were transfected with negative control siRNA(siNC) or IRF1 siRNA (si- Irf1 ) or ZBP1-plasmid (OE- Zbp1 ) or empty plasmid (OE-NC) for 24 h following TNF-α induction for 24 h. (Q-V) Western blots and quantitative analysis of the relative protein expression of AGGRECAN, COL2A1, SOX9, iNOS, COX2 MMP13, and MMP3 in chondrocytes ( n = 3). The data are shown as the means ± SDs. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01744-1'>39026271</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12964_2024_1744_fig7_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyThe effect of mtDNA on IRF1 and chondrocyte damage. Chondrocytes were treated with TNF-α alone or CsA alone or TNF-α combined with CsA for 12 h. (A, B) Western blots and quantitative analysis of expression level of IRF1 ( n = 3). (C, D) immunofluorescence staining and fluorescence intensity analysis of IRF1 nuclear location ( n = 3). (E, F) Western blots and quantitative analysis of expression level of iNOS, MMP13, and MMP3 ( n = 3). Data are shown as the means ± SDs. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01744-1'>39026271</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12967_2024_5086_fig3_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyYAP exacerbated chondrocyte damage induced by IL-1β. Chondrocytes transfected with si-NC or YAP siRNA following IL-1β induction for 24 h. A qPCR of MMP3, MMP13 and ADAMTS5 relative expression level. B Western blot and quantitative analysis of COL2A1, MMP3, ADAMTS5 and MMP13 expression level. C , D Western blot and quantitative analysis of COX2, iNOS, P62 and LC3 expression level. E , F Immunofluorescence staining and fluorescence intensity analysis of COL2A1 and MMP13 relative expression level. G , H Chondrocytes were transfected with si-NC or si-YAP and then transfected with mRFP-GFP-LC3 adenovirus following IL-1β treatment for 24 h. The representative images of fluorescence and quantitative analysis of red dots and yellow dots were shown (scale bar: 10 μm). Subsequently, Chondrocytes transfected with oe-NC or oe-YAP following IL-1β induction for 24 h. I Western blot and quantitative analysis of COL2A1, MMP3, ADAMTS5 and MMP13 expression level. J , K Western blot and quantitative analysis of COX2, iNOS, Beclin-1 and P62 expression level. L – O Immunofluorescence staining and fluorescence intensity analysis of COL2A1 and MMP13 relative expression level. Data are shown as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-024-05086-x'>38493143</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12967_2024_5086_fig6_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyLIPUS inhibits the progression of OA. A , B Western blot and quantitative analysis of MMP13, ADAMTS5 and COX2 expression level with LIPUS application for 20 min. C , D Western blot and quantitative analysis of P62, ATG5 and LC3 expression level with LIPUS application for 20 min. E , F Western blot and quantitative analysis of ACAN, COL2A1, SOX9 and COX2 expression level with 30 mW/cm 2 LIPUS application. G Western blot and quantitative analysis of ATG5 expression level with 30 mW/cm 2 LIPUS application. H qPCR of MMP3, ADAMTS5 and MMP13 relative expression level. Data are shown as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-024-05086-x'>38493143</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12967_2024_5086_fig7_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyLIPUS inhibits the progression of OA via YAP/RIPK1 axis. A Western blot and quantitative analysis of ACAN COL2A1, SOX9 and MMP3 expression level. B Western blot and quantitative analysis of COX2 and iNOS expression level. C Western blot of P-YAP and P-P65 expression level. D , E Immunofluorescence staining and fluorescence intensity analysis of COL2A1 and MMP13 relative expression level. F Chondrocytes were transfected with mRFP-GFP-LC3 adenovirus following IL-1β treatment for 24 h. The representative images of fluorescence and quantitative analysis of red dots and yellow dots were revealed (scale bar: 10 μm). G Western blot of P-YAP, YAP, P-P65, P65, P-IκB, IκB, P-RIPK1 and RIPK1 relative protein expression. H Images of IF staining for P65 relative expression and the distribution in chondrocytes with IL-1β induction for 15 min (scale bar: 25 μm). I Co-IP experiment of the binding between YAP and RIPK1 after LIPUS intervention. J YAP and RIPK1 colocalization in chondrocytes were detected by IF after LIPUS intervention (scale bar: 10 μm). K , L Immunohistochemistry staining to show the P-YAP-positive cell, P-RIPK1-positive cell and P-P65-positive cell in cartilage of the six groups (scale bar: 100 μm). Data are shown as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-024-05086-x'>38493143</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12951_2023_2050_fig1_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyLRRK2-IN-1 suppresses the IL-1β-induced inflammation and catabolism and induces anabolism without causing the inhibition of chondrocyte viability. A Schematic diagram of cell treatment and experimental procedures. B Cell viability assessed by CCK8 assay. No obvious inhibition of chondrocyte proliferation was observed when treated with 0.5, 1.0, 2.5, and 5.0 µM LRRK2-IN-1 for 24 h. Data represent mean ± SD; N = 6/group; one-way ANOVA; ns, not significant. C Western blot analyses of the protein levels of anabolic, catabolic, inflammatory factors in the IL-1β-induced chondrocytes treated with 0.5, 1.0, 2.5, and 5.0 µM LRRK2-IN-1 for 24 h. LRRK2-IN-1 suppressed MMP3, MMP13, iNOS, and COX2 and induced COL2 and SOX9 in a dose-dependent manner. D Quantitative analyses of the western blot results. Data represent mean ± SD; N = 3/group; *P < 0.05; **P < 0.01 by one-way ANOVA. E Immunofluorescence of iNOS, MMP13, and aggrecan expression in the IL-1β-induced chondrocytes treated with 5.0 µM LRRK2-IN-1 for 24 h. Scar bar: 400 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-023-02050-7'>37605203</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-12951_2023_2050_fig3_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyW-Exo-L@GelMA exhibits a strong chondrocyte-targeting effect and a pronounced action on promoting anabolism and suppressing catabolism and inflammation without causing the inhibition of chondrocyte viability. A Cell viability assessed by CCK8 assay. No obvious cytotoxicity on chondrocytes was observed when treated with W-Exo-L@GelMA loaded with 0.5, 1.0, 2.5, and 5.0 µM LRRK2-IN-1 for 48 h. Data represent mean ± SD; N = 6/group; one-way ANOVA; ns, not significant. B Immunofluorescence of Dil-labeled exosomes. The uptake of exosomes was observed in the chondrocytes when treated with Exo-L, Exo-L@GelMA or W-Exo-L@GelMA for 48 h. Dil was used for labeling exosomes (red), DAPI to label nuclei (blue), and Phalloidin to label the cytoskeleton (green). Scar bar: 200 μm. C Western blot analyses of the protein levels of anabolic, catabolic, and inflammatory factors in the IL-1β-induced chondrocytes treated with W-Exo-L@GelMA loaded with 0.5, 1.0, 2.5, and 5.0 µM LRRK2-IN-1 for 48 h. W-Exo-L@GelMA promoted COL2 and SOX9 and inhibited iNOS, COX2, MMP3, and MMP13 protein levels in a dose-dependent manner. D Quantitative analysis of the western blot results. Data represent mean ± SD; N = 3/group; *P < 0.05; **P < 0.01 by one-way ANOVA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-023-02050-7'>37605203</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-gr3.jpgAnti-MMP3 Rabbit Monoclonal AntibodyMitoQ alleviated the ECM degradation and inflammatory response in chondrocytes (A and B) iNOS protein expression. (C, D, and E) The levels of MMP3, MMP13, COL2A1, and SOX9 were detected by western blot and qRT-PCR. (F) GPX4 expression was observed by immunofluorescence (scale bar: 100 μm). (G and H) EdU staining on chondrocytes exposed to IL-1β and MitoQ (scale bar: 200 μm). ∗p < 0.05 vs. the control group, ∗∗p < 0.01 vs. the control group, #p < 0.05 vs. the IL-1β treated group, ##p < 0.01 vs. the IL-1β treated group, Data are represented as mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10483061/&orig_host=www.ncbi.nlm.nih.gov'>37694150</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-gr5.jpgAnti-MMP3 Rabbit Monoclonal AntibodyNRF2 antioxidant pathway mediated the protection of MitoQ on chondrocytes After silencing NRF2, chondrocytes were exposed to IL-1β and MitoQ for 24 h. (A and B) The chondrocytes whole-cell lysates together with nuclear lysates were prepared for western blot. The levels of NRF2, HO-1, and NQO1. (C and D) The levels of iNOS, COX2, MMP13, and MMP3. (E and F) The GPX4 expression. (G and H) The levels of Parkin and PINK1. ∗p < 0.05 vs. the IL-1β + negative control group, ∗∗p < 0.01 vs. the IL-1β + negative control group, #p < 0.05 vs. the IL-1β + MitoQ + negative control group, ##p < 0.01 vs. the IL-1β + MitoQ + negative control group, Data are represented as mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10483061/&orig_host=www.ncbi.nlm.nih.gov'>37694150</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-gr6.jpgAnti-MMP3 Rabbit Monoclonal AntibodyParkin regulated the expression of the NRF2 antioxidant pathway through negative feedback After Parkin knockdown, chondrocytes were exposed to IL-1β and MitoQ for 24 h. (A) The level of Parkin. (B and C) The levels of Parkin and PINK1. (D and E) The protein levels of iNOS, MMP3, and COL2A1. (F) The mRNA level of Col2a1. (G and H) The GPX4 level was measured by western blot and qRT-PCR. (I and J) The protein levels of NRF2, HO-1, and NQO1, and the mRNA level of Nrf2. (K and L) The levels of NRF2, HO-1, and NQO1 treated by MitoQ with negative control or si-Parkin. (M and N) The expression of iNOS, MMP13, and COL2A1. ∗p < 0.05 vs. the IL-1β + negative control group, ∗∗p < 0.01 vs. the IL-1β + negative control group, #p < 0.05 vs. the IL-1β + negative control or IL-1β + MitoQ + negative control group, ##p < 0.01 vs. the IL-1β + negative control or IL-1β + MitoQ + negative control group, Data are represented as mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10483061/&orig_host=www.ncbi.nlm.nih.gov'>37694150</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-41420_2023_1406_fig3_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyThe role of TRADD in TNF-α-mediated cellular events. The cells were transfected with siRNA and lipofectamine 3000 for 48 h. After 48 h transfection, the medium was replaced by refresh medium and chondrocytes were treated with TNF-α (5 ng/ml) for 24 h, the protein expression of TRADD, iNOS, COX2, COL2A1, MMP13, cleaved-caspase-3, and LC3 was examined ( A – C , E , F ). After 48 h transfection with siRNA and lipofectamine 3000, the medium was replaced by refresh medium and chondrocytes were pre-treated with z-VAD for 2 h and then exposed to TNF-α for 24 h, the phosphorylation of RIPK1, RIPK3, and MLKL as well as protein expression of these three markers were detected using western blot ( G ). I , K The protein expression of iNOS, COX2, COL2A1, and MMP3 was examined in chondrocytes overexpressing TRADD after TNF-α intervention. D , H , J , L Semi-quantitative analysis of protein bands by image J and data in figures were expressed as means ± SD. * p < 0.05, ** p < 0.01. NS not significant,. NC negative control. z-VAD, Z-VAD-FMK. C-caspase-3, cleaved-caspase-3. M The graphical scheme summarized the findings of the role of TRADD in TNF-α-mediated chondrocytes events. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-023-01406-0'>37002200</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-41420_2023_1406_fig7_html.pngAnti-MMP3 Rabbit Monoclonal AntibodyICCB-19 protects against TNF-α-induced detrimental events via autophagy mechanism. After a pre-treatment of ICCB-19 for 2 h, chondrocytes were stimulated by TNF-α for 24 h. A the protein expression of ATG5 and LC3 was examined. B The semi-quantitative analysis of protein bands by image J. C Representative images of immunofluorescence staining of LC3 in chondrocytes, scale bar: 50 μm. D – F After a pre-treatment of ICCB-19 and 3-MA for 2 h, chondrocytes were stimulated by TNF-α for 24 h with or without z-VAD, the protein expression of iNOS, COX2, COL2A1, MMP13, MMP3, C-caspase-9, and C-caspase-3 were examined, and the phosphorylation of RIPK1, RIPK3, and MLKL as well as protein expression of these three markers were detected by western blot. G – H After a pre-treatment of Rapa for 2 h, chondrocytes were stimulated by TNF-α for 24 h with or without z-VAD, the protein expression of iNOS, COX2, MMP13, C-caspase-3 and the phosphorylation of RIPK1, RIPK3, and MLKL as well as protein expression of these three markers were detected by western blot. I The graphical scheme summarized the findings of protective role of ICCB-19 in TNF-α-caused detrimental events. Data are expressed as means ± SD. * p < 0.05, ** p < 0.01. z-VAD, Z-VAD-FMK. C-caspase-9, cleaved-caspase-9. C-caspase-3, cleaved-caspase-3. P-, Phosphorylated-. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-023-01406-0'>37002200</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00775-ihc.jpgAnti-MMP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using MMP3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp2-rabbit-monoclonal-antibody-m00286-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00286-1-mmp2-primary-antibodies-wb-testing-1.jpgAnti-MMP2 Rabbit Monoclonal Antibody Western blot analysis of MMP2 using anti-MMP2 antibody (M00286-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP2 antigen affinity purified monoclonal antibody (Catalog # M00286-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP2 at approximately 95 kDa. The expected band size for MMP2 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00286-1-mmp2-primary-antibodies-ihc-testing-1.jpgAnti-MMP2 Rabbit Monoclonal AntibodyIHC analysis of MMP2 using anti-MMP2 antibody (M00286-1). <br>MMP2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP2 Antibody (M00286-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bmp4-rabbit-monoclonal-antibody-m00321-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00321-bmp4-primary-antibodies-wb-testing-1.jpgAnti-BMP4 Rabbit Monoclonal Antibody Western blot analysis of BMP4 using anti-BMP4 antibody (M00321). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human COLO320 whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMP4 antigen affinity purified monoclonal antibody (Catalog # M00321) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BMP4 at approximately 47 kDa. The expected band size for BMP4 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00321-BMP4-primary-antibodies-IHC-testing-1.jpgAnti-BMP4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using BMP4 Antibody(M00321)<br>BMP4 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-BMP4 Antibody (M00321)overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-psma-rabbit-monoclonal-antibody-m02846-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-icc1.jpgAnti-PSMA FOLH1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-ihc.jpgAnti-PSMA FOLH1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate carcinoma, using PSMA Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-icc2.jpgAnti-PSMA FOLH1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-wb.jpgAnti-PSMA FOLH1 Rabbit Monoclonal AntibodyWestern blot analysis of PSMA expression in LnCaP cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd34-rabbit-monoclonal-antibody-m00885-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-1-cd34-primary-antibodies-ihc-testing-1.jpgAnti-CD34 Rabbit Monoclonal Antibody IHC analysis of CD34 using anti-CD34 antibody (M00885-1). <br>
CD34 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD34 Antibody (M00885-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-1-wb.jpgAnti-CD34 Rabbit Monoclonal AntibodyWestern blot analysis of CD34 in expression NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-1-cd34-primary-antibodies-ihc-testing-2.jpgAnti-CD34 Rabbit Monoclonal Antibody IHC analysis of CD34 using anti-CD34 antibody (M00885-1). <br>
CD34 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD34 Antibody (M00885-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-1-if.jpgAnti-CD34 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HUVEC cells, using CD34 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mcl1-rabbit-monoclonal-antibody-m00712-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00712-mcl1-primary-antibodies-wb-testing-1.jpgAnti-MCL1 Rabbit Monoclonal Antibody Western blot analysis of MCL1 using anti-MCL1 antibody (M00712). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCL1 antigen affinity purified monoclonal antibody (Catalog # M00712) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MCL1 at approximately 37 kDa. The expected band size for MCL1 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00712-ihc8.jpgAnti-MCL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00712-ihc7.jpgAnti-MCL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00712-ihc.jpgAnti-MCL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using MCL1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00712-icc1.jpgAnti-MCL1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mcm2-rabbit-monoclonal-antibody-m00374-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-wb-testing-1.jpgAnti-MCM2 Rabbit Monoclonal AntibodyWestern blot analysis of MCM2 using anti-MCM2 antibody (M00374). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse thymus tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCM2 antigen affinity purified monoclonal antibody (M00374) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MCM2 at approximately 125 kDa. The expected band size for MCM2 is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-12.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-13.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-10.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-11.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-9.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-6.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-7.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-4.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-5.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-3.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-2.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-14.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00374-mcm2-primary-antibodies-ihc-testing-8.jpgAnti-MCM2 Rabbit Monoclonal AntibodyIHC analysis of MCM2 using anti-MCM2 antibody (M00374). <br>MCM2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MCM2 Antibody (M00374) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp9-rabbit-monoclonal-antibody-m00139-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-wb.jpgAnti-MMP9 Rabbit Monoclonal AntibodyWestern blot analysis of MMP9 expression in (1)Rat kidney tissue lysate;(2)Rat lung tissue lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-mmp9-primary-antibodies-ihc-testing-1.jpgAnti-MMP9 Rabbit Monoclonal AntibodyIHC analysis of MMP9 using anti-MMP9 antibody (M00139). <br>MMP9 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP9 Antibody (M00139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-fphar-16-1682504-g005.jpgAnti-MMP9 Rabbit Monoclonal AntibodyNti-inflammatory activity of PE against LPS-Induced M1 polarization in RAW264.7 macrophages. (A) Assessment of RAW264.7 cell viability after PE treatment; (B) Determination of the half-inhibitory concentration of PE on RAW264.7 cells (>200 μM) (n = 6); (C) Changes in cell morphology of RAW264.7 cells stimulated with LPS and treated with PE at concentrations of 8, 16, and 32 μM; (D) Measurement of fluorescence intensity of CD86 and INOS in RAW264.7 cells via immunofluorescence staining; (E,F) Quantification of fluorescence intensity from images (D) ; (G–K) Analysis of gene expression of INOS, IL-6, TNF-α, TGF-β, and MMP3 in RAW264.7 cells after modeling and PE treatment by RT-PCR; (L) Evaluation of protein expression of TNF-α, IL-6, MMP1, MMP9, and MMP13 in RAW264.7 cells after modeling and PE treatment; (M) Densitometric analysis of the protein expression shown in image (L) . Data are the mean ± SD of 3 independent experiments. # P < 0.05, ## P < 0.01, vs. Ctrl group; * P < 0.05, ** P < 0.01, vs. LPS group; ns, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1682504/full'>41230092</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-mmp9-primary-antibodies-ihc-testing-2.jpgAnti-MMP9 Rabbit Monoclonal AntibodyIHC analysis of MMP9 using anti-MMP9 antibody (M00139). <br>MMP9 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP9 Antibody (M00139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-if.jpgAnti-MMP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of U87-MG cells, using MMP9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-cimb-46-00840-g003.jpgAnti-MMP9 Rabbit Monoclonal AntibodyKnockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11727511/'>39727968</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-12929_2024_1040_fig3_html.pngAnti-MMP9 Rabbit Monoclonal AntibodyPDGFRB somatic mutation induce phenotypic modulation in SMCs. Immunostaining reveals the expression levels of smooth muscle markers (a-SMA and SM22a) and inflammatory markers (VCAM1, ICAM1, MMP1 and MMP9) in HBVSMCs transfected with different viruses (Control: vector; Wild Type: PDGFRB; Y562D: PDGFRB Y562D ) ( a ). The relative density of immunoblot bands about markers shown in ( A ) were display ( B ) (normalized to those in cells transfected with vector viruses). RT-qPCR ( C ) of SMCs markers (α-SMA and SM22α) and inflammatory markers (VCAM-1, ICAM1, MMP-9 and MMP-1) in HBVSMCs underwent different treatments. Student's t-test and Benjamini–Hochberg correction are employed to assess the statistical significance. Edu assay exhibit the proliferation ability of HBVSMCs under different treatment conditions ( D ). Statistical analysis of the proportion of Edu-positive cells in the different groups from 5 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is used for statistical differences ( E ). Scratch assay displays migratory ability of HBVSMCs underwent different treatment ( F ). Statistical analysis of the rate of wound healing (reduced area at 4H /area at 0H) in the different groups from 9 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is utilized to evaluate the statistical significance. * p adj < 0.05, ** p adj < 0.01, *** p adj < 0.001, **** p adj < 0.0001 ( G ). The above experiments are all repeated three times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-12929_2024_1040_fig1_html.pngAnti-MMP9 Rabbit Monoclonal AntibodySingle-cell transcriptional profiling of intracranial fusiform aneurysmal cells ( A - K ) and multi-color immunofluorescence (mIF) of smooth muscle cells (SMCs) markers and inflammatory markers between intracranial fusiform aneurysms (IFAs) and normal cerebral arteries (NCAs) ( L - M ). T-SNE visualization of intracranial fusiform aneurysmal cells type. Colored according to cell type ( A ). Visualization of specific gene expression patterns related to cell subsets identified in ( A ) using a bubble plot ( B ). T-SNE visualization of VSMC cell clusters. Colored according to clusters ( C ). Visualization of structural protein and inflammation-related genes expression patterns within the subsets of smooth muscle cells identified in ( C ) using a bubble plot ( D ). The violin plots show the expression differences of structural protein genes and inflammatory genes between the contraction subgroup (VSMC5) and the inflammatory subgroup (VSMC6) ( E ). The volcano plot specifically shows the gene expression differences between the two cell groups ( F ). The petal plot displays the GO enrichment analysis results of differential genes between the VSMC5 and VSMC6 ( G ). The bar graph shows the KEGG enrichment analysis results of differential genes between these two cell subsets ( H ). The GSEA enrichment analysis results of differential genes between the two groups. The enrichment results of differential genes related to signaling pathways ( I ). The enrichment results of differential genes related to structural protein genes ( J ). The enrichment results of differential genes related to the process of inflammatory factor secretion ( K ). α-SMA (green, SMCs marker), MMP-9 (blue, inflammatory marker) and ICAM-1 (red, inflammatory marker) in FIAs and NCAs are detected using mIF. Scale bar, 100 μm ( L ). Statistical analysis of mean fluorescence intensity about SMCs marker (α-SMA) and inflammatory markers (ICAM-1 and MMP-9) between NCAs ( n = 4) and FIAs ( n = 5). 'n' represented the number of samples. Three random fields were selected for statistical analysis in each sample, and the average value represented the detection value of this marker in this sample. The Student's t-test is utilized to examine the statistical differences among each marker. ns, no significant; ** p < 0.01, *** p < 0.01 (M). n values indicate number of independent experiments performed <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax2-rabbit-monoclonal-antibody-m01288-1-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01288-1-wb.jpgAnti-Pax2 Rabbit Monoclonal AntibodyWestern blot analysis of Pax2 expression in Human fetal kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01288-1-ihc.jpgAnti-Pax2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon using Pax2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lrp1-rabbit-monoclonal-antibody-m00829-boster.html2026-04-03T05:00:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00829-LRP1-primary-antibodies-WB-testing-1.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyWestern blot analysis of LRP1 expression in A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-lrp1-primary-antibodies-wb-testing-1.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyWestern blot analysis of LRP1/Lrp 1 Cluster Ii using anti-LRP1/Lrp 1 Cluster Ii antibody (M00829). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U87 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat heart muscle tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRP1/Lrp 1 Cluster Ii antigen affinity purified monoclonal antibody (M00829) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LRP1/Lrp 1 Cluster Ii at approximately 85 kDa. The expected band size for LRP1/Lrp 1 Cluster Ii is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-fcell-11-1224827-g004.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyMembrane-receptor LRP1 is responsible for the stimulatory effect of CD44s-tPA on lamellipodia formation (A) The distribution patterns of cortactin (red) and F-actin (green) demonstrated by immunofluorescence staining in control and LRP1 inhibitor (RAP, 200 nM), Annexin A2 inhibitor (LCKLSL, 2.5 µM), and EGFR inhibitor (AG1478, 10 µM) pretreated CD44s-overexpressing MCF7 cells. The elongated lamellipodia are highlighted by the arrows. The proportion of cells with lamellipodia in control and RAP, LCKLSL, and AG1478 pretreated groups were calculated from triplicate independent experiments, means ± SD from triplicate experiments were plotted. (B) Representative images and quantitative analysis of migration assay showing the wound closure rate of control and RAP pretreated MCF7 CD44s cells. The means ± SD of wound closure rates from triplicate experiments were plotted. (C) Analysis of LRP1 expression in control and LRP1 knockdown MCF7CD44s cells. (D) Representative images and quantitative analysis of migration assay showing the wound closure rate of control and LRP1 knockdown MCF7 CD44s cells. The means ± SD of wound closure rates from triplicate experiments were plotted. (E) Representative images and quantitative analysis of migration assay showing the wound closure rate of control and LRP1 knockdown MCF7 CD44s cells. The means ± SD of wound closure rates from triplicate experiments were plotted. n. s. Indicates no significant, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10569302/&orig_host=www.ncbi.nlm.nih.gov'>37842093</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-fcell-11-1224827-g005.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodytPA/LRP1 axis enhances the lamellipodia formation through NFκB signaling pathway. (A) Gene set enrichment analysis (GSEA) enrichment plots of the hallmark of NFκB gene sets in MCF7 CD44s compared with MCF7 vector groups. (B) Analysis of phosphorylation of p65, total p65 protein levels in MCF7 vector , MCF7 CD44s , and LRP1 knockdown MCF7 CD44s cells by western blot. (C) Analysis of phosphorylation of p65, total p65 protein levels in control and RAP pretreated MCF7 CD44s cells by western blot. (D) Analysis of phosphorylation of p65, total p65 protein levels in control and NFκB pathway inhibitor (BAY 11-7082, 10 µM) pretreated MCF7 CD44s cells by western blot. (E) The distribution patterns of cortactin (red) and F-actin (green) demonstrated by immunofluorescence staining in control and BAY 11-7082 pretreated CD44s-overexpressing MCF7 cells. The elongated lamellipodia are highlighted by the arrows. The proportion of cells with lamellipodia in control and BAY 11-7082 pretreated groups were calculated from triplicate independent experiments, means ± SD from triplicate experiments were plotted. (F) Representative images and quantitative analysis of migration assay showing the wound closure rate of control and BAY 11-7082 pretreated MCF7 CD44s cells. The means ± SD of wound closure rates from triplicate experiments were plotted. * p < 0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10569302/&orig_host=www.ncbi.nlm.nih.gov'>37842093</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-wb7.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-ihc.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver carcinoma, using LRP1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-ihc7.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-ihc8.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-ihc9.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-icc1.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00829-lrp1-primary-antibodies-fcm-testing-3.jpg.jpgAnti-LRP1/Lrp 1 Cluster Ii Rabbit Monoclonal AntibodyFlow cytometric analysis of LRP1 was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (1/50) (blue). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; red).
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-otx1-rabbit-monoclonal-antibody-m05601-boster.html2026-03-24T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05601-otx1-primary-antibodies-wb-testing-1.jpgAnti-Otx1 Rabbit Monoclonal Antibody Western blot analysis of Otx1 using anti-Otx1 antibody (M05601). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2:mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Otx1 antigen affinity purified monoclonal antibody (Catalog # M05601) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Otx1 at approximately 37 kDa. The expected band size for Otx1 is at 37 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-raf1-rabbit-monoclonal-antibody-m00446-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-1-raf1-primary-antibodies-wb-testing-1.jpgAnti-Raf1 Rabbit Monoclonal Antibody Western blot analysis of Raf1 using anti-Raf1 antibody (M00446-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Raf1 antigen affinity purified monoclonal antibody (Catalog # M00446-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Raf1 at approximately 73 kDa. The expected band size for Raf1 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-1-raf1-primary-antibodies-icc-testing-1.jpgAnti-Raf1 Rabbit Monoclonal AntibodyICC/IF analysis of Raf1 using anti-Raf1 antibody (M00446-1). <br>
Raf1 was detected in an immunocytochemical section of human HEK293T cells. The cells were fixed with 4% paraformaldehyde for 10 minutes and then treated with a membrane permeabilization agent (AR0205) for 5 minutes.The cells were blocked with 10% goat serum. And then incubated with rabbit anti-Raf1 Antibody (M00446-1) at a dilution of 1:50 overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bdnf-rabbit-monoclonal-antibody-m00035-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-wb7.jpgAnti-BDNF Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-wb.jpgAnti-BDNF Rabbit Monoclonal AntibodyWestern blot analysis of extracts of Human cerebellum lysate, using BDNF antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-41398_2023_2647_fig2_html.pngAnti-BDNF Rabbit Monoclonal AntibodyFTO mediated the BDNF-TrkB pathway in NOR memory reconsolidation. A Schematic of the experimental design for NOR memory RA and sampling. B Representative BDNF blots of each group. C Quantitative analysis of BDNF expression in WB. N = 3. *** P = 0.0004, ** P = 0.0036. D Schematic of the experimental design for the effects of ANA-12, a TrkB antagonist, administered immediately after RA on NOR memory performance. E Total exploration times in Test 1 and Test 2. F DI of each group in Test 1 and Test 2. ** P = 0.0013, *** P = 0.0006. G Distance of travelled during the tests. H Schematic of the experimental design for the effects of 7,8-dihydroxyflavone (7,8-DHF), a TrkB agonist, on MA mediated disruption of NOR memory reconsolidation. I Total exploration times in Test 1 and Test 2. J DI of each group in Test 1 and Test 2. * P = 0.0287, DI of vehicle + MA group between Test 1 and Test 2; * P = 0.0216, DI between vehicle + MA group and vehicle + 7,8-DHF group in Test 2. K Distance of travelled during the tests. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41398-023-02647-4'>37963912</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-41398_2023_2647_fig3_html.pngAnti-BDNF Rabbit Monoclonal AntibodyThe m6A-dependent mechanism of FTO in regulating the BDNF-TrkB pathway. A Western blotting shows the relative protein expression levels of FTO, BDNF, and TrkB in Control and MA treated HT22 cells ( n = 3); ** P < 0.01, * P < 0.05. B RT-PCR shows the relative levels of BDNF mRNA in Control and MA treated HT22 cells ( n = 3); *** P < 0.001. C Western blotting shows the relative protein expression levels of BDNF in LV-Vehicle and LV-FTO HT22 cells ( n = 3). ** P < 0.01, * P < 0.05. D RT-PCR shows the relative levels of BDNF mRNA in LV-Vehicle and LV-FTO HT22 cells ( n = 3); *** P < 0.001. E Prediction of m6A modification site on BDNF mRNA. F RT-PCR shows the m6A modification levels of BDNF mRNA in LV-Vehicle and LV-FTO cells ( n = 5). * P < 0.05. G Schematic of the role and mechanisms of FTO in NOR memory reconsolidation. The reactivation of NOR memory increased hippocampal FTO expression, which decrease the m6A level of BDNF mRNA and increased the protein expression of BDNF. BDNF binds to the high-affinity receptor TrkB to promote the NOR memory reconsolidation. The FTO inhibitor MA and TrkB antagonist ANA-12 disrupt NOR memory reconsolidation via targeting the FTO-BDNF-TrkB pathway. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41398-023-02647-4'>37963912</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-dddt_a_12469766_f0007_c.jpgAnti-BDNF Rabbit Monoclonal AntibodyVerification results of the WB and ELISA test. Notes: (A) Test procedure; (B) WB strip map; (C) WB gray value; (D) ELISA test results. The data are shown as the means ± SDs (n = 5). *P < 0.05, **P < 0.01 and ***P < 0.001 denote significant differences from the control group. #P < 0.05, ##P < 0.01 and ###P < 0.001 denote significant differences from the Model group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/DDDT.S537918'>40859969</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-djir_a_12469679_f0005_c.jpgAnti-BDNF Rabbit Monoclonal Antibody1 Hz rTSMS reduces astrocyte activation and neuroinflammation. (A) Representative immunofluorescence images showing GFAP (red) and Dapi (blue) staining in the injured spinal cord across groups. (B) Quantification of mean GFAP fluorescence intensity. (C) Western blot analysis of GFAP and BDNF expression. (D and E) Quantification of GFAP and BDNF relative to β-actin. (F) Western blot analysis of pro-inflammatory cytokines (TNF-α, IFN-γ and IL-6) and anti-inflammatory cytokines (IL-4 and IL-10). (G–K) Corresponding quantification of cytokine expression. n=5. Scale bar=20 μm. aP < 0.05, bP< 0.01, cP < 0.001, vs Sham group. dP < 0.05, eP < 0.01, fP < 0.001, vs SCI group. gP < 0.05, hP <0.01, vs 1 Hz group. The data are expressed as the mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S516006'>40873779</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc9.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc10.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc7.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc11.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse heart, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc8.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat pancreas, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-ihc.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using BDNF Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-icc1.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00035-1-if.jpgAnti-BDNF Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using BDNF Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pten-rabbit-monoclonal-antibody-m00006-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-11658_2025_686_fig8_html.pngAnti-PTEN Rabbit Monoclonal AntibodyOverexpression of MAF1 promoted PTEN expression, increased cellular activity, decreased cell apoptosis, and normalized autophagy. A , B qPCR and western blot analyses of MAF1 and PTEN expression in the sham-S + vector, model-S + vector, and model-S + MAF1 groups. C Western blot analyses of AKT/mTOR signaling pathway proteins. D MAF1 and PTEM expression was measured by IF. E Western blot analyses of RIG-I and IRF3, the apoptosis-related protein caspase-3, and autophagy-related proteins p62 and LC3B. F , G qPCR and flow cytometry were used to detect IFNβ expression levels. H CCK-8 analyses for detection of cellular activity in rBMECs and rAstrocytes after transfection for 0, 6, 12, 18, and 24 h. I Flow cytometry was used to detect the apoptosis of transfected cells. J Transmission electron microscopy was used to detect autophagy in rBMECs and rAstrocytes. K Schematic diagram of the mechanism by which MAF1 expression level affects BBB function in SAE. *** P < 0.001 model-S + vector versus sham-S + vector. # P < 0.05, ### P < 0.001 model-S + MAF1 versus sham-S + vector <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s11658-025-00686-x'>39833662</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-11658_2025_686_fig7_html.pngAnti-PTEN Rabbit Monoclonal AntibodyInterference with FOXO1 inhibited cellular activity and enhanced cell apoptosis. The rBMECs and rAstrocytes were treated with 10% serum harvested from the sham (sham-S) or model rats (model-S). A , B qPCR and western blot analyses of MAF1 , PTEN , and FOXO1 expression in the model-S + vector + siCtrl, model-S + PTEN + siCtrl, and model-S + PTEN + siFOXO1 groups. C MAF1 expression was measured by IF. D Western blot analyses evaluating the protein expression levels of RIG-I and IRF3 and apoptosis-related protein caspase-3. E qPCR and flow cytometry were used to detect IFNβ expression levels. F CCK-8 analyses for detection of cellular activity in rBMECs and rAstrocytes after transfection for 0, 6, 12, 18, and 24 h. G Flow cytometry was used to detect the apoptosis of transfected cells. *** P < 0.001 model-S + PTEN + siCtrl versus model-S + vector + siCtrl. # P < 0.05, ### P < 0.001 model-S + PTEN + siFOXO1 versus model-S + PTEN + siCtrl <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s11658-025-00686-x'>39833662</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-11658_2025_686_fig6_html.pngAnti-PTEN Rabbit Monoclonal AntibodyThe AKT/mTOR signaling pathway inhibited cellular activity and promoted cell apoptosis. A Levels of MAF1 expression were evaluated in the control, AKT1/2-IN, and AKT1/2-IN + CHX groups. B , C Western blot analyses were performed to assess the levels of MAF1 and FOXO1 protein expression in the control, AKT1/2-IN, and AKT1/2-IN + CHX groups. D , E The levels of cell activity and cell apoptosis in the control, AKT1/2-IN, and AKT1/2-IN + CHX groups. F An EMSA confirming the binding relationship between MAF1 and the PTEN promoter. *** P < 0.001 AKT1/2-IN versus control. # P < 0.05, ### P < 0.001 AKT1/2-IN + CHX versus AKT1/2-IN <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s11658-025-00686-x'>39833662</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-ihc.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using PTEN Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-11658_2025_686_fig5_html.pngAnti-PTEN Rabbit Monoclonal AntibodyOverexpression of PTEN attenuated the RIG-I/IRF3 signal pathway and apoptosis and recovered normal autophagy. The rBMECs and rAstrocytes were treated with 10% serum harvested from the sham (sham-S) or model rats (model-S). A , B qPCR and western blot analyses of MAF1 and PTEN expression in the sham-S + vector, model-S + vector, and model-S + PTEN groups. C Western blot analyses of AKT/mTOR signaling pathway. D MAF1 and CUL2 expression was measured by IF. E Western blot analyses of proteins RIG-I and IRF3, caspase-3, p62, and LC3B. F , G qPCR and flow cytometry were used to detect IFNβ expression levels. H CCK-8 analysis of rBMEC and rAstrocyte activity at 0, 6, 12, 18, and 24 h after transfection. I Flow cytometry analysis of apoptosis in transfected cells. J Transmission electron microscopy was used to detect autophagy in rBMECs and rAstrocytes. *** P < 0.001 model-S + vector versus sham-S + vector. # P < 0.05, ### P < 0.001 model-S + PTEN versus sham-S + vector <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s11658-025-00686-x'>39833662</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-if.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using PTEN Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-11658_2025_686_fig4_html.pngAnti-PTEN Rabbit Monoclonal AntibodyKnockdown of CUL2 increased MAF1 and PTEN expression and relieved cellular damage. A EBD extravasation and absorbance at 620 nm in brain tissues from the sham + Lv-shCtrl, model + Lv-shCtrl, and model + Lv-shCUL2 groups. B The levels of MAF1 and PTEN expression were measured by qPCR. C A Pearson correlation analysis was performed on the expression levels of MAF1 and PTEN . D , E Western blot analyses evaluating the levels of CUL2, MAF1, PTEN, AKT, p-AKT, and p-mTOR protein expression. F H&E staining showing the brain tissue morphology. G – I IHC analyses of CUL2, MAF1, and PTEN expression in brain tissues. *** P < 0.001 model + Lv-shCtrl versus sham + Lv-shCtrl. # P < 0.05, ### P < 0.001, model + Lv-shCUL2 versus model + Lv-shCtrl <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s11658-025-00686-x'>39833662</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-icc1.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-pten-primary-antibodies-wb-testing-1.jpgAnti-PTEN Rabbit Monoclonal Antibody Western blot analysis of PTEN using anti-PTEN antibody (M00006-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse heart tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified monoclonal antibody (Catalog # M00006-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTEN at approximately 54 kDa. The expected band size for PTEN is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-icc2.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-1-pten-primary-antibodies-wb-testing-2.jpgAnti-PTEN Rabbit Monoclonal AntibodyWestern blot analysis of PTEN using anti-PTEN antibody (M00006-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: control group-human mouse hippocampus tissue lysates, <br>
Lane 2: model group-human mouse hippocampus tissue lysates, <br>
Lane 3:Drug treatment (100mg/kg) – Mouse hippocampus tissue lysates, <br>
Lane 4:Drug treatment (500mg/kg) – Mouse hippocampus tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified monoclonal antibody (A04887-1) overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for PTEN at approximately 52 kDa. The expected band size for PTEN is at 54 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd86-rabbit-monoclonal-antibody-m00220-1-boster.html2026-04-01T05:01:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-cd86-primary-antibodies-wb-testing-1.jpgAnti-CD86/B7 2 Rabbit Monoclonal Antibody Western blot analysis of CD86 using anti-CD86 antibody (M00220-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Daudi whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: mouse RAW264.7 whole cell lysates,<br>
Lane 4: mouse ANA-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD86 antigen affinity purified monoclonal antibody (Catalog # M00220-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD86 at approximately 70 kDa. The expected band size for CD86 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-13046_2020_1637_fig6_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyCPEB3 attenuates tumorigenesis and TAM polarization in vivo (a) Schematic of the procedure for separating tumor cells and TAMs. (b) HCT116 cells were stably infected with Ctrl and CPEB3 lentivirus, and LoVo cells were stably infected with shCtrl and shCPEB3 sequences. Tumorigenesis assay of Balb/c nude mice subcutaneously injected with HCT116-Ctrl/CPEB3 cells and LoVo-shCtrl/shCPEB3 cells ( n = 20). Representative photos of tumors from mice in various groups. ( c) IHC staining of Ki67 positive cells was counted per high-power field (PHF), while E-cadherin and vimentin expression scores were counted in tumor tissues in a xenograft model; error bars, SEM. (d) The mice with intra-spleen injection of LoVo-shCtrl/shCPEB3 cells were treated with tocilizumab (5 mg/kg) weekly via intraperitoneally injection. The number of liver metastatic sites (indicated by arrows) was counted under the microscope; error bars, SEM. (e) Macrophages were separated from murine tumor tissues using Percoll-layered liquid. Surface expression of CD86 and CD163 was detected in macrophages using flow cytometry. The percentage of CD86 + or CD163 + cells in macrophages was reported using error bars and SEM. (f) Expression of JAK1, pJAK1, STAT3, and pSTAT3 in the tumor tissues of the two groups were analyzed by western blot analysis. (g) Schematic overview of the mechanisms by which CPEB3 modulate TAM polarization and inhibit colorectal cancer EMT. ** P < 0.01; *** P < 0.001; **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-020-01637-4'>32653013</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-fimmu-16-1538046-g007.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyWJMSCs inhibited pro-inflammatory macrophages and promoted anti-inflammatory macrophages in RV. (A) Representative images showed the CD86 + pro-inflammatory macrophages (green) and CD206 + anti-inflammatory macrophages (green) in each group. The nuclei were stained with DAPI (blue), and macrophages were stained with F4/80 (red). Scale bar, 20μm. (B–C) The percentage of CD86 + or CD206 + cells were calculated by Image-Pro Plus. (D–H) The protein level of CD86, CD206, TNF-α and IL-10 were measured by western blot, and quantification of the relative expression in the bands in different groups was calculated by Image-Pro Plus. All data were analyzed by two-way analysis of variance (ANOVA). Values are expressed as mean ± SD (n = 3-5). * p < 0.05, ** p < 0.01, *** p < 0.001. ns, not significant; HH, hypobaric hypoxia; NN, normobaric normoxia; IL-10, interleukin 10; TNF-α, tumor necrosis factor α. NS, neutral saline; WJMSCs, Wharton’s jelly-derived mesenchymal stem cells.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1538046/full'>40547034</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-13046_2020_1637_fig1_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyDecreased CPEB3 in human CRC correlates with low CD86 + TAM content and high CD163 + TAM content (a) The expression of CPEB3 and CD86 in 82 pairs of CRC tissues and adjacent non-tumor tissues was detected using qRT-PCR. Correlation between CPEB3 and CD86 or CD163 expression levels in 82 colorectal cancer tissues; error bars, SEM. (b) The protein expression of CPEB3, CD68, CD86, and CD163 in a human colorectal cancer tissue array was detected by IHC staining. Representative photos are shown (400× magnification). The number of CD68 + , CD86 + and CD163 + cells per high-power field in tissues from colorectal cancer patients with different levels of CPEB3 expression; error bars, SEM. (c) Schema for an in vitro model of stably transfected CRC cells co-cultured with TAMs. (d) Flow cytometry was used to explore the surface expression of CD86 and CD163 in SW480-Ctrl/CPEB3 and HCT116-Ctrl/CPEB3 cells; error bars, SEM. (e) Flow cytometry was used to explore the surface expression of CD86 and CD163 in LoVo-shCtrl/shCPEB3 and RKO-shCtrl/shCPEB3 cells; error bars, SEM. (f) We measured the expression of the respective inflammatory cytokines in cell culture supernatants of TAMs co-cultured HCT116-Ctrl/CPEB3 cells using ProcartaPlex combinable panels; error bars, SEM. (g) We measured the expression of the respective inflammatory cytokines in cell culture supernatants of TAM-co-cultured LoVo-shCtrl/shCPEB3 cells using ProcartaPlex combinable panels; error bars, SEM; ns, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-020-01637-4'>32653013</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-ihc.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using CD86 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-13046_2020_1637_fig5_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyCPEB3 modulates CCL2 secretion in CRC cell supernatants to regulate TAM polarization (a) We measured the expression of the respective inflammatory cytokines in cell culture supernatants of HCT116-Ctrl/CPEB3 cells by ProcartaPlex combinable panels; error bars, SEM. (b) We measured the expression of the respective inflammatory cytokines in the supernatants of LoVo-shCtrl/shCPEB3 cells by ProcartaPlex combinable panels; error bars, SEM. (c) THP-1 macrophages were co-cultured with LoVo-shCtrl/shCPEB3 with or without CCL2-neutralizing antibody (1 μg/mL) for 24 h. Flow cytometry was used to explore the surface expression of CD86 and CD163 in the differentiated macrophages; error bars, SEM. (d) THP-1 macrophages were co-cultured with RKO-shCtrl/shCPEB3 cells with or without a CCL2-neutralizing antibody (1 μg/mL) for 24 h. Flow cytometry was used to explore the surface expression of CD86 and CD163 in the differentiated macrophages. Error bars, SEM. * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-020-01637-4'>32653013</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-icc2.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-ijbms-25-781-g003.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodySanguinarine increased cellular levels of H3K4me2 and H3K9me2 and up-regulated the expression of CD86 in NSCLC cell lines. (A) and (B) Expression of H3K4me2 and H3K9me2 in H1975 and H1299 cells treated with sanguinarine for 48 hr, respectively, with H3 as loading control; (C) and (D) The expression of CD86 was detected, GADPH was used as a loading control. Data are the mean ± SEM of three independent experiments. * P <0.05, ** P <0.01, *** P <0.005 NSCLC: Non-small cell lung cancer<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9320206/&orig_host=www.ncbi.nlm.nih.gov'>35949313</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-icc3.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-fphar-15-1434568-g006.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyThe expression levels of p-mTOR/mTOR ratio, HIF-1α, and IL-1β in BV2 cells tested by western blot, the levels of GLU, LD, ATP, LDH and PDH quantified by biochemical test kit and the levels of polarization biomarkers of CD86 and CD206 detected by flow cytometry, the expression levels of IL-6 and TNF-α in BV2 cells tested by ELISA. (A) Blotting of p-mTOR, mTOR and HIF-1α protein in BV2 cells in each group; (B, C) Expression levels of p-mTOR/mTOR ratio and HIF-1α in BV2 cells in each group. (D) GLU content analysis chart; (E) LD content analysis chart; (F) ATP content analysis chart; (G) . LDH activity analysis graph; (H) PDH activity analysis graph. (I) Flow cytometry analysis charts; (J) Flow cytograms of BV2 cells in each group; (K) Blotting of IL-1β protein in BV2 cells in each group; (L) Expression level of IL-1β in BV2 cells in each group. (M, N) Expression level of IL-6 and TNF-α in BV2 cells in each group. Model group compared with control group * p < 0.05, ** p < 0.01, *** p < 0.001, HSD-containing serum-treated group compared with the model group $ p < 0.05, $$ p < 0.01, $$$ p < 0.001, Reverse validation group compared with the HSD-containing serum-treated group & p < 0.05, && p < 0.01, &&& p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1434568/full'>39130642</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-icc1.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-fphar-15-1434568-g003.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyExpression levels of CD86, Arg1 and IL-1β protein in hippocampus and cortex of SAMP8 mice detected by Western-blot, the expression levels of IL-6 and TNF-α in hippocampus and cortex of SAMP8 mice by ELISA. (A,E) Blotting of CD86, Arg1 and IL-1β protein in hippocampus and cortex of mice in each group; (B–D) Expression of CD86, Arg1 and IL-1β protein in hippocampus of mice in each group; (F–H) Expression of CD86, Arg1 and IL-1β protein in cortex of mice in each group; (I–L) Expression of IL-6 and TNF-α protein in hippocampus and cortex of mice in each group. Model group compared with the control group * p < 0.05, ** p < 0.01, *** p < 0.001, Donepezil group compared with the model group # p < 0.05, ## p < 0.01, ### p < 0.001, HSD group compared with the model group $ p < 0.05, $$ p < 0.01, $$$ p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1434568/full'>39130642</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-if.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562 cells, using CD86 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-43556_2024_203_fig6_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyMice reconstituted with FGF2 KO macrophages and subjected to CLP demonstrate increased M1 polarization in lung tissue. a - f The presence and levels of CD206, CD86, and F4/80 markers on macrophages within lung tissue were identified and quantitatively assessed using immunofluorescence staining. Bar is 20 μm. * p < 0.05, vs. WT; Δ p < 0.05 vs. WT + LPS; # p < 0.05 vs. FGF2 KO <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s43556-024-00203-0'>39436561</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-43556_2024_203_fig2_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyEffect of FGF2 deficiency on BMDM apoptosis and polarization. a – c FGF2 deletion increased BMDM apoptosis. a Apoptosis in BMDM deprived of FBS for 24 h was assessed by flow cytometry ( n = 4). b - c Percentage of PI + Annexin V + and PI- Annexin V + BMDM after starvation. d - k FGF2 deletion in BMDM promoted M1 polarization. d - g Flow cytometric analysis of macrophage markers in BMDM treated with LPS or IL4, including CD86, iNOS, CD206, and Arg1 ( n = 3). h - k The levels of CD86, iNOS, CD206 and Arg1 in BMDM after treatment with LPS or IL4. N represents no treatment; * p < 0.05, vs. WT; Ψ p < 0.05, vs. N + WT; Ω p < 0.05, vs. N + FGF2 KO <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s43556-024-00203-0'>39436561</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-41598_2025_88671_fig9_html.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyRelative expression of genes expression in GBM tissues. Expression levels of WTAP and ZC3H13 genes were compared with those of the control group on GBM tissues, 10 GBM and adjacent tissues, respectively ( A ). The expression levels of siRNA WTAP and overexpression ZC3H13 genes ( B and C ). The expression levels of CD27, CD70, CD80, CD86, ICOS, CTLA4, and LAG3 in siRNA WTAP and overexpression ZC3H13 were demonstrated in Fig. D and F, respectively. The result were determined by qRT-PCR. The data are mean ± standard deviation of six replicate experiments. * P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-cd86-primary-antibodies-wb-testing-2_1.jpgAnti-CD86/B7 2 Rabbit Monoclonal AntibodyWestern blot analysis of CD86 using anti-CD86 antibody (M00220-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Daudi whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates,<br>
Lane 7: mouse A20 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD86 antigen affinity purified monoclonal antibody (M00220-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD86 at approximately 72 kDa. The expected band size for CD86 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00220-1-cd86-primary-antibodies-wb-testing-3.jpg.pngAnti-CD86/B7 2 Rabbit Monoclonal AntibodyWestern blot analysis of CD86 using anti-CD86 antibody (A04887-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-5: mouse lung cancer tissue.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD86 antigen affinity purified polyclonal antibody (A04887-1) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a (HRP)-conjugated Anti-Rabbit IgG Secondary Antibody for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. The expected band size for CD86 is at 38 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd47-rabbit-monoclonal-antibody-m00360-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-wb7.jpgAnti-CD47 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-wb8.jpgAnti-CD47 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-wb.jpgAnti-CD47 Rabbit Monoclonal AntibodyWestern blot analysis of extracts of NIH/3T3 cell lysate, using CD47 antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc7-rabbit-monoclonal-antibody-m01190-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01190-wb.jpgAnti-CDC7 Rabbit Monoclonal AntibodyWestern blot analysis of extracts from HeLa cells, using CDC7 antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd63-rabbit-monoclonal-antibody-m01080-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01080-1-wb7.jpgAnti-CD63 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01080-1-wb.jpgAnti-CD63 Rabbit Monoclonal AntibodyWestern blot analysis of CD63 expression in A375 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01080-1-icc1.jpgAnti-CD63 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01080-1-ihc.jpgAnti-CD63 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CD63 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01080-1-icc2.jpgAnti-CD63 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nox4-rabbit-monoclonal-antibody-m00403-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-wb7.jpgAnti-NOX4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-if.jpgAnti-NOX4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using NOX4 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-jcav15p1124g002.jpgAnti-NOX4 Rabbit Monoclonal AntibodyKnockdown of AQP3 attenuated the effects of NOX4-derived H 2 O 2 on migration, invasion, and proliferation of HeLa cells. (A) Scratch was made in 6-well plates, and 24 h later, fluorescence microscopy was used to examine the migration of control or AQP3-49-shRNA cells in response to TGF-β1 training. (B) The invasion efficiency of control and AQP3-49-shRNA HeLa cells under TGF-β1 was examined with an 8-μm-pore-size transwell chamber. (C) Colony formation assays were used to test the effects of TGF-β1 on HeLa cell growth. (D) Fluorescence microscopy analysis of visualized F-actin polymerization of control or AQP3-49-shRNA cells with TRITC Phalloidin after TGF-β1 stimulation (5 ng/ml, 30 min). Data were presented as mean ± SD. *, P < 0.05, ***, P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10788729/&orig_host=www.ncbi.nlm.nih.gov'>38230207</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-jcav15p1124g003.jpgAnti-NOX4 Rabbit Monoclonal AntibodyAQP3 regulates Syk phosphorylation and activation of the PI3K/Akt signaling pathway in HeLa cells. (A) Collection of lentiviral control (sh-control) HeLa cells loaded with Green Fluorescent Protein Tag (GFP), CO-Immunoprecipitation detection analyzes the interaction of AQP3 and NOX4 complexes in HeLa cells. (B) Control and AQP3-49-shRNA HeLa cells were treated with different concentrations of TGF-β1 for 30 minutes, and the phosphorylation levels of Syk and PI3K/Akt were analyzed by western blot. (C) Western blot was used to detect the expression of Syk, PI3K p85α, and Akt phosphorylation in control and AQP3-49-shRNA HeLa cells treated with 200 μM H 2 O 2 at different times. β-Actin was used as a loading control. Data were presented as mean ± SD. *, P < 0.05, **, P < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC10788729/&orig_host=www.ncbi.nlm.nih.gov'>38230207</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-wb.jpgAnti-NOX4 Rabbit Monoclonal AntibodyWestern blot analysis of NOX4 expression in JAR cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-icc1.jpgAnti-NOX4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00403-ihc.jpgAnti-NOX4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat kidney, using NOX4 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vasp-rabbit-monoclonal-antibody-m00303-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00303-vasp-primary-antibodies-wb-testing-1.jpgAnti-VASP Rabbit Monoclonal AntibodyWestern blot analysis of VASP using anti-VASP antibody (M00303). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human SH-SY5Y whole cell lysates,<br>
Lane 6: human HEL whole cell lysates,<br>
Lane 7: human RT4 whole cell lysates.<br>
Lane 8: human K562 whole cell lysates,<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VASP antigen affinity purified monoclonal antibody (M00303) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VASP at approximately 40 kDa. The expected band size for VASP is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00303-vasp-primary-antibodies-ihc-testing-1.jpgAnti-VASP Rabbit Monoclonal AntibodyIHC analysis of VASP using anti-VASP antibody (M00303). <br>VASP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VASP Antibody (M00303) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00303-vasp-primary-antibodies-ihc-testing-2.jpgAnti-VASP Rabbit Monoclonal AntibodyIHC analysis of VASP using anti-VASP antibody (M00303). <br>VASP was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VASP Antibody (M00303) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox2-rabbit-monoclonal-antibody-m00105-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-flot1-primary-antibodies-wb-testing-1.jpgAnti-SOX2 Rabbit Monoclonal Antibody Western blot analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U251 whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX2 antigen affinity purified monoclonal antibody (Catalog # M00105-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX2 at approximately 34 kDa. The expected band size for SOX2 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-flot1-primary-antibodies-ihc-testing-1_1.jpgAnti-SOX2 Rabbit Monoclonal AntibodyIHC analysis of FLOT1 using anti-FLOT1 antibody (M00105-1). <br>
FLOT1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FLOT1 Antibody (M00105-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-1-s2.0-s2590049825000840-gr2.jpgAnti-SOX2 Rabbit Monoclonal AntibodyIdentification of NSCs. (A) NSCs were cultured in serum-free medium for 3 days (Scale bar: 200/100 μm). (B)Representative images of NSCs labelled with Nestin(red) and SOX2(green). The cell nuclei are stained blue with DAPI (Scale bar: 20/50 μm). (C) Images of NSCs-derived differentiated cells. TUBB3 (purple), GFAP (red), and Olig2 (green) are positively expressed, indicating the presence of neurons, astrocytes, and oligodendrocytes, respectively (Scale bar: 100 μm).<br><b>Index in Materials Today Advances under a CC BY license. DOI: <a href='https://www.sciencedirect.com/science/article/pii/S2590049825000840'>10.1016/j.mtadv.2025.100639</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-ihc-testing-2.jpgAnti-SOX2 Rabbit Monoclonal Antibody IHC analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-ihc-testing-3.jpgAnti-SOX2 Rabbit Monoclonal Antibody IHC analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of human tonsilitis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-ihc-testing-4.jpgAnti-SOX2 Rabbit Monoclonal Antibody IHC analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-ihc-testing-5.jpgAnti-SOX2 Rabbit Monoclonal Antibody IHC analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-flot1-primary-antibodies-ihc-testing-6.jpgAnti-SOX2 Rabbit Monoclonal AntibodyIHC analysis of FLOT1 using anti-FLOT1 antibody (M00105-1). <br>
FLOT1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FLOT1 Antibody (M00105-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-flot1-primary-antibodies-ihc-testing-7.jpgAnti-SOX2 Rabbit Monoclonal AntibodyIHC analysis of FLOT1 using anti-FLOT1 antibody (M00105-1). <br>
FLOT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FLOT1 Antibody (M00105-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-if-testing-6.jpgAnti-SOX2 Rabbit Monoclonal Antibody IF analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00105-1-sox2-primary-antibodies-if-testing-7.jpgAnti-SOX2 Rabbit Monoclonal Antibody IF analysis of SOX2 using anti-SOX2 antibody (M00105-1). <br>
SOX2 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-SOX2 Antibody (M00105-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/casestudy_m00105-1.jpgAnti-SOX2 Rabbit Monoclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ttf1-rabbit-monoclonal-antibody-m01322-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01322-1-nkx2-1-primary-antibodies-wb-testing-1.jpgAnti-TTF1 NKX2-1 Rabbit Monoclonal Antibody Western blot analysis of NKX2-1 using anti-NKX2-1 antibody (M01322-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NKX2-1 antigen affinity purified monoclonal antibody (Catalog # M01322-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NKX2-1 at approximately 39-42 kDa. The expected band size for NKX2-1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01322-1-ihc.jpgAnti-TTF1 NKX2-1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid, using TTF1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01322-1-if.jpgAnti-TTF1 NKX2-1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using TTF1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-wnt2-rabbit-monoclonal-antibody-m03226-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03226-wb.jpgAnti-WNT2 Rabbit Monoclonal AntibodyWestern blot analysis of WNT2 expression in (1) Jurkat cell lysate; (2) SKBR-3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tcf3-rabbit-monoclonal-antibody-m05152-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05152-wb.jpgAnti-TCF3 TCF7L1 Rabbit Monoclonal AntibodyWestern blot analysis of TCF3 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd22-rabbit-monoclonal-antibody-m01572-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-1-41467_2024_54150_fig4_html.pngAnti-CD22/Siglec 2 Rabbit Monoclonal AntibodyIn vivo comparison of the split-design CAR approach with ligand-based conventional CARs. a Timeline of in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). b Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). c , d Quantification of the average radiance (p/s/cm /sr) of the luminescence, related to APRIL- ( c ) and BAFF-( d )-based CAR-T-cell therapy. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. e Evaluation of serum inflammatory cytokine release by ELISA 24 h after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Tukey correction were used to assess significance. f , g Survival curves of the mice subjected to the indicated treatments. Survival curves were compared using the log-rank (Mantel‒Cox) test. h Timeline of in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). i Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). j Quantification of the average radiance (p/s/cm /sr) of the luminescence. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-BAFF) and CD19/CD22 CAR-T. k Evaluation of serum inflammatory cytokine release by ELISA 24 h after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. l Assessment of the presence of persistent human CD3 + (hCD3 + ) T cells in peripheral blood by flow cytometry over a 3-week follow-up period. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-BAFF) with BAFF-CAR-T at each time point. m Survival curves of mice subjected to the indicated treatments, compared using the log-rank (Mantel‒Cox) test. All n represents biological replicates from different mice. Data in this figure are representative of one of two independent experiments. Error bars represent mean ± SEM. NS indicates not significant. Source data are provided in the Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54150-z'>39528513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-1-cd22-primary-antibodies-wb-testing-1.jpgAnti-CD22/Siglec 2 Rabbit Monoclonal AntibodyWestern blot analysis of CD22 using anti-CD22 antibody (M01572-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Raji whole cell lysates,<br>
Lane 2: human Ramos whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD22 antigen affinity purified monoclonal antibody (M01572-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD22 at approximately 140 kDa. The expected band size for CD22 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-1-cd22-primary-antibodies-ihc-testing-1.jpgAnti-CD22/Siglec 2 Rabbit Monoclonal AntibodyIHC analysis of CD22 using anti-CD22 antibody (M01572-1). <br>CD22 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD22 Antibody (M01572-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cetp-rabbit-monoclonal-antibody-m00309-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00309-wb.jpgAnti-CETP Rabbit Monoclonal AntibodyWestern blot analysis of CETP expression in human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk1-rabbit-monoclonal-antibody-m00209-4-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-4-cdk1-2-3-primary-antibodies-wb-testing-1.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody Western blot analysis of CDK1/2/3 (Phospho-T14) using anti-CDK1/2/3 (Phospho-T14) antibody (M00209-4). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: human K562 whole cell lysates,<br>
Lane 6: human PC-3 whole cell lysates,<br>
Lane 7: human U251 whole cell lysates,<br>
Lane 8: human U2OS whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK1/2/3 (Phospho-T14) antigen affinity purified monoclonal antibody (M00209-4) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDK1/2/3 (Phospho-T14) at approximately 32-34 kDa. The expected band size for CDK1/2/3 (Phospho-T14) is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209-4-cdk1-2-3-primary-antibodies-ihc-testing-2.jpgAnti-CDK1/Cdc2 Rabbit Monoclonal Antibody IHC analysis of CDK1/2/3 (Phospho-T14) using anti-CDK1/2/3 (Phospho-T14) antibody (M00209-4). <br>CDK1/2/3 (Phospho-T14) was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK1/2/3 (Phospho-T14) Antibody (M00209-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mtor-rabbit-monoclonal-antibody-m00003-boster.html2026-03-25T05:22:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-mtor-primary-antibodies-wb-testing-1_1.jpgAnti-mTOR/Tor Rabbit Monoclonal Antibody Western blot analysis of MTOR using anti-MTOR antibody (M00003).
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human 293T whole cell lysates,
Lane 2: human Hela whole cell lysates,
Lane 3: human K562 whole cell lysates,
Lane 4: rat brain tissue lysates,
Lane 5: rat C6 whole cell lysates,
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTOR antigen affinity purified monoclonal antibody (Catalog # M00003) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MTOR at approximately 289 kDa. The expected band size for MTOR is at 289 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-fphar-16-1582677-g005.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyBECCs regulate PI3K, PDPK1, and mTOR protein levels in HAPH rats. (A–C) Primitive bands of p-PI3K, PI3K, p-PDPK1, PDPK1, p-mTOR, and mTOR by Western blots in lung tissues. (D–F) Quantitative evaluation of p-PI3K, PI3K, p-PDPK1, PDPK1, p-mTOR, and mTOR in lung tissues. n = 5. All data are represented as the mean ± SD. * p < 0.05 vs. control group and # p < 0.05 vs. hypoxia group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1582677/full'>40385484</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-fphar-16-1582677-g008.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyEriocitrin and quercetin are responsible for anti-proliferation by targeting the PI3K protein in PASMCs under hypoxic conditions. ERI, eriocitrin; QCT, quercetin. (A, B) Primitive bands and quantitative evaluation of p-mTOR, mTOR, p-AKT1 (Ser473), and AKT1 with or without PS210 (2 μM) by Western blotting in PASMCs under 3% O 2 . n = 3. All data are represented as the mean ± SD. * p < 0.05 vs. control group, # p < 0.05 vs. 3% O 2 group, and p < 0.05 vs. 3% O 2 + FLA-50 μg/ml group. (C–G) Primitive bands and quantitative densities of p-PI3K and PI3K by Western blots. n = 3. All data are represented as the mean ± SD. * p < 0.05 vs. control group and # p < 0.05 vs. 3% O 2 group. (H–N) BECC, ERI, and QCT treatment increased the stability of PI3K in PASMC protease lysates by the DARTS experiment. (H–K) Primitive Western blots of PI3K. (L–N) Quantitative evaluation of PI3K levels. n = 3. All data are represented as the mean ± SD. * p < 0.05 vs. DMSO group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1582677/full'>40385484</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-fphar-15-1506401-g005.jpgAnti-mTOR/Tor Rabbit Monoclonal Antibody(A) WB results for mTOR, RILP, LC3 and P62. (B) Relative expression levels of mTOR protein. (C) Relative expression levels of RILP protein. (D) The ratio of LC3II to LC3I. (E) Relative expression levels of P62 protein. (*: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1506401/full'>39958873</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-medi-102-e34592-g002.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyEffects of CSE on phagocytosis and miR-155-5p expression in MH-S cells. A: Phagocytosis of alveolar macrophages by Flow Cytometry. B and C: The expression of miR-155-5p, mTOR, Rictor, and RhoA were assessed by qRT-PCR. D and E: The protein expressions of mTOR, Rictor, RhoA, and p-RhoA were quantified by western blot. Data are presented as means ± SD (n = 3). ** P < .01 versus control. Blank: Alveolar macrophages without FITC-labeled E coli . CSE = cigarette smoke extract, FITC = fluorescein isothiocyanate, miRNA = microRNA, mTOR = Mammalian rapamycin target protein, qRT-PCR = quantitative real time polymerase chain reaction.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476751/'>37657048</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-medi-102-e34592-g004.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyEffects of overexpression or inhibition of miR-155-5p on phagocytosis and related proteins in MH-S cells. A: Phagocytosis of alveolar macrophages by Flow Cytometry. B: The expression of miR-155-5p, mTOR, Rictor, and RhoA was assessed by qRT-PCR. C and D: The protein expressions of mTOR, Rictor, RhoA, and p-RhoA were quantified by western blot. Data are presented as means ± SD (n = 3). ** P < .01 versus control. Blank: Alveolar macrophages without FITC-labeled E coli . CSE = cigarette smoke extract, miRNA = microRNA, mTOR = Mammalian rapamycin target protein, qRT-PCR = quantitative real time polymerase chain reaction.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476751/'>37657048</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-fcell-08-00383-g003.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyRelationship between ciRNA13761/novel-miR-3880/ ELF2 axis and PI3K/AKT/mTOR/S6K1 pathway. (A) Schematic diagram of animal treatment. C57BL/6 mice were injected with novel-miR-3880 or si ELF2 in an interval of three days and four days alternatively. Samples were harvested at day 22. (B) Immunohistochemistry of mammary gland for p-PI3K, p-AKT, p-mTOR and p-S6K1 in Normal Saline, novel-miR-3880 and si ELF2 groups. (C) Protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in mammary gland. (D,E) Effects of novel-miR-3880 and ELF2 on Bcl2/Bax pathway and protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in MEC. (F) PI3K, AKT, mTOR and S6K1 inhibitors suppressed the phosphorylation of PI3K, AKT, mTOR and S6K1 in MEC. (G–J) The role of novel-miR-3880 and si ELF2 in Bcl2/Bax and protein phosphorylation level of PI3K, AKT, mTOR and S6K1 in MEC with PI3K, AKT, mTOR or S6K1 inhibited. (K) Regulation of ciRNA13761 on Bcl2/Bax and PI3K, AKT, mTOR and S6K1 phosphorylation, and the balance effects of novel-miR-3880. (L) Effects of si DOCK1 on Bcl2/Bax and PI3K, AKT, mTOR and S6K1 phosphorylation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.00383/full'>32656203</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-fphar-09-00301-g006.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyPI3K/Akt/mTOR pathway is involved in the cardioprotective effects of LLC. (A) Expression levels of PI3K, p-Akt, Akt, p-mTOR and mTOR in hearts were analyzed. (B) Representative western blots of PI3K (p110α), p-Akt (Ser473), Akt, p-mTOR (Ser2448), mTOR, LC3, Beclin 1 and p62 in the presence or absence of 20 μmol⋅L -1 LY294002 and 40 μg⋅mL -1 LLC. (C) The cell viability was analyzed by MTT assay. (D) The cell injury was detected by LDH measurements. All experiments were repeated at least three times. Data were presented as means ± SD. ∗∗ P < 0.01 vs. Con group, ## P < 0.01 vs. OGD group, & P < 0.05, && P < 0.01 vs. OGD+LLC group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00301/full'>29651246</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003_fcell-13-1634945-g004.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyVerification of the effect of Pso on PDLSCs. (A) Representative protein expression bands for mTOR, OCN, RUNX2, ALP, and GADPH. (B–F) : Expression of LC3, PI3K, Rag C, WIPI 1, and Deptor genes. CK, blank control; L, LPS group; P, Pso group; LP, Pso/LPS co-culture group. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001 vs. control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12289674/'>40718710</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003_fcell-13-1634945-g005.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyExpression of related genes and proteins after the addition of mTOR inhibitor. (A) Expression level of the mTOR gene after adding the inhibitor rapamycin. (B) Change in the expression levels of the Rag C gene. (C–D) Changes in the expression levels of the osteogenesis-related genes ALP and RUNX2. (E) Protein expression levels for of Rag C, Deptor, ALP, and RUNX2. CK, control group; mTOR, mTOR-inhibitor group. (F) Relative expression levels of Rag C, ALP, and RUNX2 proteins. mTOR, mTOR-inhibitor group; Pso, mTOR inhibitor + Pso group. (G) Representative images of PDLSCs with Rag C lentiviral knockdown; green fluorescence indicates the lentiviral vector particles. (H–I) Expression changes in ALP and RUNX2 in PDLSCs with Rag C knockdown. CK, control group; Rag C, PDLSCs (scale bar = 200 μm). Data are presented as mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001 vs. the control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12289674/'>40718710</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-ihc.jpgAnti-mTOR/Tor Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat liver, using mTOR Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-mtor-primary-antibodies-wb-testing-2.pngAnti-mTOR/Tor Rabbit Monoclonal AntibodyWestern blot analysis of mTOR/Tor using anti-mTOR/Tor antibody (M00003). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-2: human OCI-LY1-Hmgb1 SRPK1 KOwhole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-mTOR/Tor antigen affinity purified polyclonal antibody (M00003) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for mTOR/Tor at approximately 289 kDa. The expected band size for mTOR/Tor is at 289kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-mtor-primary-antibodies-wb-testing-3.pngAnti-mTOR/Tor Rabbit Monoclonal Antibody Western blot analysis of MTOR using anti-MTOR antibody (M00003). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse 4T1 whole cell lysates, <br>
Lane 2: LPS-stimulated mouse 4T1 whole cell lysates, <br>
Lane 3: Low-dose drug mouse 4T1 whole cell lysates, <br>
Lane 4: Medium-dose drug mouse 4T1 whole cell lysates, <br>
Lane 5: High-dose drug mouse 4T1 whole cell lysates, <br>
Lane 6: Positive control drug mouse 4T1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTOR antigen affinity purified monoclonal antibody (Catalog # M00003) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with ChemiDoc MP system. A specific band was detected for MTOR at approximately 289 kDa. The expected band size for MTOR is at 289 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-mtor-primary-antibodies-wb-review-3.pngAnti-mTOR/Tor Rabbit Monoclonal AntibodyWestern blot analysis of mTOR/Tor using anti-mTOR/Tor antibody (M00003). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: normal group-Rat skeletal muscle tissue lysates, <br>
Lane 2: model group-Rat skeletal muscle tissue lysates, <br>
Lane 3: high-dose group-Rat skeletal muscle tissue lysates, <br>
Lane 4: medium-dose group-Rat skeletal muscle tissue lysates, <br>
Lane 5: low-dose group-Rat skeletal muscle tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-mTOR/Tor antigen affinity purified polyclonal antibody (M00003) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:10,000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for mTOR/Tor at approximately 289 kDa. The expected band size for mTOR/Tor is at 289kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd45-rabbit-monoclonal-antibody-m00555-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-ihc7.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-ihc10.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-ihc8.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-wb.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyWestern blot analysis of CD45 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-ihc9.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-1-ihc.jpgAnti-CD45 PTPRC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CD45 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab4-rabbit-monoclonal-antibody-m04643-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04643-1-wb.jpgAnti-Rab4 RAB4A Rabbit Monoclonal AntibodyWestern blot analysis of Rab4 expression in (1)MCF7 cell lysates (2)HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04643-1-if.jpgAnti-Rab4 RAB4A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Rab4 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04643-1-wb7.jpgAnti-Rab4 RAB4A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s6k1-rabbit-monoclonal-antibody-m01475-1-boster.html2026-03-24T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01475-1-rps6kb1-primary-antibodies-wb-testing-1.jpgAnti-S6K1 RPS6KB1 Rabbit Monoclonal AntibodyWestern blot analysis of p70 S6K/RPS6KB1 using anti-p70 S6K/RPS6KB1 antibody (M01475-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p70 S6K/RPS6KB1 antigen affinity purified monoclonal antibody (M01475-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for p70 S6K/RPS6KB1 at approximately 59 kDa. The expected band size for p70 S6K/RPS6KB1 is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp1-rabbit-monoclonal-antibody-m00733-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-wb.jpgAnti-MMP1 Rabbit Monoclonal AntibodyWestern blot analysis of MMP1 expression in MMP1 recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc10.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse kidney, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc7.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat kidney, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc11.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc8.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc9.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-ihc.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human hepatocellar carcinoma, using MMP1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00733-icc1.jpgAnti-MMP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trka-rabbit-monoclonal-antibody-m00706-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-1-trka-primary-antibodies-wb-testing-1.jpgAnti-TrkA NTRK1 Rabbit Monoclonal Antibody Western blot analysis of NTRK1 using anti-NTRK1 antibody (M00706-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NTRK1 antigen affinity purified monoclonal antibody (Catalog # M00706-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NTRK1 at approximately 145 kDa. The expected band size for NTRK1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-1-ihc.jpgAnti-TrkA NTRK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using TrkA Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd31-rabbit-monoclonal-antibody-m01513-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-1-cd31-primary-antibodies-wb-testing-1.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyWestern blot analysis of CD31 using anti-CD31 antibody (M01513-1). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD31 antigen affinity purified monoclonal antibody (M01513-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD31 at approximately 120-130 kDa. The expected band size for CD31 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-1-cd31-primary-antibodies-ihc-testing-1.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyIHC analysis of CD31 using anti-CD31 antibody (M01513-1). <br>
CD31 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD31 Antibody (M01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-1-cd31-primary-antibodies-ihc-testing-2.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyIHC analysis of CD31 using anti-CD31 antibody (M01513-1). <br>
CD31 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD31 Antibody (M01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ccr7-rabbit-monoclonal-antibody-m00390-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00390-ccr7-primary-antibodies-wb-testing-1.jpgAnti-CCR7 Rabbit Monoclonal Antibody Western blot analysis of CCR7 using anti-CCR7 antibody (M00390). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: rat spleen tissue lysates,<br>
Lane 4: rat lung tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse spleen tissue lysates,<br>
Lane 7: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR7 antigen affinity purified monoclonal antibody (Catalog # M00390) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCR7 at approximately 43 kDa. The expected band size for CCR7 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00390-ihc.jpgAnti-CCR7 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CCR7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00390-if.jpgAnti-CCR7 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CCR7 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ask1-rabbit-monoclonal-antibody-m00929-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-wb-testing-1_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody Western blot analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASK1 antigen affinity purified polyclonal antibody (Catalog # M00929) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ASK1 at approximately 95 kDa. The expected band size for ASK1 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-wb10.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-wb7.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-wb8.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ihc7.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ihc11.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-2_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-3_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-4_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-5_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-6_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-7_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-8_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-ask1-primary-antibodies-ihc-testing-9_1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal Antibody IHC analysis of ASK1 using anti-ASK1 antibody (M00929). <br>
ASK1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ASK1 Antibody (M00929) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00929-icc1.jpgAnti-ASK1 MAP3K5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mrp8-rabbit-monoclonal-antibody-m00413-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00413-1-wb.jpgAnti-MRP8 S100A8 Rabbit Monoclonal AntibodyWestern blot analysis of MRP8 expression in HL-60 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00413-1-ihc.jpgAnti-MRP8 S100A8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using MRP8 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-parp-rabbit-monoclonal-antibody-m00122-3-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-wb-testing-1_1.jpgAnti-PARP PARP1 Rabbit Monoclonal Antibody Western blot analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human SIHA whole cell lysates, <br>
Lane 4: human K562 whole cell lysates, <br>
Lane 5: human 293T whole cell lysates, <br>
Lane 6: human SH-SY5Y whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARP1 antigen affinity purified monoclonal antibody (M00122-3) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARP1 at approximately 113 kDa. The expected band size for PARP1 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-wb7.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-wb11.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-wb-testing-4_1.jpgAnti-PARP PARP1 Rabbit Monoclonal Antibody Western blot analysis of PARP1 using anti-PARP1 antibody (PB9309). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela- WT whole cell lysates,<br>
Lane 2: human Hela-GPX4 KO whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. Then the membrane was incubated with rabbit anti-PARP1 antigen affinity purified monnoclonal antibody (PB9309) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PARP1 at approximately 118 kDa. The expected band size for PARP1 is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-5_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-6_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-7_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-8_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-9_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-10_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-ihc-testing-11.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IHC analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-if-testing-12_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IF analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human pencreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-if-testing-13_1.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IF analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-parp1-primary-antibodies-if-testing-14.pngAnti-PARP PARP1 Rabbit Monoclonal Antibody IF analysis of PARP1 using anti-PARP1 antibody (M00122-3). <br>
PARP1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PARP1 Antibody (M00122-3) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG(H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-3-if_1.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PARP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lef1-rabbit-monoclonal-antibody-m00605-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00605-lef1-primary-antibodies-wb-testing-1.jpgAnti-LEF1 Rabbit Monoclonal AntibodyWestern blot analysis of LEF1 using anti-LEF1 antibody (M00605). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human REH whole cell lysates,<br>
Lane 3: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LEF1 antigen affinity purified monoclonal antibody (M00605) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LEF1 at approximately 50 kDa. The expected band size for LEF1 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00605-ihc.jpgAnti-LEF1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using LEF1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-shp1-rabbit-monoclonal-antibody-m00938-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00938-ptpn6-primary-antibodies-wb-testing-1_1.jpgAnti-SHP1 PTPN6 Rabbit Monoclonal AntibodyWestern blot analysis of PTPN6 using anti-PTPN6 antibody (M00938). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTPN6 antigen affinity purified monoclonal antibody (M00938) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PTPN6 at approximately 68 kDa. The expected band size for PTPN6 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00938-ihc.jpgAnti-SHP1 PTPN6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat spleen, using SHP1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mcsf-rabbit-monoclonal-antibody-m00620-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00620-wb.jpgAnti-MCSF Rabbit Monoclonal AntibodyWestern blot analysis of MCSF expression in MCSF recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-elk1-rabbit-monoclonal-antibody-m01426-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01426-elk1-primary-antibodies-wb-testing-1.jpgAnti-ELK1 Rabbit Monoclonal Antibody Western blot analysis of ELK1 using anti-ELK1 antibody (M01426). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human Raji whole cell lysates, <br>
Lane 3: human Daudi whole cell lysates, <br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat C6 whole cell lysates, <br>
Lane 6: mouse brain tissue lysates, <br>
Lane 7: mouse Neuro-2a whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ELK1 antigen affinity purified monoclonal antibody (M01426) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ELK1 at approximately 60 kDa. The expected band size for ELK1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01426-elk1-primary-antibodies-ihc-testing-2.jpgAnti-ELK1 Rabbit Monoclonal Antibody IHC analysis of ELK1 using anti-ELK1 antibody (M01426). <br>ELK1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ELK1 Antibody (M01426) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01426-elk1-primary-antibodies-ihc-testing-3.jpgAnti-ELK1 Rabbit Monoclonal Antibody IHC analysis of ELK1 using anti-ELK1 antibody (M01426). <br>ELK1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ELK1 Antibody (M01426) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-yap1-rabbit-monoclonal-antibody-m00116-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-yap1-primary-antibodies-wb-testing-1.jpgAnti-YAP1/Yap Rabbit Monoclonal Antibody Western blot analysis of YAP1 using anti-YAP1 antibody (M00116). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YAP1 antigen affinity purified monoclonal antibody (Catalog # M00116) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YAP1 at approximately 70 kDa. The expected band size for YAP1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-ihc.jpgAnti-YAP1/Yap Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using YAP1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig1_html.pngAnti-YAP1/Yap Rabbit Monoclonal AntibodyYAP knockdowned significantly decreased YAP expression at mRNA ( a ) and protein ( b ) levels in Hep-2 cells. c Immunofluorescence (bottom panel) was used to detect the expression of YAP (red). DAPI (blue) was used to stain the nuclei. The fluorescence intensity of YAP was stronger in YAP-NC groups, and was weaker in cells transfected with shRNA. One representative experiment out of the three performed is shown (80X). Experiments were repeated three times, and data are shown as the mean ± SD, ** P < 0.01 ( a ), ** P < 0.01 ( b ) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig2_html.pngAnti-YAP1/Yap Rabbit Monoclonal AntibodyYAP knockdowned suppresses cell proliferation, invasion and migration. Silenced YAP inhibited cell proliferation in Hep-2 cells by CCK-8 (top panel). a The OD value at 450 nm for 5 days. Hep-2 with no treatment (Control), Non-nonspecific shRNA treatment (YAP-NC), YAP knockdown (YAP-shRNA) groups, and cDNA overexpression after YAP knockdown (YAP-shRNA+YAP-cDNA), * P < 0.05. b Colony formation assays (second panel) were performed to evaluate the proliferative capability of control, YAP-NC, YAP-shRNA and YAP-shRNA+YAP-cDNA cell groups. A representative image is shown, and a statistical comparison of the indicated groups was performed across four independent experiments, ** P < 0.01. c Wound healing assays (third panel) were performed to explore the migration capability, and solid lines represented the wound edges. Images were captured by using light microscopy (40X). The migration index was calculated as described in the Materials and Methods (control, YAP-NC, YAP-shRNA and YAP-shRNA+YAP-cDNA). Statistical analysis is shown, ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig3_html.pngAnti-YAP1/Yap Rabbit Monoclonal AntibodySilencing of YAP promotes cell apoptosis and induces cell cycle arrest. a Guava easyCyte12 was used to investigate differences in cell cycle (top panel) distribution following YAP silencing or overexpression in Hep-2. Silenced YAP drove G2/M arrest in control, YAP-NC, YAP-shRNA and YAP-shRNA+YAP-cDNA cell groups. In addition, when YAP knockdown Hep-2 cells overexpressed YAP, the G2/M phase distribution was decreased, ** P < 0.01; b Apoptotic cells (medium panel) were analysed by Guava easyCyte12 via staining of annexin PE/7-AAD. The percentage of apoptotic cells is shown. ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig4_html.pngAnti-YAP1/Yap Rabbit Monoclonal Antibodya Targeted silencing of YAP inhibits the expression of mRNA and protein levels. a qRT-PCR was used to analyse the mRNA expression of YAP, GSK-3β, DDK1, E-cadherin, β-catenin and vimentin in Hep-2 cell lines after transfection or not, and GAPDH was used as the internal control. Experiments were repeated ten times, and data are shown as the mean ± SD, ** P < 0.01. b Western blot assay was employed to investigate the expression of YAP, β-catenin, E-cadherin, vimentin, DDK1 and GSK-3β. WB results indicated that the expression of vimentin and β-catenin were downregulated with YAP knockdown and were upregulated when cells were administered YAP-cDNA. Representative images are shown. Statistical analysis of the relative optical density of each band is shown. GAPDH was used as an internal control, ** P < 0.01. c Model of the role of YAP in laryngeal cancer <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig5_html.pngAnti-YAP1/Yap Rabbit Monoclonal Antibodya Targeted silencing of YAP suppresses laryngeal cancer tumourigenicity and metastasis in vivo. The effects of silenced YAP on tumour suppression in vivo. Images of tumours (left panel) formed in nude mice injected subcutaneously with Hep-2 cells transfected with control, negative vector, and YAP-shRNA. Fluorescence images (right panel) of tumours captured on the IVIS system 21 days after subcutaneous injection. Cells of each group were stably transfected with luciferase. Tumours with YAP knockdown were smaller compared to the other groups. Tumour growth curves are plotted. ** P < 0.01. b A pulmonary metastasis model (left panel) was established after 3 weeks of the indicated treatment. Images from the pulmonary metastasis model and the corresponding statistical analysis are shown. ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-12885_2019_5832_fig6_html.pngAnti-YAP1/Yap Rabbit Monoclonal AntibodyImmunohistochemistry staining for YAP, KI-67 and Bcl-2 protein in xenograft tumour model and pulmonary metastasis model. Cytoplasmic staining was considered to be positive for YAP, KI-67 and Bcl-2. b & f Higher YAP expression in both xenograft tumour and pulmonary models. c & d High YAP expression mainly in the nucleus of LSCC. e & f Low YAP expression in LSCC in both the cytoplasm and nucleus of tumour cells. g & h Low expression of YAP protein mainly in the nucleus of LSCC. [A, a, E, e] × 40; [B, b, C, c, D, d, F, f, G, g, H, h] × 100 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-019-5832-9'>31269911</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-if.jpgAnti-YAP1/Yap Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using YAP1 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-icc1.jpgAnti-YAP1/Yap Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00116-icc2.jpgAnti-YAP1/Yap Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox9-rabbit-monoclonal-antibody-m00177-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00177-sox9-primary-antibodies-wb-testing-1.jpgAnti-SOX9 Rabbit Monoclonal Antibody Western blot analysis of SOX9 using anti-SOX9 antibody (M00177). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: human SW620 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX9 antigen affinity purified monoclonal antibody (Catalog # M00177) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX9 at approximately 70 kDa. The expected band size for SOX9 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00177-sox9-primary-antibodies-ihc-testing-2.jpgAnti-SOX9 Rabbit Monoclonal Antibody IHC analysis of SOX9 using anti-SOX9 antibody (M00177). <br>
SOX9 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SOX9 Antibody (M00177) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00177-sox9-primary-antibodies-ihc-testing-3.jpgAnti-SOX9 Rabbit Monoclonal Antibody IHC analysis of SOX9 using anti-SOX9 antibody (M00177). <br>
SOX9 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SOX9 Antibody (M00177) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00177-if.jpgAnti-SOX9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of SW480 cells, using SOX9 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00177-sox9-primary-antibodies-ihc-testing-4.jpgAnti-SOX9 Rabbit Monoclonal Antibody IHC analysis of SOX9 using anti-SOX9 antibody (M00177). <br>
SOX9 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SOX9 Antibody (M00177) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk5-rabbit-monoclonal-antibody-m00511-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-cdk5-primary-antibodies-wb-testing-1.jpgAnti-CDK5 Rabbit Monoclonal AntibodyWestern blot analysis of CDK5 using anti-CDK5 antibody (M00511). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK5 antigen affinity purified monoclonal antibody (M00511) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDK5 at approximately 33 kDa. The expected band size for CDK5 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc10.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc7.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc11.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc8.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc9.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-ihc.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using CDK5 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00511-icc1.jpgAnti-CDK5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd31-rabbit-monoclonal-antibody-m01513-2-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-wb7.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-wb10.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-wb8.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-wb.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyWestern blot analysis of CD31 expression in THP1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-wb9.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01513-2-ihc.jpgAnti-CD31 PECAM1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using CD31 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ngfr-rabbit-monoclonal-antibody-m01187-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-wb7.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-wb.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyWestern blot analysis of NGFR expression in (1) C6 cell lysate; (2) PC-12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-wb8.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-wb9.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-ngfr-primary-antibodies-ihc-testing-1.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyIHC analysis of NGFR using anti-NGFR antibody (M01187-1). <br>NGFR was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NGFR Antibody (M01187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-ngfr-primary-antibodies-ihc-testing-2.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyIHC analysis of NGFR using anti-NGFR antibody (M01187-1). <br>NGFR was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NGFR Antibody (M01187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-ngfr-primary-antibodies-ihc-testing-3.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyIHC analysis of NGFR using anti-NGFR antibody (M01187-1). <br>NGFR was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NGFR Antibody (M01187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-ngfr-primary-antibodies-ihc-testing-4.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyIHC analysis of NGFR using anti-NGFR antibody (M01187-1). <br>NGFR was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NGFR Antibody (M01187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01187-1-ngfr-primary-antibodies-ihc-testing-5.jpgAnti-NGFR/P75 Rabbit Monoclonal AntibodyIHC analysis of NGFR using anti-NGFR antibody (M01187-1). <br>NGFR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NGFR Antibody (M01187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-igf1-rabbit-monoclonal-antibody-m00148-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00148-wb.jpgAnti-IGF1/Igf I Rabbit Monoclonal AntibodyWestern blot analysis of Calreticulin expression in IGF1 recombinant protein.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-brd4-rabbit-monoclonal-antibody-m00123-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-brd4-primary-antibodies-wb-testing-1.jpgAnti-Brd4 Rabbit Monoclonal Antibody Western blot analysis of Brd4 using anti-Brd4 antibody (M00123). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Brd4 antigen affinity purified monoclonal antibody (M05837-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Brd4 at approximately 240 kDa. The expected band size for Brd4 is at 152 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-brd4-primary-antibodies-wb-testing-2.jpgAnti-Brd4 Rabbit Monoclonal Antibody Western blot analysis of Brd4 using anti-Brd4 antibody (M00123). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human PC-12 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Brd4 antigen affinity purified monoclonal antibody (M05837-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Brd4 at approximately 240 kDa. The expected band size for Brd4 is at 152 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-thnov15p6839g008.jpgAnti-Brd4 Rabbit Monoclonal AntibodyO-GlcNAcylation of BRD4 inhibited NF-κB p65-mediated transcription of pro-inflammatory cytokines. (A)&(B) The expression of BRD4 in OGD-exposed cardiomyocytes was detected by RT-qPCR and Western blotting. H9C2 and AC-16 cells were transfected with shBRD4, and then subjected to OGD. (C)&(D) RT-qPCR and Western blotting analysis of BRD4 mRNA and protein levels. (E)&(F) The mRNA levels and concentrations of TNF-α, IL-1β, and IL-6 were determined by RT-qPCR and ELISA. (G) The binding of NF-κB p65 to TNF-α, IL-1β, and IL-6 promoters was confirmed by dual-luciferase reporter assay. (H)&(I) Co-IP assay verified the exogenous and endogenous interplay between OGT and BRD4 proteins. (J) O-GlcNAcylation of BRD4 protein in OGD-stimulated cardiomyocytes was evaluated. (K) YinOYang database predicated the potential O-GlcNAc sites on BRD4. OGD-challenged H9C2 and AC-16 cells were transfected with BRD4 WT plasmid or BRD4 plasmids with mutant O-GlcNAc sites (BRD4-S484R, BRD4-S784R, and BRD4-T1212R). (L) O-GlcNAcylation of BRD4 protein in H9C2 and AC-16 cells was detected. (M) Concentrations of TNF-α, IL-1β, and IL-6 were detected by ELISA. (N) The interaction between NF-κB p65 and TNF-α, IL-1β, and IL-6 promoters was validated by dual-luciferase reporter assay. n=3 for A-N. Student's t test (for A, B) and one-way ANOVA (for C-G, M, N) were performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-thnov15p6839g009.jpgAnti-Brd4 Rabbit Monoclonal AntibodyO-GlcNAcylation of BRD4 inhibited NF-κB p65-mediated transcription of pro-inflammatory cytokines. (A)&(B) The expression of BRD4 in OGD-exposed cardiomyocytes was detected by RT-qPCR and Western blotting. H9C2 and AC-16 cells were transfected with shBRD4, and then subjected to OGD. (C)&(D) RT-qPCR and Western blotting analysis of BRD4 mRNA and protein levels. (E)&(F) The mRNA levels and concentrations of TNF-α, IL-1β, and IL-6 were determined by RT-qPCR and ELISA. (G) The binding of NF-κB p65 to TNF-α, IL-1β, and IL-6 promoters was confirmed by dual-luciferase reporter assay. (H)&(I) Co-IP assay verified the exogenous and endogenous interplay between OGT and BRD4 proteins. (J) O-GlcNAcylation of BRD4 protein in OGD-stimulated cardiomyocytes was evaluated. (K) YinOYang database predicated the potential O-GlcNAc sites on BRD4. OGD-challenged H9C2 and AC-16 cells were transfected with BRD4 WT plasmid or BRD4 plasmids with mutant O-GlcNAc sites (BRD4-S484R, BRD4-S784R, and BRD4-T1212R). (L) O-GlcNAcylation of BRD4 protein in H9C2 and AC-16 cells was detected. (M) Concentrations of TNF-α, IL-1β, and IL-6 were detected by ELISA. (N) The interaction between NF-κB p65 and TNF-α, IL-1β, and IL-6 promoters was validated by dual-luciferase reporter assay. n=3 for A-N. Student's t test (for A, B) and one-way ANOVA (for C-G, M, N) were performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-thnov15p6839g010.jpgAnti-Brd4 Rabbit Monoclonal AntibodyENPP3 contributed to inflammation by inhibiting O-GlcNAcylation of BRD4. H9C2 and AC-16 cells were transfected with shENPP3, followed by exposure to OGD. (A) ENPP3 and BRD4 protein levels were measured by Western blotting. (B) The O-GlcNAc level of BRD4 protein was assessed. (C) The production of TNF-α, IL-1β, and IL-6 was determined by ELISA. (D) Dual-luciferase reporter assay evaluated the binding of NF-κB p65 to TNF-α, IL-1β, and IL-6 promoters. n=3 for A-D. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-thnov15p6839g011.jpgAnti-Brd4 Rabbit Monoclonal AntibodySRSF1/ENPP3 axis suppressed BRD4 O-GlcNAcylation to promote inflammation in CME. The OGD-stimulated cardiomyocytes were transfected with shSRSF1, ENPP3 overexpression plasmid, or a combination of them. (A) ENPP3 mRNA and lncRNA ENPP3 expression levels were detected by RT-qPCR. (B) The protein abundance of ENPP3 and BRD4 was assessed by Western blotting. (C) The O-GlcNAc level of BRD4 was determined. (D) ELISA was carried out to measure TNF-α, IL-1β, and IL-6 concentrations. n=3 for A-D. One-way ANOVA was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-thnov15p6839g012.jpgAnti-Brd4 Rabbit Monoclonal AntibodyMyocardium-specific SRSF1 knockout alleviated CME-induced inflammation via inactivation of the ENPP3/BRD4/NF-κB pathway. SRSF1 flox/flox and SRSF1-KO rats were injected with microspheres into the left ventricle to induce CME. (A) LVEF, LVFS, LVEDd, and CO were detected to evaluate cardiac function. (B) The serum cTnl level in different groups was measured by ELISA. (C) Pathological alterations in myocardial tissues were observed by HE staining (scale bar = 100 μm). (D) Myocardial infarct size was measured by HBFP staining (scale bar = 100 μm). (E) SRSF1, ENPP3, and BRD4 expression in myocardial tissues was evaluated by immunohistochemical staining (scale bar = 100 μm). (F) The protein abundance of SRSF1, ENPP3, BRD4, p65, and O-GlcNAcylation of BRD4 was detected by Western blotting or Co-IP, respectively. (G) ELISA was carried out to measure TNF-α, IL-1β, and IL-6 concentrations. n=6 for A-G. ANOVA for repeated measurement (for A, B), and one-way ANOVA (for F, G) was performed to analyze data. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12203807/'>40585977</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-if.jpgAnti-Brd4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Brd4 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00123-ihc_1.jpgAnti-Brd4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Brd4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfap-rabbit-monoclonal-antibody-m00213-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-12868_2022_733_fig5_html.pngAnti-GFAP Rabbit Monoclonal AntibodyCell-specific location of NLRP3 in the lumbar spinal cord. Representative images of double immunofluorescence staining for NLRP3 with NeuN, GFAP, or Iba1 are shown. At 60 d, NLRP3 was mainly expressed in the neuronal cytoplasm of ventral horn spinal cord of ALS mice, and low expression was found in CON mice a . Dramatic co-localization with neurons and activated GFAP + astrocytes in ALS mice was observed at 95 d b . Increased NLRP3 expression was observed in GFAP + and Iba1 + cells in the ALS spinal cord c , d . Arrows indicate double-labelled cells. Scale bar 50 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12868-022-00733-9'>35945502</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-12868_2022_733_fig6_html.pngAnti-GFAP Rabbit Monoclonal AntibodyCell-specific location of caspase-1 in the lumbar spinal cord. Representative images of double immunofluorescence staining for caspase-1 with NeuN, GFAP, or Iba1 are shown. At 60 d, caspase-1 was mainly expressed in the neuronal cytoplasm of ventral horn spinal cord of ALS mice, and low expression was found in CON mice a . Increased co-localization of caspase-1 with activated GFAP + astrocytes and Iba1 + microglia in ALS mice were observed from 95 to 122 d b , c , d . Arrows indicate double-labelled cells. Scale bar 50 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12868-022-00733-9'>35945502</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-12868_2022_733_fig8_html.pngAnti-GFAP Rabbit Monoclonal AntibodyCell specific location of IL-1β in the lumbar spinal cord. Representative images of double immunofluorescence staining for IL-1β with NeuN, GFAP, or Iba1 are shown. At 60 d, increased expression of IL-1β was observed in the neuronal cytoplasm of ventral horn spinal cord of ALS mice, and low expression was found in CON mice a . Besides NeuN + /IL-1β + double positive cells, dramatic co-localization of IL-1β with activated GFAP + astrocytes and Iba1 + microglia in transgenic ALS mice were observed from 95 to 122 d b , c , d . Arrows indicate double-labelled cells. Scale bar 50 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12868-022-00733-9'>35945502</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-nrr-14-452-g005.jpgAnti-GFAP Rabbit Monoclonal AntibodyImmunofluorescence microscopy of GFAP in the right prefrontal cortex of cerebral I/R mice following DAPT treatment. (A–I) GFAP-immunoreactive cells (arrows) were examined in the prefrontal cortex by immunofluorescence labeling at 400× magnification. GFAP-positive cells were labeled red, and the labeling was mainly localized to the cytoplasm. Nuclei were labeled blue with DAPI in A–I. Scale bars: 10 μm. (A) Sham group: A few GFAP-immunoreactive cells. (B–E) 1-day, 3-day, 7-day, and 14-day I/R subgroups, respectively: More GFAP-positive cells were visible compared with the sham group (arrows). (F–I) 1 -day, 3 -day, 7 -day, and 14 -day DAPT subgroups, respectively: fewer GFAP-positive cells were observed compared with the I/R group (arrows). (J) Quantitation analysis of GFAP-immunoreactive cells. Data are expressed as the mean ± SD ( n = 5 per subgroup; one-way analysis of variance followed by Student-Newman-Keuls test). * P < 0.01, vs . sham group; # P < 0.05, vs . I/R group. I/R: Ischemia/reperfusion; DAPT: N-[N-(3,5-difluorohenacetyl)-l-alanyl]-S-phenylglycine tert-butyl ester; GFAP: glial fibrillary acidic protein; DAPI: 4′,6-diamidino-2-phenylindole; d: day(s).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6334612/&orig_host=www.ncbi.nlm.nih.gov'>30539813</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-gfap-primary-antibodies-wb-testing-1.jpgAnti-GFAP Rabbit Monoclonal Antibody Western blot analysis of GFAP using anti-GFAP antibody (M00213-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U251 whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GFAP antigen affinity purified polyclonal antibody (Catalog # M00213-1) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GFAP at approximately 45 kDa. The expected band size for GFAP is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-gfap-primary-antibodies-ihc-testing-2.jpgAnti-GFAP Rabbit Monoclonal Antibody IHC analysis of GFAP using anti-GFAP antibody (M00213-1). <br>
GFAP was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GFAP Antibody (M00213-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-gfap-primary-antibodies-ihc-testing-3.jpgAnti-GFAP Rabbit Monoclonal Antibody IHC analysis of GFAP using anti-GFAP antibody (M00213-1). <br>
GFAP was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GFAP Antibody (M00213-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-gfap-primary-antibodies-ihc-testing-4.jpgAnti-GFAP Rabbit Monoclonal Antibody IHC analysis of GFAP using anti-GFAP antibody (M00213-1). <br>
GFAP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GFAP Antibody (M00213-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-gfap-primary-antibodies-ihc-testing-5.jpgAnti-GFAP Rabbit Monoclonal Antibody IHC analysis of GFAP using anti-GFAP antibody (M00213-1). <br>
GFAP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GFAP Antibody (M00213-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-1-if.jpgAnti-GFAP Rabbit Monoclonal AntibodyImmunofluorescent analysis of SH-SY5Y cells, using GFAP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-creb-rabbit-monoclonal-antibody-m00577-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00577-wb.jpgAnti-CREB CREB1 Rabbit Monoclonal AntibodyWestern blot analysis of CREB expression in NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00577-ihc.jpgAnti-CREB CREB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using CREB Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00577-if.jpgAnti-CREB CREB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CREB Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-igg4-rabbit-monoclonal-antibody-m11385-1-boster.html2026-03-24T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11385-1-ighg4-primary-antibodies-wb-testing-1.jpgAnti-IgG4 IGHG4 Rabbit Monoclonal AntibodyWestern blot analysis of IGHG4 using anti-IGHG4 antibody (M11385-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,<br>
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates,<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGHG4 antigen affinity purified monoclonal antibody (M11385-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IGHG4 at approximately 52 kDa. The expected band size for IGHG4 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11385-1-ihc.jpgAnti-IgG4 IGHG4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach carcinoma, using human IgG4 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek1-rabbit-monoclonal-antibody-m00292-boster.html2026-04-06T05:04:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-wb7.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-wb10.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-wb8.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-wb.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyWestern blot analysis of MEK1 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-wb9.jpgAnti-MEK1 MAP2K1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-puma-rabbit-monoclonal-antibody-m04899-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-puma-primary-antibodies-wb-testing-1.jpgAnti-PUMA BBC3 Rabbit Monoclonal Antibody Western blot analysis of PUMA using anti-PUMA antibody (M04899). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PUMA antigen affinity purified monoclonal antibody (Catalog # M04899) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PUMA at approximately 21 kDa. The expected band size for PUMA is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-bbc3-primary-antibodies-ihc-testing-2.jpgAnti-PUMA BBC3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using PUMA Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-bbc3-primary-antibodies-if-testing-3.jpgAnti-PUMA BBC3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PUMA Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-icc1.jpgAnti-PUMA BBC3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-icc2.jpgAnti-PUMA BBC3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilutionhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04899-icc3.jpgAnti-PUMA BBC3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mlkl-rabbit-monoclonal-antibody-m00535-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00535-mlkl-primary-antibodies-wb-testing-1.jpgAnti-MLKL Rabbit Monoclonal AntibodyWestern blot analysis of MLKL using anti-MLKL antibody (M00535). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MLKL antigen affinity purified monoclonal antibody (M00535) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MLKL at approximately 54 kDa. The expected band size for MLKL is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00535-ihc.jpgAnti-MLKL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using MLKL Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf1-rabbit-monoclonal-antibody-m00580-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00580-wb7.jpgAnti-IRF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00580-ihc.jpgAnti-IRF1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat kidney, using IRF1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00580-wb8.jpgAnti-IRF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00580-if.jpgAnti-IRF1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using IRF1 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00580-wb.jpgAnti-IRF1 Rabbit Monoclonal AntibodyWestern blot analysis of IRF1 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab9-rabbit-monoclonal-antibody-m05768-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05768-rab9a-primary-antibodies-wb-testing-1.jpgAnti-Rab9 RAB9A Rabbit Monoclonal AntibodyWestern blot analysis of RAB9A using anti-RAB9A antibody (M05768). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human SiHa whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse kidney tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB9A antigen affinity purified monoclonal antibody (M05768) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB9A at approximately 23 kDa. The expected band size for RAB9A is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-neun-rabbit-monoclonal-antibody-m11954-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fcell-12-1459573-g005.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyHeterochromatin changes are associated with Tau pathology in AD temporal lobes at intermediate stages. (A) WB of heterochromatin markers HP1α and H3K9me3 in human brain samples at BS1/2 (N = 7), BS3/4 (N = 6) and BS5/6 (N = 8) and relative quantification. Histone H3 and Actin are the housekeeping genes. HP1α and H3K9me3 fold change is reported in the graphs. H3K9me3 has been normalized on total H3 histone. (B) Immunofluorescence and relative quantification of H3K9me3 in human brain samples at BS1/2 (N = 6), BS3/4 (N = 5) and BS5/6 (N = 5). Red: NeuN; yellow: H3K9me3; green: pAT8; blue: DAPI. Scale bar: 20 µm * p < 0.05; ** p < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2024.1459573/full'>39830212</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-2-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyNeuN (Rbfox3) was expressed in different organs at protein level. (A) Western blot analysis; (B) semi-quantitative analysis of the results of Western blotting (Mean ± SD, n = 3); (C) β -actin expressed in different organs at protein level, * P < 0.05 vs. brain, ANOVA; (D) β -actin and Gapdh expressed in different organs at mRNA level. * P < 0.05 vs. brain, ANOVA; (E) Lambs expressed in different organs at mRNA level. FPKM = value of fragments per kilobase of transcript sequence per million base pairs sequenced, *, P < 0.05, Mann Whiteney test (two-tailed). Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-3-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyImmunofluorescence (IF) and immunohistochemistry (IHC) assays of different organs (bar = 20 µm). (A–D) Brain; (E–H) heart; (I–L), liver; (M–P) lung; (Q–T) kidney; (U–X) stomach; (Y–BB) duodenum; (CC–FF) ileum. As for IF, green fluorescence was stained to locate NeuN (BM4354, Boster) by FITC-linked secondary antibody, and blue fluorescence was stained to locate nucleus by Hoechst 33342. As for IHC, NeuN was stained in brown. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-4-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyImmunofluorescence (IF) assays verified in four organs (bar = 20 µm). (A–C) Heart; (D–F) lung; (G–I) liver; (J–L) Kidney; (M–O) kidney (Negative control). Red fluorescence was stained to locate NeuN by another rabbit anti-NeuN monoclonal antibody (ab177487, Abcam), and blue fluorescence was stained to locate nucleus by Hoechst 33342. Negative control was only stained with Alexa Fluor ® 647-linked secondary antibody and Hoechst 33342. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-5-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyDouble immunofluorescence (IF) analysis of rat heart (bar = 20 µm). (A–D) Cardiac muscle fibers in transection; (E–H) cardiac muscle fibers in longitudinal section. Red fluorescence was stained to locate Myl3 by Alexa Fluor ® 647-linked secondary antibody, green fluorescence was stained to locate NeuN by FITC-linked secondary antibody, and blue fluorescence was stained to locate nucleus by Hoechst 33342. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-6-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyQuantitative analysis of NeuN-positive cells in rat organs and cultured cells (mean ± SD, n = 3). Photos can be seen in (rat organs) and (cultured cells). (A) NeuN-positive cell rate in rat organs; (B) NeuN-positive cell rate in cultured cells. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-fig-7-1x.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyImmunofluorescence (IF) analysis of different cell lines (bar = 20 µm). (A–C) 293T cell; (D–F) A549 cell; (G–I) BRL3A cell; (J–L) Caco2 cell; (M–O) HL7702 cell; (P–R) PC12Adh cell; (S–U) atrial muscle cell. Green fluorescence was stained to locate NeuN by FITC-linked secondary antibody, and blue fluorescence was stained to locate nucleus by Hoechst 33342. Download full-size image DOI:<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://peerj.com/articles/8254/'>31938576</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-10020_2025_1301_fig1_html.pngAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyThe hippocampal neuron in DM mice showed the morphological changes. A The work flow chart of how to construct a DM mouse model. B - C The levels of blood glucose and body weight of mice were assessed. D The level of insulin of mice was assessed. E - F Morris water maze test was evaluated the learning and memory ability of mice by the escape latency time, number of crossing platform and swimming time in quadrant. G The recognition index among 4 groups in the novel object recognition test. H H&E staining evaluated the pathological changes of hippocampus. I Neuronal damage of the hippocampal region was assessed by Nissl staining. J IHC assay was used to examine the expression of NeuN in hippocampus of mice. * P < 0.05, ** P < 0.01, *** P < 0.001 Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01301-7'>40537751</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-10020_2025_1301_fig2_html.pngAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyFCGR2B were up-regulated in hippocampus of DM mice. A qRT-PCR was performed to detect the expression of ALB, AREG and FCGR2B mRNA expression in hippocampus of mice. B Western blot was conducted to detect the ALB, AREG and FCGR2B protein expression in hippocampus of mice. C IHC assay was employed to examine the ALB, AREG and FCGR2B protein expression in hippocampus of mice. D IF staining was utilized to detect the expression of FCGR2B and NeuN in hippocampus of mice. E Western blot was performed to detect the SHC1 protein expression in hippocampus of mice. F IF staining was performed to detect the expression of SHC1 and NeuN in hippocampus of mice. G Western blot was used to detect the p-PI3K and p-AKT protein expression in hippocampus of mice. *** P < 0.001 Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01301-7'>40537751</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-10020_2025_1301_fig4_html.pngAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyKnockdown FCGR2B could promote the PI3K/AKT signaling pathway in vivo. A The work flow chart of how to construct a DM mouse model. B The mRNA levels of FCGR2B and SHC1 were assessed by qRT-PCR. C The protein levels of FCGR2B and SHC1 were evaluated by Western blot. D The protein level of SHC1 was determined by Western blot. E IF staining was used to detect the expression of FCGR2B and NeuN in hippocampus of mice. F IF staining was performed to detect the expression of SHC1 and NeuN in hippocampus of mice. G The expressions of p-PI3K and p-AKT in hippocampus of mice were evaluated by Western blot. ** P < 0.01, *** P < 0.001 Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01301-7'>40537751</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-10020_2025_1301_fig5_html.pngAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyKnockdown FCGR2B improved hippocampal neuronal excitability. A Representative images of Golgi staining of the hippocampal neuronal spines from the mice. B IHC assay was performed to examine the expression of NeuN in hippocampus of mice. C IHC assay was used to examine the expression of c-fos and GABAA in hippocampus of mice. D The expressions of c-fos, CaMKII, GABAA, and GABAARAP in hippocampus of mice were detected by Western blot. E TUNEL staining was conducted to assess cell apoptosis in hippocampus. F IF was used to detect BrdU and Ki67 positive cells in hippocampaltissue to analyzecell proliferation * P < 0.05, ** P < 0.01, *** P < 0.001 Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01301-7'>40537751</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954_12985_2025_2874_fig3_html.pngAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyStable brain expression of HCMV-IE1 was associated with neuronal loss and apoptosis in the hippocampus as well as demyelination in the corpus callosum. A Nissl staining in the hippocampal and cortex region of 1-month-old IE1 mice and control mice. Scale bar, 200 μm (left); 20 μm (middle and right). B Quantification of Nissl staining. Data were presented as mean ± SEM ( n = 4 for each group). C LFB staining of corpus callosum of 1-month-old IE1 mice and control mice. Scale bar, 50 μm. D TUNEL (Pink) and Neun (Green) staining of the hippocampus region of 1-month-old IE1 mice and control mice. Scale bar, 20 μm. E Measurement of Nuen + and Tunel + cells in the hippocampus <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12985-025-02874-9'>40717094</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-djir_a_12469679_f0006_c.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal Antibody1 Hz rTSMS preserve neuronal survival and promote axonal regeneration after SCI. (A) Representative immunofluorescence images showing NeuN+ neurons (green) and Dapi (blue) in transverse spinal cord sections at 21 days post-injury across four groups (Sham, SCI, 1 Hz rTSMS, MCC950). Scare bar=200 μm. Insets show higher magnification of ventral horn neurons. Scare bar=20 μm. (B) Quantification of NeuN+ cells in the ventral horn area (n=6). (C) Representative images of cortical motor neurons retrogradely labeled by rAAV/Retro. Scare bar=1mm. (D1–K1) Display higher magnification images of the selected boxed regions. Scare bar=50 μm. (L) Quantification of GFP fluorescence intensity (n=3). (M) Number of GFP+ neurons per field (n=3). (N) Mean volume of traced neurons (n=3). aP < 0.001, vs Sham group. bP < 0.05, cP < 0.01, dP < 0.001, vs SCI group. Data are presented as mean ± SD.
<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S516006'>40873779</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-neun-primary-antibodies-wb-testing-1.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyWestern blot analysis of NeuN using anti-NeuN antibody (M11954). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NeuN antigen affinity purified monoclonal antibody (M11954) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NeuN at approximately 46, 50 kDa. The expected band size for NeuN is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-neun-primary-antibodies-ihc-testing-1.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyIHC analysis of NeuN using anti-NeuN antibody (M11954). <br>NeuN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NeuN Antibody (M11954) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-neun-primary-antibodies-ihc-testing-2.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyIHC analysis of NeuN using anti-NeuN antibody (M11954). <br>NeuN was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NeuN Antibody (M11954) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-neun-primary-antibodies-ihc-testing-3.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyIHC analysis of NeuN using anti-NeuN antibody (M11954). <br>NeuN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NeuN Antibody (M11954) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11954-neun-primary-antibodies-ihc-testing-4.jpgAnti-NeuN RBFOX3 Rabbit Monoclonal AntibodyIHC analysis of NeuN using anti-NeuN antibody (M11954). <br>NeuN was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NeuN Antibody (M11954) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-m6pr-rabbit-monoclonal-antibody-m00951-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00951-igf2r-primary-antibodies-wb-testing-1.jpgAnti-M6PR IGF2R Rabbit Monoclonal AntibodyWestern blot analysis of IGF2R using anti-IGF2R antibody (M00951). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGF2R antigen affinity purified monoclonal antibody (M00951) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IGF2R at approximately 300 kDa. The expected band size for IGF2R is at 274 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00951-ihc.jpgAnti-M6PR IGF2R Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using M6PR/IGF2R Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rps3-rabbit-monoclonal-antibody-m01542-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01542-wb.jpgAnti-RPS3/Ribosomal Protein S3 Rabbit Monoclonal AntibodyWestern blot analysis of RPS3 expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01542-ihc.jpgAnti-RPS3/Ribosomal Protein S3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using RPS3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab5-rabbit-monoclonal-antibody-m01891-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01891-rab5a-primary-antibodies-wb-testing-1.jpgAnti-Rab5 RAB5A Rabbit Monoclonal AntibodyWestern blot analysis of RAB5A using anti-RAB5A antibody (M01891). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB5A antigen affinity purified monoclonal antibody (M01891) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB5A at approximately 24 kDa. The expected band size for RAB5A is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01891-ihc.jpgAnti-Rab5 RAB5A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Rab5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pgk1-rabbit-monoclonal-antibody-m01449-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01449-wb.jpgAnti-PGK1 Rabbit Monoclonal AntibodyWestern blot analysis of PGK1 expression in (1) HepG2 cell lysate; (2) Mouse kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ki67-rabbit-monoclonal-antibody-m00254-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-wb.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyWestern blot analysis of Ki67 expression in Ramos cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-ihc7.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:3000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-12943_2020_1237_fig1_html.pngAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyPVT1 promotes pancreatic cancer cell resistance to gemcitabine in vitro and in vivo . a After nocodazole treatment for 12 h, the expression level of PVT1 in PANC-1 and SW1990 human pancreatic cancer cell lines and the PANC-1/Gem and SW1990/Gem gemcitabine resistant cell lines was examined by real-time qPCR. b and c PANC-1 cells were treated with gemcitabine at different concentrations and for different durations as indicated. Then, the expression levels of PVT1 were determined. d-g PANC-1/Gem and SW1990/Gem cells with stable PVT1knockdown and PANC-1 and SW1990 cells with stable PVT1 expression were treated with gemcitabine at different concentrations for 48 h, and cell viability was then measured by MTT assay. h PANC-1 cells stably expressing PVT1 were treated with gemcitabine (1 μM) for different durations as indicated, and cell viability was measured by MTT assay. i and j Apoptotic cells among PVT1 overexpressing PANC-1 and ASPC-1 cells treated with gemcitabine were analyzed by TUNEL assay, the number of TUNEL-positive cells was quantified. Scale bars: 100 μm. k and l Representative photographs of tumor-bearing mice in different groups and tumors excised from the mice were shown. m Growth curve showing changes in tumor volume in mice from different groups; growth was assessed every 5 days beginning from the injection and during gemcitabine (50 mg/kg) treatment. n Weight of the tumors excised from mice in each group. o and p Representative H&E staining images and immunohistochemical images of Ki67 in excised tumor tissues. Scale bars: 100 μm. Data were represented as mean ± SD, * P < 0.05; ** P < 0.01; *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-020-01237-y'>32727463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-ihc8.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver cancer, using the Antibody at 1:3000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-ihc.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using Ki67 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-ihc9.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:3000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-icc1.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00254-if.jpgAnti-Ki67 MKI67 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Ki67 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grm5-rabbit-monoclonal-antibody-m01338-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01338-wb.jpgAnti-GRM5/Mglur5 Rabbit Monoclonal AntibodyWestern blot analysis of GRM5 expression in mouse brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gfap-rabbit-monoclonal-antibody-m00213-2-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-wb7.jpgAnti-GFAP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-wb.jpgAnti-GFAP Rabbit Monoclonal AntibodyWestern blot analysis of GFAP expression in Rat brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-wb8.jpgAnti-GFAP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-ihc.jpgAnti-GFAP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human glioma, using GFAP Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-wb9.jpgAnti-GFAP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00213-2-if.jpgAnti-GFAP Rabbit Monoclonal AntibodyImmunofluorescent analysis of SNB19 cells, using GFAP Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pim1-rabbit-monoclonal-antibody-m01184-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01184-pim1-primary-antibodies-wb-testing-1.jpgAnti-PIM1 Rabbit Monoclonal AntibodyWestern blot analysis of PIM1 using anti-PIM1 antibody (M01184). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human k562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: human Caco-2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIM1 antigen affinity purified monoclonal antibody (M01184) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIM1 at approximately 34 kDa. The expected band size for PIM1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01184-ihc.jpgAnti-PIM1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate carcinoma, using PIM1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fli1-rabbit-monoclonal-antibody-m00399-1-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00399-1-wb.jpgAnti-FLI1 Rabbit Monoclonal AntibodyWestern blot analysis of FLI1 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00399-1-ihc.jpgAnti-FLI1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using FLI1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ccr3-rabbit-monoclonal-antibody-m01748-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01748-ccr3-primary-antibodies-wb-testing-1.jpgAnti-CCR3 Rabbit Monoclonal AntibodyWestern blot analysis of CCR3 using anti-CCR3 antibody (M01748). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR3 antigen affinity purified monoclonal antibody (M01748) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CCR3 at approximately 50 kDa. The expected band size for CCR3 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01748-ihc.jpgAnti-CCR3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human epidemal cells of skin, using CCR3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eea1-rabbit-monoclonal-antibody-m02296-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02296-eea1-primary-antibodies-wb-testing-1.jpgAnti-EEA1 Rabbit Monoclonal AntibodyWestern blot analysis of EEA1 using anti-EEA1 antibody (M02296). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EEA1 antigen affinity purified monoclonal antibody (M02296) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EEA1 at approximately 162 kDa. The expected band size for EEA1 is at 162 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02296-eea1-primary-antibodies-ihc-testing-1.jpgAnti-EEA1 Rabbit Monoclonal AntibodyIHC analysis of EEA1 using anti-EEA1 antibody (M02296). <br>EEA1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-EEA1 Antibody (M02296) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02296-eea1-primary-antibodies-ihc-testing-2.jpgAnti-EEA1 Rabbit Monoclonal AntibodyIHC analysis of EEA1 using anti-EEA1 antibody (M02296). <br>EEA1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-EEA1 Antibody (M02296) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02296-eea1-primary-antibodies-ihc-testing-3.jpgAnti-EEA1 Rabbit Monoclonal AntibodyIHC analysis of EEA1 using anti-EEA1 antibody (M02296). <br>EEA1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-EEA1 Antibody (M02296) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02296-eea1-primary-antibodies-ihc-testing-4.jpgAnti-EEA1 Rabbit Monoclonal AntibodyIHC analysis of EEA1 using anti-EEA1 antibody (M02296). <br>EEA1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-EEA1 Antibody (M02296) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tph1-rabbit-monoclonal-antibody-m01626-boster.html2026-04-03T05:00:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01626-tph1-primary-antibodies-wb-testing-1.jpgAnti-TPH1/Tph Rabbit Monoclonal AntibodyWestern blot analysis of TPH1 using anti-TPH1 antibody (M01626). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TPH1 antigen affinity purified monoclonal antibody (M01626) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TPH1 at approximately 70 kDa. The expected band size for TPH1 is at 51 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cox2-rabbit-monoclonal-antibody-m00084-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-wb7.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-wb.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyWestern blot analysis of COX2 expression in RAW264.7 cell lysate treated with LPS.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-12890_2024_3415_fig2_html.pngAnti-COX2 PTGS2 Rabbit Monoclonal Antibodyciprofol reduced LPS induced ferroptosis and increased antioxidant ability in mice. A - C Activities of malondialdehyde (MDA), glutathione (GSH), and superoxide dismutase (SOD) in the murine lung tissues ( n = 6 per group). D - G GPX4, 4-HNE and PTGS2 expressions in lung tissues detected by western blot ( n = 3 per group). H Expression level of Fe 2+ in murine lung tissues ( n = 6 per group). I 4-HNE expressions in lung tissues detected by immumohistochemical staining. J Transmission electron microscopy images of representative mitochondrial structures (scale bar, 1.0 μm). K quantitative analysis of 4-HNE-positive area ( n = 6 per group). Data are presented as Mean ± SD.Statistical analysis was performed using one-way ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12890-024-03415-w'>39609781</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-12890_2024_3415_fig4_html.pngAnti-COX2 PTGS2 Rabbit Monoclonal Antibodyciprofol reduced LPS induced ferroptosis and increased antioxidant ability in MLE12 cells. A ROS production detected by immunofluorescence and its quantification analysis ( n = 3 for each group). B - D Activities of malondialdehyde (MDA), glutathione (GSH), and superoxide dismutase (SOD) in MLE12 cell s ( n = 6 for each group). E , K Representative immunofluorescence images of 4-HNE, GPX4 and the quantification analysis in MLE12 cells ( n = 3 for each group). F - I GPX4, 4-HNE and PTGS2 expressions in MLE12 cells detected by western blot ( n = 3 for each group). J Expression level of Fe2 + in MLE12 cells ( n = 6 for each group). Data are presented as Mean ± SD. Statistical analysis was performed using one-way ANOVA.* p < 0.05, ** p < 0.01, *** p < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12890-024-03415-w'>39609781</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-12890_2024_3415_fig5_html.pngAnti-COX2 PTGS2 Rabbit Monoclonal Antibodyciprofol reduced LPS induced ferroptosis through Nrf2-dependent pathways in MLE12 cells. A Cell apoptosis detected by flow cytometry. B Cell viability determined by CCK8 assays ( n = 6 for each group). * P < 0.05 vs.LPS group; # P < 0.05 vs.LPS + Cip group. C Expression level of Fe 2+ in MLE12 cells. D - I GPX4, 4-HNE, PTGS2, Nrf2 and SL7A11 expressions in MLE12 cells detected by western blot ( n = 3 for each group). J Representative immunofluorescence images of Nrf2 and its quantification analysis in MLE12 cells ( n = 3 for each group). K Apoptotic rate measured by Annexin V-FITC/PI flow cytometry ( n = 3 for each group). Data are presented as Mean ± SD. Statistical analysis was performed using one-way ANOVA.* p < 0.05, ** p < 0.01, *** p < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12890-024-03415-w'>39609781</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-12890_2024_3415_fig6_html.pngAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyThe inhibition of ciprofol on ferroptosis was abolished in Nrf2 KO mice. A Representative HE staining images and lung injury score of the lung tissues ( n = 6 for each group). B Proinflammatory cytokine IL-1β, IL-6, and TNF-α levels in lung tissues ( n = 6 for each group). C Activities of MDA, GSH, SOD and Fe2 + content in lung tissues ( n = 6 for each group). D GPX4, 4-HNE expressions detected by immumohistochemical staining and the quantification analysis in lung tissues ( n = 3 for each group). E Nrf2 expressions detected by immumohistochemical staining and the quantification analysis in lung tissues ( n = 3 for each group). F GPX4, 4-HNE, PTGS2, Nrf2 and SL7A11 expressions detected by western blot in lung tissues ( n = 3 for each group). Data are presented as Mean ± SD. Statistical analysis was performed using t-test. * p < 0.05, ** p < 0.01, *** p < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12890-024-03415-w'>39609781</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-icc3.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-icc4.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-icc1.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-icc2.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00084-if.jpgAnti-COX2 PTGS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using COX2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-daxx-rabbit-monoclonal-antibody-m00439-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00439-wb7.jpgAnti-Daxx Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00439-wb.jpgAnti-Daxx Rabbit Monoclonal AntibodyWestern blot analysis of Calreticulin expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp8-rabbit-monoclonal-antibody-m01733-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01733-wb.jpgAnti-MMP8 Rabbit Monoclonal AntibodyWestern blot analysis of MMP8 expression in Human placenta lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01733-mmp8-primary-antibodies-ihc-testing-1.jpgAnti-MMP8 Rabbit Monoclonal AntibodyIHC analysis of MMP8 using anti-MMP8 antibody (M01733). <br>MMP8 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP8 Antibody (M01733) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01733-mmp8-primary-antibodies-ihc-testing-2.jpgAnti-MMP8 Rabbit Monoclonal AntibodyIHC analysis of MMP8 using anti-MMP8 antibody (M01733). <br>MMP8 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP8 Antibody (M01733) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01733-mmp8-primary-antibodies-ihc-testing-3.jpgAnti-MMP8 Rabbit Monoclonal AntibodyIHC analysis of MMP8 using anti-MMP8 antibody (M01733). <br>MMP8 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MMP8 Antibody (M01733) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aqp5-rabbit-monoclonal-antibody-m03085-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03085-wb.jpgAnti-AQP5 Rabbit Monoclonal AntibodyWestern blot analysis of AQP5 expression in SW480 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03085-ihc.jpgAnti-AQP5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse lung, using AQP5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grk2-rabbit-monoclonal-antibody-m01473-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01473-wb.jpgAnti-GRK2 ADRBK1 Rabbit Monoclonal AntibodyWestern blot analysis of GRK2 expression in THP-1 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sgk1-rabbit-monoclonal-antibody-m00673-boster.html2026-03-24T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-sgk1-primary-antibodies-wb-testing-1.jpgAnti-SGK1/Sgk Rabbit Monoclonal Antibody Western blot analysis of SGK1 using anti-SGK1 antibody (M00673). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse liver tissue lysates,<br>
Lane 4: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SGK1 antigen affinity purified monoclonal antibody (Catalog # M00673) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SGK1 at approximately 49 kDa. The expected band size for SGK1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-wb7.jpgAnti-SGK1/Sgk Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-sgk1-primary-antibodies-ihc-testing-2.jpgAnti-SGK1/Sgk Rabbit Monoclonal Antibody IHC analysis of SGK1 using anti-SGK1 antibody (M00673). <br>
SGK1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SGK1 Antibody (M00673) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-wb.jpgAnti-SGK1/Sgk Rabbit Monoclonal AntibodyWestern blot analysis of SGK1 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-sgk1-primary-antibodies-ihc-testing-3.jpgAnti-SGK1/Sgk Rabbit Monoclonal Antibody IHC analysis of SGK1 using anti-SGK1 antibody (M00673). <br>
SGK1 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SGK1 Antibody (M00673) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00673-sgk1-primary-antibodies-ihc-testing-4.jpgAnti-SGK1/Sgk Rabbit Monoclonal Antibody IHC analysis of SGK1 using anti-SGK1 antibody (M00673). <br>
SGK1 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SGK1 Antibody (M00673) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chk1-rabbit-monoclonal-antibody-m01060-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01060-wb7.jpgAnti-Chk1 CHEK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01060-wb.jpgAnti-Chk1 CHEK1 Rabbit Monoclonal AntibodyWestern blot analysis of Chk1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stk3-rabbit-monoclonal-antibody-m02224-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02224-stk3-primary-antibodies-wb-testing-1.jpgAnti-STK3/Mst2 Rabbit Monoclonal AntibodyWestern blot analysis of STK3 using anti-STK3 antibody (M02224). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human Hacat whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STK3 antigen affinity purified monoclonal antibody (M02224) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STK3 at approximately 56 kDa. The expected band size for STK3 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02224-ihc.jpgAnti-STK3/Mst2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using STK3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jnk2-rabbit-monoclonal-antibody-m02706-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-ihc9.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-mapk9-primary-antibodies-wb-testing-1.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal Antibody Western blot analysis of MAPK9 using anti-MAPK9 antibody (M02706). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: monkey COS-7 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAPK9 antigen affinity purified monoclonal antibody (Catalog # M02706) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAPK9 at approximately 48 kDa. The expected band size for MAPK9 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-ihc10.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-ihc7.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat intestine, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-ihc8.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-ihc.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using JNK2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02706-icc1.jpgAnti-JNK2 MAPK9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-msi2-rabbit-monoclonal-antibody-m02898-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02898-wb.jpgAnti-MSI2/Musashi 2 Rabbit Monoclonal AntibodyWestern blot analysis of MSI2 expression in T47 D cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02898-ihc.jpgAnti-MSI2/Musashi 2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung carcinoma, using MSI2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chk2-rabbit-monoclonal-antibody-m00277-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00277-wb.jpgAnti-Chk2 CHEK2 Rabbit Monoclonal AntibodyWestern blot analysis of Chk2 expression in (1) HeLa cell lysate; (2) 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00277-ihc.jpgAnti-Chk2 CHEK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using Chk2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00277-if.jpgAnti-Chk2 CHEK2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Chk2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jam1-rabbit-monoclonal-antibody-m02068-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02068-f11r-primary-antibodies-wb-testing-1.jpgAnti-JAM1 Rabbit Monoclonal AntibodyWestern blot analysis of F11R using anti-F11R antibody (M02068). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-F11R antigen affinity purified monoclonal antibody (M02068) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for F11R at approximately 38 kDa. The expected band size for F11R is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02068-ihc.jpgAnti-JAM1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human blader cancer, using JAM1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ku80-rabbit-monoclonal-antibody-m01275-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01275-wb7.jpgAnti-Ku80 XRCC5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01275-ihc.jpgAnti-Ku80 XRCC5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Ku80 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01275-wb8.jpgAnti-Ku80 XRCC5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01275-wb.jpgAnti-Ku80 XRCC5 Rabbit Monoclonal AntibodyWestern blot analysis of Ku80 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf7-rabbit-monoclonal-antibody-m00115-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00115-irf7-primary-antibodies-wb-testing-1.jpgAnti-IRF7 Rabbit Monoclonal AntibodyWestern blot analysis of IRF7 using anti-IRF7 antibody (M00115). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF7 antigen affinity purified monoclonal antibody (M00115) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IRF7 at approximately 54 kDa. The expected band size for IRF7 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00115-ihc.jpgAnti-IRF7 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human pancreas, using IRF7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00115-irf7-primary-antibodies-ip-testing-1.jpgAnti-IRF7 Rabbit Monoclonal AntibodyImmunoprecipitation analysis of IRF7 using anti-IRF7 (M00115).<br>
Mouse brain lysates were prepared in RIPA with protease inhibitors. Anti-IRF7 (M00115) was pre-bound to Protein A+G magnetic beads and incubated with the lysates; a normal rabbit IgG IP ran in parallel. Beads were washed with TBST and the bound proteins were eluted with SDS sample buffer by heating.
Proteins were separated on a 10% SDS-PAGE (80 V stacking / 120 V resolving) and transferred to NC membrane (≈150 mA, 50-90 min). Membranes were blocked with 5% milk/TBST, probed with M00115 (o/n, 4 °C), then with HRP anti-rabbit light-chain IgG (BM2007), and developed by ECL.<br>
Lane 1: Input (10% of starting lysate),<br>
Lane 2: Control IgG IP,<br>
Lane 3: IRF7 IP (M00115).<br>
A ~54 kDa band corresponding to IRF7 was detected in the IRF7 IP and positive-control lanes, while the IgG control showed no specific band.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hes1-rabbit-monoclonal-antibody-m01459-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-wb-testing-1.jpgAnti-Hes1 Rabbit Monoclonal Antibody Western blot analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U-87MG whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hes1 antigen affinity purified monoclonal antibody (Catalog # M01459) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hes1 at approximately 30 kDa. The expected band size for Hes1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-ihc.jpgAnti-Hes1 Rabbit Monoclonal AntibodyIHC analysis of Hes1 using anti-Hes1 antibody (M01459) on human liver.<br> Hes1 was detected in paraffin-embedded section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. Biotinylated goat anti Rabbit IgG IgG antibody was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-ihc-testing-2.jpgAnti-Hes1 Rabbit Monoclonal Antibody IHC analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-ihc-testing-3.jpgAnti-Hes1 Rabbit Monoclonal Antibody IHC analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-icc1.jpgAnti-Hes1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-ihc-testing-4.jpgAnti-Hes1 Rabbit Monoclonal Antibody IHC analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-ihc-testing-5.jpgAnti-Hes1 Rabbit Monoclonal Antibody IHC analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-ihc-testing-6.jpgAnti-Hes1 Rabbit Monoclonal Antibody IHC analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of human thyriod cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-if-testing-7.jpgAnti-Hes1 Rabbit Monoclonal Antibody IF analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-if-testing-8.jpgAnti-Hes1 Rabbit Monoclonal Antibody IF analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-if-testing-9.jpgAnti-Hes1 Rabbit Monoclonal Antibody IF analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-if-testing-10.jpgAnti-Hes1 Rabbit Monoclonal Antibody IF analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01459-hes1-primary-antibodies-if-testing-11.jpgAnti-Hes1 Rabbit Monoclonal Antibody IF analysis of Hes1 using anti-Hes1 antibody (M01459). <br>
Hes1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Hes1 Antibody (M01459) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/casestudy_m01459.jpgAnti-Hes1 Rabbit Monoclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lsp1-rabbit-monoclonal-antibody-m02992-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02992-lsp1-primary-antibodies-wb-testing-1.jpgAnti-LSP1 Rabbit Monoclonal Antibody Western blot analysis of LSP1 using anti-LSP1 antibody (M02992). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat spleen tissue lysates,<br>
Lane 2: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSP1 antigen affinity purified monoclonal antibody (Catalog # M02992) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LSP1 at approximately 52 kDa. The expected band size for LSP1 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02992-wb.jpgAnti-LSP1 Rabbit Monoclonal AntibodyWestern blot analysis of LSP1 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg7-rabbit-monoclonal-antibody-m00346-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00346-wb7.jpgAnti-ATG7/Apg7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00346-ihc.jpgAnti-ATG7/Apg7 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using ATG7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00346-wb8.jpgAnti-ATG7/Apg7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00346-wb.jpgAnti-ATG7/Apg7 Rabbit Monoclonal AntibodyWestern blot analysis of ATG7 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fntb-rabbit-monoclonal-antibody-m07620-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07620-wb.jpgAnti-FNTB Rabbit Monoclonal AntibodyWestern blot analysis of FNTB expression in (1) HepG2 cell lysate; (2) K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gars-rabbit-monoclonal-antibody-m04618-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04618-wb.jpgAnti-GARS Rabbit Monoclonal AntibodyWestern blot analysis of GARS expression in (1) Jurkat cell lysate; (2) 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04618-ihc.jpgAnti-GARS Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using GARS Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hmbs-rabbit-monoclonal-antibody-m01506-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01506-wb.jpgAnti-HMBS Rabbit Monoclonal AntibodyWestern blot analysis of HMBS expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tms1-rabbit-monoclonal-antibody-m00362-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00362-icc1.jpgAnti-TMS1 PYCARD Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00362-wb.jpgAnti-TMS1 PYCARD Rabbit Monoclonal AntibodyWestern blot analysis of TMS1 expression in U937 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gart-rabbit-monoclonal-antibody-m06061-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06061-wb.jpgAnti-GART Rabbit Monoclonal AntibodyWestern blot analysis of GART expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06061-ihc.jpgAnti-GART Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix cancer, using GART Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nsd3-rabbit-monoclonal-antibody-m05608-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05608-wb.jpgAnti-NSD3/WHSC1L1 Rabbit Monoclonal AntibodyWestern blot analysis of NSD3 expression in MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nqo2-rabbit-monoclonal-antibody-m03112-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03112-wb7.jpgAnti-NQO2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03112-wb8.jpgAnti-NQO2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03112-wb.jpgAnti-NQO2 Rabbit Monoclonal AntibodyWestern blot analysis of NQO2 expression in Mouse heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cpt2-rabbit-monoclonal-antibody-m02112-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-wb-testing-1.jpgAnti-CPT2 Rabbit Monoclonal Antibody Western blot analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CPT2 antigen affinity purified monoclonal antibody (Catalog # M02112) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CPT2 at approximately 74 kDa. The expected band size for CPT2 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-2.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-3.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-if.jpgAnti-CPT2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using CPT2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-4.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-5.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-6.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-7.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-8.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-9.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-10.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-11.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-12.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02112-cpt2-primary-antibodies-ihc-testing-13.jpgAnti-CPT2 Rabbit Monoclonal Antibody IHC analysis of CPT2 using anti-CPT2 antibody (M02112). <br>
CPT2 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CPT2 Antibody (M02112) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-asns-rabbit-monoclonal-antibody-m03302-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03302-wb.jpgAnti-ASNS/Asparagine Synthetase Rabbit Monoclonal AntibodyWestern blot analysis of ASNS expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03302-ihc.jpgAnti-ASNS/Asparagine Synthetase Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using ASNS Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-muc1-rabbit-monoclonal-antibody-m00187-1-boster.html2026-03-24T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-wb-testing-1.jpgAnti-MUC1 Rabbit Monoclonal AntibodyWestern blot analysis of CA15-3/MUC1 using anti-CA15-3/MUC1 antibody (M00187-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: rat lung tissue lysates,<br>
Lane 4: rat stomach tissue lysates,<br>
Lane 5: mouse lung tissue lysates,<br>
Lane 6: mouse stomach tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CA15-3/MUC1 antigen affinity purified monoclonal antibody (M00187-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CA15-3/MUC1 at approximately 17-30 kDa. The expected band size for CA15-3/MUC1 is at 122 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-fimmu-15-1337557-t001.jpgAnti-MUC1 Rabbit Monoclonal AntibodyCorrelation between the clinical parameters and MUC1 expression in oral tongue squamous cell carcer tissues.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1337557/full'>38390321</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-fimmu-15-1337557-g001.jpgAnti-MUC1 Rabbit Monoclonal AntibodyiPSC-derived MUC1-targeted CAR-NK cells restrict tumor growth in OTSCC xenograft mice without causing significant toxic side effects. (A) Tumor volume growth curves of OTSCC xenograft mice treated with iPSC-derived MUC1-targeted CAR-NK cells, iPSC-derived NK cells, and normal saline respectively (A left). Mouse weight changes in different treatment groups (A right). Black arrow represents the time of administration. The difference of each group (n = 10/group) was analyzed by two-way ANOVA and Sidak t test. **P < 0.01, ***P < 0.001. (B) Blood routine results of OTSCC xenograft mice after treatment with normal saline (n=4), iPSC-derived MUC1-targeted CAR-NK (n=10), iPSC-derived NK cells (n=8). *P < 0.05, **P < 0.01. One-way ANOVA and Tukey’s test. (C) IHC staining with primary antibodies to CD16, CD56 and MUC1 on sections of the tumor, liver, lung and spleen of a representative OTSCC xenograft mouse from the iPSC-derived MUC1-targeted CAR-NK cells treatment group. Scale bar: 50μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1337557/full'>38390321</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-fimmu-15-1337557-g002.jpgAnti-MUC1 Rabbit Monoclonal AntibodyMUC1 expression in human oral tongue squamous cell cancer. (A) Strong positive staining of MUC1. Positive staining of MUC1 was mainly located on the membrane and in the cytoplasm of cancer cells. (B) Moderate positive staining of MUC1. (C) Weak positive staining of MUC1. (D) Negative control. Scale bar: 30 µm. There was no significant difference of overall survival between MUC1 positive and MUC1 negative OTSCC patients either in stage III (P=0.07) (E) or in stage IV (P=0.32) (F) . Kaplan–Meier method and log-rank test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1337557/full'>38390321</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-fimmu-15-1337557-g003.jpgAnti-MUC1 Rabbit Monoclonal AntibodyEfficacy of the iPSC-derived MUC1-targeted CAR-NK cells against the MUC1-expressing human OTSCC cell lines. (A) Immunofluorescence of TSCCa cells. MUC1 positively expressed on TSCCa cell membrane. (B) Time curve of TSCCa cells killed by iPSC-derived MUC1-targeted CAR-NK cells detected by xCELLigence RTCA. Cell viability of TSCCa was calculated by xCELLigence and presented as Cell Index. ****P < 0.0001, One-way ANOVA and Tukey test. (C) The efficiency of iPSC-derived MUC1-targeted CAR-NK cells killing TSCCa cells in different ratio of cell concentration in vitro condition. Experiments were performed at the ratio of target cells to effector cells corresponding to 1:1, 1:3 and 1:10 respectively. ****P < 0.0001, One-way ANOVA and Tukey’s test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1337557/full'>38390321</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-ihc-testing-1.jpgAnti-MUC1 Rabbit Monoclonal AntibodyIHC analysis of MUC1 using anti-MUC1 antibody (M00187-1). <br>MUC1 was detected in a paraffin-embedded section of human breast cnacer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC1 Antibody (M00187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-ihc-testing-2.jpgAnti-MUC1 Rabbit Monoclonal AntibodyIHC analysis of MUC1 using anti-MUC1 antibody (M00187-1). <br>MUC1 was detected in a paraffin-embedded section of human breast cnacer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC1 Antibody (M00187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-ihc-testing-3.jpgAnti-MUC1 Rabbit Monoclonal AntibodyIHC analysis of MUC1 using anti-MUC1 antibody (M00187-1). <br>MUC1 was detected in a paraffin-embedded section of human ovarian cnacer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC1 Antibody (M00187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-ihc-testing-4.jpgAnti-MUC1 Rabbit Monoclonal AntibodyIHC analysis of MUC1 using anti-MUC1 antibody (M00187-1). <br>MUC1 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC1 Antibody (M00187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-1-muc1-primary-antibodies-ihc-testing-5.jpgAnti-MUC1 Rabbit Monoclonal AntibodyIHC analysis of MUC1 using anti-MUC1 antibody (M00187-1). <br>MUC1 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC1 Antibody (M00187-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd21-rabbit-monoclonal-antibody-m01632-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01632-wb7.jpgAnti-CD21 CR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01632-wb.jpgAnti-CD21 CR2 Rabbit Monoclonal AntibodyWestern blot analysis of CD21 expression in Raji cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01632-ihc.jpgAnti-CD21 CR2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CD21 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vav2-rabbit-monoclonal-antibody-m03014-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03014-wb.jpgAnti-VAV2 Rabbit Monoclonal AntibodyWestern blot analysis of VAV2 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03014-ihc.jpgAnti-VAV2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using VAV2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cox1-rabbit-monoclonal-antibody-m00811-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb7.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb10.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb8.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb11.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb9.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb12.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb13.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb14.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb15.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-wb.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyWestern blot analysis of COX1 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00811-ihc.jpgAnti-COX1 PTGS1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using COX1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dkk1-rabbit-monoclonal-antibody-m00632-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-wb7.jpgAnti-DKK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-ihc.jpgAnti-DKK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human placenta, using DKK1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-wb8.jpgAnti-DKK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-wb.jpgAnti-DKK1 Rabbit Monoclonal AntibodyWestern blot analysis of DKK1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd14-rabbit-monoclonal-antibody-m00137-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-wb7.jpgAnti-CD14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-ihc.jpgAnti-CD14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using CD14 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-wb8.jpgAnti-CD14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-if.jpgAnti-CD14 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562 cells, using CD14 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-wb.jpgAnti-CD14 Rabbit Monoclonal AntibodyWestern blot analysis of CD14 expression in Human tonsil cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-top1-rabbit-monoclonal-antibody-m00434-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00434-top1-primary-antibodies-wb-testing-1.jpgAnti-TOP1/Topoisomerase I Rabbit Monoclonal Antibody Western blot analysis of TOP1 using anti-TOP1 antibody (M00434). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hel whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat small intestine tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse small intestine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOP1 antigen affinity purified monoclonal antibody (Catalog # M00434) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TOP1 at approximately 100 kDa. The expected band size for TOP1 is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00434-wb7.jpgAnti-TOP1/Topoisomerase I Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00434-top1-primary-antibodies-ihc-testing-2_1.jpgAnti-TOP1/Topoisomerase I Rabbit Monoclonal Antibody IHC analysis of TOP1 using anti-TOP1 antibody (M00434). <br>
TOP1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TOP1 Antibody (M00434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00434-top1-primary-antibodies-ihc-testing-3_1.jpgAnti-TOP1/Topoisomerase I Rabbit Monoclonal Antibody IHC analysis of TOP1 using anti-TOP1 antibody (M00434). <br>
TOP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TOP1 Antibody (M00434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd13-rabbit-monoclonal-antibody-m02591-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02591-wb7.jpgAnti-CD13 ANPEP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02591-wb.jpgAnti-CD13 ANPEP Rabbit Monoclonal AntibodyWestern blot analysis of CD13 expression in THP-1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02591-ihc.jpgAnti-CD13 ANPEP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using CD13 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cybb-rabbit-monoclonal-antibody-m00328-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00328-nox2-primary-antibodies-wb-testing-1_2.jpgAnti-CYBB/Nox2 Rabbit Monoclonal AntibodyWestern blot analysis of NOX2 using anti-NOX2 antibody (M00328). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOX2 antigen affinity purified monoclonal antibody (M00328) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NOX2 at approximately 65 kDa. The expected band size for NOX2 is at 65 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd81-rabbit-monoclonal-antibody-m01281-1-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-wb7.jpgAnti-CD81 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-ihc9.jpgAnti-CD81 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-ihc7.jpgAnti-CD81 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-wb.jpgAnti-CD81 Rabbit Monoclonal AntibodyWestern blot analysis of CD81 expression in Ramos cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-ihc8.jpgAnti-CD81 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01281-1-ihc.jpgAnti-CD81 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using CD81 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd38-rabbit-monoclonal-antibody-m00193-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-cd38-primary-antibodies-wb-testing-1_1.jpgAnti-CD38 Rabbit Monoclonal Antibody Western blot analysis of CD38 anti-CD38 using antibody (M00193). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Ramos whole cell lysates, <br>
Lane 2: human Jurkat whole cell lysates, <br>
Lane 3: human THP-1 whole cell lysates, <br>
Lane 4: human Daudi whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD38 antigen affinity purified monoclonal antibody (M00193) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD38 at approximately 45 kDa. The expected band size for CD38 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-cd38-primary-antibodies-ihc-testing-1.jpgAnti-CD38 Rabbit Monoclonal AntibodyIHC analysis of CD38 using anti-CD38 antibody (M00193). <br>
CD38 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD38 Antibody (M00193) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-cd38-primary-antibodies-ihc-testing-2_1.jpgAnti-CD38 Rabbit Monoclonal AntibodyIHC analysis of CD38 using anti-CD38 antibody (M00193). <br>
CD38 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD38 Antibody (M00193) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-cd38-primary-antibodies-ihc-testing-3.jpgAnti-CD38 Rabbit Monoclonal AntibodyIHC analysis of CD38 using anti-CD38 antibody (M00193). <br>
CD38 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD38 Antibody (M00193) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-shp2-rabbit-monoclonal-antibody-m00150-1-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-wb-testing-1.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody Western blot analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHP2/PTPN11 antigen affinity purified monoclonal antibody (M00150-1) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHP2/PTPN11 at approximately 68 kDa. The expected band size for SHP2/PTPN11 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-2.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-3.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of human colon cnacer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-4.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-5.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-6.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-1-ptpn11-primary-antibodies-ihc-testing-7.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal Antibody IHC analysis of SHP2/PTPN11 using anti-SHP2/PTPN11 antibody (M00150-1). <br>SHP2/PTPN11 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SHP2/PTPN11 Antibody (M00150-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd68-rabbit-monoclonal-antibody-m00602-1-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00602-1-wb9.jpgAnti-CD68/Sr D1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00602-1-wb.jpgAnti-CD68/Sr D1 Rabbit Monoclonal AntibodyWestern blot analysis of CD68 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-shp2-rabbit-monoclonal-antibody-m00150-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-wb7.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-wb.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal AntibodyWestern blot analysis of SHP2 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00150-ihc.jpgAnti-SHP2 PTPN11 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human heart, using SHP2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkm2-rabbit-monoclonal-antibody-m01173-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01173-wb.jpgAnti-PKM2 Rabbit Monoclonal AntibodyWestern blot analysis of PKM2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01173-ihc.jpgAnti-PKM2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix cancer, using PKM2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg5-rabbit-monoclonal-antibody-m00240-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-atg5-primary-antibodies-wb-testing-1.jpgAnti-ATG5/Apg5 Rabbit Monoclonal Antibody Western blot analysis of ATG5/Apg5 using anti-ATG5/Apg5 antibody (M00240). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATG5/Apg5 antigen affinity purified monoclonal antibody (Catalog # M00240) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATG5/Apg5 at approximately 55 kDa. The expected band size for ATG5/Apg5 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-12964_2024_1628_fig3_html.pngAnti-ATG5/Apg5 Rabbit Monoclonal AntibodyHigh extracellular calcium([Ca 2+ ] o ) promotes autophagic flux. a,c RPMI8226 cells and KMS11cells were treated with or without CaCl 2 (1mM and 1.5mM) for 48h, followed by Western Blot to determin NCX1, ATG7, ATG5, P62 and LC3B-II/I levels under each condition, and summary data ( b , d ) (* p <0.05, ** p <0.01, n = 3). e , f The confocal microscopy images of RPMI8226 and KMS11 cells showed more yellow (autophagosomes) and red dots (autolysosomes) after treating with CaCl 2 (1.5mM) for 48h. Scale bar is 10µm. g The autophagosome marker protein LC3 was tandem labeled with RFP and GFP, and the autophage appeared yellow dots, while autolysosomes appeared red dots. h , i Histogram of the number of yellow dots and red dots. (** p <0.01, *** p <0.001, n = 9). j , k TEM analysis of autophagosomes (red arrow) and autolysosomes (black arrow) in RPMI8226 and KMS11 cells treated with or without CaCl 2 , and summary data ( l , m ) (* p <0.05, n = 4). Scale bar: 5 or 1μm. n , o RPMI8226 and KMS11cells were treated with BTZ (10nM) or/and CaCl 2 (1.5mM) for 24h, 48 h, 72h. The viability was detected by CCK8 assay (* p <0.05, ** p <0.01, n = 3) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01628-4'>38711131</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-12964_2024_1628_fig4_html.pngAnti-ATG5/Apg5 Rabbit Monoclonal AntibodyInhibition of NCX1 reverses the high [Ca 2+ ] o induced increase in autophagic flux in MM cells. a , b RPMI8226 and KMS11 cells were treated with 1.5mM CaCl 2 in combination with or without KB-R7943 for 48h. NCX1 protein and autophagic marker proteins (ATG7, ATG5, P62 and LC3B-II/I) were detected by western blot , and summary data ( b , d ) (* p <0.05, ** p <0.01, *** p <0.001, n = 3). e , f Representative images of confocal microscopy in RPMI8226 and KMS11 cells transduced with mRFP-GFP-LC3 lentivirus and treated with 1.5mM CaCl 2 in combination with or without KB-R7943/CQ for 48h. Scale bar is 10µm, and Histogram of the number of yellow dots (autophagosomes) and red dots (autolysosomes)( g , h ) (* p <0.05, ** p <0.01, *** p <0.001, n = 6). i , k TEM analysis of autophagosomes (red arrow) and autolysosomes (black arrow) in RPMI8226 and KMS11 cells treated with CaCl 2 in combination with or without KB-R7943/CQ, and summary data ( j , l ) (* p <0.05, ** p <0.01, n = 3). Scale bar: 5 or 1μm. m , n RPMI8226 and KMS11cells were treated with 10nM BTZ in combination with 1.5mM CaCl 2 with or without KB-7943/BAPTA for 24h, 48 h, 72h. The viability of MM cells was detected by CCK8 assay (* p <0.05, ** p <0.01, *** p <0.001, n = 3) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01628-4'>38711131</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-12964_2024_1628_fig7_html.pngAnti-ATG5/Apg5 Rabbit Monoclonal AntibodyNCX1 inhibition sensitizes MM cells to bortezomib in xenograft mouse models. a RPMI8226 and KMS11 cells(1×10 7 ) were subcutaneously injected into the right groin of NCG mice, and 10 days later were treated with intraperitoneal bortezomib injections(0.5 mg/kg), twice a week, and intraperitoneal KB-R7943 injections (5 mg/kg) three times a week. On day 35 following MM cell inoculation, mice were sacrificed and tumors were assessed for MM burden. b Photographic images of resected tumor from all the mice in each group. c Changes in tumor volume. Tumor diameters were measured with calipers once a week (5 mice per group), and tumor volumes were estimated using the following formula v=π/6 * L * W * H, where "L", "W" and "H" are the longest diameter, shortest diameter and height of the tumor respectively. Data are presented as the mean±SD from 5 mice (* p <0.05, ** p <0.01, n =5). d Mean tumor weights at day 35 after inoculation MM cells (** p <0.01, *** p <0.001, n =5). e Mean body weights at day 35 after inoculation MM cells. f Representative images of immunohistochemical staining for NCX1, CD138, Ki67, ATG5 and ATG7 in the subcutaneous tumours, and summary data (g) (* p <0.05, ** p <0.01,*** p <0.001, n =3). The magnifications are 20x. Scale bar:50μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01628-4'>38711131</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-ihc.jpgAnti-ATG5/Apg5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human ovarian cancer, using ATG5 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00240-if.jpgAnti-ATG5/Apg5 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Raji cells, using ATG5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-relb-rabbit-monoclonal-antibody-m00836-1-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00836-1-wb7.jpgAnti-RelB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00836-1-wb.jpgAnti-RelB Rabbit Monoclonal AntibodyWestern blot analysis of RelB expression in Raji cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00836-1-ihc.jpgAnti-RelB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using RelB Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gli1-rabbit-monoclonal-antibody-m00527-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00527-wb7.jpgAnti-Gli1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00527-wb8.jpgAnti-Gli1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00527-wb.jpgAnti-Gli1 Rabbit Monoclonal AntibodyWestern blot analysis of Gli1 expression in A549 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-agr2-rabbit-monoclonal-antibody-m02922-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02922-agr2-primary-antibodies-wb-testing-1.jpgAnti-AGR2/Ag 2 Rabbit Monoclonal AntibodyWestern blot analysis of AGR2 using anti-AGR2 antibody (M02922). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AGR2 antigen affinity purified monoclonal antibody (M02922) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AGR2 at approximately 17 kDa. The expected band size for AGR2 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02922-ihc.jpgAnti-AGR2/Ag 2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using AGR2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02922-icc1.jpgAnti-AGR2/Ag 2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf3-rabbit-monoclonal-antibody-m00165-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-wb7.jpgAnti-IRF3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-irf3-primary-antibodies-wb-testing-1_1.jpgAnti-IRF3 Rabbit Monoclonal Antibody Western blot analysis of IRF3 using anti-IRF3 antibody (M00165). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF3 antigen affinity purified monoclonal antibody (M00165) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IRF3 at approximately 60 kDa. The expected band size for IRF3 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-ihc9.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human ovarian cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-ihc7.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-ihc8.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-ihc.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix carcinoma, using IRF3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-icc1.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00165-if.jpgAnti-IRF3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using IRF3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-oct4-rabbit-monoclonal-antibody-m00174-boster.html2026-03-24T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00174-wb7.jpgAnti-Oct4 POU5F1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00174-if.jpgAnti-Oct4 POU5F1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of NCCIT cells, using Oct4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00174-wb.jpgAnti-Oct4 POU5F1 Rabbit Monoclonal AntibodyWestern blot analysis of Oct4 expression in NCCIT cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00174-ihc.jpgAnti-Oct4 POU5F1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human seminoma, using Oct4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ace2-rabbit-monoclonal-antibody-m00756-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-wb7.jpgAnti-ACE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-wb8.jpgAnti-ACE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-wb9.jpgAnti-ACE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-wb.jpgAnti-ACE2 Rabbit Monoclonal AntibodyWestern blot analysis of ACE2 expression in Human kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc7.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc8.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc9.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc10.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc11.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous cell carcinoma , using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00756-ihc.jpgAnti-ACE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using ACE2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd10-rabbit-monoclonal-antibody-m04065-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04065-wb.jpgAnti-CD10 MME Rabbit Monoclonal AntibodyWestern blot analysis of CD10 expression in Jurkat lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-arf1-rabbit-monoclonal-antibody-m01279-1-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01279-1-arf1-primary-antibodies-wb-testing-1.jpgAnti-ARF1 Rabbit Monoclonal AntibodyWestern blot analysis of ARF1 using anti-ARF1 antibody (M01279-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat small intestines tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse small intestines tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARF1 antigen affinity purified monoclonal antibody (M01279-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ARF1 at approximately 18 kDa. The expected band size for ARF1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01279-1-arf1-primary-antibodies-wb-testing-2.jpgAnti-ARF1 Rabbit Monoclonal AntibodyWestern blot analysis of ARF1 using anti-ARF1 antibody (M01279-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat small intestine tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse small intestine tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARF1 antigen affinity purified monoclonal antibody (M01279-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ARF1 at approximately 18 kDa. The expected band size for ARF1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01279-1-arf1-primary-antibodies-ihc-testing-4.jpgAnti-ARF1 Rabbit Monoclonal AntibodyIHC analysis of ARF1 using anti-ARF1 antibody (M01279-1). <br>ARF1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ARF1 Antibody (M01279-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01279-1-arf1-primary-antibodies-ihc-testing-2.jpgAnti-ARF1 Rabbit Monoclonal AntibodyIHC analysis of ARF1 using anti-ARF1 antibody (M01279-1). <br>ARF1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ARF1 Antibody (M01279-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01279-1-arf1-primary-antibodies-ihc-testing-3.jpgAnti-ARF1 Rabbit Monoclonal AntibodyIHC analysis of ARF1 using anti-ARF1 antibody (M01279-1). <br>ARF1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ARF1 Antibody (M01279-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-brg1-rabbit-monoclonal-antibody-m00223-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-wb-testing-1.jpgAnti-BRG1 Rabbit Monoclonal AntibodyWestern blot analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMARCA4/BRG1 antigen affinity purified monoclonal antibody (M00223) at 1: 5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SMARCA4/BRG1 at approximately 220 kDa. The expected band size for SMARCA4/BRG1 is at 185 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-wb-testing-2.jpgAnti-BRG1 Rabbit Monoclonal AntibodyWestern blot analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse RAW264.7 whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMARCA4/BRG1 antigen affinity purified monoclonal antibody (M00223) at 1: 5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SMARCA4/BRG1 at approximately 220 kDa. The expected band size for SMARCA4/BRG1 is at 185 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-1.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-2.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-3.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-4.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-5.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-6.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00223-smarca4-primary-antibodies-ihc-testing-7.jpgAnti-BRG1 Rabbit Monoclonal AntibodyIHC analysis of SMARCA4/BRG1 using anti-SMARCA4/BRG1 antibody (M00223). <br>SMARCA4/BRG1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SMARCA4/BRG1 Antibody (M00223) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd36-rabbit-monoclonal-antibody-m01189-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-wb.jpgAnti-CD36/Sr B3 Rabbit Monoclonal AntibodyWestern blot analysis of CD36 expression in 3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-wb7.jpgAnti-CD36/Sr B3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-wb8.jpgAnti-CD36/Sr B3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-cd36-primary-antibodies-ihc-testing-1.jpgAnti-CD36/Sr B3 Rabbit Monoclonal AntibodyIHC analysis of CD36 using anti-CD36 antibody (M01189). <br>CD36 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD36 Antibody (M01189) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-e2f2-rabbit-monoclonal-antibody-m02896-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02896-wb.jpgAnti-E2F2 Rabbit Monoclonal AntibodyWestern blot analysis of E2F2 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf5-rabbit-monoclonal-antibody-m00958-1-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-1-wb7.jpgAnti-IRF5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-1-wb.jpgAnti-IRF5 Rabbit Monoclonal AntibodyWestern blot analysis of IRF5 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab7-rabbit-monoclonal-antibody-m02409-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02409-rab7-primary-antibodies-wb-testing-1.jpgAnti-RAB7 RAB7A Rabbit Monoclonal Antibody Western blot analysis of RAB7 using anti-RAB7 antibody (M02409). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A375 whole cell lysates,<br>
Lane 2: human HT1080 whole cell lysates,<br>
Lane 3: human U87 whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat L6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse C2C12 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB7 antigen affinity purified monoclonal antibody (Catalog # M02409) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB7 at approximately 23 kDa. The expected band size for RAB7 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02409-ihc.jpgAnti-RAB7 RAB7A Rabbit Monoclonal Antibodymmunohistochemical analysis of paraffin-embedded human colon, using RAB7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02409-if.jpgAnti-RAB7 RAB7A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using RAB7 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf6-rabbit-monoclonal-antibody-m01822-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01822-wb.jpgAnti-IRF6 Rabbit Monoclonal AntibodyWestern blot analysis of IRF6 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smc1-rabbit-monoclonal-antibody-m02148-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02148-wb.jpgAnti-SMC1 SMC1A Rabbit Monoclonal AntibodyWestern blot analysis of SMC1 expression in (1) HeLa cell lysate; (2) Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk8-rabbit-monoclonal-antibody-m01493-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-cdk8-primary-antibodies-wb-testing-1.jpgAnti-CDK8 Rabbit Monoclonal Antibody Western blot analysis of CDK8 using anti-CDK8 antibody (M01493). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human MOLT-4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-CDK8 antigen affinity purified monoclonal antibody (Catalog # M01493) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDK8 at approximately 60 kDa. The expected band size for CDK8 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-wb7.jpgAnti-CDK8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-wb8.jpgAnti-CDK8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-icc1.jpgAnti-CDK8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-icc2.jpgAnti-CDK8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01493-icc3.jpgAnti-CDK8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk7-rabbit-monoclonal-antibody-m00552-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00552-wb.jpgAnti-CDK7 Rabbit Monoclonal AntibodyWestern blot analysis of CDK7 expression in MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf5-rabbit-monoclonal-antibody-m00958-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-wb7.jpgAnti-IRF5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-wb.jpgAnti-IRF5 Rabbit Monoclonal AntibodyWestern blot analysis of IRF5 expression in THP-1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-wb8.jpgAnti-IRF5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00958-wb9.jpgAnti-IRF5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox1-rabbit-monoclonal-antibody-m08724-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08724-sox1-primary-antibodies-wb-testing-1.jpgAnti-SOX1 Rabbit Monoclonal Antibody Western blot analysis of SOX1 using anti-SOX1 antibody (M08724). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-SOX1 antigen affinity purified monoclonal antibody (Catalog # M08724) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX1 at approximately 39 kDa. The expected band size for SOX1 is at 39 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk4-rabbit-monoclonal-antibody-m00159-1-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-1-wb7.jpgAnti-CDK4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-1-ihc.jpgAnti-CDK4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach cancer, using CDK4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-1-wb8.jpgAnti-CDK4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-1-if.jpgAnti-CDK4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using CDK4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-1-wb.jpgAnti-CDK4 Rabbit Monoclonal AntibodyWestern blot analysis of CDK4 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irs1-rabbit-monoclonal-antibody-m00268-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00268-wb.jpgAnti-IRS1 Rabbit Monoclonal AntibodyWestern blot analysis of IRS1 expression in HEK293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk9-rabbit-monoclonal-antibody-m00794-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-wb-testing-1.jpgAnti-CDK9 Rabbit Monoclonal Antibody Western blot analysis of CDK9 using anti-CDK9 antibody (M00794). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HL-60 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human A431 whole cell lysates,<br>
Lane 6: human HepG2 whole cell lysates,<br>
Lane 7: human Hacat whole cell lysates,<br>
Lane 8: human THP-1 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK9 antigen affinity purified monoclonal antibody (M00794) at a dilution of 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDK9 at approximately 38 kDa. The expected band size for CDK9 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-ihc-testing-2.jpgAnti-CDK9 Rabbit Monoclonal Antibody IHC analysis of CDK9 using anti-CDK9 antibody (M00794). <br>CDK9 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK9 Antibody (M00794) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-ihc-testing-3.jpgAnti-CDK9 Rabbit Monoclonal Antibody IHC analysis of CDK9 using anti-CDK9 antibody (M00794). <br>CDK9 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK9 Antibody (M00794) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-ihc-testing-4.jpgAnti-CDK9 Rabbit Monoclonal Antibody IHC analysis of CDK9 using anti-CDK9 antibody (M00794). <br>CDK9 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK9 Antibody (M00794) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-ihc-testing-5.jpgAnti-CDK9 Rabbit Monoclonal Antibody IHC analysis of CDK9 using anti-CDK9 antibody (M00794). <br>CDK9 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK9 Antibody (M00794) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00794-cdk9-primary-antibodies-ihc-testing-6.jpgAnti-CDK9 Rabbit Monoclonal Antibody IHC analysis of CDK9 using anti-CDK9 antibody (M00794). <br>CDK9 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK9 Antibody (M00794) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk6-rabbit-monoclonal-antibody-m00358-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00358-cdk6-primary-antibodies-wb-testing-1.jpgAnti-CDK6 Rabbit Monoclonal Antibody Western blot analysis of CDK6 using anti-CDK6 antibody (M00358). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK6 antigen affinity purified monoclonal antibody (Catalog # M00358) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDK6 at approximately 37 kDa. The expected band size for CDK6 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00358-ihc.jpgAnti-CDK6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer, using CDK6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00358-if.jpgAnti-CDK6 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562 cells, using CDK6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdk4-rabbit-monoclonal-antibody-m00159-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-cimb-46-00840-g004.jpgAnti-CDK4 Rabbit Monoclonal AntibodyLY6K knockdown inhibits cell proliferation by causing cell-cycle arrest in the G1-phase. ( A ) MTS assays showing the proliferation potential of CCSCs after siLY6K transfection. Values are the mean ± SE (n = 3). ** p < 0.01 or **** p < 0.0001 and ### p < 0.001 or #### p < 0.0001 indicate significant differences from the Mock and siNC groups, respectively, as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. ( B ) Flow cytometric analyses showing the cell-cycle progression in CCSCs and number of CCSCs in each cell-cycle phase. Values are the mean ± SE (n = 3). ## p < 0.01 and *** p < 0.001 indicate significant differences from the Mock and siNC groups, respectively, as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. ( C ) Western blot analyses showing the protein levels of cyclin D1, CDK4, cyclin E1, and CDK2 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). *** p < 0.001 or **** p < 0.0001 indicates significant differences from the Mock and siNC groups as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. ( D ) Flow cytometric analyses of Annexin V-FITC/PI staining of CCSCs following siLY6K or siNC transfection for 48 h. Values are the mean ± SE (n = 3). Lower-left quadrant: viable cells; upper-right and lower-right quadrants: apoptotic cells; upper-left quadrants: necrotic cells. ( E ) Western blot analyses showing the protein levels of caspase-3 and cleaved caspase-3 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; CDK, cyclin-dependent kinase; PI, propidium iodide; FITC, fluorescein isothiocyanate; n.s., not significant. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11727511/'>39727968</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-cdk4-primary-antibodies-wb-testing-1.jpgAnti-CDK4 Rabbit Monoclonal Antibody Western blot analysis of CDK4 using anti-CDK4 antibody (M00159). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat pancreas tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse pancreas tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK4 antigen affinity purified monoclonal antibody (Catalog # M00159) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDK4 at approximately 34 kDa. The expected band size for CDK4 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00159-if.jpgAnti-CDK4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of NIH/3T3 cells, using CDK4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irf2-rabbit-monoclonal-antibody-m02935-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02935-wb.jpgAnti-IRF2 Rabbit Monoclonal AntibodyWestern blot analysis of IRF2 expression in (1) HeLa cell lysate; (2) 3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02935-wb7.jpgAnti-IRF2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atf7-rabbit-monoclonal-antibody-m04951-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04951-wb7.jpgAnti-ATF7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04951-wb8.jpgAnti-ATF7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04951-wb.jpgAnti-ATF7 Rabbit Monoclonal AntibodyWestern blot analysis of ATF7 expression in (1) Raji cell lysate; (2) Raw 264.7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atf1-rabbit-monoclonal-antibody-m01600-boster.html2026-03-24T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01600-wb.jpgAnti-ATF1 Rabbit Monoclonal AntibodyWestern blot analysis of ATF1 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pten-rabbit-monoclonal-antibody-m00006-2-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-pten-primary-antibodies-wb-testing-1.jpgAnti-PTEN Rabbit Monoclonal Antibody Western blot analysis of PTEN using anti-PTEN antibody (M00006-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified monoclonal antibody (Catalog # M00006-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTEN at approximately 54 kDa. The expected band size for PTEN is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PTEN Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-pten-primary-antibodies-wb-testing-2.pngAnti-PTEN Rabbit Monoclonal AntibodyWestern blot analysis of PTEN using anti-PTEN antibody (M00006-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates, <br>
Lane 2: Model group-rat colon tissue lysates, <br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates, <br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates, <br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates, <br>
Lane 6: Western medicine treatment-rat colon tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified monoclonal antibody (Catalog # M00006-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for PTEN at approximately 54 kDa. The expected band size for PTEN is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc7.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat lung, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc8.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc9.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tongue cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc10.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-ihc11.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00006-2-if.jpgAnti-PTEN Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PTEN Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek2-rabbit-monoclonal-antibody-m00996-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00996-map2k2-primary-antibodies-wb-testing-1_1.jpgAnti-MEK2 MAP2K2 Rabbit Monoclonal AntibodyWestern blot analysis of MAP2K2 using anti-MAP2K2 antibody (M00996). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: mouse skeletal muscle tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP2K2 antigen affinity purified monoclonal antibody (M00996) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MAP2K2 at approximately 44 kDa. The expected band size for MAP2K2 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00996-map2k2-primary-antibodies-ihc-testing-1.jpgAnti-MEK2 MAP2K2 Rabbit Monoclonal AntibodyIHC analysis of MAP2K2 using anti-MAP2K2 antibody (M00996). <br>MAP2K2 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MAP2K2 Antibody (M00996) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00996-map2k2-primary-antibodies-ip-testing-1.jpgAnti-MEK2 MAP2K2 Rabbit Monoclonal AntibodyImmunoprecipitating (IP) MAP2K2 in K562 whole cell lysate.<br>
Western blot analysis of MAP2K2 using anti-MAP2K2 antibody (M00996); <br>
Lane 1: K562 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-MAP2K2 antibody in K562 whole cell lysate;<br>
Lane 3: anti-MAP2K2 antibody (2μg) + K562 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MAP2K2 antigen affinity purified monoclonal antibody (M00996) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MAP2K2 at approximately 44 kDa. The expected band size for MAP2K2 is at 44 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erk5-rabbit-monoclonal-antibody-m02812-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02812-wb7.jpgAnti-ERK5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02812-icc1.jpgAnti-ERK5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02812-wb.jpgAnti-ERK5 Rabbit Monoclonal AntibodyWestern blot analysis of ERK5 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek5-rabbit-monoclonal-antibody-m03980-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03980-wb7.jpgAnti-MEK5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03980-wb8.jpgAnti-MEK5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03980-wb.jpgAnti-MEK5 Rabbit Monoclonal AntibodyWestern blot analysis of MEK5 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek7-rabbit-monoclonal-antibody-m02713-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02713-map2k7-primary-antibodies-wb-testing-1.jpgAnti-MEK7 MAP2K7 Rabbit Monoclonal Antibody Western blot analysis of MKK7/MAP2K7 using anti-MKK7/MAP2K7 antibody (M02713). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MKK7/MAP2K7 antigen affinity purified monoclonal antibody (M02713) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MKK7/MAP2K7 at approximately 47 kDa. The expected band size for MKK7/MAP2K7 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atf4-rabbit-monoclonal-antibody-m00371-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-atf4-primary-antibodies-wb-testing-1.jpgAnti-ATF4 Rabbit Monoclonal Antibody Western blot analysis of ATF4 using anti-ATF4 antibody (M00371). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF4 antigen affinity purified monoclonal antibody (Catalog # M00371) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF4 at approximately 55 kDa. The expected band size for ATF4 is at 39,55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-wb7.jpgAnti-ATF4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-wb9.jpgAnti-ATF4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-atf4-primary-antibodies-wb-testing-2.pngAnti-ATF4 Rabbit Monoclonal Antibody Western blot analysis of ATF4 using anti-ATF4 antibody (M00371). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Different intestinal tissues from pigs infected with classical swine fever.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF4 antigen affinity purified monoclonal antibody (Catalog # M00371) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with ChemiDoc MP system. A specific band was detected for ATF4 at approximately 45-50 kDa. The expected band size for ATF4 is at 39,55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-ihc.jpgAnti-ATF4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using ATF4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-icc1.jpgAnti-ATF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-icc2.jpgAnti-ATF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-icc3.jpgAnti-ATF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00371-if.jpgAnti-ATF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using ATF4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek3-rabbit-monoclonal-antibody-m02916-1-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-1-mek3-primary-antibodies-wb-testing-1.jpgAnti-MEK3 MAP2K3 Rabbit Monoclonal AntibodyWestern blot analysis of MEK3 using anti-MEK3 antibody (M02916-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEK3 antigen affinity purified monoclonal antibody (M02916-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MEK3 at approximately 39 kDa. The expected band size for MEK3 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-1-ihc.jpgAnti-MEK3 MAP2K3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using MEK3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atf5-rabbit-monoclonal-antibody-m02792-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-atf5-primary-antibodies-wb-testing-1.jpgAnti-ATF5 Rabbit Monoclonal Antibody Western blot analysis of ATF5 using anti-ATF5 antibody (M02792). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human K562 whole cell lysates, <br>
Lane 3: human THP-1 whole cell lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF5 antigen affinity purified monoclonal antibody (M02792) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF5 at approximately 35 kDa. The expected band size for ATF5 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-atf5-primary-antibodies-ihc-testing-2.jpgAnti-ATF5 Rabbit Monoclonal Antibody IHC analysis of ATF5 using anti-ATF5 antibody (M02792). <br>
ATF5 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit ATF5 Antibody (M02792) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-atf5-primary-antibodies-ihc-testing-3.jpgAnti-ATF5 Rabbit Monoclonal Antibody IHC analysis of ATF5 using anti-ATF5 antibody (M02792). <br>
ATF5 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit ATF5 Antibody (M02792) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-atf5-primary-antibodies-if-testing-3.jpg.jpgAnti-ATF5 Rabbit Monoclonal AntibodyICC staining of ATF5 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (1/50) for 1 hour at room temperature, washed with PBShttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-icc1.jpgAnti-ATF5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02792-icc2.jpgAnti-ATF5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax6-rabbit-monoclonal-antibody-m00273-2-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-2-wb7.jpgAnti-PAX6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-2-wb.jpgAnti-PAX6 Rabbit Monoclonal AntibodyWestern blot analysis of PAX6 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-2-wb8.jpgAnti-PAX6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-2-wb9.jpgAnti-PAX6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-junb-rabbit-monoclonal-antibody-m01825-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01825-wb7.jpgAnti-JunB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01825-wb.jpgAnti-JunB Rabbit Monoclonal AntibodyWestern blot analysis of JunB expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax9-rabbit-monoclonal-antibody-m03356-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03356-wb7.jpgAnti-PAX9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03356-wb.jpgAnti-PAX9 Rabbit Monoclonal AntibodyWestern blot analysis of PAX9 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03356-wb8.jpgAnti-PAX9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03356-wb9.jpgAnti-PAX9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax2-rabbit-monoclonal-antibody-m01288-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01288-wb.jpgAnti-PAX2 Rabbit Monoclonal AntibodyWestern blot analysis of PAX2 expression in Human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jnk3-rabbit-monoclonal-antibody-m04297-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04297-jnk3-primary-antibodies-wb-testing-1.jpgAnti-JNK3 Rabbit Monoclonal Antibody Western blot analysis of JNK3 using anti-JNK3 antibody (M04297). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JNK3 antigen affinity purified monoclonal antibody (Catalog # M04297) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for JNK3 at approximately 50,53 kDa. The expected band size for JNK3 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04297-icc1.jpgAnti-JNK3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04297-icc2.jpgAnti-JNK3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jund-rabbit-monoclonal-antibody-m05609-1-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05609-1-wb.jpgAnti-JunD Rabbit Monoclonal AntibodyWestern blot analysis of JunD expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax6-rabbit-monoclonal-antibody-m00273-3-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-3-pax6-primary-antibodies-wb-testing-1.jpgAnti-PAX6 Rabbit Monoclonal AntibodyWestern blot analysis of PAX6 using anti-PAX6 antibody (M00273-3). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Hela whole cell lysates
Lane 5: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX6 antigen affinity purified monoclonal antibody (M00273-3) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PAX6 at approximately 49 kDa. The expected band size for PAX6 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-3-pax6-primary-antibodies-ihc-testing-1.jpgAnti-PAX6 Rabbit Monoclonal AntibodyIHC analysis of PAX6 using anti-PAX6 antibody (M00273-3). <br>
PAX6 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PAX6 Antibody (M00273-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00273-3-pax6-primary-antibodies-ihc-testing-2.jpgAnti-PAX6 Rabbit Monoclonal AntibodyIHC analysis of PAX6 using anti-PAX6 antibody (M00273-3). <br>
PAX6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PAX6 Antibody (M00273-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax7-rabbit-monoclonal-antibody-m00845-1-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00845-1-wb8.jpgAnti-PAX7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00845-1-wb9.jpgAnti-PAX7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00845-1-wb.jpgAnti-PAX7 Rabbit Monoclonal AntibodyWestern blot analysis of PAX7 expression in HeLa lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jund-rabbit-monoclonal-antibody-m05609-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05609-wb.jpgAnti-JunD Rabbit Monoclonal AntibodyWestern blot analysis of JunD expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc6-rabbit-monoclonal-antibody-m01355-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01355-wb.jpgAnti-Cdc6 Rabbit Monoclonal AntibodyWestern blot analysis of Cdc6 expression in Hela cell lysate treated with hydroxyurea.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc5-rabbit-monoclonal-antibody-m03797-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03797-wb.jpgAnti-CDC5 CDC5L Rabbit Monoclonal AntibodyWestern blot analysis of CDC5 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-uba1-rabbit-monoclonal-antibody-m02810-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-2.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-wb-testing-1.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody Western blot analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human SiHa whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UBA1 antigen affinity purified monoclonal antibody (Catalog # M02810) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for UBA1 at approximately 118 kDa. The expected band size for UBA1 is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-3.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-4.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-5.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-6.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-7.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-8.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-9.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-10.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-11.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-12.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02810-uba1-primary-antibodies-ihc-testing-13.jpgAnti-UBA1/Ube1 Rabbit Monoclonal Antibody IHC analysis of UBA1 using anti-UBA1 antibody (M02810). <br>
UBA1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-UBA1 Antibody (M02810) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-raf1-rabbit-monoclonal-antibody-m00446-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-wb7.jpgAnti-Raf1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-wb8.jpgAnti-Raf1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-wb.jpgAnti-Raf1 Rabbit Monoclonal AntibodyWestern blot analysis of Raf1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00446-raf1-primary-antibodies-icc-testing-1.jpgAnti-Raf1 Rabbit Monoclonal AntibodyICC/IF analysis of Raf1 using anti-Raf1 antibody (M00446). <br>
Raf1 was detected in an immunocytochemical section of human HEK293T cells. The cells were fixed with 4% paraformaldehyde for 10 minutes and then treated with a membrane permeabilization agent (AR0205) for 5 minutes.The cells were blocked with 10% goat serum. And then incubated with rabbit anti-Raf1 Antibody (M00446) at a dilution of 1:50 overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax5-rabbit-monoclonal-antibody-m00669-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-pax5-primary-antibodies-wb-testing-1.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyWestern blot analysis of BSAP/PAX5 using anti-BSAP/PAX5 antibody (M00669). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human MCF7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BSAP/PAX5 antigen affinity purified monoclonal antibody (M00669) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BSAP/PAX5 at approximately 45 kDa. The expected band size for BSAP/PAX5 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-pax5-primary-antibodies-ihc-testing-1.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyIHC analysis of BSAP/PAX5 using anti-BSAP/PAX5 antibody (M00669). <br>BSAP/PAX5 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BSAP/PAX5 Antibody (M00669) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-pax5-primary-antibodies-ihc-testing-2.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyIHC analysis of BSAP/PAX5 using anti-BSAP/PAX5 antibody (M00669). <br>BSAP/PAX5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BSAP/PAX5 Antibody (M00669) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-pax5-primary-antibodies-ihc-testing-3.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyIHC analysis of BSAP/PAX5 using anti-BSAP/PAX5 antibody (M00669). <br>BSAP/PAX5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BSAP/PAX5 Antibody (M00669) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-pax5-primary-antibodies-ihc-testing-4.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyIHC analysis of BSAP/PAX5 using anti-BSAP/PAX5 antibody (M00669). <br>BSAP/PAX5 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BSAP/PAX5 Antibody (M00669) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-if.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyImmunofluorescent analysis of Ramos cells, using PAX5 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00669-icc1.jpgAnti-PAX5/Bsap Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pax8-rabbit-monoclonal-antibody-m00943-2-boster.html2026-03-24T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00943-2-wb7.jpgAnti-PAX8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00943-2-wb.jpgAnti-PAX8 Rabbit Monoclonal AntibodyWestern blot analysis of PAX8 expression in SK-OV-3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sod2-rabbit-monoclonal-antibody-m00349-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-sod2-primary-antibodies-wb-testing-1.jpgAnti-SOD2/Mnsod Rabbit Monoclonal Antibody Western blot analysis of SOD2/Mnsod using anti-SOD2/Mnsod antibody (M00349). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat spleen tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse spleen tissue lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOD2/Mnsod antigen affinity purified monoclonal antibody (Catalog # M00349) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOD2/Mnsod at approximately 25 kDa. The expected band size for SOD2/Mnsod is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-sod2-primary-antibodies-wb-testing-2.jpgAnti-SOD2/Mnsod Rabbit Monoclonal Antibody Western blot analysis of SOD2/Mnsod using anti-SOD2/Mnsod antibody (M00349). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat small intestine tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 3: mouse small intestine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOD2/Mnsod antigen affinity purified monoclonal antibody (Catalog # M00349) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOD2/Mnsod at approximately 25 kDa. The expected band size for SOD2/Mnsod is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-1-s2.0-s2214388225000931-gr2.jpgAnti-SOD2/Mnsod Rabbit Monoclonal AntibodyTTM treatment reduces kidney copper content, cuproptosis-related proteins, and ROS in a CaOx deposition mouse model. (A) Renal copper content across four groups; (B) The WB analysis of cuproptosis-related proteins (Lip-DLAT, Lip-DLST, ACO2, LIAS, HSP70, FDX1, and GAPDH); no quantification performed due to obvious differences; (C) IHC staining of FDX1 ( × 200; scale bar 100 μm), NOX2 ( × 100; scale bar 200 μm) and SOD2 ( × 100; scale bar 200 μm) in the renal cortex; (D) Quantification of FDX1 IHC staining (IOD values), corresponding to panel C; (E) Quantification of NOX2 IHC staining (IOD values), corresponding to panel C; (F) Quantification of SOD2 IHC staining (IOD values), corresponding to panel C; (G) The WB analysis of ROS-related proteins NOX2, SOD2, and GAPDH; no quantification performed due to obvious differences. NC, normal control; TTM, tetrathiomolybdate; Gly, glyoxylate; lip-DLAT, lipoylated dihydrolipoamide S-acetyltransferase; lip-DLST, lipoylated dihydrolipoamide succinyltransferase; ROS, reactive oxygen species; WB, Western blot; FDX1, ferredoxin 1; ACO2, aconitase 2; LIAS, lipoic acid synthetase; HSP70, heat shock protein 70; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; IHC, immunohistochemistry; NOX2, nicotinamide adenine dinucleotide phosphate oxidase 2; SOD2, superoxide dismutase 2; IOD, integrated optical density. ∗∗∗ p<0.001.<br><b>Index in Asian Journal of Urology under a CC BY license. DOI: <a href='https://www.sciencedirect.com/science/article/pii/S2214388225000931'>10.1016/j.ajur.2025.06.006</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-1-s2.0-s2214388225000931-gr4.jpgAnti-SOD2/Mnsod Rabbit Monoclonal AntibodyTTM treatment reduces ROS level in HK-2 cells stimulated with COM. (A) Representative images of ROS detected by DCFH-DA staining in HK-2 cells under COM and TTM treatments, viewed by fluorescence microscopy; (B) Representative flow cytometry images for ROS detection under the same conditions; (C) Quantification of ROS levels by flow cytometry across groups; (D) LDH levels in HK-2 cell supernatants for each treatment; (E) MDA levels in HK-2 cell supernatants for each treatment; (F) The WB analysis of ROS-related proteins (NOX2, CAT, SOD2, and GAPDH). Data presentation: values are mean with standard error. NC, normal control; COM, calcium oxalate monohydrate; TTM, tetrathiomolybdate; DCFH-DA, 2′,7′-dichlorodihydrofluorescein diacetate; ROS, reactive oxygen species; LDH, lactate dehydrogenase; MDA, malondialdehyde; NOX2, nicotinamide adenine dinucleotide phosphate oxidase 2; CAT, catalase; SOD2, superoxide dismutase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase. ∗ p<0.05, ∗∗ p<0.01, ∗∗∗ p<0.001.<br><b>Index in Asian Journal of Urology under a CC BY license. DOI: <a href='https://www.sciencedirect.com/science/article/pii/S2214388225000931'>10.1016/j.ajur.2025.06.006</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-sod2-primary-antibodies-ihc-testing-3.jpgAnti-SOD2/Mnsod Rabbit Monoclonal Antibody IHC analysis of SOD2 using anti-SOD2 antibody (M00349). <br>
SOD2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SOD2 Antibody (M00349) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00349-sod2-primary-antibodies-ihc-testing-4.jpgAnti-SOD2/Mnsod Rabbit Monoclonal Antibody IHC analysis of SOD2 using anti-SOD2 antibody (M00349). <br>
SOD2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SOD2 Antibody (M00349) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mgmt-rabbit-monoclonal-antibody-m01012-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01012-mgmt-primary-antibodies-wb-testing-1.jpgAnti-MGMT Rabbit Monoclonal AntibodyWestern blot analysis of MGMT using anti-MGMT antibody (M01012). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: human SiHa whole cell lysates,<br>
Lane 6: human A549 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGMT antigen affinity purified monoclonal antibody (M01012) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MGMT at approximately 22 kDa. The expected band size for MGMT is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01012-mgmt-primary-antibodies-ihc-testing-1.jpgAnti-MGMT Rabbit Monoclonal AntibodyIHC analysis of MGMT using anti-MGMT antibody (M01012). <br>MGMT was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MGMT Antibody (M01012) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01012-mgmt-primary-antibodies-ihc-testing-2.jpgAnti-MGMT Rabbit Monoclonal AntibodyIHC analysis of MGMT using anti-MGMT antibody (M01012). <br>MGMT was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MGMT Antibody (M01012) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01012-mgmt-primary-antibodies-ihc-testing-3.jpgAnti-MGMT Rabbit Monoclonal AntibodyIHC analysis of MGMT using anti-MGMT antibody (M01012). <br>MGMT was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MGMT Antibody (M01012) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01012-mgmt-primary-antibodies-ihc-testing-4.jpgAnti-MGMT Rabbit Monoclonal AntibodyIHC analysis of MGMT using anti-MGMT antibody (M01012). <br>MGMT was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MGMT Antibody (M01012) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd3d-rabbit-monoclonal-antibody-m04405-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04405-cd3d-primary-antibodies-wb-testing-1.jpgAnti-CD3D Rabbit Monoclonal Antibody Western blot analysis of CD3D using anti-CD3D antibody (M04405). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human MOLT-4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD3D antigen affinity purified monoclonal antibody (Catalog # M04405) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD3D at approximately 21 kDa. The expected band size for CD3D is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04405-ihc.jpgAnti-CD3D Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CD3D Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04405-if.jpgAnti-CD3D Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using CD3D Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lc3b-rabbit-monoclonal-antibody-m01524-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-fphar-16-1526653-g007.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyAEA improved CHF via PI3K/AKT/Bnip3 axis. (A) Representative images of PI3K/AKT axis. (B, C) The phosphorylation level of PI3K and AKT. (D) Representative images of Opa1, Drp1, Bnip3, p62, Atg5 and LC3II. (E–J) The expression level of Opa1, Drp1, Bnip3, p62, Atg5 and LC3II. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-fphar-16-1526653-g010.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyAEA improved NE-induced injuries via PI3K/AKT/Bnip3 axis. (A) Representative images of PI3K/AKT axis in H9c2 cells. (B, C) The phosphorylation level of PI3K and AKT. (D) Representative images of Opa1, Drp1, TrxR2, Bnip3, p62, Atg5 and LC3II in cells. (E–K) The expression level of Opa1, Drp1, TrxR2, Bnip3, p62, Atg5 and LC3II in H9c2 cells. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-41419_2024_7200_fig8_html.pngAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyTMEM232 functions in autophagy in testis. A Western blotting analysis for the comparison of ARMC3 protein levels between Tmem232 −/− ( n = 2) and Tmem232 +/+ ( n = 2) testes and sperms at 2-months-old. α-Tubulin served as a loading control. The corresponding optical density readings for each image are shown. The representative image of biological duplicates is shown. B Western blotting analysis revealed the protein levels of four subunits (VPS15, VPS34, ATG14, and Beclin1) of PIK3C3-C1 complex in the testes of 2-month-old Tmem232 +/+ ( n = 2) and Tmem232 −/− ( n = 2) male mice. α-Tubulin served as a loading control. The representative image of biological duplicates is shown. C Co-immunoprecipitation assay results revealed the interaction between the TMEM232 and ATG14 protein in cells. Anti-Flag beads were used for immunoprecipitation. Anti-Flag and anti-GFP antibodies were used for western blotting analysis. The results shown are representative of three independent experiments. The representative image of biological duplicates is shown. D TMEM232-GFP was partly colocalized with LC3 in HeLa cells. Subcellular localization of target proteins (red) was probed with an anti-GOLGI97 antibody (upper panel, marker of Golgi apparatus), an anti-LAMP1 antibody (middle panel, marker of lysosome), and an anti-LC3 antibody (lower panel, marker of autophagosome). Cell nuclei were counterstained with DAPI. Scale bars, 10 μm. E The absence of TMEM232 in mice resulted in the accumulation of P62 and LC3. Tmem232 +/+ ( n = 2) and Tmem232 −/− ( n = 2) testes were separated and prepared for western blotting analysis. α-Tubulin served as a loading control. The corresponding optical density readings for each image are shown. The representative image of biological duplicates is shown. F Immunofluorescence staining of the P62 protein performed on frozen sections of Tmem232 +/+ ( n = 2) and Tmem232 −/− ( n = 2) testes. Blue, DAPI; green, P62. Scale bars, 20 μm. G Western blotting analysis of LC3B protein levels in HeLa cells after Flag-TMEM232 overexpression treatment with or without bafilomycin A1 (BafA1, 50 nM) treatment. HeLa cells were pretreated with Baf-A1 for 1 h and transfected with p-TMEM232×3FLAG-Myc-CMV-24 plasmid for 24 h. α-Tubulin served as a loading control. The corresponding optical density readings for each image are shown below. The results shown are representative of three independent experiments. The representative image of biological duplicates is shown. H A proposed model for the assumption that TMEM232 is involved in autophagy to regulate sperm formation in mice. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-024-07200-9'>39516485</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-lc3b-primary-antibodies-wb-testing-1_1.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyWestern blot analysis of LC3B using anti-LC3B antibody (M01524). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neurao-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LC3B antigen affinity purified monoclonal antibody (Catalog # M01524) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LC3B at approximately 15, 18 kDa. The expected band size for LC3B is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-lc3b-primary-antibodies-ihc-testing-1.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyIHC analysis of LC3B using anti-LC3B antibody (M01524). <br>
LC3B was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LC3B Antibody (M01524) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-lc3b-primary-antibodies-ihc-testing-2.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyIHC analysis of LC3B using anti-LC3B antibody (M01524). <br>
LC3B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LC3B Antibody (M01524) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-lc3b-primary-antibodies-ihc-testing-3.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyIHC analysis of LC3B using anti-LC3B antibody (M01524). <br>
LC3B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-LC3B Antibody (M01524) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-icc1.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01524-if.jpgAnti-LC3B MAP1LC3B Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells treated with choroquine, using LC3B Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-inos-rabbit-monoclonal-antibody-m00368-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-wb7.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-icc3.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-icc1.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-wb.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyWestern blot analysis of iNOS expression in Human fetal brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-icc2.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00368-if.jpgAnti-iNOS NOS2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Raw264.7 cells treated with LPS, using iNOS Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sdf1-rabbit-monoclonal-antibody-m00053-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00053-wb.jpgAnti-SDF1 CXCL12 Rabbit Monoclonal AntibodyWestern blot analysis of SDF1 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-e2f1-rabbit-monoclonal-antibody-m00257-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-wb-testing-1.jpgAnti-E2F1 Rabbit Monoclonal AntibodyWestern blot analysis of E2F1 using anti-E2F1 antibody (M00257). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HeLa whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-E2F1 antigen affinity purified monoclonal antibody (M00257) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for E2F1 at approximately 65-70 kDa. The expected band size for E2F1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-1.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-2.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-3.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-4.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-5.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-6.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-7.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-8.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-9.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-e2f1-primary-antibodies-ihc-testing-10.jpgAnti-E2F1 Rabbit Monoclonal AntibodyIHC analysis of E2F1 using anti-E2F1 antibody (M00257). <br>E2F1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-E2F1 Antibody (M00257) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-icc1.jpgAnti-E2F1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-icc2.jpgAnti-E2F1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00257-if.jpgAnti-E2F1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using E2F1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-igf2-rabbit-monoclonal-antibody-m00335-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00335-wb.jpgAnti-IGF2/IGF II Rabbit Monoclonal AntibodyWestern blot analysis of IGF2 expression in human serum lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gpx1-rabbit-monoclonal-antibody-m01019-1-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01019-1-gpx1-primary-antibodies-wb-testing-1.jpgAnti-GPX1/Glutathione Peroxidase 1 Rabbit Monoclonal Antibody Western blot analysis of GPX1 using anti-GPX1 antibody (M01019-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GPX1 antigen affinity purified monoclonal antibody (Catalog # M01019-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GPX1 at approximately 22 kDa. The expected band size for GPX1 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01019-1-gpx1-primary-antibodies-ihc-testing-2.jpgAnti-GPX1/Glutathione Peroxidase 1 Rabbit Monoclonal Antibody IHC analysis of GPX1 using anti-GPX1 antibody (M01019-1). <br>
GPX1 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GPX1 Antibody (M01019-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01019-1-gpx1-primary-antibodies-ihc-testing-3.jpgAnti-GPX1/Glutathione Peroxidase 1 Rabbit Monoclonal Antibody IHC analysis of GPX1 using anti-GPX1 antibody (M01019-1). <br>
GPX1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GPX1 Antibody (M01019-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01019-1-gpx1-primary-antibodies-ihc-testing-4.jpgAnti-GPX1/Glutathione Peroxidase 1 Rabbit Monoclonal Antibody IHC analysis of GPX1 using anti-GPX1 antibody (M01019-1). <br>
GPX1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GPX1 Antibody (M01019-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bmi1-rabbit-monoclonal-antibody-m00313-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00313-bmi1-primary-antibodies-wb-testing-1.jpgAnti-Bmi1 Rabbit Monoclonal Antibody Western blot analysis of Bmi1 using anti-Bmi1 antibody (M00313). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bmi1 antigen affinity purified monoclonal antibody (Catalog # M00313) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bmi1 at approximately 40 kDa. The expected band size for Bmi1 is at 37 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fasn-rabbit-monoclonal-antibody-m00941-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00941-wb.jpgAnti-FASN/Fatty Acid Synthase Rabbit Monoclonal AntibodyWestern blot analysis of FASN expression in A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00941-wb7.jpgAnti-FASN/Fatty Acid Synthase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gpx1-rabbit-monoclonal-antibody-m01019-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01019-wb.jpgAnti-GPX1/Glutathione Peroxidase 1 Rabbit Monoclonal AntibodyWestern blot analysis of GPX1 expression in SH SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-abl2-rabbit-monoclonal-antibody-m02715-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02715-wb.jpgAnti-ABL2 Rabbit Monoclonal AntibodyWestern blot analysis of ABL2 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mrc1-rabbit-monoclonal-antibody-m02285-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-wb8.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-wb11.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-fimmu-15-1489679-g004.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodymiR-27a-3p promotes the M2 polarization of macrophage. (A) Representative images for the immunohistochemical staining of macrophage maker CD68 and CD206 in nude mice xenografts, bar = 100 μm; and the number of CD68, CD206 positive cells per 200 × field for each group (mean ± SEM). **P < 0.01, ***P < 0.001 vs control. Below each group of images is an image showing the magnification of the corresponding box area above. (B) The expression of miR-27a-3p in mimic-miR-27a-3p or anti-miR-27a-3p treated THP1 cells was evaluated by qRT-PCR 24 h after transfection, normalized to U6 snRNA (mean ± SEM). **P < 0.01, ****P < 0.0001 vs. control. (C, D) The expression of CD206 was evaluated in mimic-miR-27a-3p or anti-miR-27a-3p treated THP1 cells by western blotting normalized to β-actin (mean ± SEM). *P < 0.05, ****P < 0.0001 vs. control. The data were from three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1489679/full'>39742261</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-wb9.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-wb.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodyWestern blot analysis of MRC1 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02285-wb10.jpgAnti-MRC1/Cd206 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-plat-rabbit-monoclonal-antibody-m02965-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02965-wb.jpgAnti-PLAT/Tpa Rabbit Monoclonal AntibodyWestern blot analysis of PLAT expression in human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rage-rabbit-monoclonal-antibody-m03438-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03438-wb.jpgAnti-RAGE Rabbit Monoclonal AntibodyWestern blot analysis of RAGE expression in mouse lung lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03438-fphar-15-1450154-g003.jpgAnti-RAGE Rabbit Monoclonal AntibodyWestern blotting results of RAGE in osteoblasts (n = 3). ** P < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1450154/full'>39525628</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03438-fphar-15-1450154-g007.jpgAnti-RAGE Rabbit Monoclonal AntibodyWestern blotting results of RAGE in osteoblasts (n = 3). ** P < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1450154/full'>39525628</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-klf4-rabbit-monoclonal-antibody-m00120-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-wb10.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-wb7.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-wb.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyWestern blot analysis of KLF4 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-wb8.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-wb9.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-ihc.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse liver, using KLF4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00120-if.jpgAnti-KLF4/Gklf Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using KLF4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd99-rabbit-monoclonal-antibody-m01724-1-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01724-1-wb.jpgAnti-CD99 Rabbit Monoclonal AntibodyWestern blot analysis of CD99 expression in HUVEC cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nefh-rabbit-monoclonal-antibody-m05307-2-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05307-2-wb.jpgAnti-NEFH/Nf H Rabbit Monoclonal AntibodyWestern blot analysis of NEFH expression in human brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd19-rabbit-monoclonal-antibody-m00154-1-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-1-wb7.jpgAnti-CD19 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-1-wb8.jpgAnti-CD19 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-1-wb.jpgAnti-CD19 Rabbit Monoclonal AntibodyWestern blot analysis of CD19 expression in (1) Jurkat cell lysate; (2) Rat spleen lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tbr1-rabbit-monoclonal-antibody-m07503-boster.html2026-03-24T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07503-wb.jpgAnti-TBR1 Rabbit Monoclonal AntibodyWestern blot analysis of TBR1 expression in human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mitf-rabbit-monoclonal-antibody-m00269-2-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00269-2-wb7.jpgAnti-MiTF Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00269-2-wb8.jpgAnti-MiTF Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00269-2-wb.jpgAnti-MiTF Rabbit Monoclonal AntibodyWestern blot analysis of MiTF expression in A375 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd80-rabbit-monoclonal-antibody-m00196-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00196-wb7.jpgAnti-CD80/B7 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00196-wb.jpgAnti-CD80/B7 1 Rabbit Monoclonal AntibodyWestern blot analysis of CD80 expression in Raji cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sod1-rabbit-monoclonal-antibody-m00238-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00238-sod1-primary-antibodies-wb-testing-1.jpgAnti-SOD1/Cu Zn Sod Rabbit Monoclonal AntibodyWestern blot analysis of SOD1/Cu Zn Sod using anti-SOD1/Cu Zn Sod antibody (M00238). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SIHA whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver muscle tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOD1/Cu Zn Sod antigen affinity purified monoclonal antibody (M00238) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SOD1/Cu Zn Sod at approximately 16-18 kDa. The expected band size for SOD1/Cu Zn Sod is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00238-sod1-primary-antibodies-wb-testing-2.jpgAnti-SOD1/Cu Zn Sod Rabbit Monoclonal AntibodyWestern blot analysis of SOD1 using anti-SOD1 antibody (M00238). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOD1 antigen affinity purified monoclonal antibody (M00238) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SOD1 at approximately 16-18 kDa. The expected band size for SOD1 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00238-sod1-primary-antibodies-ihc-testing-1.jpgAnti-SOD1/Cu Zn Sod Rabbit Monoclonal AntibodyIHC analysis of SOD1 using anti-SOD1 antibody (M00238). <br>SOD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-SOD1 Antibody (M00238) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd19-rabbit-monoclonal-antibody-m00154-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-cd19-primary-antibodies-wb-testing-1.jpgAnti-CD19 Rabbit Monoclonal Antibody Western blot analysis of CD19 using anti-CD19 antibody (M00154). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates, <br>
Lane 2: human Daudi whole cell lysates, <br>
Lane 3: human Ramos whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD19 antigen affinity purified monoclonal antibody (M00154) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD19 at approximately 95 kDa. The expected band size for CD19 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-41467_2024_54150_fig3_html.pngAnti-CD19 Rabbit Monoclonal AntibodyIn vitro comparison of the split-design CAR approach with conventional CAR. a Schematic representations of ligand-based conventional and split-design CAR approaches. The extracellular domains of BAFF and APRIL were used as target moieties to generate conventional CAR-T cells, referred to as APRIL CAR and BAFF CAR, respectively. b , d Representative images of cell‒cell conjugates captured at 100× oil objective magnification using a laser scanning confocal microscope (Nikon, A1R). APRIL or 9E10-IgG4m (pre-incubated with Myc-APRIL) CAR-T cells were co-cultured with RPMI8226-GFP cells ( b ), while BAFF or 9E10-IgG4m (pre-incubated with Myc-BAFF) CAR-T cells were co-cultured with IM9-GFP cells ( d ). Fluorescent labels included Hoechst (blue), anti-PKC-θ (red), and GFP (green) and a merged view of all stains. Scale bar = 10 μm. c , e Statistical analysis of the mean fluorescence intensity of PKC-θ at the IS in panels b and d, respectively. In panel c, sample sizes: APRIL CAR, n = 37; 9E10-IgG4m, n = 39. In panel e, BAFF CAR, n = 34; 9E10-IgG4m, n = 44. All n values represent individual cells. P values were determined by paired two-tailed t -tests. f , g Cytotoxicity assays of conventional and split-design CAR-T cells against the indicated target cells at various E:T ratios for 24 h in triplicate. h , i Inflammatory cytokine release assay. Conventional CAR-T cells or sCAR-T cells along with 1 nM corresponding switches were co-cultured with the specific target cells for 24 h at an E:T ratio of 1:1 in triplicate. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. j , l Schematic representations of ligand-based split-design CAR and FDA-approved CAR, referred to as BCMA CAR ( j ) and CD19 CAR ( l ), respectively. k , m Cytotoxicity assays of FDA-approved CAR-T cells and split-design CAR-T cells against the indicated target cells at various E:T ratios for 24 h in triplicate. Data in this figure are representative of three independent experiments. Error bars represent mean ± SD. NS indicates not significant. Source data are provided in the Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54150-z'>39528513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-41467_2024_54150_fig4_html.pngAnti-CD19 Rabbit Monoclonal AntibodyIn vivo comparison of the split-design CAR approach with ligand-based conventional CARs. a Timeline of in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). b Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). c , d Quantification of the average radiance (p/s/cm /sr) of the luminescence, related to APRIL- ( c ) and BAFF-( d )-based CAR-T-cell therapy. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. e Evaluation of serum inflammatory cytokine release by ELISA 24 h after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Tukey correction were used to assess significance. f , g Survival curves of the mice subjected to the indicated treatments. Survival curves were compared using the log-rank (Mantel‒Cox) test. h Timeline of in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). i Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). j Quantification of the average radiance (p/s/cm /sr) of the luminescence. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-BAFF) and CD19/CD22 CAR-T. k Evaluation of serum inflammatory cytokine release by ELISA 24 h after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. l Assessment of the presence of persistent human CD3 + (hCD3 + ) T cells in peripheral blood by flow cytometry over a 3-week follow-up period. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-BAFF) with BAFF-CAR-T at each time point. m Survival curves of mice subjected to the indicated treatments, compared using the log-rank (Mantel‒Cox) test. All n represents biological replicates from different mice. Data in this figure are representative of one of two independent experiments. Error bars represent mean ± SEM. NS indicates not significant. Source data are provided in the Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54150-z'>39528513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-41467_2024_54150_fig5_html.pngAnti-CD19 Rabbit Monoclonal AntibodyIn vivo comparison of the split-design CAR approach with the FDA-approved CARs. a Timeline of in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). b Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). c Evaluation of serum inflammatory cytokine release by ELISA 24 h after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. d Quantification of the average radiance (p/s/cm 2 /sr) of the luminescence. Two-way ANOVA multiple comparisons in Sidak correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-APRIL) with BCMA CAR-T. e Survival curves of mice subjected to the indicated treatments, compared using the log-rank (Mantel‒Cox) test. f Timeline of the in vivo experiments. Consistent results were obtained in two independent experiments ( n = 5 mice). g Representative bioluminescence images of mice subjected to different treatments. Colors represent the luminescence intensity (red, highest; blue, lowest). h Evaluation of serum inflammatory cytokine release by ELISA 24 hours after CAR-T-cell infusion. One-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. i Quantification of the average radiance (p/s/cm 2 /sr) of the luminescence. Two-way ANOVA multiple comparisons in Dunnett correction were used to assess significance, comparing 9E10-IgG4m CAR-T (with Myc-BAFF) with CD19 CAR-T. j Assessment of the presence of tumor cells (GFP + CD19 + or GFP + CD19 - ) in peripheral blood by flow cytometry on the 18th day of the experiment. One-way ANOVA multiple comparisons in Dunnett correction were used to assess significance. k Survival curves of the mice subjected to the indicated treatments, compared using the log-rank (Mantel‒Cox) test. All n represents biological replicates with different mice. Data are in this figure representative of one of two independent experiments. Error bars represent mean ± SEM. NS indicates not significant. Source data are provided in the Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-54150-z'>39528513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-ihc8.jpgAnti-CD19 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-ihc9.jpgAnti-CD19 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-ihc10.jpgAnti-CD19 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-ihc7.jpgAnti-CD19 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:100 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-thy1-rabbit-monoclonal-antibody-m01818-1-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-wb.jpgAnti-THY1/Cd90 Rabbit Monoclonal AntibodyWestern blot analysis of CD90 expression in human fetal brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig2_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyCharacteristics of CD90 high and CD90 low gbMSCs cultured in vitro. a , b Adherent growth patterns of CD90 high and CD90 low gbMSCs cultured in 10% DMEM (×40, scale bars = 200 µm). c FACS analysis of sorted CD90 high gbMSCs ( n ≥ 3). d FACS analysis of sorted CD90 high gbMSCs ( n ≥ 3). e Growth of CD90 high and CD90 low gbMSCs cultured in 10% DMEM ( n ≥ 3). * P < 0.05, ** P < 0.01. f Wound-healing assay of CD90 high and CD90 low gbMSCs ( n ≥ 3) for 8 h with different media (×40, scale bars = 200 µm). * P < 0.05, ** P < 0.01, *** P < 0.001 and **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig3_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyThe migration, proliferation and adhesion capacities of U87 cells incubated with different media in vitro. a Transwell assay of U87 cells cultured for 24 h in different media ( n ≥ 3) (serum-free medium, CD90 low CM and CD90 high CM). * P < 0.05, ** P < 0.01, *** P < 0.001 and **** P < 0.0001. Serum-free medium was used as a control. b CCK8 assay of U87 cells ( n ≥ 3) to evaluate proliferation in different media in vitro. U87 cells were incubated in 0%DMEM, CD90 high CM and CD90 low CM. * P < 0.05, ** P < 0.01, *** P < 0.001. Serum-free medium was used as a control. c Adhesion assay to estimate the effect of 0%DMEM, CD90 high CM and CD90 low CM on U87 cell adhesion. ( n ≥ 3) * P < 0.05, ** P < 0.01, *** P < 0.001. Serum-free medium were used as a control <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig4_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyTube formation capacity of gbMSCs and HUVECs incubated in different media. a Angiogenic capacity of CD90 high and CD90 low gbMSCs cultured in 0%DMEM, 10%DMEM, 0%gb-CM and S-gb-CM for 6 h on Matrigel (×100, scale bars = 100 µm). ( n ≥ 3) * P < 0.05, ** P < 0.01, *** P < 0.001. b Angiogenic capacity of HUVECs cultured in 0%DMEM, CD90 high CM and CD90 low CM for 6 h on Matrigel (×100, scale bars = 100 µm). ( n ≥ 3) * P < 0.05, ** P < 0.01. c Attachment capacity of DiO-labelled CD90 low and CD90 high gbMSCs onto vascular structures formed by HUVECs in 0%gb-CM (×100, scale bars = 100 µm). ( n ≥ 3) * P < 0.05 and ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig5_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyConditioned media from CD90 high and CD90 low gbMSCs have different functions in vivo. a Representative mice from intracranial xenograft experiments in which U87 cells with CD90 high CM (left) or U87 cells with CD90 low CM (right) were injected into the right frontal lobes of nude mice. Obviously, the sizes of the CD90 high CM group tumours were greater than those of their CD90 low CM counterparts. * P < 0.05. b Both the CD90 high CM and CD90 low CM tumour sections were stained with HE (×200, scale bars = 50 μm). In the CD90 high CM and CD90 low CM tumour tissues, IHC was employed to detect CD31 and Ki-67 expression (×400, scale bars = 25 µm). ( n ≥ 3) * P < 0.05, ** P < 0.01. c Survival curves of glioma-bearing mice. The survival times of mice implanted with U87 cells cultured with CD90 high CM were not significantly shorter than those of mice implanted with U87 cells cultured in CD90 low CM. d Double staining for CD105 (green) and CD90 (red) revealed that CD105 + CD90 − cells were located in the vessel walls, whereas CD105 + CD90 + cells were located around the tumour parenchyma. (×400, scale bars = 25 µm). e Kaplan–Meier survival curves for patients with low and high CD90 expression. The survival of glioma patients with different CD90 expression levels in TCGA database was not significantly different <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig6_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyThe VEGF, IL-6, bFGF, MMP9, CCL5 and SDF-1αlevels in different treatment media by ELISA. a The VEGF ( n ≥ 3) levels were significantly higher in CD90 low CM compared to those in CD90 high CM and 0%DMEM. b The bFGF ( n ≥ 3) levels were significantly higher in CD90 low CM compared to those in CD90 high CM and 0%DMEM. c The IL-6 ( n ≥ 3) levels were significantly higher in CD90 low CM compared to those in CD90 high CM and 0%DMEM. * d The SDF-1α ( n ≥ 3) levels were higher in CD90 high CM compared to those in CD90 low CM and 0%DMEM. e The CCL5 ( n ≥ 3) levels were higher in CD90 high CM compared to those in CD90 low CM and 0%DMEM. f The MMP9 ( n ≥ 3) levels were significantly higher in CD90 high CM compared to those in CD90 low CM and 0%DMEM. P < 0.05, ** P < 0.01, *** P < 0.001 and **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-41419_2018_1140_fig7_html.pngAnti-THY1/Cd90 Rabbit Monoclonal AntibodyClariom D expression profiles of CD90 high and CD90 low gbMSCs ( n = 3). a Heatmap of differentially expressed lncRNAs from a microarray assay performed on CD90 high and CD90 low gbMSCs. ‘Red’ indicates high relative expression, and ‘green’ indicates low relative expression. b GO terms for the predicted targeted genes. P < 0.05 using the two-sided Fisher’s exact test was defined as statistically significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-018-1140-6'>30368520</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-ihc.jpgAnti-THY1/Cd90 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using CD90 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-1-if.jpgAnti-THY1/Cd90 Rabbit Monoclonal AntibodyImmunofluorescent analysis of U87-MG cells, using CD90 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-arf6-rabbit-monoclonal-antibody-m00927-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00927-wb.jpgAnti-ARF6 Rabbit Monoclonal AntibodyWestern blot analysis of ARF6 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trx1-rabbit-monoclonal-antibody-m01219-1-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01219-1-wb.jpgAnti-TRX1 TXN Rabbit Monoclonal AntibodyWestern blot analysis of TRX1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01219-1-wb7.jpgAnti-TRX1 TXN Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trx1-rabbit-monoclonal-antibody-m01219-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01219-wb.jpgAnti-TRX1 TXN Rabbit Monoclonal AntibodyWestern blot analysis of TRX1 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ncam-rabbit-monoclonal-antibody-m00184-1-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-1-icc1.jpgAnti-NCAM NCAM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-1-wb.jpgAnti-NCAM NCAM1 Rabbit Monoclonal AntibodyWestern blot analysis of NCAM expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-1-icc2.jpgAnti-NCAM NCAM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-1-icc3.jpgAnti-NCAM NCAM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-numb-rabbit-monoclonal-antibody-m01206-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01206-wb.jpgAnti-NUMB Rabbit Monoclonal AntibodyWestern blot analysis of NUMB expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgf2-rabbit-monoclonal-antibody-m00121-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00121-fgf2-primary-antibodies-wb-testing-1.jpgAnti-FGF2/Fgf Basic Rabbit Monoclonal AntibodyWestern blot analysis of FGF2 using anti-FGF2 antibody (M00121). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: human U2OS whole cell lysates,<br>
Lane 6: human PC-3 whole cell lysates,<br>
Lane 7: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGF2 antigen affinity purified monoclonal antibody (M00121) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FGF2 at approximately 18,22,24 kDa. The expected band size for FGF2 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00121-fgf2-primary-antibodies-ihc-testing-1.jpgAnti-FGF2/Fgf Basic Rabbit Monoclonal AntibodyIHC analysis of FGF2 using anti-FGF2 antibody (M00121). <br>FGF2 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-FGF2 Antibody (M00121) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00121-fgf2-primary-antibodies-ihc-testing-2.jpgAnti-FGF2/Fgf Basic Rabbit Monoclonal AntibodyIHC analysis of FGF2 using anti-FGF2 antibody (M00121). <br>FGF2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-FGF2 Antibody (M00121) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bmp2-rabbit-monoclonal-antibody-m00338-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00338-wb.jpgAnti-BMP2 Rabbit Monoclonal AntibodyWestern blot analysis of BMP2 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glp1-rabbit-monoclonal-antibody-m00678-1-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00678-1-wb.jpgAnti-GLP1/GCG Rabbit Monoclonal AntibodyWestern blot analysis of GLP1 expression in human fetal pancreas lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trf1-rabbit-monoclonal-antibody-m02474-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02474-wb7.jpgAnti-TRF1 TERF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02474-wb.jpgAnti-TRF1 TERF1 Rabbit Monoclonal AntibodyWestern blot analysis of TRF1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd74-rabbit-monoclonal-antibody-m01340-2-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-wb-testing-1.jpgAnti-CD74 Rabbit Monoclonal AntibodyWestern blot analysis of CD74 using anti-CD74 antibody (M01340-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Daudi whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD74 antigen affinity purified monoclonal antibody (M01340-2) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD74 at approximately 34 kDa. The expected band size for CD74 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-2_1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-3_1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-4_1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-5_1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-2-cd74-primary-antibodies-ihc-testing-6_1.jpgAnti-CD74 Rabbit Monoclonal AntibodyIHC analysis of CD74 using anti-CD74 antibody (M01340-2). <br>CD74 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-CD74 Antibody (M01340-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apob-rabbit-monoclonal-antibody-m00100-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00100-wb.jpgAnti-ApoB/Apolipoprotein B Rabbit Monoclonal AntibodyWestern blot analysis of ApoB expression in human serum lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nqo1-rabbit-monoclonal-antibody-m00494-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-nqo1-primary-antibodies-wb-testing-1.jpgAnti-NQO1/Dt Diaphorase Rabbit Monoclonal Antibody Western blot analysis of NQO1 using anti-NQO1 antibody (M00494). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human SH-SY5Y lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NQO1 antigen affinity purified monoclonal antibody (Catalog # M00494) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NQO1 at approximately 27,31 kDa. The expected band size for NQO1 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-nqo1-primary-antibodies-ihc-testing-2.jpgAnti-NQO1/Dt Diaphorase Rabbit Monoclonal Antibody IHC analysis of NQO1 using anti-NQO1 antibody (M00494). <br>
NQO1 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NQO1 Antibody (M00494) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-12906_2023_3925_fig6_html.pngAnti-NQO1/Dt Diaphorase Rabbit Monoclonal AntibodyEffects of TMP on mRNA changes in HepG2 cells. (A) Changes in HO-1 mRNA after TMP (0.05, and 0.1 mg/mL) pre-protection. (B) Changes in NQO1 mRNA after TMP (0.05, and 0.1 mg/mL) pre-protection. (*P < 0.05, **P < 0.01) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-023-03925-w'>37046263</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-12906_2023_3925_fig7_html.pngAnti-NQO1/Dt Diaphorase Rabbit Monoclonal AntibodyEffects of TMP on PI3K/AKT/Nrf2 signaling pathway in HepG2 cells. (A-C) Effects of TMP (0.05, and 0.1 mg/mL) on HO-1 and NQO1 proteins Changes in HepG2 cells. (D-E) Effects of TMP (0.05, and 0.1 mg/mL) on nuclear Nrf2 protein Changes in HepG2 cells. (F-I) Effects of TMP (0.05, and 0.1 mg/mL) on p-AKT and p-PI3K proteins Changes in HepG2 cells. (*P < 0.05, **P < 0.01) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-023-03925-w'>37046263</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-wb8.jpgAnti-NQO1/Dt Diaphorase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1w dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00494-if.jpgAnti-NQO1/Dt Diaphorase Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using NQO1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ctcf-rabbit-monoclonal-antibody-m00132-boster.html2026-03-24T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-ctcf-primary-antibodies-wb-testing-1.jpgAnti-CTCF Rabbit Monoclonal Antibody Western blot analysis of CTCF using anti-CTCF antibody (M00132). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human Jurkat whole cell lysates, <br>
Lane 3: human MCF-7 whole cell lysates, <br>
Lane 4: human SIHA whole cell lysates, <br>
Lane 5: rat brain tissue lysates, <br>
Lane 6: rat lung tissue lysates, <br>
Lane 7: mouse brain tissue lysates, <br>
Lane 8: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTCF antigen affinity purified monoclonal antibody (M00132) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTCF at approximately 150 kDa. The expected band size for CTCF is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc4.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc1.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc5.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc2.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc6.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc3.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00132-icc7.jpgAnti-CTCF Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-xbp1-rabbit-monoclonal-antibody-m00234-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00234-wb.jpgAnti-XBP1 Rabbit Monoclonal AntibodyWestern blot analysis of XBP1 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00234-wb7.jpgAnti-XBP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00234-wb8.jpgAnti-XBP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-edg1-rabbit-monoclonal-antibody-m01502-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01502-edg1-primary-antibodies-wb-testing-1.jpgAnti-EDG1 S1PR1 Rabbit Monoclonal Antibody Western blot analysis of EDG1 using anti-EDG1 antibody (M01502). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human U-87MG whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EDG1 antigen affinity purified monoclonal antibody (Catalog # M01502) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EDG1 at approximately 43 kDa. The expected band size for EDG1 is at 43 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd32-rabbit-monoclonal-antibody-m01450-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01450-fcgr2a-primary-antibodies-wb-testing-1.jpgAnti-CD32 FCGR2A Rabbit Monoclonal AntibodyWestern blot analysis of FCGR2A using anti-FCGR2A antibody (M01450). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FCGR2A antigen affinity purified monoclonal antibody (M01450) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FCGR2A at approximately 38-40 kDa. The expected band size for FCGR2A is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd59-rabbit-monoclonal-antibody-m00914-1-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-1-wb.jpgAnti-CD59 Rabbit Monoclonal AntibodyWestern blot analysis of CD59 expression in HUVEC cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-1-if.jpgAnti-CD59 Rabbit Monoclonal AntibodyImmunofluorescent analysis of BxPC-3 cells, using CD59 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bmp7-rabbit-monoclonal-antibody-m00858-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00858-wb.jpgAnti-BMP7 Rabbit Monoclonal AntibodyWestern blot analysis of BMP7 expression in human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smc3-rabbit-monoclonal-antibody-m01930-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01930-wb.jpgAnti-SMC3 Rabbit Monoclonal AntibodyWestern blot analysis of SMC3 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ip10-rabbit-monoclonal-antibody-m00278-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00278-wb.jpgAnti-IP10 CXCL10 Rabbit Monoclonal AntibodyWestern blot analysis of IP10 expression in IP10 recombinant protein lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sdha-rabbit-monoclonal-antibody-m01753-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01753-sdha-primary-antibodies-wb-testing-1_1.jpgAnti-SDHA Rabbit Monoclonal Antibody Western blot analysis of SDHA using anti-SDHA antibody (M01753). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat kidney tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SDHA antigen affinity purified monoclonal antibody (Catalog # M01753) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SDHA at approximately 73 kDa. The expected band size for SDHA is at 73 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tlr5-rabbit-monoclonal-antibody-m00462-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00462-wb7.jpgAnti-TLR5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00462-wb8.jpgAnti-TLR5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00462-wb.jpgAnti-TLR5 Rabbit Monoclonal AntibodyWestern blot analysis of TLR5 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atpb-rabbit-monoclonal-antibody-m02937-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-wb-testing-1.jpgAnti-ATPB Rabbit Monoclonal Antibody Western blot analysis of ATPB using anti-ATPB antibody (M02937). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATPB antigen affinity purified monoclonal antibody (Catalog # M02937) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATPB at approximately 50 kDa. The expected band size for ATPB is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-ihc-testing-2.jpgAnti-ATPB Rabbit Monoclonal Antibody IHC analysis of ATPB using anti-ATPB antibody (M02937). <br>
ATPB was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ATPB Antibody (M02937) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-ihc-testing-3.jpgAnti-ATPB Rabbit Monoclonal Antibody IHC analysis of ATPB using anti-ATPB antibody (M02937). <br>
ATPB was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ATPB Antibody (M02937) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-ihc-testing-4.jpgAnti-ATPB Rabbit Monoclonal Antibody IHC analysis of ATPB using anti-ATPB antibody (M02937). <br>
ATPB was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ATPB Antibody (M02937) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-ihc-testing-5.jpgAnti-ATPB Rabbit Monoclonal Antibody IHC analysis of ATPB using anti-ATPB antibody (M02937). <br>
ATPB was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ATPB Antibody (M02937) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02937-atpb-primary-antibodies-ihc-testing-6.jpgAnti-ATPB Rabbit Monoclonal Antibody IHC analysis of ATPB using anti-ATPB antibody (M02937). <br>
ATPB was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ATPB Antibody (M02937) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-muc2-rabbit-monoclonal-antibody-m01212-1-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01212-1-muc2-primary-antibodies-wb-testing-1.jpgAnti-MUC2 Rabbit Monoclonal AntibodyWestern blot analysis of MUC2 using anti-MUC2 antibody (M01212-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Caco-2 whole cell lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUC2 antigen affinity purified monoclonal antibody (M01212-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MUC2 at approximately 110 kDa. The expected band size for MUC2 is at 540 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01212-1-muc2-primary-antibodies-ihc-testing-1.jpgAnti-MUC2 Rabbit Monoclonal AntibodyIHC analysis of MUC2 using anti-MUC2 antibody (M01212-1). <br>MUC2 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC2 Antibody (M01212-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01212-1-41598_2024_55258_fig3_html.pngAnti-MUC2 Rabbit Monoclonal AntibodyPolyamines enhance mucosal defense factors in rats with massive intestinal resection. (A-B) Fecal and serum secretory IgA was measured using ELISA. n = 5–7/group. (C) IgA in ileum tissue was assessed using western blotting. n = 4–6/group. (D) Fecal mucin was measured using a fluorometric assay. n = 4–6/group. (E) Representative images of ileal villus showing immunostaining by Muc2 (original magnification, ×400; scale bars = 200 μm). Left graphs show the number of goblet cells per unit villous area and the size of goblet cell secretion granule. (F) The expression of Claudin-3 in the ileum tissue was measured by western blot analysis. Representative images of ileal villus showing immunostaining by Claudin-3 (original magnification, ×200; scale bars = 100 μm). (G) Serum DAO was measured by ELISA. n = 5–7/group. (H) Serum GLP-2 was measured by ELISA. n = 5–7/group. (I) Fecal short-chain fatty acid (SCFA) content was measured using high-performance liquid chromatography. n = 3–6/group. Data are presented as mean ± SD. Results of one-way ANOVA are represented as follows: * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-55258-4'>38409241</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01212-1-fmicb-11-622354-g003.jpgAnti-MUC2 Rabbit Monoclonal AntibodyThe distribution of Lgr5 + ISCs in the intestinalmucosa and the subcellular localization and relative expression level detection of epithelial function proteins CDX2 and villin in the intestinal mucosa of IBD at 7 days after termination of DSS administration. (A) The Lgr5 + ISCs (brown) in the small intestinal mucosa: (A1) the normal group, the villi and the crypts were arranged compactly, and Lgr5 + ISCs were observed in the crypts; (A2) the DSS group, the villi and the crypts were scattered, with few Lgr5 + ISCs; (A3) the DSS + B. subtilis -fermented milk group, there were more Lgr5 + ISCs in villi and crypts compared with those in the DSS group. (B) The Lgr5 + ISCs (brown) in the colonic mucosa: (B1) the normal group, the glands were arranged compactly, and there were large amounts of Lgr5 + ISCs at the bottom of the glands; (B2) the DSS group: the ulcers were replaced by scars. No Lgr5 + ISCs were observed in the scars; (B3) the DSS + B. subtilis -fermented milk group: the colonic epithelium was integrated, with some regenerated glands. A number of Lgr5 + ISCs were observed at the bottom of the regenerated glands. (C) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the small intestinal mucosa: (C1) the normal group: the villi and the crypts were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the villi and the crypts; (C2) the DSS group: the villi and the crypts were scattered, and few CDX2 + epithelial cells were observed on the surface of the crypt and the villi; (C3) the DSS + B. subtilis -fermented milk group: more villi and crypts were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells covering the villi and crypts. (D) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the colonic mucosa: (D1) the normal group: the colonic glands were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the glands; (D2) the DSS group: the glands were scattered, and few CDX2 + epithelial cells were observed in the scar; (D3) the DSS + B. subtilis -fermented milk group: more colonic glands were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells in the glands. (E) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the small intestinal mucosa: (E1) the normal group, a number of Mucin2 + goblet cells observed in the epithelium; (E2) the DSS group: only few Mucin2 + goblet cells were observed in the remaining villi and crypts; (E3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered mucosa. (F) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the colonic mucosa: (F1) the normal group, large amounts of Mucin2 + goblet cells were observed in the mucosa; (F2) the DSS group: only few Mucin2 + goblet cells were observed in the scars; (F3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered colonic mucosa. (G,H) Western blotting was applied for detection of the relative expression level of Lgr5, CDX2, and Mucin2 in the samples containing equivalent ileum and colon. The expression level of Lgr5, CDX2, and Mucin2 in the DSS group was significantly lower than that of the normal (control) group. The expression level of Lgr5, CDX2, and Mucin2 in the DSS + B. subtilis -fermented milk (FM) group was significantly higher than that of the DSS group ( n = 5, ** represents p < 0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2020.622354/full'>33519783</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01212-1-muc2-primary-antibodies-ihc-testing-2.jpgAnti-MUC2 Rabbit Monoclonal AntibodyIHC analysis of MUC2 using anti-MUC2 antibody (M01212-1). <br>MUC2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MUC2 Antibody (M01212-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-drd1-rabbit-monoclonal-antibody-m00907-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00907-wb.jpgAnti-DRD1/Dopamine Receptor D1 Rabbit Monoclonal AntibodyWestern blot analysis of DRD1 expression in (1) SH-SY5Y cell lysate; (2) Mouse kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aqp1-rabbit-monoclonal-antibody-m00865-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00865-aqp1-primary-antibodies-wb-testing-1.jpgAnti-AQP1 Rabbit Monoclonal AntibodyWestern blot analysis of AQP1 using anti-AQP1 antibody (M00865). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat kidney tissue lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: mouse kidney tissue lysates,<br>
Lane 4: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AQP1 antigen affinity purified monoclonal antibody (M00865) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AQP1 at approximately 25 kDa. The expected band size for AQP1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00865-aqp1-primary-antibodies-ihc-testing-1.jpgAnti-AQP1 Rabbit Monoclonal AntibodyIHC analysis of AQP1 using anti-AQP1 antibody (M00865). <br>AQP1 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AQP1 Antibody (M00865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00865-aqp1-primary-antibodies-ihc-testing-2.jpgAnti-AQP1 Rabbit Monoclonal AntibodyIHC analysis of AQP1 using anti-AQP1 antibody (M00865). <br>AQP1 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AQP1 Antibody (M00865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00865-aqp1-primary-antibodies-ihc-testing-3.jpgAnti-AQP1 Rabbit Monoclonal AntibodyIHC analysis of AQP1 using anti-AQP1 antibody (M00865). <br>AQP1 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AQP1 Antibody (M00865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00865-aqp1-primary-antibodies-wb-testing-2.pngAnti-AQP1 Rabbit Monoclonal AntibodyWestern blot analysis of AQP1 using anti-AQP1 antibody (M00865). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: MADB106 cells under normal culture conditions,<br>
Lane 2: MADB106 cells treated with agonist,<br>
Lane 3: MADB106 cells treated with inhibitor.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AQP1 antigen affinity purified monoclonal antibody (M00865) at 1: 3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for AQP1 at approximately 25 kDa. The expected band size for AQP1 is at 25 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-noxa-rabbit-monoclonal-antibody-m02287-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02287-pmaip1-primary-antibodies-wb-testing-1.jpgAnti-Noxa Rabbit Monoclonal Antibody Western blot analysis of PMAIP1 using anti-PMAIP1 antibody (M02287). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates,<br>
Lane 4: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PMAIP1 antigen affinity purified monoclonal antibody (Catalog # M02287) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PMAIP1 at approximately 16 kDa. The expected band size for PMAIP1 is at 6 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd41-rabbit-monoclonal-antibody-m01102-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-ihc7.jpgAnti-CD41 ITGA2B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat pancreas, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-itga2b-primary-antibodies-wb-testing-1.jpgAnti-CD41 ITGA2B Rabbit Monoclonal Antibody Western blot analysis of ITGA2B using anti-ITGA2B antibody (M01102). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITGA2B antigen affinity purified monoclonal antibody (Catalog # M01102) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITGA2B at approximately 130 kDa. The expected band size for ITGA2B is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-ihc8.jpgAnti-CD41 ITGA2B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous carcinoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-ihc9.jpgAnti-CD41 ITGA2B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta, using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nefm-rabbit-monoclonal-antibody-m06821-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06821-nefm-primary-antibodies-wb-testing-1.jpgAnti-NEFM/Nf M Rabbit Monoclonal AntibodyWestern blot analysis of NF-M/NEFM using anti-NF-M/NEFM antibody (M06821). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NF-M/NEFM antigen affinity purified monoclonal antibody (M06821) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NF-M/NEFM at approximately 160 kDa. The expected band size for NF-M/NEFM is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06821-nefm-primary-antibodies-ihc-testing-1.jpgAnti-NEFM/Nf M Rabbit Monoclonal AntibodyIHC analysis of NF-M/NEFM using anti-NF-M/NEFM antibody (M06821). <br>NF-M/NEFM was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NF-M/NEFM Antibody (M06821) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06821-nefm-primary-antibodies-ihc-testing-2.jpgAnti-NEFM/Nf M Rabbit Monoclonal AntibodyIHC analysis of NF-M/NEFM using anti-NF-M/NEFM antibody (M06821). <br>NF-M/NEFM was detected in a paraffin-embedded section of pig brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-NF-M/NEFM Antibody (M06821) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tia1-rabbit-monoclonal-antibody-m02763-1-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02763-1-wb7.jpgAnti-TIA1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02763-1-wb.jpgAnti-TIA1 Rabbit Monoclonal AntibodyWestern blot analysis of TIA1 expression in (1) Jurkat cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02763-1-wb8.jpgAnti-TIA1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02763-1-wb9.jpgAnti-TIA1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ly6a-rabbit-monoclonal-antibody-m30403-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30403-ly6a-primary-antibodies-wb-testing-1.jpgAnti-LY6A/Sca1 Rabbit Monoclonal AntibodyWestern blot analysis of LY6A using anti-LY6A antibody (M30403). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse kidney tissue lysates,<br>
Lane 2: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LY6A antigen affinity purified monoclonal antibody (M30403) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LY6A at approximately 18 kDa. The expected band size for LY6A is at 14 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ku70-rabbit-monoclonal-antibody-m01732-1-boster.html2026-03-24T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01732-1-xrcc6-primary-antibodies-wb-testing-1.jpgAnti-Ku70 XRCC6 Rabbit Monoclonal AntibodyWestern blot analysis of XRCC6 using anti-XRCC6 antibody (M01732-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-XRCC6 antigen affinity purified monoclonal antibody (M01732-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for XRCC6 at approximately 70 kDa. The expected band size for XRCC6 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01732-1-ihc.jpgAnti-Ku70 XRCC6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using Ku70 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd18-rabbit-monoclonal-antibody-m00458-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00458-wb.jpgAnti-CD18 ITGB2 Rabbit Monoclonal AntibodyWestern blot analysis of CD18 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-adfp-rabbit-monoclonal-antibody-m04328-1-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04328-1-wb7.jpgAnti-ADFP PLIN2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04328-1-wb.jpgAnti-ADFP PLIN2 Rabbit Monoclonal AntibodyWestern blot analysis of ADFP expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tlr7-rabbit-monoclonal-antibody-m00376-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00376-wb.jpgAnti-TLR7 Rabbit Monoclonal AntibodyWestern blot analysis of TLR7 expression in Raji cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd73-rabbit-monoclonal-antibody-m02120-1-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-1-wb.jpgAnti-CD73 Rabbit Monoclonal AntibodyWestern blot analysis of CD73 expression in A375 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd26-rabbit-monoclonal-antibody-m00597-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00597-cd26-primary-antibodies-wb-testing-1.jpgAnti-CD26/DPP4 Rabbit Monoclonal AntibodyWestern blot analysis of CD26 using anti-CD26 antibody (M00597). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD26 antigen affinity purified monoclonal antibody (M00597) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD26 at approximately 110 kDa. The expected band size for CD26 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00597-fphar-16-1583509-g008.jpgAnti-CD26/DPP4 Rabbit Monoclonal AntibodySXD remarkably affected the ferroptosis-related markers in CoCl 2 -induced hypoxic H9c2 cells. (A–D) mRNA expressions of ACSL4, GPX4, DPP4, and HMOX1 in different groups, separately. (E) Protein expressions of ACSL4, GPX4, DPP4, and HMOX1 in different groups. *P < 0.05, **P < 0.01, and ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1583509/full'>40365322</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00597-fphar-16-1583509-g009.jpgAnti-CD26/DPP4 Rabbit Monoclonal AntibodyMolecular docking results. (A) Structure of quercetin. (B, C) Molecular docking of quercetin with DPP4 (B) and HMOX1 (C) . (D) Results of the CETSA assay.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1583509/full'>40365322</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fmrp-rabbit-monoclonal-antibody-m00192-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00192-fmr1-primary-antibodies-wb-testing-1.jpgAnti-FMRP FMR1 Rabbit Monoclonal AntibodyWestern blot analysis of FMR1 using anti-FMR1 antibody (M00192). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat NRK whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FMR1 antigen affinity purified monoclonal antibody (M00192) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FMR1 at approximately 73 kDa. The expected band size for FMR1 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00192-fmr1-primary-antibodies-ihc-testing-1.jpgAnti-FMRP FMR1 Rabbit Monoclonal AntibodyIHC analysis of FMR1 using anti-FMR1 antibody (M00192). <br>FMR1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FMR1 Antibody (M00192) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00192-fmr1-primary-antibodies-ihc-testing-2.jpgAnti-FMRP FMR1 Rabbit Monoclonal AntibodyIHC analysis of FMR1 using anti-FMR1 antibody (M00192). <br>FMR1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FMR1 Antibody (M00192) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00192-fmr1-primary-antibodies-ihc-testing-3.jpgAnti-FMRP FMR1 Rabbit Monoclonal AntibodyIHC analysis of FMR1 using anti-FMR1 antibody (M00192). <br>FMR1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FMR1 Antibody (M00192) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chat-rabbit-monoclonal-antibody-m01192-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01192-wb7.jpgAnti-CHAT/Choline Acetyltransferase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01192-wb.jpgAnti-CHAT/Choline Acetyltransferase Rabbit Monoclonal AntibodyWestern blot analysis of CHAT expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sos1-rabbit-monoclonal-antibody-m00837-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00837-sos1-primary-antibodies-wb-testing-1.jpgAnti-SOS1 Rabbit Monoclonal AntibodyWestern blot analysis of SOS1 using anti-SOS1 antibody (M00837). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOS1 antigen affinity purified monoclonal antibody (M00837) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SOS1 at approximately 170 kDa. The expected band size for SOS1 is at 152 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gclc-rabbit-monoclonal-antibody-m01722-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01722-gclc-primary-antibodies-wb-testing-1.jpgAnti-GCLC Rabbit Monoclonal Antibody Western blot analysis of GCLC using anti-GCLC antibody (M01722). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GCLC antigen affinity purified monoclonal antibody (Catalog # M01722) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GCLC at approximately 73 kDa. The expected band size for GCLC is at 73 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-g6pd-rabbit-monoclonal-antibody-m00287-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00287-g6pd-primary-antibodies-wb-testing-1.jpgAnti-G6PD/Glucose 6 Phosphate Dehydrogenase Rabbit Monoclonal Antibody Western blot analysis of G6PD using anti-G6PD antibody (M00287). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-G6PD antigen affinity purified monoclonal antibody (Catalog # M00287) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for G6PD at approximately 59 kDa. The expected band size for G6PD is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100-rabbit-monoclonal-antibody-m02503-1-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02503-1-wb.jpgAnti-S100 S100A1 Rabbit Monoclonal AntibodyWestern blot analysis of S100 expression in (1) Human skeletal muscle lysate; (2) RAW 264.7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02503-1-ihc.jpgAnti-S100 S100A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using S100 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-parp-rabbit-monoclonal-antibody-m00122-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-wb7.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-wb8.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-wb9.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-wb.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyWestern blot analysis of PARP expression in (1) HeLa cell lysate; (2) HeLa cell lysate treated with staurosporine.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc7.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat ovary, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc8.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc9.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc10.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human small cell lung cancer , using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc11.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse spleen, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-ihc.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse testis, using PARP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-icc1.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-if.jpgAnti-PARP PARP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PARP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fap1-rabbit-monoclonal-antibody-m00422-boster.html2026-03-26T05:20:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-fap1-primary-antibodies-wb-testing-1.jpgAnti-FAP1 Rabbit Monoclonal Antibody Western blot analysis of FAP1 using anti-FAP1 antibody (M00422). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U-87MG whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAP1 antigen affinity purified monoclonal antibody (Catalog # M00422) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAP1 at approximately 95 kDa. The expected band size for FAP1 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-wb7.jpgAnti-FAP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-wb9.jpgAnti-FAP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-fap1-primary-antibodies-ihc-testing-2.jpg.pngAnti-FAP1 Rabbit Monoclonal AntibodyIHC analysis of FAP1 using anti-FAP1 antibody (M01394-4).
FAP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FAP1 Antibody (M01394-4) overnight at 4°C. Two-step IHC kit was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-jcav09p3278g002.jpgAnti-FAP1 Rabbit Monoclonal AntibodyHIF-1α and FAP expression in HCC tissues determined by Wetern blot and q-RT-PCR. (A) Western blot detection of HIF-1α and FAP expression in 11 HCC tissue of different stages (I-IV). (B) Grey analysis of the Western blot results: both HIF-1α and FAP expressions significantly increased in advanced-staged (stage II-IV) HCC tissue (HIF-1α, p=0.0120; FAP, p=0.0011). (C) The mRNA expression of HIF-1α and FAP detected by q-RT-PCR shows that mRNA expression levels also increased in advanced-staged HCC tissues compared to early-staged lesions for both HIF-1α (p=0.0152) and FAP (p=0.0307). (D) The expression of HIF-1α and FAP within tumor cells in these tissues by IHC staining. (Note: T7 and T8 is stage-II tumor tissues)<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160687/'>30271487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-12964_2023_1312_fig6_html.pngAnti-FAP1 Rabbit Monoclonal AntibodyDetailed characterization of monocytes/macrophages in HPSCC. a UMAP plot of monocyte/macrophage cells colored by cell type. b Frequency (left) and proportion (right) of four major mononuclear/macrophage cell types in tumor and normal tissue samples. c Heatmap showing signature DEGs between mononuclear/macrophage cell types. d Bubble heatmap showing marker genes across mononuclear/macrophage cell types. Dot size indicates fraction of expressing cells, colored according to expression normalized to z-score. e Dot plot of representative M1, M2, angiogenic, and phagocytic signatures in monocyte/macrophage clusters [Z-score normalized log 2 (count + 1)]. f Differential pathways enriched in C1QC + and SPP1 + TAMs according to GSVA. Two-sided unpaired limma-moderated t -test. g Absolute infiltration proportion of SPP1 + TAMs compared between normal ( n = 43) and tumor ( n = 43) tissues in the TCGA-HNSC cohort. h Kaplan–Meier curve of OS in the TCGA-HNSC cohort stratified by optimal cut-off point for SPP1 expression and SPP1 + TAM infiltration. i Pseudotime trajectory analysis of mononuclear/macrophage cells. Each dot represents one cell, colored according to its cluster label. Inlet plot showed each cell with a pseudotime score from dark blue (early state) to light blue (terminal). Jitter plot showing expression changes in macrophage differentiation-associated genes over pseudotime. j Correlation of mCAF signature with SPP1 + TAMs based on TCGA-HNSC data. Each dot represents a patient (Pearson’s correlations). k Kaplan–Meier OS analyses of four subgroups in the TCGA-HNSC cohort, stratified by infiltration of both mCAFs and SPP1 + TAMs. l Dot plot of predicted ligand – receptor interactions between mCAFs and SPP1 + TAMs in tumor samples. m Representative images showing mIHC staining of panCK, FAP, and SPP1 in HPSCC tumor samples, in individual and merged channels. Scale bar = 20 μm. Significance in ( h ) and ( k ) was determined with two-sided log-rank tests <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-023-01312-z'>37853464</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-jcav09p3278g001.jpgAnti-FAP1 Rabbit Monoclonal AntibodyHIF-1α and FAP expression in HCC tissues by immunohistochemistry. Different expression features of HIF-1α in HCC tissue: low expression (A) and high expression (B) (×100). Different expression features of HIF-1α in HCC tissue within the tumor cells: low expression (C) and high expression (D) (×100). Picture reveals mesenchymal expression of FAP in HCC tissue (E). (F) Pearson' correlation test with scatter plot showing the correlation between the density of HIF-1α and FAP after IHC staining, each dot represents a case. (Pearson r2 = 0.2753, p < 0.0001)<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160687/'>30271487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-fimmu-16-1568556-g003.jpgAnti-FAP1 Rabbit Monoclonal AntibodyRepresentative multiplexed IHC staining of SMARCA2 deficiency while preserving SMARCA4 expression samples (n=2) and SMARCA2 High & SMARCA2 High sample (n=1) stained for panel A: Pan-CK, α-SMA, CD31, and CD206; panel B: Pan-CK, FAP, SPP1, CD8, and CD4.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1568556/full'>40453096</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-12964_2023_1312_fig3_html.pngAnti-FAP1 Rabbit Monoclonal AntibodyFibroblast subsets in HPSCC tumor and adjacent normal tissues. a UMAP plot of fibroblast cells colored by cell and sample type. b Heatmap showing signature DEGs among four fibroblast subsets. c Violin plots showing marker gene expression in fibroblast subsets. d Bubble heatmap showing marker gene expression in Elastic Fbs. Dot size indicates fraction of expressing cells, colored according to expression normalized based on z-scores. e Representative images showing mIHC staining of panCK, FAP, ⍶-SMA, and PLA2G2A in HPSCC samples, in individual and merged channels. Scale bar represents 50 μm. f Absolute infiltration proportion of mCAFs comparing normal ( n = 43) and tumor tissues ( n = 43) in the TCGA-HNSC cohort. g Kaplan–Meier curve of the OS in the TCGA-HNSC cohort stratified by the optimal cut-off for FAP expression and mCAF infiltration. h Representative images of the IHC staining of HPSCC tumor samples with a high and low FAP expression. i Comparing OS (Kaplan–Meier curves) among patients with HPSCC who either lowly or highly express FAP. j FaDu or SNU1076 cells were incubated for 48 h with normal and CM of NFs and CAFs; E-cadherin, N-cadherin, vimentin, Twist, and GADPH expression was evaluated using immunoblotting. Cropped blots are used here and the full-length gel images are available in Additional file (Fig. S7). k FaDu or SNU1076 cell invasion in CM relative to complete growth medium measured after 48 h. Photographs are representative of randomly chosen fields. l Representative images showing wound healing of FaDu or SNU1076 cells in CM of NFs and CAFs relative to complete growth medium, at 0, 12, 24, 48, and 72 h after wound infliction. Significance in ( g ) and ( i ) was assessed with two-sided log-rank tests. In ( j – l ), data are shown as mean ± SEM, with n = 3 paracancerous tissues and n = 4 tumor tissue columns. Differences were determined using unpaired t -tests (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-023-01312-z'>37853464</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-jcav09p3278g007.jpgAnti-FAP1 Rabbit Monoclonal AntibodyIn-vitro confirmation of FAP up-regulation in hypoxic HCC cells and association with EMT. Western blot confirmed that the cellular hypoxia in three HCC cell lines (HepG2, Huh7 and MHCC97H) after treatment, indicated by up-regulation of HIF-1α, was associated with increased FAP expression and EMT. (N, normal oxygen; H, hypoxia.)<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160687/'>30271487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-j_biol-2022-0776_fig_003.jpgAnti-FAP1 Rabbit Monoclonal AntibodyGene expression levels in fibroblasts. The mRNA expression levels of E-cadherin , α-SMA , FAP , and Cav-1 in the fibroblasts were detected by quantitative real-time PCR. Compared with HKF control, * P < 0.05; compared with HKF + EXO co-culture, # P < 0.05; and compared with HKF + siRNA negative control-EXO co-culture, & P < 0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.degruyter.com/document/doi/10.1515/biol-2022-0776/html'>38045487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g006.jpgAnti-FAP1 Rabbit Monoclonal AntibodyPan-cancer analysis of FAP + CAF and DAB2 + TAM. (A and B) Stacking plot showing the proportion of FAP + CAF and DAB2 + TAM in different sample types. (C) Gene expression analysis of FAP and DAB2 shows their expression of tumor and normal samples in different cancers, the association between gene expression and patient survival, and the correlation between FAP and DAB2 expression. (D) Circular plots showing the proportion of cancer types with different FAP and DAB2 gene expression patterns, UP indicates the proportion of cancer types in which the gene is significantly up-regulated in cancer, DOWN indicates the proportion of cancer types in which the gene is significantly down-regulated in cancer, and NS indicates the proportion of cancer types in which there is no significant difference in the expression of the gene in cancer and paracancer. (E) Spatial feature plot showing the expression of selected genes in HCC immunotherapy ST slides. (F) Spatial feature plot showing the expression of selected genes in skin cutaneous melanoma (SKCM) and breast invasive carcinoma (BRCA) ST slides. (G) Stacking plot shows the proportion of TCGA-LIHC samples in TIDE-predicted immunotherapy-responsive (R) and non-responsive (NR) samples based on the FAP and DAB2 expression groupings; quad plot shows the significance assessment of the consistency of the four grouping clusters based on the submap method. (H) Box plot comparing the difference between FAP + CAF and DAB2 + TAM scores in the response and non-response groups in the immunotherapy cohort Imvigor210. (I) Stacking plot showing the proportion of FAP + CAF and DAB2 + TAM in the response and non-response groups in our integrated pan-cancer immunotherapy scRNA-seq cohort.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g007.jpgAnti-FAP1 Rabbit Monoclonal AntibodyImmunohistochemical evaluation of FAP and DAB2. (A) Immunohistochemical staining image shows FAP + CAF and DAB2 + TAM around the tumor core. (B) KM curves show the high FAP or DAB2 average optical density (AOD) group with shorter OS. (C) KM curves show the high FAP and DAB2 AOD group had shortest overall survival. (D) Heatmap showing the distribution of clinical indicators in the sample sorted by FAP AOD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g004.jpgAnti-FAP1 Rabbit Monoclonal AntibodySpatial co-localization of TAM with FAP + CAF. (A) UMAP shows the distribution of monocyte/macrophage subtypes. (B) Bar plot shows the relative proportions of macrophage subtypes in HCC and ICC samples (left); paired dot plot shows the relative proportions of DAB2 + / SPP1 + TAMs in tumor and adjacent liver paired samples (right). *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001. (C) Distribution of DAB2 + TAMs and FAP + CAF in HCC boundary slides, and SPP1 + TAM and FAP + CAF in ICC boundary slides based on CellTrek deconvolution (left); heatmap shows the Kullback-Leibler (KL) divergence of FAP + CAF with different macrophage subtypes in ST slides, with the higher KL divergence representing the greater degree of co-localization of the two cell types (right). (D) Pie plots showing the relative proportions of different macrophage subtypes in the ST slides. (E) Unbiased clustering of ST spots and definition of cell types of each cluster (left); dot plot showing the expression of select marker genes of each cluster (right). (F) Multi-plex immunofluorescence images showing the aggregation of FAP + CAF with DAB2 + TAM at the tumor border in HCC and FAP + CAF with SPP1 + TAM at the tumor border and core in ICC. The scale bar is 200 μm and 100 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g005.jpgAnti-FAP1 Rabbit Monoclonal AntibodyCellular communication between TAM and FAP + CAF. (A) The combined heatmap shows the results after NicheNet analysis of TAM and FAP + CAF. The first part of the combined figure shows the Pearson coefficient of the macrophage ligand, and the high coefficient suggests that the ligand has a high ability to regulate the FAP + CAF target genes, the second part shows the expression of the ligand in different subtypes of macrophage, and the third part shows the comparison of the expression of the ligand in HCC and ICC, and the fourth part shows the regulated potential of the target genes. (B) Bar plot shows GO biology terms enriched for all targeted genes, PDGFB target genes, and ADM target genes. (C) Dot plot showing the expression of PDGFB receptors LRP1 , PDGFRB and PDGFRA in fibroblasts. (D) Spatial dot plot showing the spatial expression of PDGFB in DAB2 + TAM and PDGFRB in FAP + CAF. (E) KM curves showing the association of quantified ligand-receptor score (LRscore) with patient OS in five independent bulk RNA-seq cohorts.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g003.jpgAnti-FAP1 Rabbit Monoclonal AntibodySpatial distribution of FAP + CAF. (A) Bar plot shows the proportion of fibroblast subtypes that were deconvoluted by CellTrek onto hepatocellular carcinoma (HCC) spatial transcriptome sections. (B) Spatial feature plot showing the expression of FAP in tumor and paracancerous samples from four HCC patients. (C and D) Distribution of fibroblast subtypes in HCC and intrahepatic cholangiocarcinoma (ICC) border slides based on CellTrek deconvolution. The pie charts show the relative proportion of each cell subtype in the border region. (E and F) Spatial feature plot showing the expression of selected genes in HCC and ICC border samples.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g002.jpgAnti-FAP1 Rabbit Monoclonal AntibodyAssociation of FAP + CAF with clinical features and differentiation origins. (A) Forest plot showing the proportion of FAP + CAF in the single-cell discovery cohort was significantly associated with patient survival by Cox analysis. (B) KM curve shows that the high ratio of FAP + CAF group based on the best cutoff grouping had shorter overall survival; barplot shows that the FAP + CAF proportion was significantly higher in different liver cancer samples compared to adjacent liver (AL); boxplot shows the differences in FAP + CAF proportion among different clinical characteristic groups. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001. (C) UMAP shows prognostic-associated cells and their tissue-type origins identified by the Scissor algorithm. (D) KM curves show poorer survival of patients with a high proportion of Scissor + cells in the single-cell discovery cohort. (E) Bar plot showing the proportion of Scissor + cells in different tissue types. (F) Pie plot showing the percentage of different fibroblast subtypes in Scissor-related cells. (G) KM curves showing the high FAP + CAF score group usually predicted worse overall survival in the five liver cancer bulk transcriptome cohorts. (H) Fibroblast differentiation trajectories showing the distribution of cell type, sample type, Scissor type and state.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-thnov14p4822g001.jpgAnti-FAP1 Rabbit Monoclonal AntibodyIdentification of key cancer-associated fibroblasts. (A) UMAP shows the cellular clustering of major cell types in the discovery cohort and the corresponding cell numbers. (B) Heatmap showing the cell preference of different major cell types in peripheral blood (PB), adjacent liver (AL), intrahepatic cholangiocarcinoma (ICC), hepatocellular carcinoma (HCC), combined hepatocellular and cholangiocarcinoma (CHC), and secondary liver cancer (SLC). (C) Volcano plot showing the difference in the proportion of major cell types in HCC (n = 82) versus AL (n = 14). (D) UMAP shows the distribution of fibroblast subtypes in the discovery cohort. (E) Stacking plot shows the percentage of fibroblast subtypes in the five tissue types. (F) Dot plot shows top5 highly expressed genes for each fibroblast subtypes. (G) Volcano plot comparing the relative abundance of HCC/ICC versus AL fibroblast subtypes. (H) Heatmap showing the Ucell enrichment scores of key biological entries of fibroblasts in different subtypes. (I) UMAP shows the identification of fibroblasts from an integrated validated single-cell cohort (left); box plot shows the significantly higher relative abundance of fibroblast in AL, HCC and ICC (median); stacking plot shows the progressively higher proportion of FAP + CAF in HCC and ICC compared to AL (right). (J) Immunohistochemically stained pathology sections and box plot showed progressively higher FAP expression and average optical density (AOD) in AL (n = 8), HCC (n = 8) and ICC (n = 10) samples.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC11373629/&orig_host=www.ncbi.nlm.nih.gov'>39239526</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-jcav09p3278g004.jpgAnti-FAP1 Rabbit Monoclonal AntibodyKaplan-Meier survival analyses of HIF-1α and FAP in HCC patients. (A) Overall survival for postoperative HCC patients: low expression of HIF-1α (n=74, mean=70.7 months), high expression of HIF-1α (n=64, mean=35.5 months). (B) Time to recurrence for postoperative HCC patients: low expression of HIF-1α (n=74, mean=56.5 months), high expression of HIF-1α (n=64, mean=25.2 months). (C) Overall survival for HCC patients: low expression of FAP (n=65, mean=71.1 months), high expression of FAP (n=73, mean=34.8 months). (D) Time to recurrence for postoperative HCC patients: low expression of FAP (n=65, mean=58.6 months), high expression of FAP (n=73, mean=21.6 months).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160687/'>30271487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-41467_2023_43980_fig7_html.pngAnti-FAP1 Rabbit Monoclonal AntibodyFibrovascular niches within the stromal compartment of AM. a UMAP plot illustrating the landscape of all stromal cells color-coded by their associated subclusters. b Feature plots displaying classical marker genes used for the annotation of these subclusters. c UMAP plot showing the separation of stromal cells based on LN + AM and LN - AM, accompanied by a bar plot indicating the proportion of these subclusters in LN + AM and LN - AM. Source data are provided in the Source Data file. d Heatmap presenting the cluster-specific genes of these subclusters. Source data are provided in the Source Data file. e GSVA analysis of selected hallmark pathways in these subclusters. f RNA velocity analysis demonstrating the evolutionary trajectory of these subclusters. g Spatial feature plot showing the scores of endothelial cells and fibroblasts in tissue sections using ST-seq data. Scale bar, 1000 μm. h Scatter plot showing the correlation between endothelial ( x -axis) and fibroblast ( y -axis) cells, stratified by LN + AM and LN − AM. The correlation is evaluated using the two-sided Spearman correlation coefficient. The gray band represents the 95% confidence interval of the regression line. Source data are provided in the Source Data file. i Representative image of fibrovascular niches detected by anti-FAP and anti-CD31 in AM sections using the multiplex IHC assay, and violin plot showing the number of fibrovascular niches in LN − AM ( n = 73) and LN + AM ( n = 28). The box center lines, bounds of the box, and whiskers indicate medians, first and third quartiles, and minimum and maximum values within 1.5× IQR of the box limits, respectively. Significance was determined using a two-sided Mann–Whitney U -test (* P -value < 0.05; P = 0.03). Scale bar, 150 μm. The experiment was repeated once with similar results. Source data are provided in the Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41467-023-43980-y'>38065972</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-jcav09p3278g005.jpgAnti-FAP1 Rabbit Monoclonal AntibodyCombined HIF-1α and FAP expression in Kaplan-Meier survival analyses for HCC patients. (A) Overall survival for postoperative HCC patients: all low expression (n=48, mean=74.3 months), HIF-1α low/ FAP high or HIF-1α high/ FAP low expression (n=43, mean=53.9 months), all high expression (n=47, mean=28.9 months) (B) Time to recurrence for postoperative HCC patients: all low expression (n=48, mean=64.2 months), HIF-1α low/ FAP high or HIF-1α high/ FAP low expression (n=43, mean=35.4 months), all high expression (n=47, mean=18.2 months).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160687/'>30271487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-j_biol-2022-0776_fig_004.jpgAnti-FAP1 Rabbit Monoclonal AntibodyProtein expression levels in fibroblasts. The protein expression levels of E-cadherin, α-SMA, FAP, and Cav-1 in the fibroblasts were detected by Western blot analysis. Representative and quantitative Western blot results were shown. Compared with HKF control, * P < 0.05; compared with HKF + EXO co-culture, # P < 0.05; and compared with HKF + siRNA negative control-EXO co-culture, & P < 0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.degruyter.com/document/doi/10.1515/biol-2022-0776/html'>38045487</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-fimmu-16-1568556-g002.jpgAnti-FAP1 Rabbit Monoclonal Antibody(A) Kaplan-Meier survival curves generated for four subgroups of LUAD patients stratified by the expression of SMARCA2 and SMARCA4 (median cutoff), and P-values were calculated by log-rank test. (B) The volcano plot of differential gene expressions in SMARCA2 Low versus SMARCA2 High . The two vertical dashed lines represent absolute foldchange>1.5 in gene expression, and the horizontal dashed line denotes adjusted P-value cutoff 0.05. (C) GO-biological process (BP) and (D) GSEA enrichment analyses of DEGs in SMARCA2 Low and SMARCA2 High . (E) Heatmap showing the infiltration of cell subpopulations for four subgroups of LUAD patients stratified by the expression of SMARCA2 and SMARCA4 (median cutoff) using multiple algorithms including CIBERSORT, MCP-counter, EPIC, ESTIMATE, quantiseq, and TIMER. Statistical significance was determined by Kruskal-Wallis’s test. (F) The scatterplot showing the correlation between the protein levels of SMARCA2 and SMARCA4 and FAP, SPP1, ACTA2, CD3D, CD8A, and CD4. Correlation analysis was created with Pearson’s correlation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1568556/full'>40453096</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gdnf-rabbit-monoclonal-antibody-m00710-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00710-gdnf-primary-antibodies-wb-testing-1.jpgAnti-GDNF Rabbit Monoclonal AntibodyWestern blot analysis of GDNF using anti-GDNF antibody (M00710). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GDNF antigen affinity purified monoclonal antibody (M00710) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GDNF at approximately 32 kDa. The expected band size for GDNF is at 24 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mrp2-rabbit-monoclonal-antibody-m00974-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00974-abcc2-primary-antibodies-wb-testing-1.jpgAnti-MRP2 ABCC2 Rabbit Monoclonal Antibody Western blot analysis of ABCC2 using anti-ABCC2 antibody (M00974). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human HUH-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCC2 antigen affinity purified monoclonal antibody (Catalog # M00974) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABCC2 at approximately 250 kDa. The expected band size for ABCC2 is at 174 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sdhb-rabbit-monoclonal-antibody-m01090-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01090-sdhb-primary-antibodies-wb-testing-1.jpgAnti-SDHB Rabbit Monoclonal Antibody Western blot analysis of SDHB using anti-SDHB antibody (M01090). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SDHB antigen affinity purified monoclonal antibody (Catalog # M01090) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SDHB at approximately 29 kDa. The expected band size for SDHB is at 32 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tgm2-rabbit-monoclonal-antibody-m02229-1-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02229-1-wb.jpgAnti-TGM2/Transglutaminase 2 Rabbit Monoclonal AntibodyWestern blot analysis of TGM2 expression in HUVEC cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chd4-rabbit-monoclonal-antibody-m01125-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01125-wb.jpgAnti-CHD4 Rabbit Monoclonal AntibodyWestern blot analysis of CHD4 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mrp1-rabbit-monoclonal-antibody-m00872-1-boster.html2026-03-24T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00872-1-wb.jpgAnti-MRP1 ABCC1 Rabbit Monoclonal AntibodyWestern blot analysis of MRP1 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tlr9-rabbit-monoclonal-antibody-m00198-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00198-wb.jpgAnti-TLR9 Rabbit Monoclonal AntibodyWestern blot analysis of TLR9 expression in Raji cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-relb-rabbit-monoclonal-antibody-m00836-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00836-relb-primary-antibodies-wb-testing-1.jpgAnti-RelB Rabbit Monoclonal Antibody Western blot analysis of RelB using anti-RelB antibody (M00836). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human THP-1 whole cell lysates,<br>
Lane 5: mouse spleen tissue lysates,<br>
Lane 6: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RelB antigen affinity purified monoclonal antibody (Catalog # M00836) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RelB at approximately 70 kDa. The expected band size for RelB is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00836-relb-primary-antibodies-ihc-testing-2.jpgAnti-RelB Rabbit Monoclonal Antibody IHC analysis of RelB using anti-RelB antibody (M00836). <br>
RelB was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-RelB Antibody (M00836) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pai1-rabbit-monoclonal-antibody-m00637-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00637-serpine1-primary-antibodies-wb-testing-1.jpgAnti-PAI1 Rabbit Monoclonal AntibodyWestern blot analysis of PAI-1/SERPINE1 using anti-PAI-1/SERPINE1 antibody (M00637). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U251 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: human A431 whole cell lysates,<br>
Lane 6: human U-87MG whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAI-1/SERPINE1 antigen affinity purified monoclonal antibody (M00637) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PAI-1/SERPINE1 at approximately 45 kDa. The expected band size for PAI-1/SERPINE1 is at 45 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ulk1-rabbit-monoclonal-antibody-m00584-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-12943_2020_1237_fig6_html.pngAnti-ULK1/Atg1 Rabbit Monoclonal AntibodymiR-619-5p negatively regulates Pygo2 and ATG14 expression. a The predicted miR-619-5p binding sequence in the Pygo2 3’UTR and the generation of dual-luciferase reporter plasmids of wild-type (WT) or mutant (MT) were shown. b Luciferase activity assays were performed in PANC-1 cells co-transfected with Pygo2 WT or Pygo2 MT and miR-619-5p mimic or miR-619-5p inhibitor. c and d The mRNA and protein levels of Pygo2 in PANC-1 and ASPC-1 cells after transfection with miR-619-5p mimics or miR-619-5p inhibitor. e Western blotting in PANC-1 cells transfected with PVT1 siRNA was carried out using the indicated antibodies. f and g The miR-619-5p binding sequence in the ATG14 3’UTR and the generation of dual-luciferase reporter plasmids of wild-type (WT) or mutant (MT) were shown. h Luciferase activity assays were performed in PANC-1 cells co-transfected with ATG14 WT or ATG14 MT and miR-619-5p mimic or miR-619-5p inhibitor. i-k The mRNA and protein levels of ATG14 in PANC-1 and ASPC-1 cells after transfection with miR-619-5p mimics or miR-619-5p inhibitor. l and m The expression of ATG14 after co-transfection with PVT1 and miR-619-5p mimics or PVT1 siRNA and miR-619-5p inhibitor. Data were represented as mean ± SD, * P < 0.05; ** P < 0.01; *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-020-01237-y'>32727463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-12943_2020_1237_fig7_html.pngAnti-ULK1/Atg1 Rabbit Monoclonal AntibodyPVT1/miR-619-5p axis promotes autophagic activity by regulating ATG14. a Western blotting analysis of PANC-1 and ASPC-1 cells after PVT1 knockdown with or without ATG14 overexpression was carried out with the indicated antibodies. b Western blotting analysis of PANC-1 and ASPC-1 cells after PVT1 overexpression with or without ATG14 knockdown was carried out with the indicated antibodies. c and d Representative confocal images of GFP-LC3 puncta in PANC-1 cells transfected with PVT1 siRNA with or without co-transfection of ATG14 overexpression plasmid with and without gemcitabine treatment. The number of GFP-LC3 puncta was quantified using ImageJ software. ( n = 10). Scale bars: 10 μm. e and f Representative confocal images of GFP-LC3 puncta in PANC-1 cells transfected with PVT1 overexpression plasmid with or without co-transfection with ATG14 siRNA with and without gemcitabine treatment. The number of GFP-LC3 puncta was quantified using ImageJ software. (n = 10). Scale bars: 10 μm. g and h Representative electronic micrographs of the autophagosomes or autolysosomes of PANC-1 cells co-transfected with PVT1 overexpression plasmid and/or ATG14 siRNA with or without gemcitabine treatment. Red arrows indicate autophagic structures. The number of autophagic structures per cell was quantified (n = 10). Scale bars: 2 μm. i and j Representative electronic micrographs of the autophagosomes or autolysosomes of PANC-1 cells co-transfected with miR-619-5p mimics and/or ATG14 siRNA with or without gemcitabine treatment. Red arrows indicate autophagic structures. The number of autophagic structures per cell was quantified (n = 10). Scale bars: 2 μm. k and l Western blotting analysis of PANC-1 and ASPC-1 cells after transfection with miR-619-5p mimics with or without ATG14 overexpression was carried out with the indicated antibodies. Data were represented as mean ± SD, * P < 0.05; ** P < 0.01; *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-020-01237-y'>32727463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-12943_2020_1237_fig8_html.pngAnti-ULK1/Atg1 Rabbit Monoclonal AntibodyPVT1 interacts with ATG14 and promotes PtdIns3K-C1 complex assembly. a The interaction between PVT1 and ATG14 in PANC-1 and ASPC-1 cells was confirmed by RNA pulldown followed by western blotting. b and c qRT-PCR analysis of PVT1 following RNA immunoprecipitation (RIP) assays in PANC-1 and ASPC-1 cells using anti-ATG14 antibody. RNA enrichment was determined relative to the IgG control. U6 was used as a non-specific control. d and e The interaction between PIK3C3 and ATG14 or BECN1 after PVT1 knockdown in PANC-1 cells. Immunoprecipitated endogenous PIK3C3 was quantified using Image Lab software and normalized against the amount of PIK3C3 in whole-cell lysates. f and g The interaction between PIK3C3 and ATG14 or BECN1 after PVT1 overexpression and/or miR-619-5p co-transfection in PANC-1 cells with or without gemcitabine (1 μM) treatment. Immunoprecipitated endogenous PIK3C3 was quantified using Image Lab software and normalized against the amount of PIK3C3 in whole-cell lysates. h The interaction between Bcl2 and BECN1 after PVT1 overexpression in PANC-1 cells with or without gemcitabine (1 μM) treatment. Immunoprecipitated endogenous Bcl2 was quantified using Image Lab software and normalized against the amount of PIK3C3 in whole-cell lysates. i The interaction between PIK3C3 and BECN1 after the overexpression of miR-619-5p mimics in PANC-1 cells with or without gemcitabine (1 μM) treatment. Immunoprecipitated endogenous PIK3C3 was quantified using Image Lab software and normalized against the amount of PIK3C3 in whole-cell lysates. j-l Different PtdIns3K-C1 complex components were immunoprecipitated from PANC-1 and ASPC-1 cells overexpressing PVT1 or miR-619-5p mimics with or without gemcitabine (1 μM) treatment with ATG14 antibody. PIK3C3 activity was measured by analyzing PtdIns3P production using ELISA as described in the Materials and Methods section. The fold change in PtdIns3P activity was calculated based on the concentration of PtdIns3P and normalized to the amount of ATG14 used in the assay. m and n Representative confocal images of GFP-ZFYVE1 puncta in control or PVT1- or miR-619-5p-transfected PANC-1 cells with or without gemcitabine induction. The numbers of GFP-ZFYVE1 puncta was quantified ( n = 10). Scale bars: 10 μm. Data were represented as mean ± SD, * P < 0.05; ** P < 0.01; *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12943-020-01237-y'>32727463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-wb-testing-1.jpgAnti-ULK1/Atg1 Rabbit Monoclonal Antibody Western blot analysis of ULK1 using anti-ULK1 antibody (M00584). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ULK1 antigen affinity purified monoclonal antibody (Catalog # M00584) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ULK1 at approximately 130 kDa. The expected band size for ULK1 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-ihc-testing-2_1.jpgAnti-ULK1/Atg1 Rabbit Monoclonal Antibody IHC analysis of ULK1 using anti-ULK1 antibody (M00584). <br>
ULK1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ULK1 Antibody (M00584) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-ihc-testing-3.jpgAnti-ULK1/Atg1 Rabbit Monoclonal Antibody IHC analysis of ULK1 using anti-ULK1 antibody (M00584). <br>
ULK1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ULK1 Antibody (M00584) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-ihc-testing-4.jpgAnti-ULK1/Atg1 Rabbit Monoclonal Antibody IHC analysis of ULK1 using anti-ULK1 antibody (M00584). <br>
ULK1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ULK1 Antibody (M00584) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-ihc-testing-5.jpgAnti-ULK1/Atg1 Rabbit Monoclonal Antibody IHC analysis of ULK1 using anti-ULK1 antibody (M00584). <br>
ULK1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ULK1 Antibody (M00584) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584-ulk1-primary-antibodies-if-testing-3.jpgAnti-ULK1/Atg1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using ULK1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-actin-rabbit-monoclonal-antibody-m02014-1-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-1-acta1-primary-antibodies-wb-testing-1.jpgAnti-Actin ACTA1 Rabbit Monoclonal Antibody Western blot analysis of ACTA1 using anti-ACTA1 antibody (M02014-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat small intestine tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse small intestine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACTA1 antigen affinity purified monoclonal antibody (Catalog # M02014-1) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACTA1 at approximately 42 kDa. The expected band size for ACTA1 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02014-1-ACTA1-primary-antibodies-IHC-testing-1.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse heart, using Actin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-1-3.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Actin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-1-icc1.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-1-icc2.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gapdh-rabbit-monoclonal-antibody-m00227-1-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-gapdh-primary-antibodies-wb-testing-1_1.jpgAnti-GAPDH Rabbit Monoclonal Antibody Western blot analysis of GAPDH using anti-GAPDH antibody (M00227-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: human PC-3 whole cell lysates,<br>
Lane 6: monkey COS-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified monoclonal antibody (Catalog # M00227-1) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-1-s2.0-s2405844024027464-gr6.jpgAnti-GAPDH Rabbit Monoclonal AntibodyWBS inhibited the expression of TYR (A), TYRP-1 (B), TYRP-2 (C) and MITF (D) in B16F10 cells. Levels of MITF (E), TYRP-1 (F) and TYRP-2 (G) proteins in B16F10 cells treated with WBS as determined by western blotting. GAPDH was a loading control (H). The data are expressed as the mean ± S.E.M. and were analyzed by one-way. Significance was defined as *p<0.05, **p<0.01, ***p<0.001 and ****p<0.0001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2405844024027464'>38455547</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-gapdh-primary-antibodies-wb-testing-2.jpgAnti-GAPDH Rabbit Monoclonal Antibody Western blot analysis of GAPDH using anti-GAPDH antibody (M00227-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: rat RH35 whole cell lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified monoclonal antibody (Catalog # M00227-1) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-gapdh-primary-antibodies-ihc-testing-1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder cancer, using GAPDH Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-gapdh-primary-antibodies-if-testing-1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using GAPDH Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-icc1_1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-1-icc2_1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gapdh-rabbit-monoclonal-antibody-m00227-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00227-GAPDH-primary-antibodies-WB-testing-1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyWestern blot analysis of GAPDH expression in (1) Hela cell lysate; (2)Jurkat cell lysate; (3)Mouse kidney lysate; (4) Mouse spleen lysate; (5) RAW 264.7 cell lysate; (6) Rat brain lysate with GAPDH Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-wb2.jpgAnti-GAPDH Rabbit Monoclonal AntibodyAll lanes use GAPDH Antibody at 1:50000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-fnut-12-1562509-g004.jpgAnti-GAPDH Rabbit Monoclonal AntibodyEffects of n-6 PUFA on liver lipid peroxidation and the inflammatory marker NF-κB in rats with NASH induced by a choline-deficient diet. (A) Liver MDA levels, (B) PPAR-α mRNA expression in the liver. Data are expressed as mean ±SEM; n = 6/group. (C) NF-κB protein expression (~65 kDa) in the liver as analyzed by Western blotting, normalized to GAPDH, with a representative blot (left) and quantification (right). Protein molecular weight standards (kDa) are labeled on the left of each blot. Data are expressed as mean ± SEM; n = 6/group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/nutrition/articles/10.3389/fnut.2025.1562509/full'>40626231</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-fnut-12-1562509-g005.jpgAnti-GAPDH Rabbit Monoclonal AntibodyEffects of n-6 PUFA on liver macrophage phenotype in rats with NASH induced by a choline-deficient diet. (A) M1-type Kupffer cells (KCs) identified by double staining: red arrows show CD11c-positive cells, green arrows show CD68-positive cells, and yellow arrows highlight CD11c and CD68 double-positive M1-type KCs (Scale bar – 50 μM). (B) M2-type KCs identified similarly, with red arrows indicating CD163-positive cells, green arrows showing CD68-positive cells, and yellow arrows marking CD163 and CD68 double-positive M2-type KCs (Scale bar – 50 μM). For (A,B) (see ) for full-size photomicrographs. (C) M1/M2 phenotype ratio (unitless), calculated as the proportion of CD68 + CD11c + to CD68 + CD163 + cells. (D) Relative PPAR-γ2 mRNA expression (fold change normalized to GAPDH) in the liver, which is linked to macrophage polarization and inflammation. Data are expressed as mean ±SEM; n = 6/group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/nutrition/articles/10.3389/fnut.2025.1562509/full'>40626231</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-wb3.jpgAnti-GAPDH Rabbit Monoclonal AntibodyAll lanes use GAPDH Antibody at 1:50000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00227-GAPDH-primary-antibodies-IHC-testing-1.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded (1) Rat colon; (2) Mouse testis; (3) Human uterus; (4) Human kidney, using GAPDH Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-ihc7.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary adenoma, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-ihc8.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous carcinoma, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-ihc9.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00227-if.jpgAnti-GAPDH Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using GAPDH Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tgfbi-rabbit-monoclonal-antibody-m01218-2-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01218-2-tgfb1-primary-antibodies-wb-testing-1.jpgAnti-TGFBI/Beta Ig H3 Rabbit Monoclonal AntibodyWestern blot analysis of TGFB1 using anti-TGFB1 antibody (M01218-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U251 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TGFB1 antigen affinity purified monoclonal antibody (M01218-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TGFB1 at approximately 68 kDa. The expected band size for TGFB1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01218-2-ihc.jpgAnti-TGFBI/Beta Ig H3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kideny, using TGFBI Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mklp1-rabbit-monoclonal-antibody-m03483-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03483-kif23-primary-antibodies-wb-testing-1.jpgAnti-MKLP1 KIF23 Rabbit Monoclonal Antibody Western blot analysis of KIF23 using anti-KIF23 antibody (M03483). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SiHa whole cell lysates,<br>
Lane 3: human Hacat whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KIF23 antigen affinity purified monoclonal antibody (Catalog # M03483) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KIF23 at approximately 98 kDa. The expected band size for KIF23 is at 98 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kifc1-rabbit-monoclonal-antibody-m05325-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05325-kifc1-primary-antibodies-wb-testing-1.jpgAnti-KIFC1 Rabbit Monoclonal AntibodyWestern blot analysis of KIFC1 using anti-KIFC1 antibody (M05325). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human SH-SY5Y whole cell lysates,<br>
Lane 6: human U2OS whole cell lysates,<br>
Lane 7: human THP-1 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KIFC1 antigen affinity purified monoclonal antibody (M05325) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KIFC1 at approximately 74 kDa. The expected band size for KIFC1 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05325-ihc.jpgAnti-KIFC1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid carcinoma, using KIFC1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rnf20-rabbit-monoclonal-antibody-m03457-1-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03457-1-rnf20-primary-antibodies-wb-testing-1.jpgAnti-RNF20 Rabbit Monoclonal AntibodyWestern blot analysis of RNF20 using anti-RNF20 antibody (M03457-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RNF20 antigen affinity purified monoclonal antibody (M03457-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RNF20 at approximately 114 kDa. The expected band size for RNF20 is at 114 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03457-1-icc1.jpgAnti-RNF20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03457-1-icc2.jpgAnti-RNF20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad3-rabbit-monoclonal-antibody-m00059-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-41419_2020_2818_fig2_html.pngAnti-Smad3 Rabbit Monoclonal AntibodyTGF-β2 gene expression and TGF-Smad signaling are augmented in Sema7A-HUVECs. a The top 30 upregulated genes in Sema7A-HUVECs compared with Con335-HVUECs. b TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, *** p < 0.001. c The concentration of TGF-β2 in cell supernatant was detected by ELISA. N = 10. Unpaired two-tailed Student’s t tests was used to analysis the data. Data are mean ± SEM, ** p < 0.01. d GSEA based on gene ontology (GO) pathway database showed TGF-β signaling pathway was enrich in Sema7A-HUVECs. e , f Cells were treated with Oxymatrine (Oxy) (20 μmol/l) or T4442 (1 μg/ml) and the lysates were analyzed by western blotting for Smad3 phosphorylation, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. g , h CD31 and α-SMA mRNA in cells treated with inhibitors were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. i – k CD31 and α-SMA proteins in cells treated with inhibitors were analysis by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. T4442: TGF-β2 blocking antibody; Oxymatrine (Oxy): TGF/Smad signaling pathway inhibitor. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-41419_2020_2818_fig3_html.pngAnti-Smad3 Rabbit Monoclonal AntibodyInhibition of ATF3 reduced TGF-β2 expression and Sema7A-induced EndMT. a ATF3 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, *** p < 0.001 b ATF3 protein expression were analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, *** p < 0.001. c TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. d The concentration of TGF-β2 in cell supernatant was detected by ELISA among Con335-HUVECs, Sema7A-HUVECs, and Sema7A-HUVECs + ATF3-siRNA. N = 10. Data are mean ± SEM, * p < 0.05; *** p < 0.001. e Chip-qPCR product in agarose gel electrophoresis. f Chip-qPCR TGF-β2 percentage of input in con335-HUVECs and Sema7A - HUVECs were analyzed by qPCR normalized to IgG. Data are mean ± SEM, N = 3, ** p < 0.01. g Schematic graph of the constructed reporter plasmid. TGF-β2 mut indicates the TGF-β2 mutation promoter region in ATF3 binding site. The mutated nucleotides in TGF-β2 fragments are in red letters. h Luciferase reporter assays were performed on HEK 293 T cells. Data are mean ± SEM, N = 3, ** p < 0.01 vs negative control. i , j ATF3-overexpression plasmid was transfected to HUVECs, and the mRNA levels of TGF - β2 and TGF-β1 were performed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, ** p < 0.01. k , l P-Smad3 protein in cells treated with siRNA was analyzed by Western blotting, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. m – q CD31 and α-SMA RNA and proteins in cells treated with siRNA or control was analyzed by qPCR and western blotting. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-41419_2020_2818_fig4_html.pngAnti-Smad3 Rabbit Monoclonal AntibodyΒ1 integrin mediates Sema7A signal to TGF-β2 via ATF3. a Cells were treated with β1 integrin antibody (P5D2), and ATF3 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.0.1. b ATF3 protein expression was analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01. c TGF-β2 mRNA level was analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.0.1. d The concentration of TGF-β2 in cell supernatant was detected by ELISA for Con335-HUVECs, Sema7A-HUVECs, and Sema7A-HUVECs + P5D2. Data are mean ± SEM, N = 10, * p < 0.05; *** p < 0.001. e , f Smad3 phosphorylation were analyzed by western blotting, normalized to total Smad3. Data are mean ± SEM, N = 3, * p < 0.05. g , h CD31 and α-SMA mRNA level were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. i – k CD31 and α-SMA proteins were analyzed by western blotting, normalized to tubulin. Data are mean ± SEM, N = 3, * p < 0.05; ** p < 0.01; *** p < 0.001. l ATF3 overexpression plasmid was transfected into P5D2 incubated Sema7A-HUVECs, and TGF-β2 mRNA expression in Sema7A-HUVECs + P5D2 and Sema7A-HUVECs + P5D2 + ATF3 were analyzed by qPCR normalized to GAPDH. Fold changes are shown. Data are mean ± SEM, N = 3, ** p < 0.01. m – o CD31 and α-SMA protein expressions were analyzed by western blotting, normalized to GAPDH. Data are mean ± SEM, N = 3, ** p < 0.01 (Sema7A-HUVECs + P5D2 vs Sema7A-HUVECs + P5D2 + ATF3). P5D2 β1 integrin antibody. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-020-02818-x'>32826874</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-ihc7.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-smad3-primary-antibodies-wb-testing-1.jpgAnti-Smad3 Rabbit Monoclonal AntibodyWestern blot analysis of Smad3 using anti-Smad3 antibody (M00059). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human SW620 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse lung tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Smad3 antigen affinity purified monoclonal antibody (M00059) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Smad3 at approximately 50 kDa. The expected band size for Smad3 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-ihc8.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-ihc9.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-ihc.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using Smad3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-icc1.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00059-if.jpgAnti-Smad3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Smad3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad4-rabbit-monoclonal-antibody-m00074-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00074-wb.jpgAnti-Smad4 Rabbit Monoclonal AntibodyWestern blot analysis of SMAD4 expression in (1) SH-SY5Y cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00074-wb8.jpgAnti-Smad4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00074-ihc.jpgAnti-Smad4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Smad4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00074-wb7.jpgAnti-Smad4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat3-rabbit-monoclonal-antibody-m00007-2-boster.html2026-03-24T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-wb.jpgAnti-STAT3 Rabbit Monoclonal AntibodyWestern blot analysis of STAT3 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-ott-12-2011fig7.jpgAnti-STAT3 Rabbit Monoclonal AntibodyEffect of curcumin on p-JAK2/p-STAT3 signaling in MG-63 cells. Notes: MG-63 cells were treated with curcumin (0, 5, 10, or 20 µM) for 24 hours. Cell lysates were harvested, and expression of p-JAK2, JAK2, p-STAT3, and STAT3 was determined by Western blot. GAPDH was used as an internal control. ** P <0.01 and *** P <0.001. Abbreviation: p, phosphorylated.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421868/'>30936718</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-ott-12-2011fig8.jpgAnti-STAT3 Rabbit Monoclonal AntibodyExpression of p-JAK2 and STAT3 in OS tissue samples. Notes: IH staining of p-JAK2 and STAT3 in osteosarcoma tumor tissues. Positive cells contain dark-brown particles. Abbreviations: p, phosphorylated; OS, osteosarcoma; IH, immunohistochemical.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421868/'>30936718</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-ott-12-2011fig9.jpgAnti-STAT3 Rabbit Monoclonal AntibodyIn vivo effects of curcumin in nude mice. Notes: ( A ) The tumor sizes in the control group after 4 weeks of placebo treatment. ( B ) The tumor sizes in the study group after 4 weeks of curcumin treatment. ( C ) Expression of p-JAK2 in the xenograft sample. ( D ) Expression of STAT3 in the xenograft sample. After curcumin treatment for 4 weeks, the tumor sizes were significantly smaller than those in the control group. The expression of p-JAK2 and STAT3 in the curcumin group was much lower than that in the control group. Abbreviation: p, phosphorylated.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421868/'>30936718</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-ihc.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse liver, using STAT3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-2-if.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using STAT3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd11b-rabbit-monoclonal-antibody-m00144-1-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-itgam-primary-antibodies-wb-testing-1.jpgAnti-CD11b ITGAM Rabbit Monoclonal Antibody Western blot analysis of CD11B/Integrin Alpha M/ITGAM using anti-CD11B/Integrin Alpha M/ITGAM antibody (M00144-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD11B/Integrin Alpha M/ITGAM antigen affinity purified monoclonal antibody (M00144-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD11B/Integrin Alpha M/ITGAM at approximately 170 kDa. The expected band size for CD11B/Integrin Alpha M/ITGAM is at 127 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-fphar-16-1546045-g001.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyMacrophage PKM2 expression was markedly upregulated in liver tissues with ALI. (A) Log ratio–average (M–A) plots showing the changes in gene expression in ALF patients and control individual (GSE255777). (B) Gene set enrichment analysis (GSEA) of the DEGs. (C) Representative images and quantification of H&E- and immunohistochemistry staining of PKM1 and PKM2 in liver tissues of APAP- or LPS/D-GaIN-induced ALI mice and control mice. (D) Dual immunofluorescence staining for PKM2 and HNF-4α (A) or F4/80 (B) in liver tissues of APAP-induced ALI mice and control mice. (E) Representative images of H&E staining, dual immunofluorescence staining for PKM2 and F4/80, and immunohistochemistry staining for CD11b in APAP-induced mouse ALI at the indicated time points with quantification. Scale bar: 100 μm. White arrows indicate PKM2 + F4/80 + cells; Necrotic region was enclosed in dotted lines. *** P < 0.001. Error bars depict the standard deviations.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1546045/full'>40351417</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-fphar-16-1546045-g003.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyMacrophage PKM2 knockout mice showed ameliorated hepatic inflammation and hepatocyte apoptosis. ( A, B ) Representative images and quantification of TUNEL staining (A) and immunohistochemistry staining for Cleaved Caspase 3 (B) of PKM2 ΔMAC and PKM2 FL/FL mice after 24 h of APAP induction (300 mg/kg). ( C, D ) Representative images and quantification of immunohistochemistry staining for CD11b (C) and F4/80 (D) of PKM2 ΔMAC and PKM2 FL/FL mice after 24 h of APAP induction (300 mg/kg). Black arrow indicates CD11b + cells. ( E ) The mRNA levels of Tnfa, Il1b, Il6 in liver tissues of PKM2 ΔMAC and PKM2 FL/FL mice with or without APAP treatment. ( F, G ) The levels of TNF-α (F) and HMGB1 (G) in serum of PKM2 ΔMAC and PKM2 FL/FL mice with or without APAP treatment. Scale bar: 100 μm. *** P < 0.001. Error bars depict the standard deviations.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1546045/full'>40351417</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-fphar-16-1546045-g004.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyDeletion of PKM2 in macrophages reprogrammed M1 macrophages to M2 macrophages. (A) Representative images and quantification of immunofluorescence staining for iNOS and CD206 in the liver tissues of PKM2 ΔMAC and PKM2 FL/FL mice after 24 h of APAP induction (300 mg/kg). (B) Protein levels of p-STAT1, STAT1, p-STAT6 and STAT6 in liver tissues of PKM2 ΔMAC and PKM2 FL/FL mice induced by APAP or saline. (C) The mRNA levels of Tnfa , Il1b and Il6 in BMDMs of PKM2 ΔMAC and PKM2 FL/FL mice treated with or without LPS/IFN-γ. (D) Flow cytometry analysis of total macrophages (F4/80 + CD11b + ) and M1 (F4/80 + CD11b + CD86 + ) macrophages from BMDMs treated with LPS/IFN-γ, along with analysis of total macrophages (F4/80 + CD11b + ) and M2 (F4/80 + CD11b + CD206 + ) macrophages from BMDMs treated with IL-4 in vitro . (E) Schematic diagram illustrating the co-culture system of BMDMs and primary hepatocytes of indicated mice in the presence of LPS/IFN-γ. (F) The mRNA levels of Tnfa , Il1b and Il6 of hepatocytes co-cultured with indicated BMDMs. (G) The levels of HMGB1 in hepatocytes co-cultured with indicated BMDMs. Scale bar: 100 μm * P < 0.05; ** P < 0.01; *** P < 0.001. Error bars depict the standard deviations. BMDMs, bone marrow-derived macrophages.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1546045/full'>40351417</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-12872_2024_4070_figc_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyRNF5 knockout increased inflammatory response and apoptosis after MI in vivo. ( A ) Representative images (Left) and quantitative results (Right) of CD11B immunohistochemical staining of heart sections of the two groups of mice ( n = 6). Scale bar, 50 μm. (B) Representative images and quantitative results of Ly6g immunohistochemical staining of heart sections of the two groups of mice ( n = 6). Scale bar, 50 μm. ( C ) RT-PCR results of inflammatory responses associated genes including Tnf , Il6 , Il1b , and Ccl2 in WT and RNF5-KO mice subjected to MI surgery ( n = 4). ( D ) Western blot (Left) and quantification results (Right) of NF-κB signaling pathway-related proteins in wild type and RNF5-KO mice subjected to MI surgery ( n = 3). GAPDH was used as loading control. ( E ) Representative images (Up) and quantitative results (Down) of TUNEL staining of mice heart tissues sections from the indicated group ( n = 4). Scale bar, 20 μm. ( F ) RT-PCR results of apoptosis-related genes in wild type and RNF5-KO mice subjected to MI surgery ( n = 4). The RNA expression levels were normalized to Gapdh . ( G ) Western blot (Left) and quantification results (Right) of apoptosis-related proteins in wild type and RNF5-KO mice subjected to MI surgery ( n = 3). GAPDH was used as loading control. For statistical analysis, a two-tailed Student’s t -test was used. * for p < 0.05 and ** for p < 0.01 vs. WT MI 24 h group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12872-024-04070-z'>39098896</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-41419_2023_6216_fig4_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodySIRT4 regulated inflammatory response and oxidative stress during SAP in mice. A – B Statistics for the levels of inflammatory factors (IL-6, IL-1β, TNF-α and MCP-1). C – D Statistics for the levels of oxidative stress (GSH, H 2 O 2 , SOD and MDA) in the pancreas of mice. E – F Representative immunohistochemical staining of CD11b, MPO and Ly6G in the pancreas of mice. Scale bar = 100 µm. * P < 0.05, ** P < 0.01, *** P < 0.001, ns. not significant. n = 6 per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-023-06216-x'>37865653</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-41419_2023_6216_fig7_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodySIRT4 mitigated SAP by suppressing ferroptosis. A Fer-1 decreased the serum amylase level and lipase activity of SAP mice induced by L-Arg. B Representative HE staining images of pancreas. Scale bar = 100 µm. C The levels of oxidative stress (GSH, H 2 O 2 , SOD, MDA) in the pancreas of mice. D Representative IHC staining of CD11b, MPO, Ly6G and 4-HNE in the pancreas of mice in different groups. Scale bar = 100 µm. E The protein expression level of ferroptosis-related proteins (ACSL4, GPX4, SLC7A11) in the pancreas of mice in different groups. WT + SAP group, SIRT4_KO + SAP group, SIRT4_KO+Fer-1 + SAP group. E used GAPDH as the reference protein. * P < 0.05, ** P < 0.01, *** P < 0.001. n = 6 per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-023-06216-x'>37865653</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-41419_2023_6216_fig8_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyThe regulatory effect of SIRT4 on ferroptosis in SAP depends on the HIF-1α/HO-1 pathway. A – B The protein expression levels of HIF-1α, HO-1 and NQO-1 in the pancreas of mice. C Serum amylase level and lipase activity of mice in different groups after using HIF-1α inhibitor PX478 (100 mg/kg). D Representative HE staining images of mice pancreas in different groups after using HIF-1α inhibitor PX478 (100 mg/kg). Scale bar = 100 µm. E The levels of oxidative stress factors (GSH, H 2 O 2 , SOD, MDA) in the pancreas of mice in different groups after using HIF-1α inhibitor PX478 (100 mg/kg). F Representative IHC staining of CD11b, MPO, Ly6G and 4-HNE in the pancreas of mice in different groups after using HIF-1α inhibitor PX478(100 mg/kg). Scale bar = 100 µm. G The protein expression level of HIF-1α, HO-1, NQO-1, ACSL, GPX4 and SLC7A11 in the pancreas of mice in different groups after using HIF-1α inhibitor PX478 (100 mg/kg). WT + SAP group, SIRT4_KO + SAP group, SIRT4_KO + PX478 + SAP group. A – G used GAPDH as the reference protein. * P < 0.05, ** P < 0.01, *** P < 0.001, ns. not significant. n = 6 per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-023-06216-x'>37865653</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-cmh-2024-0478f6.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyThe effect of USP29 on hepatocyte lipid accumulation and MASLD is dependent on ACSL5. (A) The protein expression of USP29 and ACSL5 in WT or USP29-KO primary hepatocytes infected with ACSL5 overexpression and control adenovirus after PAOA stimulation. (b) Representative images of Nile red staining and (C) cellular TG content in indicated primary hepatocytes induced by PAOA (n=3 independent experiments). Scale bar, 25 μm. (D) The mRNA levels of Cpt1a , Ehhadh , Cxcl2 and Ccl5 in indicated primary hepatocytes induced by PAOA (n=4 mice/group). (E) The liver weight and the ratio of liver weight to body weight in USP29-KO and WT mice injected with AAV8-ACSL5 and controls fed a HFHC diet for 16 weeks (n=9 mice/group). (F) The serum lipid contents including TG and TC were detected in USP29-KO and WT mice injected with AAV8-ACSL5 and controls fed HFHC diet for 16 weeks (n=9 mice/group). (G) Representative images and relative quantitative statistical analysis of H&E, Oil red O, CD11b and PSR staining in liver tissue from USP29-KO and WT mice injected with AAV8-ACSL5 and controls fed HFHC diet for 16 weeks (n=4–6 mice/group). Scale bar, 50 μm. The data are presented as mean±SD ( * P <0.05, ** P <0.01, n.s., not significant). WT, wild type; KO, knock out; AAV, adeno-associated virus; HFHC, high-fat high cholesterol; TG, total triglyceride; TC, total cholesterol; H&E, hematoxylin and eosin; PSR, picro Sirius Red. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11791544/'>39355870</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-41467_2023_37908_fig5_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyLaptm5 -HKO exacerbates HFHC-induced NASH. a Fasting blood glucose of Laptm5 -HKO and Laptm5 -Flox mice for NC or HFHC consumptions ( n = 10 mice/group). b and c Liver weight and LW/BW ( b ), and hepatic TG, TC contents ( c ) of Laptm5 -HKO and Laptm5 -Flox mice after NC or HFHC feeding for 8 or 16 weeks ( n = 10 mice/group). d H&E (upper) and Oil Red O (lower) staining in the liver sections of mice in the indicated groups ( n = 6 mice/group). Scale bar, 100 μm. e and f NAS score analysis ( e ) and the statistical analysis of Oil red O staining ( f ) of Laptm5 -HKO and Laptm5 -Flox mice after NC or HFHC feeding for 8 or 16 weeks ( n = 6 mice/group). g Immunofluorescence staining ( g ) and statistical analysis ( h , i ) of CD11b (red) in the liver sections of mice in the indicated groups. (Nuclei, blue) ( n = 4 mice/group). Scale bar, 50 μm. PSR staining of mice liver sections in the indicated groups. (8 weeks, n = 6 mice/group, 16 weeks, n = 7 Laptm5 -Flox mice and n = 5 Laptm5 -HKO mice). Scale bars, 100 μm. j Serum ALT and AST concentrations of mice in the indicated groups ( n = 10 mice/group). k Hierarchical clustering analysis of the RNA-seq data from the mice fed the HFHC diet. l and m GSEA pathway enrichment analysis of pathways related to lipid metabolism, inflammation, apoptosis, and fibrosis. n Heatmaps of the genes related to lipid metabolism, inflammatory responses, and fibrosis (red, upregulated; blue, downregulated) in the indicated groups. Data are represented as mean ± SD. The Mann–Whitney U nonparametric statistical test was used for statistical analysis in ( c —8w, e —16w, and i —16w) and two-tailed Student’s t -test in other panels. Source data are provided as a Source data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-023-37908-9'>37156795</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-41467_2023_37908_fig8_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyAdenovirus-mediated hepatic Laptm5 over-expression alleviated non-alcoholic steatohepatitis. a Scheme of constructing Ad LAPTM5 -mediated therapeutic NASH models in HFHC mice. b Represents the WB detection results of the proteins indicated in the groups ( n = 3 mice/group). c and d Fasting blood glucose ( c ), liver weight, and LW/BW ( d ) of mice in the indicated groups ( n = 10 mice/group). e Hepatic TG and TC contents of mice in the indicated group ( n = 10 mice/group). f H&E (upper) ( n = 6 mice/group) and Oil Red O (lower) ( n = 5 mice/group) staining in the liver sections. Scale bar, 100 μm. g NAS score analysis of the group in panel ( f ) ( n = 6 mice/group). h Statistical analysis of Oil red O in the group of the panel ( f ) ( n = 5 mice/group). i Relative mRNA levels of genes related to the fatty acid metabolism in the livers of mice in the indicated groups ( n = 6 mice/group). j and k Immunofluorescence staining ( j ) and Statistical analysis ( k ) of CD11b (red) in the liver sections of HFHC-fed mice in the indicated groups ( n = 5 mice/group). Scale bar, 50 μm. l Relative mRNA levels of pro-inflammatory genes in the livers of mice in the indicated groups ( n = 6 mice/group). m Serum ALT and AST concentrations of mice in the indicated groups ( n = 10 mice/group). Data are represented as mean ± SD, two-tailed Student’s t -test was used to evaluate differences in all panels. Source data are provided as a Source data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-023-37908-9'>37156795</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig2a_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyHonokiol ameliorates high fat diet (HFD)-induced non-alcoholic fatty liver disease. A Schematic showing HFD-induced NAFLD and evaluation of therapeutic effects of honokiol in vivo (100 mg/kg). B and C Body ( B ) and liver weight ( C ) of NC- or HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. One-way ANOVA was used for statistical analysis. D Representative images of indicated mouse liver sections stained with hematoxylin and eosin (HE), oil red O (ORO), picrosirius red (PSR), and immunohistochemistry (IHC) of CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. E Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b shown in ( D ). n = 6 mice per group. Mann–Whitney U test was used for NAS, while Student’s t -test was applied to ORO, PSR, and CD11b data. F TG, TC, and non-esterified fatty acids (NEFA) in the livers of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. G Serum ALT and AST activity in HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. H Serum TC and TG concentrations in HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. I Heart weights and heart histological staining of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. Scale bar 50 μm. J Kidney and spleen weights of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. K GSVA enrichment analysis related to inflammation, lipid metabolism, and fibrosis downregulated by honokiol treatment. n = 5 mice per group. L Heatmap of gene expression profiles involved in cell damage and death, inflammation, and lipid metabolism. n = 5 mice per group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig2b_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyHonokiol ameliorates high fat diet (HFD)-induced non-alcoholic fatty liver disease. A Schematic showing HFD-induced NAFLD and evaluation of therapeutic effects of honokiol in vivo (100 mg/kg). B and C Body ( B ) and liver weight ( C ) of NC- or HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. One-way ANOVA was used for statistical analysis. D Representative images of indicated mouse liver sections stained with hematoxylin and eosin (HE), oil red O (ORO), picrosirius red (PSR), and immunohistochemistry (IHC) of CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. E Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b shown in ( D ). n = 6 mice per group. Mann–Whitney U test was used for NAS, while Student’s t -test was applied to ORO, PSR, and CD11b data. F TG, TC, and non-esterified fatty acids (NEFA) in the livers of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. G Serum ALT and AST activity in HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. H Serum TC and TG concentrations in HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. I Heart weights and heart histological staining of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. Scale bar 50 μm. J Kidney and spleen weights of HFD-fed mice treated with honokiol or vehicle after 12 weeks of their respective diets. n = 6 mice per group. Student’s t -test was applied for statistical analysis. K GSVA enrichment analysis related to inflammation, lipid metabolism, and fibrosis downregulated by honokiol treatment. n = 5 mice per group. L Heatmap of gene expression profiles involved in cell damage and death, inflammation, and lipid metabolism. n = 5 mice per group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig4a_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyHonokiol protects against mouse NASH. A Schematic of the CDAHFD-induced NASH model and evaluating the therapeutic effects of honokiol in vivo (100 mg/kg). B Body weights of NC- or CDAHFD-fed mice treated with honokiol or vehicle three weeks after subjecting them to their respective diets for one week. n = 6 mice per group. One-way ANOVA was used for statistical analysis. C Liver weights and ratio of liver weight to body weight (LW/BW) of NC- or CDAHFD-fed mice treated with honokiol or CMC three weeks after subjecting them to their respective diets for one week. n = 6 mice per group. One-way ANOVA assay was used for statistical analysis. D Blood glucose concentrations during GTT and the AUC of GTT of CDAHFD-fed mice treated with vehicle or honokiol. E Fasting blood glucose (FBG) concentrations of CDAHFD-fed mice treated with vehicle or honokiol. n = 6 mice per group. Student’s t -test was applied for statistical analysis. F TG, TC and NEFA levels in the livers of CDAHFD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. G Representative images of indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. H Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b shown in ( G ). n = 6 mice per group. The Mann–Whitney U test was used for NAS and Student’s t -test was applied to ORO, PSR, and CD11b data. I Serum ALT and AST activity and serum TG concentrations in CDAHFD-fed mice treated with honokiol or vehicles. n = 6 mice per group. Student’s t -test was applied for statistical analysis. J Schematic of the MCD-induced NASH model and evaluating the therapeutic effects of honokiol in vivo (100 mg/kg). K TG, TC. and NEFA levels in the livers of MCD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. L Representative images of the indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. M Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b data shown in ( L) . n = 6 mice per group. For statistical analysis, the Mann–Whitney U test was used for NAS and Student’s t -test was applied to ORO, PSR, and CD11b. N Serum ALT and AST activity of MCD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. O GSVA pathway enrichment analysis related to cell damage and death, inflammation, lipid metabolism, and fibrosis differentially regulated by honokiol treatment. n = 5 mice per group. P Heatmaps of gene expression profiles involved in cell damage and death, lipid metabolism, inflammation, and fibrosis <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig4b_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyHonokiol protects against mouse NASH. A Schematic of the CDAHFD-induced NASH model and evaluating the therapeutic effects of honokiol in vivo (100 mg/kg). B Body weights of NC- or CDAHFD-fed mice treated with honokiol or vehicle three weeks after subjecting them to their respective diets for one week. n = 6 mice per group. One-way ANOVA was used for statistical analysis. C Liver weights and ratio of liver weight to body weight (LW/BW) of NC- or CDAHFD-fed mice treated with honokiol or CMC three weeks after subjecting them to their respective diets for one week. n = 6 mice per group. One-way ANOVA assay was used for statistical analysis. D Blood glucose concentrations during GTT and the AUC of GTT of CDAHFD-fed mice treated with vehicle or honokiol. E Fasting blood glucose (FBG) concentrations of CDAHFD-fed mice treated with vehicle or honokiol. n = 6 mice per group. Student’s t -test was applied for statistical analysis. F TG, TC and NEFA levels in the livers of CDAHFD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. G Representative images of indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. H Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b shown in ( G ). n = 6 mice per group. The Mann–Whitney U test was used for NAS and Student’s t -test was applied to ORO, PSR, and CD11b data. I Serum ALT and AST activity and serum TG concentrations in CDAHFD-fed mice treated with honokiol or vehicles. n = 6 mice per group. Student’s t -test was applied for statistical analysis. J Schematic of the MCD-induced NASH model and evaluating the therapeutic effects of honokiol in vivo (100 mg/kg). K TG, TC. and NEFA levels in the livers of MCD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. L Representative images of the indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar 50 μm. M Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b data shown in ( L) . n = 6 mice per group. For statistical analysis, the Mann–Whitney U test was used for NAS and Student’s t -test was applied to ORO, PSR, and CD11b. N Serum ALT and AST activity of MCD-fed mice treated with honokiol or vehicle. n = 6 mice per group. Student’s t -test was applied for statistical analysis. O GSVA pathway enrichment analysis related to cell damage and death, inflammation, lipid metabolism, and fibrosis differentially regulated by honokiol treatment. n = 5 mice per group. P Heatmaps of gene expression profiles involved in cell damage and death, lipid metabolism, inflammation, and fibrosis <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig7a_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyAMPK activation is required for honokiol-mediated beneficial effects in vivo. A Schematic of the experimental procedure used with mice fed a CDAHFD diet and treated with vehicle or honokiol (100 mg/kg) in the absence or presence of compound C (CC, 10 mg/kg, every other day, i.p.). B Western blots of p-AMPKα, AMPKα, p-ACC, and ACC of mice in the indicated groups. n = 3 mice per group. C The blood glucose concentration during GTT of CDAHFD-fed mice in the indicated groups. n = 6 mice per group. One-way ANOVA was applied for statistical analysis. P -values of the red color represent the comparison of PBS-vehicle vs PBS-honokiol, while black represents CC-vehicle vs CC-honokiol. D Liver contents of TG, TC, and NEFA of CDAHFD-fed mice in the indicated groups. n = 6 mice per group. The Kruskal–Wallis test was applied for statistical analysis. E Representative images of the indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar, 50 μm. F Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b data shown in ( E ). n = 6 mice per group. For statistical analysis, the Kruskal–Wallis test was used for NAS and one-way ANOVA was applied to ORO, PSR, and CD11b data. G Serum ALT and AST activity of CDAHFD-fed mice shown in the indicated groups. n = 6 mice per group. Student’s t -test was applied for statistical analysis. H Serum TC concentrations in CDAHFD-fed mice treated with the indicated groups. n = 6 mice per group. Student’s t -test was applied for statistical analysis. I Dot plot representing pairwise GSVA comparisons of transcriptomic data from CDAHFD-fed mice shown in the indicated groups. J Heatmap of transcriptomic data from CDAHFD-fed mice shown in the indicated groups <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-13020_2023_729_fig7b_html.pngAnti-CD11b ITGAM Rabbit Monoclonal AntibodyAMPK activation is required for honokiol-mediated beneficial effects in vivo. A Schematic of the experimental procedure used with mice fed a CDAHFD diet and treated with vehicle or honokiol (100 mg/kg) in the absence or presence of compound C (CC, 10 mg/kg, every other day, i.p.). B Western blots of p-AMPKα, AMPKα, p-ACC, and ACC of mice in the indicated groups. n = 3 mice per group. C The blood glucose concentration during GTT of CDAHFD-fed mice in the indicated groups. n = 6 mice per group. One-way ANOVA was applied for statistical analysis. P -values of the red color represent the comparison of PBS-vehicle vs PBS-honokiol, while black represents CC-vehicle vs CC-honokiol. D Liver contents of TG, TC, and NEFA of CDAHFD-fed mice in the indicated groups. n = 6 mice per group. The Kruskal–Wallis test was applied for statistical analysis. E Representative images of the indicated mouse liver sections stained with HE, ORO, PSR, and IHC for CD11b-positive cells. n = 6 mice per group. Scale bar, 50 μm. F Results of NAS (HE) and quantitative analysis of ORO, PSR, and CD11b data shown in ( E ). n = 6 mice per group. For statistical analysis, the Kruskal–Wallis test was used for NAS and one-way ANOVA was applied to ORO, PSR, and CD11b data. G Serum ALT and AST activity of CDAHFD-fed mice shown in the indicated groups. n = 6 mice per group. Student’s t -test was applied for statistical analysis. H Serum TC concentrations in CDAHFD-fed mice treated with the indicated groups. n = 6 mice per group. Student’s t -test was applied for statistical analysis. I Dot plot representing pairwise GSVA comparisons of transcriptomic data from CDAHFD-fed mice shown in the indicated groups. J Heatmap of transcriptomic data from CDAHFD-fed mice shown in the indicated groups <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00729-5'>36932412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-cmh-2024-0478f3.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyUSP29 knockout accelerates hepatic steatosis, inflammation and fibrosis induced by a HFHC diet. (A) blood glucose of WT and USP29-KO mice after NC or HFHC diet treatment for 16weeks (n=8–10 mice/group). (b) GTTs of WT mice and USP29-KO mice were analyzed at the week 15 fed NC chow or HFHC diet (n=8–10 mice/group). (C) The ratio of liver weight to body weight of WT mice and USP29-KO mice fed NC chow or HFD diet for 16 weeks (n=8–10 mice/group). (D) Hepatic TG content and (E) serum TG, TC and LDL-C content were detected in WT mice and USP29-KO mice fed NC or HFHC diet for 16 weeks (n=8–10 mice/group). (F) Representative images and relative quantitative statistical analysis of H&E, Oil red O staining of liver tissue from WT and USP29-KO mice fed HFHC diet for 16 weeks (n=6 mice/group). Scale bar, 50 μm. (G) Representative images and relative quantitative statistical analysis of CD11b, F4/80, PSR and a-SMA staining of liver tissue from WT and USP29-KO mice fed HFHC diet for 16 weeks (n=4–6 mice/group). Scale bar, 50 μm. The data are presented as mean±SD, * indicates a statistical analysis between WT-NC group and WT-HFHC group ( ** P <0.01, n.s., not significant). # indicates a statistical analysis between WT-HFHC group and USP29-KO-HFHC group ( # P <0.05, ## P <0.01, n.s., not significant). WT, wild type; KO, USP29 knockout; NC, normal chow; HFHC, high-fat high cholesterol; GTT, glucose tolerance test; TG, total triglyceride; TC, total cholesterol; LDL-C, low density lipoprotein cholesterol; H&E, hematoxylin and eosin; PSR, picro Sirius Red. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11791544/'>39355870</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-ihc.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using CD11b Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-1-ihc_1.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse lung, using CD11b Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl-2-rabbit-monoclonal-antibody-m00040-1-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-wb.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyWestern blot analysis of Bcl-2 expression in (1) Jurkat cell lysate;(2) MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-wb7.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc9.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human non-Hodgkin's lymphoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc10.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous cell carcinoma , using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc7.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc11.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc8.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-ihc.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using Bcl-2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-1-if.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Bcl-2 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hmgb1-rabbit-monoclonal-antibody-m00066-1-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-wb-testing-1.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody Western blot analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HMGB1 antigen affinity purified monoclonal antibody (Catalog # M00066-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HMGB1 at approximately 25 kDa. The expected band size for HMGB1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-ihc-testing-2.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IHC analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
HMGB1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HMGB1 Antibody (M00066-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-wjg-27-815-g001.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyEffects of abdominal paracentesis drainage on pancreatic histopathology and proinflammatory cytokines. A: Representative images of rat pancreatic tissue from different groups following hematoxylin and eosin staining (bar = 100 μm); B: Histology severity score of pancreas tissue; C: Amylase; D: Lipase; E: Tumor necrosis factor-α; F: Interleukin-6; G: High mobility group box 1. All data are presented as mean ± SD ( n = 6). a P < 0.05 vs sham group; b P < 0.05 vs severe acute pancreatitis group. SAP: Severe acute pancreatitis; APD: Abdominal paracentesis drainage; TNF-α: Tumor necrosis factor-α; IL-6: Interleukin-6; PAAF: Pancreatitis-associated ascitic fluid; HMGB1: High mobility group box 1.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7941863/&orig_host=www.ncbi.nlm.nih.gov'>33727772</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-wjg-27-815-g005.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyEffects of pancreatitis-associated ascitic fluid intraperitoneal injection with or without anti-high mobility group box protein 1 neutralizing antibody on intestinal toll-like receptor 4 signaling pathway in cerulein-treated rats. A: High mobility group box protein 1 in serum; B: Toll-like receptor 4 (TLR4) mRNA measurement by real-time polymerase chain reaction; C: Immunoblotting of TLR4, myeloid differentiation factor 88 (MyD88) and p65 protein expression and p65 phosphorylation level from intestine samples; D: Representative immunohistochemical images of TLR4 in intestinal tissue (bar = 100 μm); E-G: Densitometry analysis of TLR4, MyD88 and ratio of p65 to phosphorylated p65. Data are expressed as means ± SD, n = 6 enzyme-linked immunosorbent assay results per group; means ± SD, n = 3 immunoblotting results per group. a P < 0.05 vs control group; b P < 0.05 vs pancreatitis-associated ascitic fluid injection group. HMGB1: High mobility group box protein 1; CN: Control; PI: Pancreatitis-associated ascitic fluid (PAAF) injection; PIH: PAAF and 200 μg anti-HMGB1 neutralizing antibody; PIC: PAAF + control lgY; TLR4: Toll-like receptor 4; MyD88: Myeloid differentiation factor 88; p-p65: Phosphorylated p65; GAPDH: Glyceraldehyde-3-phosphate dehydrogenase.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7941863/&orig_host=www.ncbi.nlm.nih.gov'>33727772</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-wjg-26-35-g006.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyEffects of abdominal paracentesis drainage on pancreatic histopathology and proinflammatory cytokines. A: Representative micrographs of hematoxylin-eosin stained sections of rat pancreatic tissue from different groups. Images were taken under 100 × and 200 × magnification. The arrow indicates necrotic pancreatic tissue; B: Histology severity score of pancreas; C: Amylase; D: Interleukine-1 beta; E: Tumor necrosis factor alpha; F: Endotoxin; G: High mobility group box 1. Data indicate the mean ± standard deviation obtained from six animals in each group (C-G). a P < 0.05 vs sham group; c P < 0.05 vs severe acute pancreatitis group. IL-1β: Interleukine-1 beta; TNF-α: Tumor necrosis factor alpha; HMGB1: High mobility group box 1; PAAF: Pancreatitis associated ascitic fluids; SAP: Severe acute pancreatitis; APD: Abdominal paracentesis drainage.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6952299/&orig_host=www.ncbi.nlm.nih.gov'>31933513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-wjg-26-35-g007.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyEffects of pancreatitis associated ascitic fluids intraperitoneal injection with or without anti-high mobility group box 1 neutralizing antibody on cardiac NOX expression in cerulein rats. A: High mobility group box 1 in the serum; B: Nicotinamide adenine dinucleotide phosphate oxidase-2 ( NOX2 ) and NOX4 mRNA measurement by real-time polymerase chain reaction; C: Immunoblot of NOX2 and NOX4 protein expression from heart samples; D: Densitometry analysis of NOX2 and NOX4. Data indicate the mean ± standard deviation obtained from six animals in each group (A-B). Data are representative of at least three independent experiments (C-D). a P < 0.05 vs controls group; c P < 0.05 vs pancreatitis-associated ascitic fluid injection group. HMGB1: High mobility group box 1; NOX2: Nicotinamide adenine dinucleotide phosphate oxidase-2; NOX4: Nicotinamide adenine dinucleotide phosphate oxidase-4; GAPDH: Glyceraldehyde-3-phosphate dehydrogenase; SAP: Severe acute pancreatitis; APD: Abdominal paracentesis drainage.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6952299/&orig_host=www.ncbi.nlm.nih.gov'>31933513</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-ihc-testing-3.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IHC analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
HMGB1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HMGB1 Antibody (M00066-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-ihc-testing-4.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IHC analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
HMGB1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HMGB1 Antibody (M00066-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-ihc-testing-5.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IHC analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
HMGB1 was detected in a paraffin-embedded section of human prostatic acinar adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HMGB1 Antibody (M00066-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-ihc-testing-6.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IHC analysis of HMGB1 using anti-HMGB1 antibody (M00066-1). <br>
HMGB1 was detected in a paraffin-embedded section of human cervical squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HMGB1 Antibody (M00066-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-hmgb1-primary-antibodies-if-testing-7.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal Antibody IF analysis of HMGB1 using anti-HMGB1 antibody (M00066-1) and anti-Beta Tubulin antibody (M01857-3).<br>
HMGB1 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-HMGB1 Antibody (M00066-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-ihc7.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-ihc8.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat kidney, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00066-1-ihc11.jpgAnti-HMGB1/Hmg 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:300 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac2-rabbit-monoclonal-antibody-m00325-1-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-1-hdac2-primary-antibodies-wb-testing-1.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC2 using anti-HDAC2 antibody (M00325-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human U937 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: human U2OS whole cell lysates,<br>
Lane 6: human A431 whole cell lysates,<br>
Lane 7: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDAC2 antigen affinity purified monoclonal antibody (M00325-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HDAC2 at approximately 60 kDa. The expected band size for HDAC2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-1-hdac2-primary-antibodies-ihc-testing-1.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyIHC analysis of HDAC2 using anti-HDAC2 antibody (M00325-1). <br>HDAC2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HDAC2 Antibody (M00325-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-setd7-rabbit-monoclonal-antibody-m02793-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02793-wb.jpgAnti-SETD7/Set7 Rabbit Monoclonal AntibodyWestern blot analysis of SETD7 in (1) Jurkat cell lysate; (2) HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rnf20-rabbit-monoclonal-antibody-m03457-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03457-wb.jpgAnti-RNF20 Rabbit Monoclonal AntibodyWestern blot analysis of RNF20 in (1) MCF7 cell lysate; (2) HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ptbp2-rabbit-monoclonal-antibody-m05020-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-wb7.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-wb8.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-wb.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyWestern blot analysis of PTBP2 in (1) Neuro-2a cell lysate; (2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-ihc.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PTBP2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-icc1.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-icc2.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-icc3.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-satb1-rabbit-monoclonal-antibody-m01312-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01312-stab1-primary-antibodies-wb-testing-1.jpgAnti-SATB1 Rabbit Monoclonal Antibody Western blot analysis of STAB1 using anti-STAB1 antibody (M01312). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAB1 antigen affinity purified monoclonal antibody (Catalog # M01312) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAB1 at approximately 100 kDa. The expected band size for STAB1 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01312-stab1-primary-antibodies-ihc-testing-2.jpgAnti-SATB1 Rabbit Monoclonal Antibody IHC analysis of STAB1 using anti-STAB1 antibody (M01312). <br>
STAB1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAB1 Antibody (M01312) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01312-stab1-primary-antibodies-ihc-testing-3.jpgAnti-SATB1 Rabbit Monoclonal Antibody IHC analysis of STAB1 using anti-STAB1 antibody (M01312). <br>
STAB1 was detected in a paraffin-embedded section of human prostatic acinar adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAB1 Antibody (M01312) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab4a-rabbit-monoclonal-antibody-m04643-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04643-wb.jpgAnti-Rab4A/Rab4 Rabbit Monoclonal AntibodyWestern blot analysis of Rab4A expression in (1) SH-SY5Y cell lysate; (2) MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04643-if.jpgAnti-Rab4A/Rab4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Rab4A Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad2-rabbit-monoclonal-antibody-m00090-1-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00090-1-smad2-primary-antibodies-wb-testing-1.jpgAnti-Smad2 Rabbit Monoclonal Antibody Western blot analysis of SMAD2 using anti-SMAD2 antibody (M00090-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human MDA-MB-453 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMAD2 antigen affinity purified monoclonal antibody (Catalog # M00090-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SMAD2 at approximately 52 kDa. The expected band size for SMAD2 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00090-1-if.jpgAnti-Smad2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Smad2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-olig2-rabbit-monoclonal-antibody-m02247-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02247-olig2-primary-antibodies-wb-testing-1.jpgAnti-Olig2 Rabbit Monoclonal AntibodyWestern blot analysis of OLIG2 using anti-OLIG2 antibody (M02247). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OLIG2 antigen affinity purified monoclonal antibody (M02247) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for OLIG2 at approximately 36 kDa. The expected band size for OLIG2 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02247-ihc.jpgAnti-Olig2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human mouse brain, using Olig2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-satb2-rabbit-monoclonal-antibody-m02588-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-satb2-primary-antibodies-wb-testing-1.jpgAnti-SATB2 Rabbit Monoclonal Antibody Western blot analysis of SATB2 using anti-SATB2 antibody (M02588). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SATB2 antigen affinity purified monoclonal antibody (Catalog # M02588) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SATB2 at approximately 83 kDa. The expected band size for SATB2 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-wb7.jpgAnti-SATB2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02588-SATB2-primary-antibodies-IHC-testing-1.jpgAnti-SATB2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach cancer, using SATB2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-ihc7.jpgAnti-SATB2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-ihc8.jpgAnti-SATB2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human cervical cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-satb2-primary-antibodies-if-testing-3.jpgAnti-SATB2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of SH-SY5Y cells, using SATB2 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02588-icc1.jpgAnti-SATB2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lrrk2-rabbit-monoclonal-antibody-m00221-2-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00221-2-wb.jpgAnti-LRRK2 Rabbit Monoclonal AntibodyWestern blot analysis of LRRK2 expression in U87-MG cell lysate. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00221-2-ihc.jpgAnti-LRRK2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid, using LRRK2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tacc3-rabbit-monoclonal-antibody-m02876-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02876-tacc3-primary-antibodies-wb-testing-1.jpgAnti-TACC3 Rabbit Monoclonal AntibodyWestern blot analysis of TACC3 using anti-TACC3 antibody (M02876). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TACC3 antigen affinity purified monoclonal antibody (M02876) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TACC3 at approximately 140 kDa. The expected band size for TACC3 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02876-tacc3-primary-antibodies-ihc-testing-1.jpgAnti-TACC3 Rabbit Monoclonal AntibodyIHC analysis of TACC3 using anti-TACC3 antibody (M02876). <br>TACC3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TACC3 Antibody (M02876) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02876-tacc3-primary-antibodies-ihc-testing-2.jpgAnti-TACC3 Rabbit Monoclonal AntibodyIHC analysis of TACC3 using anti-TACC3 antibody (M02876). <br>TACC3 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TACC3 Antibody (M02876) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02876-tacc3-primary-antibodies-ihc-testing-3.jpgAnti-TACC3 Rabbit Monoclonal AntibodyIHC analysis of TACC3 using anti-TACC3 antibody (M02876). <br>TACC3 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TACC3 Antibody (M02876) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02876-tacc3-primary-antibodies-ihc-testing-4.jpgAnti-TACC3 Rabbit Monoclonal AntibodyIHC analysis of TACC3 using anti-TACC3 antibody (M02876). <br>TACC3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TACC3 Antibody (M02876) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gm130-rabbit-monoclonal-antibody-m05865-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-gm130-primary-antibodies-wb-testing-1.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal Antibody Western blot analysis of GM130 using anti-GM130 antibody (M05865). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GM130 antigen affinity purified monoclonal antibody (Catalog # M05865) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GM130 at approximately 150 kDa. The expected band size for GM130 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-jev2-14-e70087-g006.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal AntibodyA‐C. Prove of urinary extracellular vesicle (uEV) particle existence in the primary analyte samples derived by different uEV isolation methods by ancillary transmission electron microscopy (TEM) (A), fluorescence microscopy (FM) (B) and Western Blotting/Immunoblotting (IB) (C) methods. TEM shows a typical cup‐shape EV morphology (EV drying artefact) at 3200 ms exposure and either medium 15,000× (bar size = 200 nm) or high 43,000× (bar size = 100 nm, inlet image) magnification; IB shows known EV protein biomarker expression such as Alix, TSG101, Flotillin‐1, CD‐9 and PKM1/2 in different subject (S1, S2) uEV samples that are free of Golgi, endoplasmic reticulum or mitochondria organelle contaminants as indicated by the absence of GM130, protein disulfide isomerase (PDI) or pyruvate dehydrogenase (PD) proteins; FM displays green fluorescent signal emitted from SYTO RNASelect‐stained internal uEV nucleic acid (RNA) cargo (bar size = 10 µm). (D) Linear relationship between raw source sample dose (pre‐clarified urine input) and isolated uEV particle concentration (output response) in samples processed by DC (left panel), SiC (middle panel) or PEG (right panel) methods.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12086329/'>40384173</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-gm130-primary-antibodies-ihc-testing-2.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal Antibody IHC analysis of GM130 using anti-GM130 antibody (M05865). <br>
GM130 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GM130 Antibody (M05865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-gm130-primary-antibodies-ihc-testing-3.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal Antibody IHC analysis of GM130 using anti-GM130 antibody (M05865). <br>
GM130 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GM130 Antibody (M05865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-gm130-primary-antibodies-ihc-testing-4.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal Antibody IHC analysis of GM130 using anti-GM130 antibody (M05865). <br>
GM130 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GM130 Antibody (M05865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-icc1.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05865-gm130-primary-antibodies-ihc-testing-5.jpgAnti-GM130 GOLGA2 Rabbit Monoclonal Antibody IHC analysis of GM130 using anti-GM130 antibody (M05865). <br>
GM130 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GM130 Antibody (M05865) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fubp1-rabbit-monoclonal-antibody-m03126-boster.html2026-03-24T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03126-fubp1-primary-antibodies-wb-testing-1.jpgAnti-FUBP1 Rabbit Monoclonal Antibody Western blot analysis of FUBP1 using anti-FUBP1 antibody (M03126). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FUBP1 antigen affinity purified monoclonal antibody (Catalog # M03126) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FUBP1 at approximately 74 kDa. The expected band size for FUBP1 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03126-fubp1-primary-antibodies-ihc-testing-2.jpgAnti-FUBP1 Rabbit Monoclonal Antibody IHC analysis of FUBP1 using anti-FUBP1 antibody (M03126). <br>
FUBP1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FUBP1 Antibody (M03126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03126-fubp1-primary-antibodies-ihc-testing-3.jpgAnti-FUBP1 Rabbit Monoclonal Antibody IHC analysis of FUBP1 using anti-FUBP1 antibody (M03126). <br>
FUBP1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FUBP1 Antibody (M03126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03126-fubp1-primary-antibodies-ihc-testing-4.jpgAnti-FUBP1 Rabbit Monoclonal Antibody IHC analysis of FUBP1 using anti-FUBP1 antibody (M03126). <br>
FUBP1 was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FUBP1 Antibody (M03126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03126-fubp1-primary-antibodies-ihc-testing-5.jpgAnti-FUBP1 Rabbit Monoclonal Antibody IHC analysis of FUBP1 using anti-FUBP1 antibody (M03126). <br>
FUBP1 was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FUBP1 Antibody (M03126) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ccl19-rabbit-monoclonal-antibody-m01605-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01605-wb.jpgAnti-CCL19/Mip 3 Beta Rabbit Monoclonal AntibodyWestern blot analysis of extracts from CCL19 recombinant protein, using CCL19 antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac1-rabbit-monoclonal-antibody-m00256-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-wb7.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-wb10.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-wb8.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-wb.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC1 expression in (1) C6 cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-wb9.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00256-ihc.jpgAnti-HDAC1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using HDAC1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat3-rabbit-monoclonal-antibody-m00007-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-stat3-primary-antibodies-wb-testing-1.jpgAnti-STAT3 Rabbit Monoclonal Antibody Western blot analysis of STAT3 using anti-STAT3 antibody (M00007). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT3 antigen affinity purified monoclonal antibody (Catalog # M00007) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT3 at approximately 88 kDa. The expected band size for STAT3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-wb7.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-stat3-primary-antibodies-wb-testing-2.pngAnti-STAT3 Rabbit Monoclonal Antibody Western blot analysis of STAT3 using anti-STAT3 antibody (M00007). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: 2h drug treated-human MCF-7 whole cell lysates,<br>
Lane 3: 4h drug treated-human MCF-7 whole cell lysates,<br>
Lane 4: 12h drug treated-human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT3 antigen affinity purified monoclonal antibody (Catalog # M00007) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT3 at approximately 88 kDa. The expected band size for STAT3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-wb8.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-wb11.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-stat3-primary-antibodies-wb-testing-1.jpg.pngAnti-STAT3 Rabbit Monoclonal AntibodyWestern blot analysis of STAT3 using anti-STAT3 antibody (M00007). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates,<br>
Lane 2: Model group-rat colon tissue lysates,<br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates,<br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates,<br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates,<br>
Lane 6: Western medicine treatment-rat colon tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT3 antigen affinity purified monoclonal antibody (Catalog # M00007) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a HRP Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for STAT3 at approximately 88 kDa. The expected band size for STAT3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-wb9.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-wb12.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-images_medium_ao4c00710_0003.gifAnti-STAT3 Rabbit Monoclonal AntibodyIn vitro cytotoxicity of CLCS nanoliposome. (a) Confocal fluorescence pictures of cell uptake of nanoliposomes (blue: cell nucleus, and red: LCS or CLCS). Scale bar: 500 nm. (b) Quantification of cell uptake of nanoliposomes through flow cytometry at different time points. (c) Representative flow cytometric images of C1498 cell uptake of nanoliposomes after being treated with LCS and CLCS for 4 and 8 h. (d) Dead/live staining of C1498 cells after various treatments (green: live cells, and red: dead cells). (e) Apoptosis/necrosis analysis of C1498 cells after multifarious treatments by flow cytometry. (f) Quantification of apoptotic cell after various treatments. (g) Western blotting analysis of JAK2/STAT3 expression in AML cells after sorts of treatments. (h) Cell viability of C1498 cells after multiple treatments. *p < 0.05, **p < 0.01, and ***p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pubs.acs.org/doi/abs/10.1021/acsomega.4c00710'>39281932</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007_12951_2025_3576_fig9_html.pngAnti-STAT3 Rabbit Monoclonal AntibodyTranscriptomic analysis elucidated the mechanism of action of FA-PPI-Ms in the treatment of RA. ( A ) Volcano plot of significantly differentially expressed genes between the model group and the FA-PPI-Ms group, where blue circles represent downregulated genes and red circles represent upregulated genes; ( B ) Heatmap of significantly differentially expressed genes in cells of the model group and the FA-PPI-Ms group, where deeper blue indicates lower expression levels and deeper red indicates higher expression levels; ( C ) Histogram of GO functional annotation of significantly differentially expressed genes between the model group and the FA-PPI-Ms group; ( D ) Histogram of GO functional enrichment of significantly different genes between the model group and the FA-PPI-Ms group; ( E ) Bubble plot of GO functional enrichment of significantly differentially expressed genes between the model group and the FA-PPI-Ms group; ( F ) Histogram of KEGG pathway enrichment of genes with significant differences between the model group and the FA-PPI-Ms group; ( G-H ) To validate the transcriptomics results, qRT-PCR was employed to measure the mRNA expression levels of JAK ( G ) and STAT3 ( H ) in RAW264.7 cells; ( I ) Western blot was utilized to assess the expression levels of proteins associated with the JAK2-STAT3 signaling pathway; ( J-K ) Statistical analysis of the ratios of p-JAK2/JAK2 ( J ) and p-STAT3/STAT3 ( K ) was conducted. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03576-8'>40660236</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007_12951_2025_3576_fig10_html.pngAnti-STAT3 Rabbit Monoclonal Antibody Validation of the mechanism by which FA-PPI-Ms reverse M1/M2 imbalance. ( A-B ) qRT-PCR analysis of CD86 and CD206 mRNA expression on activated RAW264.7 cells treated with different formulations; ( C-D ) Flow cytometric histograms of proportion of M1and M2 macrophages in different formulations; ( E-F ) Quantitative analysis of proportion of M1 and M2 macrophages in different formulations; ( G-H ) Representative fluorescence images of CD86 and CD206 staining of values with varying formulations, scale bar = 50 μm; ( I-J ) Analysis of relative fluorescence intensity in ( G-H ); ( K-L ) qRT-PCR analysis of JAK2 and STAT3 mRNA expression on activated RAW264.7 cells treated with different formulations; ( M ) Western blot analysis of JAK2-STAT3 signalling axis-related protein expression. ( N-O ) Semi-quantitative analysis of p-JAK2/ JAK2 and p-STAT3/ STAT3 levels by Image J, Data are presented as mean ± SD ( n = 3). One-way ANOVA followed by Bonferroni’s test was used. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03576-8'>40660236</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-ihc.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid carcinoma, using STAT3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-if.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using STAT3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-icc1.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-icc2.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat6-rabbit-monoclonal-antibody-m00523-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-1-wb.jpgAnti-STAT6 Rabbit Monoclonal AntibodyWestern blot analysis of STAT6 in expression (1)Daudi cell lysate;(2)HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-1-if.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using STAT6 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-traf6-rabbit-monoclonal-antibody-m00185-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-wb10.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-wb7.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-wb8.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-wb9.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-wb.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyWestern blot analysis of TRAF6 expression in NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc7.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat ovary, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc8.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc9.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc10.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc11.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-1-ihc.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma, using TRAF6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-traf6-rabbit-monoclonal-antibody-m00185-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-wb.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyWestern blot analysis of TRAF6 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-fphar-15-1435274-g004.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyThe regulatory effects of MOIG on NF-κB and JAK2/STAT3 pathway of TNF-α-stimulated FLSs cells. FLSs were incubated with TNF-α for 12 h and subsequently treated with MOIG for 24 h, the proteins were extracted to analyze expression of associated proteins by Western blot. ( A–C ) The expression of p-JAK2, JAK2, p-STAT3, STAT3. ( D–G ) The expression of TRAF6, p-p65, p65 and IκB-α, respectively. The data represents the mean ± SD (n = 3). The experiments were repeated for three times. # p < 0.05, ## p < 0.01, ### p < 0.001 vs. normal ctrl group; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. TNF-α model group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1435274/full'>39444614</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig1_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a interacts with TRAF6 and inhibits the NF-κB Signaling Pathway. a List of TRAF6 interactome based on Label-free quantification intensity (section). b , c MKC cells seeded in 6 cm 2 dishes. After 24 h, cell lysates were immunoprecipitated (IP) with anti-TRAF6 or anti-calpain2a affinity gels. Then the immunoprecipitates and cell lysates were analyzed by IB with the anti-TRAF6 and anti-calpain2a Abs, respectively. d , e HEK 293 cells seeded in 6 cm 2 dishes were transfected with the plasmids calpain2a-Flag and TRAF6-Myc (2 μg each). After 24 h, cell lysates were immunoprecipitated (IP) with anti-Myc d or anti-Flag e affinity gels. Then the immunoprecipitates and cell lysates were analyzed by IB with the anti-Myc and anti-Flag Abs, respectively. f The same amino acids among human calpain2a (Hu-calpain2), mouse calpain2a (Mu-calpain2), zebrafish calpain2a (ZF-calpain2a) and miiuy croaker calpain2a (M-calpain2a) are highlighted with black background. g – i EPC cells were transfected with calpain2a-Flag or empty vector together with the NF-κB, IL-1β, and IL-8 luciferase reporters. At 24 h post-transfection, cells were untreated (Mock) or treated with LPS for 6 h. The luciferase activity value was achieved against the Renilla luciferase activity ( n = 3 per group). Western blot analysis was used to measure the expression of transiently transfected calpain2a-Flag. The expression of Tubulin was used as a loading control. Data were analyzed by two-way ANOVA ( g , h , i ). ** p < 0.01. All experiments were performed in at least three independent experiments. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig3_html.pngAnti-TRAF6 Rabbit Monoclonal AntibodyThe interaction of calpain2a with TRAF6. a , b Schematic diagrams of domain organization in miiuy croaker calpain2a, TRAF6 and mutants used in this study. “+“ represents the interaction with TRAF6 or calpain2a, “-“ means no interaction. c HEK293 cells were transfected with mock, calpain2a-Flag wild type (WT), and calpain2a-Flag truncated mutants, or TRAF6-HA as indicated. At 24 h post-transfection, transfected cells were extracted and cell lysates were subjected to immunoprecipitation with anti-HA antibody followed by IB using anti-HA or anti-Flag antibody. d – f HEK293 cells were transfected with mock, TRAF6-HA wild type (WT), and TRAF6-HA truncated mutants, or calpain2a-Flag as indicated. At 24 h post-transfection, transfected cells were extracted and cell lysates were subjected to immunoprecipitation with anti-HA antibody d , f or anti-Flag antibody e followed by IB using anti-HA or anti-Flag antibody. g The interaction site of TRAF6 and calpain2a. h EPC cells were transfected with TRAF6-HA, calpain2a-Flag or calpain2a-Flag truncated mutants together with NF-κB and IL-1β luciferase reporters. After 36 h post-transfection, the luciferase activity value was achieved against the renilla luciferase activity ( n = 3 per group). i , j EPC cells were transfected with mock, calpain2a-mCherry, and TRAF6-GFP. DAPI-stained nuclei are shown in blue. calpain2a was detected with red fluorescence, and TRAF6 was detected with green fluorescence. Scale bar, 10 μm. All experiments were performed in at least three independent experiments. Data were analyzed by one-way ANOVA ( h ). ** p < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig6_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a attenuates autoubiquitination of TRAF6. a HEK293 cells were transfected with TRAF6-Myc, TRAF6-HA, or empty vector. After 24 h post-transfection, the cells were lysed and IP analyses with HA antibody. b HEK293 cells were transfected with TRAF6-Myc, TRAF6-HA, empty vector, or calpain2a-Flag. After 24 h post-transfection, the cells were lysed and IP analyses with HA antibody. c HEK293 cells were transfected with TRAF6-Myc, TRAF6-HA, empty vector, or different concentrations of calpain2a-ΔCysPc-Flag. After 24 h post-transfection, the cells were lysed and IP analyses with HA antibody. d , e HEK293 cells were cotransfected with TRAF6-Myc, TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. The immunoprecipitates and input immunoblot analysis with anti-Myc, anti-Flag, anti-HA, and anti-Tubulin Abs. All experiments were performed in at least three independent experiments. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig4_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a inhibits TRAF6 protein expression. a The time gradient experiment of empty vectors or calpain2a-Myc plasmids together with TRAF6-Flag was conducted in EPC cells. The cell lysates were subjected to IB with anti-Myc, anti-Flag, and anti–Tubulin Abs. RNA was extracted from cells and reverse transcribed, then TRAF6 and actin were amplified by PCR primers. b EPC cells were seeded in 12-well plates overnight and co-transfected with TRAF6-Flag and calpain2a-Myc (0.3, 0.6, or 0.9 μg) for 48 h. The expression of TRAF6-Flag and calpain2a-Myc proteins were detected by Western blotting. RNA was extracted from cells and reverse transcribed, then TRAF6 and actin were amplified by PCR primers. c calpain2a-Myc or empty vectors were co-transfected with TRAF6-Flag into EPC cells. At 36 h post-transfection, the transfected cells were treated with cycloheximide (CHX) for 2 or 4 h. d MKC cells were transfected with calpain2a-Flag or empty vectors. At 48 h post-transfection, the cell lysates were subjected to IB with anti-TRAF6, anti-Flag, and anti-Tubulin Abs. e , f EPC cells were transfected with the indicated plasmids in the presence or absence of MG132, 3-MA, NH 4 CL, E-64 (50 or 75 μM), or PMSF for 6 h before immunoblot analysis was performed. g MKC cells were transfected with calpain2a-Flag in the presence or absence of E-64 (50 or 75 μM) for 6 h before immunoblot analysis was performed. h calpain2a-Flag and calpain2a-ΔCysPc-Flag were co-transfected with TRAF6-HA into EPC cells. At 48 h post-transfection, the cell lysates were subjected to IB with indicated Abs. i calpain2a-Flag and calpain2a-ΔCysPc-Flag were co-transfected into MKC cells. At 48 h post-transfection, the cell lysates were subjected to IB with anti-TRAF6, anti-Flag, and anti-Tubulin Abs. j IL-1β , IL-8 mRNA in MKC stably transduced with calpain2a-Flag and calpain2a-ΔCysPc-Flag and treated with saline (0) or challenged with LPS for 4 h ( n = 3 per group). Relative mRNA level was normalized to the expression of the gene encoding β-actin in each sample. All experiments were performed in at least three independent experiments. Data were analyzed by two-way ANOVA ( j ). ** p < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig5_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a inhibits TRAF6 ubiquitin-ligase activity. a Ubiquitination of endogenous TRAF6 in MKC cells transduced with calpain2a-Flag and calpain2a-ΔCysPc-Flag and unchallenged (−) or challenged with LPS (+), assessed by immunoblot analysis with anti-ubiquitin after immunoprecipitation with anti-TRAF6 and input immunoblot analysis with indicated Abs. b , c HEK293 cells were cotransfected with TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. d , e HEK293 cells were cotransfected with TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag (0.5 μg, 1 μg), calpain2a-ΔCysPc-Flag (0.5 μg, 1 μg) or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. f Ubiquitination of overexpressed TRAF6 in MKC cells transduced with calpain2a-ΔCysPc-Flag, assessed by immunoblot analysis with anti-ubiquitin after immunoprecipitation with anti-Myc and input immunoblot analysis with indicated Abs. g , h HEK293 cells were cotransfected with TAK1-Myc, TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. All the immunoprecipitates and input immunoblot analysis with anti-Myc, anti-Flag, anti-HA, and anti-Tubulin Abs. All experiments were performed in at least three independent experiments. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig9_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a inhibits TRAF6-mediated ubiquitination of IRF7 and IRF3. a , b HEK293 cells were cotransfected with IRF3-Myc, TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. c , d HEK293 cells were cotransfected with IRF7-Myc, TRAF6-HA and WT-ubiquitin-His or K63O-ubiquitin-His (in which only lysine 63 is kept) together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. All the immunoprecipitates and input with anti-Myc, anti-Flag, anti-HA, and anti-Tubulin Abs. All experiments were performed in at least three independent experiments. e Model detailing the roles of calpain2a in TRAF6-mediated signaling pathways. Upon LPS and virus, TRAF6 could be activated, homo-oligomerization and auto-ubiquitination. BECN1, ECSIT, IRF7 and IRF3 are ubiquitinated by TRAF6 and trigger the activation of downstream signals. calpain2a as a negative regulator targets TRAF6 to inhibit TRAF6-mediated signaling pathways. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-42003_2023_4711_fig7_html.pngAnti-TRAF6 Rabbit Monoclonal Antibodycalpain2a inhibits TRAF6-mediated ubiquitination of ECSIT and BECN1. a HEK293 cells were transfected with ECSIT-Myc, TRAF6-Flag, or empty vector. After 24 h post-transfection, the cells were lysed and IP analyses with Flag antibody. b HEK293 cells were transfected with TAK1-Flag, ECSIT-Myc, or empty vector. After 24 h post-transfection, the cells were lysed and IP analyses with Myc antibody. c HEK293 cells were transfected with TRAF6-Myc, ECSIT-HA, empty vector, or different concentrations of calpain2a-ΔCysPc-Flag. After 24 h post-transfection, the cells were lysed and IP analyses with Myc antibody. d HEK293 cells were cotransfected with ECSIT-Myc, TRAF6-HA, WT-ubiquitin-His together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. e HEK293 cells were transfected with BECN1-Flag, TRAF6-Myc, or empty vector. After 24 h post-transfection, the cells were lysed and IP analyses with Myc antibody. f HEK293 cells were cotransfected with BECN1-HA, TRAF6-Myc, WT-ubiquitin-His together with calpain2a-Flag, calpain2a-ΔCysPc-Flag or empty vector. After 24 h post-transfection, the cells were lysed and purified with Ni-NTA agarose. The immunoprecipitates and input with anti-Myc, anti-Flag, anti-HA, and anti-Tubulin Abs. All experiments were performed in at least three independent experiments. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs42003-023-04711-7'>37002312</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-13020_2022_627_fig10_html.pngAnti-TRAF6 Rabbit Monoclonal AntibodyEffects of JTG on expression of associated proteins and NF-κB pathway of osteoclast induced from BMMs with RANKL and LPS. BMMs were incubated with RANKL and JTG for 48 h, the proteins were extracted to analyze associated proteins of osteoclast by Western blot. A : a Western blot imagines for expression of NFATc1, c-Fos, Cathepsin K and MMP9. A : b – e The quantification analysis of NFATc1, c-Fos, Cathepsin K and MMP9 based on the results of A : a by ECL detection system, respectively. B : a The images of Western blot for TRAF6, P-P65, P65 and IκBα. B : b – d The quantification analysis of TRAF6, P-P65/P65 and IκBα based on the results of B : a by using an ECL detection system, respectively. Each point represents the mean ± SD (n = 3). The experiments were repeated for three times. * P < 0.05, ** P < 0.01 compared with control group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-022-00627-2'>36195960</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00185-ihc.jpgAnti-TRAF6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung carcinoma, using TRAF6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl-6-rabbit-monoclonal-antibody-m00142-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00142-1-bcl6-primary-antibodies-wb-testing-1.jpgAnti-Bcl-6 Rabbit Monoclonal Antibody Western blot analysis of BCL6 using anti-BCL6 antibody (M00142-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Daudi whole cell lysates,<br>
Lane 2: human Raji whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL6 antigen affinity purified monoclonal antibody (Catalog # M00142-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL6 at approximately 95 kDa. The expected band size for BCL6 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00142-1-ihc.jpgAnti-Bcl-6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using Bcl-6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00142-1-if.jpgAnti-Bcl-6 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Ramos cells, using Bcl-6 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tram2-rabbit-monoclonal-antibody-m11792-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11792-wb.jpgAnti-TRAM2 Rabbit Monoclonal AntibodyWestern blot analysis of TRAM2 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lrrk2-rabbit-monoclonal-antibody-m00221-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00221-wb.jpgAnti-LRRK2 Rabbit Monoclonal AntibodyWestern blot analysis of LRRK2 in HEK293 cell lysate transfected with 3*Flag wild type, full length LRRK2.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lrrk2-rabbit-monoclonal-antibody-m00221-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00221-1-wb.jpgAnti-LRRK2 Rabbit Monoclonal AntibodyWestern blot analysis of LRRK2 expression in GFP-LRRK2 lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100b-rabbit-monoclonal-antibody-m00979-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-s100b-primary-antibodies-wb-testing-1.jpgAnti-S100B/S100 Beta Rabbit Monoclonal Antibody Western blot analysis of S100B using anti-S100B antibody (M00979-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat C6 whole cell lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-S100B antigen affinity purified monoclonal antibody (Catalog # M00979-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for S100B at approximately 11 kDa. The expected band size for S100B is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-wb.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyWestern blot analysis of S100B expression in A375 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc10.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse pancreas, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc7.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc11.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse hippocampus , using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc8.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc9.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-ihc.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat brain, using S100B Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-icc1.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00979-1-if.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyImmunofluorescent analysis of A375 cells, using S100B Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-3-sox10-primary-antibodies-if-testing-1_1.jpgAnti-S100B/S100 Beta Rabbit Monoclonal AntibodyIF analysis of S100B using anti-S100B antibody (M00979-1) . <br>
S100B was detected in an immunocytochemical section of rat C6 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes and then treated with a membrane permeabilization agent (AR0205) for 5 minutes.The cells were blocked with 10% goat serum. And then incubated with rabbit anti-S100B Antibody (M00979-1) at a dilution of 10 ug/mL overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd11c-rabbit-monoclonal-antibody-m00357-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00357-1-wb.jpgAnti-CD11c ITGAX Rabbit Monoclonal AntibodyWestern blot analysis of CD11c expression in THP-1 cell lysate treated with TPA.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00357-1-cd11c-primary-antibodies-ihc-testing-2.jpgAnti-CD11c ITGAX Rabbit Monoclonal Antibody IHC analysis of CD11c using anti-CD11c antibody (M00357-1). <br>
CD11c was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD11c Antibody (M00357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00357-1-itgax-primary-antibodies-ihc-testing-3.jpgAnti-CD11c ITGAX Rabbit Monoclonal AntibodyIHC analysis of ITGAX using anti-ITGAX antibody (M00357-1). <br>ITGAX was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGAX Antibody (M00357-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd11b-rabbit-monoclonal-antibody-m00144-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-wb.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyWestern blot analysis of CD11b expression in TF1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00144-ihc.jpgAnti-CD11b ITGAM Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma, using CD11b Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd146-rabbit-monoclonal-antibody-m01683-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-1-cd146-primary-antibodies-wb-testing-1.jpgAnti-CD146 MCAM Rabbit Monoclonal Antibody Western blot analysis of CD146 using anti-CD146 antibody (M01683-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U2OS whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat spleen tissue lysates,<br>
Lane 7: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD146 antigen affinity purified monoclonal antibody (Catalog # M01683-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD146 at approximately 120 kDa. The expected band size for CD146 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-1-cd146-primary-antibodies-ihc-testing-1.jpgAnti-CD146 MCAM Rabbit Monoclonal AntibodyIHC analysis of CD146 using anti-CD146 antibody (M01683-1). <br>CD146 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD146 Antibody (M01683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-1-cd146-primary-antibodies-ihc-testing-2.jpgAnti-CD146 MCAM Rabbit Monoclonal Antibody IHC analysis of CD146 using anti-CD146 antibody (M01683-1). <br>
CD146 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD146 Antibody (M01683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-1-if.jpgAnti-CD146 MCAM Rabbit Monoclonal AntibodyImmunofluorescent analysis of A375 cells, using CD146 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-1-cd146-primary-antibodies-icc-testing-1.jpgAnti-CD146 MCAM Rabbit Monoclonal AntibodyIF analysis of CD146 using anti-CD146 antibody (M01683-1).
CD146 was detected in a paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 5% BSA. The tissue section was then incubated with rabbit anti-CD146 Antibody (M01683-1) at a dilution of 1:50 overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad5-rabbit-monoclonal-antibody-m01423-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01423-smad5-primary-antibodies-wb-testing-1.jpgAnti-Smad5 Rabbit Monoclonal Antibody Western blot analysis of Smad5 using anti-Smad5 antibody (M01423). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 7: mouse Hepa1-6 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Smad5 antigen affinity purified monoclonal antibody (Catalog # M01423) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Smad5 at approximately 52 kDa. The expected band size for Smad5 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01423-ihc9.jpgAnti-Smad5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01423-ihc7.jpgAnti-Smad5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01423-icc1.jpgAnti-Smad5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01423-ihc8.jpgAnti-Smad5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat1-rabbit-monoclonal-antibody-m00036-1-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-wb-testing-1.jpgAnti-STAT1 Rabbit Monoclonal Antibody Western blot analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: mouse heart tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT1 antigen affinity purified monoclonal antibody (Catalog # M00036-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT1 at approximately 83, 88 kDa. The expected band size for STAT1 is at 83, 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-wb-testing-2.jpgAnti-STAT1 Rabbit Monoclonal Antibody Western blot analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T- WT whole cell lysates,<br>
Lane 2: human 293T-STAT1 KO whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. Then the membrane was incubated with rabbit anti-STAT1 antigen affinity purified monoclonal antibody (M00036-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STAT1 at approximately 91 kDa. The expected band size for STAT1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-3.jpgAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-5.pngAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-4.jpgAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human liver adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-6.pngAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-7.pngAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-8.pngAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-9.pngAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-ihc-testing-3_1.jpgAnti-STAT1 Rabbit Monoclonal Antibody IHC analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-if-testing-11.pngAnti-STAT1 Rabbit Monoclonal Antibody IF analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-if-testing-12.pngAnti-STAT1 Rabbit Monoclonal Antibody IF analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-1-stat1-primary-antibodies-if-testing-13.pngAnti-STAT1 Rabbit Monoclonal Antibody IF analysis of STAT1 using anti-STAT1 antibody (M00036-1). <br>
STAT1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-STAT1 Antibody (M00036-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp14-rabbit-monoclonal-antibody-m00656-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00656-mmp14-primary-antibodies-wb-testing-1.jpgAnti-MMP14/Mt1 Mmp Rabbit Monoclonal AntibodyWestern blot analysis of MT1-MMP/MMP14 using anti-MT1-MMP/MMP14 antibody (M00656). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>
Lane 2: rat kidney tissue lysates,<br>
Lane 3: rat heart tissue lysates,<br>
Lane 4: mouse kidney tissue lysates,<br>
Lane 5: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MT1-MMP/MMP14 antigen affinity purified monoclonal antibody (M00656) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MT1-MMP/MMP14 at approximately 55 kDa. The expected band size for MT1-MMP/MMP14 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00656-ihc.jpgAnti-MMP14/Mt1 Mmp Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kdieny, using MMP14 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00656-mmp14-primary-antibodies-icc-testing-1.jpg.pngAnti-MMP14/Mt1 Mmp Rabbit Monoclonal AntibodyIF analysis of MMP14 using anti-MMP14 antibody (M00656). <br>
MMP14 was detected in an immunocytochemical section of Mouse cell culture coverslip. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:200 rabbit anti-CBL Antibody (PB9077) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a laser confocol.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-uchl3-rabbit-monoclonal-antibody-m05004-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05004-wb.jpgAnti-UCHL3 Rabbit Monoclonal AntibodyWestern blot analysis of UCHL3 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-traf4-rabbit-monoclonal-antibody-m03069-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03069-wb7.jpgAnti-TRAF4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03069-icc2.jpgAnti-TRAF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03069-wb.jpgAnti-TRAF4 Rabbit Monoclonal AntibodyWestern blot analysis of TRAF4 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03069-icc1.jpgAnti-TRAF4 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apaf1-rabbit-monoclonal-antibody-m00889-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00889-wb7.jpgAnti-APAF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00889-wb.jpgAnti-APAF1 Rabbit Monoclonal AntibodyWestern blot analysis of APAF1 expression in (1) HeLa cell lysate; (2) MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00889-ihc.jpgAnti-APAF1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using APAF1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pelp1-rabbit-monoclonal-antibody-m02530-boster.html2026-03-24T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02530-wb7.jpgAnti-PELP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02530-wb.jpgAnti-PELP1 Rabbit Monoclonal AntibodyWestern blot analysis of PELP1 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02530-ihc.jpgAnti-PELP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using PELP1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-acadm-rabbit-monoclonal-antibody-m02383-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02383-wb.jpgAnti-ACADM/Mcad Rabbit Monoclonal AntibodyWestern blot analysis of ACADM expression in (1) HeLa cell lysate; (2) K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mertk-rabbit-monoclonal-antibody-m00489-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00489-wb.jpgAnti-MERTK/Mer Rabbit Monoclonal AntibodyWestern blot analysis of MERTK expression in HEK293 cell lysates.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00489-ihc.jpgAnti-MERTK/Mer Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lymphoma, using MERTK Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-jun-rabbit-monoclonal-antibody-m02038-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-c-jun-primary-antibodies-wb-testing-1.jpgAnti-c-Jun Rabbit Monoclonal Antibody Western blot analysis of c-Jun using anti-c-Jun antibody (M02038). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-c-Jun antigen affinity purified monoclonal antibody (Catalog # M02038) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for c-Jun at approximately 43 kDa. The expected band size for c-Jun is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-c-jun-primary-antibodies-if-testing-2.jpgAnti-c-Jun Rabbit Monoclonal Antibody IF analysis of c-Jun using anti-c-Jun antibody (M02038).<br>
c-Jun was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-c-Jun Antibody (M02038) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-ihc7.jpgAnti-c-Jun Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-ihc8.jpgAnti-c-Jun Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebellum, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-ihc9.jpgAnti-c-Jun Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous carcinoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-ihc10.jpgAnti-c-Jun Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02038-ihc11.jpgAnti-c-Jun Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat3-rabbit-monoclonal-antibody-m00007-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-wb7.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-wb8.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-wb.jpgAnti-STAT3 Rabbit Monoclonal AntibodyWestern blot analysis of STAT3 expression in (1) A431 cell lysate; (2) Human liver lysate; (3) Mouse heart lysate; (4) Rat brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-wb9.jpgAnti-STAT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-ihc7.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-ihc8.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-ihc.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat brain, using STAT3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00007-1-if.jpgAnti-STAT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells treated with IFNalpha, using STAT3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad1-rabbit-monoclonal-antibody-m00728-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00728-1-icc1.jpgAnti-Smad1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00728-1-smad1-primary-antibodies-wb-testing-1.jpgAnti-Smad1 Rabbit Monoclonal AntibodyWestern blot analysis of SMAD1 using anti-SMAD1 antibody (M00728-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMAD1 antigen affinity purified monoclonal antibody (M00728-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SMAD1 at approximately 52 kDa. The expected band size for SMAD1 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00728-1-ihc.jpgAnti-Smad1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Smad1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rad51-rabbit-monoclonal-antibody-m00088-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00088-wb.jpgAnti-Rad51 Rabbit Monoclonal AntibodyWestern blot analysis of Rad51 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-raidd-rabbit-monoclonal-antibody-m06509-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06509-1-wb.jpgAnti-RAIDD Rabbit Monoclonal AntibodyWestern blot analysis of RAIDD expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tgfbi-rabbit-monoclonal-antibody-m01218-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01218-wb.jpgAnti-TGFBI/Beta Ig H3 Rabbit Monoclonal AntibodyWestern blot analysis of TGFBI expression in human fetal kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01218-ihc.jpgAnti-TGFBI/Beta Ig H3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using TGFBI Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rad21-rabbit-monoclonal-antibody-m01864-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01864-wb.jpgAnti-Rad21 Rabbit Monoclonal AntibodyWestern blot analysis of Rad21 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-arrb1-rabbit-monoclonal-antibody-m02185-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02185-arrb1-primary-antibodies-wb-testing-1.jpgAnti-ARRB1/Beta Arrestin 1 Rabbit Monoclonal Antibody Western blot analysis of ARRB1 using anti-ARRB1 antibody (M02185). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human K562 whoel cell lysates, <br>
Lane 4: rat spleen tissue lysates, <br>
Lane 5: rat PC-12 whoel cell lysates, <br>
Lane 6: mouse EL-4 whoel cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARRB1 antigen affinity purified monoclonal antibody (M02185) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARRB1 at approximately 50 kDa. The expected band size for ARRB1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02185-ihc.jpgAnti-ARRB1/Beta Arrestin 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using ARRB1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-b-raf-rabbit-monoclonal-antibody-m00075-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00075-wb7.jpgAnti-B Raf Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00075-wb.jpgAnti-B Raf Rabbit Monoclonal AntibodyWestern blot analysis of B Raf expression in (1)Human brain lysate (2)HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00075-ihc.jpgAnti-B Raf Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human ovarian cancer, using B Raf Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rock1-rabbit-monoclonal-antibody-m00722-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-rock1-primary-antibodies-wb-testing-1.jpgAnti-ROCK1 Rabbit Monoclonal Antibody Western blot analysis of FROCK1 using anti-ROCK1 antibody (M00722). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ROCK1 antigen affinity purified monoclonal antibody (Catalog # M00722) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ROCK1 at approximately 170 kDa. The expected band size for ROCK1 is at 158 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00722-ROCK1-primary-antibodies-IHC-testing-1.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using ROCK1 Antibody(M00722)<br>ROCK1 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-ROCK1 Antibody (M00722)overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-ihc7.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-ihc8.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-ihc9.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous carcinoma, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-ihc10.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-ihc11.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse heart, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-if.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using ROCK1 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-icc1.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat6-rabbit-monoclonal-antibody-m00523-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-stat6-primary-antibodies-wb-testing-1.jpgAnti-STAT6 Rabbit Monoclonal Antibody Western blot analysis of STAT6 using anti-STAT6 antibody (M00523). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT6 antigen affinity purified polyclonal antibody (Catalog # M00523) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT6 at approximately 100 kDa. The expected band size for STAT6 is at 94 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-ihc9.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-ihc7.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-ihc.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat liver, using STAT6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-ihc8.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-if.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using STAT6 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00523-ip7.jpgAnti-STAT6 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-kit-rabbit-monoclonal-antibody-m01335-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-1-c-kit-primary-antibodies-wb-testing-1.jpgAnti-c-Kit Rabbit Monoclonal Antibody Western blot analysis of c-Kit using anti-c-Kit antibody (M01335-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-c-Kit antigen affinity purified monoclonal antibody (Catalog # M01335-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for c-Kit at approximately 145 kDa. The expected band size for c-Kit is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-1-ihc.jpgAnti-c-Kit Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using c-Kit Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glut1-rabbit-monoclonal-antibody-m00163-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-wb.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyWestern blot analysis of GLUT1 expression in HepG2 lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc10.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach, using the Antibody at 1:800 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc7.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat hippocampus , using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc11.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse kidney, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc8.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thymoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc9.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-ihc.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix cancer, using GLUT1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-icc1.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00163-if.jpgAnti-GLUT1 SLC2A1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using GLUT1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp12-rabbit-monoclonal-antibody-m01520-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01520-wb7.jpgAnti-MMP12 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01520-wb.jpgAnti-MMP12 Rabbit Monoclonal AntibodyWestern blot analysis of MMP12 expression in WI-38 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01520-wb8.jpgAnti-MMP12 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01520-wb9.jpgAnti-MMP12 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-abcg1-rabbit-monoclonal-antibody-m01227-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01227-wb7.jpgAnti-ABCG1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01227-wb8.jpgAnti-ABCG1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01227-wb.jpgAnti-ABCG1 Rabbit Monoclonal AntibodyWestern blot analysis of ABCG1 expression in HUVEC cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-epcam-rabbit-monoclonal-antibody-m30950-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-epcam-primary-antibodies-wb-testing-1.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody Western blot analysis of CD326/EPCAM using anti-CD326/EPCAM antibody (M30950-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Caco-2 whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: rat small intestine tissue lysates, <br>
Lane 4: mouse small intestine tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD326/EPCAM antigen affinity purified monoclonal antibody (M30950-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD326/EPCAM at approximately 35-40 kDa. The expected band size for CD326/EPCAM is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-2.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-3.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-4.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-5.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-6.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human breast tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-7.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human breast tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-8.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-9.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-10.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-cd326-primary-antibodies-ihc-testing-11.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal Antibody IHC analysis of EpCAM/Trop1 using anti-EpCAM/Trop1 antibody (M30950-1). <br>
EpCAM/Trop1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-EpCAM/Trop1 Antibody (M30950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-1-icc1.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using EpCAM/Trop1 Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-icam1-rabbit-monoclonal-antibody-m00171-1-boster.html2026-03-24T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-1-icam1-primary-antibodies-wb-testing-1.jpgAnti-ICAM1/Cd54 Rabbit Monoclonal AntibodyWestern blot analysis of ICAM1 using anti-ICAM1 antibody (M00171-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: human Romas whole cell lysates,<br>
Lane 6: human Hela whole cell lysates,<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM1 antigen affinity purified monoclonal antibody (M00171-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ICAM1 at approximately 100 kDa. The expected band size for ICAM1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-1-icam1-primary-antibodies-ihc-testing-1.jpgAnti-ICAM1/Cd54 Rabbit Monoclonal AntibodyIHC analysis of ICAM1 using anti-ICAM1 antibody (M00171-1). <br>ICAM1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ICAM1 Antibody (M00171-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-1-icam1-primary-antibodies-ihc-testing-2.jpgAnti-ICAM1/Cd54 Rabbit Monoclonal AntibodyIHC analysis of ICAM1 using anti-ICAM1 antibody (M00171-1). <br>ICAM1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ICAM1 Antibody (M00171-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp60-rabbit-monoclonal-antibody-m01280-1-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-wb7.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-wb10.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-wb8.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-wb.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp60 expression in (1) HeLa cell lysate; (2) 293T cell lysate; (3) NIH/3T3 cell lysate; (4) Mouse heart lysate; (5) PC-12 cell lysate; (6) Rat heart lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-wb9.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01280-1-ihc.jpgAnti-Hsp60 HSPD1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Hsp60 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-psd95-rabbit-monoclonal-antibody-m02128-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02128-dlg4-primary-antibodies-wb-testing-1.jpgAnti-PSD95 DLG4 Rabbit Monoclonal Antibody Western blot analysis of DLG4 using anti-DLG4 antibody (M02128). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat C6 whole cell lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DLG4 antigen affinity purified monoclonal antibody (Catalog # M02128) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DLG4 at approximately 95 kDa. The expected band size for DLG4 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02128-if.jpgAnti-PSD95 DLG4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of U87-MG cells, using PSD95 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vdac1-rabbit-monoclonal-antibody-m01168-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-icc1.jpgAnti-VDAC1/Porin Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-vdac1-primary-antibodies-wb-testing-1.jpgAnti-VDAC1/Porin Rabbit Monoclonal Antibody Western blot analysis of VDAC1/Porin using anti-VDAC1/Porin antibody (M01168). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat kidney tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VDAC1/Porin antigen affinity purified monoclonal antibody (Catalog # M01168) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VDAC1/Porin at approximately 31 kDa. The expected band size for VDAC1/Porin is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-vdac1-primary-antibodies-ihc-testing-2.jpgAnti-VDAC1/Porin Rabbit Monoclonal Antibody IHC analysis of VDAC1/Porin using anti-VDAC1/Porin antibody (M01168). <br>
VDAC1/Porin was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VDAC1/Porin Antibody (M01168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-vdac1-primary-antibodies-ihc-testing-3.jpgAnti-VDAC1/Porin Rabbit Monoclonal Antibody IHC analysis of VDAC1/Porin using anti-VDAC1/Porin antibody (M01168). <br>
VDAC1/Porin was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VDAC1/Porin Antibody (M01168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-vdac1-primary-antibodies-ihc-testing-4.jpgAnti-VDAC1/Porin Rabbit Monoclonal Antibody IHC analysis of VDAC1/Porin using anti-VDAC1/Porin antibody (M01168). <br>
VDAC1/Porin was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VDAC1/Porin Antibody (M01168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01168-vdac1-primary-antibodies-ihc-testing-5.jpgAnti-VDAC1/Porin Rabbit Monoclonal Antibody IHC analysis of VDAC1/Porin using anti-VDAC1/Porin antibody (M01168). <br>
VDAC1/Porin was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-VDAC1/Porin Antibody (M01168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsc70-rabbit-monoclonal-antibody-m01024-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc8.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat ovary, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-hsc70-primary-antibodies-wb-testing-1.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal Antibody Western blot analysis of HSC70/HSPA8 using anti-HSC70/HSPA8 antibody (M01024). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human Caco-2 whole cell lysates, <br>
Lane 4: human A549 whole cell lysates, <br>
Lane 5: rat heart tissue lysates, <br>
Lane 6: rat liver tissue lysates, <br>
Lane 7: mouse heart tissue lysates, <br>
Lane 8: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSC70/HSPA8 antigen affinity purified monoclonal antibody (M01024) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSC70/HSPA8 at approximately 71 kDa. The expected band size for HSC70/HSPA8 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc9.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc10.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc7.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc11.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-ihc.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Hsc70 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-icc1.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-if.jpgAnti-Hsc70 HSPA8 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using Hsc70 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dusp6-rabbit-monoclonal-antibody-m02157-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02157-wb.jpgAnti-DUSP6/Mkp 3 Rabbit Monoclonal AntibodyWestern blot analysis of DUSP6 expression in NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02157-icc2.jpgAnti-DUSP6/Mkp 3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02157-ihc.jpgAnti-DUSP6/Mkp 3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid, using DUSP6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02157-icc1.jpgAnti-DUSP6/Mkp 3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vcam1-rabbit-monoclonal-antibody-m01199-1-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-1-vcam1cd106-primary-antibodies-wb-testing-1.jpgAnti-VCAM1/Cd106 Rabbit Monoclonal Antibody Western blot analysis of VCAM1/Cd106 using anti-VCAM1/Cd106 antibody (M01199-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat kidney tissue lysates, <br>
Lane 2: rat spleen tissue lysates, <br>
Lane 3: mouse kidney tissue lysates, <br>
Lane 4: mouse spleen tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VCAM1/Cd106 antigen affinity purified monoclonal antibody (M01199-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VCAM1/Cd106 at approximately 110 kDa. The expected band size for VCAM1/Cd106 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-1-12951_2025_3725_fig1_html.pngAnti-VCAM1/Cd106 Rabbit Monoclonal AntibodyNETs are increased and related to endothelial cell injury in humans and rats with AAV. (A ) Immunofluorescence staining of neutrophil NETs in healthy individuals and patients with ANCA-GN, scale bar = 20 μm; ( B ) Level of cf-DNA in neutrophil supernatant ( n = 4); ( C ) Serum cf-DNA levels in healthy individuals ( n = 12) and patients with ANCA-GN ( n = 28); ( D ) Deposition of NETs in renal tissue by immunofluorescence staining of MPO and NE. The dashed line indicates the glomerulus, scale bar = 20 μm; ( E ) Serum cf-DNA levels in PTU-AAV rats ( n = 3); ( F ) Serum cf-DNA levels in MPO-AAV rats ( n = 3); ( G ) Correlation analysis of the between serum NETs levels and endothelial cell injury markers ICAM-1 and VCAM-1 in patients with ANCA-GN. * P < 0.05, ** P < 0.01, *** P < 0.001 AAV: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis; NETs: Neutrophil extracellular traps; MPO: Myeloperoxidase; NE: Neutrophil elastase; HC: Health control; CTRL: control; EAV: Experimental autoimmune vasculitis; HAS: Human serum albumin. PTU: Propylthiouracil. ANCA-GN: ANCA-associated glomerulonephritis <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03725-z'>41074064</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-1-12951_2025_3725_fig7_html.pngAnti-VCAM1/Cd106 Rabbit Monoclonal AntibodyGCNPs/Mn alleviates the NETs-induced ferroptosis-related endothelial cell damage by regulating MnSOD/NF-κB signaling pathway. ( A ) Effect of GCNPs/Mn on MnSOD activity in endothelial cells ( n = 4); ( B ) Representative confocal microscopy images of HUVECs incubated with 15 µg/mL DiI-GCNPs/Mn for 24 h, with lysosomes and nuclei stained with LysoTracker-Green and DAPI, respectively (scale bar = 10 μm); staining repeated three times independently with similar results; ( C ) Intracellular Mn concentration after 24 h under different condition ( n = 4); ( D ) Effect of MnSOD activity inhibition on the mitigation of NETs-induced ferroptosis in HUVEC and MRGEC cells by GCNPs/Mn ( n = 3); ( E ) Effect of MnSOD activity inhibition on the mitigation of NETs-induced activation injury in HUVEC and MRGEC cells by GCNPs/Mn (ICAM-1 n=5; VCAM-1 n=3); ( F ) Differential gene cluster analysis and KEGG enrichment analysis from HUVEC transcriptome sequencing; ( G ) Effect of GCNPs/Mn on NF-κB signaling pathway activation in HUVECs (n = 3); ( H ) Effect of BAY11-7082 (the NF-κB signaling pathway inhibitor) on cell vitality in HUVECs (n=6); ( I ) Effect of BAY11-7082 on MDA levels in HUVECs (n=3); ( J ) Effect of MnSOD activity inhibition on GCNPs/Mn-mediated NF-κB signaling pathway activation in HUVECs (n=3). *P < 0.05, **P < 0.01, ***P < 0.001, ****P< 0.0001. GCNPs/Mn: manganese-loaded glucose-based carbon nanoparticles; NETs: Neutrophil extracellular traps; HUVEC: human umbilical vein endothelial cells; MRGEC: mouse glomerular endothelial cells; MnSOD: suppressing manganese superoxide dismutase; CTRL: control <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-025-03725-z'>41074064</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-1-ihc.jpgAnti-VCAM1/Cd106 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using VCAM1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-1-if.jpgAnti-VCAM1/Cd106 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562 cells, using VCAM1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox18-rabbit-monoclonal-antibody-m04004-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04004-sox18-primary-antibodies-wb-testing-1.jpgAnti-SOX18 Rabbit Monoclonal Antibody Western blot analysis of SOX18 using anti-SOX18 antibody (M04004). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human COLO 320 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX18 antigen affinity purified monoclonal antibody (Catalog # M04004) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX18 at approximately 41 kDa. The expected band size for SOX18 is at 41 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prmt5-rabbit-monoclonal-antibody-m00635-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-prmt5-primary-antibodies-wb-testing-1.jpgAnti-PRMT5 Rabbit Monoclonal Antibody Western blot analysis of PRMT5 using anti-PRMT5 antibody (M00635). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRMT5 antigen affinity purified monoclonal antibody (Catalog # M00635) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRMT5 at approximately 71 kDa. The expected band size for PRMT5 is at 71,73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-ihc.jpgAnti-PRMT5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using PRMT5 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-icc3.jpgAnti-PRMT5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-icc4.jpgAnti-PRMT5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-icc1.jpgAnti-PRMT5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00635-icc2.jpgAnti-PRMT5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hoxb9-rabbit-monoclonal-antibody-m05689-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05689-wb.jpgAnti-HOXB9 Rabbit Monoclonal AntibodyWestern blot analysis of HOXB9 expression in MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fos-b-rabbit-monoclonal-antibody-m01569-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01569-fosb-primary-antibodies-wb-testing-1_2.jpgAnti-Fos B Rabbit Monoclonal Antibody Western blot analysis of Fos B using anti-Fos B antibody (M01569).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human U20S whole cell lysates,<br>
Lane 3: human SiHa whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Fos B antigen affinity purified monoclonal antibody (Catalog # M01569) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Fos B at approximately 45 kDa. The expected band size for Fos B is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01569-fosb-primary-antibodies-ihc-testing-2.jpgAnti-Fos B Rabbit Monoclonal Antibody IHC analysis of Fos B using anti-Fos B antibody (M01569). <br>
Fos B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Fos B Antibody (M01569) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01569-fosb-primary-antibodies-ihc-testing-3.jpgAnti-Fos B Rabbit Monoclonal Antibody IHC analysis of Fos B using anti-Fos B antibody (M01569). <br>
Fos B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Fos B Antibody (M01569) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01569-fosb-primary-antibodies-if-testing-4.jpgAnti-Fos B Rabbit Monoclonal Antibody IF analysis of Fos B using anti-Fos B antibody (M01569) and anti-Beta Tubulin antibody (M01857-3).<br>
Fos B was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-Fos B Antibody (M01569) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nup98-rabbit-monoclonal-antibody-m01301-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01301-wb.jpgAnti-NUP98 Rabbit Monoclonal AntibodyWestern blot analysis of NUP98 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01301-ihc.jpgAnti-NUP98 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using NUP98 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp70-rabbit-monoclonal-antibody-m00949-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-hsp70-primary-antibodies-wb-testing-1.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal Antibody Western blot analysis of Hsp70 using anti-Hsp70 antibody (M00949). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human MCF-7 whole cell lysates, <br>
Lane 4: human HepG2 whole cell lysates, <br>
Lane 5: rat heart tissue lysates, <br>
Lane 6: rat liver tissue lysates, <br>
Lane 7: mouse heart tissue lysates, <br>
Lane 8: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hsp70 antigen affinity purified monoclonal antibody (M00949) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hsp70 at approximately 70 kDa. The expected band size for Hsp70 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-ihc7.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous carcinoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-ihc8.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human testis cancer, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-ihc9.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-ihc.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using Hsp70 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00949-if.jpgAnti-Hsp70 HSPA1A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Hsp70 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-maf-rabbit-monoclonal-antibody-m00654-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00654-ihc.jpgAnti-c-Maf Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using c-Maf Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alas1-rabbit-monoclonal-antibody-m10405-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10405-wb.jpgAnti-Alas1/Alas H Rabbit Monoclonal AntibodyWestern blot analysis of Alas1 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ash2l-rabbit-monoclonal-antibody-m06129-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06129-wb.jpgAnti-ASH2L Rabbit Monoclonal AntibodyWestern blot analysis of ASH2L expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06129-ihc.jpgAnti-ASH2L Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kideny, using ASH2L Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dgcr8-rabbit-monoclonal-antibody-m00475-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00475-wb7.jpgAnti-DGCR8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00475-wb.jpgAnti-DGCR8 Rabbit Monoclonal AntibodyWestern blot analysis of DGCR8 expression in (1) HEK293 cell lysate; (2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00475-wb8.jpgAnti-DGCR8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00475-wb9.jpgAnti-DGCR8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sirt2-rabbit-monoclonal-antibody-m00433-1-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-1-wb7.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-1-wb.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyWestern blot analysis of SIRT2 expression in SKBR-3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-htra2-rabbit-monoclonal-antibody-m01941-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01941-wb.jpgAnti-HTRA2/Omi Rabbit Monoclonal AntibodyWestern blot analysis of HTRA2 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad2-rabbit-monoclonal-antibody-m00090-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00090-wb7.jpgAnti-Smad2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00090-icc1.jpgAnti-Smad2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00090-wb.jpgAnti-Smad2 Rabbit Monoclonal AntibodyWestern blot analysis of Smad2 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac3-rabbit-monoclonal-antibody-m00839-boster.html2026-03-24T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig1_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyEnhanced expression of HDAC3 and activation of the cGAS-STING signaling pathway in human psoriatic skin A . The hdac3 mRNA expression analysis in GEO Database datasets: healthy skin ( n = 64) and psoriatic lesions ( n = 58) (accession number: GSE13355). B . Hematoxylin and eosin (H&E) staining of healthy versus psoriatic skin sections (bright-field microscopy). C . Quantification of epidermal thickness in healthy individuals ( n = 7) and psoriasis patients ( n = 7). D - F . Immunohistochemical detection of HDAC3 ( D ), cGAS ( E ), and STING ( F ) expression in normal and psoriatic lesional skin, representative staining patterns and quantitative integrated optical density (IOD) analysis (scale bar: 100 μm). G . Western blot analysis and quantification of HDAC3, cGAS, and STING protein expression in clinical normal skin samples (N, n = 4) and psoriatic lesional skin samples (P, n = 4). GAPDH served as the loading control. Individual sample values are shown as dots, and bars represent mean ± SD (error bars). Statistical significance was determined using Student’s t-test. * p < 0.05, ***p < 0.001 vs. Normal group; ns = not significant. IOD = Integrated Optical Density; SD = Standard Deviation; GEO = Gene Expression Omnibus Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig2_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyInhibition of HDAC3 alleviates IMQ-induced psoriasis-like skin inflammation in mice. A . C57BL/6 mice were randomly divided into four groups ( n = 6 per group). The model group received topical application of 62.5 mg IMQ on the back skin for 6 consecutive days, the control group was treated with diluted basis cream, and two treatment groups received daily topical administration of RGFP966 (3/10 mg/kg) or corn oil vehicle control (IMQ group). B . After 7 days, representative macroscopic images of skin lesions. C . Splenomegaly evaluation by gross morphology. D . Body weight changes monitored daily from day 1 to day 7 were assessed. E . The Psoriasis Area and Severity Index (PASI) score was calculated daily using a 0–4 scale (0 = None; 1 = Slight; 2 = Moderate; 3 = Marked; 4 = Very marked) based on erythema, scaling, and induration components, with total scores derived from n = 5 mice/group. F - G . Spleen weight and organ coefficient (calculated as spleen weight [mg]/body weight [g] × 1000) were quantified at day 7. H - I . Histopathological analysis revealed spleen hyperplasia in H&E-stained sections ( H : scale bars 1 mm [low magnification], 100 μm [high magnification]) and epidermal hyperplasia in skin sections ( I : scale bar 100 μm). Epidermal thickness was quantified ( J ), and statistical significance was determined using one-way ANOVA with Tukey’s multiple comparisons. Data are presented as mean ± SD. ** p < 0.01, *** p < 0.001 vs. control group; # p < 0.05, ## p < 0.01 vs. model group; ns = not significant Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig3_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyHDAC3 inhibition reduces oxidative stress and inflammatory cytokine secretion in IMQ-induced psoriasis-like skin inflammation. C57BL/6 mice were treated with IMQ (62.5 mg/day for 6 days) to establish psoriasis-like inflammation, followed by daily topical application of RGFP966 or vehicle control for 6 days. ( A ). Skin tissue levels of superoxide dismutase (SOD), lactate dehydrogenase (LDH), and glutathione (GSH) were quantified as follows, SOD activity in U/mg protein, GSH content in nmol/mg protein, and LDH activity in U/mg protein. ( B ). Serum concentrations of pro-inflammatory cytokines (IL-6, IL-17 A, IL-22, and TNF-α) and anti-inflammatory cytokines (IL-10) were measured via ELISA in pg/mL. Data are presented as mean ± SD ( n = 5 mice/group). Statistical significance was determined using one-way ANOVA with Tukey’s multiple comparisons. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control group; # p < 0.05, ## p < 0.01 vs. model group; ns = not significant Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig4_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyHDAC3 inhibition disrupts cGAS-STING signaling and modulates antioxidant gene expression in IMQ-induced psoriasis-like skin inflammation. C57BL/6 mice were treated with IMQ (62.5 mg/day for 6 days) to induce psoriasis-like inflammation, followed by daily topical application of RGFP966 or vehicle control for 6 days. A . mRNA expression levels of hdac3 , cgas , sting , s od1 , and sod2 were quantified via quantitative PCR. B . Protein expression of HDAC3, cGAS, STING, p-TBK (phosphorylated TANK-binding kinase 1), SOD1, and SOD2 was analyzed by Western blot. C . Densitometric quantification of protein bands normalized to GAPDH. D - F . Immunohistochemical analysis of HDAC3 ( D ), cGAS ( E ), and STING ( F ) expression in skin lesions. Representative IHC images with 50 μm scale bar, quantitative IOD analysis (mean ± SD, n = 5). *** p < 0.001 vs. control group # p < 0.05, ## p < 0.01, ### p < 0.01 vs. model group, ns = not significant Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig5_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyHDAC3 inhibition suppresses HaCaT cells proliferation in psoriasis-like cell models. A . CCK-8 viability analysis of HaCaT cells treated with RGFP966 at concentrations ranging from 0 to 20 µM. Concentrations exceeding 20 µM caused crystallization and were excluded. B . Quantitative real-time PCR analysis of hdac3 mRNA expression in HaCaT cells after RGFP966 treatment. C . Western blot quantification of HDAC3 protein levels in HaCaT cells treated with increasing concentrations of RGFP966 (0–5 µM), normalized to GAPDH. D . Phase-contrast microscopy images of HaCaT cells treated with proinflammatory cytokines. M 1: IL-17 A (10 ng/mL) + IL-1α (10 ng/mL) + TNF-α (5 ng/mL); M 2: IL-17 A (10 ng/mL) + IL-1α (10 ng/mL) + TNF-α (5 ng/mL) + IL-6 (5 ng/mL), scale bar: 100 μm. E . Real-time PCR analysis of psoriasis-related genes ( k16 , k17 , s100a7 , tnf-α , pi3 , ki67 ) in cells treated with combination cytokines. F . Morphological changes in HaCaT cells pre-treated with combination cytokines followed by RGFP966 or vehicle. Scale bar, 100 μm G . EdU proliferation assay of HaCaT cells treated with combination cytokines with or without RGFP966. Scale bar, 50 μm. One-way ANOVA with Tukey’s multiple comparisons test was used. Data are represented by mean ± SD, * p < 0.05, *** p < 0.001, compared with the control group Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig6_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyHDAC3 inhibition alleviates mitochondrial dysfunction in psoriasis-like cell models. HaCaT cells were treated with RGFP966 (5 µM) for 24 h to evaluate its protective effects on mitochondria in psoriasis-like conditions. A . ROS levels were quantified using DCFH-DA staining and Image J analysis DCF fluorescent intensity reflected cellular ROS content, while Hoechst 33,342 staining identified nuclei (scale bar: 50 μm; n = 3). B . Flow cytometric analysis confirmed reduced intracellular ROS in RGFP966-treated cells compared to the model group. C - E . Western blot and quantitative analysis revealed that RGFP966 treatment significantly upregulated SOD1 and SOD2 protein expression (normalized to GAPDH), which was associated with decreased oxidative stress in the model group. F - G . Cell levels of SOD and GSH were quantified with U/mg protein. H . Confocal microscopy demonstrated preserved mitochondrial structure (Mitotracker Red) and reduced nuclear fragmentation (Hoechst Blue) in RGFP966-treated cells (scale bar: 20 μm). I . Transmission electron microscopy (TEM) images showed intact cristae and less vacuolation in treated cells compared to the model group. J . JC-1 staining revealed maintained mitochondrial membrane potential (red aggregates) in RGFP966-treated cells, whereas the model group exhibited depolarization (green monomers) (scale bar: 20 μm). K . Flow cytometric quantification confirmed significantly lower green-to-red fluorescence ratios in treated cells. Data are represented by mean ± SD, *** p < 0.001, compared with the control group; # p < 0.5, ## p < 0.01, ### p < 0.001, compared with the model group Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-12967_2025_6544_fig7_html.pngAnti-HDAC3 Rabbit Monoclonal AntibodyHDAC3 inhibition disrupts cGAS-STING signaling in psoriasis-like cell models. A - B . RT-qPCR analysis of cytosolic DNA content and nuclear DNA (nDNA) in HaCaT cells treated with proinflammatory cytokines. C . Immunofluorescence co-staining the expression of HDAC3 and cGAS localization in RGFP966-treated cells. D . Quantitative analysis of protein expression of cGAS, STING, TBK1, and phosphorylated form (p-TBK1), GAPDH as a loading control. One-way ANOVA with Tukey’s multiple comparisons test was used. Data are represented by mean ± SD, ** p < 0.01, *** p < 0.001, compared with the control group; # p < 0.5, ## p < 0.01, ### p < 0.001, compared with the model group Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-025-06544-w'>40457335</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00839-hdac3-primary-antibodies-wb-testing-1.jpgAnti-HDAC3 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC3 using anti-HDAC3 antibody (M00839). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDAC3 antigen affinity purified monoclonal antibody (M00839) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HDAC3 at approximately 49 kDa. The expected band size for HDAC3 is at 49 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd11a-rabbit-monoclonal-antibody-m04466-1-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04466-1-wb.jpgAnti-CD11a ITGAL Rabbit Monoclonal AntibodyWestern blot analysis of CD11a expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mlana-rabbit-monoclonal-antibody-m02033-1-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02033-1-wb7.jpgAnti-MLANA/Mart 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02033-1-wb.jpgAnti-MLANA/Mart 1 Rabbit Monoclonal AntibodyWestern blot analysis of MLANA expression in Human melanoma tissue lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02033-1-ihc.jpgAnti-MLANA/Mart 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human melanoma, using MLANA Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgfr1-rabbit-monoclonal-antibody-m00098-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-ihc7.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-icc1.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-ihc8.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thymoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-wb.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyWestern blot analysis of FGFR1 expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-ihc9.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat pancreas, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-if.jpgAnti-FGFR1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using FGFR1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nanog-rabbit-monoclonal-antibody-m00153-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00153-wb7.jpgAnti-Nanog Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00153-if.jpgAnti-Nanog Rabbit Monoclonal AntibodyImmunofluorescent analysis of NCCIT cells, using Nanog Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00153-wb.jpgAnti-Nanog Rabbit Monoclonal AntibodyWestern blot analysis of Nanog expression in NCCIT cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00153-ihc.jpgAnti-Nanog Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat testis, using Nanog Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pebp1-rabbit-monoclonal-antibody-m01668-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-wb10.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-wb7.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-wb.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyWestern blot analysis of PEBP1 expression in A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-wb8.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-wb9.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-ihc.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using PEBP1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01668-if.jpgAnti-PEBP1/Pbp Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PEBP1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gap43-rabbit-monoclonal-antibody-m01868-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01868-wb.jpgAnti-GAP43 Rabbit Monoclonal AntibodyWestern blot analysis of GAP43 expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01868-ihc.jpgAnti-GAP43 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using GAP43 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eif5a-rabbit-monoclonal-antibody-m01727-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01727-wb7.jpgAnti-eIF5A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01727-if.jpgAnti-eIF5A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using eIF5A Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01727-wb.jpgAnti-eIF5A Rabbit Monoclonal AntibodyWestern blot analysis of eIF5A expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01727-ihc.jpgAnti-eIF5A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus cancer, using eIF5A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-plcg1-rabbit-monoclonal-antibody-m00677-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00677-plcg1-primary-antibodies-wb-testing-1.jpgAnti-PLCG1/Plc Gamma 1 Rabbit Monoclonal Antibody Western blot analysis of PLCG1 using anti-PLCG1 antibody (M00677). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat RH35 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLCG1 antigen affinity purified monoclonal antibody (Catalog # M00677) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLCG1 at approximately 149 kDa. The expected band size for PLCG1 is at 149 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00677-icc1.jpgAnti-PLCG1/Plc Gamma 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rho-a-rabbit-monoclonal-antibody-m00207-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-rhoa-primary-antibodies-wb-testing-1.jpgAnti-Rho A Rabbit Monoclonal Antibody Western blot analysis of Rho A using anti-Rho A antibody (M00207). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rho A antigen affinity purified monoclonal antibody (Catalog # M00207) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Rho A at approximately 22 kDa. The expected band size for Rho A is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-if.jpgAnti-Rho A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Rho A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-irak3-rabbit-monoclonal-antibody-m02469-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02469-wb.jpgAnti-IRAK3/Irak M Rabbit Monoclonal AntibodyWestern blot analysis of SGK1 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prp19-rabbit-monoclonal-antibody-m02434-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-wb7.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-wb.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyWestern blot analysis of PRP19 expression in (1) HepG2 cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-1.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-2.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-3.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-4.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-5.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-6.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-7.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-8.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02434-prpf19-primary-antibodies-ihc-testing-9.jpgAnti-PRP19 PRPF19 Rabbit Monoclonal AntibodyIHC analysis of PRPF19 using anti-PRPF19 antibody (M02434). <br>PRPF19 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PRPF19 Antibody (M02434) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rps20-rabbit-monoclonal-antibody-m06634-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06634-rps20-primary-antibodies-wb-testing-1.jpgAnti-RPS20/Ribosomal Protein S20 Rabbit Monoclonal AntibodyWestern blot analysis of RPS20 using anti-RPS20 antibody (M06634). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse HEPA1-6 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS20 antigen affinity purified monoclonal antibody (M06634) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPS20 at approximately 18 kDa. The expected band size for RPS20 is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06634-ihc.jpgAnti-RPS20/Ribosomal Protein S20 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using RPS20 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cxcr7-rabbit-monoclonal-antibody-m02656-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02656-ackr3-primary-antibodies-wb-testing-1.jpgAnti-CXCR7 ACKR3 Rabbit Monoclonal AntibodyWestern blot analysis of CXCR7/ACKR3 using anti-CXCR7/ACKR3 antibody (M02656). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CXCR7/ACKR3 antigen affinity purified monoclonal antibody (M02656) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CXCR7/ACKR3 at approximately 38 kDa. The expected band size for CXCR7/ACKR3 is at 41 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd168-rabbit-monoclonal-antibody-m05056-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-wb7.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-ihc9.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-ihc7.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-wb.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyWestern blot analysis of CD168 expression in LnCaP cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-ihc8.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05056-ihc.jpgAnti-CD168 HMMR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using CD168 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rad18-rabbit-monoclonal-antibody-m01622-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01622-wb.jpgAnti-Rad18 Rabbit Monoclonal AntibodyWestern blot analysis of RAD18 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-wasf2-rabbit-monoclonal-antibody-m03969-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03969-wb7.jpgAnti-WASF2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03969-wb.jpgAnti-WASF2 Rabbit Monoclonal AntibodyWestern blot analysis of WASF2 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03969-ihc.jpgAnti-WASF2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using WASF2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kcna1-rabbit-monoclonal-antibody-m01813-boster.html2026-03-24T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01813-wb.jpgAnti-KCNA1/Kv1.1 Rabbit Monoclonal AntibodyWestern blot analysis of KCNA1 expression in Human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-abcf1-rabbit-monoclonal-antibody-m05358-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05358-wb.jpgAnti-ABCF1 Rabbit Monoclonal AntibodyWestern blot analysis of ABCF1 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05358-abcf1-primary-antibodies-wb-testing-1.jpgAnti-ABCF1 Rabbit Monoclonal AntibodyWestern blot analysis of ABCF1 using anti-ABCF1 antibody (M05358). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCF1 antigen affinity purified monoclonal antibody (M05358) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ABCF1 at approximately 110 kDa. The expected band size for ABCF1 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05358-ihc.jpgAnti-ABCF1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using ABCF1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05358-wb7.jpgAnti-ABCF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg9a-rabbit-monoclonal-antibody-m03757-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03757-wb.jpgAnti-ATG9A Rabbit Monoclonal AntibodyWestern blot analysis of ATG9A expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03757-ihc.jpgAnti-ATG9A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer, using ATG9A Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03757-if.jpgAnti-ATG9A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hepg2 cells, using ATG9A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mekk2-rabbit-monoclonal-antibody-m02354-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02354-map3k2-primary-antibodies-wb-testing-1.jpgAnti-MEKK2 MAP3K2 Rabbit Monoclonal AntibodyWestern blot analysis of MAP3K2 using anti-MAP3K2 antibody (M02354). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP3K2 antigen affinity purified monoclonal antibody (M02354) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MAP3K2 at approximately 78 kDa. The expected band size for MAP3K2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02354-map3k2-primary-antibodies-ihc-testing-1.jpgAnti-MEKK2 MAP3K2 Rabbit Monoclonal AntibodyIHC analysis of MAP3K2 using anti-MAP3K2 antibody (M02354). <br>MAP3K2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MAP3K2 Antibody (M02354) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mtco2-rabbit-monoclonal-antibody-m03631-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03631-wb.jpgAnti-MTCO2 Rabbit Monoclonal AntibodyWestern blot analysis of MTCO2 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03631-ihc.jpgAnti-MTCO2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using MTCO2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-agtr2-rabbit-monoclonal-antibody-m00432-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00432-agtr2-primary-antibodies-wb-testing-1.jpgAnti-AGTR2/Angiotensin Ii Type 2 Receptor Rabbit Monoclonal Antibody Western blot analysis of AGTR2 using anti-AGTR2 antibody (M00432). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human SH-SY5Y whole cell lysates, <br>
Lane 3: human Caco-2 whole cell lysates, <br>
Lane 4: rat lung tissue lysates, <br>
Lane 5: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AGTR2 antigen affinity purified monoclonal antibody (M00432) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AGTR2 at approximately 45 kDa. The expected band size for AGTR2 is at 41 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-muc16-rabbit-monoclonal-antibody-m01641-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-wb.jpgAnti-MUC16/Ca125 Rabbit Monoclonal AntibodyWestern blot analysis of MUC16 expression in Human ovary cancer lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-park7-rabbit-monoclonal-antibody-m00757-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00757-park7-primary-antibodies-wb-testing-1.jpgAnti-PARK7/Dj 1 Rabbit Monoclonal Antibody Western blot analysis of PARK7 using anti-PARK7 antibody (M00757). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARK7 antigen affinity purified monoclonal antibody (Catalog # M00757) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARK7 at approximately 20 kDa. The expected band size for PARK7 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00757-ihc.jpgAnti-PARK7/Dj 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder cancer, using PARK7 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-epcam-rabbit-monoclonal-antibody-m30950-2-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-2-wb.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal AntibodyWestern blot analysis of EpCAM expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-2-wb8.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-2-ihc.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach carcinoma, using EpCAM Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30950-2-wb7.jpgAnti-EpCAM/Trop1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl10-rabbit-monoclonal-antibody-m01616-1-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01616-1-wb.jpgAnti-Bcl10 Rabbit Monoclonal AntibodyWestern blot analysis of Bcl10 expression in (1) HeLa cell lysate; (2) Raji cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01616-1-ihc.jpgAnti-Bcl10 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Bcl10 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ap2m1-rabbit-monoclonal-antibody-m06179-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06179-wb.jpgAnti-AP2M1/Ap 2 Mu 1 Rabbit Monoclonal AntibodyWestern blot analysis of AP2M1 expression in (1) HEK293 cell lysate; (2) MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp11-rabbit-monoclonal-antibody-m04490-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04490-mmp11-primary-antibodies-wb-testing-1.jpgAnti-MMP11 Rabbit Monoclonal AntibodyWestern blot analysis of MMP11 using anti-MMP11 antibody (M04490). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP11 antigen affinity purified monoclonal antibody (M04490) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MMP11 at approximately 55 kDa. The expected band size for MMP11 is at 55 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il1ra-rabbit-monoclonal-antibody-m00651-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00651-wb.jpgAnti-IL1RA Rabbit Monoclonal AntibodyWestern blot analysis of IL1RA expression in (1) HeLa cell lysate; (2) 3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00651-gr4.jpgAnti-IL1RA Rabbit Monoclonal AntibodySSD treatment ameliorated RA rats. Representative images of hind paws from different groups and changes in foot circumference. Hematoxylin eosin staining and immunohistochemical staining (CD31, CD39, CD73, CCR6 and IL1R1) of knee joint synovial slices. *P < 0.05, **P < 0.01 vs Model group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/heliyon/fulltext/S2405-8440(24)13288-4'>39296024</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-oprd1-rabbit-monoclonal-antibody-m03505-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03505-oprd1-primary-antibodies-wb-testing-1.jpgAnti-OPRD1/Delta Opioid Receptor Rabbit Monoclonal AntibodyWestern blot analysis of OPRD1 using anti-OPRD1 antibody (M03505). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U87MG whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse spleen tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OPRD1 antigen affinity purified monoclonal antibody (M03505) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for OPRD1 at approximately 42 kDa. The expected band size for OPRD1 is at 40 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glur1-rabbit-monoclonal-antibody-m02677-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02677-wb7.jpgAnti-GluR1 GRIA1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02677-wb8.jpgAnti-GluR1 GRIA1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02677-wb.jpgAnti-GluR1 GRIA1 Rabbit Monoclonal AntibodyWestern blot analysis of GluR1 expression in Human brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erbb4-rabbit-monoclonal-antibody-m00296-1-boster.html2026-03-24T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00296-1-wb7.jpgAnti-ErbB4/Her4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00296-1-wb8.jpgAnti-ErbB4/Her4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00296-1-wb.jpgAnti-ErbB4/Her4 Rabbit Monoclonal AntibodyWestern blot analysis of ErbB4 expression in Human brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox11-rabbit-monoclonal-antibody-m02603-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02603-wb.jpgAnti-SOX11 Rabbit Monoclonal AntibodyWestern blot analysis of SOX11 expression in SHSY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox10-rabbit-monoclonal-antibody-m00758-1-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-1-sox10-primary-antibodies-wb-testing-1.jpgAnti-SOX10 Rabbit Monoclonal Antibody Western blot analysis of SOX10 using anti-SOX10 antibody (M00758-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A375 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX10 antigen affinity purified monoclonal antibody (Catalog # M00758-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX10 at approximately 60-65 kDa. The expected band size for SOX10 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-1-if.jpgAnti-SOX10 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HT-29 cells, using SOX10 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-1-sox10-primary-antibodies-if-testing-2.jpgAnti-SOX10 Rabbit Monoclonal AntibodyIF analysis of SOX10 using anti-SOX10 antibody (M00758-1) . <br>
SOX10 was detected in an immunocytochemical section of human A-375 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes and then treated with a membrane permeabilization agent (AR0205) for 5 minutes.The cells were blocked with 10% goat serum. And then incubated with rabbit anti-SOX10 Antibody (M00758-1) at a dilution of 10 μg/mL overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sox10-rabbit-monoclonal-antibody-m00758-2-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-2-wb7.jpgAnti-SOX10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-2-wb10.jpgAnti-SOX10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-2-wb8.jpgAnti-SOX10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-2-ihc.jpgAnti-SOX10 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using SOX10 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00758-2-wb9.jpgAnti-SOX10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdpk1-rabbit-monoclonal-antibody-m01159-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01159-wb.jpgAnti-PDPK1/Pdk 1 Rabbit Monoclonal AntibodyWestern blot analysis of PDPK1 expression in HEK293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01159-pdpk1-primary-antibodies-wb-testing-1.jpgAnti-PDPK1/Pdk 1 Rabbit Monoclonal AntibodyWestern blot analysis of PDPK1 using anti-PDPK1 antibody (M01159). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human SIHA whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDPK1 antigen affinity purified monoclonal antibody (M01159) at 1:1000 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDPK1 at approximately 63 kDa. The expected band size for PDPK1 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01159-ihc.jpgAnti-PDPK1/Pdk 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using PDPK1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01159-if.jpgAnti-PDPK1/Pdk 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of PC-12 cells, using PDPK1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-traf2-rabbit-monoclonal-antibody-m00400-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00400-traf2-primary-antibodies-wb-testing-1.jpgAnti-TRAF2 Rabbit Monoclonal AntibodyWestern blot analysis of TRAF2 using anti-TRAF2 antibody (M00400). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAF2 antigen affinity purified monoclonal antibody (M00400) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRAF2 at approximately 50 kDa. The expected band size for TRAF2 is at 56 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sirt6-rabbit-monoclonal-antibody-m00611-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00611-sirt6-primary-antibodies-wb-testing-1.jpgAnti-SIRT6 Rabbit Monoclonal AntibodyWestern blot analysis of SIRT6 using anti-SIRT6 antibody (M00611). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HCT116 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIRT6 antigen affinity purified monoclonal antibody (M00611) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SIRT6 at approximately 39 kDa. The expected band size for SIRT6 is at 39 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sirt2-rabbit-monoclonal-antibody-m00433-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-wb7.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-wb.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyWestern blot analysis of SIRT2 expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-wb8.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00433-wb9.jpgAnti-SIRT2/Sirtuin 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat2-rabbit-monoclonal-antibody-m01360-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01360-wb.jpgAnti-STAT2 Rabbit Monoclonal AntibodyWestern blot analysis of STAT2 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01360-ihc.jpgAnti-STAT2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer, using STAT2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01360-if.jpgAnti-STAT2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using STAT2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat4-rabbit-monoclonal-antibody-m00734-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00734-wb.jpgAnti-STAT4 Rabbit Monoclonal AntibodyWestern blot analysis of STAT4 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smad1-rabbit-monoclonal-antibody-m00728-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00728-wb.jpgAnti-Smad1 Rabbit Monoclonal AntibodyWestern blot analysis of Smad1 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00728-ihc.jpgAnti-Smad1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Smad1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac2-rabbit-monoclonal-antibody-m00325-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-wb7.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-wb10.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-wb8.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-wb.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00325-wb9.jpgAnti-HDAC2/Histone Deacetylase 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac6-rabbit-monoclonal-antibody-m00595-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00595-hdac6-primary-antibodies-wb-testing-1.jpgAnti-HDAC6/Histone Deacetylase 6 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC6 using anti-HDAC6 antibody (M00595). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: human SIHA whole cell lysates,<br>
Lane 6: human A431 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDAC6 antigen affinity purified monoclonal antibody (M00595) at 1: 5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HDAC6 at approximately 160 kDa. The expected band size for HDAC6 is at 131 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac9-rabbit-monoclonal-antibody-m02177-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02177-wb.jpgAnti-HDAC9 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC9 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02177-ihc.jpgAnti-HDAC9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain, using HDAC9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02177-if.jpgAnti-HDAC9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using HDAC9 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxo4-rabbit-monoclonal-antibody-m01819-1-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01819-1-foxo4-primary-antibodies-wb-testing-1.jpgAnti-FoxO4/Afx Rabbit Monoclonal Antibody Western blot analysis of FOXO4 using anti-FOXO4 antibody (M01819-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates, <br>
Lane 2: human Hela whole cell lysates, <br>
Lane 3: human 293T whole cell lysates, <br>
Lane 4: human Caco-2 whole cell lysates, <br>
Lane 5: rat skeletal muscle tissue lysates, <br>
Lane 6: mouse heart tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXO4 antigen affinity purified monoclonal antibody (M01819-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FOXO4 at approximately 65 kDa. The expected band size for FOXO4 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01819-1-if.jpgAnti-FoxO4/Afx Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using FoxO4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxo4-rabbit-monoclonal-antibody-m01819-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01819-wb.jpgAnti-FoxO4/Afx Rabbit Monoclonal AntibodyWestern blot analysis of FoxO4 expression in 293T cell lysate transfected with FoxO4.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac7-rabbit-monoclonal-antibody-m01913-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01913-wb7.jpgAnti-HDAC7/Histone Deacetylase 7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01913-wb.jpgAnti-HDAC7/Histone Deacetylase 7 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC7 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac8-rabbit-monoclonal-antibody-m01843-1-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01843-1-HDAC8-primary-antibodies-WB-testing-1.jpgAnti-HDAC8/Histone Deacetylase 8 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC8 expression in HeLa cell lysate (M01843-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDAC8 monoclonal antibody (Catalog # M01843-1) overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDAC8https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01843-1-hdac8-primary-antibodies-if-testing-2.jpgAnti-HDAC8/Histone Deacetylase 8 Rabbit Monoclonal AntibodyIF analysis of HDAC8 using anti-HDAC8 antibody (M01843-1) and anti-Beta Tubulin antibody (M01857-3).<br>
HDAC8 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-HDAC8 Antibody (M01843-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac4-rabbit-monoclonal-antibody-m00971-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00971-wb7.jpgAnti-HDAC4/Histone Deacetylase 4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00971-wb.jpgAnti-HDAC4/Histone Deacetylase 4 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC4 expression in Hela lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mekk3-rabbit-monoclonal-antibody-m03586-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03586-wb.jpgAnti-MEKK3 MAP3K3 Rabbit Monoclonal AntibodyWestern blot analysis of MEKK3 expression in Hela cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03586-djir_a_12304658_f0005_c.jpgAnti-MEKK3 MAP3K3 Rabbit Monoclonal AntibodyWestern blot analysis of curcumin regulation of the p38MAPK pathway. (A–C) Western blot and quantitative analysis of p38 and p-p38. (D–F) Western blot and quantitative analysis of ASK1 and MEKK3. (G and H) Western blot images and quantitative analysis of PKCδ and p-PKCδ. (I–L) Western blot and quantitative analysis of BCL-2 and caspase-3. (n = 3). *p < 0.05,** p < 0.01,***p < 0.001.
<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S459867'>39081871</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sirt5-rabbit-monoclonal-antibody-m02395-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02395-wb.jpgAnti-SIRT5/Sirtuin 5 Rabbit Monoclonal AntibodyWestern blot analysis of SIRT5 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac8-rabbit-monoclonal-antibody-m01843-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01843-wb7.jpgAnti-HDAC8/Histone Deacetylase 8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01843-wb8.jpgAnti-HDAC8/Histone Deacetylase 8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01843-wb.jpgAnti-HDAC8/Histone Deacetylase 8 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC8 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp27-rabbit-monoclonal-antibody-m00676-2-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-hspb1-primary-antibodies-wb-testing-1.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal Antibody Western blot analysis of HSPB1 using anti-HSPB1 antibody (M00676-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPB1 antigen affinity purified monoclonal antibody (Catalog # M00676-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPB1 at approximately 27 kDa. The expected band size for HSPB1 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-icc3.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-hspb1-primary-antibodies-ihc-testing-2.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal Antibody IHC analysis of HSPB1 using anti-HSPB1 antibody (M00676-2). <br>
HSPB1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPB1 Antibody (M00676-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-icc1.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-hspb1-primary-antibodies-ihc-testing-3.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal Antibody IHC analysis of HSPB1 using anti-HSPB1 antibody (M00676-2). <br>
HSPB1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPB1 Antibody (M00676-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00676-2-icc2.jpgAnti-Hsp27 HSPB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sumo4-rabbit-monoclonal-antibody-m06740-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06740-wb.jpgAnti-SUMO4 Rabbit Monoclonal AntibodyWestern blot analysis of SUMO4 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc45-rabbit-monoclonal-antibody-m01367-boster.html2026-03-24T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01367-wb.jpgAnti-CDC45/Cdc45L Rabbit Monoclonal AntibodyWestern blot analysis of CDC45 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc40-rabbit-monoclonal-antibody-m07786-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07786-cdc40-primary-antibodies-wb-testing-1.jpgAnti-CDC40 Rabbit Monoclonal AntibodyWestern blot analysis of CDC40 using anti-CDC40 antibody (M07786). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDC40 antigen affinity purified monoclonal antibody (M07786) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDC40 at approximately 69 kDa. The expected band size for CDC40 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07786-cdc40-primary-antibodies-ihc-testing-1.jpgAnti-CDC40 Rabbit Monoclonal AntibodyIHC analysis of CDC40 using anti-CDC40 antibody (M07786). <br>CDC40 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDC40 Antibody (M07786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07786-cdc40-primary-antibodies-ihc-testing-2.jpgAnti-CDC40 Rabbit Monoclonal AntibodyIHC analysis of CDC40 using anti-CDC40 antibody (M07786). <br>CDC40 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDC40 Antibody (M07786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07786-cdc40-primary-antibodies-ihc-testing-3.jpgAnti-CDC40 Rabbit Monoclonal AntibodyIHC analysis of CDC40 using anti-CDC40 antibody (M07786). <br>CDC40 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CDC40 Antibody (M07786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspa4-rabbit-monoclonal-antibody-m03618-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03618-wb.jpgAnti-HSPA4 Rabbit Monoclonal AntibodyWestern blot analysis of HSPA4 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp20-rabbit-monoclonal-antibody-m07981-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07981-wb.jpgAnti-Hsp20 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp20 expression in mouse skeletal muscle lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc42-rabbit-monoclonal-antibody-m00119-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-wb10.jpgAnti-CDC42 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-wb7.jpgAnti-CDC42 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-wb8.jpgAnti-CDC42 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-wb9.jpgAnti-CDC42 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-wb.jpgAnti-CDC42 Rabbit Monoclonal AntibodyWestern blot analysis of CDC42 expression in (1) Jurkat cell lysate; (2) Mouse spleen lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc7.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat skin, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc8.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc9.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc10.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc11.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00119-ihc12.jpgAnti-CDC42 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:200 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdca3-rabbit-monoclonal-antibody-m10074-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10074-cdca3-primary-antibodies-wb-testing-1.jpgAnti-CDCA3 Rabbit Monoclonal Antibody Western blot analysis of CDCA3 using anti-CDCA3 antibody (M10074). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDCA3 antigen affinity purified monoclonal antibody (Catalog # M10074) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDCA3 at approximately 29 kDa. The expected band size for CDCA3 is at 29 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdca5-rabbit-monoclonal-antibody-m05043-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05043-cdca5-primary-antibodies-wb-testing-1.jpgAnti-CDCA5/Sororin Rabbit Monoclonal Antibody Western blot analysis of CDCA5 using anti-CDCA5 antibody (M05043). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDCA5 antigen affinity purified monoclonal antibody (Catalog # M05043) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDCA5 at approximately 35 kDa. The expected band size for CDCA5 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05043-ihc.jpgAnti-CDCA5/Sororin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using CDCA5 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05043-if.jpgAnti-CDCA5/Sororin Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CDCA5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc34-rabbit-monoclonal-antibody-m03038-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03038-cdc34-primary-antibodies-wb-testing-1.jpgAnti-CDC34/Ubch3 Rabbit Monoclonal AntibodyWestern blot analysis of CDC34 using anti-CDC34 antibody (M03038). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: human SH-SY5Y whole cell lysates,<br>
Lane 6: human U251 whole cell lysates,<br>
Lane 7: rat testis tissue lysates,<br>
Lane 8: mouse testis tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDC34 antigen affinity purified monoclonal antibody (M03038) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDC34 at approximately 35 kDa. The expected band size for CDC34 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03038-if.jpgAnti-CDC34/Ubch3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CDC34 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-a-raf-rabbit-monoclonal-antibody-m02061-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02061-wb.jpgAnti-A-RAF Rabbit Monoclonal AntibodyWestern blot analysis of A-RAF expression in A375 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp75-rabbit-monoclonal-antibody-m02426-1-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02426-1-wb.jpgAnti-Hsp75 TRAP1 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp75 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc37-rabbit-monoclonal-antibody-m02169-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02169-wb.jpgAnti-Cdc37 Rabbit Monoclonal AntibodyWestern blot analysis of Cdc37 expression in (1) Jurkat cell lysate; (2) SW480 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspa2-rabbit-monoclonal-antibody-m03474-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03474-hspa2-primary-antibodies-wb-testing-1.jpgAnti-HSPA2 Rabbit Monoclonal AntibodyWestern blot analysis of HSPA2 using anti-HSPA2 antibody (M03474). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA2 antigen affinity purified monoclonal antibody (M03474) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HSPA2 at approximately 70 kDa. The expected band size for HSPA2 is at 70 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mmp13-rabbit-monoclonal-antibody-m00420-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00420-wb7.jpgAnti-MMP13 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00420-wb.jpgAnti-MMP13 Rabbit Monoclonal AntibodyWestern blot analysis of MMP13 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-suz12-rabbit-monoclonal-antibody-m00583-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00583-wb.jpgAnti-SUZ12 Rabbit Monoclonal AntibodyWestern blot analysis of SUZ12 expression in (1) HeLa cell lysate; (2) SW480 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-acss2-rabbit-monoclonal-antibody-m02809-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig2_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyACSS2 deficiency blunts CCF formation during senescence. a , b IMR90 cells were induced to senesce by oncogene RAS ( a ) or Etoposide ( b ). The proliferating cells and senescent cells expressing non-targeting shRNA, ACSS2 , or ACLY -targeted shRNAs were infected with cGAS-FLAG encoding lentivirus. All groups of cells were subjected to γH2AX and cGAS-FLAG immunostaining. CCFs were indicated by arrows. Scale bar = 20 μm. c , d the CCF-positive cells were quantified among groups as described in ( a , b ). Randomly imaged fields with over 100 cells were analysed. Data represent the mean values of six different fields ± s.d. The P values were calculated using One-way ANOVA (Tukey’s multiple-comparison test). Representative of n = 3 independent experiments were shown ( c, d ). Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig1_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyACSS2 regulates SASP during senescence. a ER:RAS-expressing IMR90 cells were induced to senesce by adding 100 nM 4-OHT, expressing non-targeting shRNA (shCtrl) or ACSS2 targeted shRNA (shACSS2). The puromycin-selected cells were harvested and analysed for expression of the indicated proteins by immunoblots. b – d The indicated cells were examined by SA-β-gal staining and colony formation ( b ). SA-β-gal-positive cells were quantified ( c ), the integrated intensity of the colonies was quantified using NIH Image J software ( d ). e , f Heat map of the RNA-seq data of the genes for which expression was significantly changed among proliferating and senescent cells with or without ACSS2 knockdown ( e ), KEGG analysis of genes altered by ACSS2 knockdown is shown (fold change, FC ≥ 2, P < 0.05) ( f ). g Heat map of SASP genes in senescent cells with ACSS2 knockdown vs. control knockdown determined by RNA-seq analysis. h The secretion of SASP components under the indicated conditions was detected by antibody arrays. The relative FC in comparison to the senescent cell with control shRNA was shown ( n = 2 indepe n dent repeats). i Average signal from ChIP-seq analysis of H3K27ac occupancy in proliferating and senescent cells with or without knockdown of ACSS2 . j Overlap between genes with expression upregulated in senescence while decreased by ACSS2 knockdown and genes with increased H3K27ac signal while decreased by ACSS2 knockdown (FC ≥ 2). RNA-seq and ChIP-seq analysis, n = 3 biologically independent repeats. k Gene ontology analysis of the overlap genes from ( j ). l Tracks of H3K27ac distribution on the representative SASP genes in groups of proliferating and senescent cells with or without ACSS2 knockdown. Data represent the mean ± s.d. of three biologically independent experiments. The P values were calculated using One-way ANOVA (Tukey’s multiple-comparison test) ( c, d ) or two-tailed Fisher Exact test ( j ) or one-sided Fisher exact test with Benjamini-Hochberg adjustment ( f, k ). Representative blot of n = 3 indepe n dent experiments was shown ( a ). Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig3_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyACSS2 deficiency increases purine biosynthesis in senescence. a ER:RAS-expressing cells were induced to senesce by adding 100 nM 4-OHT. At day 8 post-induction, cells were infected with lentivirus encoding non-targeting shRNA, ACSS2 , or ACLY -targeted shRNAs. The puromycin-selected cells were harvested to perform targeted metabolomics analysis. Hierarchical clustering of significantly altered metabolites among groups was shown ( n = 3 each group). b Top-ranked metabolic pathways in senescent cells with ACSS2 knockdown compared to control shRNA knockdown. P values were calculated using hypergeometric distribution (MetaboAnalyst v6.0). c , d Heat map analysis of the metabolites involved in the pyrimidine pathway ( c ) and the purine pathway ( d ). e ER:RAS-expressing cells were induced to senesce by adding 100 nM 4-OHT. On day 8 post-induction, cells were infected with lentivirus-encoding non-targeting shRNA or ACSS2 -targeted shRNA. The puromycin-selected cells were harvested to measure cellular dNTP levels. f – h ER:RAS-expressing cells were induced to senesce by adding 100 nM 4-OHT. At day 8 post-induction, cells were supplemented with or without nucleosides or purine-only nucleosides for 14 days. Cells were stained for γH2AX ( f ). Three randomly imaged fields were analysed ( g ). The SASP mRNA expression was examined by qRT-PCR ( h ). Scale bar = 20 μm. Data represent mean ± s.d. of three biologically independent experiments. The P values were calculated using an unpaired two-tailed Student’s t -test ( e ) or One-way ANOVA (Tukey’s multiple-comparison test) ( g, h ). Pro, proliferating cells; Sen, RAS induced senescence; NS, nucleosides; A + G, Adenosine+Guanosine. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig4_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyDNPB enzymes partially mediate the effects of ACSS2 knockdown on CCF formation and SASP gene expression. a Volcano plot showing Log 2 fold changes in protein intensities on the X-axis and −Log 10 P values on the Y-axis. Significantly enriched proteins were in blue ( P < 0.05) and non-significant in gray. P values were calculated using a two-tailed Student’s t -test. b – e ER:RAS-expressing cells were induced to senesce by adding 100 nM 4-OHT, and the proliferating cells and senescent cells expressing non-targeting shRNA, ACSS2 targeting shRNA together with PAICS or AK1 specific shRNAs were subjected to immunoblots for the indicated proteins ( b ), or CCF detection ( c ). Scale bar = 10 μm. d The CCF-positive cells were quantified among groups. Four Randomly imaged fields with over 100 cells were analysed. Bar graphs represent mean values of different fields ± s.d. e Proliferating and senescent cells, as described in ( b ), were subjected to qRT-PCR analysis for expression of the indicated SASP genes. f Proliferating and OIS cells with shCtrl or shACSS2 were harvested and the labeled 15 N-Glutamine incorporation into purine intermediates were analysed by LC-MS/MS. Data represent mean ± s.d. of three biologically independent experiments. The P values were calculated using One-way ANOVA (Tukey’s multiple-comparison test) ( d – f ). Representative of n = 3 indepe n dent experiments were shown ( b, d ). Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig5_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyACSS2 promotes acetylation of PAICS and decreases its protein stability. a Proliferating and OIS cells with or without ACSS2 knockdown were harvested. Co-immunoprecipitation analysis of endogenous PAICS and ACSS2 in extracts from the indicated IMR90 cells was performed and subjected to immunoblots of the indicated proteins. b Purified human protein of ACSS2 and PAICS was subjected to in vitro pull-down assay. Immunoblot of the indicated proteins was shown. c Proliferating and OIS cells were infected with HA-PAICS encoding lentivirus, and then treated with or without ACSS2i for 48 h. PAICS protein was immunoprecipitated, and the acetylation was analysed by immunoblot with the indicated antibody. d HEK293T cells were transfected with HA-tagged wildtype (WT) or K36R, K47R, and K36RK47R mutants of PAICS. HA-PAICS protein was immunoprecipitated, and the acetylation was analyzed by immunoblot with the indicated antibody. e , f ER:RAS-expressing cells were induced to senesce by adding 100 nM 4-OHT. On day 8 after the induction, the senescent cell was infected with lentivirus encoding non-targeting shRNA or ACSS2 targeted shRNA ( e ) or treated with ACSS2i for 48 h ( f ). The cells were harvested and analysed by immunoblot for expression of the indicated proteins. g , h Proliferating and senescent cells described in ( e ) were treated with CHX (100 μg/mL) for 0, 6, or 12 h, and the expression of the indicated proteins was analysed by immunoblot ( g ) and quantified ( h ). i OIS cells were subjected to co-immunoprecipitation analysis of endogenous PAICS and PCAF, immunoblots of the indicated proteins were shown. j , k OIS cells expressing non-targeting shRNA or PCAF -targeted shRNA were infected with HA-PAICS encoding lentivirus. PAICS protein was immunoprecipitated, and the acetylation was analyzed by immunoblot with the indicated antibody ( j ) and quantified ( k ). l Proliferating and OIS cells expressing non-targeting shRNA or PCAF -targeted shRNA were subjected to immunoblots of the indicated proteins. Data represent mean ± s.d. of three biologically independent experiments. The P values were calculated using an unpaired two-tailed Student’s t -test ( k ). Representative of n = 3 independent experiments were shown ( a – g, i, j, l ). Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-41467_2025_57334_fig7_html.pngAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal AntibodyACSS2 is required for the in vivo function of SASP. a , b TOV21G cells were co-injected with proliferating or senescent IMR90 cells into NCG mice. The tumor volume was measured ( a ) and the tumor weight was measured, ( b ). n = 5 mice per group. c A scheme of the experimental procedure. d – f One week after ionizing irradiation, Livers from vehicle or ACSS2i treated mice were analysed by immunohistochemistry for γH2AX ( d ), the mean values of γH2AX positive cells from nine randomly imaged fields were quantified per mouse ( e ), and SASP mRNA expression was analysed ( f ). Scale bar = 20 μm. n = 5 for non-IR group, n = 7 per IR group. g – j 18-month-old mice were administered with vehicle or ACSS2i for one week ( g ). Livers were harvested and analyzed by immunohistochemistry for γH2AX ( h ), and the mean values of γH2AX positive cells from ten randomly imaged fields were quantified per mouse ( i ) and SASP mRNA expression was analysed ( j ). Scale bar = 20 μm. n = 5 for the young or vehicle-treated old mice group, n = 7 for the treated old mice group. k Schematic model of the constructs and the experimental design. l – n Representative images of SA-β-gal staining of the liver tissues at day 7 and 14 post-injection ( l ), and quantified ( m, n ). n = 6 each group. o , p Representative images of CD45 immunofluorescence staining and NRas-dsRed at day 7 post-injection ( o ), and the mean value of the double positive clusters from five randomly imaged fields per mouse were calculated ( p ). Scale bar = 100 μm. q , r Representative images of CD45 IHC staining of the liver tissues at day 7 and 14 post-injection ( q ). Arrows point to examples of immune clusters. CD45 + cells in the indicated groups at day 7 post-injection were quantified ( r ). Scale bar = 100 μm. n = 6 each group. Data represent the mean ± s.d. The P values were calculated using One-way ANOVA (Tukey’s multiple-comparison test) ( a, b, e, f, i, j ) or an unpaired two-tailed Student’s t -test ( m, n, p, r ). Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-57334-3'>40021646</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02809-acss2-primary-antibodies-wb-testing-1.jpgAnti-ACSS2/Acetyl Coa Synthetase Rabbit Monoclonal Antibody Western blot analysis of ACSS2 using anti-ACSS2 antibody (M02809). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human HEL whole cell lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: rat kidney tissue lysates, <br>
Lane 6: mouse liver tissue lysates, <br>
Lane 7: mouse kidney tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACSS2 antigen affinity purified monoclonal antibody (M02809) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACSS2 at approximately 79 kDa. The expected band size for ACSS2 is at 79 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-znrf2-rabbit-monoclonal-antibody-m11505-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11505-wb7.jpgAnti-ZNRF2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11505-wb.jpgAnti-ZNRF2 Rabbit Monoclonal AntibodyWestern blot analysis of ZNRF2 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dusp1-rabbit-monoclonal-antibody-m02276-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02276-wb7.jpgAnti-DUSP1/Mkp 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02276-wb8.jpgAnti-DUSP1/Mkp 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02276-wb.jpgAnti-DUSP1/Mkp 1 Rabbit Monoclonal AntibodyWestern blot analysis of DUSP1 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02276-dusp1-primary-antibdodies-ihc-testing-1.jpgAnti-DUSP1/Mkp 1 Rabbit Monoclonal AntibodyIHC analysis of DUSP1 using anti-DUSP1 antibody (M02276).<br>
DUSP1 expression was detected in paraffin-embedded sections of human breast cancer tissues, with human placenta tissue serving as the positive control. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 5% BSA . The tissue section was then incubated with rabbit anti-DUSP1 antibody (M02276) at 5 μg/ml overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ptp1b-rabbit-monoclonal-antibody-m00613-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00613-wb.jpgAnti-PTP1B PTPN1 Rabbit Monoclonal AntibodyWestern blot analysis of PTP1B expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-fos-rabbit-monoclonal-antibody-m00297-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00297-fos-primary-antibodies-wb-testing-1.jpgAnti-c-Fos Rabbit Monoclonal AntibodyWestern blot analysis of FOS using anti-FOS antibody (M00297). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOS antigen affinity purified monoclonal antibody (M00297) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOS at approximately 41 kDa. The expected band size for FOS is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00297-fos-primary-antibodies-wb-testing-2.pngAnti-c-Fos Rabbit Monoclonal AntibodyWestern blot analysis of FOS using anti-FOS antibody (M00297). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse hippocampus tissue lysates,<br>
Lane 2: mouse Alzheimer’s disease tissue lysates,<br>
Lane 3-5: mouse Alzheimer’s disease hippocampi treated with increasing doses of Qianlenta herbal formula tissue lysates,
<br>
Lane 6:mouse Alzheimer’s disease hippocampi treated with positive control drug.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOS antigen affinity purified monoclonal antibody (M00297) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for FOS at approximately 41 kDa. The expected band size for FOS is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00297-qihang_yang.pngAnti-c-Fos Rabbit Monoclonal AntibodyIF analysis of c-Fos using anti-c-Fos antibody (M00297). <br>
c-Fos was detected in an immunocytochemical section of mouse brain tissue. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:200 rabbit anti-c-Fos Antibody (M00297) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 45 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lamp1-rabbit-monoclonal-antibody-m00780-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00780-wb7.jpgAnti-LAMP1/Cd107A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00780-wb.jpgAnti-LAMP1/Cd107A Rabbit Monoclonal AntibodyWestern blot analysis of LAMP1 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prdx1-rabbit-monoclonal-antibody-m01845-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01845-prdx1-primary-antibodies-wb-testing-1.jpgAnti-PRDX1/Peroxiredoxin 1 Rabbit Monoclonal Antibody Western blot analysis of PRDX1/Peroxiredoxin 1 using anti-PRDX1/Peroxiredoxin 1 antibody (M01845). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: mouse liver tissue lysates,<br>
Lane 6: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRDX1/Peroxiredoxin 1 antigen affinity purified monoclonal antibody (Catalog # M01845) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRDX1/Peroxiredoxin 1 at approximately 24 kDa. The expected band size for PRDX1/Peroxiredoxin 1 is at 22,24 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ebp50-rabbit-monoclonal-antibody-m02427-boster.html2026-03-24T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02427-wb.jpgAnti-EBP50 SLC9A3R1 Rabbit Monoclonal AntibodyWestern blot analysis of EBP50 expression in (1) HepG2 cell lysate; (2) PC12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-timp1-rabbit-monoclonal-antibody-m00561-1-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00561-1-wb7.jpgAnti-TIMP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00561-1-wb8.jpgAnti-TIMP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00561-1-wb.jpgAnti-TIMP1 Rabbit Monoclonal AntibodyWestern blot analysis of TIMP1 expression in HL60 cell lysate treated with TPA.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lama3-rabbit-monoclonal-antibody-m04194-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04194-wb.jpgAnti-LAMA3/Laminin 5 Rabbit Monoclonal AntibodyWestern blot analysis of LAMA3 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nedd8-rabbit-monoclonal-antibody-m00547-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00547-nedd8-primary-antibodies-wb-testing-1.jpgAnti-NEDD8 Rabbit Monoclonal Antibody Western blot analysis of NEDD8 using anti-NEDD8 antibody (M00547). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NEDD8 antigen affinity purified monoclonal antibody (M00547) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NEDD8 at approximately 10 kDa. The expected band size for NEDD8 is at 9 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bmp11-rabbit-monoclonal-antibody-m02355-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02355-gdf11-primary-antibodies-wb-testing-1.jpgAnti-BMP11 GDF11 Rabbit Monoclonal AntibodyWestern blot analysis of BMP11/GDF11 using anti-BMP11/GDF11 antibody (M02355). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat C6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMP11/GDF11 antigen affinity purified monoclonal antibody (M02355) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BMP11/GDF11 at approximately 45 kDa. The expected band size for BMP11/GDF11 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02355-gdf11-primary-antibodies-ihc-testing-1.jpgAnti-BMP11 GDF11 Rabbit Monoclonal AntibodyIHC analysis of BMP11/GDF11 using anti-BMP11/GDF11 antibody (M02355). <br>BMP11/GDF11 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BMP11/GDF11 Antibody (M02355) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02355-gdf11-primary-antibodies-ihc-testing-2.jpgAnti-BMP11 GDF11 Rabbit Monoclonal AntibodyIHC analysis of BMP11/GDF11 using anti-BMP11/GDF11 antibody (M02355). <br>BMP11/GDF11 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BMP11/GDF11 Antibody (M02355) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02355-gdf11-primary-antibodies-ihc-testing-3.jpgAnti-BMP11 GDF11 Rabbit Monoclonal AntibodyIHC analysis of BMP11/GDF11 using anti-BMP11/GDF11 antibody (M02355). <br>BMP11/GDF11 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BMP11/GDF11 Antibody (M02355) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02355-gdf11-primary-antibodies-ihc-testing-4.jpgAnti-BMP11 GDF11 Rabbit Monoclonal AntibodyIHC analysis of BMP11/GDF11 using anti-BMP11/GDF11 antibody (M02355). <br>BMP11/GDF11 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-BMP11/GDF11 Antibody (M02355) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vamp8-rabbit-monoclonal-antibody-m02338-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02338-vamp8-primary-antibodies-wb-testing-1.jpgAnti-VAMP8/Endobrevin Rabbit Monoclonal Antibody Western blot analysis of VAMP8 using anti-VAMP8 antibody (M02338). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates,<br>
Lane 6: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VAMP8 antigen affinity purified monoclonal antibody (Catalog # M02338) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VAMP8 at approximately 11 kDa. The expected band size for VAMP8 is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02338-vamp8-primary-antibodies-ihc-testing-2.jpgAnti-VAMP8/Endobrevin Rabbit Monoclonal Antibody IHC analysis of VAMP8 using anti-VAMP8 antibody (M02338). <br>
VAMP8 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VAMP8 Antibody (M02338) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02338-vamp8-primary-antibodies-ihc-testing-3.jpgAnti-VAMP8/Endobrevin Rabbit Monoclonal Antibody IHC analysis of VAMP8 using anti-VAMP8 antibody (M02338). <br>
VAMP8 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VAMP8 Antibody (M02338) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02338-ip7.jpgAnti-VAMP8/Endobrevin Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution).
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdia6-rabbit-monoclonal-antibody-m03813-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03813-wb.jpgAnti-PDIA6/Erp5 Rabbit Monoclonal AntibodyWestern blot analysis of PDIA6 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lyve1-rabbit-monoclonal-antibody-m04027-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04027-lyve1-primary-antibodies-wb-testing-1.jpgAnti-LYVE1 Rabbit Monoclonal Antibody Western blot analysis of LYVE1 using anti-LYVE1 antibody (M04027). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYVE1 antigen affinity purified monoclonal antibody (Catalog # M04027) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYVE1 at approximately 29 kDa. The expected band size for LYVE1 is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-actn2-rabbit-monoclonal-antibody-m03673-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03673-wb.jpgAnti-ACTN2 Rabbit Monoclonal AntibodyWestern blot analysis of ACTN2 expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03673-actn2-primary-antibodies-wb-testing-1.jpgAnti-ACTN2 Rabbit Monoclonal Antibody Western blot analysis of ACTN2 using anti-ACTN2 antibody (M03673). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat skeletal muscle tissue lysates,<br>
Lane 2: rat heart tissue lysates,<br>
Lane 3: mouse skeletal muscle tissue lysates,<br>
Lane 4: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACTN2 antigen affinity purified monoclonal antibody (Catalog # M03673) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACTN2 at approximately 104 kDa. The expected band size for ACTN2 is at 104 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hmgcr-rabbit-monoclonal-antibody-m00643-boster.html2026-04-03T05:00:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00643-wb.jpgAnti-HMGCR/Hmg Coa Reductase Rabbit Monoclonal AntibodyWestern blot analysis of HMGCR expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100p-rabbit-monoclonal-antibody-m01963-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01963-wb.jpgAnti-S100P Rabbit Monoclonal AntibodyWestern blot analysis of S100P expression in SW480 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01963-s100p-primary-antibodies-wb-testing-1.jpgAnti-S100P Rabbit Monoclonal AntibodyWestern blot analysis of S100P using anti-S100P antibody (M01963). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-S100P antigen affinity purified monoclonal antibody (M01963) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for S100P at approximately 10 kDa. The expected band size for S100P is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01963-ihc.jpgAnti-S100P Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder carcinoma, using S100P Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01963-if.jpgAnti-S100P Rabbit Monoclonal AntibodyImmunofluorescent analysis of SW480 cells, using S100P Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dnmt1-rabbit-monoclonal-antibody-m00172-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00172-dnmt1-primary-antibodies-wb-testing-1.jpgAnti-Dnmt1 Rabbit Monoclonal Antibody Western blot analysis of DNMT1 using anti-DNMT1 antibody (M00172). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat NRK whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNMT1 antigen affinity purified monoclonal antibody (M00172) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNMT1 at approximately 200 kDa. The expected band size for DNMT1 is at 183 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00172-ihc9.jpgAnti-Dnmt1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00172-ihc10.jpgAnti-Dnmt1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00172-ihc7.jpgAnti-Dnmt1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat spleen, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00172-ihc8.jpgAnti-Dnmt1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:100 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ctip2-rabbit-monoclonal-antibody-m01485-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01485-wb.jpgAnti-Ctip2 Rabbit Monoclonal AntibodyWestern blot analysis of Ctip2 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-abcg2-rabbit-monoclonal-antibody-m00457-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00457-wb.jpgAnti-ABCG2/Bcrp Rabbit Monoclonal AntibodyWestern blot analysis of ABCG2 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdha1-rabbit-monoclonal-antibody-m01906-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01906-wb7.jpgAnti-PDHA1/Pdh E1Alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01906-wb.jpgAnti-PDHA1/Pdh E1Alpha Rabbit Monoclonal AntibodyWestern blot analysis of PDHA1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01906-wb8.jpgAnti-PDHA1/Pdh E1Alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01906-wb9.jpgAnti-PDHA1/Pdh E1Alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aspp2-rabbit-monoclonal-antibody-m02609-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02609-wb.jpgAnti-ASPP2 Rabbit Monoclonal AntibodyWestern blot analysis of ASPP2 expression in MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxa1-rabbit-monoclonal-antibody-m00266-1-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00266-1-foxa1-primary-antibodies-ihc-testing-2.jpgAnti-FOXA1/Hnf 3 Alpha Rabbit Monoclonal Antibody IHC analysis of FOXA1 using anti-FOXA1 antibody (M00266-1). <br>
FOXA1 was detected in a paraffin-embedded section of human esophageal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOXA1 Antibody (M00266-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00266-1-foxa1-primary-antibodies-wb-testing-1.jpgAnti-FOXA1/Hnf 3 Alpha Rabbit Monoclonal Antibody Western blot analysis of FOXA1 using anti-FOXA1 antibody (M00266-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXA1 antigen affinity purified monoclonal antibody (Catalog # M00266-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FOXA1 at approximately 49 kDa. The expected band size for FOXA1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00266-1-foxa1-primary-antibodies-ihc-testing-3.jpgAnti-FOXA1/Hnf 3 Alpha Rabbit Monoclonal Antibody IHC analysis of FOXA1 using anti-FOXA1 antibody (M00266-1). <br>
FOXA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOXA1 Antibody (M00266-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00266-1-foxa1-primary-antibodies-ihc-testing-4.jpgAnti-FOXA1/Hnf 3 Alpha Rabbit Monoclonal Antibody IHC analysis of FOXA1 using anti-FOXA1 antibody (M00266-1). <br>
FOXA1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOXA1 Antibody (M00266-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00266-1-foxa1-primary-antibodies-ihc-testing-5.jpgAnti-FOXA1/Hnf 3 Alpha Rabbit Monoclonal Antibody IHC analysis of FOXA1 using anti-FOXA1 antibody (M00266-1). <br>
FOXA1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOXA1 Antibody (M00266-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ercc1-rabbit-monoclonal-antibody-m00388-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00388-wb.jpgAnti-ERCC1 Rabbit Monoclonal AntibodyWestern blot analysis of ERCC1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxp1-rabbit-monoclonal-antibody-m00723-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00723-foxp1-primary-antibodies-wb-testing-1.jpgAnti-FOXP1 Rabbit Monoclonal Antibody Western blot analysis of FOXP1 using anti-FOXP1 antibody (M00723). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse spleen tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXP1 antigen affinity purified monoclonal antibody (Catalog # M00723) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FOXP1 at approximately 90 kDa. The expected band size for PFOXP1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00723-foxp1-primary-antibodies-if-testing-2.jpgAnti-FOXP1 Rabbit Monoclonal Antibody IF analysis of FOXP1 using anti-FOXP1 antibody (M00723) and anti-Beta Tubulin antibody (M01857-3).<br>
FOXP1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-FOXP1 Antibody (M00723) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prox1-rabbit-monoclonal-antibody-m01985-1-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01985-1-prox1-primary-antibodies-wb-testing-1.jpgAnti-PROX1 Rabbit Monoclonal AntibodyWestern blot analysis of PROX1 using anti-PROX1 antibody (M01985-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PROX1 antigen affinity purified monoclonal antibody (M01985-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PROX1 at approximately 90 kDa. The expected band size for PROX1 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01985-1-prox1-primary-antibodies-ihc-testing-4.jpgAnti-PROX1 Rabbit Monoclonal AntibodyIHC analysis of PROX1 using anti-PROX1 antibody (M01985-1). <br>PROX1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PROX1 Antibody (M01985-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01985-1-prox1-primary-antibodies-ihc-testing-3.jpgAnti-PROX1 Rabbit Monoclonal AntibodyIHC analysis of PROX1 using anti-PROX1 antibody (M01985-1). <br>PROX1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PROX1 Antibody (M01985-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01985-1-prox1-primary-antibodies-ihc-testing-2.jpgAnti-PROX1 Rabbit Monoclonal AntibodyIHC analysis of PROX1 using anti-PROX1 antibody (M01985-1). <br>PROX1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PROX1 Antibody (M01985-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-agtr1-rabbit-monoclonal-antibody-m01213-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01213-wb.jpgAnti-AGTR1 Rabbit Monoclonal AntibodyWestern blot analysis of AGTR1 expression in (1) HeLa cell lysate; (2) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hla-g-rabbit-monoclonal-antibody-m01235-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01235-wb.jpgAnti-HLA G Rabbit Monoclonal AntibodyWestern blot analysis of HLA G expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tgn46-rabbit-monoclonal-antibody-m06591-boster.html2026-03-24T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06591-wb7.jpgAnti-TGN46 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06591-wb.jpgAnti-TGN46 Rabbit Monoclonal AntibodyWestern blot analysis of TGN46 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ddit3-rabbit-monoclonal-antibody-m00311-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00311-fphar-12-685895-g005.jpgAnti-DDIT3/Chop Rabbit Monoclonal AntibodyCHOP siRNA partially decreases MCT-induced apoptosis of primary rat hepatocytes. After pretreatment with CHOP siRNA (100 nM) or siNC (100 nM) for 24 h, the hepatocytes were treated with or without 300 μM of MCT for another 36 h. (A) Representative immunofluorescence photomicrographs showing the location of CHOP in hepatocytes from different groups. Scale bar = 20 μM. (B) Western blot was used to detect the expression of CHOP and cleaved caspase-3. (C) Quantitative analysis of protein levels in A. (D) The apoptosis rate of primary rat hepatocytes was detected by Annexin-V/PI staining. The Q1 quadrant stands for cell death induced by mechanical damage or necrotic cells, the Q2 quadrant stands for late apoptosis cells, the Q3 quadrant stands for early apoptosis cells, and the Q4 quadrant stands for normal cells. The sum of cell apoptosis included early and late apoptosis cells (E) The percentages of apoptosis cells were measured by flow cytometry. (F) Hepatocytes viability was detected by CCK-8 assay. Data are presented as mean ± SD error of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.685895/full'>34108882</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00311-fphar-12-685895-g004.jpgAnti-DDIT3/Chop Rabbit Monoclonal AntibodyInhibition of MCT-induced ER stress can partly protect primary rat hepatocytes from apoptosis. After pretreatment with 4-PBA (0.5 mM) for 4 h, the hepatocytes were treated with or without 300 μM of MCT for another 36 h. (A) Representative immunofluorescence photomicrographs showing the location of GRP78 in hepatocytes from different groups. (B) Representative immunofluorescence photomicrographs showing the location of CHOP in hepatocytes from different groups. Scale bar = 20 μM. (C) Detection of ER stress-related proteins, including GRP78, IRE1 α, p-IRE1 α, ATF6, eIF2 α, p-eIF2 α, ATF4, and CHOP by western blot. (D–F) Quantitative analysis of protein levels in C. (G) The hepatocytes viability was detected by CCK-8 assay. (H) Representative western blot of cleaved-caspase eight and cleaved-caspase three in hepatocytes. (I) Quantitative analysis of protein levels in G. (J) Representative apoptosis rate measured by Annexin-V/PI staining. The Q1 quadrant stands for cell death induced by mechanical damage or necrotic cells, the Q2 quadrant stands for late apoptosis cells, the Q3 quadrant stands for early apoptosis cells, and the Q4 quadrant stands for normal cells. The sum of cell apoptosis included early and late apoptosis cells. (K) The results of quantitative analyses of apoptosis rate. Data are presented as mean ± SD error of three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.685895/full'>34108882</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00311-ddit3-primary-antibodies-wb-testing-1.jpgAnti-DDIT3/Chop Rabbit Monoclonal Antibody Western blot analysis of DDIT3 using anti-DDIT3 antibody (M00311). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDIT3 antigen affinity purified monoclonal antibody (Catalog # M00311) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DDIT3 at approximately 29 kDa. The expected band size for DDIT3 is at 20 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd147-rabbit-monoclonal-antibody-m00248-1-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00248-1-cd147-primary-antibodies-wb-testing-1.jpgAnti-CD147 BSG Rabbit Monoclonal Antibody Western blot analysis of CD147 using anti-CD147 antibody (M00248-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: rat kidney tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse kidney tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD147 antigen affinity purified monoclonal antibody (Catalog # M00248-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD147 at approximately 65 kDa. The expected band size for CD147 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00248-1-ihc.jpgAnti-CD147 BSG Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach cancer, using CD147 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00248-1-if.jpgAnti-CD147 BSG Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using using CD147 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-timp1-rabbit-monoclonal-antibody-m00561-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00561-wb.jpgAnti-TIMP1 Rabbit Monoclonal AntibodyWestern blot analysis of TIMP1 expression in human prostate cancer lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00561-cimb-46-00840-g003.jpgAnti-TIMP1 Rabbit Monoclonal AntibodyKnockdown of LY6K inhibits migration and invasion of CCSCs in vitro. Optical micrographs and the number of migrated ( A ) and invaded ( B ) CCSCs following siLY6K or siNC transfection for 48 h according to Transwell migration and invasion assay. n = 3. ( C ) Western blot analyses showing the protein levels of MMP-2, MMP-9, and TIMP-1 in CCSCs after treatment with siLY6K or siNC for 48 h. Values are the mean ± SE (n = 3). ** p < 0.01, *** p < 0.001, or **** p < 0.0001 indicates significant differences from the Mock and siNC group as assessed by one-way ANOVA with Tukey–Kramer multiple comparisons tests. LY6K, lymphocyte antigen 6, locus K; CCSC, colon cancer stem cells; MMP, matrix metalloproteinase; TIMP-1, tissue inhibitor of MMP-1; n.s., not significant. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11727511/'>39727968</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-actin-rabbit-monoclonal-antibody-m02014-2-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-2-wb.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyWestern blot analysis of Actin expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-actin-rabbit-monoclonal-antibody-m02014-3-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-3-wb.jpgAnti-Actin ACTA1 Rabbit Monoclonal AntibodyWestern blot analysis of Actin expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl-2-rabbit-monoclonal-antibody-m00040-2-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-wb11.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-wb8.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-43556_2024_203_fig7_html.pngAnti-Bcl-2 Rabbit Monoclonal AntibodyMice reconstituted with FGF2 KO macrophages and subjected to CLP exhibit increased proinflammatory gene expression and apoptosis. a - c The expression of the inflammatory factors CXCL1, IL1β, and IL6 in lung tissue was detected by real-time PCR ( n = 3 per group). d TUNEL staining was used to evaluate apoptosis in the lung tissue. e - f The apoptosis-associated genes BCL2 and Bax were identified by western blot analysis. Bar is 20 μm. * p < 0.05, vs. WT; Δ p < 0.05, vs. WT + LPS; # p < 0.05 vs. FGF2 KO <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s43556-024-00203-0'>39436561</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-41598_2024_69356_fig2_html.pngAnti-Bcl-2 Rabbit Monoclonal AntibodySuidical iBAT ablation significantly inhibited the cardioprotective effect of DEX. ( A ) Representative echocardiographic M-mode images were obtained 24 h after myocardial ischemia/reperfusion (MI/R), n = 6/group. ( B ) Left ventricular ejection fraction (LVEF) and fractional shortening (LVFS), n = 6/group. ( C ) Representative images of TTC staining 24 h after MI/R. Myocardial infarction area was calculated as a percentage of the myocardial area at risk, n = 6/group. ( D ) The levels of serum CK-MB, n = 6/group. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3 expression, n = 3/group. ( F ) Representative photographs of cardiomyocyte apoptosis examined by TUNEL assay. Bar graphs present the quantification analysis of cell apoptosis, n = 6/group. Scale bar = 200 μm. ( G ) Morphological changes in myocardium was determined by HE staining. Scale bar = 100 μm. ( H ) The levels of serum FGF21 in Mice, n = 6/group.* means P < 0.05 vs Control, † means P < 0.05 vs I/R group, ‡ means P < 0.05 vs. I/R + DEX group, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-12906_2019_2544_fig2_html.pngAnti-Bcl-2 Rabbit Monoclonal Antibodya Representative photographs of P53 and Bcl-2 expression on xenograft tumor lysate. b : Normalize grey values of P53 and Bcl-2 expression. * P < 0.05, ** P < 0.01 vs control group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-019-2544-2'>31215421</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-41598_2024_69356_fig3_html.pngAnti-Bcl-2 Rabbit Monoclonal AntibodyExogenous administration of FGF21 neutralizing antibody significantly inhibited the cardioprotective effect of DEX. ( A ) Representative echocardiographic M-mode images were obtained 24 h after myocardial ischemia/reperfusion (MI/R), n = 6/group. ( B ) Left ventricular ejection fraction (LVEF) and fractional shortening (LVFS), n = 6/group. ( C ) Representative images of TTC staining 24 h after MI/R. Myocardial infarction area was calculated as a percentage of the myocardial area at risk, n = 6/group. ( D ) The levels of serum CK-MB, n = 6/group. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group. ( F ) Representative photographs of cardiomyocyte apoptosis examined by TUNEL assay. Bar graphs present the quantification analysis of cell apoptosis, n = 6/group. scale bar = 200 μm. ( G ) Morphological changes in myocardium was determined by HE staining. scale bar = 100 μm.* means P < 0.05 vs Control,† means P < 0.05 vs I/R group,‡ means P < 0.05 vs. I/R + DEX group, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-41598_2024_69356_fig5_html.pngAnti-Bcl-2 Rabbit Monoclonal AntibodyDEX had minimal effect on the H/R-induced injury in HL-1 cells. ( A ) Representative photographs of flow cytometry apoptosis assay. ( B ) Statistics of Cell apoptosis rate. ( C ) CCK-8 cell viability assay. ( D ) lactate dehydrogenase (LDH) release assay.( E ) Representative photographs of PI staining. Scale bar = 100 μm. ( F ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group.* means P < 0.05 vs Control, the value is expressed as Mean ± SD. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-41598_2024_69356_fig6_html.pngAnti-Bcl-2 Rabbit Monoclonal AntibodyFGF21 release from DEX-treated brown adipocytes attenuated H/R-induced injury in HL-1 cells through regulating the Keap1/Nrf2 complex. ( A ) Representative photographs of flow cytometry apoptosis assay. ( B ) Statistics of Cell apoptosis rate. ( C ) CCK-8 cell viability assay. ( D ) Lactate dehydrogenase (LDH) release assay. ( E ) The protein expression of Bax, Bcl-2, cleaved caspase 3, were determined by western blot analysis. Bar graphs present the quantification analysis of Bax, Bcl-2, cleaved caspase 3, n = 3/group. ( F ) Representative photographs of DHE staining. Scale bar = 100 μm. ( G ) The protein expression of Keap1 were determined by western blot. ( H ) The interaction of Keap1 with Nrf2 was determined by Co-IP. ( I ) The protein expression of Nrf2 in nucleus and cytoplasm were determined by western blot. ( J ) Relative mRNA levels of antioxidant genes in cardiomyocytes after CM-DEX treatment. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-69356-w'>39112671</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-thnov10p3980g006.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyTMEM16A bound with p62 and modulated p62-Bcl-2-Beclin-1-VPS43 complex formation. (A and B) Immunoprecipitation (IP) followed by immunoblotting (IB) in MASMC lysates showing presence of p62 in TMEM16A immunoprecipitates (A), and reciprocal immunoprecipitation showing the presence of TMEM16A in p62 immunoprecipitates (B). (C and D) MASMCs were co-transfected with vectors expressing TMEM16A tagged with HA and RFP, and p62 tagged with His. Western blot analysis for His (C) or HA (D) after immunoprecipitation with an HA or His antibody, respectively. n=5. (E-H) The cells were infected with Ad-Lacz or Ad-TM adenovirus (E and F, respectively), or transfected with scr.RNA or TM siRNA (G and H, respectively) for 48 h and then treated with AngII for another 24 h. Lysates were immunoprecipitated with a Bcl-2 (E and G) or Beclin-1 (F and H) antibody and immunoblotted with the indicated antibodies. **P < 0.01 vs. control; ##P < 0.01 vs. AngII, one-way ANOVA. n = 7. (I) Schematic representation of the study findings. TMEM16A bound with p62 and sequestered it from the p62-Bcl-2 complex. AngII-induced TMEM16A downregulation and led to reduced TMEM16A-p62 association and facilitated the binding of p62-Bcl-2, which limited formation of Bcl-2-Beclin-1 complexes. Finally, the enhanced Beclin-1-VPS34 association increased the kinase activity of VPS34 and initiated autophagy, leading to VSMC hyperplasia and remodeling.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7086348/&orig_host=www.ncbi.nlm.nih.gov'>32226533</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-12906_2019_2544_fig5_html.pngAnti-Bcl-2 Rabbit Monoclonal Antibodya Representative photographs of Bcl-2 immunological histological chemistry examination (200 ×). I: Control group, II: Elemene 20 mg/kg group, III: Elemene 40 mg/kg group, IV: Elemene 60 mg/kg group. b Quantification of P53 stained cells. * P < 0.05, ** P < 0.01 vs control group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12906-019-2544-2'>31215421</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-oncotarget-08-29785-g002.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyTGF-β1 suppresses the HCC cells proliferative capacity but does not promote apoptosis. SMMC-7721 and BEL-7402 cells were treated with 0, 5ng/mL and 10ng/mL TGF-β1 for 48 hours. A . apoptosis B . western blotting examined the expression levels of Bcl-2 and Bax. Data are expressed as the mean ± SEM of three independent experiments, #P>0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5444703/&orig_host=www.ncbi.nlm.nih.gov'>28076850</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-wb9.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-wb10.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-wb.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyWestern blot analysis of Bcl-2 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-ihc7.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-ihc8.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-ihc9.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tonsil, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-ihc.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using Bcl-2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-icc1.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00040-2-if.jpgAnti-Bcl-2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Bcl-2 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgfr2-rabbit-monoclonal-antibody-m00231-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-wb7.jpgAnti-FGFR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-wb.jpgAnti-FGFR2 Rabbit Monoclonal AntibodyWestern blot analysis of FGFR2 expression in (1) MCF-7 cell lysate; (2) Mouse brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lin28-rabbit-monoclonal-antibody-m01966-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01966-csdd1-primary-antibodies-wb-testing-1.jpgAnti-Lin28 LIN28A Rabbit Monoclonal Antibody Western blot analysis of Lin28 using anti-Lin28 antibody (M01966). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Caco-2 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lin28 antigen affinity purified monoclonal antibody (Catalog # M01966) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lin28 at approximately 26 kDa. The expected band size for Lin28 is at 24 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxa2-rabbit-monoclonal-antibody-m01032-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01032-foxa2-primary-antibodies-wb-testing-1.jpgAnti-FOXA2/Hnf3B Rabbit Monoclonal AntibodyWestern blot analysis of FOXA2 using anti-FOXA2 antibody (M01032). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: rat RH35 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXA2 antigen affinity purified monoclonal antibody (M01032) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXA2 at approximately 50 kDa. The expected band size for FOXA2 is at 48 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ezrin-rabbit-monoclonal-antibody-m01750-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01750-wb.jpgAnti-Ezrin Rabbit Monoclonal AntibodyWestern blot analysis of Ezrin expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myod1-rabbit-monoclonal-antibody-m00964-1-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00964-1-wb7.jpgAnti-MyoD1/Myod Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00964-1-wb8.jpgAnti-MyoD1/Myod Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00964-1-wb.jpgAnti-MyoD1/Myod Rabbit Monoclonal AntibodyWestern blot analysis of MyoD1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fabp1-rabbit-monoclonal-antibody-m02477-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02477-fabp-primary-antibodies-wb-testing-1.jpgAnti-FABP1/L Fabp Rabbit Monoclonal Antibody Western blot analysis of FABP1/L using anti-FABP1/L antibody (M02477). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HCCT whole cell lysates, <br>
Lane 2: human HCCP whole cell lysates, <br>
Lane 3: human HepG2 whole cell lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: human RH35 whole cell lysates, <br>
Lane 6: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FABP1/L antigen affinity purified monoclonal antibody (M02477) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FABP1/L at approximately 14 kDa. The expected band size for FABP1/L is at 14 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgfr3-rabbit-monoclonal-antibody-m00200-1-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-1-fgfr3-primary-antibodies-wb-testing-1.jpgAnti-FGFR3 Rabbit Monoclonal Antibody Western blot analysis of FGFR3 using anti-FGFR3 antibody (M00200-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: human HEL whole cell lysates,<br>
Lane 6: human 293T whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGFR3 antigen affinity purified monoclonal antibody (M00200-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGFR3 at approximately 125 kDa. The expected band size for FGFR3 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-1-wb8.jpgAnti-FGFR3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-1-fgfr3-primary-antibodies-ihc-testing-3.jpgAnti-FGFR3 Rabbit Monoclonal Antibody IHC analysis of FGFR3 using anti-FGFR3 antibody (M00200-1). <br>FGFR3 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FGFR3 Antibody (M00200-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-1-fgfr3-primary-antibodies-ihc-testing-4.jpgAnti-FGFR3 Rabbit Monoclonal Antibody IHC analysis of FGFR3 using anti-FGFR3 antibody (M00200-1). <br>FGFR3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FGFR3 Antibody (M00200-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-timp2-rabbit-monoclonal-antibody-m01037-1-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01037-1-wb.jpgAnti-TIMP2 Rabbit Monoclonal AntibodyWestern blot analysis of TIMP2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01037-1-jcav13p2281g004.jpgAnti-TIMP2 Rabbit Monoclonal AntibodyEffect of LASS2 on cell migration, invasion and apoptosis. (A) Wound healing assay of pLV-vector or pLV-LASS2-transfected glioma/glioblastoma cells at 0 h, 12 h and 24 h after scratch. The images were taken from an inverted microscope under 10× magnification (*P < 0.05 and **P < 0.01, vs. pLV control; unpaired two-tailed Student's t-test; n = 3). Scale bar = 200 µm. (B) Colony formation assay in pLV-vector or pLV-LASS2-transfected U251 and U-87 MG cells. Images were acquired at 4× magnification (*P <0.05, vs. pLV control; unpaired two-tailed Student's t-test; n = 3). (C) Transwell assay demonstrated that LASS2 inhibits the migration of U251 and U-87 MG cells compared with the pLV control (*P <0.05; unpaired two-tailed Student's t-test; n = 3). Scale bar = 200 µm. (D) The immunofluorescence staining of MMP9 and SPHK1 was shown in both U251 and U-87 MG cells. Scale bar = 200 µm. (E) RNA-Seq shows that LASS2 influenced cell migration/invasion, apoptosis, epithelial- mesenchymal transition (EMT) conversion and cellular life activity. (F) Overexpression of LASS2 reduced the protein levels of MMP2, MMP9, and SPHK1 while increasing that of TIMP2 in both U251 and U-87 MG cells. (G) LASS2 overexpression increased the levels of Bax, cleaved Caspase-3, TNF-α, and p53 while reducing that of Bcl-2 in both U251 and U-87 MG cells. (H) Overexpression of LASS2 reduced the protein levels of Vimentin and N-cadherin while increasing that of E-cadherin in both U251 and U-87 MG cells (F, G, and H, *P <0.05 and **P < 0.01, vs. pLV control in each cell line; unpaired two-tailed Student's t-test; n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9066216/&orig_host=www.ncbi.nlm.nih.gov'>35517425</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01037-1-jcav13p2281g005.jpgAnti-TIMP2 Rabbit Monoclonal AntibodyLASS2 inhibited tumor growth in a pLV-LASS2-U-87 MG glioblastoma xenograft nude mouse model. (A) Representative photographs showing the gross pLV-LASS2-U-87 MG and empty scramble control glioblastoma xenografts from the nude mouse. (B) The tumor volume was evaluated between the scrambled control and pLV-LASS2 groups (**P < 0.05 and **P < 0.01 vs. pLV control group; unpaired two-tailed Student's t-test; n = 5 animals). (C) The final tumor weight was measured after dissection. The average final weight of tumors derived from pLV-LASS2-transcfected U-87 MG cells was significantly lower than those derived from the scrambled control (**P < 0.01, vs. pLV control group; unpaired two-tailed Student's t-test; n = 5 animals). (D) Representative images for H&E staining from either group were shown. (E) IHC staining of LASS2, TIMP2, MMP9, and SPHK1 in xenografted tumors derived from U-87 MG cells transfected with either pLV-LASS2 or scrambled control. Scale bar = 20 µm. (F) Western blot analysis of LASS2, SPHK1, TIMP2, MMP2, and MMP9 in xenografted tumors derived from U-87 MG cells transfected with either pLV or pLV-LASS2. (G) Western blot analysis of Bax, Bcl-2, pro-Caspase-3, cleaved Caspase-3, TNF-α and p53 in xenografted tumors derived from U-87 MG cells transfected with either pLV or pLV-LASS2. (H) Western blot analysis of EMT conversion-related proteins Vimentin, E-cadherin, and N-cadherin in xenografted tumors derived from U-87 MG cells transfected with either pLV or pLV-LASS2 ( F, G, and H, *P <0.05, **P < 0.01, and ***P < 0.001, vs. pLV control; unpaired two-tailed Student's t-test; n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9066216/&orig_host=www.ncbi.nlm.nih.gov'>35517425</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd62p-rabbit-monoclonal-antibody-m01241-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01241-selp-primary-antibodies-wb-testing-1.jpgAnti-CD62P SELP Rabbit Monoclonal AntibodyWestern blot analysis of P-Selectin/SELP using anti-P-Selectin/SELP antibody (M01241). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: human K562 whole cell lysates,<br>
Lane 6: human Jurkat whole cell lysates,<br>
Lane 7: human SIHA whole cell lysates,<br>
Lane 8: human RT4 whole cell lysates,<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-Selectin/SELP antigen affinity purified monoclonal antibody (M01241) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-Selectin/SELP at approximately 91 kDa. The expected band size for P-Selectin/SELP is at 91 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgf21-rabbit-monoclonal-antibody-m00802-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00802-wb7.jpgAnti-FGF21 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00802-wb8.jpgAnti-FGF21 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00802-wb.jpgAnti-FGF21 Rabbit Monoclonal AntibodyWestern blot analysis of FGF21 expression in (1) HeLa cell lysate; (2) Mouse spleen lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fabp4-rabbit-monoclonal-antibody-m01528-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01528-fabp4-primary-antibodies-wb-testing-1.jpgAnti-FABP4/A Fabp Rabbit Monoclonal Antibody Western blot analysis of FABP4 using anti-FABP4 antibody (M01528). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: rat thymus tissue lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: mouse thymus tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FABP4 antigen affinity purified monoclonal antibody (Catalog # M01528) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FABP4 at approximately 15 kDa. The expected band size for FABP4 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01528-fabp4-primary-antibodies-ihc-testing-2.jpgAnti-FABP4/A Fabp Rabbit Monoclonal Antibody IHC analysis of FABP4 using anti-FABP4 antibody (M01528). <br>
FABP4 was detected in a paraffin-embedded section of adipose of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FABP4 Antibody (M01528) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01528-fabp4-primary-antibodies-ihc-testing-3.jpgAnti-FABP4/A Fabp Rabbit Monoclonal Antibody IHC analysis of FABP4 using anti-FABP4 antibody (M01528). <br>
FABP4 was detected in a paraffin-embedded section of adipose of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-FABP4 Antibody (M01528) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vamp2-rabbit-monoclonal-antibody-m02331-1-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02331-1-wb.jpgAnti-VAMP2 Rabbit Monoclonal AntibodyWestern blot analysis of VAMP2 expression in mouse brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bnip3-rabbit-monoclonal-antibody-m01469-boster.html2026-03-24T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-wb7.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-wb8.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-wb.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyWestern blot analysis of BNIP3 expression in (1) Jurkat cell lysate; (2) Mouse spleen lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-ihc8.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pancreatic cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-ihc9.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-ihc7.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-ihc.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using BNIP3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01469-icc1.jpgAnti-BNIP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-l1cam-rabbit-monoclonal-antibody-m00729-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00729-l1cam-primary-antibodies-wb-testing-1.jpgAnti-L1CAM Rabbit Monoclonal AntibodyWestern blot analysis of L1CAM using anti-L1CAM antibody (M00729). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SiHa whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-L1CAM antigen affinity purified monoclonal antibody (M00729) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for L1CAM at approximately 250 kDa. The expected band size for L1CAM is at 140 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00729-l1cam-primary-antibodies-ihc-testing-1.jpgAnti-L1CAM Rabbit Monoclonal AntibodyIHC analysis of L1CAM using anti-L1CAM antibody (M00729). <br>L1CAM was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-L1CAM Antibody (M00729) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00729-l1cam-primary-antibodies-ihc-testing-2.jpgAnti-L1CAM Rabbit Monoclonal AntibodyIHC analysis of L1CAM using anti-L1CAM antibody (M00729). <br>L1CAM was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-L1CAM Antibody (M00729) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00729-l1cam-primary-antibodies-ihc-testing-3.jpgAnti-L1CAM Rabbit Monoclonal AntibodyIHC analysis of L1CAM using anti-L1CAM antibody (M00729). <br>L1CAM was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-L1CAM Antibody (M00729) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nfat1-rabbit-monoclonal-antibody-m00969-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00969-wb7.jpgAnti-NFAT1 NFATC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00969-wb8.jpgAnti-NFAT1 NFATC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00969-wb.jpgAnti-NFAT1 NFATC2 Rabbit Monoclonal AntibodyWestern blot analysis of NFAT1 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gad67-rabbit-monoclonal-antibody-m02002-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02002-gad1-primary-antibodies-wb-testing-1.jpgAnti-GAD67 GAD1 Rabbit Monoclonal AntibodyWestern blot analysis of GAD1 using anti-GAD1 antibody (M02002). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAD1 antigen affinity purified monoclonal antibody (M02002) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GAD1 at approximately 70 kDa. The expected band size for GAD1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02002-gad1-primary-antibodies-ihc-testing-1.jpgAnti-GAD67 GAD1 Rabbit Monoclonal AntibodyIHC analysis of GAD1 using anti-GAD1 antibody (M02002). <br>GAD1 was detected in a paraffin-embedded section of pig brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GAD1 Antibody (M02002) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prdx6-rabbit-monoclonal-antibody-m01847-boster.html2026-04-01T05:01:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01847-prdx6-primary-antibodies-wb-testing-1.jpgAnti-PRDX6/Peroxiredoxin 6 Rabbit Monoclonal Antibody Western blot analysis of PRDX6 using anti-PRDX6 antibody (M01847). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRDX6 antigen affinity purified polyclonal antibody (Catalog # M01847) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRDX6 at approximately 25 kDa. The expected band size for PRDX6 is at 25 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prmt1-rabbit-monoclonal-antibody-m01417-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01417-wb7.jpgAnti-PRMT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01417-wb8.jpgAnti-PRMT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01417-wb.jpgAnti-PRMT1 Rabbit Monoclonal AntibodyWestern blot analysis of PRMT1 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mre11-rabbit-monoclonal-antibody-m00731-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00731-wb.jpgAnti-Mre11 MRE11A Rabbit Monoclonal AntibodyWestern blot analysis of Mre11 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grp94-rabbit-monoclonal-antibody-m02393-1-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02393-1-wb7.jpgAnti-GRP94 HSP90B1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02393-1-wb10.jpgAnti-GRP94 HSP90B1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02393-1-wb8.jpgAnti-GRP94 HSP90B1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02393-1-wb.jpgAnti-GRP94 HSP90B1 Rabbit Monoclonal AntibodyWestern blot analysis of GRP94 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02393-1-wb9.jpgAnti-GRP94 HSP90B1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-axin2-rabbit-monoclonal-antibody-m01772-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01772-wb.jpgAnti-Axin2/Conductin Rabbit Monoclonal AntibodyWestern blot analysis of Axin2 expression in (1) SW480 cell lysate; (2) PC-12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01772-fnmol-13-596039-g005.jpgAnti-Axin2/Conductin Rabbit Monoclonal AntibodyAx increases the expression of GCase and β-catenin when NSCs exposed to OGD. (A–C) Statistical analysis of GCase (A) , β-catenin (B) and Axin2 (C) mRNA expression using RT-qPCR assays in different groups. * P < 0.05, ** P < 0.01 vs. control group; # P < 0.05 vs. OGD + Vehicle; @ P < 0.05 vs. OGD + Ax-30 μM. (D) Bands depicted the expression of GCase, β-catenin, p-β-catenin and Axin2 in different groups. GAPDH was used as an internal control. (E–H) Semi-quantitative analysis of β-catenin (E) , p-β-catenin (F) , GCase (G) and Axin2 (H) expression from (D) . * P < 0.05, ** P < 0.01 vs. control group; # P < 0.05 vs. OGD + Vehicle; @ P < 0.05 vs. OGD + Ax-30 μM. (I) Representative immunostaining images of GCase (green), β-catenin (red) and Nestin (white) in various groups. Scale bar: 20 μm. Ax, ambroxol; OGD, oxygen glucose deprivation.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2020.596039/full'>33551744</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgfr3-rabbit-monoclonal-antibody-m00200-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-wb7.jpgAnti-FGFR3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-wb8.jpgAnti-FGFR3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-wb.jpgAnti-FGFR3 Rabbit Monoclonal AntibodyWestern blot analysis of FGFR3 expression in (1) A549 cell lysate; (2) Mouse brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd40l-rabbit-monoclonal-antibody-m01114-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-wb7.jpgAnti-CD40L CD40LG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-wb.jpgAnti-CD40L CD40LG Rabbit Monoclonal AntibodyWestern blot analysis of CD40L expression in MOLT-4 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-wb8.jpgAnti-CD40L CD40LG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-wb9.jpgAnti-CD40L CD40LG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gata4-rabbit-monoclonal-antibody-m00499-1-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00499-1-gata4-primary-antibodies-wb-testing-1.jpgAnti-GATA4 Rabbit Monoclonal Antibody Western blot analysis of GATA4 using anti-GATA4 antibody (M00499-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: rat liver tissue lysates,<br>
Lane 4: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATA4 antigen affinity purified polyclonal antibody (Catalog # M00499-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GATA4 at approximately 54 kDa. The expected band size for GATA4 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00499-1-if.jpgAnti-GATA4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using GATA4 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erp57-rabbit-monoclonal-antibody-m01464-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01464-pdia3-primary-antibodies-wb-testing-1.jpgAnti-ERp57 PDIA3 Rabbit Monoclonal AntibodyWestern blot analysis of PDIA3 using anti-PDIA3 antibody (M01464). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U251 whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: human RT4 whole cell lysates,<br>
Lane 6: human HEL whole cell lysates,<br>
Lane 7: human SH-SY5Y whole cell lysates,<br>
Lane 8: human K562 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDIA3 antigen affinity purified monoclonal antibody (M01464) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDIA3 at approximately 57 kDa. The expected band size for PDIA3 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01464-pdia3-primary-antibodies-ihc-testing-1.jpgAnti-ERp57 PDIA3 Rabbit Monoclonal AntibodyIHC analysis of PDIA3 using anti-PDIA3 antibody (M01464). <br>PDIA3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PDIA3 Antibody (M01464) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01464-pdia3-primary-antibodies-ihc-testing-2.jpgAnti-ERp57 PDIA3 Rabbit Monoclonal AntibodyIHC analysis of PDIA3 using anti-PDIA3 antibody (M01464). <br>PDIA3 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PDIA3 Antibody (M01464) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-xrcc1-rabbit-monoclonal-antibody-m00571-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00571-xrcc1-primary-antibodies-wb-testing-1.jpgAnti-XRCC1 Rabbit Monoclonal AntibodyWestern blot analysis of XRCC1 using anti-XRCC1 antibody (M00571). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-XRCC1 antigen affinity purified monoclonal antibody (M00571) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for XRCC1 at approximately 90 kDa. The expected band size for XRCC1 is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00571-ihc.jpgAnti-XRCC1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using XRCC1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00571-if.jpgAnti-XRCC1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using XRCC1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tdp43-rabbit-monoclonal-antibody-m01001-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-wb-testing-1.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyWestern blot analysis of TARDBP using anti-TARDBP antibody (M01001). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TARDBP antigen affinity purified monoclonal antibody (M01001) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TARDBP at approximately 40 kDa. The expected band size for TARDBP is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-1.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-2.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-3.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-4.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-5.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-6.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-7.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-8.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-9.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-10.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-11.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-12.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01001-tardbp-primary-antibodies-ihc-testing-13.jpgAnti-TDP43 TARDBP Rabbit Monoclonal AntibodyIHC analysis of TARDBP using anti-TARDBP antibody (M01001). <br>TARDBP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TARDBP Antibody (M01001) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-g-csf-rabbit-monoclonal-antibody-m02280-1-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02280-1-wb.jpgAnti-G-CSF CSF3 Rabbit Monoclonal AntibodyWestern blot analysis of G-CSF expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rpe65-rabbit-monoclonal-antibody-m00824-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00824-wb.jpgAnti-RPE65 Rabbit Monoclonal AntibodyWestern blot analysis of RPE65 expression in mouse eyeball lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-53bp1-rabbit-monoclonal-antibody-m00397-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-wb-testing-1.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody Western blot analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human U251 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-53BP1 antigen affinity purified polyclonal antibody (Catalog # M00397) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for 53BP1 at approximately 450 kDa. The expected band size for 53BP1 is at 214 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-2.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-3.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-4.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-5.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-6.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-7.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-8.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-9.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-10.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-11.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-12.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-13.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-14.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-15.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-16.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-17.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-18.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-19.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-20.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-ihc-testing-21.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal Antibody IHC analysis of 53BP1 using anti-53BP1 antibody (M00397). <br>
53BP1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-53BP1 Antibody (M00397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00397-53bp1-primary-antibodies-if-testing-1.jpgAnti-53BP1 TP53BP1 Rabbit Monoclonal AntibodyIF analysis of 53BP1 using anti-53BP1 antibody (M00397) and anti-Tubulin Alpha antibody (M03989-3).<br>
53BP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-53BP1 Antibody (M00397) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and Fluoro488 Conjugated Goat Anti-Mouse IgG Secondary Antibody (red)(BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sfrp1-rabbit-monoclonal-antibody-m01968-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01968-wb7.jpgAnti-SFRP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01968-wb.jpgAnti-SFRP1 Rabbit Monoclonal AntibodyWestern blot analysis of SFRP1 expression in A375 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gata3-rabbit-monoclonal-antibody-m00593-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-wb7.jpgAnti-GATA3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-wb.jpgAnti-GATA3 Rabbit Monoclonal AntibodyWestern blot analysis of GATA3 expression in (1) SH-SY5Y cell lysate; (2) Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-gata3-primary-antibodies-wb-testing-1.jpgAnti-GATA3 Rabbit Monoclonal AntibodyWestern blot analysis of GATA3 using anti-GATA3 antibody (M00593). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATA3 antigen affinity purified monoclonal antibody (M00593) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GATA3 at approximately 48 kDa. The expected band size for GATA3 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc9.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc10.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human small cell lung cancer , using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc7.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat intestine, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc11.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse pancreas, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc8.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-ihc.jpgAnti-GATA3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder cancer, using GATA3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00593-gata3-custom-antibodies-wb-testing-9.jpgAnti-GATA3 Rabbit Monoclonal Antibody Western blot analysis of GATA3 using anti-GATA3 rabbit monoclonal antibody (M00593). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% milk for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATA3 rabbit monoclonal antibody (M00593) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000, room temperature for 1 h. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GATA3 at approximately 47 kDa. The expected band size for GATA3 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prox1-rabbit-monoclonal-antibody-m01985-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01985-wb.jpgAnti-PROX1 Rabbit Monoclonal AntibodyWestern blot analysis of PROX1 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gata1-rabbit-monoclonal-antibody-m00408-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00408-ihc.jpgAnti-GATA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse spleen, using GATA1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00408-gata1-primary-antibodies-wb-testing-1_1.jpgAnti-GATA1 Rabbit Monoclonal AntibodyWestern blot analysis of GATA1 using anti-GATA1 antibody (M00408). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human CCRF-CEM whole cell lysates,<br>
Lane 4: human Raji whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATA1 antigen affinity purified monoclonal antibody (M00408) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GATA1 at approximately 43 kDa. The expected band size for GATA1 is at 43 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd163-rabbit-monoclonal-antibody-m00812-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00812-wb.jpgAnti-CD163 Rabbit Monoclonal AntibodyWestern blot analysis of CD163 expression in Human fetal kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00812-ihc.jpgAnti-CD163 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse liver, using CD163 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nfat2-rabbit-monoclonal-antibody-m00340-boster.html2026-03-24T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00340-wb.jpgAnti-NFAT2 NFATC1 Rabbit Monoclonal AntibodyWestern blot analysis of NFAT2 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gcet1-rabbit-monoclonal-antibody-m09606-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09606-wb.jpgAnti-GCET1 SERPINA9 Rabbit Monoclonal AntibodyWestern blot analysis of GCET1 expression in MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eaat2-rabbit-monoclonal-antibody-m01713-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01713-wb7.jpgAnti-EAAT2/GLT-1/SLC1A2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01713-wb.jpgAnti-EAAT2/GLT-1/SLC1A2 Rabbit Monoclonal AntibodyWestern blot analysis of EAAT2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01713-wb8.jpgAnti-EAAT2/GLT-1/SLC1A2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01713-icc1.jpgAnti-EAAT2/GLT-1/SLC1A2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-wnt5a-rabbit-monoclonal-antibody-m00549-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-wb7.jpgAnti-Wnt5a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-wb10.jpgAnti-Wnt5a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-12951_2024_2438_fig1_html.pngAnti-Wnt5a Rabbit Monoclonal AntibodyThe mechanism of regulatory relationships among EZH2, SFRP1, and WNT5A. (A) The miR26a level in C4-2B and C4-2B EnzR cells. n = 3, mean ± SD, *** p < 0.001, one-way ANOVA. (B) Statistical analysis of each group. n = 5, mean ± SD, * p < 0.05, **** p < 0.0001, one-way ANOVA. (C) In vitro cell migration and invasion assays. Microscope images of anti-migration and anti-invasion effects in each group (visualized with 0.1% crystal violet, scale bar: 100 μm). C4-2B EnzR cells were incubated with miR26a mimic and miR26a inhibitor, respectively (miR26a mimic/inhibitor: 1 µg·mL − 1 ). (D) Dual luciferase reporter assays were used to verify the direct targeting of miR26a on EZH2 and WNT5A, h-EZH2-3’UTR/h-WNT5A-3’UTR: 0.16 µg, hsa-miR-26a-5p/NC: 5 pmol. n = 3, mean ± SD, **** p < 0.0001, one-way ANOVA. (E) Protein expressions of EZH2, WNT5A, H3K27me3, and SFRP1 were detected via western blotting in siEZH2, siSFRP1, and their negative control groups (siNC1: EZH2 negative control, siNC2: SFRP1 negative control). (F) Statistical difference of the ratio of gray values. (G) Protein expressions of WNT5A were detected via western blotting in siEZH2 + siSFRP1 and siEZH2 + siNC1 groups. (H) Statistical difference of the ratio of gray values. n = 3, mean ± SD, ** p < 0.01, *** p < 0.001, **** p < 0.0001, one-way ANOVA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-024-02438-z'>38566211</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-wb8.jpgAnti-Wnt5a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-wb.jpgAnti-Wnt5a Rabbit Monoclonal AntibodyWestern blot analysis of Wnt5a expression in (1) HeLa cell lysate; (2) SK-OV-3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00549-wb9.jpgAnti-Wnt5a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eaat1-rabbit-monoclonal-antibody-m02133-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02133-SLC1A3-primary-antibodies-WB-testing-1.jpgAnti-EAAT1 SLC1A3 Rabbit Monoclonal AntibodyWestern blot analysis of EAAT1 expression in Mouse brain lysate.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02133-wb7.jpgAnti-EAAT1 SLC1A3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02133-slc1a3-primary-antibodies-ihc-testing-2.jpgAnti-EAAT1 SLC1A3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Rabbit anti-EAAT1 antibody at 1/200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02133-slc1a3-primary-antibodies-ihc-testing-3.jpgAnti-EAAT1 SLC1A3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain tissue using anti-EAAT1 antibody. <br>The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody ( 1/50) for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pcsk9-rabbit-monoclonal-antibody-m00085-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-pcsk9-primary-antibodies-wb-testing-1.jpgAnti-PCSK9/Proprotein Convertase 9 Rabbit Monoclonal Antibody Western blot analysis of PCSK9 using anti-PCSK9 antibody (M00085). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCSK9 antigen affinity purified monoclonal antibody (Catalog # M00085) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCSK9 at approximately 75 kDa. The expected band size for PCSK9 is at 75 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bace1-rabbit-monoclonal-antibody-m00322-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00322-wb7.jpgAnti-BACE1/Bace Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00322-wb8.jpgAnti-BACE1/Bace Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00322-wb.jpgAnti-BACE1/Bace Rabbit Monoclonal AntibodyWestern blot analysis of BACE1 expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bubr1-rabbit-monoclonal-antibody-m01564-1-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01564-1-wb.jpgAnti-BubR1 BUB1B Rabbit Monoclonal AntibodyWestern blot analysis of BubR1 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd276-rabbit-monoclonal-antibody-m02220-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-wb.jpgAnti-CD276/B7 H3 Rabbit Monoclonal AntibodyWestern blot analysis of CD276 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nur77-rabbit-monoclonal-antibody-m00626-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00626-wb7.jpgAnti-NUR77 NR4A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00626-wb.jpgAnti-NUR77 NR4A1 Rabbit Monoclonal AntibodyWestern blot analysis of NUR77 expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00626-wb8.jpgAnti-NUR77 NR4A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00626-wb9.jpgAnti-NUR77 NR4A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-usp14-rabbit-monoclonal-antibody-m03042-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03042-usp14-primary-antibodies-wb-testing-1.jpgAnti-USP14 Rabbit Monoclonal AntibodyWestern blot analysis of USP14 using anti-USP14 antibody (M03042). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human SK-OV-3 whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates,<br>
Lane 8: mouse Raw264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP14 antigen affinity purified monoclonal antibody (M03042) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP14 at approximately 60 kDa. The expected band size for USP14 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03042-usp14-primary-antibodies-ihc-testing-1.jpgAnti-USP14 Rabbit Monoclonal AntibodyIHC analysis of USP14 using anti-USP14 antibody (M03042). <br>USP14 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-USP14 Antibody (M03042) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nr5a2-rabbit-monoclonal-antibody-m01332-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01332-nr5a2-primary-antibodies-wb-testing-1.jpgAnti-NR5A2/Lrh 1 Rabbit Monoclonal AntibodyWestern blot analysis of NR5A2 using anti-NR5A2 antibody (M01332). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat ovary tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse ovary tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR5A2 antigen affinity purified monoclonal antibody (M01332) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NR5A2 at approximately 70 kDa. The expected band size for NR5A2 is at 61 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fgfr4-rabbit-monoclonal-antibody-m00769-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00769-fgfr4-primary-antibodies-wb-testing-1.jpgAnti-FGFR4 Rabbit Monoclonal Antibody Western blot analysis of FGFR4 using anti-FGFR4 antibody (M00769). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGFR4 antigen affinity purified monoclonal antibody (Catalog # M00769) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FGFR4 at approximately 88 kDa. The expected band size for FGFR4 is at 88 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glut3-rabbit-monoclonal-antibody-m03259-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03259-slc2a3-primary-antibodies-wb-testing-1.jpgAnti-GLUT3 SLC2A3 Rabbit Monoclonal Antibody Western blot analysis of GLUT3 using anti-GLUT3 antibody (M03259). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse kidney tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLUT3 antigen affinity purified monoclonal antibody (Catalog # M03259) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLUT3 at approximately 54 kDa. The expected band size for GLUT3 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03259-slc2a3-primary-antibodies-ihc-testing-2.jpgAnti-GLUT3 SLC2A3 Rabbit Monoclonal Antibody IHC analysis of GLUT3/SLC2A3 using anti-GLUT3/SLC2A3 antibody (M03259). <br>
GLUT3/SLC2A3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GLUT3/SLC2A3 Antibody (M03259) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03259-slc2a3-primary-antibodies-ihc-testing-3.jpgAnti-GLUT3 SLC2A3 Rabbit Monoclonal Antibody IHC analysis of GLUT3/SLC2A3 using anti-GLUT3/SLC2A3 antibody (M03259). <br>
GLUT3/SLC2A3 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GLUT3/SLC2A3 Antibody (M03259) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cryab-rabbit-monoclonal-antibody-m03496-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03496-wb7.jpgAnti-CRYAB/Alpha B Crystallin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03496-wb.jpgAnti-CRYAB/Alpha B Crystallin Rabbit Monoclonal AntibodyWestern blot analysis of CRYAB expression in human fetal heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myh11-rabbit-monoclonal-antibody-m02422-1-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02422-1-wb.jpgAnti-MYH11 Rabbit Monoclonal AntibodyWestern blot analysis of MYH11 expression in Human testis lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bnip1-rabbit-monoclonal-antibody-m09220-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09220-wb.jpgAnti-BNIP1 Rabbit Monoclonal AntibodyWestern blot analysis of BNIP1 expression in (1) Jurkat cell lysate; (2) C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg4b-rabbit-monoclonal-antibody-m02885-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02885-wb7.jpgAnti-Atg4B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02885-wb.jpgAnti-Atg4B Rabbit Monoclonal AntibodyWestern blot analysis of Atg4B expression in Ramos cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02885-wb8.jpgAnti-Atg4B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02885-icc1.jpgAnti-Atg4B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg4c-rabbit-monoclonal-antibody-m09728-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09728-wb.jpgAnti-Atg4C Rabbit Monoclonal AntibodyWestern blot analysis of Atg4C expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ha-tag-rabbit-monoclonal-antibody-mt0012-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/T/MT0012-HA-Tag-primary-antibodies-WB-testing-1.jpgAnti-HA-Tag Rabbit Monoclonal AntibodyWestern blot analysis of HA-tag fusion protein, using HA tag Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-v5-tag-rabbit-monoclonal-antibody-mt0013-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/T/MT0013-V5-Tag-primary-antibodies-WB-testing-1.jpgAnti-V5-Tag Rabbit Monoclonal AntibodyWestern blot analysis of extracts from v5-tag fusion protein, using V5 tag antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dnmt3b-rabbit-monoclonal-antibody-rabbit-monoclonal-antibody-m00319-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb7.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb10.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb8.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb11.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb9.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb12.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00319-wb.jpgAnti-Dnmt3b Rabbit Monoclonal Antibody Rabbit Monoclonal AntibodyWestern blot analysis of Dnmt3b expression in (1) A549 cell lysate; (2) A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac11-rabbit-monoclonal-antibody-m06209-boster.html2026-03-24T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06209-wb7.jpgAnti-HDAC11/Histone Deacetylase 11 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06209-wb8.jpgAnti-HDAC11/Histone Deacetylase 11 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06209-wb.jpgAnti-HDAC11/Histone Deacetylase 11 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC11 expression in (1) Jurkat cell lysate;(2) MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl-xl-rabbit-monoclonal-antibody-m00181-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-bcl2l1-primary-antibodies-wb-testing-1.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal Antibody Western blot analysis of BCL2L1 using anti-BCL2L1 antibody (M00181-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL2L1 antigen affinity purified monoclonal antibody (Catalog # M00181-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL2L1 at approximately 30 kDa. The expected band size for BCL2L1 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-bcl2l1-primary-antibodies-wb-testing-2.pngAnti-Bcl-XL BCL2L1 Rabbit Monoclonal Antibody Western blot analysis of BCL2L1 using anti-BCL2L1 antibody (M00181-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Control group-rat colon tissue lysates,<br>
Lane 2: Model group-rat colon tissue lysates,<br>
Lane 3: Traditional Chinese medicine treatment-rat colon tissue lysates,<br>
Lane 4: Western medicine treatment-rat colon tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL2L1 antigen affinity purified monoclonal antibody (Catalog # M00181-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for BCL2L1 at approximately 30 kDa. The expected band size for BCL2L1 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-ihc8.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human liver cancer, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-ihc7.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-ihc.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using Bcl-XL Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-icc1.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-1-if.jpgAnti-Bcl-XL BCL2L1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Bcl-XL Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat5a-rabbit-monoclonal-antibody-m01087-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-1-stat5a-primary-antibodies-wb-testing-1.jpgAnti-STAT5a Rabbit Monoclonal AntibodyWestern blot analysis of STAT5A using anti-STAT5A antibody (M01087-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: rat thymus tissue lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse thymus tissue lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5A antigen affinity purified monoclonal antibody (M01087-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STAT5A at approximately 91 kDa. The expected band size for STAT5A is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-1-stat5a-primary-antibodies-ip-testing-1.jpgAnti-STAT5a Rabbit Monoclonal AntibodyImmunoprecipitating (IP) STAT5a in K562 whole cell lysate.<br>
Western blot analysis of STAT5a using anti-STAT5a antibody (M01087-1); <br>
Lane 1: K562 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-STAT5a antibody in K562 whole cell lysate;<br>
Lane 3: anti-STAT5a antibody (2μg) + K562 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-STAT5a antigen affinity purified monoclonal antibody (M01087-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for STAT5a at approximately 91 kDa. The expected band size for STAT5a is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-1-stat5a-primary-antibodies-ihc-testing-2.jpgAnti-STAT5a Rabbit Monoclonal AntibodyIHC analysis of STAT5a using anti-STAT5a antibody (M01087-1). <br>
STAT5a was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-STAT5a Antibody (M01087-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-1-stat5a-primary-antibodies-ihc-testing-1.jpgAnti-STAT5a Rabbit Monoclonal AntibodyIHC analysis of STAT5a using anti-STAT5a antibody (M01087-1). <br>
STAT5a was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-STAT5a Antibody (M01087-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxo3a-rabbit-monoclonal-antibody-m00252-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-1-wb7.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-1-if.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using FoxO3a Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-1-wb.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyWestern blot analysis of FoxO3a in (1) Jurkat cell lysate; (2) SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-1-ihc.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder carcinoma, using FoxO3a Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cox-iv-rabbit-monoclonal-antibody-m05442-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-cox4-primary-antibodies-wb-testing-1.jpgAnti-COX IV COX4I1 Rabbit Monoclonal Antibody Western blot analysis of COX IV using anti-COX IV antibody (M05442). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human SW620 whole cell lysates,<br>
Lane 4: human CACO-2 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COX IV antigen affinity purified monoclonal antibody (Catalog # M05442) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for COX IV at approximately 17 kDa. The expected band size for COX IV is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-cox4-primary-antibodies-ihc-testing-2.jpgAnti-COX IV COX4I1 Rabbit Monoclonal Antibody IHC analysis of COX IV using anti-COX IV antibody (M05442). <br>
COX IV was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-COX IV Antibody (M05442) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-cox4-primary-antibodies-ihc-testing-3.jpgAnti-COX IV COX4I1 Rabbit Monoclonal Antibody IHC analysis of COX IV using anti-COX IV antibody (M05442). <br>
COX IV was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-COX IV Antibody (M05442) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-if.jpgAnti-COX IV COX4I1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using COX IV Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-cox4-primary-antibodies-ihc-testing-4.jpgAnti-COX IV COX4I1 Rabbit Monoclonal Antibody IHC analysis of COX IV using anti-COX IV antibody (M05442). <br>
COX IV was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-COX IV Antibody (M05442) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05442-icc1.jpgAnti-COX IV COX4I1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek1-2-rabbit-monoclonal-antibody-m00292-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-advs71038-fig-0008-m.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyBioinformatic and mechanistic analysis of BMSCs differentiation with HAw and the magnetic HAw/Fe3O4 under the activation of an MF. A) Heatmap of Pearson correlation between BMSCs co-cultured with HAw and the magnetic HAw/Fe3O4 in the MF. B) Enriched KEGG pathways of HAw versus the magnetic HAw/Fe3O4 under MF stimulation. C) Fluorescence and D) the fluorescent intensity values of the intracellular Ca2+ with BMSCs cultured on HAw and the magnetic HAw/Fe3O4 via different MF patterns (“OFF” and “ON”) for 24 and 48 h (n = 4). E) Western blot analysis and F) the corresponding quantification of Piezo1 and G) MAPK pathway-related proteins with/without inhibitor (GsMTx4) of Piezo1 via different MF patterns for 7 days (n = 3). *p < 0.05; **p < 0.01, ***p < 0.001, and ****p < 0.0001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://advanced.onlinelibrary.wiley.com/doi/abs/10.1002/advs.202509715'>40788056</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-mek1-2-primary-antibodies-wb-testing-1.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal Antibody Western blot analysis of MEK1-2 using anti-MEK1-2 antibody (M00292-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEK1-2 antigen affinity purified monoclonal antibody (Catalog # M00292-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MEK1-2 at approximately 43 kDa. The expected band size for MEK1-2 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-ihc.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using MEK1/2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-if.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using MEK1/2 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-icc1.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-icc2.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00292-1-icc3.jpgAnti-MEK1/2 MAP2K1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-desmin-rabbit-monoclonal-antibody-m01948-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01948-1-des-primary-antibodies-wb-testing-1.jpgAnti-Desmin Rabbit Monoclonal AntibodyWestern blot analysis of Desmin/DES using anti-Desmin/DES antibody (M01948-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates,<br>
Lane 2: rat skeletal muscle tissue lysates,<br>
Lane 3: mouse heart tissue lysates,<br>
Lane 4: mouse skeletal muscle tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Desmin/DES antigen affinity purified monoclonal antibody (M01948-1) at 1: 10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Desmin/DES at approximately 54 kDa. The expected band size for Desmin/DES is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01948-1-ihc.jpgAnti-Desmin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate, using Desmin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sumo-1-rabbit-monoclonal-antibody-m00631-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-sumo1-primary-antibodies-wb-testing-1.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyWestern blot analysis of SUMO1 using anti-SUMO1 antibody (M00631-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse lung tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SUMO1 antigen affinity purified monoclonal antibody (M00631-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SUMO1 at approximately 18,80 kDa. The expected band size for SUMO1 is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-sumo1-primary-antibodies-ihc-testing-1.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyIHC analysis of SUMO1 using anti-SUMO1 antibody (M00631-1). <br>SUMO1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SUMO1 Antibody (M00631-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-sumo1-primary-antibodies-ihc-testing-2.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyIHC analysis of SUMO1 using anti-SUMO1 antibody (M00631-1). <br>SUMO1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SUMO1 Antibody (M00631-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-sumo1-primary-antibodies-ihc-testing-3.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyIHC analysis of SUMO1 using anti-SUMO1 antibody (M00631-1). <br>SUMO1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SUMO1 Antibody (M00631-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-sumo1-primary-antibodies-ihc-testing-4.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyIHC analysis of SUMO1 using anti-SUMO1 antibody (M00631-1). <br>SUMO1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SUMO1 Antibody (M00631-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc1.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc2.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc3.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc4.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc5.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00631-1-icc6.jpgAnti-Sumo 1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hapln1-rabbit-monoclonal-antibody-m05980-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-hapln1-primary-antibodies-wb-testing-1.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyWestern blot analysis of HAPLN1 using anti-HAPLN1 antibody (M05980-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Caco-2 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAPLN1 antigen affinity purified monoclonal antibody (M05980-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HAPLN1 at approximately 48 kDa. The expected band size for HAPLN1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-hapln1-primary-antibodies-ihc-testing-1.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyIHC analysis of HAPLN1 using anti-HAPLN1 antibody (M05980-1). <br>HAPLN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HAPLN1 Antibody (M05980-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-hapln1-primary-antibodies-ihc-testing-2.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyIHC analysis of HAPLN1 using anti-HAPLN1 antibody (M05980-1). <br>HAPLN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HAPLN1 Antibody (M05980-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-hapln1-primary-antibodies-ihc-testing-3.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyIHC analysis of HAPLN1 using anti-HAPLN1 antibody (M05980-1). <br>HAPLN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HAPLN1 Antibody (M05980-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-icc1.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-1-icc2.jpgAnti-HAPLN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab11a-rabbit-monoclonal-antibody-m01436-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01436-wb7.jpgAnti-RAB11A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01436-wb8.jpgAnti-RAB11A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01436-wb.jpgAnti-RAB11A Rabbit Monoclonal AntibodyWestern blot analysis of RAB11A expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-camkii-rabbit-monoclonal-antibody-m03964-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03964-wb7.jpgAnti-CaMKII CAMK2B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03964-if.jpgAnti-CaMKII CAMK2B Rabbit Monoclonal AntibodyImmunofluorescent analysis of PC-12 cells, using CaMKII Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03964-wb.jpgAnti-CaMKII CAMK2B Rabbit Monoclonal AntibodyWestern blot analysis of CaMKII expression in (1)Mouse brain tissue lysate ;(2)Rat brain tissue lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03964-ihc.jpgAnti-CaMKII CAMK2B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse colon, using CaMKII Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-scarb1-rabbit-monoclonal-antibody-m01093-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01093-wb7.jpgAnti-SCARB1/Sr Bi Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01093-wb.jpgAnti-SCARB1/Sr Bi Rabbit Monoclonal AntibodyWestern blot analysis of SCARB1 expression in (1) Human fetal liver lysate; (2) Mouse liver lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01093-wb8.jpgAnti-SCARB1/Sr Bi Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01093-ihc.jpgAnti-SCARB1/Sr Bi Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using SCARB1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01093-wb9.jpgAnti-SCARB1/Sr Bi Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxo1a-rabbit-monoclonal-antibody-m00073-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00073-foxo1-primary-antibodies-wb-testing-1.jpgAnti-FoxO1a Rabbit Monoclonal AntibodyWestern blot analysis of FOXO1 using anti-FOXO1 antibody (M00073). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse pancreas tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXO1 antigen affinity purified monoclonal antibody (M00073) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXO1 at approximately 80 kDa. The expected band size for FOXO1 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00073-12967_2019_2170_fig1_html.pngAnti-FoxO1a Rabbit Monoclonal AntibodyThe FXR agonist GW4064 improved fasting blood glucose and inhibited the translocation of PGC1α and FOXO1 from the nucleus to the cytoplasm in gluconeogenesis with FK506 treatment in mice for 3 months. a After FK506 was administered at a dose of 1 mg/kg/day to the C57BL/6J mice for 3 months, the fasting blood glucose levels obviously increased gradually compared with those of the control group, and the FXR agonist GW4064 downregulated the blood glucose levels. No significant difference was found for b body weights and c morphological alterations among the control group, the FK506 group and the FK506 + GW4064 group. The C-1, C-2 and C-3 groups were the control group, the FK506 group and the FK506 + GW4064 group, respectively. d , f – h , j , k Western blotting and quantitative analysis show the protein subcellular localization of PGC1α and FOXO1. Original magnification, ×3400 in each group. e , i IF staining for PGC1α ( e ) and FOXO1 ( i ) in sections of 3 groups. DAPI was used to locate the nuclei of the cells. Data are presented as the mean ± SD (n = 7). * P < 0.05 vs. the control group, # P < 0.05 vs. the FK506 group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-019-02170-5'>31836014</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00073-ihc.jpgAnti-FoxO1a Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain carcinoma, using FoxO1a Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00073-if.jpgAnti-FoxO1a Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using FoxO1a Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ifnar1-rabbit-monoclonal-antibody-m00306-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-1-wb.jpgAnti-IFNAR1/Beta R1 Rabbit Monoclonal AntibodyWestern blot analysis of IFNAR1 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-1-wb7.jpgAnti-IFNAR1/Beta R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-1-wb8.jpgAnti-IFNAR1/Beta R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erk1-2-rabbit-monoclonal-antibody-m00104-1-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-wb.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyWestern blot analysis of ERK1/2 Antibody expression in HepG2 whole cell lysates.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-wb7.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-41420_2025_2508_fig6_html.pngAnti-ERK1/2 Rabbit Monoclonal AntibodyERK/NF-κB signaling is involved in Kv1.3-related M1 macrophages. A Respective western blotting image and densitometry analysis of ERK/NF-κB signaling after transfection with LV-Kv1.3 in THP-1 cells. Data were expressed as mean ± SD (n = 4). B The phosphorylation signal data are depicted in the form of stacked histogram overlaid plots. The mean fluorescence intensity (MFI) of the ERK1/2 and NF-κB p65 phosphorylation signal was expressed as the mean ± SD (n = 3). C Effects of MgTx, PD98059, and Licochalcone B on Kv1.3 and ERK/NF-κB signaling in LV-Kv1.3-transduced THP-1 cells were analyzed by western blotting. Data were expressed as mean ± SD (n = 3). D Respective western blotting image and densitometry analysis of ERK/NF-κB signaling in HK-2 cells co-cultured with the supernatant from LV-Kv1.3-transduced THP-1 cells for 48 h. Data were expressed as mean ± SD (n = 4). E Respective western blotting image and densitometry analysis of ERK/NF-κB signaling in mice subjected to UUO (7 days post-surgery) and IRI. Data were expressed as mean ± SD (n = 4). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-025-02508-7'>40324999</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-41398_2023_2624_fig4_html.pngAnti-ERK1/2 Rabbit Monoclonal AntibodyEffects of knocking-down ADRB1 CaMKII on mPFC activity and subsequent signals in METH-sired male F1. a Levels of c-Fos protein. b The c-Fos immunostaining. Scale bar, 500 μm /100 μm. c Density of dendritic spine. Scale bar, 50 μm /10 μm. d Levels of β-arestin2 and PKA protein. e Levels of ERK1/2, p-ERK1/2, ERK1/2/p-ERK1/2, CREB, p-CREB, p-CREB/ CREB and ΔFosB protein. F1-METH-Ctrl, METH-sired male F1 mice injected with Ctrl virus. F1-METH-KD, METH-sired male F1 mice injected with KD virus. The data are presented as the Mean ± SD. N.S., P > 0.05. * P < 0.05, ** P < 0.01 vs F1-METH-Ctrl. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41398-023-02624-x'>37857642</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-m_rsob.230427.f005.pngAnti-ERK1/2 Rabbit Monoclonal AntibodyEffect of MYH7 R453C mutation on TGF-β/Smad2/3, ERK1/2, NF-κB and PI3K/AKT pathways. (a) The protein expression of TGF-β/Smad2/3 and ERK1/2 cascades were detected by western blotting. (b–d) The protein expression of TGF-β1/2, p-Smad2/3/Smad2/3 and p-ERK1/2/ERK1/2 were quantitated using densitometry. (e) The protein expression of NF-κB signalling was detected by western blotting. (f) Quantitative analysis of the protein expression of p-NF-κB p65 and NF-κB p65. **p < 0.01, ****p < 0.0001. n = 3 biologically independent samples. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://royalsocietypublishing.org/doi/abs/10.1098/rsob.230427'>38862020</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-feb413914-fig-0010-m.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyEffects of OPN and OVE on activation of MAPK signaling pathways in LPS-stimulated RAW264.7 cells. Expression levels of p-ERK, ERK, p-p38, p-38, p-JNK, and JNK were detected in the same samples for COX-2 detection after 24 h of LPS stimulation. (A) OVE treatment. (B) OPN treatment. All experiments were carried out in triplicates and data are presented as means ± SDs; one-way ANOVA analysis was adopted for multiple comparisons; ###P < 0.001, ####P < 0.0001, compared to the untreated control group; ***P < 0.001 and ****P < 0.0001, compared to the LPS control group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://febs.onlinelibrary.wiley.com/doi/abs/10.1002/2211-5463.13914'>39455284</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-if.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using ERK1/2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-wb8.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-wb9.jpgAnti-ERK1/2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-6.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-7.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-8.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-9.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-10.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-ihc-testing-11.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IHC analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-12.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-13.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-14_1.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-15.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-16.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-17.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-18.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-19.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-20.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00104-1-erk12-primary-antibodies-if-testing-21_1.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody IF analysis of ERK1/2 using anti-ERK1/2 antibody (M00104-1). <br>
ERK1/2 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-ERK1/2 Antibody (M00104-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/a/casestudy_m00104-1.jpgAnti-ERK1/2 Rabbit Monoclonal Antibody
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tomm20-rabbit-monoclonal-antibody-m04039-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-tomm20-primary-antibodies-wb-testing-1.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal Antibody Western blot analysis of TOMM20/Tom20 using anti-TOMM20/Tom20 antibody (M04039). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: rat stomach tissue lysates,<br>
Lane 7: mouse kidney tissue lysates,<br>
Lane 8: mouse stomach tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOMM20/Tom20 antigen affinity purified monoclonal antibody (Catalog # M04039) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TOMM20/Tom20 at approximately 16 kDa. The expected band size for TOMM20/Tom20 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-tomm20-primary-antibodies-ihc-testing-2.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal Antibody IHC analysis of TOMM20 using anti-TOMM20 antibody (M04039). <br>
TOMM20 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TOMM20 Antibody (M04039) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-tomm20-primary-antibodies-ihc-testing-3.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal Antibody IHC analysis of TOMM20 using anti-TOMM20 antibody (M04039). <br>
TOMM20 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TOMM20 Antibody (M04039) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-icc2.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-icc3.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-icc4.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-icc1.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04039-if.jpgAnti-TOMM20/Tom20 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using TOMM20 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dnmt3a-rabbit-monoclonal-antibody-m00136-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00136-dnmt3a-primary-antibodies-wb-testing-1.jpgAnti-Dnmt3a Rabbit Monoclonal Antibody Western blot analysis of Dnmt3a using anti-Dnmt3a antibody (M00136). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: mouse brain tissue lysates,<br>
Lane 5: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dnmt3a antigen affinity purified monoclonal antibody (Catalog # M00136) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Dnmt3a at approximately 130 kDa. The expected band size for Dnmt3a is at 130 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lin28b-rabbit-monoclonal-antibody-m00896-boster.html2026-03-24T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00896-lin28b-primary-antibodies-wb-testing-1_1.jpgAnti-Lin28B Rabbit Monoclonal Antibody Western blot analysis of LIN28B using anti-LIN28B antibody (M00896). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human HUH-7 whole cell lysates,<br>
Lane 5: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIN28B antigen affinity purified monoclonal antibody (Catalog # M00896) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIN28B at approximately 35 kDa. The expected band size for LIN28B is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00896-if.jpgAnti-Lin28B Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using Lin28B Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dynll1-rabbit-monoclonal-antibody-m03454-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-wb-testing-1.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyWestern blot analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DYN1L1 antigen affinity purified monoclonal antibody (M03454) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DYN1L1 at approximately 12 kDa. The expected band size for DYN1L1 is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-10.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-11.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-8.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-9.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-6.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-7.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-5.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-4.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-3.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dyn1l1-primary-antibodies-ihc-testing-2.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyIHC analysis of DYN1L1 using anti-DYN1L1 antibody (M03454). <br>DYN1L1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DYN1L1 Antibody (M03454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03454-dynll1-primary-antibodies-ip-testing-1.jpgAnti-DYNLL1/Pin Rabbit Monoclonal AntibodyImmunoprecipitating DYNLL1 in A549 whole cell lysate.<br>
Western blot analysis of DYNLL1 using anti-DYNLL1 antibody (M03454).<br>
Lane 1: A549 whole cell lysates (30ug),<br>
Lane 2: Rabbit control IgG instead of anti-DYNLL1 antibody in A549 whole cell lysate,<br>
Lane 3: anti-DYNLL1 antibody (2μg) + A549 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DYNLL1 antigen affinity purified monoclonal antibody (M03454) at a dilution of 1:50 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for DYNLL1 at approximately 12 kDa. The expected band size for DYNLL1 is at 10 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-golph2-rabbit-monoclonal-antibody-m02975-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02975-wb.jpgAnti-GOLPH2 Rabbit Monoclonal AntibodyWestern blot analysis of GOLPH2 expression in LnCaP cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl2a1-rabbit-monoclonal-antibody-m03850-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03850-bcl2a1-primary-antibodies-wb-testing-1.jpgAnti-BCL2A1/Bcl 2 Related Protein A1 Rabbit Monoclonal Antibody Western blot analysis of BCL2A1 using anti-BCL2A1 antibody (M03850). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL2A1 antigen affinity purified monoclonal antibody (Catalog # M03850) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL2A1 at approximately 27 kDa. The expected band size for BCL2A1 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03850-wb8.jpgAnti-BCL2A1/Bcl 2 Related Protein A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03850-bcl2a1-primary-antibodies-wb-testing-2.jpgAnti-BCL2A1/Bcl 2 Related Protein A1 Rabbit Monoclonal AntibodyWestern blot analysis of Bcl2A1 using anti-Bcl2A1 antibody (M03850).<br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: huamn OE19 whole cell lysates,<br>
Lane 2: human OE19 whole cell lysates,<br>
Lane 3: human OE33 whole cell lysates,<br>
Lane 4: human OE33 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bcl2A1 antigen affinity purified monoclonal antibody (M03850) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Bcl2A1 at approximately ~27 kDa. The expected band size for Bcl2A1 is at ~20 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-raptor-rabbit-monoclonal-antibody-m01463-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01463-wb.jpgAnti-Raptor RPTOR Rabbit Monoclonal AntibodyWestern blot analysis of Raptor expression in MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nestin-rabbit-monoclonal-antibody-m00806-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-wb-testing-1.jpgAnti-Nestin Rabbit Monoclonal AntibodyWestern blot analysis of Nestin using anti-Nestin antibody (M00806). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U251 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: rat C6 whole cell lysates,<br>
Lane 4: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Nestin antigen affinity purified monoclonal antibody (M00806) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Nestin at approximately 270-300 kDa. The expected band size for Nestin is at 177 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-1.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of human diffuse large B-cell lymphoma of the intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-2.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-3.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-4.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-5.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-ihc-testing-6.jpgAnti-Nestin Rabbit Monoclonal AntibodyIHC analysis of Nestin using anti-Nestin antibody (M00806). <br>Nestin was detected in a paraffin-embedded section of pig brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-if-testing-1_1.jpgAnti-Nestin Rabbit Monoclonal AntibodyIF analysis of Nestin using anti-Nestin antibody (M00806).<br>
Nestin was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with rabbit anti-Nestin Antibody (M00806) at a dilution of 1:50 overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00806-nestin-primary-antibodies-if-testing-1.jpgAnti-Nestin Rabbit Monoclonal AntibodyIF analysis of Nestin using anti-Nestin antibody (M00806). <br>
Nestin was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated at 1:50 rabbit anti-Nestin Antibody (M00806) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ralbp1-rabbit-monoclonal-antibody-m01403-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01403-wb.jpgAnti-RALBP1 Rabbit Monoclonal AntibodyWestern blot analysis of RALBP1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01403-ihc.jpgAnti-RALBP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using RALBP1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-akap14-rabbit-monoclonal-antibody-m15886-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15886-akap14-primary-antibodies-wb-testing-1.jpgAnti-AKAP14 Rabbit Monoclonal Antibody Western blot analysis of AKAP14 using anti-AKAP14 antibody (M15886). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AKAP14 antigen affinity purified monoclonal antibody (Catalog # M15886) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AKAP14 at approximately 21,23 kDa. The expected band size for AKAP14 is at 21 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tcf7l2-rabbit-monoclonal-antibody-m00431-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00431-wb.jpgAnti-TCF7L2 Rabbit Monoclonal AntibodyWestern blot analysis of TCF7L2 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00431-ihc.jpgAnti-TCF7L2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colonic cancer, using TCF7L2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-moesin-rabbit-monoclonal-antibody-m00766-1-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00766-1-wb.jpgAnti-Moesin Rabbit Monoclonal AntibodyWestern blot analysis of Moesin expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00766-1-ihc.jpgAnti-Moesin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid cancer, using Moesin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fancd2-rabbit-monoclonal-antibody-m00563-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00563-fancd2-primary-antibodies-wb-testing-1.jpgAnti-FANCD2 Rabbit Monoclonal Antibody Western blot analysis of FANCD2 using anti-FANCD2 antibody (M00563). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FANCD2 antigen affinity purified monoclonal antibody (Catalog # M00563) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FANCD2 at approximately 164kDa. The expected band size for FANCD2 is at 164 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00563-ihc.jpgAnti-FANCD2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using FANCD2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-inpp4b-rabbit-monoclonal-antibody-m06336-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06336-inpp4b-primary-antibodies-wb-testing-1.jpgAnti-INPP4B/Type Ii 4 Phosphatase Rabbit Monoclonal Antibody Western blot analysis of INPP4B using anti-INPP4B antibody (M06336). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INPP4B antigen affinity purified monoclonal antibody (Catalog # M06336) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INPP4B at approximately 105 kDa. The expected band size for INPP4B is at 105,107 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tweakr-rabbit-monoclonal-antibody-m06261-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig1_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyTh17/Treg cell differentiation ratio and TWEAK/Fn14 signaling level in AC mice. ( A ) The state of mice ocular surface was observed by slit-lamp. ( B ) The clinical scores of mice were performed according to the status of eyelid, conjunctiva and cornea. ( C ) HE staining was utilized to evaluate the pathological changes of conjunctival tissue in mice. ( D ) The proportion of Th17 or Treg cells in spleen of mice was assessed by flow cytometry. ( E ) The levels of Th17 and Treg cytokines in mice spleen were evaluated by ELISA. ( F-H ) TWEAK and Fn14 levels in ocular conjunctival tissue were measured by qRT-PCR and WB. ( I ) IHC was used to observe the protein level of TWEAK and Fn14 in ocular conjunctival tissue. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. Control<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig2_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyTWEAK knockdown affected conjunctivitis in AC mice. ( A ) The effect of TWEAK knockdown on the state of mice ocular surface was observed under slit-lamp. ( B ) Clinical score of eyelid, conjunctiva and cornea to assess the effect of TWEAK knockdown in AC mice. ( C-D ) HE staining and TB staining were utilized to evaluate the effect of TWEAK knockdown on conjunctivitis in mice. ( E-G ) The levels of TWEAK and Fn14 in conjunctival tissue were detected by qRT-PCR, IHC and WB. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. Con + AAV-shNC; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. AC + AAV-shNC; ns, no significant difference<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig3_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyTWEAK regulated the Th17/Treg cell ratio in AC mice. ( A ) The effect of TWEAK knockdown on Th17 and Treg cell ratio in spleen of AC mice was observed by flow cytometry. ( B-C ) WB and IHC were employed to evaluate the expression levels of FoxP3 and RORγt in mice conjunctival tissue. ( D ) The effect of TWEAK knockdown on the levels of Th17 and Treg cytokines in mice spleen were evaluated by ELISA. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. Con + AAV-shNC; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. AC + AAV-shNC; ns, no significant difference<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig4_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyTWEAK knockdown promoted Nrf2/HO-1 signaling pathway in AC mice. ( A ) qRT-PCR was utilized to measure the effect of TWEAK knockdown on Nrf2 and HO-1 mRNA levels in conjunctival tissue of mice. ( B-C ) The effect of TWEAK knockdown on protein levels of Nrf2 and HO-1 in conjunctival tissue of mice were detected by WB and IHC. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. Con + AAV-shNC; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. AC + AAV-shNC; ns, no significant difference<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig5_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyInhibition of Nrf2/HO-1 signaling pathway affected the improvement of conjunctivitis in AC mice from TWEAK knockdown. ( A ) The effect of Nrf2 inhibitor on ocular surface status was observed by slit-lamp in AC mice with TWEAK knockdown. ( B ) Clinical score of eyelid, conjunctiva and cornea to assess the effect of Nrf2 inhibitor in AC mice with TWEAK knockdown. ( C-D ) HE staining and TB staining were employed to evaluate the effect of Nrf2 inhibitor on conjunctivitis in AC mice with TWEAK knockdown. ( E-G ) The levels of Nrf2 and HO-1 in conjunctival tissue were detected by qRT-PCR, IHC and WB. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. AC + AAV-shNC; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. AC + AAV-shTWEAK<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-10020_2024_1004_fig6_html.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyInhibition of Nrf2/HO-1 signaling pathway affected Th17/Treg cell ratio in AC mice with TWEAK knockdown. ( A ) The effect of Nrf2 inhibitor on Th17/Treg cell ratio in AC mice with TWEAK knockdown was assessed by flow cytometry. ( B-C ) WB and IHC assays were employed to evaluate the expression of FoxP3 and RORγt in conjunctival tissue of AC mice. ( D ) The levels of Th17 and Treg cytokines in mice spleen were detected by ELISA. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. AC + AAV-shNC; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. AC + AAV-shTWEAK<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11590473/'>39592944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-fimmu-16-1649327-g005.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyEffects of ISO on the TWEAK/Fn14 signaling pathway in TGF-β1-induced HK-2 cells. (A, B) ISO directly interacts with Fn14, dose–response sensorgrams, and the affinity constant ( K d = 5.47 μM) of ISO with Fn14. (C–F) Western blot analysis of TWEAK, Fn14, and the phosphorylation levels of ERK1/2 in TGF-β1-induced HK-2 cells. β-actin was used as the loading control. Data are expressed as mean ± SD ( n = 3). # p < 0.05, ## p < 0.01 versus the sham group, * p < 0.05, ** p < 0.01 versus the UUO group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1649327/full'>40977693</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-fimmu-16-1649327-g006.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyEffect of ISO on the expression of TWEAK/Fn14 signaling pathway-related proteins in UUO rats. Representative images and quantification of Western blot results of the protein expression of TWEAK, Fn14, TRAF2, and BRAF (A–D) , and phosphorylation of MER1/2 and ERK1/2 (E–H) . β-actin was used as the loading control for total protein. (I–L) Relative optical density analysis of the nucleoprotein expression of p-SP1, Snail, and β-catenin. PCNA was used as the loading control for nucleoprotein. All data are expressed as the mean ± SD ( n = 5). ## p < 0.01 versus the sham group, * p < 0.05, ** p < 0.01 versus the UUO group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1649327/full'>40977693</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-fimmu-16-1649327-g007.jpgAnti-TWEAKR Rabbit Monoclonal AntibodyFn14 overexpression compromises the therapeutic effects of ISO and the regulation of ISO on the TWEAK/Fn14 pathway-related proteins on UUO model rats. (A, B) Serum Scr and BUN levels in different groups. (C, D) Representative images and the CVF of Masson staining (×400). (E–H) Representative and quantification analysis of Col III and FN immunohistochemical staining (×400). Nuclei were counterstained with DAPI (blue). (I–K) Western blot and the relative optical densities analysis of E-cadherin and α-SMA in kidney tissue. (L–O) Representative images and quantification of Western blot results of the protein expression of TWEAK, Fn14, and phosphorylation of ERK1/2. β-actin was used as the loading control. (P–R) Relative optical density analysis of the nucleoprotein expression of Snail and β-catenin. PCNA was used as the loading control for nucleoprotein. Data were shown as mean ± SD ( n = 3). ## p < 0.01 versus the sham group, * p < 0.05, ** p < 0.01 versus the UUO group, △ p < 0.05, △△ p < 0.01 versus the ISO group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1649327/full'>40977693</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-tweakr-primary-antibodies-wb-testing-1.jpgAnti-TWEAKR Rabbit Monoclonal Antibody Western blot analysis of TWEAKR using anti-TWEAKR antibody (M06261). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HUVEC whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates,<br>
Lane 6: mouse 4T1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TWEAKR antigen affinity purified monoclonal antibody (Catalog # M06261) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TWEAKR at approximately 17,20 kDa. The expected band size for TWEAKR is at 17,20 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100a4-rabbit-monoclonal-antibody-m01217-1-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-wb7.jpgAnti-S100A4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-wb.jpgAnti-S100A4 Rabbit Monoclonal AntibodyWestern blot analysis of S100A4 expression in A375 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-ihc9.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-ihc10.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-ihc7.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-ihc8.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-ihc.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma, using S100A4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-1-if.jpgAnti-S100A4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using S100A4 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eif2c3-rabbit-monoclonal-antibody-m04191-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04191-wb.jpgAnti-EIF2C3 AGO3 Rabbit Monoclonal AntibodyWestern blot analysis of EIF2C3 expression in Human brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04191-ago3-primary-antibodies-ihc-testing-1.jpgAnti-EIF2C3 AGO3 Rabbit Monoclonal AntibodyIHC analysis of AGO3 using anti-AGO3 antibody (M04191). <br>AGO3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AGO3 Antibody (M04191) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat5b-rabbit-monoclonal-antibody-m00681-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00681-stat5b-primary-antibodies-wb-testing-1_1.jpgAnti-STAT5b Rabbit Monoclonal AntibodyWestern blot analysis of STAT5B using anti-STAT5B antibody (M00681). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human Raji whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse lung tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5B antigen affinity purified monoclonal antibody (M00681) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STAT5B at approximately 90 kDa. The expected band size for STAT5B is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00681-stat5b-primary-antibodies-wb-testing-2.jpgAnti-STAT5b Rabbit Monoclonal AntibodyWestern blot analysis of STAT5B using anti-STAT5B antibody (M00681). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat skeletal muscle tissue lysates,<br>
Lane 7: mouse thymus tissue lysates,<br>
Lane 8: mouse skeletal muscle tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5B antigen affinity purified monoclonal antibody (M00681) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STAT5B at approximately 90-95 kDa. The expected band size for STAT5B is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00681-ihc.jpgAnti-STAT5b Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using STAT5b Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00681-stat5b-primary-antibodies-ip-testing-1.jpgAnti-STAT5b Rabbit Monoclonal AntibodyImmunoprecipitating (IP) STAT5B in K562 whole cell lysate.<br>
Western blot analysis of STAT5B using anti-STAT5B antibody (M00681); <br>
Lane 1: K562 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-STAT5B antibody in K562 whole cell lysate;<br>
Lane 3: anti-STAT5B antibody (2μg) + K562 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-STAT5B antigen affinity purified monoclonal antibody (M00681) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for STAT5B at approximately 90 kDa. The expected band size for STAT5B is at 90 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hdac10-rabbit-monoclonal-antibody-m05215-boster.html2026-03-24T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05215-wb7.jpgAnti-HDAC10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05215-wb.jpgAnti-HDAC10 Rabbit Monoclonal AntibodyWestern blot analysis of HDAC10 expression in (1) HeLa cell lysate; (2) 3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05215-if.jpgAnti-HDAC10 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using HDAC10 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-foxo3a-rabbit-monoclonal-antibody-m00252-boster.html2026-03-31T05:01:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-12860_2022_448_fig7_html.pngAnti-FoxO3a Rabbit Monoclonal AntibodyRPL5 regulates colon cancer cell proliferation and migration through MAPK/ERK signaling pathway. A HCT116 and RKO cells were treated with RPL5-targeting siRNAs (siRPL5–1 and siRPL5–2) or negative control siRNA (siNC). After 48 h, cell lysates were harvested, and the protein samples were separated by SDS-PAGE. The levels of MAPK/ERK signaling pathway related proteins P-MEK1/2, MEK1/2, P-ERK, ERK, FOXO3 and c-Myc were detected by western blotting. The band intensities of P-MEK1/2, MEK1/2, P-ERK, ERK, FOXO3 and c-Myc proteins were quantified relative to β-Tubulin and normalized to the siNC sample. The blots were cut prior to hybridization with antibodies during blotting. B TBHQ (50 μM) was added to HCT116 and RKO cells after 6 h transfection of siRPL5, and the proteins of each group were extracted 48 h later. Changes of proteins related to MAPK/ERK signaling pathway were detected by western blotting. The blots were cut prior to hybridization with antibodies during blotting. C HCT116 and RKO cells were transfected with siRPL5 and then added TBHQ (20 μM) to detect the effect of TBHQ on the proliferation inhibition of colon cancer cells caused by siRPL5 at 24 h and 48 h. D HCT116 and RKO cells were transfected with siRPL5 and then added TBHQ (20uM) to detect the effect of TBHQ on the inhibition of colon cancer cell migration caused by siRPL5 at 24 h and 48 h. (E) TBHQ (50 μM) was added to HCT116 and RKO cells after transfection of siRPL5 for 6 h, and cell cycle-related proteins (CDK4 and CyclinD1) and migration-related proteins (MMP2 and MMP9) were detected by western blotting. The band intensities of CDK4, CyclinD1, MMP2 and MMP9 proteins were quantified relative to β-Tubulin and normalized to the siNC sample. The blots were cut prior to hybridization with antibodies during blotting. The data are representative of three independent experiments. (* P < 0.05, ** P < 0.01, *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12860-022-00448-z'>36384455</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-wb7.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-wb.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyWestern blot analysis of FOXO3A expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-if.jpgAnti-FoxO3a Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using FoxO3a Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00252-foxo3a-primary-antibodies-wb-review-1.pngAnti-FoxO3a Rabbit Monoclonal AntibodyWestern blot analysis of FoxO3a using anti-FoxO3a antibody (M00252). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: control group-normal mouse hippocampal tissue lysates,<br>
Lane 2: hippocampal tissue from Alzheimer’s disease model mouse,<br>
Lane 3: hippocampal tissue from Alzheimer’s disease model mouse treated with a self-developed drug.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FoxO3a antigen affinity purified polyclonal antibody (Catalog # PA1079) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for FoxO3a at approximately 80-100 kDa. The expected band size for FoxO3a is at 71.3 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-rabbit-monoclonal-antibody-m02431-1-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02431-1-wb.jpgAnti-14-3-3 YWHAB Rabbit Monoclonal AntibodyWestern blot analysis of 14-3-3 expression in Hela lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02431-1-ihc.jpgAnti-14-3-3 YWHAB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using 14-3-3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-rabbit-monoclonal-antibody-m02431-2-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02431-2-wb.jpgAnti-14-3-3 YWHAB Rabbit Monoclonal AntibodyWestern blot analysis of 14-3-3 expression in (1) HeLa cell lysate; (2) 3T3 cell lysate; (3) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspa14-rabbit-monoclonal-antibody-m09630-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09630-wb.jpgAnti-HSPA14 Rabbit Monoclonal AntibodyWestern blot analysis of HSPA14 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc25c-rabbit-monoclonal-antibody-m01343-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01343-cdc25c-primary-antibodies-wb-testing-1.jpgAnti-Cdc25C Rabbit Monoclonal AntibodyWestern blot analysis of CDC25C using anti-CDC25C antibody (M01343). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDC25C antigen affinity purified monoclonal antibody (M01343) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDC25C at approximately 53 kDa. The expected band size for CDC25C is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01343-cdc25c-primary-antibodies-ihc-testing-1.jpgAnti-Cdc25C Rabbit Monoclonal AntibodyIHC analysis of CDC25C using anti-CDC25C antibody (M01343). <br>CDC25C was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CDC25C Antibody (M01343) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01343-cdc25c-primary-antibodies-ihc-testing-2.jpgAnti-Cdc25C Rabbit Monoclonal AntibodyIHC analysis of CDC25C using anti-CDC25C antibody (M01343). <br>CDC25C was detected in a paraffin-embedded section of human lymph node tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CDC25C Antibody (M01343) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01343-cdc25c-primary-antibodies-ihc-testing-3.jpgAnti-Cdc25C Rabbit Monoclonal AntibodyIHC analysis of CDC25C using anti-CDC25C antibody (M01343). <br>CDC25C was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CDC25C Antibody (M01343) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc25b-rabbit-monoclonal-antibody-m01899-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01899-wb7.jpgAnti-Cdc25B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01899-wb8.jpgAnti-Cdc25B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01899-wb.jpgAnti-Cdc25B Rabbit Monoclonal AntibodyWestern blot analysis of Cdc25B expression in U937 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-notch4-rabbit-monoclonal-antibody-m02582-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02582-wb.jpgAnti-NOTCH4 Rabbit Monoclonal AntibodyWestern blot analysis of NOTCH4 expression in Mouse lung lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp105-rabbit-monoclonal-antibody-m04168-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-wb-testing-1.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyWestern blot analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPH1 antigen affinity purified monoclonal antibody (M04168) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HSPH1 at approximately 108 kDa. The expected band size for HSPH1 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-ihc-testing-1.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyIHC analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>HSPH1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPH1 Antibody (M04168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-ihc-testing-2.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyIHC analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>HSPH1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPH1 Antibody (M04168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-ihc-testing-3.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyIHC analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>HSPH1 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPH1 Antibody (M04168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-ihc-testing-4.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyIHC analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>HSPH1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPH1 Antibody (M04168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04168-hsph1-primary-antibodies-ihc-testing-5.jpgAnti-Hsp105 Rabbit Monoclonal AntibodyIHC analysis of HSPH1 using anti-HSPH1 antibody (M04168). <br>HSPH1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HSPH1 Antibody (M04168) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tsg101-rabbit-monoclonal-antibody-m01233-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-tsg101-primary-antibodies-wb-testing-1.jpgAnti-TSG101 Rabbit Monoclonal Antibody Western blot analysis of TSG101 using anti-TSG101 antibody (M01233). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human COLO320 whole cell lysates,<br>
Lane 3: human SW620 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSG101 antigen affinity purified monoclonal antibody (Catalog # M01233) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSG101 at approximately 44 kDa. The expected band size for TSG101 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-ihc10.jpgAnti-TSG101 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-ihc7.jpgAnti-TSG101 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-ihc11.jpgAnti-TSG101 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse kidney, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-ihc8.jpgAnti-TSG101 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-ihc9.jpgAnti-TSG101 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tongue cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-jev2-14-e70087-g008.jpgAnti-TSG101 Rabbit Monoclonal AntibodyRepeatability of selected urinary extracellular vesicle (uEV) protein content measurements by Multi‐Strip Western Blotting (MSWB). (A) The principle of MSWB analysis. Multiple gels were loaded with molecular weight marker (Mr, lanes 1 and 10) and lysates of either individual technical replicate (TR) samples (lanes 3–8) or pooled master TR7 sample in duplicate (lanes 2 and 9) prepared by mixing equal amounts of TR1–TR6 lysates of either uMV or uEXO fractions to resolve proteins by their molecular weight (left panel). After electrophoresis, these gels were cut into strips. Strips that contained the identical antigen of interest, were aligned onto single assembling filter paper, and then transferred onto single nitrocellulose membrane. Following protein transfer, the membrane was blocked and probed with appropriate primary and HRP‐conjugated secondary antibodies. For visualization, some strips were rearranged to alternate between male ( M ) and female ( F ) subjects and between uEXO and uMV series, because paired samples were loaded in a randomised manner. Black line strokes around the individual strips were drawn to improve readability. The representative blot shows 50 kDa TSG101 protein level distribution across TR1‐TR7 samples of paired uEV fractions of individual subjects (right panel). (B) Comparison of procedural sample processing precision for selected endogenous uEV protein detection following uEV isolation by DC method. Relative uncertainty of chemiluminescent protein band signal measurements was expressed as CV TR to assess average procedural sample processing precision in six uMV ( left panel ) or six uEXO ( right panel ) TR samples obtained from male ( teal bars ) ( N = 3) or female ( pink bars ) urine ( N = 3) by differential velocity centrifugation (DC) method. (C) Comparative uEV‐associated protein marker expression levels before and after elimination of procedural sample processing variations by sample pooling. Average percentage difference calculated between the arithmetic mean of signal detected across six individual TR samples for PKM1/2 ( upside triangle symbols ), GAPDH ( triangle symbols ), TSG101 ( square symbols ) and ALIX ( circle symbols ) protein bands and an average signal of pooled (TR7) sample, which was loaded in duplicate. The analysis was performed on 8 data points (4 uMV and 4 uEXO series).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12086329/'>40384173</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-jev2-14-e70087-g006.jpgAnti-TSG101 Rabbit Monoclonal AntibodyA‐C. Prove of urinary extracellular vesicle (uEV) particle existence in the primary analyte samples derived by different uEV isolation methods by ancillary transmission electron microscopy (TEM) (A), fluorescence microscopy (FM) (B) and Western Blotting/Immunoblotting (IB) (C) methods. TEM shows a typical cup‐shape EV morphology (EV drying artefact) at 3200 ms exposure and either medium 15,000× (bar size = 200 nm) or high 43,000× (bar size = 100 nm, inlet image) magnification; IB shows known EV protein biomarker expression such as Alix, TSG101, Flotillin‐1, CD‐9 and PKM1/2 in different subject (S1, S2) uEV samples that are free of Golgi, endoplasmic reticulum or mitochondria organelle contaminants as indicated by the absence of GM130, protein disulfide isomerase (PDI) or pyruvate dehydrogenase (PD) proteins; FM displays green fluorescent signal emitted from SYTO RNASelect‐stained internal uEV nucleic acid (RNA) cargo (bar size = 10 µm). (D) Linear relationship between raw source sample dose (pre‐clarified urine input) and isolated uEV particle concentration (output response) in samples processed by DC (left panel), SiC (middle panel) or PEG (right panel) methods.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12086329/'>40384173</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01233-13287_2025_4205_fig2_html.pngAnti-TSG101 Rabbit Monoclonal AntibodyIllustrates the characterization of DFATs and exosomes. DFATs exhibited a spindle-shaped morphology ( A-B ). Flow cytometry analysis showed that DFATs were positive for markers CD90, CD105, and CD73, and negative for CD34, CD11b, CD19, CD45, and HLA-DR ( C ). NTA showed that the average diameter of the exosomes was 136.3 nm ( D ). TEM showed that DFATs-Exos exhibited a typical bilayer membrane structure ( E ). Western blot analysis revealed that DFATs exosomes were enriched in markers such as CD63, CD9, and TSG101, while lacking the marker Calnexin ( F ). Full-length blots are presented in Supplementary Digital Material 1 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04205-9'>40022232</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cited2-rabbit-monoclonal-antibody-m02966-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02966-wb.jpgAnti-CITED2 Rabbit Monoclonal AntibodyWestern blot analysis of CITED2 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mglur2-rabbit-monoclonal-antibody-m06123-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06123-wb.jpgAnti-mGluR2 GRM2 Rabbit Monoclonal AntibodyWestern blot analysis of mGluR2 expression in Mouse brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06123-wb7.jpgAnti-mGluR2 GRM2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mglur1-rabbit-monoclonal-antibody-m03049-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03049-wb7.jpgAnti-mGluR1 GRM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03049-wb8.jpgAnti-mGluR1 GRM1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03049-wb.jpgAnti-mGluR1 GRM1 Rabbit Monoclonal AntibodyWestern blot analysis of mGluR1 expression in Mouse brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03049-grm1-primary-antibodies-ihc-testing-1_1.jpgAnti-mGluR1 GRM1 Rabbit Monoclonal AntibodyIHC analysis of GRM1 using anti-GRM1 antibody (M03049). <br>GRM1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GRM1 Antibody (M03049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03049-grm1-primary-antibodies-ihc-testing-2_1.jpgAnti-mGluR1 GRM1 Rabbit Monoclonal AntibodyIHC analysis of GRM1 using anti-GRM1 antibody (M03049). <br>GRM1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GRM1 Antibody (M03049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100a9-rabbit-monoclonal-antibody-m00380-1-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00380-1-wb.jpgAnti-S100A9 Rabbit Monoclonal AntibodyWestern blot analysis of S100A9 expression in human tonsil lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00380-1-wb7.jpgAnti-S100A9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-parkin-rabbit-monoclonal-antibody-m00127-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00127-wb7.jpgAnti-Parkin PARK2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00127-wb.jpgAnti-Parkin PARK2 Rabbit Monoclonal AntibodyWestern blot analysis of Parkin expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00127-wb8.jpgAnti-Parkin PARK2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00127-wb9.jpgAnti-Parkin PARK2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pgp9-5-rabbit-monoclonal-antibody-m01018-1-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-1-wb.jpgAnti-PGP9.5 Rabbit Monoclonal AntibodyWestern blot analysis of PGP9.5 expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-1-ihc.jpgAnti-PGP9.5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain, using PGP9.5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-serca2-rabbit-monoclonal-antibody-m01176-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01176-wb.jpgAnti-SERCA2 ATP2A2 Rabbit Monoclonal AntibodyWestern blot analysis of SERCA2 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cnpase-rabbit-monoclonal-antibody-m01017-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01017-wb.jpgAnti-CNPase Rabbit Monoclonal AntibodyWestern blot analysis of CNPase expression in C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-adam17-rabbit-monoclonal-antibody-m00604-boster.html2026-03-24T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00604-adam17-primary-antibodies-wb-testing-1.jpgAnti-ADAM17/Tace Rabbit Monoclonal Antibody Western blot analysis of ADAM17 using anti-ADAM17 antibody (M00604). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: rat liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM17 antigen affinity purified polyclonal antibody (Catalog # M00604) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM17 at approximately 93 kDa. The expected band size for ADAM17 is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00604-wb7.jpgAnti-ADAM17/Tace Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00604-if.jpgAnti-ADAM17/Tace Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using ADAM17 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mina53-rabbit-monoclonal-antibody-m00783-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00783-wb7.jpgAnti-MINA53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00783-wb8.jpgAnti-MINA53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00783-wb.jpgAnti-MINA53 Rabbit Monoclonal AntibodyWestern blot analysis of MINA53 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pgp9-5-rabbit-monoclonal-antibody-m01018-2-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-pgp95-primary-antibodies-wb-testing-1.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal Antibody Western blot analysis of PGP95 using anti-PGP95 antibody (M01018-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat testis tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGP95 antigen affinity purified monoclonal antibody (Catalog # M01018-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGP95 at approximately 25 kDa. The expected band size for PGP95 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-ihc.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate cancer, using PGP9.5 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-ihc7.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-ihc8.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-ihc9.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human ovarian cancer, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-ihc10.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tonsil, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01018-2-if.jpgAnti-PGP9.5 UCHL1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of U87-MG cells, using PGP9.5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hbg1-2-rabbit-monoclonal-antibody-m02830-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02830-wb7.jpgAnti-HBG1/2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02830-wb.jpgAnti-HBG1/2 Rabbit Monoclonal AntibodyWestern blot analysis of HBG1/2 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyp2e1-rabbit-monoclonal-antibody-m00672-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00672-wb.jpgAnti-CYP2E1 Rabbit Monoclonal AntibodyWestern blot analysis of CYP2E1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00672-cyp2e1-primary-antibodies-ihc-testing-1.jpgAnti-CYP2E1 Rabbit Monoclonal AntibodyIHC analysis of CYP2E1 using anti-CYP2E1 antibody (M00672). <br>CYP2E1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CYP2E1 Antibody (M00672) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atp5a1-rabbit-monoclonal-antibody-m03598-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03598-atp5f1a-primary-antibodies-wb-testing-1.jpgAnti-ATP5A1/Atp5A Rabbit Monoclonal AntibodyWestern blot analysis of ATP5F1A using anti-ATP5F1A antibody (M03598). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified monoclonal antibody (M03598) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ATP5F1A at approximately 50 kDa. The expected band size for ATP5F1A is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03598-icc1.jpgAnti-ATP5A1/Atp5A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03598-icc2.jpgAnti-ATP5A1/Atp5A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fkbp12-rabbit-monoclonal-antibody-m04492-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04492-fkbp1a-primary-antibodies-wb-testing-1.jpgAnti-FKBP12 Rabbit Monoclonal AntibodyWestern blot analysis of FKBP1A using anti-FKBP1A antibody (M04492). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FKBP1A antigen affinity purified monoclonal antibody (M04492) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FKBP1A at approximately 12 kDa. The expected band size for FKBP1A is at 12 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nmdar1-rabbit-monoclonal-antibody-m01808-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01808-wb7.jpgAnti-NMDAR1 GRIN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01808-wb.jpgAnti-NMDAR1 GRIN1 Rabbit Monoclonal AntibodyWestern blot analysis of NMDAR1 expression in mouse brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pabpn1-rabbit-monoclonal-antibody-m02445-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-wb-testing-1.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyWestern blot analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse Raw264.7 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PABPN1 antigen affinity purified monoclonal antibody (M02445) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PABPN1 at approximately 50 kDa. The expected band size for PABPN1 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-ihc-testing-1.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyIHC analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>PABPN1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PABPN1 Antibody (M02445) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-ihc-testing-2.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyIHC analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>PABPN1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PABPN1 Antibody (M02445) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-ihc-testing-3.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyIHC analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>PABPN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PABPN1 Antibody (M02445) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-ihc-testing-4.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyIHC analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>PABPN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PABPN1 Antibody (M02445) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02445-pabpn1-primary-antibodies-ihc-testing-5.jpgAnti-PABPN1 Rabbit Monoclonal AntibodyIHC analysis of PABPN1 using anti-PABPN1 antibody (M02445). <br>PABPN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PABPN1 Antibody (M02445) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-adam10-rabbit-monoclonal-antibody-m00566-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00566-adam10-primary-antibodies-wb-testing-1.jpgAnti-ADAM10 Rabbit Monoclonal Antibody Western blot analysis of ADAM10 using anti-ADAM10 antibody (M00566). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates, <br>
Lane 2: human Hacat whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM10 antigen affinity purified monoclonal antibody (M00566) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM10 at approximately 84 kDa. The expected band size for ADAM10 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00566-adam10-primary-antibodies-ihc-testing-1.jpgAnti-ADAM10 Rabbit Monoclonal AntibodyIHC analysis of ADAM10 using anti-ADAM10 antibody (M00566) . <br> ADAM10 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ADAM10 Antibody (M00566) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00566-adam10-primary-antibodies-ihc-testing-2.jpgAnti-ADAM10 Rabbit Monoclonal AntibodyIHC analysis of ADAM10 using anti-ADAM10 antibody (M00566) . <br> ADAM10 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ADAM10 Antibody (M00566) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00566-adam10-primary-antibodies-ihc-testing-3.jpgAnti-ADAM10 Rabbit Monoclonal AntibodyIHC analysis of ADAM10 using anti-ADAM10 antibody (M00566) . <br> ADAM10 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ADAM10 Antibody (M00566) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00566-adam10-primary-antibodies-ihc-testing-4.jpgAnti-ADAM10 Rabbit Monoclonal AntibodyIHC analysis of ADAM10 using anti-ADAM10 antibody (M00566) . <br> ADAM10 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ADAM10 Antibody (M00566) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-muc5ac-rabbit-monoclonal-antibody-m00612-1-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00612-1-wb.jpgAnti-MUC5AC/Mucin 5Ac Rabbit Monoclonal AntibodyWestern blot analysis of MUC5AC expression in human stomach lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-drosha-rabbit-monoclonal-antibody-m00111-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00111-drosha-primary-antibodies-wb-testing-1.jpgAnti-Drosha Rabbit Monoclonal Antibody Western blot analysis of Drosha using anti-Drosha antibody (M00111). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Drosha antigen affinity purified monoclonal antibody (Catalog # M00111) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Drosha at approximately 159 kDa. The expected band size for Drosha is at 159 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00111-drosha-primary-antibodies-ihc-testing-2.jpgAnti-Drosha Rabbit Monoclonal Antibody IHC analysis of Drosha using anti-Drosha antibody (M00111). <br>
Drosha was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Drosha Antibody (M00111) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00111-drosha-primary-antibodies-ihc-testing-3.jpgAnti-Drosha Rabbit Monoclonal Antibody IHC analysis of Drosha using anti-Drosha antibody (M00111). <br>
Drosha was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Drosha Antibody (M00111) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-snap25-rabbit-monoclonal-antibody-m01625-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-snap25-primary-antibodies-wb-testing-1.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyWestern blot analysis of SNAP25 using anti-SNAP25 antibody (M01625). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse brain tissue lysates,<br>
Lane 2: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNAP25 antigen affinity purified monoclonal antibody (M01625) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SNAP25 at approximately 25 kDa. The expected band size for SNAP25 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-nrr-12-969-g005.jpgAnti-SNAP25 Rabbit Monoclonal AntibodySignificant genes in the spinal cord of rats with spinal cord contusion injury. (A) The fold change shows that SNCB was highest among SNAP-25, PEBP1, SNCB and AQP4 genes. (B) The expression of SNAP-25, PRBP1, SNCB and AQP4. SNAP-25 had the highest expression in both groups based on the gene array. Data are shown as the logarithmic function of 2. (C) Quantitative real time-polymerase chain reaction was used to verify the accuracy of the gene array. The levels of SNAP-25, PRBP1, SNCB and AQP4 were significantly decreased in the SCI group when compared with the sham group, and SNAP-25 was most highly expressed in the two groups. Thus, SNAP-25 was selected for further research in this study. Data are relative to beta-actin. Data are presented as the mean ± SEM and were analyzed using Student's t -test. *** P < 0.001. SCI: Spinal cord injury; SNAP-25: synaptosomal-associated protein 25 kDa; PEBP1: phosphatidylethanolamine binding protein 1; SNCB: beta-synuclein; AQP4: aquaporin 4.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514873/'>28761431</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-nrr-12-969-g006.jpgAnti-SNAP25 Rabbit Monoclonal AntibodySNAP-25 expression in rats with spinal cord injury. (A) SNAP-25 expression in spinal cord tissue of rats detected by quantitative real time-polymerase chain reaction. Data are relative to beta-actin. Data are presented as the mean ± SEM and were analyzed using one-way analysis of variance with Dunnett T3. (B) Western blot assay was used to detect SNAP-25 protein expression in the spinal cord. Data represent the optical density ratio to beta-actin. Data are presented as the mean ± SEM and were analyzed using one-way analysis of variance with the least significant difference. * P < 0.05, vs . sham group. SNAP-25: Synaptosomal-associated protein 25 kDa; d: day(s).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514873/'>28761431</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-nrr-12-969-g008.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyDistribution of SNAP-25 in the posterior horn of spinal cord. Immunohistochemistry was performed to investigate the location of SNAP-25 in the spinal cord of rat. (A) The region of SNAP-25-immunoreactivity located in the posterior horn of spinal cord. The squares correspond to the location of images in B–G. (B–G) A large amount of immunoreactivity was found on axons of neurons and glial cells in the dorsal horn of the spinal cord in both the sham and spinal cord injury groups. Scale bar: 100 μm. Black arrows indicate SNAP-25 immunoreactivity. (H) Quantitative results of the density of SNAP-25 immunoreactivity. Data are presented as the mean ± SEM and were analyzed using one-way analysis of variance with the least significant difference. * P < 0.05, vs . sham group. SNAP-25: Synaptosomal-associated protein 25 kDa; d: day(s).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514873/'>28761431</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-nrr-12-969-g010.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyDistribution and role of SNAP-25 in the anterior horn of spinal cord. (A) SNAP-25 immunoreactivity was located in the anterior horn of spinal cord. The squares correspond to the location of images in B–G. (B–G) Representative images of SNAP-25 immunohistochemistry in the anterior horn of the spinal cord, in which the majority of immunoreactivity was localized in neuronal axons and cytoplasm. Scale bar: 100 μm. Black arrows indicate SNAP-25 immunoreactivity in axons or cytoplasm. (H) Quantitative results of SNAP-25 immunoreactivity. Data are presented as the mean ± SEM and were analyzed using one-way analysis of variance with the least significant difference. * P < 0.05, vs . sham group. SNAP-25: Synaptosomal-associated protein 25 kDa; d: day(s).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514873/'>28761431</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-icc1.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-icc2.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-icc3.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-icc4.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pras40-rabbit-monoclonal-antibody-m03629-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03629-wb.jpgAnti-PRAS40 AKT1S1 Rabbit Monoclonal AntibodyWestern blot analysis of PRAS40 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bnip3l-rabbit-monoclonal-antibody-m03107-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-wb7.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-fphar-16-1526653-g008.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyAEA suppressed elevation of Bnip3. (A) Immunohistochemistry of Bnip3. (B–F) Expression of Nppa, Nppb, Tgfb1, and Bnip3 mRNA. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-fphar-16-1526653-g007.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyAEA improved CHF via PI3K/AKT/Bnip3 axis. (A) Representative images of PI3K/AKT axis. (B, C) The phosphorylation level of PI3K and AKT. (D) Representative images of Opa1, Drp1, Bnip3, p62, Atg5 and LC3II. (E–J) The expression level of Opa1, Drp1, Bnip3, p62, Atg5 and LC3II. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-fphar-16-1526653-g010.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyAEA improved NE-induced injuries via PI3K/AKT/Bnip3 axis. (A) Representative images of PI3K/AKT axis in H9c2 cells. (B, C) The phosphorylation level of PI3K and AKT. (D) Representative images of Opa1, Drp1, TrxR2, Bnip3, p62, Atg5 and LC3II in cells. (E–K) The expression level of Opa1, Drp1, TrxR2, Bnip3, p62, Atg5 and LC3II in H9c2 cells. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-fphar-16-1526653-g011.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyImmunofluorescence of Bnip3, Drp1, and p62 in H9c2 cells. (A) Immunofluorescence of Bnip3. (B) Immunofluorescence of Drp1. (C) Immunofluorescence of p62. (D) Quantitative analysis of Bnip3. (E) Quantitative analysis of Drp1. (F) Quantitative analysis of p62. (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1526653/full'>40206063</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-wb.jpgAnti-BNIP3L/Nix Rabbit Monoclonal AntibodyWestern blot analysis of BNIP3L expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-3.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-4.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-5.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-6.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-7.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-8.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-9.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-10.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-11.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-12.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of mouse adrenal tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-13.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-14.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-15.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-16.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of rat hippocampus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03107-bnip3l-primary-antibodies-ihc-testing-17.jpgAnti-BNIP3L/Nix Rabbit Monoclonal Antibody IHC analysis of BNIP3L using anti-BNIP3L antibody (M03107). <br>BNIP3L was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-BNIP3L Antibody (M03107) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cubilin-rabbit-monoclonal-antibody-m03670-1-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03670-1-wb.jpgAnti-Cubilin CUBN Rabbit Monoclonal AntibodyWestern blot analysis of Cubilin expression in Human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cubilin-rabbit-monoclonal-antibody-m03670-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03670-wb.jpgAnti-Cubilin CUBN Rabbit Monoclonal AntibodyWestern blot analysis of Cubilin expression in Human fetal kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03670-ihc.jpgAnti-Cubilin CUBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Cubilin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-plectin-rabbit-monoclonal-antibody-m01924-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01924-wb.jpgAnti-Plectin Rabbit Monoclonal AntibodyWestern blot analysis of Plectin expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aldh1a1-rabbit-monoclonal-antibody-m01392-1-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01392-1-aldh1a1-primary-antibodies-wb-testing-1.jpgAnti-ALDH1A1 Rabbit Monoclonal AntibodyWestern blot analysis of ALDH1A1 using anti-ALDH1A1 antibody (M01392-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: rat kidney tissue lysates,<br>
Lane 4: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALDH1A1 antigen affinity purified monoclonal antibody (M01392-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALDH1A1 at approximately 50 kDa. The expected band size for ALDH1A1 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01392-1-ihc.jpgAnti-ALDH1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using ALDH1A1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-talin-2-rabbit-monoclonal-antibody-m06080-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06080-wb.jpgAnti-Talin 2 TLN2 Rabbit Monoclonal AntibodyWestern blot analysis of Talin 2 in expression HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspa12a-rabbit-monoclonal-antibody-m13632-boster.html2026-03-24T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13632-wb.jpgAnti-HSPA12A Rabbit Monoclonal AntibodyWestern blot analysis of HSPA12A expression in U-87 MG cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13632-ihc.jpgAnti-HSPA12A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using HSPA12A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dnajc15-rabbit-monoclonal-antibody-m08200-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08200-dnajc15-primary-antibodies-wb-testing-1.jpgAnti-DNAJC15 Rabbit Monoclonal Antibody Western blot analysis of DNAJC15 using anti-DNAJC15 antibody (M08200). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJC15 antigen affinity purified monoclonal antibody (Catalog # M08200) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DNAJC15 at approximately 16 kDa. The expected band size for DNAJC15 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08200-wb.jpgAnti-DNAJC15 Rabbit Monoclonal AntibodyWestern blot analysis of DNAJC15 expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08200-ihc.jpgAnti-DNAJC15 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma, using DNAJC15 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p16-arc-rabbit-monoclonal-antibody-m02096-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02096-arpc5-primary-antibodies-wb-testing-1.jpgAnti-p16 ARC ARPC5 Rabbit Monoclonal AntibodyWestern blot analysis of ARPC5 using anti-ARPC5 antibody (M02096). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: rat spleen tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse spleen tissue lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARPC5 antigen affinity purified monoclonal antibody (M02096) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ARPC5 at approximately 16 kDa. The expected band size for ARPC5 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02096-ihc.jpgAnti-p16 ARC ARPC5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using p16 ARC Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-darpp32-rabbit-monoclonal-antibody-m03424-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03424-ppp1r1b-primary-antibodies-wb-testing-1_1.jpgAnti-DARPP32 PPP1R1B Rabbit Monoclonal Antibody Western blot analysis of PPP1R1B using anti-PPP1R1B antibody (M03424). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1R1B antigen affinity purified monoclonal antibody (Catalog # M03424) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1R1B at approximately 32 kDa. The expected band size for PPP1R1B is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-insulin-rabbit-monoclonal-antibody-m00067-1-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00067-1-ihc.jpgAnti-Insulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse pancreas, using Insulin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00067-1-insulin-primary-antibodies-if-testing-1.jpgAnti-Insulin Rabbit Monoclonal AntibodyIF analysis of Insulin using anti-Insulin antibody (M00067-1). <br>
Insulin was detected in an immunocytochemical section of Beta-TC-6 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 rabbit anti-Insulin Antibody (M00067-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gata2-3-rabbit-monoclonal-antibody-m01415-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01415-gata2-3-primary-antibodies-wb-testing-1.jpgAnti-GATA2/3 Rabbit Monoclonal AntibodyWestern blot analysis of GATA2/3 using anti-GATA2/3 antibody (M01415). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATA2/3 antigen affinity purified monoclonal antibody (M01415) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GATA2/3 at approximately 51 kDa. The expected band size for GATA2/3 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01415-ihc.jpgAnti-GATA2/3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using GATA2/3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01415-if.jpgAnti-GATA2/3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562 cells, using GATA2/3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-midkine-rabbit-monoclonal-antibody-m01823-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-wb.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodyWestern blot analysis of Midkine expression in Midkine Recombinant protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-fimmu-16-1546382-g003.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodySingle-cell communication networks. (A) Incoming communication patterns of target cells, showing pathways to which each cell type responds. (B) Outgoing communication patterns of secreting cells, illustrating the pathways through which cells send signals, MIF, MK and CXCL pathway exhibit high activity. (C) Network diagram showing the strength of intercellular communication, with connections between various cell types. (D) Scatter plot comparing outgoing and incoming communication strengths across cell populations, with bubble size indicating the number of interactions, malignant cells have higher strength of intercellular communication. (E) Chord diagram depicting communication via the MK pathway between different cell types. (F) Ligand-receptor interaction probabilities within the MK pathway between malignant and other cell types. Dot size represents significance (P-value), and color represents communication probability highlighting the MDK-NCL signaling pathway. (G) Violin plots of MK pathway gene expression levels across cell types, showing gene activity variations, MDK has advancer expression level in malignant cells.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12089103/'>40396179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-fimmu-16-1546382-g004.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodySpatial transcriptomics and MDK-NCL signal communication. (A) Niche clustering in spatial transcriptomics samples, identifying distinct ecological zones. (B) Spatial expression of representative markers in key regions: MUC1 (tumor region), LYZ (immune region), COL14A1 (stromal region), and SFTPC (normal region). (C) Violin plots displaying the expression of MUC1, LYZ, COL14A1, and SFTPC across different niches. (D) MCPcounter analysis showing the infiltration of six cell types (e.g., endothelial cells, fibroblasts, immune lineages) across spatial regions. (E) Spatial niche classification, distinguishing tumor, immune-stromal, and normal regions. (F) MDK-NCL ligand-receptor interaction analysis, spatially mapping MDK ligands, NCL receptors, and their binding regions.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12089103/'>40396179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-fimmu-16-1546382-g005.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodySingle-cell pseudotime analysis. (A) Pseudotime trajectory analysis showing the 6 differentiation states of cells. (B) Subtype classification of malignant cells along the pseudotime trajectory. (C) Pseudotime scores mapped along the differentiation trajectory. (D) UMAP plot visualizing pseudotime scores across individual cells. (E) Box plots comparing pseudotime scores across different malignant cell clusters, cluster 0, 1, and 5 had higher pseudotime scores. (F) UMAP plot of differentiation states, with colors representing distinct states. (G) Stacked bar plots showing the proportion of differentiation states within each malignant cell cluster, cluster 0, 1, and 5 have larger proportion of state 6. (H) Expression dynamics of MK pathway genes (e.g., MDK, NCL, ITG genes) along the pseudotime trajectory, highlighting gene expression changes during differentiation, MDK and NCL express more in the later time.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12089103/'>40396179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-fimmu-16-1546382-g006.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodyAssociation of MDK-NCL with the immune microenvironment. (A) Boxplot shows the expression levels of MDK and NCL genes in tumor and control groups, it exhibit higher activity in tumor group. (B) MDK-NCL enrichment scores in tumor and control groups. (C) Relative mRNA expression levels of MDK and NCL in tumor and control groups from in-house data. (D) Relative protein expression levels of MDK and NCL in tumor and control groups from in-house data. (E) Comparison of MDK protein expression levels between tumor and control groups. (F) Comparison of NCL protein expression levels between tumor and control groups. (G) Correlation of MDK and NCL expression with ImmuneScore, StromalScore, ESTIMATEScore, and TumorPurity. (H) Scatter plots depicting the relationship between MDK and NCL expression and immune-related scores (ImmuneScore, StromalScore, ESTIMATEScore) as well as TumorPurity. (I) Comparison of immune cell infiltration scores across high and low MDK-NCL expression groups for 28 immune cell types. *P < 0.05, **P < 0.01, ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12089103/'>40396179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-fimmu-16-1546382-g007.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodyAssociation of MDK-NCL with immunotherapy response. (A) Comparison of tumor mutation burden (TMB) between high and low MDK-NCL expression groups. (B) Comparison of microsatellite instability (MSI) between high and low MDK-NCL groups. (C) Comparison of dysfunction scores between high and low MDK-NCL groups. (D) Comparison of exclusion scores between high and low MDK-NCL groups. (E) Expression of immunogenic cell death (ICD)-related genes in high and low MDK-NCL groups. (F) Expression levels of CTLA4 and PD1 in high and low MDK-NCL groups. (G) Comparison of immune checkpoint gene expression between high and low MDK-NCL expression groups. *P < 0.05, **P < 0.01, ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12089103/'>40396179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01823-ihc.jpgAnti-Midkine MDK Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver carcinoma, using Midkine Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tuberin-rabbit-monoclonal-antibody-m00229-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229-wb.jpgAnti-Tuberin TSC2 Rabbit Monoclonal AntibodyWestern blot analysis of Tuberin expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229-ihc.jpgAnti-Tuberin TSC2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate carcinoma, using Tuberin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-islet-1-rabbit-monoclonal-antibody-m02969-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02969-isl1-primary-antibodies-wb-testing-1.jpgAnti-Islet 1 Rabbit Monoclonal Antibody Western blot analysis of Islet 1 using anti-Islet 1 antibody (M02969). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Islet 1 antigen affinity purified monoclonal antibody (Catalog # M02969) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Islet 1 at approximately 39 kDa. The expected band size for Islet 1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02969-isl1-primary-antibodies-ihc-testing-1.jpgAnti-Islet 1 Rabbit Monoclonal AntibodyIHC analysis of ISL1 using anti-ISL1 antibody (M02969). <br>ISL1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ISL1 Antibody (M02969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02969-isl1-primary-antibodies-ihc-testing-2.jpgAnti-Islet 1 Rabbit Monoclonal AntibodyIHC analysis of ISL1 using anti-ISL1 antibody (M02969). <br>ISL1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ISL1 Antibody (M02969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02969-isl1-primary-antibodies-ihc-testing-3.jpgAnti-Islet 1 Rabbit Monoclonal AntibodyIHC analysis of ISL1 using anti-ISL1 antibody (M02969). <br>ISL1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ISL1 Antibody (M02969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hnrnp-k-rabbit-monoclonal-antibody-m01793-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-wb-testing-1.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyWestern blot analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HNRNPK antigen affinity purified monoclonal antibody (M01793) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HNRNPK at approximately 60 kDa. The expected band size for HNRNPK is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-1.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-2.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-3.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-4.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-5.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-6.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-7.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-8.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-9.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-10.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-11.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01793-hnrnpk-primary-antibodies-ihc-testing-12.jpgAnti-hnRNP K Rabbit Monoclonal AntibodyIHC analysis of HNRNPK using anti-HNRNPK antibody (M01793). <br>HNRNPK was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPK Antibody (M01793) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-radixin-rabbit-monoclonal-antibody-m01926-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01926-rdx-primary-antibodies-wb-testing-1.jpgAnti-Radixin Rabbit Monoclonal Antibody Western blot analysis of Radixin using anti-Radixin antibody (M01926). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HUVEC whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Radixin antigen affinity purified monoclonal antibody (Catalog # M01926) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Radixin at approximately 80 kDa. The expected band size for Radixin is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01926-radixin-primary-antibodies-ihc-testing-2.jpgAnti-Radixin Rabbit Monoclonal Antibody IHC analysis of smc4 using anti-smc4 antibody (M01926). <br>
smc4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-smc4 Antibody (M01926) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hla-dra-rabbit-monoclonal-antibody-m01195-2-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-hla-dra-primary-antibodies-wb-testing-1.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal Antibody Western blot analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HLA-DRA antigen affinity purified monoclonal antibody (Catalog # M01195-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HLA-DRA at approximately 36 kDa. The expected band size for HLA-DRA is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-wb7.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-hla-dra-primary-antibodies-ihc-testing-2.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal Antibody IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-2). <br>
HLA-DRA was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HLA-DRA Antibody (M01195-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-if.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal AntibodyImmunofluorescent analysis of Raji cells, using HLA-DRA Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-hla-dra-primary-antibodies-ihc-testing-3.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal Antibody IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-2). <br>
HLA-DRA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HLA-DRA Antibody (M01195-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-hla-dra-primary-antibodies-ihc-testing-4.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal Antibody IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-2). <br>
HLA-DRA was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HLA-DRA Antibody (M01195-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-2-hla-dra-primary-antibodies-ihc-testing-5.jpgAnti-HLA-DRA/Hla Dr Rabbit Monoclonal Antibody IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-2). <br>
HLA-DRA was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HLA-DRA Antibody (M01195-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-adipor1-rabbit-monoclonal-antibody-m01869-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-wb7.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-ihc.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using ADIPOR1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-fcell-09-762335-g006.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyMechanisms for local medulla injection of ADPN promoting bone healing. (A) Serum Osteoprotegerin (OPG) levels at weeks 2, 4, and 6. (B) WB analysis of alkaline phosphatase (ALP), bone morphogenic protein 2 (BMP-2), osteocalcin (OCN), and adiponectin receptor 1 (AdipoR1) expressions with corresponding quantification, (C) Immunofluorescent staining of ALP, OCN, BMP-2, and AdipoR1 in G2 (ADPN 1 mg/kg) and G3 (ADPN 2 mg/kg), and the corresponding quantification, n = 5. The white arrow indicates the periosteum, and the blue arrow indicates the lacuna, scale bar = 100 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2021.762335/full'>34790669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-fcell-09-762335-g007.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyThe immunofluorescent staining of ALP, OCN, BMP-2, and AdipoR1 on BMSCs with ADPN 10 μg/ml and AdipoR1 siRNA + ADPN 10 μg/ml, and the corresponding quantification, scale bar = 100 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2021.762335/full'>34790669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-12974_2019_1492_fig1_html.pngAnti-ADIPOR1 Rabbit Monoclonal AntibodyExpression of AdipoR1 and AdipoR2 in BV2 cells and microglia in mice brain. a RT-PCR analysis of AdipoR1 and AdipoR2 in BV2 cells. b Western blot analysis of AdipoR1 and AdipoR2 expression in BV2 cells. Expression of AdipoR1 and AdipoR2 from cerebral cortex homogenates was used as a positive control. α-Tubulin was used as a loading control. c , d Co-immunocytochemistry staining of microglia (Iba1) and AdipoR1 or AdipoR2 in BV2 cells and microglia in the cortex of WT mice. Scale bar 50 μm <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12974-019-1492-6'>31128596</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-12974_2019_1492_fig4_html.pngAnti-ADIPOR1 Rabbit Monoclonal AntibodyAPN suppressed AβO-induced proinflammatory cytokine release in BV2 cells via AdipoR1. a , b Representative Western blot analysis of AdipoR1 and AdipoR2. BV2 cells were transfected with control siRNA, AdipoR1 siRNA, or AdipoR2 siRNA in a concentration-dependent manner (25, 50, 100 nM). c , d ELISA assays of TNFα and IL-1β were conducted after knockdown of AdipoR1. e , f ELISA assays of TNFα and IL-1β were conducted after knockdown of AdipoR2. Data were presented as the mean ± SEM for at least three independent experiments, and each performed in duplicates ( n = 3). Two-way ANOVA with Tukey’s multiple comparison test revealed a difference between groups . *p < 0.05, **p < 0.01, ***p < 0.001; ns, statistically not significant <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12974-019-1492-6'>31128596</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-wb8.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01869-wb.jpgAnti-ADIPOR1 Rabbit Monoclonal AntibodyWestern blot analysis of ADIPOR1 expression in Human heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nedd4-2-rabbit-monoclonal-antibody-m01595-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01595-nedd4l-primary-antibodies-wb-testing-1.jpgAnti-NEDD4-2 NEDD4L Rabbit Monoclonal Antibody Western blot analysis of NEDD4L using anti-NEDD4L antibody (M01595). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NEDD4L antigen affinity purified monoclonal antibody (Catalog # M01595) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NEDD4L at approximately 130 kDa. The expected band size for NEDD4L is at 112 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01595-nedd4l-primary-antibodies-wb-testing-2.pngAnti-NEDD4-2 NEDD4L Rabbit Monoclonal AntibodyWestern blot analysis of NEDD4-2 expression in mouse spleen tissue.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tnfaip3-rabbit-monoclonal-antibody-m00224-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-tnfaip3-primary-antibodies-wb-testing-1.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal Antibody Western blot analysis of TNFAIP3 using anti-TNFAIP3 antibody (M00224). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Caco-2 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNFAIP3 antigen affinity purified monoclonal antibody (M00224) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TNFAIP3 at approximately 82 kDa. The expected band size for TNFAIP3 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-fnins-13-00347-g001.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodymiR-873a-5p is upregulated, while A20 is downregulated in the spinal cord of morphine-tolerant (MT) mice. (A) Morphine-induced antinociception was assessed by the tail-flick test. Tail-flick latency was converted to MPE%. n = 8, ∗∗∗ P < 0.001 compared with the NS group. (B) Real-time qPCR showed that miR-873a-5p expression increased in the morphine group 3, 5, and 7 days after chronic morphine administration, especially on day 7 compared to the expression in the control group. Data are expressed as the mean ± SD, n = 6 mice per group, ∗∗ P < 0.01. (C) The staining of miR-873a-5p in the spinal cord, Scale bar = 100 μm. (D) Changes in the A20 protein expression level in the L4-L6 spinal cord were gradually decreased after the development of morphine tolerance, especially on day 7. n = 4 mice per group. Samples were collected on days 3, 5, and 7 following chronic morphine injection, ∗ P < 0.05, ∗∗ P < 0.01. (E) miR-873a-5p was assessed by in situ hybridization and staining of miR-873a-5p (red) with neurons (green, identified using NeuN), astrocytes (green, identified using GFAP) and microglia (green, identified using Iba1) of the spinal cord in morphine-tolerant mice. The data showed that miR-873a-5p was mainly expressed in neurons and astrocytes, whereas no expression was observed in microglia. Scale bar = 100 μm. Samples were collected on day 7 following chronic morphine injection.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fnins.2019.00347/full'>31024249</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-fnins-13-00347-g002.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodymiR-873a-5p directly targets the A20 3′-UTR. (A) The 3′-UTR sequences of A20 containing the miR-873a-5p target regions and the binding sites of miR-873a-5p with the target sequence are well conserved among mammals. The binding site sequence is indicated in red bold letters. (B) Diagram of the seed sequence of miR-873a-5p matching the 3′-UTR of A20. Positions of the mutated nucleotides in miR-873a-5p and the 3′-UTR of A20. (C) The decreased luciferase activity induced by transfection with miR-873a-5p mimics was completely reversed by the mutant A20 3′-UTR vector. Data are expressed as the means ± SD, ∗∗∗ P < 0.001, n = 6. (D) MiR-873a-5p costaining with A20 in the spinal cord. Samples were collected on day 7 following chronic morphine injection, n = 3, scale bars = 100 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fnins.2019.00347/full'>31024249</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-fnins-13-00347-g003.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodyDownregulated miR-873a-5p significantly attenuates and partly reverses morphine tolerance in mice. (A) Preintrathecal injection of the miR-873a-5p antagomir for 3 consecutive days (from days 1 to 3 when morphine was injected) attenuated morphine-induced tolerance. n = 10, ∗∗∗ P < 0.001 vs. the MT + control (pre) group. (B) Postintrathecal injection of the miR-873a-5p antagomir for 3 consecutive days (from days 5 to 7 after morphine injection) significantly reversed morphine-induced analgesic tolerance. n = 8, ∗∗∗ P < 0.001 vs. the MT + control group. (C) The validation of miR-873a-5p antagomir transfection efficiency in vivo was tested by RT-qPCR. The MT + antagomir group had significantly lower miR-873a-5p expression than the MT + control group. n = 5, ∗∗∗ P < 0.001 vs. the NS group; ∗ P < 0.05 vs. the MT + control group. (D) RT-qPCR showing that miR-873a-5p antagomir administration reversed A20 mRNA expression in the spinal cord. (E,F) Western blot demonstrating that miR-873a-5p antagomir administration reversed A20 protein expression levels and downregulated p-NF-κB. n = 4, ∗∗ P < 0.01, ∗∗∗ P < 0.001 vs. the NS group; ∗ P < 0.05, ∗∗ P < 0.01 vs. the MT + control group. (G) In situ hybridization staining of miR-873a-5p in the spinal cord from the NS, MT + control and MT + antagomir groups. Images showing that miR-873a-5p expression was significantly downregulated in the mice treated with the antagomir; n = 3 mice per group, ∗∗ P < 0.01, vs. the NS group; ∗ P < 0.05 vs. the MT + control group, scale bars = 100 μm. Samples were collected 4 days after antagomir administration.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fnins.2019.00347/full'>31024249</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-fnins-13-00347-g004.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodyOverexpressed A20 prevents and reverses morphine tolerance in mice. (A) Mice were pretreated with the LV-control or LV-A20 vector before morphine tolerance was established. MT + LV-A20 (pre) treatment prevented the development of morphine tolerance compared with MT-LV-control (pre) treatment. n = 10, ∗∗∗ P < 0.001 compared with the MT + LV-control (pre) group. (B) Mice were injected with morphine twice a day for 15 consecutive days, and LV-control vector or LV-A20 vector was administered on day 7 after the establishment of morphine tolerance. MT + LV-A20 treatment attenuated morphine tolerance compared with MT + LV-control treatment. n = 10, ∗∗∗ P < 0.001 compared with the MT + LV-control group. (C) Image of enhanced green fluorescent immunofluorescence in the spinal cord after injection of LV-A20 or LV-control, indicating that the lentivirus was successfully transfected. n = 3, scale bars = 100 μm. (D,E) MT + LV-A20 upregulated A20 protein expression levels after lentiviral LV-A20 was injected. n = 4, ∗∗ P < 0.01 compared with the NS group, ∗∗ P < 0.01 compared with MT + LV-control. (D,F) p-NF-κB was significantly decreased when A20 was upregulated in the MT + LV-A20 group. n = 4, ∗ P < 0.05 compared with the NS group, ∗ P < 0.05 compared with MT + LV-control. Samples were collected 8 days after lentiviral vector administration.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fnins.2019.00347/full'>31024249</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-fnins-13-00347-g005.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodymiR-873a-5p targets A20 to participate in morphine tolerance in mice. (A) Staining of the spinal cord for A20 (green), neurons using the NeuN antibody (red), astrocytes using the GFAP antibody (red), and microglia using the Iba1 antibody (red) in morphine-tolerant mice. A20 was mainly expressed in neurons and astrocytes and barely expressed in microglia. Scale bars = 100 μm. (B) GFP was detected in HT22 cells after transfection with lentivirus LV-shA20 and LV-NC (control); scale bars = 100 μm. (C) Western blot analysis showed that A20 protein expression was significantly decreased in HT22 cells after lentivirus (LV-shA20) transfection; n = 3, ∗∗ P < 0.01 compared with the LV-NC group. (D) A20 is responsible for miR-873a-5p-mediated morphine tolerance in mice. LV-shA20 or LV-NC was intrathecally injected on day 1 with morphine injection, and the miR-873a-5p antagomir was intrathecally injected on day 9 when chronic morphine tolerance was established. MT + LV-shA20 or LV-NC was intrathecally injected 7 days before morphine was first injected, and the miR-873a-5p antagomir was intrathecally injected from days 9 to 11. n = 8, ∗∗ P < 0.01, ∗∗∗ P < 0.001 compared with the MT + LV-NC + antagomir group. ## P < 0.01, ### P < 0.001 compared with the MT + LV-shA20 + NS group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fnins.2019.00347/full'>31024249</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-ihc.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using TNFAIP3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00224-if.jpgAnti-TNFAIP3/A20 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Histone H3 (di methyl K9) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ppp1r1a-rabbit-monoclonal-antibody-m11390-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11390-wb8.jpgAnti-PPP1R1A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11390-ppp1r1a-primary-antibodies-wb-testing-1.jpgAnti-PPP1R1A Rabbit Monoclonal Antibody Western blot analysis of PPP1R1A using anti-PPP1R1A antibody (M11390). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: mouse brain tissue lysates, <br>
Lane 3: rat small intestine tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1R1A antigen affinity purified monoclonal antibody (M11390) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1R1A at approximately 27 kDa. The expected band size for PPP1R1A is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11390-ppp1r1a-primary-antibodies-ihc-testing-2.jpgAnti-PPP1R1A Rabbit Monoclonal Antibody IHC analysis of PPP1R1A using anti-PPP1R1A antibody (M11390) . <br> PPP1R1A was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PPP1R1A Antibody (M11390) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11390-ppp1r1a-primary-antibodies-ihc-testing-3.jpgAnti-PPP1R1A Rabbit Monoclonal Antibody IHC analysis of PPP1R1A using anti-PPP1R1A antibody (M11390) . <br> PPP1R1A was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PPP1R1A Antibody (M11390) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11390-ppp1r1a-primary-antibodies-ihc-testing-4.jpgAnti-PPP1R1A Rabbit Monoclonal Antibody IHC analysis of PPP1R1A using anti-PPP1R1A antibody (M11390) . <br> PPP1R1A was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PPP1R1A Antibody (M11390) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sumo2-3-rabbit-monoclonal-antibody-m01282-2-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-wb7.jpgAnti-Sumo2/3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-wb.jpgAnti-Sumo2/3 Rabbit Monoclonal AntibodyWestern blot analysis of Sumo2/3 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-3.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-4.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-5.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-6.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-7.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-8.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-9.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01282-2-sumo2-3-primary-antibodies-ihc-testing-10.jpgAnti-Sumo2/3 Rabbit Monoclonal Antibody IHC analysis of SUMO2/3 using anti-SUMO2/3 antibody (M01282-2). <br>SUMO2/3 was detected in a paraffin-embedded section of human baldder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-SUMO2/3 Antibody (M01282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100a10-rabbit-monoclonal-antibody-m02787-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02787-wb.jpgAnti-S100A10 Rabbit Monoclonal AntibodyWestern blot analysis of S100A10 expression in (1) A431 cell lysate; (2) RAW264.7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dcamkl1-rabbit-monoclonal-antibody-m03089-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03089-dclk1-primary-antibodies-wb-testing-1.jpgAnti-DCAMKL1 Rabbit Monoclonal Antibody Western blot analysis of DCLK1 using anti-DCLK1 antibody (M03089). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DCLK1 antigen affinity purified monoclonal antibody (M03089) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DCLK1 at approximately 82 kDa. The expected band size for DCLK1 is at 82 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-neurod1-rabbit-monoclonal-antibody-m01038-boster.html2026-03-24T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01038-wb7.jpgAnti-NeuroD1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01038-wb.jpgAnti-NeuroD1 Rabbit Monoclonal AntibodyWestern blot analysis of NeuroD1 expression in Y79 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-drebrin-rabbit-monoclonal-antibody-m05530-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05530-dbn1-primary-antibodies-wb-testing-1.jpgAnti-Drebrin DBN1 Rabbit Monoclonal Antibody Western blot analysis of DBN1 using anti-DBN1 antibody (M05530). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DBN1 antigen affinity purified polyclonal antibody (Catalog # M05530) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DBN1 at approximately 120 kDa. The expected band size for DBN1 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05530-wb10.jpgAnti-Drebrin DBN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05530-wb7.jpgAnti-Drebrin DBN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05530-wb.jpgAnti-Drebrin DBN1 Rabbit Monoclonal AntibodyWestern blot analysis of Drebrin expression in (1) HeLa cell lysate; (2) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atg16l1-rabbit-monoclonal-antibody-m00526-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00526-atg16l1-primary-antibodies-wb-testing-1.jpgAnti-Atg16L1/Atg16 Rabbit Monoclonal AntibodyWestern blot analysis of ATG16L1 using anti-ATG16L1 antibody (M00526). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human Daudi whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATG16L1 antigen affinity purified monoclonal antibody (M00526) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ATG16L1 at approximately 68 kDa. The expected band size for ATG16L1 is at 68 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lamin-b1-rabbit-monoclonal-antibody-m02778-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-wb.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyAll lanes use Lamin B1 Antibody at 1:10000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-wb2.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyAll lanes use Lamin B1 Antibody at 1:20000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-wb3.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyAll lanes use Lamin B1 Antibody at 1:10000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02778-LMNB1-primary-antibodies-IHC-testing-1.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat liver, using Lamin B1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-ihc7.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat ovary, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-ihc8.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human non-Hodgkin's lymphoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-ihc9.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-ihc10.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-lmnb1-primary-antibodies-if-testing-3.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using Lamin B1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02778-icc1.jpgAnti-Lamin B1 LMNB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aurora-b-rabbit-monoclonal-antibody-m00762-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-wb-testing-1.jpgAnti-Aurora B AURKB Rabbit Monoclonal Antibody Western blot analysis of Aurora B using anti-Aurora B antibody (M00762-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human U251 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Aurora B antigen affinity purified monoclonal antibody (Catalog # M00762-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Aurora B at approximately 39 kDa. The expected band size for Aurora B is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-ihc-testing-2.jpgAnti-Aurora B AURKB Rabbit Monoclonal Antibody IHC analysis of AURKB using anti-AURKB antibody (M00762-1). <br>
AURKB was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AURKB Antibody (M00762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-ihc-testing-3.jpgAnti-Aurora B AURKB Rabbit Monoclonal Antibody IHC analysis of AURKB using anti-AURKB antibody (M00762-1). <br>
AURKB was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AURKB Antibody (M00762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-ihc-testing-4.jpgAnti-Aurora B AURKB Rabbit Monoclonal AntibodyIHC analysis of AURKB using anti-AURKB antibody (M00762-1). <br>
AURKB was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AURKB Antibody (M00762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-ihc-testing-5.jpgAnti-Aurora B AURKB Rabbit Monoclonal AntibodyIHC analysis of AURKB using anti-AURKB antibody (M00762-1). <br>
AURKB was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AURKB Antibody (M00762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00762-1-aurkb-primary-antibodies-ihc-testing-6.jpgAnti-Aurora B AURKB Rabbit Monoclonal AntibodyIHC analysis of AURKB using anti-AURKB antibody (M00762-1). <br>
AURKB was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-AURKB Antibody (M00762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-er-alpha-rabbit-monoclonal-antibody-m00057-2-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb7.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb10.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb8.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb11.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb9.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-wb.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyWestern blot analysis of ER alpha expression in (1) MCF7 cell lysate; (2)T47-D cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-er-alpha-primary-antibodies-wb-testing-1.pngAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyWestern blot analysis of ER alpha using anti-ER alpha antibody (M00057-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: control group-mouse brain tissue lysates,<br>
Lane 2: model group-model mouse brain tissue lysates,<br>
Lane 3: high dose A medicine treated group-model mouse brain tissue lysates,<br>
Lane 4: low dose A medicine treated group-model mouse brain tissue lysates,<br>
Lane 5: high dose B medicine treated group-model mouse brain tissue lysates,<br>
Lane 6: low dose B medicine treated group-model mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ER alpha antigen affinity purified monoclonal antibody (M00057-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:2000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for ER alpha at approximately 70 kDa. The expected band size for ER alpha is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-ihc.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix carcinoma, using ER alpha Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00057-2-if.jpgAnti-ER alpha ESR1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using ER alpha Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-survivin-rabbit-monoclonal-antibody-m00379-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-1-birc5-primary-antibodies-wb-testing-1.jpgAnti-Survivin BIRC5 Rabbit Monoclonal Antibody Western blot analysis of BIRC5 using anti-BIRC5 antibody (M00379-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: human U20S whole cell lysates,<br>
Lane 6: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BIRC5 antigen affinity purified monoclonal antibody (Catalog # M00379-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BIRC5 at approximately 16 kDa. The expected band size for BIRC5 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-1-ihc.jpgAnti-Survivin BIRC5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human gastric carcinoma, using Survivin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-1-if.jpgAnti-Survivin BIRC5 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Survivin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-1-icc1.jpgAnti-Survivin BIRC5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vimentin-rabbit-monoclonal-antibody-m00235-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-wb-testing-1.jpgAnti-Vimentin Rabbit Monoclonal Antibody Western blot analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vimentin antigen affinity purified monoclonal antibody (Catalog # M00235-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vimentin at approximately 54 kDa. The expected band size for Vimentin is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-41467_2023_41529_fig5_html.pngAnti-Vimentin Rabbit Monoclonal AntibodyTherapeutic potentials of Pg-Fe-hMSC in both monocellular and multicellular humanized fibrotic models. a Schematic illustration and representative image of EpCAM immunostaining in primary human lung epithelial cells (hLECs). Scale bar, 50 μm. b Mitochondrial transfer rates from the indicated hMSC to the primary hLEC ( n = 3 biologically independent cells). c Relative intracellular ROS levels ( n = 3 biologically independent cells), d TGF- β expression levels ( n = 4 biologically independent cells), and e Viability of BLM-treated hLEC after the indicated treatment using different engineered hMSCs ( n = 3 biologically independent cells). f Schematic illustration showing the preparation of the 3D multicellular human fibrotic model. g Representative immunostaining images showing the expression of α -smooth muscle actin ( α -SMA), vimentin, collagen-I, and Ki-67 in the healthy and fibrotic multicellular human spheroid models. Blue fluorescent signals indicate the cell nuclei and green signals indicate the biomarkers. Scale bar, 20 μm. h Mitochondrial transfer rates of different engineered hMSC in fibrotic human lung spheroids ( n = 3 biologically independent experiments). i Relative intracellular ROS levels ( n = 3 biologically independent experiments) and j TGF- β expression levels of fibrotic human lung spheroids after the indicated treatment using different engineered hMSCs ( n = 4 biologically independent experiments). k Viability of fibrotic human lung spheroids after the indicated treatment using different engineered hMSCs ( n = 3 biologically independent experiments). Data are presented as means ± SD. Statistical significance was analyzed using ordinary one-way ANOVA. ECs epithelial cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-023-41529-7'>37723135</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-2.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-3.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-4.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-5.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human non small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-6.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-7.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-8.jpgAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin using anti-Vimentin antibody (M00235-1). <br>
Vimentin was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Vimentin Antibody (M00235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-9.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-10.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-11.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-12.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-13.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-14.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-15.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-16.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-ihc-testing-17.pngAnti-Vimentin Rabbit Monoclonal Antibody IHC analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-18.jpgAnti-Vimentin Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Vimentin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-19.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-20_1.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-21.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-22.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human liver caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-23.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human lung caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-24.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human thyroid caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-25.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human cervical caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-26.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human pancreatic caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235-1-vimentin-primary-antibodies-if-testing-27.pngAnti-Vimentin Rabbit Monoclonal Antibody IF analysis of Vimentin/VIM using anti-Vimentin/VIM antibody (M00235-1). <br>
Vimentin/VIM was detected in a paraffin-embedded section of human stomach caner tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 25 μg/mL rabbit anti-Vimentin/VIM Antibody (M00235-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vinculin-rabbit-monoclonal-antibody-m01207-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01207-vinculin-primary-antibodies-wb-testing-1.jpgAnti-Vinculin VCL Rabbit Monoclonal Antibody Western blot analysis of Vinculin using anti-Vinculin antibody (M01207). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vinculin antigen affinity purified monoclonal antibody (Catalog # M01207) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vinculin at approximately 124 kDa. The expected band size for Vinculin is at 124 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01207-vinculin-primary-antibodies-ihc-testing-2.jpgAnti-Vinculin VCL Rabbit Monoclonal Antibody IHC analysis of Vinculin using anti-Vinculin antibody (M01207). <br>
Vinculin was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Vinculin Antibody (M01207) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01207-vinculin-primary-antibodies-ihc-testing-3.jpgAnti-Vinculin VCL Rabbit Monoclonal Antibody IHC analysis of Vinculin using anti-Vinculin antibody (M01207). <br>
Vinculin was detected in a paraffin-embedded section of human renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Vinculin Antibody (M01207) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01207-if.jpgAnti-Vinculin VCL Rabbit Monoclonal AntibodyImmunofluorescent analysis of A673 cells, using Vinculin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-torsin-a-rabbit-monoclonal-antibody-m01381-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01381-wb7.jpgAnti-Torsin A TOR1A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01381-wb8.jpgAnti-Torsin A TOR1A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01381-wb.jpgAnti-Torsin A TOR1A Rabbit Monoclonal AntibodyWestern blot analysis of Torsin A expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calponin-rabbit-monoclonal-antibody-m08065-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08065-1-cnn1-primary-antibodies-wb-testing-1.jpgAnti-Calponin CNN1 Rabbit Monoclonal Antibody Western blot analysis of CNN1 using anti-CNN1 antibody (M08065-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: mouse stomach tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CNN1 antigen affinity purified monoclonal antibody (Catalog # M08065-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CNN1 at approximately 35 kDa. The expected band size for CNN1 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08065-1-wb9.jpgAnti-Calponin CNN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08065-1-calponin-primary-antibodies-ihc-testing-2.jpgAnti-Calponin CNN1 Rabbit Monoclonal AntibodyIHC analysis of Calponin using anti-Calponin antibody (M08065-1). <br>
Calponin was detected in a paraffin-embedded section of human appendicitis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Calponin Antibody (M08065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-paxillin-rabbit-monoclonal-antibody-m01033-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01033-pxn-primary-antibodies-wb-testing-1.jpgAnti-Paxillin PXN Rabbit Monoclonal AntibodyWestern blot analysis of PXN using anti-PXN antibody (M01033). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PXN antigen affinity purified monoclonal antibody (M01033) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PXN at approximately 65 kDa. The expected band size for PXN is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01033-ihc.jpgAnti-Paxillin PXN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Paxillin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il1-beta-rabbit-monoclonal-antibody-m00101-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-1-wb.jpgAnti-IL1 beta Rabbit Monoclonal AntibodyWestern blot analysis of extracts from recombinant IL1 beta, using IL1 beta antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-1-il1beta-primary-antibodies-wb-testing-1.pngAnti-IL1 beta Rabbit Monoclonal AntibodyWestern blot analysis of IL1 beta using anti-IL1 beta antibody (M00101-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-6: Mouse PACs whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1 beta antigen affinity purified polyclonal antibody (M00101-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL1 beta at approximately 30 kDa. The expected band size for IL1 beta is at 30.7 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p95-nbs1-rabbit-monoclonal-antibody-m00732-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-nbn-primary-antibodies-wb-testing-1.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal Antibody Western blot analysis of NBN using anti-NBN antibody (M00732). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NBN antigen affinity purified monoclonal antibody (Catalog # M00732) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NBN at approximately 95 kDa. The expected band size for NBN is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc10.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc7.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat kidney, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc11.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse heart, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc8.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat heart, using p95/NBS1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-ihc9.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00732-icc1.jpgAnti-p95/NBS1 NBN Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jnk1-2-3-rabbit-monoclonal-antibody-m02608-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-1-jnk1-2-3-primary-antibodies-wb-testing-1.jpgAnti-JNK1/2/3 MAPK8 Rabbit Monoclonal Antibody Western blot analysis of JNK1/2/3 using anti-JNK1/2/3 antibody (M02608-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U87 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JNK1/2/3 antigen affinity purified monoclonal antibody (Catalog # M02608-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for JNK1/2/3 at approximately 40, 48 kDa. The expected band size for JNK1/2/3 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-1-ajcr0006-0924-f6.jpgAnti-JNK1/2/3 MAPK8 Rabbit Monoclonal AntibodySP+N: SP600125+NDV; SP+R: SP600125+rL-RVG. The autophagy induced by rL-RVG was mediated by the IRE1/JNK/beclin-1 signaling pathway. A. For SGC; B. For HGC. The phosphorylation of JNK and bcl-2 was upregulated in the rL-RVG- or NDV-infected SGC and HGC cells. The expression of the autophagy-associated proteins beclin-1 and LC3-II/I decreased in cells after treatment with a specific inhibitor of JNK, or SP600125, compared with cells without the treatment. The same was observed for apoptosis-associated proteins. C. The ultrastructure of the SGC cells after infection with virus or pretreatment with SP600125. rL-RVG infection increased the number of autophagosomes in SGC cells, but the number of rL-RVG-induced autophagosomes was markedly decreased after pretreatment with SP600125.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4889710/&orig_host=www.ncbi.nlm.nih.gov'>27293989</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-1-feb413914-fig-0010-m.jpgAnti-JNK1/2/3 MAPK8 Rabbit Monoclonal AntibodyEffects of OPN and OVE on activation of MAPK signaling pathways in LPS-stimulated RAW264.7 cells. Expression levels of p-ERK, ERK, p-p38, p-38, p-JNK, and JNK were detected in the same samples for COX-2 detection after 24 h of LPS stimulation. (A) OVE treatment. (B) OPN treatment. All experiments were carried out in triplicates and data are presented as means ± SDs; one-way ANOVA analysis was adopted for multiple comparisons; ###P < 0.001, ####P < 0.0001, compared to the untreated control group; ***P < 0.001 and ****P < 0.0001, compared to the LPS control group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://febs.onlinelibrary.wiley.com/doi/abs/10.1002/2211-5463.13914'>39455284</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-1-icc1.jpgAnti-JNK1/2/3 MAPK8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-1-if.jpgAnti-JNK1/2/3 MAPK8 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using JNK1/2/3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-survivin-rabbit-monoclonal-antibody-m00379-2-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00379-2-Birc5-primary-antibodies-WB-testing-1.jpgAnti-Survivin Birc5 Rabbit Monoclonal AntibodyWestern blot analysis of Survivin expression in Neuro-2a cell lysate (M00379-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Birc5 monoclonal antibody (Catalog # M00379-2) overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Birc5https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-2-birc5-primary-antibodies-ihc-testing-2.jpgAnti-Survivin Birc5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse colon tissue using anti-Survivin antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody ( 1/100) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-2-birc5-primary-antibodies-ihc-testing-3.jpgAnti-Survivin Birc5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-Survivin antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/100) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00379-2-ihc.jpgAnti-Survivin Birc5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse ovarian cancer, using Survivin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aurora-a-rabbit-monoclonal-antibody-m00246-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00246-wb.jpgAnti-Aurora A AURKA Rabbit Monoclonal AntibodyWestern blot analysis of Aurora A expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-map1lc3a-rabbit-monoclonal-antibody-m01543-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-41420_2025_2386_figa_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyCharacteristics of the tongue dorsum mucosal cell landscape in the rats with gastric intestinal metaplasia. The abundances of T cells, neutrophils, and macrophages were upregulated, and the autophagy marker gene Map1lc3a in T cells and neutrophils was downregulated, which indicated an actively inflammatory immune response. Downregulation of cuprotosis marker gene Dlst in fibroblasts suggested potential damage to the mucosal barrier. Meanwhile, the expression of bitter receptor Rtp4 and sweet receptor Tas1r2 in mesenchymal stem cells was downregulated. The cell communication ability was reduced, especially between mesenchymal stem cells and epithelial cells. In a word, the abnormal status of tongue dorsum mucosa may accompany the development of gastric intestinal metaplasia.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-025-02386-z'>40090940</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-41420_2025_2386_fig3_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyCharacterization of cell death in the tongue dorsal mucosal tissue of GIM rats. Based on the cell-death-related marker genes, differential analysis was conducted between the control and GIM groups. A Differential analysis of apoptosis-related genes. B Differential analysis of pyroptosis-related genes. C Differential analysis of autophagy-related genes. D Differential analysis of ferroptosis-related genes. E Differential analysis of necroptosis-related genes. F Differential analysis of cuproptosis-related genes. G Immunofluorescence staining of Mapllc3a and Gpx4 expression in tongue dorsal mucosal tissue (magnification: ×20, scale bar: 50 μm). Data with error bars are shown as mean ± standard deviation. * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001 as determined by independent t -tests. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-025-02386-z'>40090940</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-13046_2018_1012_fig3_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyXAG induces HCC cell autophagy. Cells were co-cultured with 10 and 20 μM of XAG or vehicle for 48 h. a Effect of XAG on the development of acidic vesicle organelles (AVO) in Bel 7402 and SMMC 7721 cells was examined by Acridine orange (AO) staining. Red plot represents AVO. b Western blotting demonstrated expression of autophagy-related proteins, including LC3B-I, LC3B-II, p62/SQSTM1, Beclin-1, and Atg5. GAPDH was used as control group as well. ** p <0.01. c Bel 7402 and SMMC 7721 cells were infected with an adenovirus expression of mRFP-GFP-LC3. Effect of XAG on the formation of autolysosome was observed under a fluorescence microscope, with 400× magnification. mRFP was used to label and track the LC3B-II in HCC cells, decrease of GFP indicates the fusion of lysosome and autophagosome, as well as formation of autolysosome. Yellow puncta and red puncta imply to autophagosome and autolysosome, respectively. Results represent independent experiments in triplicate <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-018-1012-z'>30621754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-13046_2018_1012_fig7_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal Antibodyp-JNK is required for the autophagy-induced by XAG in HCC cells. Cells were pre-treated with or without JNK inhibitor, SP600125 (20 μM), for 6 h, then were co-cultured with 20 μM of XAG for 48 h. a Expression levels of LC3B-II, p62/SQSTM1, Beclin-1, and Atg5 in HCC cells were analyzed by Western blotting, and GAPDH was severed as control group. ** p <0.01. b Flow cytometry was performed to quantify the apoptotic cell ratio. ** p <0.01. c The expression levels of Bax, Bcl-2, and cleaved caspase-3 in HCC cells were analyzed by Western blotting. GAPDH was served as control group as well. ** p <0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-018-1012-z'>30621754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-13046_2018_1012_fig5_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyApoptosis-inducing effect of XAG on HCC cells was abrogated by autophagy mediated by triggering ERS signaling pathway. a Bel 7402 and SMMC 7721 cells were co-cultured with 10 and 20 μM of XAG or vehicle. Western blotting analysis detected the expression of ERS-related proteins, including CHOP, GRP78, ATF-6, p-eIF2α, IRE1α, and cleaved caspase-12. GAPDH was used as control group. ** p <0.01. b After cells were pre-treated with or without 2.5 mM of TUDCA (as ERS inhibitor), then co-cultured with 20 μM of XAG for 48 h. The expression levels of LC3B-II, p62/SQSTM1, Beclin 1, Atg5 were analyzed by Western blotting, and GAPDH was used as control group. ** p <0.01. (c) After cells were transfected with shRNA targeting CHOP, then were treated with or without 20 μM of XAG for 48 h. Expression of autophagy-associated proteins (LC3B-II, p62/SQSTM1, Beclin-1, and Atg5) was detected by Western blotting, and GAPDH was used as control group. ** p <0.01. d After cells were pre-treated with or without 2.5 mM of TUDCA (an ERS inhibitor), then were co-cultured with 20 μM of XAG for 48 h. Cell apoptotic ratio in each treatment group was quantified by flow cytometry. ** p <0.01. e After cells were pre-treated with or without 2.5 mM of TUDCA, then were co-cultured with 20 μM of XAG for 48 h. The expression of Bax, Bcl-2, and cleaved caspase-3 was analyzed by Western blotting, and GAPDH was used as control group. ** p <0.01. f After cells were transfected with shRNA targeting CHOP, then were treated with or without 20 μM of XAG for 48 h. Cell apoptotic ratio was quantified by flow cytometry. ** p <0.01. g After cells were transfected with shRNA targeting CHOP, then were treated with or without 20 μM of XAG for 48 h. The expression levels of Bax, Bcl-2, and cleaved caspase-3 were analyzed by Western blotting, and GAPDH was used as control group. ** p <0.01 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-018-1012-z'>30621754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-13046_2018_1012_fig8_html.pngAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyXAG suppresses tumor growth in HCC xenograft model. a Mice were respectively given vehicle (0.9% sodium chloride plus 1% DMSO) orally, and injected intraperitoneally with 40 or 80 mg/kg XAG, tumor volume and body weight (e) were measured every 3 days for 24 days. ** p <0.01. b After tumor was isolated from mice, the weight of tumor tissues was measured. ** p <0.01. c TUNEL staining measured cell apoptosis in tumor tissues. ** p <0.01. d IHC detected the expression levels of Ki-67, cleaved caspase-3, Beclin 1, CHOP, GRP78, p-JNK, p-c-jun in tumor tissues. LC3 expression in tumor tissues was detected by Immunofluorescence. ** p <0.01. f The levels of ALT, AST, and urea nitrogen in tumor tissues were detected using all-automatic biochemical analyzer. ** p <0.01. g HE staining examined the histopathologic characteristics of lung, liver, spleen, kindey, heart in each treatment groups <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13046-018-1012-z'>30621754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-map1lc3a-primary-antibodies-wb-testing-1.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal Antibody Western blot analysis of MAP1LC3A using anti-MAP1LC3A antibody (M01543-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP1LC3A antigen affinity purified monoclonal antibody (Catalog # M01543-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP1LC3A at approximately 18 kDa. The expected band size for MAP1LC3A is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-ihc.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using MAP1LC3A Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-icc1.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-icc2.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-icc3.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-1-if.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using MAP1LC3A Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lysozyme-rabbit-monoclonal-antibody-m01811-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-lysozyme-primary-antibodies-wb-testing-1.jpgAnti-Lysozyme LYZ Rabbit Monoclonal Antibody Western blot analysis of Lysozyme using anti-Lysozyme antibody (M01811). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human U937 whole cell lysates,<br>
Lane 3: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lysozyme antigen affinity purified monoclonal antibody (Catalog # M01811) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lysozyme at approximately 15 kDa. The expected band size for Lysozyme is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-lyz-primary-antibodies-if-testing-2.jpgAnti-Lysozyme LYZ Rabbit Monoclonal Antibody IF analysis of Lysozyme using anti-Lysozyme antibody (M01811).
Lysozyme was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated at 1:50 rabbit anti-Lysozyme Antibody (M01811) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig1_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyMG53 attenuates intestinal injury in mouse models. a Serum IL-6 and IL-18 levels of MG53-TG and their WT littermates at the indicated time points following DSS treatment. n = 3 for each group. Overexpression of MG53 attenuated DSS-induced IBD symptoms, including disease activity index (DAI; b ), body weight change ( c ), disruption of intestinal structure as demonstrated by H&E staining of the jejunum, ileum, and colon ( d ; scale bar, 100 μm), and shortening of the colon as evidenced by the representative images ( e ) and statistic results of colon length ( f ) in MG53-TG and WT mice. n = 7 for each group. g , h Depletion of MG53 exacerbated DSS-induced IBD symptoms. The DAI ( g ) and body weight change ( h ) of MG53-KO and the WT littermates at the indicated time points after DSS challenge. n = 5 for each group. Immunofluorescence staining of Ki-67 (red) to indicate the TA zone and the statistic results of its length in MG53-TG ( i , n = 20 for each group) or MG53-KO ( j , n = 13 for each group) as compared with their corresponding WT littermates. The nuclei were indicated by DAPI staining (blue); scale bar, 100 μm. Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using two tailed paired t test ( a – c , f – j ). All data were presented as mean ± s.e.m. * p < 0.05, ** p < 0.01, and *** p < 0.001 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig4_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyPPARα mediates the effect of MG53 in promoting asymmetric division of Lgr5 + cells. Representative images ( a ) and statistic results ( b , n = 3 for each group) of asymmetric division of Lgr5 + cells with or without GW6471 (10 μM, 24 h) treatment. Lgr5 + cells were in green; all the cells were visualized by tubulin (red). Scale bar, 10 μm. c FACS analysis of Lgr5 + , Atoh1 + , and Notch1 + cells in the Lgr5 and MG53;Lgr5 organoids treated with GW6471 or vehicle. d Immunofluorescence staining of Ki-67 (red) and PPARα (green) and statistic results of PPARα positive cells ( n = 3 for each group) and the length of TA zone ( n = 18 for each group) in mice treated GW6471 or vehicle. Nuclei were stained with DAPI (blue); scale bar, 100 μm. Representative images and statistic results of PAS staining of goblet cells in the ileum ( e ; n = 10 for each group; TG, MG53-TG; scale bar, 50 μm) and colon ( f ; n = 10 for each group; scale bar, 100 μm). Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using one-way ANOVA with Tukey post hoc test ( b , d , e , and f ) and were presented as mean ± s.e.m. ns not significant and *** p < 0.001 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig2_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyMG53 overexpression promotes secretory lineage commitment. a Immunofluorescence staining of BrdU (red) and EdU (yellow) in the ileum of MG53-TG and their WT littermates subjected to DSS treatment and administered BrdU 48 h and EdU 24 h before euthanasia. n = 10 for each group. Scale bar, 100 μm. b UMAP of scRNA-seq of Epcam + CD45 − intestinal epithelial cells collected from MG53-TG and their WT littermates on Day 7 of DSS treatment, n = 5 for each group. c Proportions of stem, secretory, and absorptive cells in general and each particular cell clusters. d Representative images and statistic results of PAS staining of goblet cells of MG53-TG and WT mice in the colon. n = 10 for each group. Scale bar, 100 μm. e Representative images of intestinal organoids derived from MG53;Lgr5 mice and their Lgr5 littermates at the indicated time points. f Relative mRNA levels of the marker genes in the transcriptome analysis of the crypt organoids. n = 4 for each group. g Representative images of colonic organoids derived from MG53;Lgr5 mice and their Lgr5 littermates at the indicated time points. h Representative FACS profiles and statistic results of Lgr5 + cells in the colonic organoids derived from MG53;Lgr5 and the control Lgr5 mice. n = 6 for each group. Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using two tailed paired t test ( a , d , f , and h ), and were presented as mean ± s.e.m. * p < 0.05, ** p < 0.01, and *** p < 0.001 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig3_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyPPAR signaling is enhanced by MG53 overexpression. a Trajectory analysis of Epcam + CD45 − intestinal epithelial cells Using Monocle 2. b KEGG pathway enrichment analysis of the differentially expressed genes between the secretory and absorptive branches. GSEA results ( c ) and the heatmap of differentially expressed genes ( d ) related to fatty acid oxidation and PPAR signaling derived from the bulk RNAseq data of the intestinal organoids from MG53-TG and WT mice. n = 4 for each group. Representative images ( e ) and statistic results of signal intensity of the immunofluorescence staining of MG53 (green) and PPARα (red) determined by Aperio Scanscope scanner and Halo software ( f ), as well as the correlation of the levels of these two proteins ( g ) in the human small intestine of normal subjects ( n = 5) and patients with intestinal inflammation ( n = 8). Nuclei were stained with DAPI (blue); scale bars as indicated. Representative images ( h ) and statistic results of signal intensity of the immunofluorescence staining of MG53 (green) and PPARα (red) determined by Aperio Scanscope scanner and Halo software ( i ), as well as the correlation of the levels of these two proteins ( j ) in the human colon of normal subjects ( n = 4) and patients with intestinal inflammation ( n = 12). Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using Mann–Whitney U test ( f , i ) and Pearson correlation analysis ( g , j ). Data were presented as mean ± s.e.m. * p < 0.05 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig5_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyActivation of PPARα signaling is required for MG53-induced alleviation of intestinal injury. Body weight change and DAI ( a ) as well as the representative images and statistic results of the intestinal length ( b ) of ISC-MG53-TG and the control MG53 tg-fl mice. n = 7 for each group. Body weight change and DAI ( c ) as well as the representative images and statistic results of the intestinal length ( d ) of the Lgr5 mice with ISC-specific inhibition of MG53 expression via infection with adeno-associated virus with inducible expression of shRNA targeting MG53 (AAV-shMG53) or the control mice infected with control shRNA (AAV-shCON). n = 6 for each group. Body weight change and DAI ( e ) as well as the intestinal length ( f ) of ISC-Ppara-KO mice with or without ISC-specific MG53 overexpression via injecting AAV-MG53 or AAV-CON. n = 8 for each group. Body weight change and DAI ( g ) as well as the intestinal length ( h ) of MG53-KO and control WT mice treated with PPARα agonist fenofibrate or vehicle following DSS treatment. n = 8 for each group. Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using two-tailed paired t test ( a – e , g ), Mann–Whitney U test ( f , h ), and were presented as mean ± s.e.m. ns not significant, * p < 0.05 and ** p < 0.01 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-41392_2025_2268_fig6_html.pngAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyEnhanced PPARα activation by palmitoleic acid contributes to MG53-mediated amelioration of intestinal injury. a Heatmap of free fatty acids (FFA) in MG53-TG and WT intestinal tissues at the indicated time points during DSS treatment. n = 3 for each group. b Changes in the intestinal content of FFA in the MG53-TG and their WT littermates at day 7 after DSS treatment. n = 3 for each group. c Relative change in POA concentrations in the serum of IBD patients in remission ( n = 11) or flare ( n = 26). d Luciferase reporter activity driven by the PPARα-responsive element in the presence of different FFA in HEK293 cells. n = 3 for each group. Body weight change and DAI ( e ) as well as the colon length ( f ) of MG53-TG (TG) and their WT littermates challenged with DSS with or without POA treatment. n = 12 for each group. g Immunofluorescence staining of Ki-67 (red) and statistic results of the length of TA zone of MG53-TG and their WT littermates with or without POA treatment. n = 15 for each group. The nuclei were indicated by DAPI staining (blue); scale bar, 100 μm. h Representative images and statistic results of PAS staining of goblet cells in the colon after POA treatment. n = 10 for each group. Scale bar, 100 μm. Normal distribution was confirmed by Shapiro–Wilk test. Data were analyzed using one-way ANOVA with Tukey post hoc test ( c , e ), two tailed t test ( d , f – h ) and were presented as mean ± s.e.m. ns not significant, * p < 0.05, ** p < 0.01, and *** p < 0.001 as compared with the corresponding controls Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41392-025-02268-x'>40494851</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01811-LYZ-primary-antibodies-IHC-testing-1.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using Lysozyme Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-ihc7.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-ihc8.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:4000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-ihc9.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta, using the Antibody at 1:4000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-ihc10.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-ihc11.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse heart, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01811-icc1.jpgAnti-Lysozyme LYZ Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p38-mapk-rabbit-monoclonal-antibody-m00176-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-mapk14-primary-antibodies-wb-testing-1.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal Antibody Western blot analysis of p38 MAPK using anti-p38 MAPK antibody (M00176-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human SW620 whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p38 MAPK antigen affinity purified monoclonal antibody (Catalog # M00176-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for p38 MAPK at approximately 41, 38 kDa. The expected band size for p38 MAPK is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-ihc.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyIHC analysis of p38 MAPK using anti-p38 MAPK antibody (M00176-1) on human brain.<br> p38 MAPK was detected in paraffin-embedded section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-p38 MAPK Antibody (M00176-1) overnight at 4°C. Biotinylated goat anti Rabbit IgG IgG antibody was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-ihc7.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-ihc8.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-ihc9.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-if.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyIF analysis of immunocytochemical section of Hela cells using anti-p38 MAPK antibody (M00176-1) <br> p38 MAPK was detected in immunocytochemical section. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-p38 MAPK Antibody (M00176-1) overnight at 4 °https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176-1-icc1.jpgAnti-p38 MAPK MAPK14 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dna-pkcs-rabbit-monoclonal-antibody-m00645-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00645-wb.jpgAnti-DNA-PKcs PRKDC Rabbit Monoclonal AntibodyWestern blot analysis of DNA-PKcs expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00645-ihc.jpgAnti-DNA-PKcs PRKDC Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using DNA-PKcs Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikk-beta-rabbit-monoclonal-antibody-m00118-1-boster.html2026-03-24T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00118-1-wb.jpgAnti-IKK beta IKBKB Rabbit Monoclonal AntibodyWestern blot analysis of IKK beta expression in Daudi cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ferritin-rabbit-monoclonal-antibody-m02401-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-41419_2022_5037_fig2_html.pngAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyIron-overloaded EMFF induced ferritinophagy-dependent ferroptosis in granulosa cells. A – C Levels of total iron, hepcidin, and transferrin in EMFF ( n = 15) and COFF ( n = 15). Data are expressed as means ± SD and analyzed by Student’s t test. D Results of mouse granulosa cells proliferation under different intervention conditions (each group in the figure is compared with COFF group). DFO, iron chelators; FER, ferroptosis inhibitor; NEC, necrosis inhibitor; ZDF, apoptosis inhibitor; ME, autophagy inhibitor. Data are expressed as means ± SD and analyzed by one-way ANOVA. E – H Comparison of ferritinophagy-related proteins FTH1, NCOA4, and ATG5 between human granulosa cells of infertile patients with EMs (EMGC) and of control group (COGC). The expression of β-actin was used as an internal control. Data are expressed as means ± SD and analyzed by Student’s t test. I – L Detection of ferroptosis-related indicators iron, GSH, GPX4, and MDA in COGC and EMGC. Data are expressed as means ± SD and analyzed by Student’s t test. M Representative images of the mitochondrial morphology of mouse granulosa cells intervened by COFF and EMFF were observed under TEM. Yellow arrows indicate mitochondrion. Scale bar = 1.0 µm. Scale bar = 5.0 µm. N Representative images of ROS and ferrous ion fluorescence staining after COFF and EMFF intervention in mouse granulosa cells. Scale bar = 100 µm. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns, no significance. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-022-05037-8'>35787614</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-41419_2022_5037_fig5_html.pngAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyConstruction of an iron overload mouse model. A – C Serum levels of E 2 , FSH, and LH in standard iron (STD), low iron (LID), and high iron (HID) diet feeding groups ( n = 8). D – F Total iron, GSH, and MDA levels in the ovary tissues of mice in each group ( n = 8). G Representative images of ROS fluorescence staining of ovarian mouse granulosa cells in three groups of mice. Scale bar = 20 µm. H – K Western blot analysis of ferritinophagy-related proteins, FTH1, NCOA4, and ATG5 in mouse ovary tissues in the STD, LID, and HID group. The expression of β-actin was used as an internal control. All data are expressed as means ± SD and analyzed by one-way ANOVA. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns, no significance. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-022-05037-8'>35787614</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-fphar-15-1392123-g005.jpgAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyKidney tea attenuated ferroptosis in the kidney. (A) Representative images of transmission electron microscopy of kidney samples (scale bar: 2 μm/500 nm). (B) SOD activity in kidney samples. (C, D) MDA and 4-HNE levels in kidney samples. (E–H) The mRNA expression of NCOA4, FTH1, ACSL4 and GPX4 in kidney samples. (I–M) The protein levels of NCOA4, FTH1, ACSL4 and GPX4 in kidney samples. * p < 0.05, ** p < 0.01, *** p < 0.001 compared with the Mod group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1392123/full'>38962302</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-fth1-primary-antibodies-wb-testing-1.jpgAnti-Ferritin FTH1 Rabbit Monoclonal Antibody Western blot analysis of Ferritin using anti-Ferritin antibody (M02401). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human MCF-7 whole cell lysates, <br>
Lane 4: human K562 whole cell lysates, <br>
Lane 5: rat liver tissue lysates, <br>
Lane 6: rat RH35 whole cell lysates, <br>
Lane 7: mouse liver tissue lysates, <br>
Lane 8: mouse HEPA1-6 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ferritin antigen affinity purified monoclonal antibody (M02401) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ferritin at approximately 19 kDa. The expected band size for Ferritin is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-fth1-primary-antibodies-wb-testing-2.pngAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyWestern blot analysis of FTH1 using anti-FTH1 antibody (M02401). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-5: model group-Human uterine tissue lysates, <br>
Lane 2: young group-Human uterine tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FTH1 antigen affinity purified monoclonal antibody (M02401) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FTH1 at approximately 21 kDa. The expected band size for FTH1 is at 21 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-if.jpgAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Ferritin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02401-icc1.jpgAnti-Ferritin FTH1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikb-beta-rabbit-monoclonal-antibody-m05766-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05766-nfkbib-primary-antibodies-wb-testing-1.jpgAnti-IKB beta Rabbit Monoclonal AntibodyWestern blot analysis of NFKBIB using anti-NFKBIB antibody (M05766). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human A549 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFKBIB antigen affinity purified monoclonal antibody (M05766) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NFKBIB at approximately 48 kDa. The expected band size for NFKBIB is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05766-ihc.jpgAnti-IKB beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using IKB beta Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mad2l1bp-rabbit-monoclonal-antibody-m06825-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06825-wb.jpgAnti-MAD2L1BP/Mad2L1 Binding Protein Rabbit Monoclonal AntibodyWestern blot analysis of MAD2L1BP expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06825-ihc.jpgAnti-MAD2L1BP/Mad2L1 Binding Protein Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using MAD2L1BP Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-map1lc3a-rabbit-monoclonal-antibody-m01543-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-wb7.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-wb.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyWestern blot analysis of MAP1LC3A expression in Human brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01543-ihc.jpgAnti-MAP1LC3A/Lc3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using MAP1LC3A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-psa-klk3-rabbit-monoclonal-antibody-m01505-1-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01505-1-wb.jpgAnti-PSA/KLK3 Rabbit Monoclonal AntibodyWestern blot analysis of PSA/KLK3 expression in Human prostate carcinoma tissue lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-h-rabbit-monoclonal-antibody-m03013-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03013-wb.jpgAnti-Cyclin H Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin H expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calnexin-rabbit-monoclonal-antibody-m03372-1-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03372-1-canx-primary-antibodies-wb-testing-1.jpgAnti-Calnexin CANX Rabbit Monoclonal Antibody Western blot analysis of CANX using anti-CANX antibody (M03372-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CANX antigen affinity purified monoclonal antibody (Catalog # M03372-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CANX at approximately 97 kDa. The expected band size for CANX is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03372-1-icc1.jpgAnti-Calnexin CANX Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03372-1-icc2.jpgAnti-Calnexin CANX Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat5a-b-rabbit-monoclonal-antibody-m01087-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-stat5a-primary-antibodies-wb-testing-1.jpgAnti-STAT5A/B Rabbit Monoclonal Antibody Western blot analysis of STAT5A using anti-STAT5A antibody (M01087). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: rat C6 whole cell lysates, <br>
Lane 4: rat heart tissue lysates, <br>
Lane 5: rat liver tissue lysates, <br>
Lane 6: mouse heart tissue lysates, <br>
Lane 7: mouse liver tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5A antigen affinity purified monoclonal antibody (M01087) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT5A at approximately 91 kDa. The expected band size for STAT5A is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01087-ihc.jpgAnti-STAT5A/B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast, using STAT5A/B Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trka-b-c-rabbit-monoclonal-antibody-m00706-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-wb7.jpgAnti-TrkA+B+C NTRK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-if.jpgAnti-TrkA+B+C NTRK1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Neuro-2a cells, using TrkA+B+C Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-wb.jpgAnti-TrkA+B+C NTRK1 Rabbit Monoclonal AntibodyWestern blot analysis of TrkA+B+C expression in Human fetal brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-ihc.jpgAnti-TrkA+B+C NTRK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using TrkA+B+C Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc42ep1-rabbit-monoclonal-antibody-m08856-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08856-wb.jpgAnti-CDC42EP1/Mse55 Rabbit Monoclonal AntibodyWestern blot analysis of CDC42EP1 expression in HUVEC cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il1-beta-rabbit-monoclonal-antibody-m00101-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-wb7.jpgAnti-IL1 beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-wb8.jpgAnti-IL1 beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-wb.jpgAnti-IL1 beta Rabbit Monoclonal AntibodyWestern blot analysis of IL1 beta expression in recombinant IL1 beta protein.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-il1beta-primary-antibodies-wb-testing-1.pngAnti-IL1 beta Rabbit Monoclonal AntibodyWestern blot analysis of IL1 beta using anti-IL1 beta antibody ( M00101). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-6: mouse PACs whole cell lysates, <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1 beta antigen affinity purified polyclonal antibody (M00101) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system.The expected band size for IL1 beta is at 30 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-occludin-rabbit-monoclonal-antibody-m01246-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01246-ocln-primary-antibodies-wb-testing-1.jpgAnti-Occludin OCLN Rabbit Monoclonal AntibodyWestern blot analysis of OCLN using anti-OCLN antibody (M01246). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OCLN antigen affinity purified monoclonal antibody (M01246) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for OCLN at approximately 59 kDa. The expected band size for OCLN is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eif4ebp1-rabbit-monoclonal-antibody-m00968-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00968-wb.jpgAnti-eIF4EBP1/4Ebp1 Rabbit Monoclonal AntibodyWestern blot analysis of eIF4EBP1 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00968-ihc.jpgAnti-eIF4EBP1/4Ebp1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using eIF4EBP1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00968-if.jpgAnti-eIF4EBP1/4Ebp1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using eIF4EBP1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikk-beta-rabbit-monoclonal-antibody-m00118-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00118-ikbkb-primary-antibodies-wb-testing-1.jpgAnti-IKK beta IKBKB Rabbit Monoclonal Antibody Western blot analysis of IKBKB using anti-IKBKB antibody (M00118). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKBKB antigen affinity purified monoclonal antibody (Catalog # M00118) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IKBKB at approximately 87 kDa. The expected band size for IKBKB is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00118-ihc.jpgAnti-IKK beta IKBKB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using IKK beta Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00118-if.jpgAnti-IKK beta IKBKB Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using IKK beta Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glucagon-rabbit-monoclonal-antibody-m00678-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00678-wb.jpgAnti-Glucagon GCG Rabbit Monoclonal AntibodyWestern blot analysis of Glucagon expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00678-glucagon-primary-antibodies-ihc-testing-2.jpgAnti-Glucagon GCG Rabbit Monoclonal Antibody IHC analysis of Glucagon using anti-Glucagon antibody (M00678). <br>
Glucagon was detected in a paraffin-embedded section of mouse pancrease tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Glucagon Antibody (M00678) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-serpina1-rabbit-monoclonal-antibody-m00720-1-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00720-1-wb.jpgAnti-SERPINA1/Alpha 1 Antitrypsin Rabbit Monoclonal AntibodyWestern blot analysis of SERPINA1 expression in human fetal kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00720-1-serpina1-primary-antibodies-wb-testing-1.jpgAnti-SERPINA1/Alpha 1 Antitrypsin Rabbit Monoclonal AntibodyWestern blot analysis of SERPINA1 using anti-SERPINA1 antibody (M00720-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPINA1 antigen affinity purified monoclonal antibody (M00720-1) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SERPINA1 at approximately 47 kDa. The expected band size for SERPINA1 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-catalase-rabbit-monoclonal-antibody-m03123-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03123-ihc.jpgAnti-Catalase Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat liver, using Catalase Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03123-cat-primary-antibodies-wb-testing-1.jpgAnti-Catalase Rabbit Monoclonal AntibodyWestern blot analysis of CAT using anti-CAT antibody (M03123). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAT antigen affinity purified monoclonal antibody (M03123) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CAT at approximately 60-65 kDa. The expected band size for CAT is at 60 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hepcidin-rabbit-monoclonal-antibody-m01347-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01347-wb.jpgAnti-Hepcidin HAMP Rabbit Monoclonal AntibodyWestern blot analysis of Hepcidin expression in Human Hepcidin Full-length Recombinant Protein (GFP Tagged).
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rac1-2-3-rabbit-monoclonal-antibody-m00041-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00041-wb7.jpgAnti-Rac1/2/3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00041-wb8.jpgAnti-Rac1/2/3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00041-wb.jpgAnti-Rac1/2/3 Rabbit Monoclonal AntibodyWestern blot analysis of Rac1/2/3 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hnrnp-a1-rabbit-monoclonal-antibody-m01476-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-wb-testing-1.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyWestern blot analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Daudi whole cell lysates,<br>
Lane 3: human MOLT-4 whole cell lysates,<br>
Lane 4: human HL-60 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse HEPA1-6 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HNRNPA1 antigen affinity purified monoclonal antibody (M01476) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HNRNPA1 at approximately 36 kDa. The expected band size for HNRNPA1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-1.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-2.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-3.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-4.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-6.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-7.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01476-hnrnpa1-primary-antibodies-ihc-testing-8.jpgAnti-hnRNP A1 Rabbit Monoclonal AntibodyIHC analysis of HNRNPA1 using anti-HNRNPA1 antibody (M01476). <br>HNRNPA1 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPA1 Antibody (M01476) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vsv-g-tag-rabbit-monoclonal-antibody-mt0017-boster.html2026-03-24T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/T/MT0017-VSV-G-Tag-primary-antibodies-WB-testing-1.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyWestern blot analysis of extracts from VSV-G tag fusion protein, using VSV-G tag antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0017-fcimb-15-1603530-g002.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyBT restricts the VSV infection in 2fTGH cells. (A) RT-qPCR analysis of VSV-N mRNA levels in 2fTGH cells infected with VSV (MOI = 0.1) and treated with DMSO or increasing concentrations of BT (30 and 60 μM for 12 h; 10, 30, 60, and 100 μM for 24 h). Black triangles indicate increasing BT concentrations. Data normalized to ACTB. Fold changes relative to VSV-treated control samples were calculated using the 2^-ΔΔCT method. (B) Western blotting analysis of VSV glycoprotein (G) protein expression in 2fTGH cells infected with VSV (MOI = 0.1) and treated with DMSO or BT (30 and 60 μM for 12 h; 60 and 100 μM for 24 h). (C) Plaque assay quantification of infectious viral particles from supernatants of BT-treated cells for 12 h. Culture supernatants were serially diluted and adsorbed onto fresh 2fTGH cells for 1 h, then overlaid with 0.5% carboxymethyl cellulose and incubated for an additional 48 h. (D) HeLa cells infected with VSV-GFP at an MOI of 0.1 and treated with BT (20 and 100 μM) for 24 (h) The percentage of VSV-GFP-positive cells was determined by flow cytometry analysis. (E) Representative bright-field and green fluorescence images of HeLa cells infected with VSV-GFP (MOI = 0.1, 12 h) with BT (0-60 μM). Scale bar, 100 μm. Data are presented as mean ± SEM, with n = 3. **P < 0.01; ***P < 0.001. ns, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12408630/'>40918260</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0017-fcimb-15-1603530-g003.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyBT inhibits a range of viral infections in vitro . (A) RT-qPCR analysis of VSV-N mRNA levels in VSV-infected (MOI = 0.1) A549, HeLa, HT29, and RAW264.7 cells treated with BT (50 μM) or DMSO (vehicle control) for 12 h. Data normalized to ACTB and expressed as fold change relative to control (VSV+DMSO, set as 1). (B) Representative plaque assay images quantifying infectious VSV particles in supernatants from (A) . (C) RT-qPCR analysis of viral RNA in HSV-1 (MOI = 0.5), IAV (MOI = 0.1), EMCV (MOI = 0.1)-infected 2fTGH cells as well as MHV-A59 (MOI = 0.1)-infected J774A.1 cells, all treated with either BT (40, 60, or 100 μM) or DMSO (vehicle control) for 12 (h) Data normalized to ACTB and expressed as fold change relative to control (virus+DMSO, set as 1). (D) HSV-1 envelope glycoprotein- and MHV-A59 spike protein-mediated cell-cell fusion and syncytium formation in the presence or absence of 60 μM BT for 12 h (Scale bar, 100 μm. The arrow points to fused cells). Data are presented as mean ± SEM, with n = 3. **P < 0.01; ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12408630/'>40918260</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0017-fcimb-15-1603530-g004.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyBT arrests viral replication in an FXa independent manner. (A) Schematic diagram illustrating the potential antiviral mechanism of BT. (B) 2fTGH cells infected with VSV (MOI=0.1) were treated with 50 μM direct oral anticoagulants (DOACs) for 12 h. Antiviral effects quantified by RT-qPCR. Data normalized to ACTB and expressed as fold change relative to DMSO-treated control (set as 1). RIV: Rivaroxaban, BTM: Betrixaban maleate. (C) Left: RT-qPCR analysis of FXa mRNA levels in 2fTGH cells transfected with non-targeting control siRNA or FXa siRNA (100 nM). Right: RT-qPCR analysis of VSV-N mRNA levels in 2fTGH cells transfected with non-targeting control siRNA or FXa siRNA (100 nM) followed by VSV infection (MOI = 0.1, 12 h). Data normalized to ACTB and expressed as fold change relative to Scramble-treated (set as 1). (D) 2fTGH cells were transfected with 1 μg of FXa-mCherry or an empty plasmid for 48 h, followed by infection with VSV-GFP at an MOI of 0.1 for 12 h. RT-qPCR analysis of FXa mRNA levels and viral replication. Data normalized to ACTB and expressed as fold change relative to empty plasmid-treated (Mock, set as 1). Western blotting analysis of VSV-G protein expression. (E, F) HeLa cells were transfected with 1 μg of FXa-mCherry or an empty plasmid for 48 h, followed by infection with VSV-GFP at an MOI of 0.1 for 12 h. Quantification of the percentage of VSV-GFP positive cells in HeLa cells with FXa overexpression via fluorescence microscopy (E) and ImageJ (F) . Scale bar, 100 μm. The number of VSV-GFP-positive cells in the empty-vector transfection control group (Mock) was normalized to 100% to determine the infection rate. Data are presented as mean ± SEM, with n = 3. ***P < 0.001. ns, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12408630/'>40918260</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0017-fcimb-15-1603530-g007.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyThe antiviral protective effects of BT treatment in vivo . (A) Schematic representation of a mouse model of VSV infection treated with BT in vivo . C57BL/6 mice were infected intraperitoneally (i.p.) with VSV (1 × 10 8 PFU per mouse), followed by daily i.p. injections of BT (10 mg/kg/day) or PBS (vehicle control) for three consecutive days. (B) Survival curves of VSV-infected mice treated with BT or PBS (n = 8 per group). Survival comparisons were performed using the log-rank (Mantel-Cox) test. (C) RT-qPCR analysis of the VSV-N mRNA levels in the blood tissues of VSV-infected mice treated with BT or not (n = 3 per group). Data normalized to ACTB and expressed as fold change relative to PBS-treated control (VSV alone, set as 1). (D) IFNB1 mRNA levels in the liver, lung, and spleen tissues harvested from C57BL/6J mice 24 h after a single i.p. injection of BT (10 mg/kg) or PBS were quantified by RT-qPCR (n = 3 per group). Data normalized to ACTB and expressed as fold change relative to PBS-treated control (Mock, set as 1). Data are presented as mean ± SEM, with n = 3. *P < 0.05; **P < 0.01; ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12408630/'>40918260</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0017-fcimb-15-1603530-g006.jpgAnti-VSV-G-Tag Rabbit Monoclonal AntibodyBT elicits antiviral immune response via TBK1/IRF3 signaling axis. (A) RT-qPCR analysis of ISG15 mRNA expression in 2fTGH cells pretreated with TBK1 inhibitor for 6 h, followed by treatment with BT (100 μM, 12 h). Data normalized to ACTB and expressed as fold change relative to DMSO-treated control (set as 1). (B) Luciferase activity in 2fTGH cells treated as described in (A) . Relative luciferase activity was expressed as fold change relative to the control (DMSO, set as 1.0). (C) IRF3 protein levels in IRF3 knockout (IRF3 –/– ) 2fTGH cells and WT cells. (D, E) The Luciferase reporter activity and gene expression of ISG15 in WT and IRF3 –/– 2fTGH cells after 16 h of BT (60 μM) or SeV (MOI = 0.1) treatment. Data normalized to ACTB and expressed as fold change relative to DMSO-treated control (set as 1). Relative luciferase activity was expressed as fold change relative to the control (DMSO, set as 1.0). (F) RT-qPCR analysis of Mx mRNA levels in WT and IRF3 –/– 2fTGH cells following treatment with BT (60 μM) for 16 h. Data normalized to ACTB and expressed as fold change relative to DMSO-treated control (set as 1). (G, H) RT-qPCR (G) and flow cytometry analysis (H) evaluating virus (VSV or VSV-GFP, MOI = 0.1) infection in WT and IRF3-depleted 2fTGH cells treated with BT (60 μM) for 12 h. Data normalized to ACTB and expressed as fold change relative to VSV-treated control (set as 1). Data are presented as mean ± SEM, with n = 3. **P < 0.01; ***P < 0.001. ns, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12408630/'>40918260</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikb-alpha-rabbit-monoclonal-antibody-m01139-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01139-nfkbia-primary-antibodies-wb-testing-1.jpgAnti-IKB alpha NFKBIA Rabbit Monoclonal Antibody Western blot analysis of IKB alpha using anti-IKB alpha antibody (M01139). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKB alpha antigen affinity purified monoclonal antibody (Catalog # M01139) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IKB alpha at approximately 36, 39 kDa. The expected band size for IKB alpha is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01139-feb413914-fig-0010-m.jpgAnti-IKB alpha NFKBIA Rabbit Monoclonal AntibodyEffects of OPN and OVE on activation of MAPK signaling pathways in LPS-stimulated RAW264.7 cells. Expression levels of p-ERK, ERK, p-p38, p-38, p-JNK, and JNK were detected in the same samples for COX-2 detection after 24 h of LPS stimulation. (A) OVE treatment. (B) OPN treatment. All experiments were carried out in triplicates and data are presented as means ± SDs; one-way ANOVA analysis was adopted for multiple comparisons; ###P < 0.001, ####P < 0.0001, compared to the untreated control group; ***P < 0.001 and ****P < 0.0001, compared to the LPS control group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://febs.onlinelibrary.wiley.com/doi/abs/10.1002/2211-5463.13914'>39455284</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01139-NFKBIA-primary-antibodies-IHC-testing-1.jpgAnti-IKB alpha NFKBIA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse stomach, using IKB alpha Antibody(M01139)<br>NFKBIA was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-NFKBIA Antibody (M01139)overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01139-if.jpgAnti-IKB alpha NFKBIA Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using IKB alpha Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-8-rabbit-monoclonal-antibody-m00042-2-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-2-wb7.jpgAnti-Caspase-8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-2-wb.jpgAnti-Caspase-8 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-8 expression in(1) Jurkat cell lysate; (2)HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-2-if.jpgAnti-Caspase-8 Rabbit Monoclonal AntibodyImmunofluorescent analysis of K562cells, using Caspase-8 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-9-rabbit-monoclonal-antibody-m00080-3-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-wb7.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-wb8.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-wb.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-9 in HeLa cell lysate treated with Camptothecin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-wb9.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-ihc.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using Caspase-9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-icc2.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-icc3.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-icc4.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-icc1.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-3-if.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 3T3 cells, using Caspase-9 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-3-rabbit-monoclonal-antibody-m00334-5-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-5-caspase-3-primary-antibodies-wb-testing-1.jpgAnti-Caspase-3 CASP3 Rabbit Monoclonal Antibody Western blot analysis of Caspase-3 using anti-Caspase-3 antibody (M00334-5). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: human HepG2 whole cell lysates,<br>
Lane 6: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase-3 antigen affinity purified monoclonal antibody (Catalog # M00334-5) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase-3 at approximately 32 kDa. The expected band size for Caspase-3 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-5-casp3-primary-antibodies-ihc-testing-2.jpgAnti-Caspase-3 CASP3 Rabbit Monoclonal Antibody IHC analysis of CASP3 using anti-CASP3 antibody (M00334-5). <br>
CASP3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CASP3 Antibody (M00334-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-5-casp3-primary-antibodies-ihc-testing-3.jpgAnti-Caspase-3 CASP3 Rabbit Monoclonal Antibody IHC analysis of CASP3 using anti-CASP3 antibody (M00334-5). <br>
CASP3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CASP3 Antibody (M00334-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-5-if.jpgAnti-Caspase-3 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Caspase-3 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-5-ip7.jpgAnti-Caspase-3 CASP3 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cebp-beta-rabbit-monoclonal-antibody-m01100-1-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01100-1-wb.jpgAnti-CEBP Beta Rabbit Monoclonal AntibodyWestern blot analysis of CEBP Beta in (1) PC-12 cell lysate; (2) Human spleen lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pygopus-2-rabbit-monoclonal-antibody-m05260-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00283-pygo2-primary-antibodies-wb-testing-1.jpgAnti-Pygopus 2 Rabbit Monoclonal Antibody Western blot analysis of Pygopus 2 using anti-Pygopus 2 antibody (M00283). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human SH-SY5Y whole cell lysates, <br>
Lane 4: human PC-3 whole cell lysates, <br>
Lane 5: huamn U2OS whole cell lysates, <br>
Lane 6: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Pygopus 2 antigen affinity purified monoclonal antibody (M00283) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Pygopus 2 at approximately 50 kDa. The expected band size for Pygopus 2 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05260-ihc.jpgAnti-Pygopus 2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using Pygopus 2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-filamin-a-rabbit-monoclonal-antibody-m00502-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00502-flna-primary-antibodies-wb-testing-1.jpgAnti-Filamin A FLNA Rabbit Monoclonal Antibody Western blot analysis of Filamin A using anti-Filamin A antibody (M00502). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human MCF-7 whole cell lysates, <br>
Lane 3: human 293T whole cell lysates, <br>
Lane 4: human Jurkat whole cell lysates, <br>
Lane 5: rat C6 whole cell lysates, <br>
Lane 6: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Filamin A antigen affinity purified monoclonal antibody (M00502) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Filamin A at approximately 281 kDa. The expected band size for Filamin A is at 281 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grp78-bip-rabbit-monoclonal-antibody-m00955-1-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-1-wb7.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-1-ihc.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using GRP78 BiP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-1-wb8.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-1-wb.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyWestern blot analysis of GRP78 BiP expression in (1) HeLa cell lysate; (2) C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grp78-bip-rabbit-monoclonal-antibody-m00955-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-wb8.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-wb7.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-wb.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyWestern blot analysis of GRP78 BiP expression in (1) LnCaP cell lysate;(2) HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc8.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human non-Hodgkin's lymphoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc9.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc10.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc7.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat testis, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc11.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-ihc.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human pancreas, using GRP78 BiP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-icc1.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00955-if.jpgAnti-GRP78 BiP HSPA5 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using GRP78 BiP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd8-alpha-rabbit-monoclonal-antibody-m02236-2-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-2-ihc7.jpgAnti-CD8 alpha Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-2-cd8a-primary-antibodies-ihc-testing-1.jpgAnti-CD8 alpha Rabbit Monoclonal Antibody IHC analysis of CD8A using anti-CD8A antibody (M02236-2). <br>
CD8A was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD8A Antibody (M02236-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-2-ihc11.jpgAnti-CD8 alpha Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse testis, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-2-cd8a-primary-antibodies-ihc-testing-2.jpgAnti-CD8 alpha Rabbit Monoclonal Antibody IHC analysis of CD8A using anti-CD8A antibody (M02236-2). <br>
CD8A was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD8A Antibody (M02236-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02236-2-cd8a-primary-antibodies-ihc-testing-3.jpgAnti-CD8 alpha Rabbit Monoclonal Antibody IHC analysis of CD8A using anti-CD8A antibody (M02236-2). <br>
CD8A was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD8A Antibody (M02236-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lamin-a-c-rabbit-monoclonal-antibody-m00438-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamina-c-primary-antibodies-wb-testing-1.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyWestern blot analysis of LaminA/C using anti-LaminA/C antibody (M00438). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human SK-OV-3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LaminA/C antigen affinity purified monoclonal antibody (M00438) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LaminA/C at approximately 70-74 kDa. The expected band size for LaminA/C is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-1.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogenhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-icc1.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-2.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-3.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-4.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-5.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-6.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-7.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-8.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00438-lamin-a-c-primary-antibodies-ihc-testing-9.jpgAnti-Lamin A/C LMNA Rabbit Monoclonal AntibodyIHC analysis of Lamin A/C using anti-Lamin A/C antibody (M00438). <br>Lamin A/C was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Lamin A/C Antibody (M00438) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-musashi-1-rabbit-monoclonal-antibody-m05052-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05052-wb.jpgAnti-Musashi 1 MSI1 Rabbit Monoclonal AntibodyWestern blot analysis of Musashi 1 expression in SH-SY-5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05052-mis1-primary-antibodies-ihc-testing-1.jpgAnti-Musashi 1 MSI1 Rabbit Monoclonal AntibodyIHC analysis of MIS1 using anti-MIS1 antibody (M05052). <br>MIS1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MIS1 Antibody (M05052) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05052-mis1-primary-antibodies-ihc-testing-2.jpgAnti-Musashi 1 MSI1 Rabbit Monoclonal AntibodyIHC analysis of MIS1 using anti-MIS1 antibody (M05052). <br>MIS1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MIS1 Antibody (M05052) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cebp-beta-rabbit-monoclonal-antibody-m01100-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01100-wb7.jpgAnti-CEBP beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01100-wb.jpgAnti-CEBP beta Rabbit Monoclonal AntibodyWestern blot analysis of CEBP beta expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01100-if.jpgAnti-CEBP beta Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using CEBP beta Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p27-kip-1-rabbit-monoclonal-antibody-m00173-1-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-cdkn1b-primary-antibodies-wb-testing-1.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal Antibody Western blot analysis of CDKN1B using anti-CDKN1B antibody (M00173-1).<br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDKN1B antigen affinity purified monoclonal antibody (Catalog # M00173-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDKN1B at approximately 25 kDa. The expected band size for CDKN1B is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-cdkn1b-primary-antibodies-ihc-testing-2.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal Antibody IHC analysis of CDKN1B using anti-CDKN1B antibody (M00173-1). <br>
CDKN1B was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDKN1B Antibody (M00173-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-cdkn1b-primary-antibodies-ihc-testing-3.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal Antibody IHC analysis of CDKN1B using anti-CDKN1B antibody (M00173-1). <br>
CDKN1B was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDKN1B Antibody (M00173-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-cdkn1b-primary-antibodies-ihc-testing-4.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal Antibody IHC analysis of CDKN1B using anti-CDKN1B antibody (M00173-1). <br>
CDKN1B was detected in a paraffin-embedded section of human urothelial carcinoma with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDKN1B Antibody (M00173-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-cdkn1b-primary-antibodies-ihc-testing-5.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal Antibody IHC analysis of CDKN1B using anti-CDKN1B antibody (M00173-1). <br>
CDKN1B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDKN1B Antibody (M00173-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00173-1-if.jpgAnti-p27 KIP 1 CDKN1B Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using p27 KIP 1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-alpha-rabbit-monoclonal-antibody-m00743-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-ihc7.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-prkca-primary-antibodies-wb-testing-1.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal Antibody Western blot analysis of PRKCA using anti-PRKCA antibody (M00743). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat spleen tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKCA antigen affinity purified monoclonal antibody (Catalog # M00743) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRKCA at approximately 77 kDa. The expected band size for PRKCA is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-ihc9.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human melanoma, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-ihc8.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thymoma, using the Antibody at 1:300 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-ihc.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PKC alpha Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-icc1.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-if.jpgAnti-PKC alpha PRKCA Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using PKC alpha Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caldesmon-rabbit-monoclonal-antibody-m04578-1-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04578-1-wb.jpgAnti-Caldesmon CALD1 Rabbit Monoclonal AntibodyWestern blot analysis of Caldesmon expression in (1)NIH3T3 cell lysate; (2)HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-b1-rabbit-monoclonal-antibody-m00745-3-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-3-wb7.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-3-wb.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin B1 expression in (1)HaCaT cell lysates; (2)HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-3-ihc.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Cyclin B1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-d1-rabbit-monoclonal-antibody-m00149-1-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ccnd1-primary-antibodies-wb-testing-1.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal Antibody Western blot analysis of Cyclin D1 using anti-Cyclin D1 antibody (M00149-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human LNCAP whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclin D1 antigen affinity purified monoclonal antibody (Catalog # M00149-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclin D1 at approximately 34 kDa. The expected band size for Cyclin D1 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ccnd1-primary-antibodies-wb-testing-1_1.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin D1 using anti-Cyclin D1 antibody (M00149-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates, <br>
Lane 2: Model group-rat colon tissue lysates, <br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates, <br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates, <br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates, <br>
Lane 6: Western medicine-rat colon tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclin D1 antigen affinity purified monoclonal antibody (Catalog # M00149-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for Cyclin D1 at approximately 36 kDa. The expected band size for Cyclin D1 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-fendo-10-00091-g008.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyCombined effects of FSH and SCF on the expressions of cell cycling proteins CCND1 and CDK2. (A–D) 4-day-old chickens were treated by FSH in vivo . Brown staining represents the immunohistochemical antigen. (E,F) 4-day-old chicken ovaries were treated by FSH or SCF for 2 days in vitro . (A) Arrowheads represent oocytes stained with CDK2 antibody. (B) Arrowheads and arrows represent oocytes and somatic cells stained with CCND1 antibody. (C,D) Western blot and gray analysis indicate that FSH promoted the CDK2 and CCND1 protein expression in vivo . (E,F) Western blot and gray analysis indicate that SCF enhanced the effect of FSH on promoting the CDK2 and CCND1 protein expression in vitro . T -tests were used to determine statistically significant differences. The values are the mean ± SEM of six experiments. Asterisks indicate significant differences (* P < 0.05, ** P < 0.01). Scale bars: 50 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2019.00091/full'>30837955</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ott-13-1637-g0006.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyOverexpression of miR-1294 inhibited tumorigenicity of osteosarcoma cells. ( A, B ) Tumor volume in nude mice after subcutaneous injection of ME63 and U2O2 cells with or without overexpression of miR-1294. ( C ) The expression of miR-1294 in tumor tissues was determined by real-time PCR. ( D, E ) The expression of PKM2, c-Myc, cyclin D1, MMP-2, and MMP-9 in tumor tissues was assessed using immunohistochemistry and Western blot analysis. Data are shown as mean ± SD from 6 mice/group. ∗P < 0.05, ∗∗∗P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7041606/&orig_host=www.ncbi.nlm.nih.gov'>32110059</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ott-13-1637-g0005.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyOverexpression of PKM2 reversed the actions of miR-1294 upregulation on osteosarcoma cells. ( A ) Cell proliferation was evaluated by CCK-8 assay. ( B ) Cell apoptosis was examined by flow cytometry using Annexin V and PI staining. ( C ) Cell migration was assessed by a wound-healing assay. ( D ) Cell invasiveness was determined by transwell assay. ( E ) Expression levels of c-Myc, cyclin D1, cleaved-caspase 3, MMP-2, and MMP-9 were texted by Western blotting. Data are shown as mean ± SD. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7041606/&orig_host=www.ncbi.nlm.nih.gov'>32110059</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ott-13-1637-g0002.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodymiR-1294 upregulation inhibited proliferation and promoted apoptosis of osteosarcoma cells. ( A ) Overexpression of miR-1294 in MG63 and U2OS cells by transfection of miR-1294 mimic. ( B ) Cell proliferation was assessed using the CCK-8 assay. ( C ) Cell cycle distribution was analyzed by flow cytometry using propidium iodide (PI) staining. ( D ) Cell apoptosis was determined by flow cytometry using Annexin V and PI staining. ( E ) Expression levels of PCNA, c-Myc, cyclin D1, cleaved caspase 3, and cleaved PARP were examined by Western blotting. Data are shown as mean ± SD. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7041606/&orig_host=www.ncbi.nlm.nih.gov'>32110059</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-13578_2022_744_fig4_html.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyAIF blocks hypoxia-induced progression of PH in vitro and in vivo. A Hypoxia increased the viability of PASMCs after growth arrest for 24 h, and this effect was decreased by AIF (n = 4). B Pretreatment with an AIF overexpression plasmid blocked the effects of hypoxia on EdU incorporation in cells (n = 6). Scale bars: 50 μm. C Cell cycle analysis by flow cytometry indicated that hypoxia stimulated cell progression into G 2 /M + S phase, and this effect was inhibited by AIF overexpression (n = 3). D Effects of AIF on the expression of PCNA, Cyclin A and Cyclin D under hypoxia (n = 4–5). E Represents weight ratio of the right ventricular (RV)/left ventricular (LV) + Septum (n = 6); F Represents the right ventricular systolic pressure (RVSP) from mice (n = 5); G pulmonary artery velocity time integral (PAVTI), pulmonary artery acceleration time (PAAT) and left ventricular ejection fraction (LVEF) of the hypoxic mouse model infected with AAV5-NC and AAV5-AIF (n = 6). All data are presented as the means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001; Nor normoxia, Hyp hypoxia, NC negative control <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13578-022-00744-3'>35090552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-41419_2024_7113_fig6_html.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyThe MAT1A/CCND1 signaling axis promotes glycolysis and tumorigenesis in NSCLC. The xenograft tumor model in nude mice established by A549 cells that interfered with MAT1A and CCND1 expression. After 39 days of monitoring, A tumor volume and B tumor weight was measured. C HE, IHC staining and D WB analysis was performed to determine the expression of MAT1A, CCND1, proliferation marker Ki67 and glycolytic enzymes (ALDOC, HK2) after tumor tissue sections or protein extraction. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-024-07113-7'>39438468</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-41419_2024_7113_fig5_html.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyMAT1A enhances the glycolysis of NSCLC cells through CCND1. The metabolic profile of glycolysis in MAT1A knockdown A549 cells was analyzed, including ( A ) glucose utilization, lactic acid production, PA, PGK, GAPDH activity and ( B ) expression of pivotal glycolytic enzymes (PKM2, ALDOC, ADH6). C , D Measurement of glucose utilization, lactic acid production and ( D ) expression of pivotal glycolytic enzymes (PKM2, ALDOC, ADH6) in A549 cells (NC, as negative control; MAT1A-overexpressing; CCND1 knockdown; MAT1A-overexpressing and CCND1 knockdown). E , F MAT1A-overexpresed A549 cells treated with AKT inhibitor (perifosine) and measurement of ( E ) glucose utilization, lactic acid production and ( F ) expression of pivotal glycolytic enzymes (PKM2, ALDOC, ADH6). G , H MAT1A-overexpresed A549 cells treated with glycolysis inhibitor 2-deoxy-d-glucose (2-DG) and measurement of ( G ) glucose utilization, lactic acid production and ( H ) expression of pivotal glycolytic enzymes (PKM2, ALDOC, ADH6). Results were shown as mean ± SD. * p < 0.05, ** p < 0.05, *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-024-07113-7'>39438468</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-41419_2024_7113_fig4_html.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyMAT1A inhibited the ubiquitination of CCND1 by blocking the binding of SKP2 to CCND1. In co-immunoprecipitation experiments, the total lysates of A549 and NCI-H1299 cells were immunized with ( A ) anti-CCND1 or ( B ) anti-SKP2 and WB, respectively. In the co-immunoprecipitation experiments, total lysates of A549 and NCI-H1299 cells were immunized with ( C ) anti-MAT1A or ( D ) anti-SKP2 and WB. E MAT1A knockdown and control A549 and NCI-H1299 cells were treated with protein synthesis inhibitor (CHX, cycloheximide from microbial, 10 μmol/L) and then subjected to cycloheximide chase assays. F SKP2 overexpressed and control A549 and NCI-H1299 cells were treated with CHX (10 μmol/L) to detect the relative protein levels of CCND1 at indicated time points. CCND1 protein level was determined in ( G ) MAT1A-depleted or ( H ) SKP2-overexpresed A549 and NCI-H1299 cells treated with or without proteasome inhibitor (MG132, 10 μmol/L). The ubiquitin of CCND1 immunoprecipitated in ( I ) MAT1A-depleted or ( J ) SKP2-overexpresed A549 and NCI-H1299 cells was detected. K Total lysates of A549 and NCI-H1299 cells with or without MAT1A knockdown were immunized with anti-CCND1 and WB. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-024-07113-7'>39438468</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-41419_2024_7113_fig3_html.pngAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyMAT1A facilitated NSCLC cell proliferation and migration through CCND1. A Relative mRNA levels of top 4 DEGs were detected by qPCR analysis in A549 and NCI-H1299 cell after MAT1A depletion. B Relative protein levels of CCND1, BIRC5, E2F1 and MCM2 in A549 and NCI-H1299 cell after MAT1A depletion were determined by WB assays. C Cell viabilities of A549 cell after depletion of CCND1, BIRC5, E2F1 and MCM2 were assessed by Celigo cell count assays at indicated times. D CCND1 expression levels in human NSCLC cell lines (A549, NCI-H1299 and NCI-H1944) and normal human lung epithelial cell line (BEAS-2B) were determined by qPCR. A549 and NCI-H1299 cells were grouped as NC (empty vector, as negative control), MAT1A (MAT1A-overexpressing), shCCND1 (CCND1 knockdown) and MAT1A+shCCND1 (MAT1A-overexpressing and CCND1-knockdown) groups, performed ( E ) Celigo cell count assays, ( F ) flow cytometry, ( G ) wound-healing assays. Results were shown as mean ± SD. * p < 0.05, ** p < 0.05, *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-024-07113-7'>39438468</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00149-1-CCND1-primary-antibodies-IHC-testing-1.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using Cyclin D1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ihc7.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ihc8.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous cell carcinoma , using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-ihc9.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human ovarian cancer, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-if.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using Cyclin D1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00149-1-icc1.jpgAnti-Cyclin D1 CCND1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-1-rabbit-monoclonal-antibody-m00048-boster.html2026-03-24T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00048-casp1-primary-antibodies-wb-testing-1.jpgAnti-Caspase-1 CASP1 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase 1/CASP1 using anti-Caspase 1/CASP1 antibody (M00048). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 1/CASP1 antigen affinity purified monoclonal antibody (M00048) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Caspase 1/CASP1 at approximately 35-48 kDa. The expected band size for Caspase 1/CASP1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00048-ihc.jpgAnti-Caspase-1 CASP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Caspase-1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-e1-rabbit-monoclonal-antibody-m00543-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00543-1-wb.jpgAnti-Cyclin E1 CCNE1 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin E1 expression in HeLa cell lysates.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-2-rabbit-monoclonal-antibody-m02384-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02384-1-wb.jpgAnti-Caspase-2 CASP2 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-2 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02384-1-wb7.jpgAnti-Caspase-2 CASP2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02384-1-ihc.jpgAnti-Caspase-2 CASP2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse testis, using Caspase-2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02384-1-if.jpgAnti-Caspase-2 CASP2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Caspase-2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hp1-alpha-rabbit-monoclonal-antibody-m02780-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02780-cbx5-primary-antibodies-wb-testing-1.jpgAnti-HP1 alpha CBX5 Rabbit Monoclonal Antibody Western blot analysis of CBX5 using anti-CBX5 antibody (M02780). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CBX5 antigen affinity purified monoclonal antibody (Catalog # M02780) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CBX5 at approximately 22 kDa. The expected band size for CBX5 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02780-icc2.jpgAnti-HP1 alpha CBX5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02780-cbx5-primary-antibodies-ihc-testing-2.jpgAnti-HP1 alpha CBX5 Rabbit Monoclonal Antibody IHC analysis of CBX5 using anti-CBX5 antibody (M02780). <br>
CBX5 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CBX5 Antibody (M02780) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02780-cbx5-primary-antibodies-ihc-testing-3.jpgAnti-HP1 alpha CBX5 Rabbit Monoclonal Antibody IHC analysis of CBX5 using anti-CBX5 antibody (M02780). <br>
CBX5 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CBX5 Antibody (M02780) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02780-icc1.jpgAnti-HP1 alpha CBX5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kdm1-lsd1-rabbit-monoclonal-antibody-m00532-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00532-1-kdm1a-primary-antibodies-wb-testing-1.jpgAnti-KDM1/LSD1 KDM1A Rabbit Monoclonal AntibodyWestern blot analysis of KDM1/KDM1A using anti-KDM1/KDM1A antibody (M00532-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SIHA whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KDM1/KDM1A antigen affinity purified monoclonal antibody (M00532-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KDM1/KDM1A at approximately 100 kDa. The expected band size for KDM1/KDM1A is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00532-1-ihc.jpgAnti-KDM1/LSD1 KDM1A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using KDM1/LSD1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ubiquitin-rabbit-monoclonal-antibody-m02848-3-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-ubb-primary-antibodies-wb-testing-1.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyWestern blot analysis of Ubiquitin/UBB using anti-Ubiquitin/UBB antibody (M02848-3). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ubiquitin/UBB antigen affinity purified monoclonal antibody (M02848-3) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Ubiquitin/UBB at approximately 10 kDa. The expected band size for Ubiquitin/UBB is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-ihc7.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-13578_2022_744_fig1_html.pngAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyHypoxia results in decreased AIF expression. A Activity of mitochondrial respiratory chain complexes I–V after exposure to hypoxia, with complex I showing the most severe damage (n = 6). B Schematic structural model of AIF protein. C Decreased AIF expression was found in plasma from the hypoxic group (n = 5). D , E AIF protein and RNA levels in the lung tissues of the hypoxic model (n = 8). F , G The location of AIF in the smooth muscle layer of lung tissues from the hypoxic model was determined by immunofluorescence ( F , Scale bar = 100 μm) and immunohistochemical staining analysis ( G , Scale bar = 200 μm) (n = 3). H , I Time course of AIF protein and RNA levels in PASMCs 0, 24, 48, and 72 h after hypoxia treatment. J Subcellular distribution of AIF in PASMCs as determined by immunofluorescence analysis. Scale bars: 50 μm (n = 3). All data are presented as the means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001; Nor normoxia, Hyp hypoxia <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13578-022-00744-3'>35090552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-13578_2022_744_fig6_html.pngAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyUBA52 participates in AIF ubiquitination, leading to its degradation by the proteasome system. A The colocalization of ubiquitin (UB) and Tom20 was determined using immunofluorescence (n = 3). Scale bars: 50 μm. B PASMCs were exposed to normoxia or hypoxia for 24 h, and co-IP assay was performed using anti-AIF, followed by probing with anti-UB (n = 3). C Cells were treated with or without PS-341 for 24 h, and the expression levels of AIF and β-actin were examined (n = 6). D , E GO and KEGG analysis of proteins interacting with AIF. F Mass spectrometry of specific segments of AIF and UBA52. G After PASMCs were exposed to normoxia or hypoxia, whole cell lysates were extracted for co-IP assay with anti-AIF or anti-UBA52, followed by probing with anti-UBA52 or anti-AIF (n = 3). H Representative predicted binding sites and structures of UBA52 and AIF. I PASMCs were transfected with si-UBA52 and then exposed to hypoxia, and the protein expression of AIF was estimated with β-actin serving as the standard (n = 6). All data are presented as the means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001; Nor normoxia, Hyp hypoxia, NC negative control, si small interfering RNA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13578-022-00744-3'>35090552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-13578_2022_744_fig7_html.pngAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyUBA52/AIF axis is responsible for increased cell autophagy and proliferation in response to hypoxia treatment. A Mitochondrial ROS was visualized by the mitochondrially targeted superoxide indicator (MitoSOX). Treatment with UBA52 siRNA blocked the increase in MitoSOX under hypoxia, whereas UBA52 plus AIF siRNA reversed this effect (n = 6). Scale bars: 50 μm. B Representative autophagic flux monitored by eGFP-mRFP LC3 plasmid transfection. The formation of autophagosomes was calculated (n = 6). Scale bars: 50 μm. C Western blot analysis of LC3BII and Pink in PASMCs cotransfected with UBA52 and AIF siRNA (n = 5). D , E CCK8 and 5-ethynyl-2-deoxyuridine (EdU) assays were used to determine the effects of UBA52 and AIF on cell proliferation (n = 6). F The number of cells in each phase of the cell cycle was examined by flow cytometry (n = 3). All data are presented as the means ± standard deviation. *p < 0.05; **p < 0.01; ***p < 0.001; Nor normoxia, Hyp hypoxia, NC negative control, si small interfering RNA <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13578-022-00744-3'>35090552</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-ihc8.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-ihc.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Ubiquitin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-ihc9.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human stomach, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-3-if.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunofluorescent analysis of Raji cells, using Ubiquitin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-b1-rabbit-monoclonal-antibody-m00745-2-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-wb7.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-wb.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin B1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-kd1.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc9.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc10.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc7.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc11.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse lung, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc8.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-ihc.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using Cyclin B1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-icc1.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00745-2-if.jpgAnti-Cyclin B1 CCNB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cyclin B1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-e2-rabbit-monoclonal-antibody-m04536-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-1-wb7.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-1-wb8.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-1-wb.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin E2 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-7-rabbit-monoclonal-antibody-m01044-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01044-1-wb.jpgAnti-Caspase-7 Casp7 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-7 expression in NIH/3T3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-8-rabbit-monoclonal-antibody-m00042-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-casp8-primary-antibodies-wb-testing-1.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyWestern blot analysis of CASP8 using anti-CASP8 antibody (M00042). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: human A549 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CASP8 antigen affinity purified monoclonal antibody (M00042) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CASP8 at approximately 50 kDa. The expected band size for CASP8 is at 55 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dysferlin-rabbit-monoclonal-antibody-m01234-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01234-dysf-primary-antibodies-wb-testing-1.jpgAnti-Dysferlin Rabbit Monoclonal Antibody Western blot analysis of Dysferlin using anti-Dysferlin antibody (M01234). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse skeletal muscle tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dysferlin antigen affinity purified monoclonal antibody (Catalog # M01234) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Dysferlin at approximately 280 kDa. The expected band size for Dysferlin is at 237 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-6-rabbit-monoclonal-antibody-m02631-2-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-2-wb.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-6 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-2-ihc.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Caspase-6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-err-alpha-rabbit-monoclonal-antibody-m03339-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03339-wb7.jpgAnti-ERR alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03339-wb8.jpgAnti-ERR alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03339-wb.jpgAnti-ERR alpha Rabbit Monoclonal AntibodyWestern blot analysis of ERR alpha expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myoglobin-rabbit-monoclonal-antibody-m04058-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04058-mb-primary-antibodies-wb-testing-1.jpgAnti-Myoglobin MB Rabbit Monoclonal Antibody Western blot analysis of MB using anti-MB antibody (M04058). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates,<br>
Lane 2: rat skeletal muscle tissue lysates,<br>
Lane 3: mouse heart tissue lysates,<br>
Lane 4: mouse skeletal muscle tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MB antigen affinity purified monoclonal antibody (Catalog # M04058) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MB at approximately 15 kDa. The expected band size for MB is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04058-wb.jpgAnti-Myoglobin MB Rabbit Monoclonal AntibodyWestern blot analysis of Myoglobin expression in Human heart muscle lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04058-ihc.jpgAnti-Myoglobin MB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human skeletal muscle, using Myoglobin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cortactin-rabbit-monoclonal-antibody-m01253-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01253-cttn-primary-antibodies-wb-testing-1.jpgAnti-Cortactin CTTN Rabbit Monoclonal Antibody Western blot analysis of Cortactin using anti-Cortactin antibody (M01253). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cortactin antigen affinity purified monoclonal antibody (Catalog # M01253) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cortactin at approximately 85 kDa. The expected band size for Cortactin is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01253-ihc.jpgAnti-Cortactin CTTN Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Cortactin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikk-alpha-rabbit-monoclonal-antibody-m01918-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-1-chuk-primary-antibodies-wb-testing-1.jpgAnti-IKK alpha CHUK Rabbit Monoclonal Antibody Western blot analysis of IKK alpha using anti-IKK alpha antibody (M01918-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human A375 whole cell lysates,<br>
Lane 4: human Daudi whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKK alpha antigen affinity purified monoclonal antibody (Catalog # M01918-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IKK alpha at approximately 85 kDa. The expected band size for IKK alpha is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-1-ihc.jpgAnti-IKK alpha CHUK Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using IKK alpha Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-1-icc1.jpgAnti-IKK alpha CHUK Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-5-rabbit-monoclonal-antibody-m05259-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05259-casp5-primary-antibodies-wb-testing-1.jpgAnti-Caspase 5 CASP5 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase 5/CASP5 using anti-Caspase 5/CASP5 antibody (M05259). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HT1080 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 5/CASP5 antigen affinity purified monoclonal antibody (M05259) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Caspase 5/CASP5 at approximately 50 kDa. The expected band size for Caspase 5/CASP5 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05259-ihc.jpgAnti-Caspase 5 CASP5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Caspase 5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-8-rabbit-monoclonal-antibody-m00042-1-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-1-wb7.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-1-ihc.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using Caspase-8 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-1-wb8.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-1-if.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Caspase-8 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00042-1-wb.jpgAnti-Caspase-8 CASP8 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-8 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-2-rabbit-monoclonal-antibody-m02384-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02384-wb.jpgAnti-Caspase-2 CASP2 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-2 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-9-rabbit-monoclonal-antibody-m00080-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080_12672_2025_3032_fig3_html.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal Antibody(a) The representative cell apoptosis photos using flow cytometry, (i) The blank control group; (ii) The miR-NC transfection group; (iii) The miR-145 mimics transfection group. (b) The apoptosis rate of the miR-145 mimics transfection group increased significantly, ** p < 0.01. (c) The representative protein expression (Caspase-9: 46 kD, Caspase-3: 32 kD, GAPDH: 36 kD) photos using western blot. (d) The expression of Caspase-9 and Caspase-3 in three groups, ** p < 0.01<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12214196/'>40591050</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-casp9-primary-antibodies-wb-testing-1.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal Antibody Western blot analysis of Caspase-9 using anti-Caspase-9 antibody (M00080). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human SiHa whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: human Jurkat whole cell lysates,<br>
Lane 6: human Jurkat whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase-9 antigen affinity purified monoclonal antibody (Catalog # M00080) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase-9 at approximately 46 kDa. The expected band size for Caspase-9 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-ihc.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Caspase-9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-if.jpgAnti-Caspase-9 CASP9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells treated with staurosporine, using Caspase-9 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-e1-rabbit-monoclonal-antibody-m00543-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00543-wb7.jpgAnti-Cyclin E1 CCNE1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00543-wb.jpgAnti-Cyclin E1 CCNE1 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin E1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00543-if.jpgAnti-Cyclin E1 CCNE1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cyclin E1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-e2-rabbit-monoclonal-antibody-m04536-boster.html2026-03-24T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-wb.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyWestern blot analysis of Cyclin E2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-ihc.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Cyclin E2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04536-if.jpgAnti-Cyclin E2 CCNE2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cyclin E2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-d3-rabbit-monoclonal-antibody-m01744-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01744-ccnd3-primary-antibodies-wb-testing-1.jpgAnti-Cyclin D3 CCND3 Rabbit Monoclonal AntibodyWestern blot analysis of CCND3 using anti-CCND3 antibody (M01744). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: mouse thymus tissue lysates,<br>
Lane 5: mouse Raw264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCND3 antigen affinity purified monoclonal antibody (M01744) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CCND3 at approximately 33 kDa. The expected band size for CCND3 is at 33 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-b2-rabbit-monoclonal-antibody-m02040-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-wb-testing-1.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody Western blot analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCNB2 antigen affinity purified polyclonal antibody (Catalog # M02040) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCNB2 at approximately 45 kDa. The expected band size for CCNB2 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-2.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-3.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-icc1.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-4.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-5.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-icc2.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-6.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-7.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-8.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-9.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-10.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-11.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-12.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02040-ccnb2-primary-antibodies-ihc-testing-13.jpgAnti-Cyclin B2 CCNB2 Rabbit Monoclonal Antibody IHC analysis of CCNB2 using anti-CCNB2 antibody (M02040). <br>
CCNB2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CCNB2 Antibody (M02040) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-a2-rabbit-monoclonal-antibody-m00700-1-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-ccna2-primary-antibodies-wb-testing-1.jpgAnti-Cyclin A2 Rabbit Monoclonal Antibody Western blot analysis of Cyclin A2 using anti-Cyclin A2 antibody (M00700-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat NRK whole cell lysates,<br>
Lane 7: mouse RAW264.7 whole cell lysates,<br>
Lane 8: mouse ANA-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclin A2 antigen affinity purified monoclonal antibody (Catalog # M00700-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclin A2 at approximately 55 kDa. The expected band size for Cyclin A2 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-ccna2-primary-antibodies-ihc-testing-2.jpgAnti-Cyclin A2 Rabbit Monoclonal Antibody IHC analysis of Cyclin A2 using anti-Cyclin A2 antibody (M00700-1). <br>
Cyclin A2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cyclin A2 Antibody (M00700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-ccna2-primary-antibodies-ihc-testing-3.jpgAnti-Cyclin A2 Rabbit Monoclonal Antibody IHC analysis of Cyclin A2 using anti-Cyclin A2 antibody (M00700-1). <br>
Cyclin A2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cyclin A2 Antibody (M00700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-ccna2-primary-antibodies-ihc-testing-4.jpgAnti-Cyclin A2 Rabbit Monoclonal Antibody IHC analysis of Cyclin A2 using anti-Cyclin A2 antibody (M00700-1). <br>
Cyclin A2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cyclin A2 Antibody (M00700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-ccna2-primary-antibodies-ihc-testing-5.jpgAnti-Cyclin A2 Rabbit Monoclonal Antibody IHC analysis of Cyclin A2 using anti-Cyclin A2 antibody (M00700-1). <br>
Cyclin A2 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cyclin A2 Antibody (M00700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-icc1.jpgAnti-Cyclin A2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-1-icc2.jpgAnti-Cyclin A2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-6-rabbit-monoclonal-antibody-m02631-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-wb7.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-if.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Caspase-6 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-wb.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-6 expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-ihc.jpgAnti-Caspase-6 CASP6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Caspase-6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mek3-mek6-rabbit-monoclonal-antibody-m02916-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-map2k3-6-primary-antibodies-wb-testing-1.jpgAnti-MEK3/MEK6 MAP2K3 Rabbit Monoclonal AntibodyWestern blot analysis of MEK3/6 using anti-MEK3/6 antibody (M02916). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat skeletal muscle tissue lysates,<br>
Lane 7: mouse skeletal muscle tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEK3/6 antigen affinity purified monoclonal antibody (M02916) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MEK3/6 at approximately 38,39 kDa. The expected band size for MEK3/6 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-map2k3-primary-antibodies-ihc-testing-1.jpgAnti-MEK3/MEK6 MAP2K3 Rabbit Monoclonal AntibodyIHC analysis of MAP2K3 using anti-MAP2K3 antibody (M02916). <br>MAP2K3 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MAP2K3 Antibody (M02916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-map2k3-primary-antibodies-ihc-testing-2.jpgAnti-MEK3/MEK6 MAP2K3 Rabbit Monoclonal AntibodyIHC analysis of MAP2K3 using anti-MAP2K3 antibody (M02916). <br>MAP2K3 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MAP2K3 Antibody (M02916) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02916-if.jpgAnti-MEK3/MEK6 MAP2K3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using MEK3/MEK6 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ubiquitin-rabbit-monoclonal-antibody-m02848-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-wb.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyWestern blot analysis of Ubiquitin expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-ihc.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Ubiquitin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-if.jpgAnti-Ubiquitin UBB Rabbit Monoclonal AntibodyImmunofluorescent analysis of Jurkat cells, using Ubiquitin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-jnk1-jnk3-rabbit-monoclonal-antibody-m02608-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-wb.jpgAnti-JNK1/JNK3 MAPK8 Rabbit Monoclonal AntibodyWestern blot analysis of JNK1/JNK3 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02608-jnk1-jnk3-primary-antibodies-wb-testing-1.jpgAnti-JNK1/JNK3 MAPK8 Rabbit Monoclonal AntibodyWestern blot analysis of JNK using anti-JNK antibody (M02608).<br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions..<br>
Lane 1: mouse spleen tissue lysates,.<br>
Lane 2: mouse RAW264.7 whole cell lysates..<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JNK antigen affinity purified monoclonal antibody (M02608) at a dilution of 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for JNK at approximately 48 and 54 kDa. The expected band size for JNK is at 48 and 54 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fus-tls-rabbit-monoclonal-antibody-m00771-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00771-fus-primary-antibodies-wb-testing-1.jpgAnti-FUS / TLS Rabbit Monoclonal AntibodyWestern blot analysis of FUS using anti-FUS antibody (M00771). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FUS antigen affinity purified monoclonal antibody (M00771) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FUS at approximately 70 kDa. The expected band size for FUS is at 70 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-delta-rabbit-monoclonal-antibody-m00822-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00822-djir_a_12304658_f0005_c.jpgAnti-PKC delta PRKCD Rabbit Monoclonal AntibodyWestern blot analysis of curcumin regulation of the p38MAPK pathway. (A–C) Western blot and quantitative analysis of p38 and p-p38. (D–F) Western blot and quantitative analysis of ASK1 and MEKK3. (G and H) Western blot images and quantitative analysis of PKCδ and p-PKCδ. (I–L) Western blot and quantitative analysis of BCL-2 and caspase-3. (n = 3). *p < 0.05,** p < 0.01,***p < 0.001.
<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S459867'>39081871</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00822-prkcd-primary-antibodies-wb-testing-1.jpgAnti-PKC delta PRKCD Rabbit Monoclonal Antibody Western blot analysis of PRKCD using anti-PRKCD antibody (M00822). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: rat lung tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKCD antigen affinity purified polyclonal antibody (Catalog # M00822) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRKCD at approximately 78 kDa. The expected band size for PRKCD is at 78 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-human-igm-rabbit-monoclonal-antibody-m07469-1-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07469-1-wb.jpgAnti-Human IgM IGHM Rabbit Monoclonal AntibodyWestern blot analysis of Human IgM expression in human plasma lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07469-1-ihc.jpgAnti-Human IgM IGHM Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tonsil, using Human IgM Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gc-vdbp-rabbit-monoclonal-antibody-m03364-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03364-wb.jpgAnti-GC / VDBP Rabbit Monoclonal AntibodyWestern blot analysis of GC/VDBP expression in Human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calbindin-rabbit-monoclonal-antibody-m03047-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03047-wb7.jpgAnti-Calbindin CALB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03047-wb.jpgAnti-Calbindin CALB1 Rabbit Monoclonal AntibodyWestern blot analysis of Calbindin expression in human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-annexin-v-rabbit-monoclonal-antibody-m00744-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00744-anxa5-primary-antibodies-wb-testing-2.jpgAnti-Annexin V ANXA5 Rabbit Monoclonal AntibodyWestern blot analysis of ANXA5 using anti-ANXA5 antibody (M00744). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANXA5 antigen affinity purified monoclonal antibody (M00744) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ANXA5 at approximately 36 kDa. The expected band size for ANXA5 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00744-anxa5--primary-antibodies-wb-testing-1.jpgAnti-Annexin V ANXA5 Rabbit Monoclonal AntibodyWestern blot analysis of Annexin V using anti-Annexin V antibody (M00744). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin V antigen affinity purified monoclonal antibody (M00744) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Annexin V at approximately 36kDa. The expected band size for Annexin V is at 36 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aromatase-rabbit-monoclonal-antibody-m00071-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00071-cyp19a1-primary-antibodies-wb-testing-1.jpgAnti-Aromatase CYP19A1 Rabbit Monoclonal AntibodyWestern blot analysis of CYP19A1 using anti-CYP19A1 antibody (M00071). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP19A1 antigen affinity purified monoclonal antibody (M00071) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CYP19A1 at approximately 50 kDa. The expected band size for CYP19A1 is at 58 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-urokinase-rabbit-monoclonal-antibody-m04352-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04352-wb.jpgAnti-Urokinase Rabbit Monoclonal AntibodyWestern blot analysis of Urokinase expression in LnCaP cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04352-plau-primary-antibodies-ihc-testing-1.jpgAnti-Urokinase Rabbit Monoclonal AntibodyIHC analysis of PLAU using anti-PLAU antibody (M04352). <br>PLAU was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PLAU Antibody (M04352) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04352-plau-primary-antibodies-ihc-testing-2.jpgAnti-Urokinase Rabbit Monoclonal AntibodyIHC analysis of ERK1 using anti-ERK1 antibody (M00104). <br>ERK1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ERK1 Antibody (M00104) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rhodopsin-rabbit-monoclonal-antibody-m00083-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00083-wb.jpgAnti-Rhodopsin Rabbit Monoclonal AntibodyWestern blot analysis of Rhodopsin expression in rat eyeball lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-claudin-5-rabbit-monoclonal-antibody-m03260-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03260-wb7.jpgAnti-Claudin 5 CLDN5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03260-wb.jpgAnti-Claudin 5 CLDN5 Rabbit Monoclonal AntibodyWestern blot analysis of Claudin 5 expression in human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikk-gamma-rabbit-monoclonal-antibody-m00874-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00874-wb.jpgAnti-IKK gamma IKBKG Rabbit Monoclonal AntibodyWestern blot analysis of IKK gamma expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00874-ihc.jpgAnti-IKK gamma IKBKG Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse colon, using IKK gamma Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-profilin1-rabbit-monoclonal-antibody-m01480-boster.html2026-03-24T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01480-pfn1-primary-antibodies-wb-testing-1.jpgAnti-Profilin1 PFN1 Rabbit Monoclonal Antibody Western blot analysis of PFN1 using anti-PFN1 antibody (M01480). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PFN1 antigen affinity purified monoclonal antibody (Catalog # M01480) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PFN1 at approximately 15 kDa. The expected band size for PFN1 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01480-icc1.jpgAnti-Profilin1 PFN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lxr-alpha-rabbit-monoclonal-antibody-m03331-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03331-wb7.jpgAnti-LXR alpha NR1H3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03331-wb8.jpgAnti-LXR alpha NR1H3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03331-wb.jpgAnti-LXR alpha NR1H3 Rabbit Monoclonal AntibodyWestern blot analysis of LXR alpha expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-claudin-1-rabbit-monoclonal-antibody-m01585-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01585-fmicb-16-1594012-g005.jpgAnti-Claudin 1 CLDN1 Rabbit Monoclonal AntibodyOral administration of SA-Q-CS MPs improves the levels of colonic tight-junction proteins. (A) IHC staining images of ZO-1 protein, black arrows indicate positive signal of ZO-1 protein (scale bar 100 μm); (B) Protein bands of Occludin, Claudin-1 and ZO-1; (C) IOD was counted of ZO-1 by immunohistochemical staining; (D) FITC fluorescence intensity in blood of C57/BL6 mice in each FITC group; ( E–G ) Protein statistical analysis of proteins Occludin, Claudin-1, and ZO-1. Data was represented as mean ± SD ( * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001 by one-way ANOVA with Dunnett’s multiple comparisons test, n ≥ 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2025.1594012/full'>40842836</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01585-cldn1-primary-antibodies-wb-testing-1.jpgAnti-Claudin 1 CLDN1 Rabbit Monoclonal Antibody Western blot analysis of Claudin 1 using anti-Claudin 1 antibody (M01585). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-Claudin 1 antigen affinity purified monoclonal antibody (Catalog # M01585) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Claudin 1 at approximately 23 kDa. The expected band size for Claudin 1 is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calpain-1-rabbit-monoclonal-antibody-m01943-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01943-wb7.jpgAnti-Calpain 1 CAPN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01943-wb.jpgAnti-Calpain 1 CAPN1 Rabbit Monoclonal AntibodyWestern blot analysis of Calpain 1 expression in Human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-human-igg-rabbit-monoclonal-antibody-m04575-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04575-ihc7.jpgAnti-Human IgG IGHG1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04575-ihc.jpgAnti-Human IgG IGHG1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using Human IgG Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04575-ihc8.jpgAnti-Human IgG IGHG1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04575-wb.jpgAnti-Human IgG IGHG1 Rabbit Monoclonal AntibodyWestern blot analysis of Human IgG expression in Human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-actin-rabbit-monoclonal-antibody-m01263-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-beta_actin-primary-antibodies-wb-testing-1_1.jpgAnti-beta Actin ACTB Rabbit Monoclonal Antibody Western blot analysis of Beta Actin using anti-Beta Actin antibody (M01263). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human GES-1 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Beta Actin antigen affinity purified monoclonal antibody (Catalog # M01263) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Beta Actin at approximately 42 kDa. The expected band size for Beta Actin is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-fendo-16-1528768-g003.jpgAnti-beta Actin ACTB Rabbit Monoclonal AntibodyEffects of 1,25 VD3 supplementation on hepatic lipid peroxidation, inflammation and fatty acid metabolizing genes in NASH rats. To assess oxidative stress, hepatic (A) MDA was measured using a thiobarbituric acid kit and (B) TAOC levels measured using the FRAP method. (C) NF-κB expression in liver tissue, analyzed by Western blotting and normalized to β-actin (left panel showing representative blot and right panel showing quantification by densitometry of 65 kDa band). Antibodies used and their dilutions: primary antibodies against NF-κB (anti-rabbit, 1:1000) and β-actin (anti-rabbit, 1:1000), followed by HRP-conjugated secondary antibody (1:2000). (D) PPARα and (E) CPT-1 mRNA levels were quantified by qPCR in liver tissues of indicated groups, and expressed as relative mRNA levels following normalization to GAPDH mRNA levels. Data are presented as mean ± SEM, n=6. *p < 0.05, **p<0.01 and ***p < 0.001 vs CG; ##p < 0.01 and ###p < 0.001 vs CDG.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2025.1528768/full'>40190400</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-fphar-15-1361561-g007.jpgAnti-beta Actin ACTB Rabbit Monoclonal AntibodyMSMP-containing serum inhibited NF-κB pathway in macrophages after LPS induction. (A) Western blot analysis of p-p65, p65 and β-actin; (B) Statistical analysis of the Western blot results for p-p65/β-actin (%); (C) Statistical analysis of the Western blot results for p-p65/p65 (%); Quantification of the proteins was analyzed by the ImageJ software. (D) The immunofluorescence assay shows the blue fluorescence for DAPI, the red fluorescence for p-p65 and finally the merge plot; (E, F) The expression of p-p65 was analyzed by the ImageJ software. Scale bar represents 100 μm (Date are mean ± SD, #### p < 0.0001, versus Control group; *** p < 0.001, **** p < 0.0001, versus LPS group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1361561/full'>38974041</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-12967_2018_1645_fig4_html.pngAnti-beta Actin ACTB Rabbit Monoclonal AntibodyIncreased β-catenin expression in HBV-infected hepatic cells. a Western blot analysis of β-catenin expression in hepatic L02 cells transfected with and without pcDNA3.1-HBV (1.3 and 1.1) or its control pcDNA3.1 for 48 h. β-actin served as a loading control. b Immunofluorescence staining for β-catenin in L02 cells transfected with and without pcDNA3.1-HBV (1.3 and 1.1) or its control pcDNA3.1 for 48 h. White scale bars = 50 µm. c ELISA assay for β-catenin expression in L02 cells transfected with and without pcDNA3.1-HBV (1.3 and 1.1) or its control pcDNA3.1 for 48 h. d LDH assay for LDH from L02 cells transfected with and without pcDNA3.1-HBV (1.3 and 1.1) or its control pcDNA3.1 for 48 h. e Flow cytometry analysis for apoptotic L02 cells transfected with and without pcDNA3.1-HBV (1.3 and 1.1) or its control pcDNA3.1 for 72 h. f Apoptosis index for L02 cells with different treatment. Ns no statistical significance <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-018-1645-x'>30268125</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-fphys-09-00941-g005.jpgAnti-beta Actin ACTB Rabbit Monoclonal Antibody(A–D) Cisatracurium alters migration and invasion regulatory genes transcription and protein expression levels in HCT116 cells. (A) Representative densities of SNAI-1, SLUG, E-Cadherin, CALD1, and β-actin proteins following western blot experiment. (B,C) Cluster bar charts of SNAI-1, SLUG, E-Cadherin, and CALD1 proteins expression and mRNA transcription levels of untreated and cisatracurium-treated (10 or 20 μM) HCT116 cells. β-Actin was used as internal control during western blot and qRT-PCR experiments. (D) Immunofluorescence was performed using FITC-labeled phalloidin, SNAI-1, SLUG, E-Cadherin, and CALD1 were stained with DAPI (Scale bar: 20 μm). Data are expressed as Mean ± SEM ( n = 3). ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 versus untreated (0).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2018.00941/full'>30108509</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-fphys-09-00941-g006.jpgAnti-beta Actin ACTB Rabbit Monoclonal Antibody(A–F) Cisatracurium inhibits metastatic ability of CRC in vivo . (A) Line graph of subcutaneous tumor volume. (B) Weight of subcutaneous tumors in grams. Data are expressed as mean tumor volume or weight ± SE. ∗ p < 0.05. (C–F) Representative densities of tumor viability and migration regulatory proteins (p53, p21 and CD1, SNAI-1, CALD1, E-Cadherin) in tumor tissue samples. β-Actin was used as internal control. The cluster bar chats in (D , F) indicates the levels of viability and migration regulatory proteins in the treatment group. Data are expressed as Mean ± SEM ( n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 versus control.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2018.00941/full'>30108509</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-1-s2.0-s2405844024033073-gr7.jpgAnti-beta Actin ACTB Rabbit Monoclonal AntibodyThe expression levels of FTH1 protein in different treated groups over time. The expression levels of FTH1 protein in different treated groups of HFL1 cells over time (Western Blot). The β-actin protein was used as an internal reference protein. The relative expression levels of FTH1 protein quantified by image analysis, and corrected by internal reference protein and control. The trend of levels of FTH1 protein expression were consistent with the results of immunofluorescence after TGF-β1 and DHA treatments. Data are presented as mean ± SEM (n = 3). Compared with the control group, *P < 0.05, **P < 0.01; compared with TGF-β1treatment group, △△P < 0.01, compared with DHA treated group, ##P < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2405844024033073'>38463857</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-40769220-figure-6.jpgAnti-beta Actin ACTB Rabbit Monoclonal AntibodyEffect of C15/ChemR23 on HMGB1 levels and ROS production in vivo. (A) Western blot was used to measure the protein expression of HMGB1 after I/R in mice.
(B) Densitometric quantification of HMGB1/β-actin expression (n = 4, independent samples).
(C) Representative DHE staining images show the production of ROS (red) after I/R in mice. Scale bar: 100 μm.
(D) The bar graph represents the mean fluorescent intensity (MFI) of ROS (n = 6, independent samples). Data are presented as means ± SDs and were analyzed using one-way ANOVA with post hoc Tukey’s multiple comparison test. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01657-8'>40970195</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01263-ACTB-primary-antibodies-IHC-testing-1.jpgAnti-beta Actin ACTB Rabbit Monoclonal Antibody
Immunohistochemical analysis of paraffin-embedded (1) Human heart; (2) Mouse testis; (3) Human bladder cancer; (4) Mouse heart, using beta Actin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01263-icc1.jpgAnti-beta Actin ACTB Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-e-cadherin-rabbit-monoclonal-antibody-m00063-4-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-4-wb7.jpgAnti-E Cadherin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-4-cdh1-primary-antibodies-ihc-testing-2.jpgAnti-E Cadherin Rabbit Monoclonal Antibody IHC analysis of E Cadherin using anti-E Cadherin antibody (M00063-4). <br>
E Cadherin was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:5000 rabbit anti-E Cadherin Antibody (M00063-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-4-cdh1-primary-antibodies-ihc-testing-3.jpgAnti-E Cadherin Rabbit Monoclonal Antibody IHC analysis of E Cadherin using anti-E Cadherin antibody (M00063-4). <br>
E Cadherin was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:5000 rabbit anti-E Cadherin Antibody (M00063-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-4-icc1.jpgAnti-E Cadherin Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-4-wb.jpgAnti-E Cadherin Rabbit Monoclonal AntibodyWestern blot analysis of E-cadherin expression in MCF7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caveolin-2-rabbit-monoclonal-antibody-m01574-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01574-wb7.jpgAnti-Caveolin-2 CAV2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01574-wb.jpgAnti-Caveolin-2 CAV2 Rabbit Monoclonal AntibodyWestern blot analysis of Caveolin 2 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01574-ihc.jpgAnti-Caveolin-2 CAV2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Caveolin-2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caveolin-3-rabbit-monoclonal-antibody-m00990-1-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00990-1-wb7.jpgAnti-Caveolin-3 CAV3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00990-1-wb8.jpgAnti-Caveolin-3 CAV3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00990-1-wb.jpgAnti-Caveolin-3 CAV3 Rabbit Monoclonal AntibodyWestern blot analysis of Caveolin 3 expression in Human fetal heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caveolin-3-rabbit-monoclonal-antibody-m00990-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00990-wb.jpgAnti-Caveolin-3 CAV3 Rabbit Monoclonal AntibodyWestern blot analysis of Caveolin 3 expression in Human fetal heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-n-cadherin-rabbit-monoclonal-antibody-m01577-1-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc7.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat testis, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-cdh2-primary-antibodies-wb-testing-1.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal Antibody Western blot analysis of CDH2 using anti-CDH2 antibody (M01577-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDH2 antigen affinity purified polyclonal antibody (Catalog # M01577-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDH2 at approximately 140 kDa. The expected band size for CDH2 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc8.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc9.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc10.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc11.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-ihc.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using N Cadherin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01577-1-icc1.jpgAnti-N-Cadherin-2 CDH2 CD325-Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caveolin-1-rabbit-monoclonal-antibody-m00179-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00179-wb7.jpgAnti-Caveolin-1 CAV1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00179-if.jpgAnti-Caveolin-1 CAV1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using Caveolin-1 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00179-wb.jpgAnti-Caveolin-1 CAV1 Rabbit Monoclonal AntibodyWestern blot analysis of Caveolin-1 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00179-wb8.jpgAnti-Caveolin-1 CAV1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00179-ihc.jpgAnti-Caveolin-1 CAV1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse lung, using Caveolin-1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mutant-p53-rabbit-monoclonal-antibody-m00001-3-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-3-wb7.jpgAnti-Mutant p53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00001-3-wb.jpgAnti-Mutant p53 Rabbit Monoclonal AntibodyWestern blot analysis of p53 in (1) A431 cell lysate; (2) HEK293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-collagen-i-rabbit-monoclonal-antibody-m00624-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00624-COL1A2-primary-antibodies-WB-testing-1.jpgAnti-Collagen I COL1A1 Rabbit Monoclonal AntibodyWestern blot analysis of Collagen I in Human stomach tissue lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00624-col1a1-primary-antibodies-ihc-testing-2.jpgAnti-Collagen I COL1A1 Rabbit Monoclonal Antibody IHC analysis of Collagen I using anti-Collagen I antibody (M00624). <br>
Collagen I was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Collagen I Antibody (M00624) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00624-col1a1-primary-antibodies-ihc-testing-3.jpgAnti-Collagen I COL1A1 Rabbit Monoclonal Antibody IHC analysis of Collagen I using anti-Collagen I antibody (M00624). <br>
Collagen I was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Collagen I Antibody (M00624) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00624-col1a1-primary-antibodies-ihc-testing-4.jpgAnti-Collagen I COL1A1 Rabbit Monoclonal Antibody IHC analysis of Collagen I using anti-Collagen I antibody (M00624). <br>
Collagen I was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Collagen I Antibody (M00624) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00624-col1a1-primary-antibodies-ihc-testing-5.jpgAnti-Collagen I COL1A1 Rabbit Monoclonal Antibody IHC analysis of Collagen I using anti-Collagen I antibody (M00624). <br>
Collagen I was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Collagen I Antibody (M00624) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-beta-rabbit-monoclonal-antibody-m01692-1-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-1-wb.jpgAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp90 beta expression in (1)HeLa cell lysate;(2)Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-1-ihc.jpgAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using Hsp90 beta Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-1-if.jpgAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Hsp90 beta Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ckii-alpha-rabbit-monoclonal-antibody-m02398-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02398-csnk2a1-primary-antibodies-wb-testing-1.jpgAnti-CKII alpha CSNK2A1 Rabbit Monoclonal AntibodyWestern blot analysis of CSNK2A1 using anti-CSNK2A1 antibody (M02398). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human AGS whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CSNK2A1 antigen affinity purified monoclonal antibody (M02398) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CSNK2A1 at approximately 40 kDa. The expected band size for CSNK2A1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02398-csnk2a1-primary-antibodies-ihc-testing-1.jpgAnti-CKII alpha CSNK2A1 Rabbit Monoclonal AntibodyIHC analysis of CSNK2A1 using anti-CSNK2A1 antibody (M02398). <br>CSNK2A1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CSNK2A1 Antibody (M02398) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02398-csnk2a1-primary-antibodies-ihc-testing-2.jpgAnti-CKII alpha CSNK2A1 Rabbit Monoclonal AntibodyIHC analysis of CSNK2A1 using anti-CSNK2A1 antibody (M02398). <br>CSNK2A1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CSNK2A1 Antibody (M02398) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02398-csnk2a1-primary-antibodies-ihc-testing-3.jpgAnti-CKII alpha CSNK2A1 Rabbit Monoclonal AntibodyIHC analysis of CSNK2A1 using anti-CSNK2A1 antibody (M02398). <br>CSNK2A1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CSNK2A1 Antibody (M02398) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02398-csnk2a1-primary-antibodies-ihc-testing-4.jpgAnti-CKII alpha CSNK2A1 Rabbit Monoclonal AntibodyIHC analysis of CSNK2A1 using anti-CSNK2A1 antibody (M02398). <br>CSNK2A1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CSNK2A1 Antibody (M02398) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calmodulin-rabbit-monoclonal-antibody-m06609-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06609-calmodulin-primary-antibodies-wb-testing-1.jpgAnti-Calmodulin Rabbit Monoclonal Antibody Western blot analysis of Calmodulin using anti-Calmodulin antibody (M06609). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human U20S whole cell lysates,<br>
Lane 5: rat skeletal muscle tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse skeletal muscle tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calmodulin antigen affinity purified monoclonal antibody (Catalog # M06609) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calmodulin at approximately 17 kDa. The expected band size for Calmodulin is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M06609-CALM1-primary-antibodies-IHC-testing-1.jpgAnti-Calmodulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Calmodulin Antibody (M06609)<br>CALM1 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Calmodulin Antibody (M06609)overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-beta-rabbit-monoclonal-antibody-m01692-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-hsp90ab1-primary-antibodies-wb-testing-1.jpgAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal Antibody Western blot analysis of HSP90AB1 using anti-HSP90AB1 antibody (M01692). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSP90AB1 antigen affinity purified monoclonal antibody (Catalog # M01692) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSP90AB1 at approximately 90 kDa. The expected band size for HSP90AB1 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-12953_2023_213_fig2_html.pngAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyThe differential abundance of HSP90AB1, HSPD1 and HSPA13 in villi tissues was verified by Western blot. A The representative of Western blot analysis to verify selected differentially expressed proteins HSP90AB1, HSPD1 and HSPA13 in the villi tissue of embryo from EMA ( n = 6) and control( n = 6). B The scatter plot of HSP90AB1 abundance in the villi tissue of embryo from EMA ( n = 22) vs control ( n = 22) ( P < 0.01). C The scatter plot of HSPD1 abundance in the villi tissue of embryo from EMA ( n = 22) vs control ( n = 22) ( P < 0.01). D The scatter plot of HSPA13 abundance in the villi tissue of embryo from EMA ( n = 22) vs control ( n = 22) ( P < 0.01) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12953-023-00213-w'>37587463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-12953_2023_213_fig3_html.pngAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyA , B , C Immunohistochemical staining for HSP90AB1, HSPD1, and HSPA13 observed in the cytoplasm of syncytiotrophoblast and cytotrophoblast cells (× 200, × 400). Villus from 22 patients with EMA showed lower; D - F Quantitative scoring results of IHC analyses w shown as box plots <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12953-023-00213-w'>37587463</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01692-ihc.jpgAnti-Hsp90 beta HSP90AB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Hsp90 beta antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tenascin-c-rabbit-monoclonal-antibody-m00936-1-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00936-1-wb.jpgAnti-Tenascin C TNC Rabbit Monoclonal AntibodyWestern blot analysis of Cytotactin C expression in (1)Human fetal brain lysate;(2)Human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lgr5-gpr49-rabbit-monoclonal-antibody-m00239-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00239-wb.jpgAnti-LGR5/GPR49 Rabbit Monoclonal AntibodyWestern blot analysis of GPR49 expression in Human fetal skeletal muscle lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00239-12951_2024_2854_fig4_html.pngAnti-LGR5/GPR49 Rabbit Monoclonal AntibodySI protects IECs against radiation-induced DNA damage and apoptotic death. ( a , b ) TUNEL staining was employed to evaluate the impact of SI on apoptosis in the context of RIII. ( c - f ) IHC staining results for Lgr5 + and Ki67 + cells in samples of murine small intestinal tissue. ( g ) Cumulative Zn 2+ release profiles. ( h ) Blood glucose levels over time after oral administration.Representative RT-PCR of NLRP3 ( i ), Caspase-3 ( j ) and γ-H2AX(k) mRNA levels in the RIII. ( n = 5,* P < 0.05) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12951-024-02854-1'>39415273</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00239-fmicb-11-622354-g003.jpgAnti-LGR5/GPR49 Rabbit Monoclonal AntibodyThe distribution of Lgr5 + ISCs in the intestinalmucosa and the subcellular localization and relative expression level detection of epithelial function proteins CDX2 and villin in the intestinal mucosa of IBD at 7 days after termination of DSS administration. (A) The Lgr5 + ISCs (brown) in the small intestinal mucosa: (A1) the normal group, the villi and the crypts were arranged compactly, and Lgr5 + ISCs were observed in the crypts; (A2) the DSS group, the villi and the crypts were scattered, with few Lgr5 + ISCs; (A3) the DSS + B. subtilis -fermented milk group, there were more Lgr5 + ISCs in villi and crypts compared with those in the DSS group. (B) The Lgr5 + ISCs (brown) in the colonic mucosa: (B1) the normal group, the glands were arranged compactly, and there were large amounts of Lgr5 + ISCs at the bottom of the glands; (B2) the DSS group: the ulcers were replaced by scars. No Lgr5 + ISCs were observed in the scars; (B3) the DSS + B. subtilis -fermented milk group: the colonic epithelium was integrated, with some regenerated glands. A number of Lgr5 + ISCs were observed at the bottom of the regenerated glands. (C) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the small intestinal mucosa: (C1) the normal group: the villi and the crypts were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the villi and the crypts; (C2) the DSS group: the villi and the crypts were scattered, and few CDX2 + epithelial cells were observed on the surface of the crypt and the villi; (C3) the DSS + B. subtilis -fermented milk group: more villi and crypts were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells covering the villi and crypts. (D) The CDX2 was localized in the epithelial cellular nuclei (brown) by immunohistochemistry staining in the colonic mucosa: (D1) the normal group: the colonic glands were arranged compactly, and CDX2 + epithelial cells were observed on the surface of the glands; (D2) the DSS group: the glands were scattered, and few CDX2 + epithelial cells were observed in the scar; (D3) the DSS + B. subtilis -fermented milk group: more colonic glands were observed in comparison with the DSS group, and there were more CDX2 + epithelial cells in the glands. (E) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the small intestinal mucosa: (E1) the normal group, a number of Mucin2 + goblet cells observed in the epithelium; (E2) the DSS group: only few Mucin2 + goblet cells were observed in the remaining villi and crypts; (E3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered mucosa. (F) The Mucin2 was localized in the cytoplasm of the goblet cells (brown) by immunohistochemistry staining in the colonic mucosa: (F1) the normal group, large amounts of Mucin2 + goblet cells were observed in the mucosa; (F2) the DSS group: only few Mucin2 + goblet cells were observed in the scars; (F3) the DSS + B. subtilis -fermented milk group: more Mucin2 + goblet cells were observed in the recovered colonic mucosa. (G,H) Western blotting was applied for detection of the relative expression level of Lgr5, CDX2, and Mucin2 in the samples containing equivalent ileum and colon. The expression level of Lgr5, CDX2, and Mucin2 in the DSS group was significantly lower than that of the normal (control) group. The expression level of Lgr5, CDX2, and Mucin2 in the DSS + B. subtilis -fermented milk (FM) group was significantly higher than that of the DSS group ( n = 5, ** represents p < 0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2020.622354/full'>33519783</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-beta-2-rabbit-monoclonal-antibody-m01940-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01940-prkcb-primary-antibodies-wb-testing-1.jpgAnti-PKC beta 2 PRKCB Rabbit Monoclonal Antibody Western blot analysis of PRKCB using anti-PRKCB antibody (M01940). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKCB antigen affinity purified monoclonal antibody (Catalog # M01940) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRKCB at approximately 77 kDa. The expected band size for PRKCB is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01940-fphar-11-556074-g004.jpgAnti-PKC beta 2 PRKCB Rabbit Monoclonal AntibodyIodixanol triggered PKC phosphorylation, NOX activation, and eNOS dysregulation in HUVECs. HUVECs were incubated with iodixanol (30 mg I/ml) for 0, 5, 15, 30, 60, or 120 min. The phosphorylation of PKC beta II, p47, Rac1, eNOS (Thr495), and eNOS (Ser1177) was assayed by Western blot analysis (A-E) .<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2020.556074/full'>33658920</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01940-fphar-11-556074-g006.jpgAnti-PKC beta 2 PRKCB Rabbit Monoclonal AntibodyD-4F inhibited iodixanol-induced NOX activation and eNOS dysregulation through the AMPK/PKC pathway in HUVECs. HUVECs were preincubated in the absence or presence of Compound C (2 μmol/L) for 1 h. Then, cells were incubated with or without D-4F (20 μg/ml) for 8 h and treated with iodixanol (30 mg I/ml) for 30 min. The phosphorylation of PKC beta II, p47, Rac1, and eNOS (Thr495) was assayed by Western blot analysis (A-D) .<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2020.556074/full'>33658920</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stathmin-1-rabbit-monoclonal-antibody-m01194-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-wb-testing-1.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody Western blot analysis of Stathmin 1 using anti-Stathmin 1 antibody (M00994). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MDA-MB-453 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Stathmin 1 antigen affinity purified monoclonal antibody (Catalog # M00994) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Stathmin 1 at approximately 17 kDa. The expected band size for Stathmin 1 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-2.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-3.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-4.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-5.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-6.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-7.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-8.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-9.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-10.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-11.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-12.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01194-stmn1-primary-antibodies-ihc-testing-13.jpgAnti-Stathmin 1 STMN1 Rabbit Monoclonal Antibody IHC analysis of STMN1 using anti-STMN1 antibody (M01194). <br>
STMN1 was detected in a paraffin-embedded section of neuroplexus of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-STMN1 Antibody (M01194) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prohibitin-rabbit-monoclonal-antibody-m01178-boster.html2026-03-24T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01178-phb-primary-antibodies-wb-testing-1.jpgAnti-Prohibitin PHB Rabbit Monoclonal Antibody Western blot analysis of PHB using anti-PHB antibody (M01178). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Ramos whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human A549 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHB antigen affinity purified monoclonal antibody (Catalog # M01178) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHB at approximately 30 kDa. The expected band size for PHB is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01178-phb-primary-antibodies-ihc-testing-2.jpgAnti-Prohibitin PHB Rabbit Monoclonal Antibody IHC analysis of PMB using anti-PMB antibody (M01178). <br>
PMB was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PMB Antibody (M01178) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01178-phb-primary-antibodies-if-testing-1.jpgAnti-Prohibitin PHB Rabbit Monoclonal AntibodyIF analysis of PHB using anti-PHB antibody (M01178). <br>
PHB was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 rabbit anti-PHB Antibody (M01178) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hif-1-beta-rabbit-monoclonal-antibody-m02263-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02263-arnt-primary-antibodies-wb-testing-1.jpgAnti-HIF-1 beta ARNT Rabbit Monoclonal AntibodyWestern blot analysis of ARNT using anti-ARNT antibody (M02263). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human SIHA whole cell lysates,<br>
Lane 5: human Hela whole cell lysates,<br>
Lane 6: human Jurkat whole cell lysates,<br>
Lane 7: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARNT antigen affinity purified monoclonal antibody (M02263) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ARNT at approximately 87 kDa. The expected band size for ARNT is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02263-arnt-primary-antibodies-ihc-testing-2.jpgAnti-HIF-1 beta ARNT Rabbit Monoclonal AntibodyIHC analysis of ARNT using anti-ARNT antibody (M02263). <br>ARNT was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ARNT Antibody (M02263) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02263-arnt-primary-antibodies-ihc-testing-3.jpgAnti-HIF-1 beta ARNT Rabbit Monoclonal AntibodyIHC analysis of ARNT using anti-ARNT antibody (M02263). <br>ARNT was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ARNT Antibody (M02263) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p62-sqstm1-rabbit-monoclonal-antibody-m00300-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-ijms-26-04630-g002.jpgAnti-p62/SQSTM1 Rabbit Monoclonal AntibodyThe depletion of β-catenin triggered by PPI is mediated through the process of autophagy. ( A , B ) The effect of different concentrations of PPI on the expression levels of β-catenin protein in HO-8910PM cells following a 6-h treatment was assessed using a Western blot assay, and the resulting data were further subjected to quantitative analysis. ( C ) qRT-PCR analysis of β-catenin mRNA levels in PPI-treated cells. ( D ) Assessment of the impact of PPI on β-catenin protein degradation: HO-8910PM cells were exposed to PPI (1 μM) either alone or in combination with either MG132 (20 μM), which is a proteasome inhibitor, or BAF (200 nM), which is an autophagy inhibitor, for 6 h. Subsequently, the cells were subjected to CHX (100 µg/mL) treatment for the indicated durations. ( E ) The quantification results of ( D ). ( F , G ) The effect of different concentrations of PPI on the expression levels of p62 protein in HO-8910PM cells following a 6-h treatment was assessed by WB, and the resulting data were subjected to quantitative analysis. ( H – J ) The effect of different concentrations of PPI on the expression levels of LC3 I and LC3 II proteins in HO-8910PM cells following a 6-h treatment was assessed by WB, and the resulting data were subjected to quantitative analysis. Data from six independent experiments are presented as mean ± S.D. *: p < 0.05; **: p < 0.01; ***: p < 0.001 vs. control; ###: p < 0.001 vs. 1 μM PPI.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12110821/'>40429774</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-1-s2.0-s2319417025001015-gr3.jpgAnti-p62/SQSTM1 Rabbit Monoclonal AntibodyImmunohistochemistry of piriformis muscle tissue sections.
(A) Parkin expression was higher in the ACP and FSN groups than in the MOD group, with the FSN group showing significantly stronger Parkin immunoreactivity. (B) PINK1 expression was higher in the ACP and FSN groups than in the MOD group, with the FSN group surpassing the ACP group. (C) P62 staining was higher in the MOD and ACP groups than in the COT group. The FSN group showed significantly reduced P62 staining compared to the MOD group. (D-F) Relative protein expression and statistical results. Compared with the COT group, the MOD group had lower Parkin/PINK1 expression and higher P62 expression. Compared with the MOD group, the FSN group had higher Parkin/PINK1 expression and lower P62 expression. Compared with the ACP group, the FSN group showed higher Parkin/PINK1 expression and lower P62 expression. *P<0.05; **P<0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2319417025001015'>41177207</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-1-s2.0-s2319417025001015-gr4.jpgAnti-p62/SQSTM1 Rabbit Monoclonal AntibodyImmunofluorescence of piriformis muscle tissue sections.
(A) PINK1 fluorescence intensity was higher in the FSN group than the MOD and ACP groups. (B) Parkin fluorescence intensity was higher in the FSN group than in the MOD and ACP groups. (C) P62 fluorescence intensity was higher in the MOD and ACP groups than in the MOD group. (D-F) Relative protein expression and statistical results. Compared with the COT group, the MOD group had lower PINK1/Parkin expression and higher P62 expression. Compared with the MOD group, the FSN group had higher PINK1/Parkin expression and lower P62 expression. Compared with the ACP group, the FSN group showed higher PINK1/Parkin expression and lower P62 expression. *P<0.05; **P<0.01; ***P<0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2319417025001015'>41177207</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-sqstm1-primary-antibodies-wb-testing-1.jpgAnti-p62/SQSTM1 Rabbit Monoclonal Antibody Western blot analysis of p62/SQSTM1 using anti-p62/SQSTM1 antibody (M00300). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p62/SQSTM1 antigen affinity purified monoclonal antibody (Catalog # M00300) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for p62/SQSTM1 at approximately 62 kDa. The expected band size for p62/SQSTM1 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-sqstm1-primary-antibodies-ihc-testing-2.jpgAnti-p62/SQSTM1 Rabbit Monoclonal Antibody IHC analysis of p62/SQSTM1 using anti-p62/SQSTM1 antibody (M00300). <br>
p62/SQSTM1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p62/SQSTM1 Antibody (M00300) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-sqstm1-primary-antibodies-ihc-testing-3.jpgAnti-p62/SQSTM1 Rabbit Monoclonal Antibody IHC analysis of p62/SQSTM1 using anti-p62/SQSTM1 antibody (M00300). <br>
p62/SQSTM1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p62/SQSTM1 Antibody (M00300) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-if.jpgAnti-p62/SQSTM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using p62/SQSTM1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-sqstm1-primary-antibodies-ihc-testing-4.jpgAnti-p62/SQSTM1 Rabbit Monoclonal Antibody IHC analysis of p62/SQSTM1 using anti-p62/SQSTM1 antibody (M00300). <br>
p62/SQSTM1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-p62/SQSTM1 Antibody (M00300) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00300-icc1.jpgAnti-p62/SQSTM1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-troponin-i-rabbit-monoclonal-antibody-m01720-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01720-wb.jpgAnti-Troponin I Rabbit Monoclonal AntibodyWestern blot analysis of Troponin I expression in fetal heart cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01720-ihc.jpgAnti-Troponin I Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human heart, using Troponin I Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-troponin-t-rabbit-monoclonal-antibody-m01154-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01154-tnnt2-primary-antibodies-wb-testing-1.jpgAnti-Troponin T TNNT2 Rabbit Monoclonal Antibody Western blot analysis of Troponin T using anti-Troponin T antibody (M01154). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates, <br>
Lane 2: mouse heart whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Troponin T antigen affinity purified monoclonal antibody (M01154) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Troponin T at approximately 40 kDa. The expected band size for Troponin T is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01154-ihc.jpgAnti-Troponin T TNNT2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human heart muscle, using Troponin T Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cebp-alpha-rabbit-monoclonal-antibody-m00386-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00386-wb.jpgAnti-CEBP alpha Rabbit Monoclonal AntibodyWestern blot analysis of CEBP alpha expression in U937 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h4-rabbit-monoclonal-antibody-m14495-2-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-wb-testing-1.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody Western blot analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human Hacat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse 3T3-L1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H4 antigen affinity purified monoclonal antibody (Catalog # M14495-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Histone H4 at approximately 11 kDa. The expected band size for Histone H4 is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-2.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-3.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-4.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-5.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-6.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-7.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-8.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-9.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-hist1h4a-primary-antibodies-ihc-testing-11.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-if.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Histone H4 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-h4c1-primary-antibodies-ihc-testing-10.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-2-hist1h4a-primary-antibodies-ihc-testing-12.jpgAnti-Histone H4 HIST1H4A Rabbit Monoclonal Antibody IHC analysis of Histone H4 using anti-Histone H4 antibody (M14495-2). <br>
Histone H4 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Histone H4 Antibody (M14495-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-rabbit-monoclonal-antibody-m12477-10-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-wb7.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-wb.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 expression in (1) HeLa cell lysate; (2) 3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc9.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tonsil, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc10.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer, using the Antibody at 1:6000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc7.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat thymus, using the Antibody at 1:3000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc11.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse spleen, using the Antibody at 1:3000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc8.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:2000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-ihc.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using Histone H3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-10-if.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Histone H3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc27-apc3-rabbit-monoclonal-antibody-m03905-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03905-wb.jpgAnti-Cdc27/APC3 Rabbit Monoclonal AntibodyWestern blot analysis of Cdc27/APC3 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc16-apc6-rabbit-monoclonal-antibody-m04573-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04573-wb7.jpgAnti-Cdc16/APC6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04573-wb8.jpgAnti-Cdc16/APC6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04573-wb.jpgAnti-Cdc16/APC6 Rabbit Monoclonal AntibodyWestern blot analysis of Cdc16/APC6 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cdc23-apc8-rabbit-monoclonal-antibody-m05798-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05798-icc1.jpgAnti-Cdc23/APC8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05798-icc2.jpgAnti-Cdc23/APC8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05798-wb.jpgAnti-Cdc23/APC8 Rabbit Monoclonal AntibodyWestern blot analysis of Cdc23/APC8 expression in (1)HepG2 cell lysate; (2)Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-10-rabbit-monoclonal-antibody-m02190-1-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02190-1-wb7.jpgAnti-Caspase-10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02190-1-wb8.jpgAnti-Caspase-10 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02190-1-wb.jpgAnti-Caspase-10 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-10 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-14-rabbit-monoclonal-antibody-m05143-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05143-wb7.jpgAnti-Caspase-14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:8K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05143-wb.jpgAnti-Caspase-14 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-14 expression in Human skin lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05143-wb8.jpgAnti-Caspase-14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:8K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cystatin-c-rabbit-monoclonal-antibody-m00961-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00961-cst3-primary-antibodies-wb-testing-1.jpgAnti-Cystatin C CST3 Rabbit Monoclonal Antibody Western blot analysis of Cystatin C/CST3 using anti-Cystatin C/CST3 antibody (M00961). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: rat testis tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cystatin C/CST3 antigen affinity purified monoclonal antibody (M00961) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cystatin C/CST3 at approximately 16 kDa. The expected band size for Cystatin C/CST3 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00961-wb.jpgAnti-Cystatin C CST3 Rabbit Monoclonal AntibodyWestern blot analysis of Cystatin C expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-rabbit-monoclonal-antibody-m12477-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-wb.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) Rat brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc10.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human squamous cell carcinoma , using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc7.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc11.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse hippocampus , using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc8.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat pancreas, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc9.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human cervical cancer, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-ihc.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Histone H3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-if.jpgAnti-Histone H3 HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using Histone H3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-collagen-x-rabbit-monoclonal-antibody-m01026-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01026-col10a1-primary-antibodies-wb-testing-1.jpgAnti-Collagen X COL10A1 Rabbit Monoclonal Antibody Western blot analysis of COL10A1 using anti-COL10A1 antibody (M01026). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COL10A1 antigen affinity purified monoclonal antibody (Catalog # M01026) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for COL10A1 at approximately 66 kDa. The expected band size for COL10A1 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01026-wb.jpgAnti-Collagen X COL10A1 Rabbit Monoclonal AntibodyWestern blot analysis of Collagen X expression in human fetal skin lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pgc1-alpha-rabbit-monoclonal-antibody-m00236-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-fgene-13-922807-g004.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal AntibodyArbutin exerted protective effects via the SIRT1/FOXO3A/PGC-1α/β and NF-κB/p65 signaling pathway. (A) qRT-PCR was used to measure transcript levels of the SIRT1/FOXO3a/PGC-1α/β pathway and NF-κB/p65 genes. TBHP decreased the expression of SIRT1, FOXO3a, and PGC-1α/β and increased the expression of NF-κB/p65, whereas mRNA levels in the groups that were pretreated with Arbutin showed reversed trend. (B) western blots were conducted to detect the proteins level of SIRT1, FOXO3a, PGC-1α/β, p-ERK, and NFKB1/P65. (C) imageJ was used to analyze the relative expression level of the proteins mentioned above (* p < 0.05, ** p < 0.01, *** p < 0.001, n = 3, bars represent SD).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2022.922807/full'>36051689</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-fgene-13-922807-g005.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal AntibodySirtinol diminished the capability of Arbutin to assist ARPE-19 cells to defend against oxidative stress. (A) (B) flow cytometric analysis showed that cells treated with only sirtinol, TBHP, cotreated with sirtinol, and TBHP displayed decreased cellular viability. However, sirtinol conduction diminished the protective capacity of Arbutin. (C) ARPE-19 cells were seeded in a 24-well plate and applied wounds at the confluence of 80%. The cells were pretreated with or without Arbutin and then subjected to TBHP (350 µM); meanwhile, cells in certain groups were incubated with sirtinol. Photos were taken at different time points post distinct treatments. (D) fluorescence images observed that ARPE-19 treated with Arbutin while subjected to sirtinol and then exposed to TBHP was unable to recuperate ΔΨm. (E) with sirtinol administration, the protein levels of the SIRT1/FOXO3a/PGC-1α/β pathway decreased in the presence of Arbutin (* p < 0.05, ** p < 0.01, *** p < 0.001, n = 3, bars represent SD).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2022.922807/full'>36051689</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-wb8.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-icc1.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-ppargc1a-primary-antibodies-wb-testing-1.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal Antibody Western blot analysis of PGC1 Alpha/PPARGC1A using anti-PGC1 Alpha/PPARGC1A antibody (M00236). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: mouse heart tissue lysates,<br>
Lane 4: mouse liver tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGC1 Alpha/PPARGC1A antigen affinity purified monoclonal antibody (M00236) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGC1 Alpha/PPARGC1A at approximately 113 kDa. The expected band size for PGC1 Alpha/PPARGC1A is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-wb.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal AntibodyWestern blot analysis of PGC1 alpha/beta expression in (1) HeLa cell lysate; (2) NIH 3T3 cell lysate; (3) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00236-ppargc1a-primary-antibodies-wb-testing-2.jpgAnti-PGC1 alpha PPARGC1A Rabbit Monoclonal Antibody Western blot analysis of PGC1 Alpha/PPARGC1A using anti-PGC1 Alpha/PPARGC1A antibody (M00236). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>
Lane 2: rat C6 whole cell lysates,<br>
Lane 3: mouse liver tissue lysates,<br>
Lane 4: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGC1 Alpha/PPARGC1A antigen affinity purified monoclonal antibody (M00236) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGC1 Alpha/PPARGC1A at approximately 113 kDa. The expected band size for PGC1 Alpha/PPARGC1A is at 91 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ppar-gamma-rabbit-monoclonal-antibody-m00449-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-wb7.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-wb.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyWestern blot analysis of PPAR gamma expression in (1) HeLa cell lysate; (2) PC-3 cell lysate; (3) THP-1 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prealbumin-rabbit-monoclonal-antibody-m00290-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00290-wb.jpgAnti-Prealbumin TTR Rabbit Monoclonal AntibodyWestern blot analysis of Prealbumin gamma expression in human fetal kidney lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dystrophin-rabbit-monoclonal-antibody-m00069-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00069-wb.jpgAnti-Dystrophin DMD Rabbit Monoclonal AntibodyWestern blot analysis of Dystrophin expression in human fetal heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-galectin-3-rabbit-monoclonal-antibody-m00621-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00621-wb7.jpgAnti-Galectin 3 LGALS3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00621-lgals3-primary-antibodies-wb-testing-1.jpgAnti-Galectin 3 LGALS3 Rabbit Monoclonal Antibody Western blot analysis of LGALS3 using anti-LGALS3 antibody (M00621). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U-87MG whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LGALS3 antigen affinity purified monoclonal antibody (Catalog # M00621) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LGALS3 at approximately 29 kDa. The expected band size for LGALS3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00621-wb9.jpgAnti-Galectin 3 LGALS3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-podoplanin-rabbit-monoclonal-antibody-m01124-1-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01124-1-wb7.jpgAnti-Podoplanin PDPN Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01124-1-wb.jpgAnti-Podoplanin PDPN Rabbit Monoclonal AntibodyWestern blot analysis of Podoplanin expression in human placenta lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-syndecan-1-rabbit-monoclonal-antibody-m00991-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00991-icc1.jpgAnti-Syndecan 1 SDC1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00991-icc2.jpgAnti-Syndecan 1 SDC1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00991-wb.jpgAnti-Syndecan 1 SDC1 Rabbit Monoclonal AntibodyWestern blot analysis of Syndecan 1 expression in Ramos cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-podoplanin-rabbit-monoclonal-antibody-m01124-2-boster.html2026-03-24T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01124-2-wb.jpgAnti-Podoplanin PDPN Rabbit Monoclonal AntibodyWestern blot analysis of Podoplanin expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tyrosinase-rabbit-monoclonal-antibody-m00326-1-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00326-1-tyr-primary-antibodies-wb-testing-1.jpgAnti-Tyrosinase Rabbit Monoclonal AntibodyWestern blot analysis of TYR using anti-TYR antibody (M00326-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: mouse B16-F10 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TYR antigen affinity purified monoclonal antibody (M00326-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TYR at approximately 50-80 kDa. The expected band size for TYR is at 60 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pka-2-beta-rabbit-monoclonal-antibody-m04943-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04943-wb.jpgAnti-PKA 2 beta PRKAR2B Rabbit Monoclonal AntibodyWestern blot analysis of PKA 2 beta expression in human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-annexin-a2-rabbit-monoclonal-antibody-m00868-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00868-anxa2-primary-antibodies-wb-testing-1.jpgAnti-Annexin A2 ANXA2 Rabbit Monoclonal Antibody Western blot analysis of ANXA2 using anti-ANXA2 antibody (M00868). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 7: rat liver tissue lysates,<br>
Lane 8: mouse lung tissue lysates,<br>
Lane 9: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANXA2 antigen affinity purified monoclonal antibody (Catalog # M00868) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANXA2 at approximately 36 kDa. The expected band size for ANXA2 is at 39 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-involucrin-rabbit-monoclonal-antibody-m02628-1-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02628-1-ivl-primary-antibodies-wb-testing-1.jpgAnti-Involucrin IVL Rabbit Monoclonal Antibody Western blot analysis of IVL using anti-IVL antibody (M02628-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IVL antigen affinity purified monoclonal antibody (Catalog # M02628-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IVL at approximately 120 kDa. The expected band size for IVL is at 68 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-flotillin-2-rabbit-monoclonal-antibody-m06107-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06107-flot2-primary-antibodies-wb-testing-1.jpgAnti-Flotillin 2 FLOT2 Rabbit Monoclonal Antibody Western blot analysis of FLOT2 using anti-FLOT2 antibody (M06107). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: rat skin tissue lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: mouse skin tissue lysates,<br>
Lane 7: mouse heart tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FLOT2 antigen affinity purified monoclonal antibody (Catalog # M06107) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FLOT2 at approximately 47 kDa. The expected band size for FLOT2 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erbb-her4-rabbit-monoclonal-antibody-m00296-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00296-erbb4-primary-antibodies-wb-testing-1.jpgAnti-ErbB (HER4) ERBB4 Rabbit Monoclonal AntibodyWestern blot analysis of ERBB4 using anti-ERBB4 antibody (M00296). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human T-47D whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERBB4 antigen affinity purified monoclonal antibody (M00296) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ERBB4 at approximately 180 kDa. The expected band size for ERBB4 is at 147 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00296-if.jpgAnti-ErbB (HER4) ERBB4 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A673 cells, using ErbB4 (HER4) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aconitase-1-rabbit-monoclonal-antibody-m02781-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02781-wb7.jpgAnti-Aconitase 1 ACO1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02781-wb8.jpgAnti-Aconitase 1 ACO1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02781-wb.jpgAnti-Aconitase 1 ACO1 Rabbit Monoclonal AntibodyWestern blot analysis of Aconitase 1 in (1) mouse kidney lysate; (2) HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hif-2-alpha-rabbit-monoclonal-antibody-m01248-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01248-wb7.jpgAnti-HIF-2 alpha EPAS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01248-wb.jpgAnti-HIF-2 alpha EPAS1 Rabbit Monoclonal AntibodyWestern blot analysis of HIF-2 alpha in (1)MCF-7 cell lysate;(2)HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01248-wb8.jpgAnti-HIF-2 alpha EPAS1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01248-icc1.jpgAnti-HIF-2 alpha EPAS1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-alpha-rabbit-monoclonal-antibody-m01103-3-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-3-wb.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp90 alpha expression in (1)PC-12 cell lysate; (2)HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-3-if.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Hsp90 alpha Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-alpha-rabbit-monoclonal-antibody-m01103-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-wb.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyWestern blot analysis of Hsp90 alpha expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mhc-class-1-rabbit-monoclonal-antibody-m00194-1-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-1-hla-a-primary-antibodies-wb-testing-1.jpgAnti-MHC class 1 HLA-A Rabbit Monoclonal Antibody Western blot analysis of HLA-A using anti-HLA-A antibody (M00194-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Raji whole cell lysates,<br>
Lane 5: human Daudi whole cell lysates,<br>
Lane 6: human A431 whole cell lysates,<br>
Lane 7: human HEL whole cell lysates,<br>
Lane 8: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HLA-A antigen affinity purified monoclonal antibody (M00194-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HLA-A at approximately 41 kDa. The expected band size for HLA-A is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-1-hla-a-primary-antibodies-ihc-testing-2.jpgAnti-MHC class 1 HLA-A Rabbit Monoclonal Antibody IHC analysis of HLA-A using anti-HLA-A antibody (M00194-1). <br>HLA-A was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HLA-A Antibody (M00194-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gtpase-hras-rabbit-monoclonal-antibody-m00114-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00114-wb.jpgAnti-GTPase HRAS Rabbit Monoclonal AntibodyWestern blot analysis MCF7 cell lysate using HRAS Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-met-c-met-rabbit-monoclonal-antibody-m01488-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-met-primary-antibodies-ihc-testing-1.jpgAnti-Met (c-Met) Rabbit Monoclonal Antibody IHC analysis of MET using anti-MET antibody (M01488). <br>
MET was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-MET Antibody (M01488) overnight at 4°C. HRP Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-wb7.jpgAnti-Met (c-Met) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-met-primary-antibodies-if-testing-2.jpgAnti-Met (c-Met) Rabbit Monoclonal Antibody IF analysis of MET using anti-MET antibody (M01488). <br>
MET was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MET Antibody (M01488) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-wb.jpgAnti-Met (c-Met) Rabbit Monoclonal AntibodyWestern blot analysis of c-Met expression in 293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-icc1.jpgAnti-Met (c-Met) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-met-primary-antibodies-if-testing-3.jpgAnti-Met (c-Met) Rabbit Monoclonal Antibody IF analysis of MET using anti-MET antibody (M01488). <br>
MET was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MET Antibody (M01488) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-ihc.jpgAnti-Met (c-Met) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using Met (c-Met) Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-met-primary-antibodies-if-testing-4.jpgAnti-Met (c-Met) Rabbit Monoclonal Antibody IF analysis of MET using anti-MET antibody (M01488). <br>
MET was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MET Antibody (M01488) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-met-primary-antibodies-if-testing-5.jpgAnti-Met (c-Met) Rabbit Monoclonal Antibody IF analysis of MET using anti-MET antibody (M01488). <br>
MET was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MET Antibody (M01488) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-flotillin-1-rabbit-monoclonal-antibody-m05980-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-flot1-primary-antibodies-wb-testing-1.jpgAnti-Flotillin 1 FLOT1 Rabbit Monoclonal Antibody Western blot analysis of Flotillin 1 using anti-Flotillin 1 antibody (M05980). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U2OS whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Flotillin 1 antigen affinity purified monoclonal antibody (Catalog # M05980) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Flotillin 1 at approximately 47 kDa. The expected band size for Flotillin 1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-flot1-primary-antibodies-ihc-testing-2.jpgAnti-Flotillin 1 FLOT1 Rabbit Monoclonal Antibody IHC analysis of Flotillin 1 using anti-Flotillin 1 antibody (M05980). <br>
Flotillin 1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Flotillin 1 Antibody (M05980) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-flot1-primary-antibodies-ihc-testing-3.jpgAnti-Flotillin 1 FLOT1 Rabbit Monoclonal Antibody IHC analysis of Flotillin 1 using anti-Flotillin 1 antibody (M05980). <br>
Flotillin 1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Flotillin 1 Antibody (M05980) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05980-flot1-primary-antibodies-ihc-testing-4.jpgAnti-Flotillin 1 FLOT1 Rabbit Monoclonal Antibody IHC analysis of Flotillin 1 using anti-Flotillin 1 antibody (M05980). <br>
Flotillin 1 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Flotillin 1 Antibody (M05980) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-flotillin-1-rabbit-monoclonal-antibody-m04517-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04517-wb.jpgAnti-Flotillin 1 FLOT1 Rabbit Monoclonal AntibodyWestern blot analysis of Flotillin 1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erbb-her3-rabbit-monoclonal-antibody-m00539-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-wb.jpgAnti-ErbB (HER3) Rabbit Monoclonal AntibodyWestern blot analysis of ErbB3 (HER3) expression in MCF-7 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd3-epsilon-rabbit-monoclonal-antibody-m02675-1-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-1-cd3e-primary-antibodies-ihc-testing-1.jpgAnti-CD3 epsilon Rabbit Monoclonal Antibody IHC analysis of CD3E using anti-CD3E antibody (M02675-1). <br>CD3E was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CD3E Antibody (M02675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-1-cd3e-primary-antibodies-ihc-testing-2.jpgAnti-CD3 epsilon Rabbit Monoclonal Antibody IHC analysis of CD3E using anti-CD3E antibody (M02675-1). <br>CD3E was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CD3E Antibody (M02675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-1-cd3e-primary-antibodies-ihc-testing-3.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyIHC analysis of CD3E using anti-CD3E antibody (M02675-1). <br>
CD3E was detected in a paraffin-embedded section of human intestinal lymph nodes tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3E Antibody (M02675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-1-cd3e-primary-antibodies-ihc-testing-4.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyIHC analysis of CD3E using anti-CD3E antibody (M02675-1). <br>
CD3E was detected in a paraffin-embedded section of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3E Antibody (M02675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-1-cd3e-primary-antibodies-ihc-testing-5.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyIHC analysis of CD3E using anti-CD3E antibody (M02675-1). <br>
CD3E was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD3E Antibody (M02675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-alpha-rabbit-monoclonal-antibody-m01103-1-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-1-wb.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyWestern blot analysis on HeLa cell lysate using HSP90A Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-1-ihc.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Hsp90 alpha antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-1-if.jpgAnti-Hsp90 alpha HSP90AA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using Hsp90 alpha Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-osteopontin-rabbit-monoclonal-antibody-m00634-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-osteopontin-spp1-primary-antibodies-wb-testing-1.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal Antibody Western blot analysis of Osteopontin SPP1 using anti-Osteopontin SPP1 antibody (M00634). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human MCF-7 whole cell lysates, <br>
Lane 4: mouse kidney tissue lysates,<br>
Lane 5: mouse small intestine tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates, <br>
Lane 7: mouse RAW264.7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Osteopontin SPP1 antigen affinity purified monoclonal antibody (M00634) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Osteopontin SPP1 at approximately 35 kDa. The expected band size for Osteopontin SPP1 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-spp1-primary-antibodies-ihc-testing-2.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal Antibody IHC analysis of SPP1 using anti-SPP1 antibody (M00634). <br>SPP1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SPP1 Antibody (M00634) overnight:50 at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-images_medium_s1793545824420021figf6.pngAnti-Osteopontin SPP1 Rabbit Monoclonal AntibodyIF staining images of (a) BMP-2, (b) COL-1, (c) OCN, and (d) OPN in BMSCs (red: osteogenic proteins and genes; green: cytoskeleton; blue: nucleus). <br><b>Index in World Scientific under a CC BY license. DOI: <a href='https://www.worldscientific.com/doi/abs/10.1142/S1793545824420021'>10.1142/S1793545824420021</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-fcell-12-1503481-g001.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal AntibodyDFSC regulated tooth eruption through EVs. (A) Experimental design and schedule for model construction and result assessment. (B) Methods of measuring tooth eruption distance. (C) Representative micro-CT images of detecting tooth eruption distance. (D) Analysis of tooth eruption distance based on micro-CT. (E) Representative H&E staining images of the first mandibular molar area. (F) Analysis of tooth eruption distance based on H&E staining. (G) Representative immunohistochemistry staining images of OPN expression in the first mandibular molar area. (H) Quantitative analysis of OPN expression in the first mandibular molar area. (I) Representative images of TRAP staining. (J) Quantitative analysis of TRAP-positive distance. Scale bar = 1 mm ns, not significant. ** p < 0. 01. n = 3.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2024.1503481/full'>39834384</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-icc1.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-ihc.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal AntibodyProstaglandin E1 Inhibited Diabetes-Induced Phenotypic Switching of Vascular Smooth Muscle Cells Through Activating Autophagy. -Cellular Physiology and Biochemistryhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-icc2.jpgAnti-Osteopontin SPP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd90-thy1-rabbit-monoclonal-antibody-m01818-boster.html2026-03-24T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-thy1-primary-antibodies-wb-testing-1.jpgAnti-CD90 / Thy1 Rabbit Monoclonal AntibodyWestern blot analysis of CD90/THY1 using anti-CD90/THY1 antibody (M01818). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U251 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD90/THY1 antigen affinity purified monoclonal antibody (M01818) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD90/THY1 at approximately 18 kDa. The expected band size for CD90/THY1 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01818-ihc.jpgAnti-CD90 / Thy1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using CD90 / Thy1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cathepsin-d-rabbit-monoclonal-antibody-m01361-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01361-ctsd-primary-antibodies-wb-testing-1.jpgAnti-Cathepsin D CTSD Rabbit Monoclonal Antibody Western blot analysis of Cathepsin D/CTSD using anti-Cathepsin D/CTSD antibody (M01361). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cathepsin D/CTSD antigen affinity purified monoclonal antibody (M01361) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cathepsin D/CTSD at approximately 28 kDa. The expected band size for Cathepsin D/CTSD is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01361-ihc.jpgAnti-Cathepsin D CTSD Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human ovarian cancer, using Cathepsin D Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-transferrin-rabbit-monoclonal-antibody-m00094-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00094-wb.jpgAnti-Transferrin TF Rabbit Monoclonal AntibodyWestern blot analysis of Transferrin expression in Human serum lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00094-ihc.jpgAnti-Transferrin TF Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human breast carcinoma, using Transferrin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vitronectin-rabbit-monoclonal-antibody-m02271-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02271-wb.jpgAnti-Vitronectin VTN Rabbit Monoclonal AntibodyWestern blot analysis of Vitronectin expression in human Serum membrane lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2a-rabbit-monoclonal-antibody-m16777-2-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-wb-testing-1.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human LNCAP whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H2A.2 antigen affinity purified monoclonal antibody (M16777-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H2A.2 at approximately 14 kDa. The expected band size for Histone H2A.2 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-1.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-2.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-3.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-4.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-5.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-6.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-7.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-8.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-9.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-histone_h2a-2-primary-antibodies-ihc-testing-10.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyIHC analysis of Histone H2A.2 using anti-Histone H2A.2 antibody (M16777-2). <br>Histone H2A.2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H2A.2 Antibody (M16777-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-2-if.jpgAnti-Histone H2A HIST1H2AB Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Histone H2A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fibrillarin-rabbit-monoclonal-antibody-m03178-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03178-ihc.jpgAnti-Fibrillarin FBL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using Fibrillarin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03178-fbl-primary-antibodies-wb-testing-1.jpgAnti-Fibrillarin FBL Rabbit Monoclonal Antibody Western blot analysis of Fibrillarin using anti-Fibrillarin antibody (M03178). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat spleen tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Fibrillarin antigen affinity purified monoclonal antibody (Catalog # M03178) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Fibrillarin at approximately 36 kDa. The expected band size for Fibrillarin is at 34,36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03178-fbl-primary-antibodies-if-testing-1.jpgAnti-Fibrillarin FBL Rabbit Monoclonal AntibodyIF analysis of Fibrillarin using anti-Fibrillarin antibody (M03178). <br>
Fibrillarin was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 rabbit anti-Fibrillarin Antibody (M03178) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd3-epsilon-rabbit-monoclonal-antibody-m02675-2-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-wb7.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-wb8.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-wb.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyWestern blot analysis of CD3 epsilon expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-ihc8.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse intestine, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-ihc9.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-ihc7.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-2-ihc.jpgAnti-CD3 epsilon Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using CD3 epsilon Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fibronectin-rabbit-monoclonal-antibody-m00564-1-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-wb.jpgAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyWestern blot analysis of Fibronectin expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-fphar-16-1565569-g007.jpgAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEffects of DBT on the expression of α-SMA, FN1, p-SMAD3 and TGF-β1 in rat lung tissue. α-SMA protein expression after (A) 28 and (B) 42 days of DBT administration. FN1 protein expression after (C) 28 and (D) 42 days of DBT administration; n = 4. (E) TGF-β1 and (F) p-SMAD3, n = 5. TGF-β1 protein expression after (G) 28 and (H) 42 days of DBT administration; n = 4 (G, H) , * P < 0.05 or ** P < 0.01; N.S. , not statistically significant, compared with the silica group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1565569/full'>40206091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig1_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyFN1 is distinctive expression in PTC cells and positively correlated with p53 signaling pathway. ( A , B ) FN1 mRNA and protein levels in pan-cancer cell lines analyzed by semiquantitative PCR ( A ) and western blotting ( B ) respectively. ( C ) GSEA pathway enrichment plot showing the positive correlation between FN1 expression and p53 signaling pathway in PTC patients from TCGA dataset. ( D ) The TP53 mutation rate of PTC tissues of TCGA dataset from cBioPortal database. ( E ) Knockdown of FN1 in K1 and KTC-1 cells verified by western blotting with GAPDH loading control. ( F ) GSEA pathway enrichment plot showing significant downregulation of p53 signaling pathway following FN1 knockdown in PTC cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig2_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB region is exclusively expressed in tumor, EDB(+)FN1 and EDB(−)FN1 two isoforms enriched in different signaling pathways. ( A ) The simple schematic diagram showing FN1 containing three alternative splicing domains, EDB, EDA and IIICS. ( B , C ) Semiquantitative PCR analysis of EDB domain expression in normal and papillary thyroid tissues ( B ) and cells ( C ) respectively, EDB(+) representing FN1 including EDB domain and EDB(−) representing FN1 skipping EDB domain. ( D ) Overexpression of two isoforms of FN1, EDB(+)FN1 and EDB(−)FN1, verified by western blotting and Semiquantitative PCR with GAPDH loading control. ( E ) KEGG enrichment showing ECM-receptor interaction upregulated after co-culture with conditional medium (CM) from OE-EDB(+)FN1 cells. ( F ) GSEA pathway enrichment plot showing significant upregulation of p53 signaling pathway following EDB(−)FN1 overexpression in shFN1 cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig3_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB(−)FN1 inhibits cell proliferation by upregulating p53-targeted protein p21 expression. ( A ) The Venn plot showing the genes in p53 signaling pathway downregulated after knockdown of FN1 and re-upregulated after overexpression of EDB(−)FN1. ( B ) qRT-PCR analysis verifying P21, BAX, ZMAT3 and MDM2 expression in indicated cells. ( C ) Knockdown of alternative splicing EDB domain of FN1 verified by western blotting and semiquantitative PCR with GAPDH loading control in K1 and KTC-1 cells. ( D , E ) Western blot analysis of P53 and p21 expression level in different transfection cells. ( F , G ) PTC cells treated with DNA-induced damage drug cis-platinum for 24 h, then Western blotting analyzed P53 and p21 expression in shFN1 and shEDB cells. ( H ) Cell proliferation ability of shFN1 cell overexpressed EDB(−)FN1 or EDB(+)FN1 isoform measured by CCK8 assays. ( I , J ) After shEDB and shFN1 cells transduced with sgRNAs targeting p53 and p21, the cell growth capability tested by CCK8 assays. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig4_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB(+)FN1 promotes migration, invasion and tube formation extracellularly via VEGF signaling pathway. ( A , B ) After overexpressing EDB(+)FN1 or EDB(−)FN1 in shFN1 cells, the migration and invasion ability examined by wound healing and transwell assays. ( C ) Representative images and quantifications of tube formation by LECS and HECV cultured with conditional medium (CM) collected from two isoforms EDB(+)FN1 and EDB(−)FN1 cells. Scale bars: 50 μm. ( D ) GSEA pathway enrichment plot showing significant upregulation of VEGF signaling pathway following EDB(+)FN1 overexpression in shFN1 cells. ( E , F ) Western blot analysis of VEGFC expression in LECS and HECV cells after co-culture with CM collected from the indicated PTC cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig5_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB region deficiency inhibits the binding of ITGB1 and FN1 and its secretion. ( A ) Flag tag with EDB(+)FN1 and His tag with EDB(−)FN1, using anti-flag and anti-his antibodies to pull down corresponding bound proteins for PAGE. ( B , C ) After transfecting Flag-EDB(+)FN1 or His-EDB(−)FN1 plasmids, then using FN1, flag and his antibodies for immunoprecipitation and western blotting assays. ( D ) After transfecting Flag-EDB(+)FN1 or His-EDB(−)FN1 plasmids, then using ITGB1 antibody for immunoprecipitation and western blotting assays. ( E , F ) Western blot analysis of secreted FN1 expression in cultured medium collected from the indicated cells with transferrin loading control. ( G ) Knockdown of ITGB1 in OE-EDB(+)FN1 cells verified by western blotting with GAPDH loading control. ( H ) Western blot analysis of VEGFC expression level in LECS cells after co-culture with CM from the indicated cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig6_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB region of FN1 is modulated by splicing factor ZMAT3 which promotes cell migration and invasion. ( A ) GSEA pathway enrichment plot showing the positive correlation between ZMAT3 expression level and P53 signaling pathway from TCGA database. ( B ) GSEA pathway enrichment plot showing the positive correlation between ZMAT3 expression and ECM-receptor interaction from TCGA database. ( C ) rMATS plot showing the decrease in Including level (InLevel) of the alternative splicing EDB region of FN1 upon ZMAT3 silencing. ( D ) The expression of EDB(+)FN1 and EDB(−)FN1 isoforms in shZMAT3 and control groups from RNA-seq data and verified by qRT-PCR. ( E ) Semiquantitative PCR analysis of EDB(+)FN1 and EDB(−)FN1 isoforms expression of K1 and KTC-1 cells following ZMAT3 knockdown. ( F ) Western blot analysis of ZMAT3 expression and Semiquantitative PCR analysis of EDB(+)FN1 and EDB(−)FN1 expression following p53 knockout. ( G ) Representative images and quantifications of tube formation by LECS and HECV cultured with CM collected from the indicated cells. Scale bars: 50 μm. ( H ) qRT-PCR analysis of VEGFR3 expression of LECS and HECV after co-cultured with CM derived from indicated cells. ( I , J ) Western blot analysis of VEGFC expression of LECS after co-cultured with CM from the indicated PTC cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig7_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyEDB(−)FN1 impairs tumor growth while EDB(+)FN1 promotes LNM in mice models. ( A ) Tumor formation by shFN1 or shEDB cells injected into the subcutaneous tissue of nude mice, and tumor growth curves are shown. ( B ) The expression of p53 and p21 in subcutaneous tumor tissues were evaluated by IHC. Scale bars: 50 μm. ( C ) Representative images of popliteal lymph node (LN) metastasis model of nude mouse, the indicated K1 cells were injected into the footpads, and images of popliteal LNs and histogram analysis of the LN volume in the indicated cells ( n = 3). ( D ) The image of LYVE-1 expression in popliteal LNs tested by IHC. ( E ) The expression of VEGFC and CK7 in popliteal LNs of indicated groups. Scale bars: 50 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-41598_2024_83369_fig8_html.pngAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyThe expression of EDB(−)FN1, EDB(+)FN1 and ZMAT3 in PTC patients. ( A ) The percentage of EDB(−)FN1 and EDB(+)FN1 accounting for FN1 in tumors with-LNM (N1) and without-LNM (N0) respectively in TCGA dataset from the TSVdb database. ( B ) The ratio of EDB(−)FN1 and EDB(+)FN1 in different tumor size stage (T1–T4) in TCGA dataset from the TSVdb database. ( C ) Representative images of EDB region expression in PTC tumors with-LNM (N1) and without-LNM (N0), and statistical diagram was shown. Scale bars: 50 μm. ( D ) Diagnostic efficacy of EDB region expression in PTC with LNM evaluated by ROC curve. ( E ) The differential expression of ZMAT3 in normal and tumor tissues, tumor with-LNM and without-LNM PTC tissues from TCGA dataset. ( F ) The differential expression of ZMAT3 in normal and tumor tissues, normal LN and metastatic LN from GSE60542 dataset. ( G ) qRT-PCR analysis of ZMAT3 mRNA expression in paired tumor and paracancerous tissues ( n = 10). ( H ) ZMAT3 protein expression in normal and PTC tissues from the Protein Atlas database. ( I ) The correlation analysis of FN1 and ZMAT3 expression levels from cBioPortal database. ( J , K ) Kaplan-Meier analyses of the correlations between FN1 ( I ), ZMAT3 ( J ) expression and recurrence-free survival of PTC patients from Kmplot database. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-83369-5'>39747903</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-ihc.jpgAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using Fibronectin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-1-wb7.jpgAnti-Fibronectin FN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hnrnp-c1-c2-rabbit-monoclonal-antibody-m02726-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-wb-testing-1.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyWestern blot analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HNRNPC antigen affinity purified monoclonal antibody (M02726) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HNRNPC at approximately 40 kDa. The expected band size for HNRNPC is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-1.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-2.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-3.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-4.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-5.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-6.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-7.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-8.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-9.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02726-hnrnpc-primary-antibodies-ihc-testing-10.jpgAnti-hnRNP C1/C2 Rabbit Monoclonal AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (M02726). <br>HNRNPC was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-HNRNPC Antibody (M02726) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-annexin-a10-rabbit-monoclonal-antibody-m13560-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13560-wb.jpgAnti-Annexin A10 Rabbit Monoclonal AntibodyWestern blot analysis of Annexin A10 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-smac-diablo-rabbit-monoclonal-antibody-m03790-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03790-wb.jpgAnti-Smac/Diablo Rabbit Monoclonal AntibodyWestern blot analysis of Smac/Diablo expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03790-ihc.jpgAnti-Smac/Diablo Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Smac/Diablo Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glutaminase-rabbit-monoclonal-antibody-m01272-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-wb.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyWestern blot analysis of Glutaminase expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-5.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-6.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-4.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-3.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-2.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01272-gls-primary-antibodies-ihc-testing-1.jpgAnti-Glutaminase GLS Rabbit Monoclonal AntibodyIHC analysis of GLS using anti-GLS antibody (M01272). <br>GLS was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-GLS Antibody (M01272) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hnf-4-alpha-rabbit-monoclonal-antibody-m00389-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00389-wb.jpgAnti-HNF-4-alpha Rabbit Monoclonal AntibodyWestern blot analysis of HNF-4-alpha expression in A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00389-ihc.jpgAnti-HNF-4-alpha Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using HNF-4-alpha Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-rabbit-monoclonal-antibody-m11068-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-wb-testing-1_1.jpgAnti-Histone H2B Rabbit Monoclonal Antibody Western blot analysis of Histone H2B/H2BC12 using anti-Histone H2B/H2BC12 antibody (M11068). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse Nerro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H2B/H2BC12 antigen affinity purified monoclonal antibody (M11068) at a dilution of 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H2B/H2BC12 at approximately 17 kDa. The expected band size for Histone H2B/H2BC12 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-ihc-testing-1.jpgAnti-Histone H2B Rabbit Monoclonal AntibodyIHC analysis of Histone H2B/H2BC12 using anti-Histone H2B/H2BC12 antibody (M11068). <br>Histone H2B/H2BC12 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H2B/H2BC12 Antibody (M11068) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-ihc-testing-2_1.jpgAnti-Histone H2B Rabbit Monoclonal AntibodyIHC analysis of Histone H2B/H2BC12 using anti-Histone H2B/H2BC12 antibody (M11068). <br>Histone H2B/H2BC12 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H2B/H2BC12 Antibody (M11068) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-histone-h2b-primary-antibodies-ihc-testing-3.jpgAnti-Histone H2B Rabbit Monoclonal AntibodyIHC analysis of H2B/H2BC12 using anti-H2B/H2BC12 antibody (M11068). <br>
H2B/H2BC12 was detected in a paraffin-embedded section of rat uterus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2B/H2BC12 Antibody (M11068) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-ihc-testing-4.jpgAnti-Histone H2B Rabbit Monoclonal Antibody IHC analysis of Histone H2B/H2BC12 using anti-Histone H2B/H2BC12 antibody (M11068). <br>Histone H2B/H2BC12 was detected in a paraffin-embedded section of human colon cnacer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H2B/H2BC12 Antibody (M11068) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-ip-testing-1.jpgAnti-Histone H2B Rabbit Monoclonal AntibodyImmunoprecipitating (IP) Histone H2B in K562 whole cell lysate.<br>
Western blot analysis of Histone H2B using anti-Histone H2B antibody (M11068); <br>
Lane 1: K562 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-Histone H2B antibody in K562 whole cell lysate;<br>
Lane 3: anti-Histone H2B antibody (2μg) + K562 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Histone H2B antigen affinity purified monoclonal antibody (M11068) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for Histone H2B at approximately 17 kDa. The expected band size for Histone H2B is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11068-h2bc12-primary-antibodies-ihc-testing-5.jpgAnti-Histone H2B Rabbit Monoclonal Antibody IHC analysis of Histone H2B/H2BC12 using anti-Histone H2B/H2BC12 antibody (M11068). <br>Histone H2B/H2BC12 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H2B/H2BC12 Antibody (M11068) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stat1-alpha-rabbit-monoclonal-antibody-m00036-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00036-stat1-primary-antibodies-wb-testing-1.jpgAnti-STAT1 alpha Rabbit Monoclonal Antibody Western blot analysis of STAT1 using anti-STAT1 antibody (M00036). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Caco-2 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: human A431 whole cell lysates,<br>
Lane 6: human MCF-7 whole cell lysates,<br>
Lane 7: human RT4 whole cell lysates,<br>
Lane 8: human HEL whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT1 antigen affinity purified monoclonal antibody (Catalog # M00036) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT1 at approximately 91 kDa. The expected band size for STAT1 is at 91 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ampk-beta-1-rabbit-monoclonal-antibody-m03741-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03741-wb.jpgAnti-AMPK beta 1 PRKAB1 Rabbit Monoclonal AntibodyWestern blot analysis of AMPK beta 1 expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-collagen-vi-rabbit-monoclonal-antibody-m02226-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-wb-testing-1.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyWestern blot analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: rat ovary tissue lysates,<br>
Lane 3: mouse ovary tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Collagen Type VI/COL6A1 antigen affinity purified monoclonal antibody (M02226) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Collagen Type VI/COL6A1 at approximately 147 kDa. The expected band size for Collagen Type VI/COL6A1 is at 109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-wb-testing-2_1.pngAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyWestern blot analysis of COL6A1 using anti-COL6A1 antibody (M02226). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: control group-Mouse hippocampus tissue lysates, <br>
Lane 2: model group-Mouse hippocampus tissue lysates, <br>
Lane 3: Drug treatment (0.1g/kg) – Mouse hippocampus tissue lysates, <br>
Lane 4: Drug treatment (0.3g/kg) – Mouse hippocampus tissue lysates, <br>
Lane 5: Drug treatment (0.6g/kg) – Mouse hippocampus tissue lysates, <br>
Lane 6: Drug treatment (1.2g/kg) – Mouse hippocampus tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COL6A1 antigen affinity purified monoclonal antibody (M02226) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for COL6A1 at approximately 147 kDa. The expected band size for COL6A1 is at 108 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-1.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-2.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-3.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-4.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-5.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-6.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-7.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-8.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-9.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-10.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-11.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-12.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-13.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-14.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-15.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02226-col6a1-primary-antibodies-ihc-testing-16.jpgAnti-Collagen VI COL6A1 Rabbit Monoclonal AntibodyIHC analysis of Collagen Type VI/COL6A1 using anti-Collagen Type VI/COL6A1 antibody (M02226). <br>Collagen Type VI/COL6A1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Collagen Type VI/COL6A1 Antibody (M02226) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ubiquitin-d-rabbit-monoclonal-antibody-m01970-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig1_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyHigh FAT10 expression is associated with poor prognosis in patients with PC. A The GEPIA2 server was used to analyze the expression of FAT10 in PAAD (T, tumor; N, nontumorous tissues; * p < 0.05). B Representative IHC image showing the increase in FAT10 protein levels in PC tissue (magnification: 100×, inset magnification: 200×). Scale bar, 200 μm. C Immunofluorescence localization of FAT10 protein expression in PC and paracancerous tissues using the anti-FAT10 antibody (1:100, green) and anti-Maspin antibody (1:100, red), followed by DAPI nuclear counterstaining (blue). Merged images of FAT10 (green) and Maspin (red) with DAPI (blue) are also shown. Scale bar, 100 μm. D qRT–PCR analysis of FAT10 mRNA levels in PC tissues and corresponding adjacent tissues ( n = 40, p = 0.001; Wilcoxon signed-rank test). GAPDH was used as a loading control. E Western blot analysis of FAT10 protein expression in PC tissues and corresponding adjacent noncancerous tissues ( n = 40; Student’s t-test). GAPDH was used as a loading control. F Kaplan–Meier survival curve of the relationship between FAT10 high and low expression groups and the prognosis of PC patients ( n = 89, p = 0.003; Log-rank test). G Kaplan–Meier survival curves of prognosis-related FAT10 expression in the Kaplan–Meier plotter cohort ( n = 177, p = 0.016; Log-rank test). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig2_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyFAT10 expression is correlated with chemoresistance of PC cells to GEM. A Protein expression of FAT10 in noncancerous pancreatic ductal epithelial cells and PC cell lines was analyzed by western blotting. B The mRNA expression of FAT10 in normal pancreatic ductal epithelial cells and PC cell lines was analyzed by qRT–PCR. C Viabilities of PC cells were determined in response to different concentrations of GEM. Inhibition curves were fitted by nonlinear regression, and GEM IC50s were calculated using GraphPad Prism 8 software. D Western blotting was used to analyze expression levels of FAT10 in GEM-resistant (GR) PC cells. Data represent the mean ± SD of triplicate experiments and were statistically analyzed with Student’s t-test, * p < 0.05, ** p < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig3_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyInhibition of FAT10 increases the chemotherapeutic sensitivity of PC to GEM. A – C The IC50 of PC cells (FAT10 knockdown or overexpression) exposed to different concentrations of GEM was determined by cell viability experiments. D – F The effect of knocking down FAT10 on the proliferation rate of PC cells treated with GEM was detected by EdU staining. G – I The apoptosis rate of PC cells with FAT10 knockdown was detected by AO/EB staining after GEM treatment. Data represent the mean ± SD of triplicate experiments and were statistically analyzed by one-way ANOVA. J Representative images of different groups of tumors removed from mice are shown. K Growth curve showing changes in tumor volume in mice from different groups. Growth was assessed every 5 days beginning from the day of injection and during GEM treatment. At the end of the experiment, the tumor was dissected and photographed, and the tumor volume (V) was calculated as follows: V = 0.52 × length × width 2 and analyzed by one-way ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig4_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyFAT10 regulates EMT to promote chemotherapeutic resistance in PC cells. A Spearman correlation analysis of the correlation between FAT10 ( UBD ) and EMT pathway score. FAT10 expression is represented by the abscissa, and the EMT pathway score is represented by the ordinate. A density curve to the right represents the trend in the distribution of pathway scores, a density curve to the upper part represents the trend in the distribution of gene expression. The top part shows the p -value, correlation coefficient, and correlation calculation method. B Immunofluorescence analysis of the effect of inhibiting FAT10 on the expression of EMT-related proteins (E-cadherin and Vimentin) in PC cells. Scale bar, 50 μm. C – F GEM-resistant PC cell lines (PANC-1/GR and BxPC-3/GR) were transfected with interfering plasmid sh-FAT10#2 and or EMT activator (TGF-β, 10 ng/mL) for 48 h. C , E Western blot analysis was used to observe the expression of EMT-related proteins in each treatment group. D , F Cell viability experiments were used to calculate the half-inhibitory concentration (IC50) of GEM-treated PC-resistant cells in each treatment group. Data represent the mean ± SD of triplicate experiments and were statistically analyzed by one-way ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig5_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyFAT10 regulates EMT through FOXM1. A Top 10 proteins co-precipitated with FAT10 analyzed by LC-MS/MS. #PSMs, peptide spectrum matches. B Mass spectrum showing unique peptides of FOXM1 identified by 2D-LC-MS/MS from the protein lysates prepared from PANC-1 cells following immunoprecipitation with anti-FAT10. C Representative western blot analysis of FAT10 and FOXM1 protein expression in PC and paired paracancerous tissues (T, tumor; NT, non-tumor tissue). D Scatter plots showing a positive correlation between FAT10 and FOXM1 protein expression levels in 40 PC samples ( n = 40, r = 0.4642, p = 0.0025, Pearson test). E , F Western blot analyses were used to detect FAT10 and FOXM1 protein expression in cells stably transfected with the shFAT10 or HA-FAT10 plasmid. G Western blot analysis confirming FAT10 silencing and FOXM1 restoration and their effects on EMT-related proteins. H Western blot analysis showing the levels of FAT10 overexpression and FOXM1 inhibition and their effects on EMT-related proteins. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig6_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyFAT10 increases FOXM1 protein levels by inhibiting the ubiquitination and degradation of FOXM1 in PC cells. A Co-IP was used to detect the interaction between FOXM1 and ubiquitin in PANC-1 and BxPC-3 cells. HC, heavy chain. B With MG132 (10 μM) added to PANC-1 and BxPC-3 cells, western blotting was used to detect protein levels of FOXM1 at different times. C MG132 (10 μM) was added to PANC-1 and BxPC-3 cells while the expression of FAT10 was altered. Western blotting was used to detect protein expression levels of FOXM1. D PANC-1 and BxPC-3 cells were treated with CHX (20 μM) for a specified time with or without the addition of the FAT10 overexpression plasmid, and FOXM1 protein levels were detected by western blotting. Data represent the mean ± SD of triplicate experiments and were statistically analyzed with Student’s t-test, * p < 0.05, ** p < 0.01. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-41419_2022_4960_fig7_html.pngAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyFAT10 competes with ubiquitin to bind and stabilize FOXM1. A Co-IP was used to detect the interaction between FOXM1 and FAT10 in PANC-1 and BxPC-3 cells. HC, heavy chain. B MG132 (10 μM) was added to PANC-1 and BxPC-3 cells, shFAT10 or HA-FAT10 plasmid was transfected at the same time, and then co-IP was used to detect the levels of ubiquitin bound to FOXM1 protein. C PANC-1 and BxPC-3 cells were transfected with different amounts of HA-FAT10 plasmid, and the level of FAT10 binding to FOXM1 protein was detected by co-IP. D PANC-1 and BxPC-3 cells were transfected with different amounts of HA-FAT10 plasmid, and the level of Ub binding to FOXM1 protein was detected by co-IP. E Docking conformation of the first ranking score. Three-dimensional structure of FAT10 and FOXM1. FAT10 is shown in green. FOXM1 is shown in cyan. F The Flag-FOXM1 plasmid was transfected into PANC-1 and BxPC-3 cells, the HA-FAT10 or HA-FAT10ΔGG plasmid was transfected at the same time, and then the protein level of Flag-FOXM1 bound to the HA-tagged protein was detected by co-IP. HC, heavy chain. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-022-04960-0'>35614040</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01970-ubd-primary-antibodies-wb-testing-1.jpgAnti-Ubiquitin D UBD Rabbit Monoclonal AntibodyWestern blot analysis of Ubiquitin D using anti-Ubiquitin D antibody (M04905-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human SH-SY5Y whole cell lysates,<br>
Lane 6: human K562 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse HEPA1/6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ubiquitin D antigen affinity purified monoclonal antibody (M04905-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Ubiquitin D at approximately 23 kDa. The expected band size for Ubiquitin D is at 18 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspb8-hsp22-rabbit-monoclonal-antibody-m02492-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02492-wb.jpgAnti-HSPB8/HSP22 Rabbit Monoclonal AntibodyWestern blot analysis of HSPB8/HSP22 expression in Human fetal heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kmt6-ezh2-rabbit-monoclonal-antibody-m00050-1-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00050-1-wb.jpgAnti-KMT6 / EZH2 Rabbit Monoclonal AntibodyWestern blot analysis of KMT6 / EZH2 expression in HEK293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00050-1-ihc.jpgAnti-KMT6 / EZH2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human tonsil, using KMT6 / EZH2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00050-1-if.jpgAnti-KMT6 / EZH2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using KMT6 / EZH2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ve-cadherin-rabbit-monoclonal-antibody-m02632-boster.html2026-03-24T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02632-fphar-12-653035-g003.jpgAnti-VE-Cadherin Cdh5-Rabbit Monoclonal AntibodyThe upregulation of angiogenesis in the skin flaps via Andro (A,C) IHC of Cadherin5 and VEGF in both groups of ischemic skin flaps (original magnification, ×200; scan bar, 50 μm). (B,D) The total absorbance of Cadherin5 and VEGF in IHC. (E) The results of immunoblotting i.e., the expressions of cadherin 5, MMP9, VEGF in the control as well as Andro groups. (F–H) The quantification of Cadherin5, MMP9, and VEGF expressions in the flaps by measuring their optical densities. The obtained data were presented as means ± SEM. Significance: * p -value < 0.05 and ** p -value < 0.01, vs. control group (n = 6 per group).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2021.653035/full'>33796027</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02632-cdh5-primary-antibodies-wb-testing-1.jpgAnti-VE-Cadherin Cdh5-Rabbit Monoclonal Antibody Western blot analysis of Cdh5 using anti-Cdh5 antibody (M02632). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cdh5 antigen affinity purified monoclonal antibody (Catalog # M02632) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cdh5 at approximately 88 kDa. The expected band size for Cdh5 is at 88 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kmt6-ezh2-rabbit-monoclonal-antibody-m00050-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00050-wb.jpgAnti-KMT6 / EZH2 Rabbit Monoclonal AntibodyWestern blot analysis of KMT6 / EZH2 expression in Hela cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mitofusin-2-rabbit-monoclonal-antibody-m00461-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00461-mfn2-primary-antibodies-wb-testing-1_1.jpgAnti-Mitofusin 2 MFN2 Rabbit Monoclonal Antibody Western blot analysis of Mitofusin 2 using anti-Mitofusin 2 antibody (M00461). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: rat brain tissue lysates, <br>
Lane 3: rat kidney tissue lysates, <br>
Lane 4: rat liver tissue lysates, <br>
Lane 5: mouse brain tissue lysates, <br>
Lane 6: mouse kidney tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Mitofusin 2 antigen affinity purified monoclonal antibody (M00461) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Mitofusin 2 at approximately 86 kDa. The expected band size for Mitofusin 2 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00461-ihc.jpgAnti-Mitofusin 2 MFN2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Mitofusin 2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00461-13287_2025_4422_fig3_html.pngAnti-Mitofusin 2 MFN2 Rabbit Monoclonal AntibodyDMOG treatment ameliorates mitochondrial dysfunction and enhances mitophagy and ATP production in aged MSCs. ( A ) Representative JC-1 fluorescence images showing mitochondrial membrane potential in different groups: CCCP (positive control for mitochondrial depolarization), P5 MSCs, P5 + H₂O₂-treated MSCs, P5 + H₂O₂+DMOG-treated MSCs, P15 MSCs, and P15 + DMOG-treated MSCs. JC-1 red fluorescence indicates high mitochondrial membrane potential, whereas green fluorescence indicates depolarized mitochondria. Scale bar = 100 μm. ( B ) Representative MitoSox Red fluorescence images showing mitochondrial ROS levels in different treatment groups. Scale bar = 10 μm. ( C , D ) Quantitative analysis of the mitochondrial membrane potential ( C ) and mitochondrial ROS levels ( D ). ( E ) Western blot analysis showing the expression levels of mitophagy-related proteins (MFN1, MFN2, and Fis1) in P5 and P15 MSCs with or without H₂O₂ and DMOG treatment. GAPDH was used as a loading control. ( F ) Representative confocal images of co-staining with LysoTracker Red (lysosomes) and MitoTracker Green (mitochondria) in MSCs under different conditions. Scale bar = 10 μm. ( G ) Quantitative analysis of the number of mitophagosomes per cell in the different groups. ( H ) Quantitative analysis of ATP production per cell in the different groups. Data are expressed as the mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01. *** p < 0.001. Full-length blots are presented in Supplementary Materials - WB Raw Data Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04422-2'>40457488</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00461-if.jpgAnti-Mitofusin 2 MFN2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Mitofusin 2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-argonaute-2-rabbit-monoclonal-antibody-m00189-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00189-ago2-primary-antibodies-wb-testing-1.jpgAnti-Argonaute 2 AGO2 Rabbit Monoclonal Antibody Western blot analysis of AGO2 using anti-AGO2 antibody (M00189). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AGO2 antigen affinity purified monoclonal antibody (Catalog # M00189) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AGO2 at approximately 97 kDa. The expected band size for AGO2 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00189-wb7.jpgAnti-Argonaute 2 AGO2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00189-fonc-11-663114-g005.jpgAnti-Argonaute 2 AGO2 Rabbit Monoclonal AntibodyMTORT1 serves as a miRNA sponge. (A) Enrichment of miRNA candidates in mitochondria in MCF-7 cells. Candidates of miRNA were predicted using miRDB ( ). Relative expression levels of miRNA were measured by quantitative RT-PCR and compared to that of miR-181c , which was reported as a mitochondrial miRNA. (B) Relative expression levels of miRNA candidates in MTORT1 knockdown cells were measured by quantitative RT-PCR and normalized to 18S rRNA. (C–E) RNA immunoprecipitation analysis of MTORT1 (C) , miR-26a-5p (D) , and miR-1297 (E) using antibody against AGO2 in MCF-7 cells. Relative expression levels of AGO2-enriched non-coding RNA were measured by quantitative RT-PCR and compared to those pulled down by IgG. The results are means ± SDs (n = 3). * P < 0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.663114/full'>34141617</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00189-41419_2022_5253_fig4_html.pngAnti-Argonaute 2 AGO2 Rabbit Monoclonal AntibodyNDRG1-OT1 serves as a sponge for miR-875-3p . A , B Distribution of NDRG1-OT1 in MDA-MB-231 cells under normoxia ( A ) and hypoxia ( B ). Cytoplasmic and nuclear RNA were fractionated in MDA-MB-231 cells under normoxia ( A ) and hypoxia ( B ). Relative abundance of RNA was normalized to the total amount of RNA and detected by qPCR. GAPDH : cytoplasmic marker; BCAR4 : nuclear marker. C Relative expression levels of six predicted miRNAs in MDA-MB-231 cells overexpressing NDRG1-OT1 . The candidate miRNAs binding NDRG1-OT1 were predicted by miRDB ( ). The expression levels of miRNAs were measured by qPCR and normalized to U6 . D RIP analysis of NDRG1-OT1 using antibody against AGO2 in normoxia. The RIP enrichment of the AGO2-associated lncRNA was measured by qPCR and normalized to 18 S rRNA. The relative fold enrichment was calculated as compared to the IgG group. E Expression levels of miR-875-3p in five breast cancer cell lines under hypoxia and normoxia, detected by qPCR. Loading control: U6 snRNA. The relative expression levels in each cell line were compared with those of the normoxic group, respectively. F Relative expression of NDRG1-OT1 in MDA-MB-231 cells overexpressing miR-875-3p , and followed by treatment of miR-875-3p inhibitor (50 nM). Loading control: GAPDH . ( n = 5). G Schematic representation of firefly luciferase constructs containing the sequence of NDRG1-OT1 (WT) and two mutations of miR-875-3p binding sites (sites 1 and 2). H Luciferase reporter assays of NDRG1-OT1 in HEK293T cells overexpressing miR-875-3p . All data shown are the means ± SDs. * P < 0.05. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-022-05253-2'>36127332</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00189-wb.jpgAnti-Argonaute 2 AGO2 Rabbit Monoclonal AntibodyWestern blot analysis of Argonaute 2 expression in (1) HeLa cell lysate; (2) RAW 264.7 cell lysate; (3) C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-parvalbumin-rabbit-monoclonal-antibody-m04041-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04041-wb.jpgAnti-Parvalbumin PVALB Rabbit Monoclonal AntibodyWestern blot analysis of Parvalbumin expression in human cerebellum lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04041-pvalb-primary-antibodies-ihc-testing-1_1.jpgAnti-Parvalbumin PVALB Rabbit Monoclonal AntibodyIHC analysis of PVALB using anti-PVALB antibody (M04041). <br>PVALB was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PVALB Antibody (M04041) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04041-pvalb-primary-antibodies-ihc-testing-2_2.jpgAnti-Parvalbumin PVALB Rabbit Monoclonal AntibodyIHC analysis of PVALB using anti-PVALB antibody (M04041). <br>PVALB was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PVALB Antibody (M04041) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mhc-class-i-rabbit-monoclonal-antibody-m00194-2-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-2-wb7.jpgAnti-MHC class I HLA-A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-2-wb.jpgAnti-MHC class I HLA-A Rabbit Monoclonal AntibodyWestern blot analysis of MHC class I expression in Raji cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-2-wb8.jpgAnti-MHC class I HLA-A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-2-icc1.jpgAnti-MHC class I HLA-A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00194-2-wb9.jpgAnti-MHC class I HLA-A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cea-cd66e-rabbit-monoclonal-antibody-m00356-1-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-1-wb.jpgAnti-CEA (CD66e) CEACAM5 Rabbit Monoclonal AntibodyWestern blot analysis of CEA(CD66e) expression in Human colon cancer lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-1-icc1.jpgAnti-CEA (CD66e) CEACAM5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-1-ihc.jpgAnti-CEA (CD66e) CEACAM5 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon carcinoma, using CEA(CD66e) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-1-icc2.jpgAnti-CEA (CD66e) CEACAM5 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-1-if.jpgAnti-CEA (CD66e) CEACAM5 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using CEA(CD66e) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdgfr-alpha-rabbit-monoclonal-antibody-m00366-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-pdgfra-primary-antibodies-wb-testing-1.jpgAnti-PDGFR alpha Rabbit Monoclonal Antibody Western blot analysis of PDGFR alpha/PDGFRA using anti-PDGFR alpha/PDGFRA antibody (M00366). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Caco-2 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: rat ovary tissue lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse ovary tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDGFR alpha/PDGFRA antigen affinity purified monoclonal antibody (M00366) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDGFR alpha/PDGFRA at approximately 180 kDa. The expected band size for PDGFR alpha/PDGFRA is at 123 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lipocalin-2-rabbit-monoclonal-antibody-m00452-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00452-lcn2-primary-antibodies-wb-testing-1.jpgAnti-Lipocalin-2 LCN2 Rabbit Monoclonal AntibodyWestern blot analysis of LCN2 using anti-LCN2 antibody (M00452). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LCN2 antigen affinity purified monoclonal antibody (M00452) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LCN2 at approximately 23 kDa. The expected band size for LCN2 is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-haptoglobin-rabbit-monoclonal-antibody-m00062-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00062-wb.jpgAnti-Haptoglobin HP Rabbit Monoclonal AntibodyWestern blot analysis of Haptoglobin expression in human plasma lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-perilipin-a-rabbit-monoclonal-antibody-m03918-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03918-wb7.jpgAnti-Perilipin A PLIN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03918-wb.jpgAnti-Perilipin A PLIN1 Rabbit Monoclonal AntibodyWestern blot analysis of Perilipin A expression in human fetal liver lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03918-plin1-primary-antibodies-wb-testing-1.pngAnti-Perilipin A PLIN1 Rabbit Monoclonal AntibodyWestern blot analysis of PLIN1 using anti-PLIN1 antibody (M03918). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-3: mouse Brown Adipose Tissue-f/f, <br>
Lane 4-6: mouse Brown Adipose Tissue-mko, <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLIN1 antigen affinity purified polyclonal antibody (A04887-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a Goat Anti-Rabbit IgG Antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Abbkine system.The expected band size for PLIN1 is at 56 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cathepsin-b-rabbit-monoclonal-antibody-m01456-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01456-ctsb-primary-antibodies-wb-testing-1.jpgAnti-Cathepsin B CTSB Rabbit Monoclonal Antibody Western blot analysis of Cathepsin B using anti-Cathepsin B antibody (M01456). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U-87MG whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cathepsin B antigen affinity purified monoclonal antibody (Catalog # M01456) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cathepsin B at approximately 38 kDa. The expected band size for Cathepsin B is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01456-ctsb-primary-antibodies-ihc-testing-2.jpgAnti-Cathepsin B CTSB Rabbit Monoclonal Antibody IHC analysis of Cathepsin B using anti-Cathepsin B antibody (M01456). <br>
Cathepsin B was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cathepsin B Antibody M01456) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01456-ctsb-primary-antibodies-ihc-testing-3.jpgAnti-Cathepsin B CTSB Rabbit Monoclonal Antibody IHC analysis of Cathepsin B using anti-Cathepsin B antibody (M01456). <br>
Cathepsin B was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cathepsin B Antibody M01456) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01456-ctsb-primary-antibodies-ihc-testing-4.jpgAnti-Cathepsin B CTSB Rabbit Monoclonal Antibody IHC analysis of Cathepsin B using anti-Cathepsin B antibody (M01456). <br>
Cathepsin B was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Cathepsin B Antibody M01456) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lactoferrin-rabbit-monoclonal-antibody-m00633-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00633-wb.jpgAnti-Lactoferrin LTF Rabbit Monoclonal AntibodyWestern blot analysis of Lactoferrin expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apg3-atg3-rabbit-monoclonal-antibody-m01768-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01768-atg3-primary-antibodies-wb-testing-1.jpgAnti-Apg3 (Atg3) Rabbit Monoclonal Antibody Western blot analysis of Apg3 using anti-Apg3 antibody (M01768). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human Raji whole cell lysates,<br>
Lane 4: monkey COS-7 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse kidney tissue lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Apg3 antigen affinity purified monoclonal antibody (Catalog # M01768) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Apg3 at approximately 40 kDa. The expected band size for Apg3 is at 36 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-crispr-cas9-rabbit-monoclonal-antibody-m30929-1-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30929-1-wb.jpgAnti-CRISPR-Cas9 Rabbit Monoclonal AntibodyWestern blot analysis of CRISPR-Cas9 SA expression in (1) 293T cell lysate transfected with CRISPR-Cas9 SA; (2) 293T cell lysate; (3) 3T3 cell lysate; (4) PC12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30929-1-if.jpgAnti-CRISPR-Cas9 Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293T cells transfected with CRISPR-Cas9 SA, using CRISPR-Cas9 SA Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mef2a-mef2c-rabbit-monoclonal-antibody-m01131-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01131-mef2a-mef2c-primary-antibodies-wb-testing-1.jpgAnti-MEF2A+MEF2C Rabbit Monoclonal Antibody Western blot analysis of MEF2A+MEF2C using anti-MEF2A+MEF2C antibody (M01131). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEF2A+MEF2C antigen affinity purified monoclonal antibody (Catalog # M01131) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MEF2A+MEF2C at approximately 52 kDa. The expected band size for MEF2A+MEF2C is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01131-mef2a-mef2c-primary-antibodies-ihc-testing-2.jpgAnti-MEF2A+MEF2C Rabbit Monoclonal Antibody IHC analysis of MEF2A+MEF2C using anti-MEF2A+MEF2C antibody (M01131). <br>
MEF2A+MEF2C was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MEF2A+MEF2C Antibody (M01131) overnight at 4°C. Peroxidase Conjugated Goat Anti-mouse IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01131-mef2a-mef2c-primary-antibodies-ihc-testing-3.jpgAnti-MEF2A+MEF2C Rabbit Monoclonal Antibody IHC analysis of MEF2A+MEF2C using anti-MEF2A+MEF2C antibody (M01131). <br>
MEF2A+MEF2C was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MEF2A+MEF2C Antibody (M01131) overnight at 4°C. Peroxidase Conjugated Goat Anti-mouse IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01131-mef2a-mef2c-primary-antibodies-ihc-testing-4.jpgAnti-MEF2A+MEF2C Rabbit Monoclonal Antibody IHC analysis of MEF2A+MEF2C using anti-MEF2A+MEF2C antibody (M01131). <br>
MEF2A+MEF2C was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MEF2A+MEF2C Antibody (M01131) overnight at 4°C. Peroxidase Conjugated Goat Anti-mouse IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Mouse IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-tubulin-rabbit-monoclonal-antibody-m05613-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05613-TUBB-primary-antibodies-IHC-testing-1.jpgAnti-beta Tubulin TUBB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded (1) Human glioma; (2) Rat brain; (3) Mouse kidney; (4) Human uterus cancer, using beta Tubulin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05613-_-tubulin-primary-antibodies-wb-testing-1.jpgAnti-beta Tubulin TUBB Rabbit Monoclonal AntibodyWestern blot analysis of beta-Tubulin using anti-beta-Tubulin antibody (M05613). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: monkey COS-7 whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-beta-Tubulin antigen affinity purified monoclonal antibody (M05613) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for beta-Tubulin at approximately 50 kDa. The expected band size for beta-Tubulin is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05613-if.jpgAnti-beta Tubulin TUBB Rabbit Monoclonal AntibodyImmunofluorescent analysis of NIH/3T3 cells, using beta Tubulin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-catenin-rabbit-monoclonal-antibody-m00004-1-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-ctnnb1-primary-antibodies-wb-testing-1.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody Western blot analysis of beta Catenin using anti-beta Catenin antibody (M00004-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: rat PC-12 whole cell lysates,<br>
Lane 4: rat RH35 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-beta Catenin antigen affinity purified monoclonal antibody (Catalog # M00004-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for beta Catenin at approximately 85 kDa. The expected band size for beta Catenin is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-beta_catenin-primary-antibodies-ihc-testing-2.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody IHC analysis of Beta Catenin using anti-Beta Catenin antibody (M00004-1). <br>
Beta Catenin was detected in a paraffin-embedded section of human bladder squamous cell carcinomar tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Beta Catenin Antibody (M00004-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-beta_catenin-primary-antibodies-ihc-testing-3.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody IHC analysis of Beta Catenin using anti-Beta Catenin antibody (M00004-1). <br>
Beta Catenin was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Beta Catenin Antibody (M00004-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-beta_catenin-primary-antibodies-ihc-testing-4.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody IHC analysis of Beta Catenin using anti-Beta Catenin antibody (M00004-1). <br>
Beta Catenin was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Beta Catenin Antibody (M00004-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-beta_catenin-primary-antibodies-ihc-testing-5.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody IHC analysis of Beta Catenin using anti-Beta Catenin antibody (M00004-1). <br>
Beta Catenin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Beta Catenin Antibody (M00004-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-beta_catenin-primary-antibodies-ihc-testing-6.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal Antibody IHC analysis of Beta Catenin using anti-Beta Catenin antibody (M00004-1). <br>
Beta Catenin was detected in a paraffin-embedded section of rat intestines tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Beta Catenin Antibody (M00004-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004-1-if.jpgAnti-beta Catenin CTNNB1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using beta Catenin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cleaved-parp-rabbit-monoclonal-antibody-m00122-1-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-1-parp1-primary-antibodies-wb-testing-1.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal Antibody Western blot analysis of PARP1 using anti-PARP1 antibody (M00122-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: mouse Raw264.7 whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARP1 antigen affinity purified polyclonal antibody (Catalog # M00122-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARP1 at approximately 25 kDa. The expected band size for PARP1 is at 25,113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-1-ihc.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Cleaved PARP Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-1-12885_2025_14920_fig1_html.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal Antibodyα-hederin effectively inhibit proliferation and promotes apoptosis of cervical cancer cells. A Chemical molecular structure formula of α-hederin. B CCK8 detection of α-hederin action on SiHa and HeLa cells. C Fluorescence staining images of hoechst and edu after α-hederin treatment of. Scale bar is 200 μm. D - E Statistical analysis of fluorescent area by EDU staining. F - G Statistical analysis of fluorescence intensity by Hoechst staining. H Immunoblotting strip image of apoptosis key proteins after α-hederin treatment. I - L Statistical analysis of gray scale values of apoptosis key protein immunostaining bands. Results are expressed as mean ± SD ( n = 3). ns, p > 0.05; *, p < 0.05. M Flow cytometry analysis of the effect of α-hederin on apoptosis of cells. N – O Quantitative analysis of the number of apoptotic cells in different concentration groups and control group. ****, p < 0.0001. P Clone formation in α-hederin-treated SiHa and HeLa cells. Q - R Statistical analysis of the number of clone formation in SiHa and HeLa cells. Results are expressed as mean ± SD ( n = 3). ns, p > 0.05; *, p < 0.05; **, p < 0.01; ***, p < 0.001; and ****, p < 0.0001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12885-025-14920-4'>41044707</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ldl-receptor-rabbit-monoclonal-antibody-m00076-boster.html2026-03-24T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00076-wb.jpgAnti-LDL Receptor Rabbit Monoclonal AntibodyWestern blot analysis of LDLR expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00076-ihc.jpgAnti-LDL Receptor Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver carcinoma, using LDL Receptor Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-neuropilin-1-rabbit-monoclonal-antibody-m01324-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-nrp1-primary-antibodies-wb-testing-1.jpgAnti-Neuropilin 1 NRP1 Rabbit Monoclonal Antibody Western blot analysis of NRP1 using anti-NRP1 antibody (M01324). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human U251 whole cell lysates,<br>
Lane 4: rat heart tissue lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse heart tissue lysates,<br>
Lane 7: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRP1 antigen affinity purified monoclonal antibody (Catalog # M01324) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NRP1 at approximately 120 kDa. The expected band size for NRP1 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-nrp1-primary-antibodies-ihc-testing-2.jpgAnti-Neuropilin 1 NRP1 Rabbit Monoclonal Antibody IHC analysis of NRP1 using anti-NRP1 antibody (M01324). <br>
NRP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NRP1 Antibody (M01324) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-nrp1-primary-antibodies-ihc-testing-3.jpgAnti-Neuropilin 1 NRP1 Rabbit Monoclonal Antibody IHC analysis of NRP1 using anti-NRP1 antibody (M01324). <br>
NRP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NRP1 Antibody (M01324) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-nrp1-primary-antibodies-ihc-testing-4.jpgAnti-Neuropilin 1 NRP1 Rabbit Monoclonal Antibody IHC analysis of NRP1 using anti-NRP1 antibody (M01324). <br>
NRP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NRP1 Antibody (M01324) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-nrp1-primary-antibodies-ihc-testing-5.jpgAnti-Neuropilin 1 NRP1 Rabbit Monoclonal Antibody IHC analysis of NRP1 using anti-NRP1 antibody (M01324). <br>
NRP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NRP1 Antibody (M01324) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cleaved-parp-rabbit-monoclonal-antibody-m00122-2-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-wb7.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-wb8.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-wb9.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-wb.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyWestern blot analysis of Cleaved PARP expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-ihc7.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat skin, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-ihc8.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-ihc9.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-ihc10.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-icc1.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00122-2-if.jpgAnti-Cleaved PARP PARP1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using Cleaved PARP Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dap-kinase-1-rabbit-monoclonal-antibody-m01161-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01161-wb.jpgAnti-DAP Kinase 1 DAPK1 Rabbit Monoclonal AntibodyWestern blot analysis of DAP Kinase 1 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01161-ihc.jpgAnti-DAP Kinase 1 DAPK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using DAP Kinase 1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01161-if.jpgAnti-DAP Kinase 1 DAPK1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using DAP Kinase 1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pan-cadherin-rabbit-monoclonal-antibody-m00063-1-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-1-wb7.jpgAnti-pan Cadherin 1 CDH1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-1-ihc.jpgAnti-pan Cadherin 1 CDH1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded colon cancer, using pan Cadherin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-1-wb8.jpgAnti-pan Cadherin 1 CDH1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-1-wb.jpgAnti-pan Cadherin 1 CDH1 Rabbit Monoclonal AntibodyWestern blot analysis of pan Cadherin expression in C6 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kmt4-dot1l-rabbit-monoclonal-antibody-m00840-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00840-wb.jpgAnti-KMT4 / Dot1L Rabbit Monoclonal AntibodyWestern blot analysis of KMT4/Dot1L expression in RAW264.7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00840-dot1l-primary-antibodies-ihc-testing-1.jpgAnti-KMT4 / Dot1L Rabbit Monoclonal AntibodyIHC analysis of DOT1L using anti-DOT1L antibody (M00840). <br>DOT1L was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-DOT1L Antibody (M00840) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ampk-alpha-1-rabbit-monoclonal-antibody-m00994-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-fonc-10-573127-g004.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyInvolvement of the AMPK-ULK1-LC3 signaling cascade in TRPM8-stimulated autophagy. (A, B) The construct for Flag-AMPK expression was transiently transfected into MCF7 cells. After 48 h of transfection, the AMPK-ULK1-LC3 signaling cascade-related proteins were detected by WB (N = 3). (C, D) MCF7 cells were transiently transfected with wild type TRPM8, mutant V976W, or control vector. After 48 h of transfection, protein lysates were used for WB analysis (N = 3). (E, F) MDA-MB-231 cells treated with 2 μM icilin, 0.5 μM AMTB, or their combination for 48 h were extracted for WB analysis (N = 3). (G, H) MCF7 cells were transfected with siRNA against human TRPM8; siRNA against TRPM8 (siTRPM8-1 and siTRPM8-2) successfully knocked down TRPM8 expression compared with that in the control scramble siRNA samples according to WB analysis using an anti-TRPM8 antibody. The AMPK-ULK1-LC3 signaling cascade-related proteins detected by WB analysis using the indicated antibodies (N = 3). N represents the number of replicate experiments. *P < 0.05; NS, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.573127/full'>33344232</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-fonc-10-573127-g005.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyInfluence of AMPK impairment on the stimulatory effect of TRPM8 on autophagy. (A, B) MCF7 cells were transiently transfected with siRNA against human AMPK and a Flag-TRPM8 construct. After 48 h of transfection, protein lysates were extracted for WB analysis to determine the effect of TRPM8 overexpression on basal autophagy in the presence of AMPK knockdown (N = 3). (C, D) WB analysis of cell lysates of MDA-MB-231 cells treatment with 2 μM icilin, 10 μM menthol, or a combination of 10 M compound C for 48 h (N = 3). N represents the number of replicate experiments. *P < 0.05; NS, not significant.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.573127/full'>33344232</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-fonc-10-573127-g006.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyAMPK interacts with TRPM8. (A, B) Co-IP analysis. (A) Constructs for GFP-TRPM8 and Flag-AMPK expression were transiently transfected into MCF7 cells. After 48 h of transfection, protein lysates were immunoprecipitated with an anti-GFP antibody and assayed by immunoblot with an anti-Flag antibody (lower panel). Reciprocal Co-IP with an anti-Flag antibody used for immunoprecipitation and anti-GFP used for WB analysis (upper panel) (N = 3). (B) The construct for GFP-AMPK expression was cotransfected with M8-N, M8-LI, M8-LII, or M8-C into MCF7 cells. Protein lysates were immunoprecipitated with an anti-Flag antibody and assayed by immunoblot with an anti-GFP antibody (upper). The constructs for GFP-AMPK and Flag-M8-C expression were cotransfected into MCF7 cells. Protein lysates were immunoprecipitated with an anti-GFP antibody and assayed by immunoblot with an anti-Flag antibody (upper) (N = 3). (C) GST pull-down analysis. Protein lysates of MCF7 cells transiently expressing Flag-AMPK were incubated with purified cytoplasmic C-terminus of TRPM8 GST fusion protein (GST-M8C). GST-M8C, but not control GST, successfully pulled down Flag-AMPK. PD: pull-down. The lysate was used as a positive control (N = 3). N represents the number of replicate experiments. PD, pull down; WCL, whole cell lysates.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.573127/full'>33344232</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-prkaa1-primary-antibodies-wb-testing-1.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal Antibody Western blot analysis of AMPK alpha 1 using anti-AMPK alpha 1 antibody (M00994). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U-87MG whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AMPK alpha 1 antigen affinity purified monoclonal antibody (Catalog # M00994) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AMPK alpha 1 at approximately 64 kDa. The expected band size for AMPK alpha 1 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-ihc7.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-ihc8.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human tonsil, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-ihc9.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-ihc.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using AMPK alpha 1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00994-if.jpgAnti-AMPK alpha 1 PRKAA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using AMPK alpha 1 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calreticulin-rabbit-monoclonal-antibody-m00894-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-bmr.0151.fig.006.jpgAnti-Calreticulin Rabbit Monoclonal Antibody(A) CFRI-mediated ICD and DCs matured in vitro. Mechanism scheme of PTT-induced immunogenic death; 1,064-nm laser irradiation (1.0 W/cm 2 ) with or without treatment with DMEM, FR837, FIR1048, FRI, and CFRI (2 μg/ml). (B) The efflux of HMGB1 was quantitatively analyzed by flow cytometry. (C) CLSM images of CRT expression on the 4T1 cell surface after different treatments (scale bar: 100 μm). (D) Mean fluorescence intensity of CRT expression in 4T1 cells after different treatments. (E) The average fluorescence intensity of ATP exposure in 4T1 cells after different treatments. (F) The corresponding quantification (CD80 + CD86 + ) of mature DCs was quantitatively analyzed by flow cytometry. (G) After different treatments by enzyme-linked immunosorbent assay (ELISA), secretion levels of TNF-ɑ in the cell supernatant. (H) After different treatments by ELISA, the secretion level of IL-6 in the cell supernatant. (I) After different treatments by ELISA, the secretion level of IL-10 in the cell supernatant. Information of each group: I, control; II, control + L; III, FR837; IV, FR837 + L; V, FIR1048; VI, FIR1048 + L; VII, FRI; VII, FRI + L; IX, CFRI; X, CFRI + L. Significance is determined using one-way analysis of variance (* P < 0.05, ** P < 0.01, and *** P < 0.001). HSPs, heat shock proteins.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11876542/'>40040955</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-bmr.0151.fig.009.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyIn vivo CFRI-mediated PTT-enhanced immunotherapy elicited an immune response after 16 d of treatment. (A) Schematic diagram of immunity induced by damage-associated molecular patterns (DAMPs). (B and C) Analysis of DC maturity (CD11 + CD80 + CD86 + ) using flow cytometry in the primary tumor of 4T1 tumor-bearing mice. (D and E) Regulatory T cells (Tregs) (CD4 + CD25 + ) in the spleen. (F and G) T cell proliferation in the blood (CD4 + CD8 + ). (H) The content of TNF-α in the spleen of 4T1 tumor-bearing mice. (I) The content of IL-6 in the spleen of 4T1 tumor-bearing mice. (J) The content of IL-10 in the spleen of 4T1 tumor-bearing mice. (K) Heat map of TNF-α and IL-10 content in the blood of 4T1 tumor-bearing mice. (L) CRT and HMGB1 staining images of 4T1 tumor-bearing mice after different treatments. Scale bar: 100 μm. Group information: I, PBS; II, PBS + L; III, FR837; IV, FR837 + L; V, FIR1048; VI, FIR1048 + L; VII, FRI; VIII, FRI + L; IX, CFRI; X, CFRI + L (* P < 0.05, ** P < 0.01, and *** P < 0.001). CTL, cytotoxic T lymphocyte; TCR, T cell receptor.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11876542/'>40040955</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-calreticulin-primary-antibodies-wb-testing-1.jpgAnti-Calreticulin Rabbit Monoclonal Antibody Western blot analysis of Calreticulin using anti-Calreticulin antibody (M00894). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human COLO320 whole cell lysates,<br>
Lane 2: human HL-60 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calreticulin antigen affinity purified monoclonal antibody (Catalog # M00894) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calreticulin at approximately 60 kDa. The expected band size for Calreticulin is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-ihc7.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-ihc8.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human renal cancer, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-ihc9.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human placenta, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-ihc10.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse testis, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-ihc11.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse cerebellum, using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00894-icc1.jpgAnti-Calreticulin Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hexokinase-1-rabbit-monoclonal-antibody-m01504-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-wb7.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-wb10.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-wb8.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-wb.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyWestern blot analysis of Hexokinase 1 expression in (1) MCF-7 cell lysate; (2) 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-wb9.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01504-ihc.jpgAnti-Hexokinase 1 HK1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung carcinoma, using Hexokinase 1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-3-rabbit-monoclonal-antibody-m06819-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06819-wb7.jpgAnti-Histone H3.3 H3F3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06819-wb.jpgAnti-Histone H3.3 H3F3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3.3 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06819-wb8.jpgAnti-Histone H3.3 H3F3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06819-ihc.jpgAnti-Histone H3.3 H3F3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse stomach, using Histone H3.3 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06819-wb9.jpgAnti-Histone H3.3 H3F3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytochrome-c-rabbit-monoclonal-antibody-m03529-1-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-wb7.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-icc1.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-wb8.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-wb.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyWestern blot analysis of Cytochrome C expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-wb9.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-1-ihc.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colonic cancer, using Cytochrome C Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytochrome-c-rabbit-monoclonal-antibody-m03529-2-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-cycs-primary-antibodies-wb-testing-1.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal Antibody Western blot analysis of CYCS using anti-CYCS antibody (M03529-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human HT-1080 whole cell lysates,<br>
Lane 5: rat kidney tissue lysates,<br>
Lane 6: rat skeletal muscle tissue lysates,<br>
Lane 7: mouse kidney tissue lysates,<br>
Lane 8: mouse skeletal muscle tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYCS antigen affinity purified monoclonal antibody (Catalog # M03529-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYCS at approximately 14 kDa. The expected band size for CYCS is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-ihc.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Cytochrome C Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-icc1.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-icc2.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-if.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cytochrome C Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03529-2-icc3.jpgAnti-Cytochrome C CYCS Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ampk-gamma-1-rabbit-monoclonal-antibody-m04467-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04467-wb.jpgAnti-AMPK gamma 1 Rabbit Monoclonal AntibodyWestern blot analysis of AMPK gamma 1 expression in HEK293 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclin-a1-a2-rabbit-monoclonal-antibody-m00700-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-ccna2-primary-antibodies-wb-testing-1.jpgAnti-Cyclin A1/A2 Rabbit Monoclonal Antibody Western blot analysis of Cyclin A1/A2 using anti-Cyclin A1/A2 antibody (M00700). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclin A1/A2 antigen affinity purified monoclonal antibody (Catalog # M00700) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclin A1/A2 at approximately 55 kDa. The expected band size for Cyclin A1/A2 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00700-ihc.jpgAnti-Cyclin A1/A2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using Cyclin A1/A2 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h1-0-rabbit-monoclonal-antibody-m08821-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08821-wb.jpgAnti-Histone H1.0 H1F0 Rabbit Monoclonal AntibodyWestern blot analysis of Histone H1.0 expression in Human kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08821-ihc.jpgAnti-Histone H1.0 H1F0 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using Histone H1.0 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08821-if.jpgAnti-Histone H1.0 H1F0 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using Histone H1.0 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-gamma-rabbit-monoclonal-antibody-m04148-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04148-wb.jpgAnti-14-3-3 gamma YWHAG Rabbit Monoclonal AntibodyWestern blot analysis of 14-3-3 gamma expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-sigma-rabbit-monoclonal-antibody-m01127-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01127-wb7.jpgAnti-14-3-3 sigma SFN Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01127-wb8.jpgAnti-14-3-3 sigma SFN Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01127-wb.jpgAnti-14-3-3 sigma SFN Rabbit Monoclonal AntibodyWestern blot analysis of 14-3-3 sigma expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-theta-rabbit-monoclonal-antibody-m03904-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03904-ywhaq-primary-antibodies-wb-testing-1.jpgAnti-14-3-3 Theta YWHAQ Rabbit Monoclonal AntibodyWestern blot analysis of YWHAQ using anti-YWHAQ antibody (M03904). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YWHAQ antigen affinity purified monoclonal antibody (M03904) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for YWHAQ at approximately 28 kDa. The expected band size for YWHAQ is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03904-ywhaq-primary-antibodies-ihc-testing-1.jpgAnti-14-3-3 Theta YWHAQ Rabbit Monoclonal AntibodyIHC analysis of YWHAQ using anti-YWHAQ antibody (M03904). <br>YWHAQ was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-YWHAQ Antibody (M03904) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-s100-alpha-6-rabbit-monoclonal-antibody-m02043-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02043-s100a6-primary-antibodies-wb-testing-1.jpgAnti-S100 alpha 6 S100A6 Rabbit Monoclonal Antibody Western blot analysis of S100A6 using anti-S100A6 antibody (M02043). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SW620 whole cell lysates,<br>
Lane 3: human placenta tissue lysates,<br>
Lane 4: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-S100A6 antigen affinity purified monoclonal antibody (Catalog # M02043) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for S100A6 at approximately 10 kDa. The expected band size for S100A6 is at 10 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mhc-class-ii-rabbit-monoclonal-antibody-m00487-1-boster.html2026-03-24T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00487-1-wb.jpgAnti-MHC Class II HLA-DPB1 Rabbit Monoclonal AntibodyWestern blot analysis of MHC Class II expression in Daudi cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-camkii-alpha-rabbit-monoclonal-antibody-m03241-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241-camk2a-primary-antibodies-wb-testing-1.jpgAnti-CaMKII alpha CAMK2A Rabbit Monoclonal AntibodyWestern blot analysis of CAMK2A using anti-CAMK2A antibody (M03241). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat Hippocampus tissue lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: rat C6 whole cell lysates,<br>
Lane 4: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAMK2A antigen affinity purified monoclonal antibody (Catalog # M03241) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CAMK2A at approximately 54 kDa. The expected band size for CAMK2A is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241-camk2a-primary-antibodies-ihc-testing-1.jpgAnti-CaMKII alpha CAMK2A Rabbit Monoclonal AntibodyIHC analysis of CAMK2A using anti-CAMK2A antibody (M03241). <br>CAMK2A was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CAMK2A Antibody (M03241) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241-camk2a-primary-antibodies-ihc-testing-2.jpgAnti-CaMKII alpha CAMK2A Rabbit Monoclonal AntibodyIHC analysis of CAMK2A using anti-CAMK2A antibody (M03241). <br>CAMK2A was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CAMK2A Antibody (M03241) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-camkii-delta-rabbit-monoclonal-antibody-m02611-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02611-camk2d-primary-antibodies-wb-testing-1.jpgAnti-CaMKII delta CAMK2D Rabbit Monoclonal Antibody Western blot analysis of CaMKII delta/CAMK2D using anti-CaMKII delta/CAMK2D antibody (M02611). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Daudi whole cell lysates, <br>
Lane 2: human U-87MG whole cell lysates, <br>
Lane 3: human HUVEC whole cell lysates, <br>
Lane 4: human A549 whole cell lysates, <br>
Lane 5: rat C6 whole cell lysates, <br>
Lane 6: mouse Neuro-2a whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CaMKII delta/CAMK2D antigen affinity purified monoclonal antibody (M02611) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CaMKII delta/CAMK2D at approximately 50 kDa. The expected band size for CaMKII delta/CAMK2D is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02611-camk2d-primary-antibodies-wb-testing-2.jpgAnti-CaMKII delta CAMK2D Rabbit Monoclonal AntibodyWestern blot analysis of CAMK2D using anti-CAMK2D antibody (M02611).<br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: mouse MH-S whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAMK2D antigen affinity purified monoclonal antibody (M02611) at a dilution of 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CAMK2D at approximately 50 kDa. The expected band size for CAMK2D is at 50-56 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02611-camk2d-primary-antibodies-wb-testing-3.jpgAnti-CaMKII delta CAMK2D Rabbit Monoclonal AntibodyWestern blot analysis of CAMK2D using anti-CAMK2D antibody (M02611).<br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.<br>
Lane 1: mouse RAW264.7 whole cell lysates,<br>
Lane 2: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAMK2D antigen affinity purified monoclonal antibody (M02611) at a dilution of 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CAMK2D at approximately 50 kDa. The expected band size for CAMK2D is at 56 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02611-camk2d-primary-antibodies-icc-testing-1.jpgAnti-CaMKII delta CAMK2D Rabbit Monoclonal AntibodyICC/IF analysis of CAMK2D using anti- CAMK2D antibody (M02611). <br>
CAMK2D was detected in an immunocytochemical section of mouse MH-S cells. The cells were blocked with 10% goat serum. And then incubated with rabbit anti- CAMK2D Antibody (M02611) at a dilution of 1:50 overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-tubulin-rabbit-monoclonal-antibody-m08382-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-1-tuba1b-primary-antibodies-wb-testing-1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal Antibody Western blot analysis of Alpha Tubulin using anti-Alpha Tubulin antibody (M08382-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha Tubulin antigen affinity purified monoclonal antibody (Catalog # M08382-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha Tubulin at approximately 55 kDa. The expected band size for Alpha Tubulin is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M08382-1-TUBA1B-primary-antibodies-IHC-testing-1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using alpha Tubulin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-1-if.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells, using alpha Tubulin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-tubulin-rabbit-monoclonal-antibody-m08382-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M08382-TUBA1B-primary-antibodies-IHC-testing-1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using alpha Tubulin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M08382-TUBA1B-primary-antibodies-WB-testing-1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyWestern blot analysis of alpha Tubulin in (1) HeLa cell lysate; (2) HepG2 cell lysate; (3) NIH/3T3 cell lysate; (4) Mouse brain lysate; (5) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-tuba1b-primary-antibodies-if-testing-1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using alpha Tubulin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc1_1.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc2.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc3.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc4.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc5.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc6.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-icc7.jpgAnti-alpha Tubulin TUBA1B Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pro-caspase-3-rabbit-monoclonal-antibody-m00334-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-pro_caspase_3-primary-antibodies-wb-testing-1.jpgAnti-pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyWestern blot analysis of Pro Caspase 3 using anti-Pro Caspase 3 antibody (M00334). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Pro Caspase 3 antigen affinity purified monoclonal antibody (M00334) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Pro Caspase 3 at approximately 30 kDa. The expected band size for Pro Caspase 3 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-if.jpgAnti-pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A673 cells, using pro Caspase 3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ppp1ca-ppp1cb-rabbit-monoclonal-antibody-m02801-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02801-ppp1ca-ppp1cb-primary-antibodies-wb-testing-1.jpgAnti-PPP1CA+PPP1CB Rabbit Monoclonal Antibody Western blot analysis of PPP1CA + PPP1CB using anti-PPP1CA + PPP1CB antibody (M02801). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human U87 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1CA + PPP1CB antigen affinity purified monoclonal antibody (Catalog # M02801) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1CA + PPP1CB at approximately 38 kDa. The expected band size for PPP1CA + PPP1CB is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M02801-PPP1CA-primary-antibodies-IHC-testing-1.jpgAnti-PPP1CA+PPP1CB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human pancreas, using PPP1CA+PPP1CB Antibody(M02801)<br>PPP1CA was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-PPP1CA Antibody (M02801)overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-synaptophysin-rabbit-monoclonal-antibody-m05049-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-1-wb.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyWestern blot analysis of Synaptophysin expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-1-ihc.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using Synaptophysin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-1-if.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyImmunofluorescent analysis of PC-12 cells, using Synaptophysin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2a-x-rabbit-monoclonal-antibody-m00241-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00241-1-h2afx-primary-antibodies-wb-testing-1.jpgAnti-Histone H2A.X H2AFX Rabbit Monoclonal Antibody Western blot analysis of H2AFX using anti-H2AFX antibody (M00241-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human U20S whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse thymus tissues lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H2AFX antigen affinity purified monoclonal antibody (Catalog # M00241-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for H2AFX at approximately 15 kDa. The expected band size for H2AFX is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00241-1-h2afx-primary-antibodies-ihc-testing-2.jpgAnti-Histone H2A.X H2AFX Rabbit Monoclonal Antibody IHC analysis of H2AFX using anti-H2AFX antibody (M00241-1). <br>
H2AFX was detected in a paraffin-embedded section of human breast hyperplasia tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-H2AFX Antibody (M00241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00241-1-h2afx-primary-antibodies-ihc-testing-3.jpgAnti-Histone H2A.X H2AFX Rabbit Monoclonal Antibody IHC analysis of H2AFX using anti-H2AFX antibody (M00241-1). <br>
H2AFX was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-H2AFX Antibody (M00241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00241-1-h2afx-primary-antibodies-ihc-testing-4.jpgAnti-Histone H2A.X H2AFX Rabbit Monoclonal Antibody IHC analysis of H2AFX using anti-H2AFX antibody (M00241-1). <br>
H2AFX was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-H2AFX Antibody (M00241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00241-1-h2afx-primary-antibodies-ihc-testing-5.jpgAnti-Histone H2A.X H2AFX Rabbit Monoclonal Antibody IHC analysis of H2AFX using anti-H2AFX antibody (M00241-1). <br>
H2AFX was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-H2AFX Antibody (M00241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-synaptophysin-rabbit-monoclonal-antibody-m05049-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-syp-primary-antibodies-wb-testing-1.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyWestern blot analysis of Synaptophysin/SYP using anti-Synaptophysin/SYP antibody (M05049). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Synaptophysin/SYP antigen affinity purified monoclonal antibody (M05049) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Synaptophysin/SYP at approximately 38 kDa. The expected band size for Synaptophysin/SYP is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-syp-primary-antibodies-ihc-testing-1.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyIHC analysis of Synaptophysin/SYP using anti-Synaptophysin/SYP antibody (M05049). <br>Synaptophysin/SYP was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Synaptophysin/SYP Antibody (M05049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-syp-primary-antibodies-ihc-testing-2.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyIHC analysis of Synaptophysin/SYP using anti-Synaptophysin/SYP antibody (M05049). <br>Synaptophysin/SYP was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Synaptophysin/SYP Antibody (M05049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05049-if.jpgAnti-Synaptophysin SYP Rabbit Monoclonal AntibodyImmunofluorescent analysis of PC-12 cells, using Synaptophysin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p70-s6-kinase-rabbit-monoclonal-antibody-m01475-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01475-rps6kb1-primary-antibodies-wb-testing-1.jpgAnti-p70 S6 Kinase RPS6KB1 Rabbit Monoclonal AntibodyWestern blot analysis of p70 S6K/RPS6KB1 using anti-p70 S6K/RPS6KB1 antibody (M01475). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p70 S6K/RPS6KB1 antigen affinity purified monoclonal antibody (M01475) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for p70 S6K/RPS6KB1 at approximately 70 kDa. The expected band size for p70 S6K/RPS6KB1 is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-8-rabbit-monoclonal-antibody-m01421-2-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-wb7.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-wb.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 8 expression in HaCaT cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-krt8-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyIHC analysis of KRT8 using anti-KRT8 antibody (M01421-2). <br>KRT8 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT8 Antibody (M01421-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-krt8-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyIHC analysis of KRT8 using anti-KRT8 antibody (M01421-2). <br>KRT8 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT8 Antibody (M01421-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-krt8-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyIHC analysis of KRT8 using anti-KRT8 antibody (M01421-2). <br>KRT8 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT8 Antibody (M01421-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-krt8-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyIHC analysis of KRT8 using anti-KRT8 antibody (M01421-2). <br>KRT8 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT8 Antibody (M01421-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-icc1.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01421-2-icc2.jpgAnti-Cytokeratin 8 KRT8 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclophilin-b-rabbit-monoclonal-antibody-m03229-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03229-wb.jpgAnti-Cyclophilin B PPIB Rabbit Monoclonal AntibodyWestern blot analysis of Cyclophilin B expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tubulin-gamma-rabbit-monoclonal-antibody-m06313-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06313-fgene-16-1646991-g007.jpgAnti-Tubulin gamma Rabbit Monoclonal AntibodyConstruction of animal models and analysis of pathological damage. (A) TTC staining plots of the Sham and VD group. (B) Motion trajectory diagram. (C) Representative images stained with HE (scale bars = 50 μm). (D) Representative histopathological images obtained from TUNEL staining (scale bars = 50 μm), showing changes in the cortex hippocampus CA1. (E) Quantification of TUNEL+ cells in the hippocampal CA1 (n = 3). (F) Expression profile of CD31 between Sham and VD groups (qPCR). **P < 0.01. (G) Expression profile of HIF-1α between Sham and VD groups (qPCR; n = 6). ***P < 0.001. (H) WB strips. (I) Expression profile of CD31 between Sham and VD groups (WB). *P < 0.05. (J) Expression profile of HIF-1α between Sham and VD groups (WB; n = 3). ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1646991/full'>40988927</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06313-fgene-16-1646991-g008.jpgAnti-Tubulin gamma Rabbit Monoclonal AntibodyExperimental validation of the key genes in vivo . (A) Representative images of immunofluorescence. (B–F) Expression profile of CCL2, VEGFA, SPP1, ANGPT2, and ANGPTL4 between Sham and VD groups (qPCR; n = 6). *P < 0.05; **P < 0.01; ***P < 0.001. (G) Immunofluorescence quantification of CD31. ***P < 0.001. (H) WB representative strips of the 5 key genes. (I–M) Protein expression level of CCL2, VEGFA, SPP1, ANGPT2, and ANGPTL4 between Sham and VD groups (WB; n = 3). *P < 0.05; **P < 0.01; ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1646991/full'>40988927</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06313-tubg1-primary-antibodies-wb-testing-1.jpgAnti-Tubulin gamma Rabbit Monoclonal AntibodyWestern blot analysis of TUBG1 using anti-TUBG1 antibody (M06313). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: monkey COS-7 whole cell lysates,<br>
Lane 4: fish embryo tissue lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBG1 antigen affinity purified monoclonal antibody (M06313) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TUBG1 at approximately 47 kDa. The expected band size for TUBG1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06313-ihc.jpgAnti-Tubulin gamma Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Tubulin gamma Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rho-a-b-c-rabbit-monoclonal-antibody-m00207-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-rhoabc-primary-antibodies-wb-testing-1.jpgAnti-Rho A + B + C Rabbit Monoclonal Antibody Western blot analysis of Rho A+B+C using anti-Rho A+B+C antibody (M00207-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HUVEC whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rho A+B+C antigen affinity purified monoclonal antibody (M00207-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Rho A+B+C at approximately 22 kDa. The expected band size for Rho A+B+C is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-rho-a_b_c-primary-antibodies-wb-testing-2_1.jpgAnti-Rho A + B + C Rabbit Monoclonal Antibody Western blot analysis of Rho A+B+C using anti-Rho A+B+C antibody (M00207-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates,<br>
Lane 4: human U251 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse neuro-2a whole cell.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rho A+B+C antigen affinity purified monoclonal antibody (Catalog # M00207-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Rho A+B+C at approximately 22 kDa. The expected band size for Rho A+B+C is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-if.jpgAnti-Rho A + B + C Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Rho A + B + C Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-rhoabc-primary-antibodies-wb-testing-1.pngAnti-Rho A + B + C Rabbit Monoclonal Antibody Western blot analysis of Rho A+B+C using anti-Rho A+B+C antibody (M00207-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human 293T cells transfected with RHOP whole cell lysayes,<br>
Lane 3: human 293T cells transfected with RHOP whole cell lysayes.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rho A+B+C antigen affinity purified monoclonal antibody (M00207-1) at 1:2500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for Rho A+B+C at approximately 22 kDa. The expected band size for Rho A+B+C is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-rho-a_b_c-primary-antibodies-wb-testing-3_1.pngAnti-Rho A + B + C Rabbit Monoclonal Antibody Western blot analysis of Rho A+B+C using anti-Rho A+B+C antibody (M00207-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates, <br>
Lane 2: Model group-rat colon tissue lysates, <br>
Lane 3: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates, <br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates, <br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates, <br>
Lane 6: Western medicine treatment-rat colon tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Rho A+B+C antigen affinity purified monoclonal antibody (Catalog # M00207-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a HRP Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # AR1196-200) with ChemiDoc MP system. A specific band was detected for Rho A+B+C at approximately 22 kDa. The expected band size for Rho A+B+C is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00207-1-ihc_1.jpgAnti-Rho A + B + C Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung carcinoma, using Rho A + B + C Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-collagen-xvii-rabbit-monoclonal-antibody-m03031-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03031-wb7.jpgAnti-Collagen XVII Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03031-ihc.jpgAnti-Collagen XVII Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse skin, using Collagen XVII Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03031-wb8.jpgAnti-Collagen XVII Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03031-if.jpgAnti-Collagen XVII Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using Collagen XVII Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03031-wb.jpgAnti-Collagen XVII Rabbit Monoclonal AntibodyWestern blot analysis of Collagen XVII expression in Human skin lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2a-z-rabbit-monoclonal-antibody-m16777-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-wb-testing-1.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyWestern blot analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human REH whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H2AZ1 antigen affinity purified monoclonal antibody (M16777) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for H2AZ1 at approximately 14 kDa. The expected band size for H2AZ1 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-1.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-2.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-3.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-4.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-5.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-6.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-7.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-8.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-9.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-10.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-11.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-h2az1-primary-antibodies-ihc-testing-12.jpgAnti-Histone H2A.Z H2afz Rabbit Monoclonal AntibodyIHC analysis of H2AZ1 using anti-H2AZ1 antibody (M16777). <br>H2AZ1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-H2AZ1 Antibody (M16777) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-7-rabbit-monoclonal-antibody-m02416-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-1-wb7.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-1-if.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cytokeratin 7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-1-wb.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 7 expression in T47 D cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-1-ihc.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using Cytokeratin 7 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-prion-protein-rabbit-monoclonal-antibody-m02447-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02447-prnp-primary-antibodies-wb-testing-1.jpgAnti-Prion Protein PRNP Rabbit Monoclonal AntibodyWestern blot analysis of PRNP using anti-PRNP antibody (M02447). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRNP antigen affinity purified monoclonal antibody (M02447) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PRNP at approximately 30 kDa. The expected band size for PRNP is at 28 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-5-rabbit-monoclonal-antibody-m00398-1-boster.html2026-03-24T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-wb-testing-1_2.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody Western blot analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT5 antigen affinity purified polyclonal antibody (Catalog # M00398-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KRT5 at approximately 62 kDa. The expected band size for KRT5 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-wb7.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-wb8.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-2_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-3_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-4_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-5_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-6_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-7_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-8_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-1-krt5-primary-antibodies-ihc-testing-9_1.jpgAnti-Cytokeratin 5 KRT5 Rabbit Monoclonal Antibody IHC analysis of KRT5 using anti-KRT5 antibody (M00398-1). <br>
KRT5 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-6-rabbit-monoclonal-antibody-m30943-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30943-1-krt6a-b-c-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 6 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 6 using anti-Cytokeratin 6 antibody (M30943-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 6 antigen affinity purified monoclonal antibody (M30943-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 6 at approximately 60 kDa. The expected band size for Cytokeratin 6 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30943-1-krt6a-b-c-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 6 Rabbit Monoclonal AntibodyIHC analysis of Cytokeratin 6 using anti-Cytokeratin 6 antibody (M30943-1). <br>Cytokeratin 6 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Cytokeratin 6 Antibody (M30943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pro-caspase-3-rabbit-monoclonal-antibody-m00334-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-1-wb.jpgAnti-pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyWestern blot analysis of pro Caspase 3 expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-1-ihc.jpgAnti-pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using pro Caspase 3 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-1-if.jpgAnti-pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using pro Caspase 3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pro-caspase-9-rabbit-monoclonal-antibody-m00080-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-1-wb7.jpgAnti-pro Caspase 9 CASP9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-1-ihc.jpgAnti-pro Caspase 9 CASP9 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using pro Caspase 9 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-1-wb8.jpgAnti-pro Caspase 9 CASP9 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-1-wb.jpgAnti-pro Caspase 9 CASP9 Rabbit Monoclonal AntibodyWestern blot analysis of pro Caspase 9 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-6-p18-rabbit-monoclonal-antibody-m02631-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-1-wb.jpgAnti-Caspase-6 p18 CASP6 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-6 p18 expression in Jurkat cell treated with 1uM staurosporine lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-1-rabbit-monoclonal-antibody-m01639-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01639-1-wb7.jpgAnti-Cytokeratin 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01639-1-wb.jpgAnti-Cytokeratin 1 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 1 expression in Human skin lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01639-1-ihc.jpgAnti-Cytokeratin 1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat skin, using Cytokeratin 1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-4-rabbit-monoclonal-antibody-m07410-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07410-1-wb7.jpgAnti-Cytokeratin 4 KRT4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07410-1-wb.jpgAnti-Cytokeratin 4 KRT4 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 4 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-3-p12-rabbit-monoclonal-antibody-m00334-2-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-dmso-14-1253-g0006.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyEffects of Emo on the protein expression of Bax and Cleaved caspase-3 in the kidney. Notes: ( A ) Western blot analysis of Bax, Cleaved caspase-3 and caspase-3 protein expression. ( B and C ) Quantitative analysis of Bax and Cleaved caspase-3 protein expression. Data are expressed as mean ± SEM. * P < 0.05, # P < 0.01. Abbreviations: Emo, Emodin; LD-Emo, low-dose Emodin; HD-Emo, high-dose Emodin.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987270/'>33776462</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-jgo-16-03-1060-f2.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyLncRNA RMRP knockdown promoted cell apoptosis and cell cycle arrest. (A) Apoptosis of HCCLM3 and HepG2 cells with or without lncRNA RMRP knockdown was detected via flow cytometry. (B) The expression of several apoptosis-related proteins including p53, caspase-3, cleaved caspase-3 (C-caspase-3), and Bcl-XL in the shCtrl and shRMRP groups of HCCLM3 and HepG2 cells was detected by WB. (C) Flow cytometry was used for examining the cell cycle distribution of HCCLM3 and HepG2 cells with or without lncRNA RMRP knockdown. Data are presented as the mean and standard deviation. *, P<0.05; **, P<0.01; ***, P<0.001. HCC, hepatocellular carcinoma; lncRNA, long noncoding RNA; shCtrl, HCC cells transfected with negative control lentivirus; shRMRP, HCC cells transfected with lncRNA RMRP knockdown lentivirus; WB, Western blotting.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12260943/'>40672090</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-casp3-primary-antibodies-wb-testing-1.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase 3/CASP3 (p12) using anti-Caspase 3/CASP3 (p12) antibody (M00334-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human HEL whole cell lysates,<br>
Lane 3: human RT4 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse lung tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 3/CASP3 (p12) antigen affinity purified monoclonal antibody (M00334-2) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Caspase 3/CASP3 (p12) at approximately 35 kDa. The expected band size for Caspase 3/CASP3 (p12) is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-ihc.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Caspase-3 p12 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-icc1.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-2-if.jpgAnti-Caspase-3 p12 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using Caspase-3 p12 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-7-rabbit-monoclonal-antibody-m02416-2-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-2-krt7-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 7/KRT7 using anti-Cytokeratin 7/KRT7 antibody (M02416-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SIHA whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: rat kidney tissue lysates,<br>
Lane 7: mouse lung tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 7/KRT7 antigen affinity purified monoclonal antibody (M02416-2) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 7/KRT7 at approximately 40-50 kDa. The expected band size for Cytokeratin 7/KRT7 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-2-ihc.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using Cytokeratin 7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-2-if.jpgAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HeLa cells, using Cytokeratin 7 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02416-2-krt7-primary-antibodies-wb-testing-2.pngAnti-Cytokeratin 7 KRT7 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 7/KRT7 using anti-Cytokeratin 7/KRT7 antibody (M02416-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-4: control group-human HTR8 whole cell lysates, <br>
Lane 5-9: model group-human HTR8 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 7/KRT7 antigen affinity purified polyclonal antibody (M02416-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate with ChemiDoc MP system. A specific band was detected for Cytokeratin 7/KRT7 at approximately 51 kDa. The expected band size for Cytokeratin 7/KRT7 is at 40-50 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-4-rabbit-monoclonal-antibody-m07410-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07410-wb.jpgAnti-Cytokeratin 4 KRT4 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 4 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07410-wb7.jpgAnti-Cytokeratin 4 KRT4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tissue-factor-rabbit-monoclonal-antibody-m00342-boster.html2026-04-03T05:00:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-f3-primary-antibodies-ihc-testing-2.jpgAnti-Tissue Factor Rabbit Monoclonal Antibody IHC analysis of Tissue Factor using anti-Tissue Factor antibody (M00342). <br>
Tissue Factor was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Tissue Factor Antibody (M00342) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-f3-primary-antibodies-ihc-testing-3.jpgAnti-Tissue Factor Rabbit Monoclonal Antibody IHC analysis of Tissue Factor using anti-Tissue Factor antibody (M00342). <br>
Tissue Factor was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Tissue Factor Antibody (M00342) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-f3-primary-antibodies-wb-testing-1.jpgAnti-Tissue Factor Rabbit Monoclonal Antibody Western blot analysis of Tissue Factor using anti-Tissue Factor antibody (M00342). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human PANC-1 whole cell lysates,<br>
Lane 4: rat lung tissue lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: mouse lung tissue lysates,<br>
Lane 7: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tissue Factor antigen affinity purified monoclonal antibody (Catalog # M00342) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tissue Factor at approximately 50 kDa. The expected band size for Tissue Factor is at 35 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-9-rabbit-monoclonal-antibody-m03692-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03692-krt9-primary-antibodies-wb-testing-1_1.jpgAnti-Cytokeratin 9 KRT9 Rabbit Monoclonal AntibodyWestern blot analysis of KRT9 using anti-KRT9 antibody (M03692). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human SIHA whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse thymus tissue lysates,<br>
Lane 8: mouse RAW264.7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT9 antigen affinity purified monoclonal antibody (M03692) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT9 at approximately 62 kDa. The expected band size for KRT9 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03692-krt9-primary-antibodies-ihc-testing-1_1.jpgAnti-Cytokeratin 9 KRT9 Rabbit Monoclonal AntibodyIHC analysis of KRT9 using anti-KRT9 antibody (M03692). <br>KRT9 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT9 Antibody (M03692) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-1-rabbit-monoclonal-antibody-m01639-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01639-wb.jpgAnti-Cytokeratin 1 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 1 expression in Human skin lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pd-l1-cd274-rabbit-monoclonal-antibody-m00109-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-12885_2022_10353_fig11_html.pngAnti-PD-L1 (CD274) Rabbit Monoclonal AntibodyIGF2BP3 expression was significantly associated with PD-L1 expression. A heatmap of immune checkpoints based on IGF2BP3 expression. B - F the correlation between IGF2BP3 expression and CD274 (PDL-1), PDCD1LG2 (PDL-2), LAG3, CTLA4, and HAVCR2. G, PD-L1 mRNA expression increased by IGF2BP3 upregulation <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://bmccancer.biomedcentral.com/articles/10.1186/s12885-022-10353-5'>36732736</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-cd274-primary-antibodies-wb-testing-1.jpgAnti-PD-L1 (CD274) Rabbit Monoclonal Antibody Western blot analysis of PD-L1 using anti-PD-L1 antibody (M00109). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Ramos whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat thymus tissue lysates,<br>
Lane 6: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PD-L1 antigen affinity purified monoclonal antibody (Catalog # M00109) at 1:100 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PD-L1 at approximately 40 kDa. The expected band size for PD-L1 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-ihc.jpgAnti-PD-L1 (CD274) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thymoma, using PD-L1 (CD274) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-cd274-primary-antibodies-wb-testing-2_1.pngAnti-PD-L1 (CD274) Rabbit Monoclonal Antibody Western blot analysis of PD-L1 using anti-PD-L1 antibody (M00109). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Human periodontal ligament fibroblasts whole cell lysates,<br>
Lane 2: TGF-β1-induced with human periodontal ligament fibroblasts whole cell lysates,<br>
Lane 3: Brefeldin A-treated with human periodontal ligament fibroblasts whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PD-L1 antigen affinity purified monoclonal antibody (Catalog # M00109) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for PD-L1 at approximately 40-50 kDa. The expected band size for PD-L1 is at 33 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-catenin-gamma-rabbit-monoclonal-antibody-m01901-1-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01901-1-jup-primary-antibodies-wb-testing-1.jpgAnti-Catenin gamma JUP Rabbit Monoclonal AntibodyWestern blot analysis of JUP using anti-JUP antibody (M01901-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human HT-29 whole cell lysates,<br>
Lane 3: human Hacat whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JUP antigen affinity purified monoclonal antibody (M01901-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for JUP at approximately 82 kDa. The expected band size for JUP is at 82 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cyclophilin-a-rabbit-monoclonal-antibody-m01308-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01308-ppia-primary-antibodies-wb-testing-1.jpgAnti-Cyclophilin A PPIA Rabbit Monoclonal Antibody Western blot analysis of Cyclophilin A/PPIA using anti-Cyclophilin A/PPIA antibody (M01308). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human HUVEC whole cell lysates, <br>
Lane 3: human Hela whole cell lysates, <br>
Lane 4: human THP-1 whole cell lysates, <br>
Lane 5: rat kidney tissue lysates, <br>
Lane 6: rat brain tissue lysates, <br>
Lane 7: mouse kidney tissue lysates, <br>
Lane 8: mouse brain tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cyclophilin A/PPIA antigen affinity purified monoclonal antibody (M01308) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cyclophilin A/PPIA at approximately 18 kDa. The expected band size for Cyclophilin A/PPIA is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01308-ppia-primary-antibodies-ihc-testing-2.jpgAnti-Cyclophilin A PPIA Rabbit Monoclonal Antibody IHC analysis of Cyclophilin A/PPIA using anti-Cyclophilin A/PPIA antibody (M01308) . <br> Cyclophilin A/PPIA was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Cyclophilin A/PPIA Antibody (M01308) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01308-ppia-primary-antibodies-ihc-testing-3.jpgAnti-Cyclophilin A PPIA Rabbit Monoclonal Antibody IHC analysis of Cyclophilin A/PPIA using anti-Cyclophilin A/PPIA antibody (M01308) . <br> Cyclophilin A/PPIA was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Cyclophilin A/PPIA Antibody (M01308) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-calcineurin-a-rabbit-monoclonal-antibody-m03026-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03026-ppp3ca-primary-antibodies-wb-testing-1.jpgAnti-Calcineurin A Rabbit Monoclonal AntibodyWestern blot analysis of PPP3CA using anti-PPP3CA antibody (M03026). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP3CA antigen affinity purified monoclonal antibody (M03026) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PPP3CA at approximately 59 kDa. The expected band size for PPP3CA is at 59 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apg10-atg10-rabbit-monoclonal-antibody-m07803-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07803-atg10-primary-antibodies-wb-testing-1.jpgAnti-Apg10 (Atg10) Rabbit Monoclonal Antibody Western blot analysis of Apg10 using anti-Apg10 antibody (M07803). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human SH-SY5Y whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Apg10 antigen affinity purified monoclonal antibody (Catalog # M07803) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Apg10 at approximately 28 kDa. The expected band size for Apg10 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07803-ip7.jpgAnti-Apg10 (Atg10) Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apg12-atg12-rabbit-monoclonal-antibody-m00820-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00820-wb7.jpgAnti-Apg12 (Atg12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00820-wb8.jpgAnti-Apg12 (Atg12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00820-wb.jpgAnti-Apg12 (Atg12) Rabbit Monoclonal AntibodyWestern blot analysis of Apg12 expression in HepG2 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-i-tubulin-rabbit-monoclonal-antibody-m05397-boster.html2026-03-24T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-wb-testing-1.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody Western blot analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBB1 antigen affinity purified polyclonal antibody (Catalog # M05397) at 1:3000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TUBB1 at approximately 50 kDa. The expected band size for TUBB1 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-2.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody <a href="https://www.bosterbio.com/services/assay-services/ihc-histology-services/analyzing-ihc-data-from-halo-to-pathologist-review">IHC analysis</a> of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-if.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal AntibodyIF analysis of immunocytochemical section of Hela cells using anti-beta I Tubulin antibody (M05397) <br> beta I Tubulin was detected in immunocytochemical section. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-beta I Tubulin Antibody (M05397) overnight at 4 °https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-3.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-4.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal AntibodyIHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-5.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal AntibodyIHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-6.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-7.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-8.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-9.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-10.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-11.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-12.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05397-tubb1-primary-antibodies-ihc-testing-13.jpgAnti-beta I Tubulin TUBB1 Rabbit Monoclonal Antibody IHC analysis of TUBB1 using anti-TUBB1 antibody (M05397). <br>
TUBB1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TUBB1 Antibody (M05397) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lrp2-megalin-rabbit-monoclonal-antibody-m02463-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02463-wb.jpgAnti-Lrp2 / Megalin Rabbit Monoclonal AntibodyWestern blot analysis of Lrp2 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-18-rabbit-monoclonal-antibody-m01357-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-1-wb7.jpgAnti-Cytokeratin 18 KRT18 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-1-wb.jpgAnti-Cytokeratin 18 KRT18 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 18 expression in (1) HT-29 cell lysate;(2) human kidney lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-1-wb8.jpgAnti-Cytokeratin 18 KRT18 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-1-if_1.jpgAnti-Cytokeratin 18 KRT18 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HACAT cells, using Cytokeratin 18 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-1-wb9.jpgAnti-Cytokeratin 18 KRT18 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nf-kappa-b-p65-rabbit-monoclonal-antibody-m00284-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb10.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb7.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12885_2025_14066_fig7_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodymRNA and Protein expression in H460 cells after DET intervention in vitro. A RT-qPCR analysis of Bcl2, Bax, CASP3, ICAM1, JUN, PTGS2 and TNFα mRNA expression in H460 cells after stimulation with DET (10, 20 and 40 μM) for 24 h. B Western blotting analysis of Bcl2, Bax and CASP3 protein expression in H460 cells after stimulation with DET (10, 20 and 40 μM) for 24 h. C Western blotting analysis of p-p65 and NFκB(p65) protein expression in H460 cells after stimulation with DET (10, 20 and 40 μM) for 24 h.All Data are represented as mean ± SD (n = 3). * P < 0.05, ** P < 0.01, *** P < 0.001, ns = no significant differences versus the non-treated group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://bmccancer.biomedcentral.com/articles/10.1186/s12885-025-14066-3'>40259252</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12957_2022_2722_fig5_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyA Correlation of ASCL2 with immune-associated cells in STAD. B Correlation of ASCL2 with target protein of macrophage M2, T cell follicular helper, neutrophils, dendritic cells, monocytes, T cells CD8, and macrophage M1. C , D GSEA assay of ASCL2 with gastric cancer, inflammation, and TLR4 in STAD <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12957-022-02722-y'>36008864</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12957_2022_2722_fig7_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyA ASCL2, TLR4, NF-κB, IL-1β, and IL-18 expressed in different groups, and B quantificated in vitro. C ASCL2, TLR4, NF-κB, IL-1β, and IL-18 expressed in different groups and D quantificated in vivo (sh-ASCL2 vs. Con, n = 6, * P < 0.05; Spa. + sh-ASCL2 vs. sh-ASCL2, n = 6,. # P < 0.05) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12957-022-02722-y'>36008864</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12957_2022_2722_fig8_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyA Correlation analysis between ASCL2 with CNTNAP3, CLIP1, C9orf84, ARIH2, and IL1R2 in STAD. B Expression of ASCL2 in CNTNAP3, CLIP1, C9orf84, ARIH2, and IL1R2 mutant and wild-type STAD patients <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12957-022-02722-y'>36008864</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12957_2021_2477_fig5_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyGSEA of TMED2 with A inflammation, B TLR4, and C NF-κB in LUAD <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://wjso.biomedcentral.com/articles/10.1186/s12957-021-02477-y'>35135563</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-12957_2021_2477_fig6_html.pngAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyA Western blot assay of TMED2, TLR4, NF-κB-p-p65, IL-1β, and IL-18 expression in the Con, sh-TMED2, control-shTMED2, and Spa. + sh-TMED2 groups in vitro. B Quantification of TMED2, TLR4, NF-κB-p-p65, IL-1β, and IL-18 protein expression. C Western blot assay of TMED2, TLR4, NF-κB-p-p65, IL-1β, and IL-18 expression in vivo. D Quantification of TMED2, TLR4, NF-κB-p-p65, IL-1β, and IL-18 protein expression. Protein levels were normalized to β-actin. (sh-TMED2 vs. Con group, * P < 0.05; Spa. + sh-TMED2 vs. sh-TMED2 group, # P < 0.05, n = 6 per group) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://wjso.biomedcentral.com/articles/10.1186/s12957-021-02477-y'>35135563</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb11.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb8.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb9.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-wb.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyWestern blot analysis of NF-κB p65 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-ihc.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human transitional cell carcinoma of bladder, using NF-κB p65 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-icc1.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00284-if.jpgAnti-NF-Kappa B p65 RELA Rabbit Monoclonal AntibodyImmunofluorescent analysis of HT-1080 cells, using NF-κB p65 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-liver-arginase-rabbit-monoclonal-antibody-m01106-2-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01106-2-arg1-primary-antibodies-wb-testing-1.jpgAnti-Liver Arginase ARG1 Rabbit Monoclonal Antibody Western blot analysis of ARG1 using anti-ARG1 antibody (M01106-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates,<br>
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARG1 antigen affinity purified monoclonal antibody (Catalog # M01106-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARG1 at approximately 38 kDa. The expected band size for ARG1 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01106-2-gr3_lrg.jpgAnti-Liver Arginase ARG1 Rabbit Monoclonal Antibody(C) Expression of ASS1 and ARG in AQP5+ and AQP5− AGS cells detected by western blotting.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/cell-reports-medicine/fulltext/S2666-3791(25)00406-9'>40961922</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01106-2-ihc.jpgAnti-Liver Arginase ARG1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Liver Arginase Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sonic-hedgehog-rabbit-monoclonal-antibody-m00058-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00058-shh-primary-antibodies-wb-testing-1.jpgAnti-Sonic Hedgehog SHH Rabbit Monoclonal AntibodyWestern blot analysis of SHH using anti-SHH antibody (M00058). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHH antigen affinity purified monoclonal antibody (M00058) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHH at approximately 50 kDa. The expected band size for SHH is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00058-shh-primary-antibodies-ihc-testing-1.jpgAnti-Sonic Hedgehog SHH Rabbit Monoclonal AntibodyIHC analysis of SHH using anti-SHH antibody (M00058). <br>SHH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SHH Antibody (M00058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00058-shh-primary-antibodies-ihc-testing-2.jpgAnti-Sonic Hedgehog SHH Rabbit Monoclonal AntibodyIHC analysis of SHH using anti-SHH antibody (M00058). <br>SHH was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SHH Antibody (M00058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00058-shh-primary-antibodies-ihc-testing-3.jpgAnti-Sonic Hedgehog SHH Rabbit Monoclonal AntibodyIHC analysis of SHH using anti-SHH antibody (M00058). <br>SHH was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SHH Antibody (M00058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00058-shh-primary-antibodies-ihc-testing-4.jpgAnti-Sonic Hedgehog SHH Rabbit Monoclonal AntibodyIHC analysis of SHH using anti-SHH antibody (M00058). <br>SHH was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SHH Antibody (M00058) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pmel17-gp100-rabbit-monoclonal-antibody-m01262-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-wb.jpgAnti-PMEL17 / GP100 Rabbit Monoclonal AntibodyWestern blot analysis of PMEL17 / GP100 expression in human melanoma lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-ihc.jpgAnti-PMEL17 / GP100 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human melanoma, using PMEL17 / GP100 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-thrombomodulin-rabbit-monoclonal-antibody-m01325-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01325-1-thbd-primary-antibodies-wb-testing-1.jpgAnti-Thrombomodulin THBD Rabbit Monoclonal AntibodyWestern blot analysis of Thrombomodulin/THBD using anti-Thrombomodulin/THBD antibody (M01325-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Thrombomodulin/THBD antigen affinity purified monoclonal antibody (M01325-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Thrombomodulin/THBD at approximately 100 kDa. The expected band size for Thrombomodulin/THBD is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01325-1-ihc.jpgAnti-Thrombomodulin THBD Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using Thrombomodulin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-19-rabbit-monoclonal-antibody-m02101-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02101-1-wb.jpgAnti-Cytokeratin 19 KRT19 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 19 expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02101-1-krt19-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 19 KRT19 Rabbit Monoclonal AntibodyIHC analysis of Cytokeratin 19/KRT19 using anti-Cytokeratin 19/KRT19 antibody (M02101-1). <br>Cytokeratin 19/KRT19 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Cytokeratin 19/KRT19 Antibody (M02101-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02101-1-krt19-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 19 KRT19 Rabbit Monoclonal AntibodyIHC analysis of Cytokeratin 19/KRT19 using anti-Cytokeratin 19/KRT19 antibody (M02101-1). <br>Cytokeratin 19/KRT19 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-Cytokeratin 19/KRT19 Antibody (M02101-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02101-1-if.jpgAnti-Cytokeratin 19 KRT19 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using Cytokeratin 19 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-20-rabbit-monoclonal-antibody-m02828-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-krt20-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal Antibody Western blot analysis of KRT20 using anti-KRT20 antibody (M02828). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT20 antigen affinity purified monoclonal antibody (Catalog # M02828) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KRT20 at approximately 48 kDa. The expected band size for KRT20 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-wb7.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-if.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Cytokeratin 20 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-krt20-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal Antibody IHC analysis of KRT20 using anti-KRT20 antibody (M02828). <br>
KRT20 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT20 Antibody (M02828) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-icc1.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-krt20-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal Antibody IHC analysis of KRT20 using anti-KRT20 antibody (M02828). <br>
KRT20 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KRT20 Antibody (M02828) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02828-ihc.jpgAnti-Cytokeratin 20 KRT20 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Cytokeratin 20 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-15-rabbit-monoclonal-antibody-m06791-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06791-1-krt15-primary-antibodies-wb-testing-1_1.jpgAnti-Cytokeratin 15 Rabbit Monoclonal AntibodyWestern blot analysis of KRT15 using anti-KRT15 antibody (M06791-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT15 antigen affinity purified monoclonal antibody (M06791-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT15 at approximately 49 kDa. The expected band size for KRT15 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06791-1-krt15-primary-antibodies-ihc-testing-1_1.jpgAnti-Cytokeratin 15 Rabbit Monoclonal AntibodyIHC analysis of KRT15 using anti-KRT15 antibody (M06791-1). <br>KRT15 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT15 Antibody (M06791-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06791-1-krt15-primary-antibodies-ihc-testing-2_1.jpgAnti-Cytokeratin 15 Rabbit Monoclonal AntibodyIHC analysis of KRT15 using anti-KRT15 antibody (M06791-1). <br>KRT15 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT15 Antibody (M06791-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06791-1-krt15-primary-antibodies-ihc-testing-3_1.jpgAnti-Cytokeratin 15 Rabbit Monoclonal AntibodyIHC analysis of KRT15 using anti-KRT15 antibody (M06791-1). <br>KRT15 was detected in a paraffin-embedded section of mouse skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT15 Antibody (M06791-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06791-1-krt15-primary-antibodies-ihc-testing-4_1.jpgAnti-Cytokeratin 15 Rabbit Monoclonal AntibodyIHC analysis of KRT15 using anti-KRT15 antibody (M06791-1). <br>KRT15 was detected in a paraffin-embedded section of rat skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT15 Antibody (M06791-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-17-rabbit-monoclonal-antibody-m02289-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-krt17-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 17 Rabbit Monoclonal AntibodyWestern blot analysis of KRT17 using anti-KRT17 antibody (M02289-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT17 antigen affinity purified monoclonal antibody (M02289-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT17 at approximately 48 kDa. The expected band size for KRT17 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-cytokeratin-17-primary-antibodies-ihc-testing-2.pngAnti-Cytokeratin 17 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 17 using anti-Cytokeratin 17 antibody (M02289-1). <br>
Cytokeratin 17 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 17 Antibody (M02289-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-cytokeratin-17-primary-antibodies-ihc-testing-3.pngAnti-Cytokeratin 17 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 17 using anti-Cytokeratin 17 antibody (M02289-1). <br>
Cytokeratin 17 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/ml rabbit anti-Cytokeratin 17 Antibody (M02289-1) overnight at 4°C. HRP-AffiniPure Goat Anti-Rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-cytokeratin-17-primary-antibodies-if-testing-5_1.pngAnti-Cytokeratin 17 Rabbit Monoclonal Antibody IF analysis of Cytokeratin-17 using anti-Cytokeratin-17 antibody (M02289-1). <br>
Cytokeratin-17 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin-17 Antibody (M02289-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-cytokeratin-17-primary-antibodies-if-testing-6.pngAnti-Cytokeratin 17 Rabbit Monoclonal Antibody IF analysis of Cytokeratin-17 using anti-Cytokeratin-17 antibody (M02289-1). <br>
Cytokeratin-17 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Cytokeratin-17 Antibody (M02289-1) overnight at 4°C. DyLight 594 Conjugated AffiniPure Goat Anti-rabbit IgG (H+L) (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02289-1-cytokeratin-17-primary-antibodies-if-testing-7.jpgAnti-Cytokeratin 17 Rabbit Monoclonal Antibody Immunofluorescent analysis of Hela cells, using Cytokeratin 17 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kras-hras-nras-rabbit-monoclonal-antibody-m00099-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00099-1-kras-hras-nras-primary-antibodies-wb-testing-1.jpgAnti-KRAS+HRAS+NRAS Rabbit Monoclonal Antibody Western blot analysis of KRAS+HRAS+NRAS using anti-KRAS+HRAS+NRAS antibody (M00099-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human SW620 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRAS+HRAS+NRAS antigen affinity purified monoclonal antibody (Catalog # M00099-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KRAS+HRAS+NRAS at approximately 21 kDa. The expected band size for KRAS+HRAS+NRAS is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/y/cy5549-if.jpgAnti-KRAS+HRAS+NRAS Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using KRAS+HRAS+NRAS Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00099-1-kras_hras_nras-primary-antibodies-ip-testing-3.pngAnti-KRAS+HRAS+NRAS Rabbit Monoclonal AntibodyKRAS+HRAS+NRAS was immunoprecipitated from 1mg of A549 whole cell lysate. A549 whole cell lysate 10ug (Input). The second antibody be without interference from denatured IgG.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-16-rabbit-monoclonal-antibody-m03393-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03393-krt16-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 16 KRT16 Rabbit Monoclonal AntibodyWestern blot analysis of KRT16 using anti-KRT16 antibody (M03393). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hacat whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT16 antigen affinity purified monoclonal antibody (M03393) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT16 at approximately 51 kDa. The expected band size for KRT16 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03393-ihc.jpgAnti-Cytokeratin 16 KRT16 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human skin, using Cytokeratin 16 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-14-rabbit-monoclonal-antibody-m01432-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-1-wb.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal AntibodyWestern blot analysis of Cytokeratin 14 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-1-ihc.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human skin, using Cytokeratin 14 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-10-rabbit-monoclonal-antibody-m02305-1-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02305-1-krt10-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 10 KRT10 Rabbit Monoclonal Antibody Western blot analysis of KRT10 using anti-KRT10 antibody (M02305-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT10 antigen affinity purified monoclonal antibody (Catalog # M02305-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KRT10 at approximately 59 kDa. The expected band size for KRT10 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02305-1-if.jpgAnti-Cytokeratin 10 KRT10 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HACAT cells, using Cytokeratin 10 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02305-1-ihc.jpgAnti-Cytokeratin 10 KRT10 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder, using Cytokeratin 10 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ikk-alpha-beta-rabbit-monoclonal-antibody-m01918-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-icc1.jpgAnti-IKK alpha+beta CHUK Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-chuk-ikbkb-primary-antibodies-wb-testing-1.jpgAnti-IKK alpha+beta CHUK Rabbit Monoclonal AntibodyWestern blot analysis of IKK Alpha/Beta using anti-IKK Alpha/Beta antibody (M01918). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKK Alpha/Beta antigen affinity purified monoclonal antibody (M01918) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IKK Alpha/Beta at approximately 87 kDa. The expected band size for IKK Alpha/Beta is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-icc2.jpgAnti-IKK alpha+beta CHUK Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-icc3.jpgAnti-IKK alpha+beta CHUK Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01918-icc4.jpgAnti-IKK alpha+beta CHUK Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p-glycoprotein-rabbit-monoclonal-antibody-m00049-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-wb7.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-wb8.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-wb.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyWestern blot analysis of P Glycoprotein expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-ihc8.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-abcb1-primary-antibodies-ihc-testing-4.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal Antibody IHC analysis of ABCB1 using anti-ABCB1 antibody (M00049). <br>
ABCB1 was detected in a paraffin-embedded section of human adrenal gland tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCB1 Antibody (M00049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-abcb1-primary-antibodies-ihc-testing-5.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal Antibody IHC analysis of ABCB1 using anti-ABCB1 antibody (M00049). <br>
ABCB1 was detected in a paraffin-embedded section of human cardiac muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCB1 Antibody (M00049) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-ihc10.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:1000 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00049-ihc7.jpgAnti-P Glycoprotein ABCB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat spleen, using the Antibody at 1:1000 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-14-rabbit-monoclonal-antibody-m01432-2-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-2-krt14-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal Antibody Western blot analysis of KRT14 using anti-KRT14 antibody (M01432-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT14 antigen affinity purified monoclonal antibody (Catalog # M01432-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KRT14 at approximately 52 kDa. The expected band size for KRT14 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-2-wb7.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-2-ihc.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using Cytokeratin 14 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01432-2-if.jpgAnti-Cytokeratin 14 KRT14 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HACAT cells, using Cytokeratin 14 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-angiopoietin-1-rabbit-monoclonal-antibody-m00853-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00853-angpt1-primary-antibodies-wb-testing-1.jpgAnti-Angiopoietin 1 ANGPT1 Rabbit Monoclonal Antibody Western blot analysis of Angiopoietin-1/ANGPT1 using anti-Angiopoietin-1/ANGPT1 antibody (M00853). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates, <br>
Lane 2: human HEL whole cell lysates, <br>
Lane 3: human K562 whole cell lysates, <br>
Lane 4: human Caco-2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Angiopoietin-1/ANGPT1 antigen affinity purified monoclonal antibody (M00853) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Angiopoietin-1/ANGPT1 at approximately 70 kDa. The expected band size for Angiopoietin-1/ANGPT1 is at 58 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-13-rabbit-monoclonal-antibody-m04299-boster.html2026-03-24T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04299-krt13-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 13 Rabbit Monoclonal Antibody Western blot analysis of Cytokeratin 13/KRT13 using anti-Cytokeratin 13/KRT13 antibody (M04299). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: mouse skin tissue lysates,<br>
Lane 4: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 13/KRT13 antigen affinity purified monoclonal antibody (M04299) at 1:50000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 13/KRT13 at approximately 50 kDa. The expected band size for Cytokeratin 13/KRT13 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04299-krt13-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 13 Rabbit Monoclonal Antibody IHC analysis of KRT13 using anti-KRT13 antibody (M04299). <br>KRT13 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT13 Antibody (M04299) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pro-caspase-10-rabbit-monoclonal-antibody-m02190-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02190-wb.jpgAnti-pro Caspase 10 Rabbit Monoclonal AntibodyWestern blot analysis of pro Caspase 10 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02190-if.jpgAnti-pro Caspase 10 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using pro Caspase 10 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-18-rabbit-monoclonal-antibody-m01357-2-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Cytokeratin 18 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Cytokeratin 18 Antibody (M01357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Cytokeratin 18 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Cytokeratin 18 Antibody (M01357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Cytokeratin 18 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Cytokeratin 18 Antibody (M01357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody Western blot analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human HT-1080 whole cell lysates,<br>
Lane 4: human U2OS whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat thymus tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 18 antigen affinity purified monoclonal antibody (Catalog # M01357-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cytokeratin 18 at approximately 48 kDa. The expected band size for Cytokeratin 18 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-ihc-testing-5.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Cytokeratin 18 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Cytokeratin 18 Antibody (M01357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-krt18-primary-antibodies-ihc-testing-6.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal Antibody IHC analysis of Cytokeratin 18 using anti-Cytokeratin 18 antibody (M01357-2). <br>
Cytokeratin 18 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Cytokeratin 18 Antibody (M01357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-icc1.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-icc2.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-icc3.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01357-2-if.jpgAnti-Cytokeratin 18 Krt18 Rabbit Monoclonal AntibodyImmunofluorescent analysis of pc-12 cells, using Cytokeratin 18 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-trk-fused-gene-rabbit-monoclonal-antibody-m02870-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02870-wb.jpgAnti-TRK fused gene TFG Rabbit Monoclonal AntibodyWestern blot analysis of TRK fused gene expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-epsilon-rabbit-monoclonal-antibody-m01687-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01687-wb.jpgAnti-14-3-3 epsilon YWHAE Rabbit Monoclonal AntibodyWestern blot analysis of 14-3-3 epsilon expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-laminin-beta-1-rabbit-monoclonal-antibody-m03894-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03894-wb.jpgAnti-Laminin beta 1 LAMB1 Rabbit Monoclonal AntibodyWestern blot analysis of Laminin beta 1 expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-chromogranin-a-rabbit-monoclonal-antibody-m01256-1-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01256-1-wb.jpgAnti-Chromogranin A CHGA Rabbit Monoclonal AntibodyWestern blot analysis of Chromogranin A expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-growth-hormone-rabbit-monoclonal-antibody-m00851-1-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00851-1-gh1-primary-antibodies-wb-testing-1.jpgAnti-Growth Hormone GH1 Rabbit Monoclonal Antibody Western blot analysis of GH1 using anti-GH1 antibody (M00851-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GH1 antigen affinity purified monoclonal antibody (Catalog # M00851-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GH1 at approximately 22 kDa. The expected band size for GH1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00851-1-ihc.jpgAnti-Growth Hormone GH1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human placenta, using Growth Hormone Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-crispr-cas9-sp-rabbit-monoclonal-antibody-m30929-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30929-wb.jpgAnti-CRISPR-Cas9 SP Rabbit Monoclonal AntibodyWestern blot analysis of CRISPR-Cas9 SP expression in (1) 293T cell lysate transfected with CRISPR-Cas9; (2) 293T cell lysate; (3) 3T3 cell lysate; (4) PC12 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30929-if.jpgAnti-CRISPR-Cas9 SP Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293T cells transfected with CRISPR-SpCas9, using CRISPR-Cas9 SP Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30929-crspr-cas9-primary-antibodies-wb-testing-1.pngAnti-CRISPR-Cas9 SP Rabbit Monoclonal AntibodyWestern blot analysis of CRISPR-Cas9 SP using anti-CRISPR-Cas9 SP antibody (A04887-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-3: 24h human HEK293T whole cell lysates, <br>
Lane 4-6: 48h human HEK293T whole cell lysates, <br>
Lane 7-9: 60h human HEK293T whole cell lysates, <br>
Lane 10-12: 72h human A549 whole cell lysates, <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRISPR-Cas9 SP antigen affinity purified polyclonal antibody (A04887-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate with Azure Biosystems c600 system. A specific band was detected for CRISPR-Cas9 SP at approximately 158 kDa. The expected band size for CRISPR-Cas9 SP is at 158 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vegf-receptor-1-rabbit-monoclonal-antibody-m00534-boster.html2026-03-27T05:07:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-41598_2016_article_bfsrep26722_fig7_html.jpgAnti-VEGF Receptor 1 FLT1 Rabbit Monoclonal AntibodyThe anti-angiogenic activity of SPS on HUVECs in vitro . ( a ) Dose- and time-dependent growth-inhibiting effects of SPS on HUVECs. Cells were cultured in 96-well plate and treated with different concentrations of SPS (0–1.5 mg/ml) for 12 and 24 h. The cell viability was analyzed by MTT assay. Each data indicated the mean ± SD of three independent experiments (n = 3). * P < 0.05, ** P < 0.01 versus medium control. After A549 cells were treated without (I) or with 0.2 (II), 0.3 (III) and 0.4 (IV) mg/ml of SPS for 8–10 h, cell migration was analyzed using scratch-wound assay ( b ) as well as Transwell assay ( c ). Quantitative evaluations of HUVECs migration induced by SPS in the scratch-wound assay ( d ) and Transwell assay ( e ). ( f ) SPS inhibited the formation of new capillary tube of HUVECs. HUVECs were plated on the surface of the Matrigel in a 96-well plate, where endothelial cells could align and form cords and treated without (I) or with 0.2 (II), 0.3 (III) and 0.4 (IV) mg/ml of SPS for 6 h. ( g ) SPS did not disrupt the preformed vascular network of HUVECs. After the new tube-like structures established, various concentrations of SPS, 0 (I), 0.2 (II), 0.4 (III) and 0.6 (IV) mg/ml were added and incubated for another 12 h. The disruption on the preformed tubes was observed and recorded using an inverted microscope. ( h ) After treated with SPS for 24 h, HUVECs were lysed and western blotting analysis was performed to detect the expressions of VEGF and VEGFR. ( i ) Histograms showed the quantitative evaluation of VEGF and VEGFR protein levels, which were measured by Image J and results were normalized to untreated cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fsrep26722'>27216943</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-flt1-primary-antibodies-wb-testing-1.jpgAnti-VEGF Receptor 1 FLT1 Rabbit Monoclonal AntibodyWestern blot analysis of VEGFR1/FLT1 using anti-VEGFR1/FLT1 antibody (M00534). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: rat heart tissue lysates,<br>
Lane 4: mouse lung tissue lysates,<br>
Lane 5: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGFR1/FLT1 antigen affinity purified monoclonal antibody (M00534) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VEGFR1/FLT1 at approximately 180 kDa. The expected band size for VEGFR1/FLT1 is at 151 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-flt1-primary-antibodies-ihc-testing-1.jpgAnti-VEGF Receptor 1 FLT1 Rabbit Monoclonal AntibodyIHC analysis of VEGFR1/FLT1 using anti-VEGFR1/FLT1 antibody (M00534). <br>VEGFR1/FLT1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-VEGFR1/FLT1 Antibody (M00534) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-flt1-primary-antibodies-ihc-testing-2_1.jpgAnti-VEGF Receptor 1 FLT1 Rabbit Monoclonal AntibodyIHC analysis of VEGFR1/FLT1 using anti-VEGFR1/FLT1 antibody (M00534). <br>VEGFR1/FLT1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-VEGFR1/FLT1 Antibody (M00534) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-1-rabbit-monoclonal-antibody-m00772-2-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-2-wb7.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-2-ihc.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human bladder carcinoma, using Integrin beta 1 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-2-wb8.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-2-wb.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyWestern blot analysis of using Integrin beta1 expression in U937 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-1-rabbit-monoclonal-antibody-m00772-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-wb.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyWestern blot analysis of using Integrin beta1 expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-synuclein-rabbit-monoclonal-antibody-m00215-1-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-wb-testing-1.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyWestern blot analysis of SNCA using anti-SNCA antibody (M00215-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human HEL whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNCA antigen affinity purified monoclonal antibody (M00215-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SNCA at approximately 18 kDa. The expected band size for SNCA is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-ihc-testing-1.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyIHC analysis of SNCA using anti-SNCA antibody (M00215-1). <br>SNCA was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-ihc-testing-2.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyIHC analysis of SNCA using anti-SNCA antibody (M00215-1). <br>SNCA was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-ihc-testing-3.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyIHC analysis of SNCA using anti-SNCA antibody (M00215-1). <br>SNCA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-ihc-testing-4.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyIHC analysis of SNCA using anti-SNCA antibody (M00215-1). <br>SNCA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-snca-primary-antibodies-ihc-testing-5.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyIHC analysis of SNCA using anti-SNCA antibody (M00215-1). <br>SNCA was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-icc1_1.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-icc2_1.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-1-icc3_1.jpgAnti-Alpha Synuclein SNCA Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-3-rabbit-monoclonal-antibody-m00587-1-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00587-1-wb7.jpgAnti-Integrin beta 3 ITGB3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00587-1-wb.jpgAnti-Integrin beta 3 ITGB3 Rabbit Monoclonal AntibodyWestern blot analysis of Integrin beta3 expression in human spleen lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00587-1-ihc.jpgAnti-Integrin beta 3 ITGB3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using Integrin beta 3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-amyloid-beta-a4-rabbit-monoclonal-antibody-m00081-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-wb7.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-wb.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyWestern blot analysis of Amyloid beta A4 expression in mouse brain lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-wb8.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-wb9.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-ihc.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain, using Amyloid beta A4 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-if.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyImmunofluorescent analysis of SH-SY5Y cells, using Amyloid beta A4 Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-ip7.jpgAnti-Amyloid beta A4 APP Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vegf-receptor-2-rabbit-monoclonal-antibody-m00901-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-vegfr2-primary-antibodies-wb-testing-1.jpgAnti-VEGF Receptor 2 KDR Rabbit Monoclonal Antibody Western blot analysis of VEGFR2 using anti-VEGFR2 antibody (M00901). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGFR2 antigen affinity purified monoclonal antibody (Catalog # M00901) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGFR2 at approximately 180-250 kDa. The expected band size for VEGFR2 is at 156 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-ii-tubulin-rabbit-monoclonal-antibody-m09008-boster.html2026-03-24T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09008-tubb4b-primary-antibodies-wb-testing-1_1.jpgAnti-Tubulin beta 4B/2A/2B Rabbit Monoclonal AntibodyWestern blot analysis of Tubulin beta 4B/2A/2B using anti-Tubulin beta 4B/2A/2B antibody (M09008). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: rat C6 whole cell lysates,<br>
Lane 4: mouse brain tissue lysates,<br>
Lane 5: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tubulin beta 4B/2A/2B antigen affinity purified monoclonal antibody (Catalog # M09008) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tubulin beta 4B/2A/2B at approximately 50 kDa. The expected band size for Tubulin beta 4B/2A/2B is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09008-ihc.jpgAnti-Tubulin beta 4B/2A/2B Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse brain, using beta II Tubulin Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-1-rabbit-monoclonal-antibody-m00772-1-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-1-itgb1-primary-antibodies-wb-testing-1.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal Antibody Western blot analysis of Integrin beta 1 using anti-Integrin beta 1 antibody (M00772-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HT-1080 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Integrin beta 1 antigen affinity purified monoclonal antibody (Catalog # M00772-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Integrin beta 1 at approximately 140 kDa. The expected band size for Integrin beta 1 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-1-ihc.jpgAnti-Integrin beta 1 ITGB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast cancer, using Integrin beta 1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-catenin-alpha-1-rabbit-monoclonal-antibody-m01617-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01617-ctnna1-primary-antibodies-wb-testing-1.jpgAnti-Catenin alpha 1 CTNNA1 Rabbit Monoclonal AntibodyWestern blot analysis of CTNNA1 using anti-CTNNA1 antibody (M01617). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human U-87MG whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTNNA1 antigen affinity purified monoclonal antibody (M01617) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CTNNA1 at approximately 100 kDa. The expected band size for CTNNA1 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01617-ihc.jpgAnti-Catenin alpha 1 CTNNA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human lung cancer, using Catenin alpha 1 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-angiotensinogen-rabbit-monoclonal-antibody-m02103-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02103-wb.jpgAnti-Angiotensinogen AGT Rabbit Monoclonal AntibodyWestern blot analysis of Angiotensinogen expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-peroxiredoxin-2-rabbit-monoclonal-antibody-m01982-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01982-prdx2-primary-antibodies-wb-testing-1.jpgAnti-Peroxiredoxin 2 Rabbit Monoclonal AntibodyWestern blot analysis of PRDX2 using anti-PRDX2 antibody (M01982). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRDX2 antigen affinity purified monoclonal antibody (M01982) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PRDX2 at approximately 22 kDa. The expected band size for PRDX2 is at 22 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myeloperoxidase-rabbit-monoclonal-antibody-m00372-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M00372-MPO-primary-antibodies-WB-testing-1.jpgAnti-Myeloperoxidase MPO Rabbit Monoclonal Antibody Western blot analysis of MPO using anti-MPO antibody (M00372). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPO antigen affinity purified monoclonal antibody (Catalog # M00372) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPO at approximately 84 kDa. The expected band size for MPO is at 84 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-interferon-beta-rabbit-monoclonal-antibody-m02041-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02041-wb.jpgAnti-Interferon beta Rabbit Monoclonal AntibodyWestern blot analysis of Interferon beta expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-4-rabbit-monoclonal-antibody-m01015-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01015-itgb4-primary-antibodies-wb-testing-1_1.jpgAnti-Integrin beta 4 ITGB4 Rabbit Monoclonal AntibodyWestern blot analysis of Integrin Beta 4/ITGB4 using anti-Integrin Beta 4/ITGB4 antibody (M01015). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human PC-3 whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Integrin Beta 4/ITGB4 antigen affinity purified monoclonal antibody (M01015) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Integrin Beta 4/ITGB4 at approximately 210 kDa. The expected band size for Integrin Beta 4/ITGB4 is at 202 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01015-itgb4-primary-antibodies-ihc-testing-1.jpgAnti-Integrin beta 4 ITGB4 Rabbit Monoclonal AntibodyIHC analysis of Integrin Beta 4/ITGB4 using anti-Integrin Beta 4/ITGB4 antibody (M01015). <br>Integrin Beta 4/ITGB4 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Integrin Beta 4/ITGB4 Antibody (M01015) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tnf-receptor-ii-rabbit-monoclonal-antibody-m01437-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01437-wb.jpgAnti-TNF Receptor II TNFRSF1B Rabbit Monoclonal AntibodyWestern blot analysis of TNF Receptor II expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-serum-amyloid-a-rabbit-monoclonal-antibody-m01362-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01362-saa1-primary-antibodies-wb-testing-1.jpgAnti-Serum Amyloid A SAA1 Rabbit Monoclonal AntibodyWestern blot analysis of SAA1 using anti-SAA1 antibody (M01362). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat blood tissue lysates<br>
Lane 2: mouse blood tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SAA1 antigen affinity purified monoclonal antibody (M01362) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SAA1 at approximately 12 kDa. The expected band size for SAA1 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01362-ihc.jpgAnti-Serum Amyloid A SAA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver cancer, using Serum Amyloid A Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-leptin-receptor-rabbit-monoclonal-antibody-m00350-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00350-lepr-primary-antibodies-wb-testing-1.jpgAnti-Leptin Receptor LEPR Rabbit Monoclonal Antibody Western blot analysis of Leptin Receptor using anti-Leptin Receptor antibody (M00350). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates, <br>
Lane 2: human K562 whole cell lysates, <br>
Lane 3: human HEL whole cell lysates, <br>
Lane 4: rat kidney tissue lysates, <br>
Lane 5: rat spleen tissue lysates, <br>
Lane 6: mouse kidney tissue lysates, <br>
Lane 7: mouse spleen tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Leptin Receptor antigen affinity purified monoclonal antibody (M00350) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Leptin Receptor at approximately 150 kDa. The expected band size for Leptin Receptor is at 132 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-iii-tubulin-rabbit-monoclonal-antibody-m01857-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01857-TUBB3-primary-antibodies-IHC-testing-1.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human ovarian cancer, using beta III Tubulin Antibody(M01857)<br>TUBB3 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TUBB3 Antibody (M01857)overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01857-TUBB3-primary-antibodies-WB-testing-1.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal AntibodyWestern blot analysis of beta III Tubulin expression in HeLa cell lysate (M01857). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBB3 monoclonal antibody (Catalog # M01857) overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TUBB3https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-ihc7.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-ihc8.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-ihc9.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-ihc10.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibodyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-if.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal AntibodyAB0042Immunofluorescent analysis of PC12 cells, using beta Tubulin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-icc1.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-iii-tubulin-rabbit-monoclonal-antibody-m01857-1-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-wb-testing-1.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody Western blot analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human SIHA whole cell lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TUBB3 antigen affinity purified polyclonal antibody (Catalog # M01857-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TUBB3 at approximately 50 kDa. The expected band size for TUBB3 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-2.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-3.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-4.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-5.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-6.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-7.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-8.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-9.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-10.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-tubb3-primary-antibodies-ihc-testing-11.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal Antibody IHC analysis of TUBB3 using anti-TUBB3 antibody (M01857-1). <br>
TUBB3 was detected in a paraffin-embedded section of non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-TUBB3 Antibody (M01857-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01857-1-if.jpgAnti-beta III Tubulin TUBB3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using beta III Tubulin Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-active-caspase-3-rabbit-monoclonal-antibody-m00334-3-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-3-wb.jpgAnti-active Caspase-3 CASP3 Rabbit Monoclonal AntibodyWestern blot analysis of active Caspase-3 expression in Jurkat cell lysate treated with Camptothecin.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-3-if.jpgAnti-active Caspase-3 CASP3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of HepG2 cells, using active Caspase-3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-heme-oxygenase-1-rabbit-monoclonal-antibody-m00253-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00253-ho-1-primary-antibodies-wb-testing-1.jpgAnti-Heme Oxygenase 1 HMOX1 Rabbit Monoclonal AntibodyWestern blot analysis of HO-1 using anti-HO-1 antibody (M00253). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U87-MG whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human Hela whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HO-1 antigen affinity purified monoclonal antibody (M00253) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HO-1 at approximately 33 kDa. The expected band size for HO-1 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00253-fphar-16-1583509-g008.jpgAnti-Heme Oxygenase 1 HMOX1 Rabbit Monoclonal AntibodySXD remarkably affected the ferroptosis-related markers in CoCl 2 -induced hypoxic H9c2 cells. (A–D) mRNA expressions of ACSL4, GPX4, DPP4, and HMOX1 in different groups, separately. (E) Protein expressions of ACSL4, GPX4, DPP4, and HMOX1 in different groups. *P < 0.05, **P < 0.01, and ***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1583509/full'>40365322</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00253-fphar-16-1583509-g009.jpgAnti-Heme Oxygenase 1 HMOX1 Rabbit Monoclonal AntibodyMolecular docking results. (A) Structure of quercetin. (B, C) Molecular docking of quercetin with DPP4 (B) and HMOX1 (C) . (D) Results of the CETSA assay.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1583509/full'>40365322</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00253-ho-1-primary-antibodies-ihc-testing-2.jpgAnti-Heme Oxygenase 1 HMOX1 Rabbit Monoclonal AntibodyIHC analysis of Heme Oxygenase 1 using anti-Heme Oxygenase 1 antibody (M00253). <br>
Heme Oxygenase 1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Heme Oxygenase 1 Antibody (M00253) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-v-rabbit-monoclonal-antibody-m01561-1-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-itgav-primary-antibodies-wb-testing-2.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-wb.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyWestern blot analysis of integrin alpha V expression in A549 cell lysates.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-itgav-primary-antibodies-wb-testing-1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-wb8_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-wb7_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-ihc9_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human ovarian cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-ihc8_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-ihc11_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse cerebral cortex, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-ihc7_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-ihc10_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human esophageal carcinoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-1-icc1_1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-6-rabbit-monoclonal-antibody-m01693-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01693-ITGA6-primary-antibodies-WB-testing-1.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal AntibodyWestern blot analysis of Integrin alpha 6 expression in SW480 cell lysate (M01693). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITGA6 monoclonal antibody (Catalog # M01693) overnight at 4 then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITGA6https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01693-wb7.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperaturehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01693-wb8.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperaturehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01693-wb9.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01693-ITGA6-primary-antibodies-IHC-testing-1.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using Integrin alpha 6 Antibody(M01693)<br>ITGA6 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-ITGA6 Antibody (M01693)overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01693-itga6-primary-antibodies-if-testing-3.jpgAnti-Integrin alpha 6 ITGA6 Rabbit Monoclonal Antibody IF analysis of ITGA6 using anti-ITGA6 antibody (M01693).<br>
ITGA6 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 with rabbit anti-ITGA6 Antibody (M01693) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lamin-b-receptor-rabbit-monoclonal-antibody-m01238-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01238-wb.jpgAnti-Lamin B Receptor LBR Rabbit Monoclonal AntibodyWestern blot analysis of Lamin B Receptor expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-e-rabbit-monoclonal-antibody-m07091-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07091-itgae-primary-antibodies-ihc-testing-1.jpgAnti-Integrin alpha E ITGAE Rabbit Monoclonal AntibodyIHC analysis of ITGAE using anti-ITGAE antibody (M07091). <br>
ITGAE was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ITGAE Antibody (M07091) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07091-itgae-primary-antibodies-ihc-testing-2.jpgAnti-Integrin alpha E ITGAE Rabbit Monoclonal AntibodyIHC analysis of ITGAE using anti-ITGAE antibody (M07091). <br>
ITGAE was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ITGAE Antibody (M07091) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-2-rabbit-monoclonal-antibody-m01933-boster.html2026-03-24T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-itga2-primary-antibodies-wb-testing-1.jpgAnti-Integrin alpha 2 ITGA2 Rabbit Monoclonal AntibodyWestern blot analysis of ITGA2 using anti-ITGA2 antibody (M01933). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat lung tissue lysates,<br>
Lane 2: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITGA2 antigen affinity purified monoclonal antibody (M01933) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ITGA2 at approximately 165 kDa. The expected band size for ITGA2 is at 129 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-itga2-primary-antibodies-ihc-testing-1.jpgAnti-Integrin alpha 2 ITGA2 Rabbit Monoclonal AntibodyIHC analysis of ITGA2 using anti-ITGA2 antibody (M01933). <br>ITGA2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGA2 Antibody (M01933) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-itga2-primary-antibodies-ihc-testing-2.jpgAnti-Integrin alpha 2 ITGA2 Rabbit Monoclonal AntibodyIHC analysis of ITGA2 using anti-ITGA2 antibody (M01933). <br>ITGA2 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGA2 Antibody (M01933) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-itga2-primary-antibodies-ihc-testing-3.jpgAnti-Integrin alpha 2 ITGA2 Rabbit Monoclonal AntibodyIHC analysis of ITGA2 using anti-ITGA2 antibody (M01933). <br>ITGA2 was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGA2 Antibody (M01933) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-icc1.jpgAnti-Integrin alpha 2 ITGA2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-insulin-receptor-rabbit-monoclonal-antibody-m00447-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00447-wb7.jpgAnti-Insulin Receptor INSR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00447-if.jpgAnti-Insulin Receptor INSR Rabbit Monoclonal AntibodyImmunofluorescent analysis of BxPC-3 cells, using Insulin Receptor Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00447-wb8.jpgAnti-Insulin Receptor INSR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00447-wb.jpgAnti-Insulin Receptor INSR Rabbit Monoclonal AntibodyWestern blot analysis of Insulin Receptor expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-5-rabbit-monoclonal-antibody-m01911-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-wb.jpgAnti-Integrin alpha 5 ITGA5 Rabbit Monoclonal AntibodyWestern blot analysis of Integrin alpha 5 expression in Mouse heart lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-if.jpgAnti-Integrin alpha 5 ITGA5 Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using Integrin alpha 5 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-4-rabbit-monoclonal-antibody-m00468-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-wb.jpgAnti-Integrin alpha 4 ITGA4 Rabbit Monoclonal AntibodyWestern blot analysis of Integrin alpha 4 expression in Jurkat cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-interferon-gamma-rabbit-monoclonal-antibody-m00393-1-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-1-wb7.jpgAnti-Interferon gamma IFNG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-1-wb.jpgAnti-Interferon gamma IFNG Rabbit Monoclonal AntibodyWestern blot analysis of Interferon gamma expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-1-ifng-primary-antibodies-wb-testing-1.jpgAnti-Interferon gamma IFNG Rabbit Monoclonal AntibodyWestern blot analysis of IFNG using anti-IFNG antibody (M00393-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: recombinant human IFNG protein.After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFNG antigen affinity purified monoclonal antibody (M00393-1) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IFNG at approximately 17 kDa. The expected band size for IFNG is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-1-wb8.jpgAnti-Interferon gamma IFNG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-1-wb9.jpgAnti-Interferon gamma IFNG Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-alpha-v-rabbit-monoclonal-antibody-m01561-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-itgav-primary-antibodies-wb-testing-1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal Antibody Western blot analysis of ITGAV using anti-ITGAV antibody (M01561). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: rat spleen tissue lysates,<br>
Lane 6: rat brain tissue lysates,<br>
Lane 7: mouse spleen tissue lysates,<br>
Lane 8: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITGAV antigen affinity purified monoclonal antibody (Catalog # M01561) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITGAV at approximately 130, 140, 150 kDa. The expected band size for ITGAV is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-icc1.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-icc2.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-icc3.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-icc4.jpgAnti-Integrin alpha V ITGAV Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-androgen-receptor-rabbit-monoclonal-antibody-m00542-1-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb10.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb7.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb11.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb8.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb12.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb9.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-wb.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyWestern blot analysis of Androgen Receptor expression in (1) T47D cell lysate;(2) LnCaP cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-ihc.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate carcinoma, using Androgen Receptor Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-icc1.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-icc2.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-1-if.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis of Lncap cells, using Androgen Receptor Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nak-tbk1-n-term-rabbit-monoclonal-antibody-m00261-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-fcimb-14-1393680-g003.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyEV71 infection inhibits the TLR4/MYD88/NF-κB and TBK1 pathway. (A) The network of TLR4 interacting proteins; (B) MYD88 gene expression of the GSE15323 dataset from the GEO database; (C–F) Western blot analysis of MYD88, p-NF-κB p65, NF-κB p65 and VP1 protein expression in EV71 infected RD cells at different MOIs. (G–I) Western blot analysis of p-TBK1/TBK1 and VP1 protein expression in EV71 infected RD cells at different MOIs. Data are presented as the mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2024.1393680/full'>38938877</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-41419_2023_6418_fig3_html.pngAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyPOLE mutations promote the occurrence of endogenous DNA breaks. A Immunohistochemical analysis of γH2AX expression in human EC specimens. The images are sequentially magnified from left to right and the black frames indicate the amplification area. Scale bar, 100 μm. B Quantification of nuclear γH2AX staining intensity in the ( A ). C Immunofluorescence analysis of micronucleus in human EC cells with WT POLE or P286R mutation. Scale bar, 25 μm. D Quantification of genomic damage by the micronucleus assay. E Western blot analyses of γH2AX and H2AX proteins in human EC cells with POLE mutation or WT POLE. F Quantification of γH2AX and H2AX expression levels in the EC cells treated as in ( E ). G Western blot analyses of γH2AX and H2AX proteins in human EC cells bearing POLE mutant or WT POLE in the absence or presence of Etoposide (100 μM). H Quantification of γH2AX expression level in the EC cells treated as in ( G ). I Western blotting of TBK1 and its phosphorylation in human EC cells with WT or mutant POLE. J Quantification of TBK1 phosphorylation level in the EC cells treated as in ( I ). Data are shown as mean ± SD. * p < 0.05, ** p < 0.005, *** p < 0.001 significantly different from Control. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-023-06418-3'>38238314</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc7.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat liver, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-tbk1-primary-antibodies-wb-testing-1.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal Antibody Western blot analysis of NAK/TBK1 using anti-NAK/TBK1 antibody (M00261). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAK/TBK1 antigen affinity purified monoclonal antibody (Catalog # M00261) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAK/TBK1 at approximately 84 kDa. The expected band size for NAK/TBK1 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc8.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat stomach, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc9.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc10.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc11.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skin, using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-ihc.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human testis, using NAK/TBK1 (N-term) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-icc1.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00261-if.jpgAnti-NAK/TBK1 (N-term) Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using NAK/TBK1 (N-term) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-androgen-receptor-rabbit-monoclonal-antibody-m00542-2-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ijpharm-42-312-g001.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyEffect of E 2 on prostate pathology when TP was 0.15 mg/kg/rat. Compared with the control (a) and castrated control (b) group, the area of prostate glandular cavity and the height of prostate epithelia had no obvious change. 7 groups which were all administered TP 0.15 mg/kg, and E 2 were 0 (c), 0.4 (d), 2.0 (e), 10 (f), 50 (g), 250 (h) and 1250µg/kg (j). Magnification ×100.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC2959216/&orig_host=www.ncbi.nlm.nih.gov'>21206625</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ijpharm-42-312-g002.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyEffect of E 2 on prostate pathology when TP was 0.74 mg/kg/rat. Control group is picture (a) and castrated control group is picture (b). And the other 7 groups which were all administered TP 0.74 mg/kg/rat, and E 2 were 0 (c), 0.4 (d), 2.0 (e), 10 (f), 50 (g), 250 (h) and 1250µg/kg (j). Compared with the control (a) and castrated control (b) group, the area of prostate glandular cavity of the last thee groups (g, h, and j) increased significantly. Magnification ×100.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC2959216/&orig_host=www.ncbi.nlm.nih.gov'>21206625</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ijpharm-42-312-g003.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyEffect of E 2 on prostate pathology when TP was 3.7 mg/kg/rat. Control group is picture (a) and castrated control group is picture (b). And the other 7 groups which were all administered TP 3.7 mg/kg/rat, and E 2 were 0 (c), 0.4 (d), 2.0 (e),10 (f), 50 (g), 250 (h), 1250µg/kg (j). Compared with control group (a), the area of prostate glandular cavity were significant differences. Magnification ×100.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC2959216/&orig_host=www.ncbi.nlm.nih.gov'>21206625</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ijpharm-42-312-g004.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyEffect of E 2 on prostate pathology when TP was 18.5 mg/kg/rat. Control group is picture (a) and castrated control group is picture (b). And the other 7 groups which were all administered TP 18.5 mg/kg/rat, and E 2 were 0 (c), 0.4 (d), 2.0 (e), 10 (f), 50 (g), 250 (h) and 1250 µg/kg (j). Compared with the control group (a), the area of prostate glandular cavity were all significant differences. Magnification ×100.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC2959216/&orig_host=www.ncbi.nlm.nih.gov'>21206625</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ijpharm-42-312-g005.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyEffect of E 2 on prostate pathology when TP was 92.6 mg/kg/rat. Control group is picture (a) and castrated control group is picture (b). And the other 7 groups which were all administered TP 92.6 mg/kg/rat, and E 2 were 0 (c), 0.4 (d), 2.0 (e), 10 (f), 50 (g), 250 (h) and 1250µg/kg (j). Compared with the castrated control group (a), the area of prostate glandular cavity were all significant differences. Magnification ×100.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC2959216/&orig_host=www.ncbi.nlm.nih.gov'>21206625</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ihc.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate, using Androgen Receptor Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-ar-primary-antibodies-wb-testing-1.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyWestern blot analysis of Androgen Receptor using anti-Androgen Receptor antibody (M00542-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U251 whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: mouse C2C12 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Androgen Receptor antigen affinity purified monoclonal antibody (M00542-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Androgen Receptor at approximately 110-120 kDa. The expected band size for Androgen Receptor1 is at 99 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-icc1.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-icc2.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-2-if.jpgAnti-Androgen Receptor AR Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF7 cells, using Androgen Receptor Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-runx1-runx2-runx3-rabbit-monoclonal-antibody-m00086-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00086-wb7.jpgAnti-RUNX1/RUNX2/RUNX3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00086-wb.jpgAnti-RUNX1/RUNX2/RUNX3 Rabbit Monoclonal AntibodyWestern blot analysis of RUNX1/RUNX2/RUNX3 expression in MOLT4 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00086-ihc.jpgAnti-RUNX1/RUNX2/RUNX3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse lung, using RUNX1/RUNX2/RUNX3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p53-acetyl-k370-rabbit-monoclonal-antibody-p00001-1-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-wb7.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-icc2.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-41419_2022_5037_fig6_html.pngAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyEMs combined with iron overload modeling affected pregnancy. A The average body weight of the pregnant mice was calculated from control (CON, n = 10), EMs model (EMs, n = 10), EMs combined with iron overload model (IRON, n = 10), DFO treatment after IRON model (IRON + DFO, n = 10), and VITE treatment after IRON model (IRON + VITE, n = 10). B Representative photographs of the uterus after pregnancy in each of the five groups of female mice. C , D Total litter size and specific number of litters per in five groups ( n = 10). E For Prussian blue, H&E, and GPX4 immunohistochemical staining, ovarian tissues were observed from the five groups of mice. Scale bar = 50 µm; Scale bar = 200 µm; Scale bar = 20 µm. F Western blot analysis of TP53 expression in the ovarian tissues of mice in each group. Expression of GAPDH was used as an internal control. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-022-05037-8'>35787614</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-12967_2014_article_287_fig2_html.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyMethylating effect of daphnetin and 5-aza-dc on DR3, PDCD5, FasL and p53 in CIA rat synovial cells. Four experimental groups consisting of untreated cell control, or treated with 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). Cells were cultured, treated and harvested as described in Materials and Methods. Total DNA was extracted and used for MSP after bisulphite modification. M: methylated amplification products, U: hypomethylated amplification products. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-12967_2014_article_287_fig3_html.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyEffect of daphnetin and 5-aza-dc on expression of DR3, PDCD5, FasL, p53 (A) and DNMT1, DNMT3a, DNMT3b (B) in CIA rat synovial cells. Four experimental groups consisting of untreated cell control, or treated with 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). Cells were cultured, treated and harvested as described in Matreials and Methods. Total RNA was extracted and cDNA was synthesized. After reverse transcription, cDNA was used for real time-PCR. Relative quantification of gene expression was performed by the 2-ΔΔCt method. The results show the mean ± S.D. of six independent experiments. ▲P < 0.05 compared with control, ●P < 0.05 compared with 5-aza-dc, ☆P > 0.05 compared with 5-aza-dc, ★P > 0.05 compared with daphnetin, *P < 0.05 compared with daphnetin. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-12967_2014_article_287_fig4_html.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyEffect of daphnetin on DR3, PDCD5, FasL and p53 protein expression in CIA rats synovial cells. Cells were cultured, treated and harvested as described Materials and Methods. Four experimental groups consisting of untreated cell control, 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). The results show the mean ± S.D. of six independent experiments. ▲P < 0.05 compared with control, ●P < 0.05 compared with 5-aza-dc, ★P > 0.05 compared with 5-aza-dc, *P < 0.05 compared with daphnetin. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-13287_2025_4422_fig1_html.pngAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyShort-term DMOG treatment reduces MSC senescence by activating HIF-1α and decreasing apoptosis. ( A , B ) Representative images of SA-β-gal staining showing the proportion of senescent cells in H₂O₂-treated MSCs before and after DMOG treatment. Scale bar = 500 μm. ( C ) Western blot analysis of p53 and p21 protein expression during oxidative stress-induced senescence. ( D , E ) SA-β-gal staining in replicative senescence (P15) MSCs, demonstrating the effect of DMOG in reducing senescence markers. Scale bar = 500 μm. ( F ) Western blot analysis of p53 and p21 protein levels in P5 (young) and P15 (senescent) MSCs. ( G ) Expression levels of senescence-associated genes (IL6, CXCL1, and MMP3) in both senescence models as assessed by qRT-PCR. ( H ) Western blotting and qPCR analysis showing increased HIF-1α protein and mRNA levels in both senescence models after DMOG treatment. ( I ) Calcein/PI live-dead staining revealed an increase in the proportion of live cells following DMOG treatment in both senescence models. ( J , K ) Flow cytometric analysis of apoptosis. Error bars represent the mean ± SD of three independent experiments. Statistical significance was set as p < 0.05. Full-length blots are presented in Supplementary Materials - WB Raw Data Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04422-2'>40457488</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-wb8.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-icc3.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-icc1.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-1-wb.jpgAnti-p53 (acetyl K370) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of p53 (acetyl K370) expression in HeLa cell lysate treated with Trichostatin A.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-p53-acetyl-k382-rabbit-monoclonal-antibody-p00001-2-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/0/p00001-2-wb.jpgAnti-p53 (acetyl K382) TP53 Rabbit Monoclonal AntibodyWestern blot analysis of p53 (acetyl K382) expression in Jurkat cell lysate treated with etopside and TSA.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-atp-citrate-lyase-rabbit-monoclonal-antibody-m02372-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02372-acly-primary-antibodies-wb-testing-1.jpgAnti-ATP citrate lyase ACLY Rabbit Monoclonal Antibody Western blot analysis of ACLY using anti-ACLY antibody (M02372). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACLY antigen affinity purified monoclonal antibody (Catalog # M02372) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACLY at approximately 121 kDa. The expected band size for ACLY is at 121 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02372-ihc.jpgAnti-ATP citrate lyase ACLY Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain carcinoma, using ATP citrate lyase Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02372-ip7.jpgAnti-ATP citrate lyase ACLY Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:3K dilution)
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pp2a-alpha-beta-rabbit-monoclonal-antibody-m07661-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07661-wb.jpgAnti-PP2A alpha + beta Rabbit Monoclonal AntibodyWestern blot analysis of PP2A alpha+beta expression in T47 D cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07661-ihc.jpgAnti-PP2A alpha + beta Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using PP2A alpha + beta Antibody.
https://www.bosterbio.com/products/primary-antibodies/monoclonal-primary-antibodies/anti-apolipoprotein-picoband-trade-antibody-monoclonal-m00717-1-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00717-1-apoa1-primary-antibodies-wb-testing-1.jpgAnti-Apolipoprotein A I APOA1 Antibody Picoband® (monoclonal, 17G5) Western blot analysis of APOA1 using anti-APOA1 antibody (M00717-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: human CACO-2 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-APOA1 antigen affinity purified monoclonal antibody (M00717-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1051) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for APOA1 at approximately 25 kDa. The expected band size for APOA1 is at 31 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cleaved-caspase-9-rabbit-monoclonal-antibody-m00080-2-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00080-2-casp9-primary-antibodies-wb-testing-1.jpgAnti-cleaved Caspase-9 p35 CASP9 Rabbit Monoclonal Antibody Western blot analysis of Caspase 9/CASP9 using anti-Caspase 9/CASP9 antibody (M00080-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human HEL whole cell lysates,<br>
Lane 5: human Jurkat whole cell lysates,<br>
Lane 6: human Jurkat treated with staurosporine,<br>
Lane 7: mouse NIH/3T3 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 treated with staurosporine.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 9/CASP9 antigen affinity purified monoclonal antibody (M00080-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase 9/CASP9 at approximately 46 kDa. The expected band size for Caspase 9/CASP9 is at 46 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glycogen-synthase-rabbit-monoclonal-antibody-m03512-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03512-wb.jpgAnti-Glycogen synthase GYS1 Rabbit Monoclonal AntibodyWestern blot analysis of Glycogen synthase expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-58k-golgi-protein-rabbit-monoclonal-antibody-m05499-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05499-wb.jpgAnti-58K Golgi protein Rabbit Monoclonal AntibodyWestern blot analysis of 58K Golgi protein expression in human fetal liver lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cathepsin-l-v-k-h-rabbit-monoclonal-antibody-m01589-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01589-ctsl-primary-antibodies-wb-testing-1.jpgAnti-Cathepsin L/V/K/H Rabbit Monoclonal Antibody Western blot analysis of Cathepsin L/V/K/H using anti-Cathepsin L/V/K/H antibody (M01589). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat PC-12 whole cell lysates,<br>
Lane 2: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cathepsin L/V/K/H antigen affinity purified monoclonal antibody (Catalog # M01589) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cathepsin L/V/K/H at approximately 38 kDa. The expected band size for Cathepsin L/V/K/H is at 36,38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01589-wb7.jpgAnti-Cathepsin L/V/K/H Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01589-wb10.jpgAnti-Cathepsin L/V/K/H Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01589-wb9.jpgAnti-Cathepsin L/V/K/H Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01589-wb.jpgAnti-Cathepsin L/V/K/H Rabbit Monoclonal AntibodyWestern blot analysis of Cathepsin L/V/K/H expression in (1) HepG2 cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate;
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-kappa-light-chain-rabbit-monoclonal-antibody-m05470-1-boster.html2026-03-24T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05470-1-wb.jpgAnti-Kappa light chain IGKC Rabbit Monoclonal AntibodyWestern blot analysis of Kappa light chain expression in human plasma lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05470-1-igkc-primary-antibodies-ihc-testing-1.jpgAnti-Kappa light chain IGKC Rabbit Monoclonal AntibodyIHC analysis of ig Kappa light chain using anti-ig Kappa light chain antibody (M05470-1). <br>ig Kappa light chain was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ig Kappa light chain Antibody (M05470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05470-1-igkc-primary-antibodies-ihc-testing-2.jpgAnti-Kappa light chain IGKC Rabbit Monoclonal AntibodyIHC analysis of ig Kappa light chain using anti-ig Kappa light chain antibody (M05470-1). <br>ig Kappa light chain was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ig Kappa light chain Antibody (M05470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05470-1-igkc-primary-antibodies-ihc-testing-3.jpgAnti-Kappa light chain IGKC Rabbit Monoclonal AntibodyIHC analysis of ig Kappa light chain using anti-ig Kappa light chain antibody (M05470-1). <br>ig Kappa light chain was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ig Kappa light chain Antibody (M05470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05470-1-igkc-primary-antibodies-ihc-testing-4.jpgAnti-Kappa light chain IGKC Rabbit Monoclonal AntibodyIHC analysis of ig Kappa light chain using anti-ig Kappa light chain antibody (M05470-1). <br>ig Kappa light chain was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ig Kappa light chain Antibody (M05470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pias1-pias2-pias3-rabbit-monoclonal-antibody-m01707-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias123-primary-antibodies-wb-testing-1.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody Western blot analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human A431 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIAS1+PIAS2+PIAS3 antigen affinity purified polyclonal antibody (Catalog # M01707) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIAS1+PIAS2+PIAS3 at approximately 76 kDa. The expected band size for PIAS1+PIAS2+PIAS3 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-2.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-3.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-4.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-5.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-6.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-7.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-8.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-9.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-10.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-11.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-12.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01707-pias2-primary-antibodies-ihc-testing-13.jpgAnti-PIAS1+PIAS2+PIAS3 Rabbit Monoclonal Antibody IHC analysis of PIAS1+PIAS2+PIAS3 using anti-PIAS1+PIAS2+PIAS3 antibody (M01707). <br>
PIAS1+PIAS2+PIAS3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PIAS1+PIAS2+PIAS3 Antibody (M01707) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gamma-sarcoglycan-rabbit-monoclonal-antibody-m05934-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05934-SGCG-primary-antibodies-WB-testing-1.jpgAnti-gamma Sarcoglycan Rabbit Monoclonal AntibodyWestern blot analysis of gamma Sarcoglycan expression in Human skeletal muscle lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05934-sgcg-primary-antibodies-ihc-testing-2.jpgAnti-gamma Sarcoglycan Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue using anti-gamma Sarcoglycan antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody ( 1/100) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05934-wb7.jpgAnti-gamma Sarcoglycan Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-sarcoglycan-rabbit-monoclonal-antibody-m04756-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04756-wb7.jpgAnti-alpha Sarcoglycan Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04756-wb10.jpgAnti-alpha Sarcoglycan Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04756-wb8.jpgAnti-alpha Sarcoglycan Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04756-wb.jpgAnti-alpha Sarcoglycan Rabbit Monoclonal AntibodyWestern blot analysis of alpha Sarcoglycan expression in Human skeletal muscle lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04756-wb9.jpgAnti-alpha Sarcoglycan Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-delta-sarcoglycan-rabbit-monoclonal-antibody-m05297-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M05297-SGCD-primary-antibodies-WB-testing-1.jpgAnti-delta Sarcoglycan SGCD Rabbit Monoclonal AntibodyWestern blot analysis of delta Sarcoglycan expression in Human fetal heart lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05297-sgcd-primary-antibodies-ihc-testing-2.jpgAnti-delta Sarcoglycan SGCD Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach carcinoma tissue using anti-delta Sarcoglycan antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody ( 1/100) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdgf-receptor-beta-rabbit-monoclonal-antibody-m00096-1-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-1-wb.jpgAnti-PDGF Receptor beta PDGFRB Rabbit Monoclonal AntibodyWestern blot analysis of PDGF Receptor beta expression in SH-SY5Y cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-1-ihc.jpgAnti-PDGF Receptor beta PDGFRB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human uterus, using PDGF Receptor beta Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-1-if.jpgAnti-PDGF Receptor beta PDGFRB Rabbit Monoclonal AntibodyImmunofluorescent analysis of 3T3 cells, using PDGF Receptor beta Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-reactive-protein-rabbit-monoclonal-antibody-m00249-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00249-crp-primary-antibodies-wb-testing-1.jpgAnti-C Reactive Protein CRP Rabbit Monoclonal AntibodyWestern blot analysis of CRP using anti-CRP antibody (M00249). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human hepatocellular carcinoma tumor tissue lysates,<br>
Lane 2: human hepatocellular carcinoma paracancerous tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRP antigen affinity purified monoclonal antibody (M00249) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CRP at approximately 25 kDa. The expected band size for CRP is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00249-crp-primary-antibodies-ihc-testing-1.jpgAnti-C Reactive Protein CRP Rabbit Monoclonal AntibodyIHC analysis of CRP using anti-CRP antibody (M00249). <br>CRP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CRP Antibody (M00249) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-firefly-luciferase-rabbit-monoclonal-antibody-mt0021-1-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0021-1-wb.jpgAnti-Firefly Luciferase Rabbit Monoclonal AntibodyWestern blot analysis of Firefly Luciferase Antibody - N-terminal expression in (1) Firefly Luciferase transfected 293T cell lysate; (2) HeLa cell lysate; (3) NIH/3T3 cell lysate; (4) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0021-1-if.jpgAnti-Firefly Luciferase Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells transfected with Firefly Luciferase, using Firefly Luciferase Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-firefly-luciferase-rabbit-monoclonal-antibody-mt0021-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0021-wb.jpgAnti-Firefly Luciferase Rabbit Monoclonal AntibodyWestern blot analysis of Firefly Luciferase Antibody expression in (1) Firefly Luciferase transfected 293T cell lysate; (2) HeLa cell lysate; (3) NIH/3T3 cell lysate; (4) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0021-if.jpgAnti-Firefly Luciferase Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells transfected with Firefly Luciferase, using Firefly Luciferase Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-renilla-luciferase-rabbit-monoclonal-antibody-mt0022-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0022-wb.jpgAnti-Renilla Luciferase Rabbit Monoclonal AntibodyWestern blot analysis of Renilla Luciferase expression in (1) Renilla Luciferase transfected 293 cell lysate; (2) HeLa cell lysate; (3) NIH/3T3 cell lysate; (4) C6 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/t/mt0022-if.jpgAnti-Renilla Luciferase Rabbit Monoclonal AntibodyImmunofluorescent analysis of 293 cells transfected with Renilla Luciferase, using Renilla Luciferase Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp90-alpha-beta-rabbit-monoclonal-antibody-m01103-2-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90-primary-antibodies-wb-testing-1.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody Western blot analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human SiHa whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates,<br>
Lane 6: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hsp90 antigen affinity purified monoclonal antibody (Catalog # M01103-2) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hsp90 at approximately 80-100 kDa. The expected band size for Hsp90 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-wb-testing-1.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal AntibodyWestern blot analysis of HSP90AA1 using anti-HSP90AA1 antibody (M01103-2).<br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: huamn MDA-MB-231 whole cell lysates,<br>
Lane 2: human MDA-MB-231 whole cell lysates,<br>
Lane 3: human HCC1937 whole cell lysates,<br>
Lane 4: human HCC1937 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSP90AA1 antigen affinity purified monoclonal antibody (M01103-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HSP90AA1 at approximately 90 kDa. The expected band size for HSP90AA1 is at 90 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-ijbsv21p0175g003.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal AntibodyHA induces tolerance to high temperatures via the HIF-1α/HSP70 signaling. A & B. The bEnd.3 cells were exposed to 40℃ for 2 h daily, continuously for 1 day, 3 days, and 5 days. RT-qPCR was used to detect the expression of Hif-1α and Hspa1a mRNA. C. WB was used to detect the expression of HIF-1α, HSP90AA1, and HSP70 protein. β-actin was used as an internal control. D. IF was used to detect the expression of HIF-1α and HSP70 protein. E. WB was used to detect the expression of HIF-1α and HSP70 protein. β-actin was used as an internal control. F. bEnd.3 HA cells were exposed to HS for 4 h and treated with LW6, VER-155088, or a combination of both. Cell viability was detected using the CCK-8 assay. G. bEnd.3 HA cells were exposed to HS for 4 h and treated with si- Hif-1α , si- Hspa1a , or a combination of both. Cell viability was detected using the CCK-8 assay. H. Flow cytometry with Annexin V and PI staining was used to determine the apoptotic index of cells. ** P < 0.01, *** P < 0.001, **** P < 0.0001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11667810/'>39744422</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-2.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-3.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of human brest cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-4.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-5.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-6.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-hsp90aa1-primary-antibodies-ihc-testing-7.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal Antibody IHC analysis of Hsp90 using anti-Hsp90 antibody (M01103-2). <br>
Hsp90 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Hsp90 Antibody (M01103-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-if.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Hsp90 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-icc1.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01103-2-icc2.jpgAnti-Hsp90 alpha + beta HSP90AA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mast-cell-tryptase-rabbit-monoclonal-antibody-m08039-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08039-wb.jpgAnti-Mast Cell Tryptase Rabbit Monoclonal AntibodyWestern blot analysis of Mast Cell Tryptase expression in Human tonsil lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08039-ihc.jpgAnti-Mast Cell Tryptase Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Mast Cell Tryptase Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-thymidine-kinase-1-rabbit-monoclonal-antibody-m04850-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04850-tk1-primary-antibodies-wb-testing-1.jpgAnti-Thymidine Kinase 1 Rabbit Monoclonal Antibody Western blot analysis of Thymidine Kinase 1 using anti-Thymidine Kinase 1 antibody (M04850). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human U20S whole cell lysates,<br>
Lane 3: human PC-3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Thymidine Kinase 1 antigen affinity purified monoclonal antibody (Catalog # M04850) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Thymidine Kinase 1 at approximately 25 kDa. The expected band size for Thymidine Kinase 1 is at 25 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myosin-heavy-chain-rabbit-monoclonal-antibody-m02808-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02808-myh6-primary-antibodies-wb-testing-1.jpgAnti-Myosin heavy chain MYH6 Rabbit Monoclonal AntibodyWestern blot analysis of MYH6 using anti-MYH6 antibody (M02808). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates,<br>
Lane 2: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYH6 antigen affinity purified monoclonal antibody (M02808) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYH6 at approximately 224 kDa. The expected band size for MYH6 is at 224 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02808-myh6-primary-antibodies-ihc-testing-1.jpgAnti-Myosin heavy chain MYH6 Rabbit Monoclonal AntibodyIHC analysis of MYH6 using anti-MYH6 antibody (M02808). <br>MYH6 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MYH6 Antibody (M02808) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02808-myh6-primary-antibodies-ihc-testing-2.jpgAnti-Myosin heavy chain MYH6 Rabbit Monoclonal AntibodyIHC analysis of MYH6 using anti-MYH6 antibody (M02808). <br>MYH6 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MYH6 Antibody (M02808) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02808-myh6-primary-antibodies-ihc-testing-3.jpgAnti-Myosin heavy chain MYH6 Rabbit Monoclonal AntibodyIHC analysis of MYH6 using anti-MYH6 antibody (M02808). <br>MYH6 was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MYH6 Antibody (M02808) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02808-myh6-primary-antibodies-ihc-testing-4.jpgAnti-Myosin heavy chain MYH6 Rabbit Monoclonal AntibodyIHC analysis of MYH6 using anti-MYH6 antibody (M02808). <br>MYH6 was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-MYH6 Antibody (M02808) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vitamin-d-receptor-rabbit-monoclonal-antibody-m00210-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00210-vdr-primary-antibodies-wb-testing-1.jpgAnti-Vitamin D Receptor VDR Rabbit Monoclonal Antibody Western blot analysis of VDR using anti-VDR antibody (M00210). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VDR antigen affinity purified monoclonal antibody (Catalog # M00210) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VDR at approximately 48 kDa. The expected band size for VDR is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00210-wb7.jpgAnti-Vitamin D Receptor VDR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lipoprotein-lipase-rabbit-monoclonal-antibody-m00316-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00316-wb7.jpgAnti-Lipoprotein lipase LPL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00316-wb.jpgAnti-Lipoprotein lipase LPL Rabbit Monoclonal AntibodyWestern blot analysis of Lipoprotein lipase expression in Human fetal liver lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00316-wb8.jpgAnti-Lipoprotein lipase LPL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00316-wb9.jpgAnti-Lipoprotein lipase LPL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-actin-alpha-actin-rabbit-monoclonal-antibody-m02014-4-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-acta1-primary-antibodies-ihc-testing-1.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyIHC analysis of Actin (Alpha-Actin) using anti-Actin (Alpha-Actin) antibody (M02014-4). <br>Actin (Alpha-Actin) was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Actin (Alpha-Actin) Antibody (M02014-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-acta1-primary-antibodies-ihc-testing-2.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyIHC analysis of Actin (Alpha-Actin) using anti-Actin (Alpha-Actin) antibody (M02014-4). <br>Actin (Alpha-Actin) was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Actin (Alpha-Actin) Antibody (M02014-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-acta1-primary-antibodies-ihc-testing-3.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyIHC analysis of Actin (Alpha-Actin) using anti-Actin (Alpha-Actin) antibody (M02014-4). <br>Actin (Alpha-Actin) was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Actin (Alpha-Actin) Antibody (M02014-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-acta1-primary-antibodies-ihc-testing-4.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyIHC analysis of Actin (Alpha-Actin) using anti-Actin (Alpha-Actin) antibody (M02014-4). <br>Actin (Alpha-Actin) was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Actin (Alpha-Actin) Antibody (M02014-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-wb_1.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyWestern blot analysis of Actin (Alpha-Actin) expression in (1) A431 cell lysate; (2) MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02014-4-if_1.jpgAnti-Actin (Alpha-Actin) ACTA1 Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Actin (Alpha-Actin) Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pi-3-kinase-class-3-rabbit-monoclonal-antibody-m02356-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02356-wb.jpgAnti-PI 3 Kinase Class 3 PIK3C3 Rabbit Monoclonal AntibodyWestern blot analysis of PI 3 Kinase Class 3 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02356-ihc.jpgAnti-PI 3 Kinase Class 3 PIK3C3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using PI 3 Kinase Class 3 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-wilms-tumor-protein-rabbit-monoclonal-antibody-m00199-1-boster.html2026-03-24T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00199-1-wb7.jpgAnti-Wilms Tumor Protein WT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00199-1-ihc.jpgAnti-Wilms Tumor Protein WT1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse kidney, using Wilms Tumor Protein Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00199-1-ijbsv21p3852g001.jpgAnti-Wilms Tumor Protein WT1 Rabbit Monoclonal AntibodyConstruction of db/db model to evaluate changes in renal pathology lipid metabolism. Two groups of twenty-week-old mice were analyzed: db/m (n=6) and db/db (n=6). A-B. Representative PAS staining of glomeruli in each group, and the semiquantitative analysis of mesangial area ratio. (**<0.01, scale bar: 50 μm). C-G. Biochemical examination: (C) UACR, (D) serum creatinine, (E) blood glucose, (F) serum cholesterol, (G) serum triglycerides. (**<0.01). H. Representative transmission electron microscopy (TEM) images of podocyte foot processes and glomerular basement membrane (GBM) in each group. (**<0.01, scale bar: 10 μm). I-J. Representative immunofluorescence double staining of BODIPY and WT1 in the glomeruli of db/m and db/db mice, and semiquantitative analysis. (**<0.01, scale bar:50μm). K-L. Oil Red O staining of lipid droplets (LDs) in the glomeruli of db/m and db/db mice, and semiquantitative analysis. (**<0.01, scale bar: 40 μm).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12210380/'>40607256</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00199-1-wb8.jpgAnti-Wilms Tumor Protein WT1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00199-1-wb.jpgAnti-Wilms Tumor Protein WT1 Rabbit Monoclonal AntibodyWestern blot analysis of WT1 expression in K562 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-yeast-rabbit-monoclonal-antibody-m30930-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30930-wb.jpgAnti-Histone H2B (yeast) HIST1H2BC Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B expression in Saccharomyces cerevisiae cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-14-3-3-alpha-beta-rabbit-monoclonal-antibody-m02431-3-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02431-3-ywhab-primary-antibodies-wb-testing-1.jpgAnti-14-3-3 alpha + beta YWHAB Rabbit Monoclonal Antibody Western blot analysis of YWHAB using anti-YWHAB antibody (M02431-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Caco-2 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human Hacat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat lung tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse lung tissue lysates,<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YWHAB antigen affinity purified monoclonal antibody (Catalog # M02431-3) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YWHAB at approximately 28 kDa. The expected band size for YWHAB is at 28 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-neutrophil-elastase-rabbit-monoclonal-antibody-m01607-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01607-tau-primary-antibodies-wb-testing-1.jpgAnti-Neutrophil Elastase ELANE Rabbit Monoclonal Antibody Western blot analysis of Neutrophil Elastase using anti-Neutrophil Elastase antibody (M01607). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HL-60 whole cell lysates,<br>
Lane 2: human THP-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Neutrophil Elastase antigen affinity purified monoclonal antibody (Catalog # M01607) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Neutrophil Elastase at approximately 29 kDa. The expected band size for Neutrophil Elastase is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01607-wb7.jpgAnti-Neutrophil Elastase ELANE Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-tubulinyeast-rabbit-monoclonal-antibody-m30932-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/3/M30932-TUB1-primary-antibodies-WB-testing-1.jpgAnti-alpha Tubulin (yeast) TUB1 Rabbit Monoclonal AntibodyWestern blot analysis of alpha Tubulin expression in Saccharomyces cerevisiae (yeast) cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-glutamine-synthetase-rabbit-monoclonal-antibody-m03191-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-wb7.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-wb.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyWestern blot analysis of Glutamine Synthetase expression in (1)Jurkat cell lysate;(2) HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc9.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human glioblastoma, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc10.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human prostate cancer, using the Antibody at 1:250 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc7.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat kidney, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc11.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse ovary, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc8.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:400 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-ihc.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Glutamine Synthetase Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03191-icc1.jpgAnti-Glutamine Synthetase GLUL Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-2-microglobulin-rabbit-monoclonal-antibody-m00456-1-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00456-1-b2m-primary-antibodies-wb-testing-1.jpgAnti-beta 2 Microglobulin B2M Rabbit Monoclonal AntibodyWestern blot analysis of Beta-2 Microglobulin/B2M using anti-Beta-2 Microglobulin/B2M antibody (M00456-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human U937 whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human THP-1 whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Beta-2 Microglobulin/B2M antigen affinity purified monoclonal antibody (M00456-1) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Beta-2 Microglobulin/B2M at approximately 12 kDa. The expected band size for Beta-2 Microglobulin/B2M is at 14 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alkaline-phosphatase-rabbit-monoclonal-antibody-m01008-1-boster.html2026-04-06T05:04:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01008-1-alpl-primary-antibodies-wb-testing-1_1.jpgAnti-Alkaline Phosphatase ALPL Rabbit Monoclonal Antibody Western blot analysis of ALPL using anti-ALPL antibody (M01008-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat spleen tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALPL antigen affinity purified monoclonal antibody (Catalog # M01008-1) at 1:5000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ALPL at approximately 80 kDa. The expected band size for ALPL is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01008-1-ihc.jpgAnti-Alkaline Phosphatase ALPL Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Alkaline Phosphatase Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01008-1-if.jpgAnti-Alkaline Phosphatase ALPL Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Alkaline Phosphatase Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pi-3-kinase-p85-beta-rabbit-monoclonal-antibody-m03363-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-wb7.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-icc2.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-wb8.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-wb.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyWestern blot analysis of PI 3 Kinase p85 beta expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-icc1.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03363-ihc.jpgAnti-PI 3 Kinase p85 beta PIK3R2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using PI 3 Kinase p85 beta Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tyrosine-hydroxylase-rabbit-monoclonal-antibody-m01917-1-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-wb10.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-wb7.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-wb.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyWestern blot analysis of Tyrosine Hydroxylase expression in PC-3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-wb8.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-wb9.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-ihc.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using Tyrosine Hydroxylase Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-1-if.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyImmunofluorescent analysis of PC-12 cells, using Tyrosine Hydroxylase Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pi3-kinase-p110-beta-rabbit-monoclonal-antibody-m01091-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01091-pik3cb-primary-antibodies-wb-testing-1.jpgAnti-PI3 Kinase p110 beta PIK3CB Rabbit Monoclonal Antibody Western blot analysis of PIK3CB using anti-PIK3CB antibody (M01091). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human MCF-7 whole cell lysates,<br>
Lane 5: human HEL whole cell lysates,<br>
Lane 6: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3CB antigen affinity purified monoclonal antibody (Catalog # M01091) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIK3CB at approximately 110 kDa. The expected band size for PIK3CB is at 123 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myosin-light-chain-2-rabbit-monoclonal-antibody-m03215-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03215-wb7.jpgAnti-Myosin Light Chain 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03215-ihc.jpgAnti-Myosin Light Chain 2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human heart, using Myosin Light Chain 2 Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03215-wb8.jpgAnti-Myosin Light Chain 2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03215-wb.jpgAnti-Myosin Light Chain 2 Rabbit Monoclonal AntibodyWestern blot analysis of Myosin Light Chain 2 expression in Mouse heart lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tyrosine-hydroxylase-rabbit-monoclonal-antibody-m01917-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-th-primary-antibodies-wb-testing-1.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal Antibody Western blot analysis of TH using anti-TH antibody (M01917). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TH antigen affinity purified monoclonal antibody (M01917) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TH at approximately 59 kDa. The expected band size for TH is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-ihc.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain, using Tyrosine Hydroxylase Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-icc1.jpgAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01917-th-primary-antibodies-if-testing-1.jpg.pngAnti-Tyrosine Hydroxylase TH Rabbit Monoclonal AntibodyIF analysis of TH using anti-TH antibody (M01917). <br>
TH was detected in an immunocytochemical section of mouse brain tissue. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:200 rabbit anti-TH Antibody (M01917) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 45 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myelin-basic-protein-rabbit-monoclonal-antibody-m00211-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00211-wb7.jpgAnti-Myelin Basic Protein MBP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00211-ihc.jpgAnti-Myelin Basic Protein MBP Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human brain, using Myelin Basic Protein Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00211-wb8.jpgAnti-Myelin Basic Protein MBP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00211-wb.jpgAnti-Myelin Basic Protein MBP Rabbit Monoclonal AntibodyWestern blot analysis of Myelin Basic Protein expression in Human fetal brain lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bovine-serum-albumin-rabbit-monoclonal-antibody-m01245-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-10020_2025_1301_fig2_html.pngAnti-Albumin Rabbit Monoclonal AntibodyFCGR2B were up-regulated in hippocampus of DM mice. A qRT-PCR was performed to detect the expression of ALB, AREG and FCGR2B mRNA expression in hippocampus of mice. B Western blot was conducted to detect the ALB, AREG and FCGR2B protein expression in hippocampus of mice. C IHC assay was employed to examine the ALB, AREG and FCGR2B protein expression in hippocampus of mice. D IF staining was utilized to detect the expression of FCGR2B and NeuN in hippocampus of mice. E Western blot was performed to detect the SHC1 protein expression in hippocampus of mice. F IF staining was performed to detect the expression of SHC1 and NeuN in hippocampus of mice. G Western blot was used to detect the p-PI3K and p-AKT protein expression in hippocampus of mice. *** P < 0.001 Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01301-7'>40537751</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-albumin-primary-antibodies-wb-testing-1.jpgAnti-Albumin Rabbit Monoclonal AntibodyWestern blot analysis of Albumin using anti-Albumin antibody (M01245). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat blood lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: mouse blood lysates,<br>
Lane 4: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Albumin antigen affinity purified monoclonal antibody (M01245) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Albumin at approximately 69 kDa. The expected band size for Albumin is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-ihc.jpgAnti-Albumin Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Serum Albumin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-albumin-primary-antibodies-wb-testing-2.pngAnti-Albumin Rabbit Monoclonal AntibodyWestern blot analysis of Albumin using anti-Albumin antibody (M01245). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1-2: Human keratinocytes isolated from skin.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Albumin antigen affinity purified monoclonal antibody (M01245) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate with ChemiDoc MP system. A specific band was detected for Albumin at approximately 69 kDa. The expected band size for Albumin is at 69 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-clathrin-heavy-chain-rabbit-monoclonal-antibody-m03134-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-cltc-primary-antibodies-ihc-testing-2.jpgAnti-Clathrin heavy chain Rabbit Monoclonal Antibody IHC analysis of CLTC using anti-CLTC antibody (M03134). <br>
CLTC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CLTC Antibody (M03134) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-cltc-primary-antibodies-wb-testing-1.jpgAnti-Clathrin heavy chain Rabbit Monoclonal Antibody Western blot analysis of CLTC using anti-CLTC antibody (M03134). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates.<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat kidney tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLTC antigen affinity purified monoclonal antibody (Catalog # M03134) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CLTC at approximately 192 kDa. The expected band size for CLTC is at 192 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-cltc-primary-antibodies-ihc-testing-3.jpgAnti-Clathrin heavy chain Rabbit Monoclonal Antibody IHC analysis of CLTC using anti-CLTC antibody (M03134). <br>
CLTC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CLTC Antibody (M03134) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-icc1.jpgAnti-Clathrin heavy chain Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-cltc-primary-antibodies-ihc-testing-4.jpgAnti-Clathrin heavy chain Rabbit Monoclonal Antibody IHC analysis of CLTC using anti-CLTC antibody (M03134). <br>
CLTC was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CLTC Antibody (M03134) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-cltc-primary-antibodies-ihc-testing-5.jpgAnti-Clathrin heavy chain Rabbit Monoclonal Antibody IHC analysis of CLTC using anti-CLTC antibody (M03134). <br>
CLTC was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CLTC Antibody (M03134) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-icc2.jpgAnti-Clathrin heavy chain Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tgf-beta-receptor-ii-rabbit-monoclonal-antibody-m00759-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00759-wb7.jpgAnti-TGF beta Receptor II TGFBR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00759-wb8.jpgAnti-TGF beta Receptor II TGFBR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00759-wb.jpgAnti-TGF beta Receptor II TGFBR2 Rabbit Monoclonal AntibodyWestern blot analysis of TGF beta Receptor II expression in A549 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nf-kappa-b-p105-p50-rabbit-monoclonal-antibody-m00283-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00283-nfkb1-primary-antibodies-wb-testing-1.jpgAnti-NF-Kappa B (p105/p50) NFKB1 Rabbit Monoclonal Antibody Western blot analysis of NF-κB p105/p50 using anti-NF-κB p105/p50 antibody (M00283). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human SiHa whole cell lysates, <br>
Lane 4: human CACO-2 whole cell lysates, <br>
Lane 5: rat PC-12 whole cell lysates, <br>
Lane 6: rat NRK whole cell lysates, <br>
Lane 7: mouse NIH/3T3 whole cell lysates, <br>
Lane 8: mouse RAW264.7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NF-κB p105/p50 antigen affinity purified monoclonal antibody (M00283) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NF-κB p105/p50 at approximately 50, 105 kDa. The expected band size for NF-κB p105/p50 is at 50, 105 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00283-ihc.jpgAnti-NF-Kappa B (p105/p50) NFKB1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human kidney, using NF-κB p105/p50 Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lactate-dehydrogenase-rabbit-monoclonal-antibody-m00825-boster.html2026-03-24T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00825-ldha-primary-antibodies-wb-testing-1.jpgAnti-Lactate Dehydrogenase LDHA Rabbit Monoclonal Antibody Western blot analysis of LDHA using anti-LDHA antibody (M00825). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LDHA antigen affinity purified monoclonal antibody (Catalog # M00825) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LDHA at approximately 37 kDa. The expected band size for LDHA is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00825-ldha-primary-antibodies-wb-testing-2_1.jpgAnti-Lactate Dehydrogenase LDHA Rabbit Monoclonal AntibodyWestern blot analysis of LDHA using anti-LDHA antibody (M00825). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: rat lung tissue lysates,<br>
Lane 6: mouse liver tissue lysates,<br>
Lane 7: mouse lung tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LDHA antigen affinity purified monoclonal antibody (M00825) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LDHA at approximately 36 kDa. The expected band size for LDHA is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00825-ldha-primary-antibodies-ihc-testing-2.jpgAnti-Lactate Dehydrogenase LDHA Rabbit Monoclonal Antibody IHC analysis of LDHA using anti-LDHA antibody (M00825). <br>
LDHA was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-LDHA Antibody (M00825) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pi-3-kinase-p85-alpha-rabbit-monoclonal-antibody-m00318-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00318-wb7.jpgAnti-PI 3 Kinase p85 alpha PIK3R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00318-wb10.jpgAnti-PI 3 Kinase p85 alpha PIK3R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00318-wb8.jpgAnti-PI 3 Kinase p85 alpha PIK3R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00318-wb.jpgAnti-PI 3 Kinase p85 alpha PIK3R1 Rabbit Monoclonal AntibodyWestern blot analysis of PI 3 Kinase p85 alpha expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00318-wb9.jpgAnti-PI 3 Kinase p85 alpha PIK3R1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pi-3-kinase-p55-gamma-rabbit-monoclonal-antibody-m06707-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-pik3r3-primary-antibodies-wb-testing-1.jpgAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyWestern blot analysis of PIK3R3 using anti-PIK3R3 antibody (M06707). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human Raji whole cell lysates,<br>
Lane 3: human Daudi whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3R3 antigen affinity purified monoclonal antibody (M06707) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIK3R3 at approximately 50 kDa. The expected band size for PIK3R3 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-41598_2025_97643_fig8_html.pngAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyDetermination of the relative gene expression. The levels of PIK3R3, AKT2, TGF-β1, E-cadherin, MMP2, TIMP2, BAD, BCL-2, and COLI were detected by qPCR after myopia induction. Significance refers to comparisons of the LIM group to the NC group (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). N = 3. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-97643-7'>40216914</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-41598_2025_97643_fig9_html.pngAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyThe relevant protein expression measured by western blot analysis. After 2- and 4-week myopia induction, expression of PIK3R3 and p-AKT2 ( A ), BAD and BCL-2 ( B ), TGF-β1 and E-cadherin ( C ), and COLI ( D ) in the sclera of the guinea pigs in the NC and LIM groups were detected by western blot analysis. Significance refers to comparisons of the LIM group to the NC group (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). N = 4. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-97643-7'>40216914</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-ihc7.jpgAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-ihc8.jpgAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody at 1:200 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-ihc9.jpgAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody at 1:800 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06707-if.jpgAnti-PI 3 Kinase p55 gamma PIK3R3 Rabbit Monoclonal AntibodyImmunofluorescent analysis of C6 cells, using PI 3 Kinase p55 gamma Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-progesterone-receptor-rabbit-monoclonal-antibody-m00541-1-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00541-1-pgr-primary-antibodies-wb-testing-1.jpgAnti-Progesterone Receptor PGR Rabbit Monoclonal AntibodyWestern blot analysis of PGR using anti-PGR antibody (M00541-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human T-47D whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGR antigen affinity purified monoclonal antibody (M00541-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PGR at approximately 118 kDa. The expected band size for PGR is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00541-1-pgr-primary-antibodies-ihc-testing-1.jpgAnti-Progesterone Receptor PGR Rabbit Monoclonal AntibodyIHC analysis of PGR using anti-PGR antibody (M00541-1). <br>PGR was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PGR Antibody (M00541-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-endothelin-b-receptor-rabbit-monoclonal-antibody-m01041-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01041-wb.jpgAnti-Endothelin B Receptor EDNRB Rabbit Monoclonal AntibodyWestern blot analysis of Endothelin B Receptor expression in 293T cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-topoisomerase-ii-alpha-rabbit-monoclonal-antibody-m00953-1-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00953-1-wb.jpgAnti-Topoisomerase II alpha TOP2A Rabbit Monoclonal AntibodyWestern blot analysis of Topoisomerase II alpha expression in (1) HeLa cell lysate; (2) Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00953-1-ihc.jpgAnti-Topoisomerase II alpha TOP2A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon cancer, using Topoisomerase II alpha Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cytokeratin-5-c-term-rabbit-monoclonal-antibody-m00398-2-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-2-krt5-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 5 (C-term) KRT5 Rabbit Monoclonal AntibodyWestern blot analysis of KRT5 using anti-KRT5 antibody (M00398-2). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: rat skin tissue lysates,<br>
Lane 4: mouse skin tissue lysates,<br>
Lane 5: mouse thymus tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT5 antigen affinity purified monoclonal antibody (M00398-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT5 at approximately 62 kDa. The expected band size for KRT5 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-2-krt5-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 5 (C-term) KRT5 Rabbit Monoclonal AntibodyIHC analysis of KRT5 using anti-KRT5 antibody (M00398-2). <br>KRT5 was detected in a paraffin-embedded section of human skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-2-krt5-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 5 (C-term) KRT5 Rabbit Monoclonal AntibodyIHC analysis of KRT5 using anti-KRT5 antibody (M00398-2). <br>KRT5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-2-krt5-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 5 (C-term) KRT5 Rabbit Monoclonal AntibodyIHC analysis of KRT5 using anti-KRT5 antibody (M00398-2). <br>KRT5 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00398-2-krt5-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 5 (C-term) KRT5 Rabbit Monoclonal AntibodyIHC analysis of KRT5 using anti-KRT5 antibody (M00398-2). <br>KRT5 was detected in a paraffin-embedded section of rat skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-KRT5 Antibody (M00398-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-beta-synuclein-rabbit-monoclonal-antibody-m00215-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00215-snca-b-primary-antibodies-wb-testing-1.jpgAnti-alpha + beta Synuclein SNCA Rabbit Monoclonal AntibodyWestern blot analysis of SNCA/B using anti-SNCA/B antibody (M00215). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNCA/B antigen affinity purified monoclonal antibody (M00215) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SNCA/B at approximately 18 kDa. The expected band size for SNCA/B is at 18 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-active-pro-caspase-3-rabbit-monoclonal-antibody-m00334-4-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-4-ihc8.jpgAnti-active + pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human melanoma, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-4-casp3-primary-antibodies-wb-testing-1.jpgAnti-active + pro Caspase 3 CASP3 Rabbit Monoclonal Antibody Western blot analysis of CASP3 using anti-CASP3 antibody (M00334-4). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat liver tissue lysates,<br>
Lane 6: rat spleen tissue lysates,<br>
Lane 7: mouse liver tissue lysates,<br>
Lane 8: mouse spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CASP3 antigen affinity purified monoclonal antibody (Catalog # M00334-4) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CASP3 at approximately 17,35 kDa. The expected band size for CASP3 is at 17,35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-4-ihc9.jpgAnti-active + pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human colon, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-4-ihc7.jpgAnti-active + pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human lung large cell cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00334-4-ihc.jpgAnti-active + pro Caspase 3 CASP3 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using active + pro Caspase 3 Antibody .
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k4-rabbit-monoclonal-antibody-p12477-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-wb.jpgAnti-Histone H3 (acetyl K4) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (acetyl K4) expression in HeLa+TSA cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-estrogen-receptor-beta-rabbit-monoclonal-antibody-m00786-1-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00786-1-esr2-primary-antibodies-wb-testing-1.jpgAnti-Estrogen Receptor beta ESR2 Rabbit Monoclonal Antibody Western blot analysis of ESR2 using anti-ESR2 antibody (M00786-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ESR2 antigen affinity purified monoclonal antibody (Catalog # M00786-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ESR2 at approximately 59 kDa. The expected band size for ESR2 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00786-1-zoolstud-57-041-g006.jpgAnti-Estrogen Receptor beta ESR2 Rabbit Monoclonal AntibodyImmuno-expression of AR (A:3.5yr.) and ERβ (B: 0.1yr., C: 3.5yr.
and D: 8yr.) in testes. Scale bar = 50 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6517756/&orig_host=www.ncbi.nlm.nih.gov'>31966281</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00786-1-ihc.jpgAnti-Estrogen Receptor beta ESR2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human cervix cancer, using Estrogen Receptor beta Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00786-1-wb9.jpgAnti-Estrogen Receptor beta ESR2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-67kda-laminin-receptor-rabbit-monoclonal-antibody-m01691-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01691-rpsa-primary-antibodies-wb-testing-1.jpgAnti-67kDa Laminin Receptor RPSA Rabbit Monoclonal Antibody Western blot analysis of 67kDa Laminin Receptor using anti-67kDa Laminin Receptor antibody (M01691). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human COLO320 whole cell lysates,<br>
Lane 5: mouse liver tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-67kDa Laminin Receptor antigen affinity purified monoclonal antibody (Catalog # M01691) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for 67kDa Laminin Receptor at approximately 40 kDa. The expected band size for 67kDa Laminin Receptor is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01691-wb7.jpgAnti-67kDa Laminin Receptor RPSA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01691-wb.jpgAnti-67kDa Laminin Receptor RPSA Rabbit Monoclonal AntibodyWestern blot analysis of 67kDa Laminin Receptor expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate; (3) PC-12 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phd1-prolyl-hydroxylase-rabbit-monoclonal-antibody-m03015-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03015-41598_2024_80160_fig5_html.pngAnti-PHD1/prolyl hydroxylase Rabbit Monoclonal AntibodyMT1G overexpression in GC cell line intervenes in GPX4/SQSTM1 axis to initiate iron autophagy. ( a ) Comparison of protein associations between TCGA non cancerous tissue and gastric cancer tissue. ( b ) Correlation heatmap between MT1G and GPX4/SQSTM1 axis related proteins. ( c ) The expression status of GPX4/SQSTM1 axis related proteins in the high and low expression queue of gastric adenocarcinoma. ( d ) The expression of GPX4/SQSTM1 axis related proteins in different GC cell lines. ( e ) The ratio of GPX4 protein expression in different GC cell lines. ( f ) The expression of SQSTM1 protein in different GC cell lines. ( g ) The expression of ARNTL protein in different GC cell lines. ( h ) The expression of EGLN2 protein in different GC cell lines. ( i ) Co-IP detection of the correlation between SQSTM1 and ARNTL in GC cell lines. * p < 0.05; ** p < 0.01; *** p < 0.001.The original images for western blot analysis were shown in “Supplementary information”. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-80160-4'>39558129</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03015-41598_2024_80160_fig6_html.pngAnti-PHD1/prolyl hydroxylase Rabbit Monoclonal AntibodyIntervention of GPX4 blocks ferroptosis induced by MT1G overexpression. ( a ) The CCK-8 method was used to detect the survival of GC cells intervened with DFOM for 24 h. ( b ) The CCK-8 method was used to detect the survival of GC cells intervened with RSL3 for 24 h. ( c ) The CCK-8 method was used to detect the survival of GC cells intervened with Fer-1 for 24 h. ( d ) The effects of different ferroptosis inhibitors on the activity of GC cells. ( e ) RT-qPCR was used to examine the effects of small molecule compounds RSL3 and Fer-1 on MT1G transfection. ( f ) The effects of small molecule compounds RSL3 and Fer-1 on GPX4 protein expression in different GC cell lines. ( g ) Statistical analysis of GPX4 protein expression in different cell lines. ( h ) The effect of small molecule compound Fer-1 on the expression of GPX4/SQSTM1 axis protein. ( i ) The expression of GPX4 protein in different GC cell lines. ( j ) The expression of SQSTM1 protein in different GC cell lines. ( k ) The expression of ARNTL protein in different GC cell lines. ( l ) The expression of EGLN2 protein in different GC cell lines. ( m ) Fluorescence expression of different GC cell lines JC-1. Scale bar = 50 μm. ( n ) Fluorescence statistics of different GC cell lines JC-1. ( o ) MDA expression in different GC cell lines. ( p ) SOD expression in different GC cell lines. ( q ) The expression of GSH in different GC cell lines. * p < 0.05; ** p < 0.01; *** p < 0.001.The original images for western blot analysis were shown in “Supplementary information”. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-024-80160-4'>39558129</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03015-egln2-primary-antibodies-wb-testing-1.jpgAnti-PHD1/prolyl hydroxylase Rabbit Monoclonal AntibodyWestern blot analysis of PHD1/EGLN2 using anti-PHD1/EGLN2 antibody (M03015). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human SIHA whole cell lysates,<br>
Lane 4: human RT4 whole cell lysates,<br>
Lane 5: rat testis tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse testis tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHD1/EGLN2 antigen affinity purified monoclonal antibody (M03015) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PHD1/EGLN2 at approximately 48 kDa. The expected band size for PHD1/EGLN2 is at 44 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sodium-potassium-atpase-rabbit-monoclonal-antibody-m00956-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-wb7.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-wb8.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-wb9.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc7.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat cerebral cortex, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc8.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Rat heart, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc9.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human cervical cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc10.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Human thyroid cancer, using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc11.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded Mouse skeletal muscle - gastrocnemius , using the Antibody at 1:100 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-ihc.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human thyroid carcinoma, using Sodium Potassium ATPase Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00956-icc1.jpgAnti-Sodium Potassium ATPase ATP1A1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-maltose-binding-protein-rabbit-monoclonal-antibody-m30934-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30934-wb.jpgAnti-Maltose Binding Protein malE Rabbit Monoclonal AntibodyWestern blot analysis of Maltose Binding Protein expression in E.coli lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k56-rabbit-monoclonal-antibody-p12477-1-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-1-icc1.jpgAnti-Histone H3 (acetyl K56) HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-1-ihc.jpgAnti-Histone H3 (acetyl K56) HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Histone H3 (acetyl K56) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-1-icc2.jpgAnti-Histone H3 (acetyl K56) HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-1-if.jpgAnti-Histone H3 (acetyl K56) HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis of Hela cells, using Histone H3 (acetyl K56) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-1-wb.jpgAnti-Histone H3 (acetyl K56) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (acetyl K56) expression in C6 cell lysate, treated with TSA.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k14-rabbit-monoclonal-antibody-p12477-2-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-wb-testing-1_1.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody Western blot analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates,<br>
Lane 2: human U2OS whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: mouse brain tissue lysates,<br>
Lane 7: mouse heart tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 (acetyl K14) antigen affinity purified monoclonal antibody (P12477-2) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H3 (acetyl K14) at approximately 17 kDa. The expected band size for Histone H3 (acetyl K14) is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-3.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-4.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-5.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-6.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-7.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-8.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-9.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-10.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-11.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-12.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12477-2-histone-h3-primary-antibodies-ihc-testing-13_1.jpgAnti-Histone H3 (acetyl K14) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K14) using anti-Histone H3 (acetyl K14) antibody (P12477-2). <br>Histone H3 (acetyl K14) was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K14) Antibody (P12477-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-somatostatin-receptor-2-rabbit-monoclonal-antibody-m01689-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01689-sstr2-primary-antibodies-wb-testing-1.jpgAnti-Somatostatin Receptor 2 SSTR2 Rabbit Monoclonal Antibody Western blot analysis of SSTR2 using anti-SSTR2 antibody (M01689). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human SH-SY5Y whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SSTR2 antigen affinity purified monoclonal antibody (Catalog # M01689) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SSTR2 at approximately 41 kDa. The expected band size for SSTR2 is at 41 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-maltose-binding-protein-rabbit-monoclonal-antibody-m30934-1-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30934-1-wb.jpgAnti-Maltose Binding Protein malE Rabbit Monoclonal AntibodyWestern blot analysis of MBP expression in Escherichia coli lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hemoglobin-subunit-alpha-rabbit-monoclonal-antibody-m00233-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00233-hba1-primary-antibodies-wb-testing-1.jpgAnti-Hemoglobin subunit alpha HBA1 Rabbit Monoclonal AntibodyWestern blot analysis of Hemoglobin subunit alpha expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00233-2.jpgAnti-Hemoglobin subunit alpha HBA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human spleen, using hemoglobin subunit alpha Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00233-hba1-primary-antibodies-ihc-testing-3.jpgAnti-Hemoglobin subunit alpha HBA1 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse embryo tissue using anti-Hemoglobin subunit alpha antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-acetyl-k20-rabbit-monoclonal-antibody-p12718-boster.html2026-03-24T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12718-wb.jpgAnti-Histone H2B (acetyl K20) HIST1H2BB Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B (acetyl K20) expression in Hela cell treated with TSA lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/1/p12718-ihc.jpgAnti-Histone H2B (acetyl K20) HIST1H2BB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Histone H2B (acetyl K20) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-smooth-muscle-actin-rabbit-monoclonal-antibody-m01072-1-boster.html2026-03-25T05:22:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-sma-primary-antibodies-wb-testing-1_1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody Western blot analysis of ACTA2 using anti-ACTA2 antibody (M01072-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: human Caco-2 whole cell lysates,<br>
Lane 6: human SH-SY5Y whole cell lysates,<br>
Lane 7: human U251 whole cell lysates,<br>
Lane 8: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACTA2 antigen affinity purified monoclonal antibody (Catalog # M01072-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACTA2 at approximately 42 kDa. The expected band size for ACTA2 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-sma-primary-antibodies-wb-review-2.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyWestern blot analysis of ACTA2 using anti-ACTA2 antibody (M01072-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: cardiac tissue lysayes from 3-month-old mouse,<br>
Lane 2: cardiac tissue lysayes from 6-month-old mouse,<br>
Lane 3: cardiac tissue lysayes from 12-month-old mouse,<br>
Lane 4: cardiac tissue lysayes from 18-month-old mouse.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACTA2 antigen affinity purified monoclonal antibody (Catalog # M01072-1) at 1:2000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) withChemiDoc MP system. A specific band was detected for ACTA2 at approximately 42 kDa. The expected band size for ACTA2 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-6.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(H) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, and HIF-1α in LX-2 cells was analyzed using western blotting.
(I) Immunofluorescence double staining of α-SMA and HIF-1α in TGF-β1-stimulated and DMSO or AZD8055-treated LX-2 cells transducted with LV-control-shRNA or LV-4EBP1-shRNA (×400 magnification).
(L and M) (L) The apoptosis of LX-2 cells determined using flow cytometry and (M) percentages of apoptotic cells (early and late apoptotic cells). NC, LV-control-shRNA; KD, LV-4EBP1-shRNA. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-3.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(A) Illustration of AAV transduction and BDL administration in mouse models.
(B) Images of H&E, Masson’s trichrome, Sirius red, and IHC of α-SMA and vimentin staining of representative liver sections (×200 magnification).
(C) Representative Masson and Sirius red staining of liver tissues and positive content (%) of α-SMA.
and vimentin staining (n = 5).
(D and E) Serum (D) ALT, AST, TBIL, DBIL, and (E) TGF-β1, IL-6 in each group.
(F) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in liver tissues was analyzed using western blotting.
(G) Immunofluorescence double staining of α-SMA and HIF-1α in the liver sections of mice (×100 magnification). The arrowheads represent colocalization of staining.
(H) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; BDL, bile duct ligation; DAPI, 4′,6-diamidino-2-phenylindole; DBIL, direct bilirubin; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin-eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, Interleukin 6; TBIL, total bilirubin; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-ihc.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using alpha smooth muscle Actin Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-2.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(A) Illustration of adeno-associated virus,AAV transduction and CCl4 administration in mice models.
(B and C) RT-qPCR analysis of 4ebp1-4A levels and (C) western blotting analysis of FLAG-tagged protein levels with saline, AAV2/8-scramble, or AAV2/8-4ebp1-4A-3xflag administration.
(D) Images of H&E, Masson’s trichrome, Sirius red, and IHC of α-SMA and vimentin staining of representative liver sections (×200 magnification).
(E) Representative Masson and Sirius red staining of liver tissues and positive content (%) of α-SMA.
and vimentin staining (n = 5).
(F and G) Serum (F) ALT, AST and (G) TGF-β1, IL-6 in each group.
(H) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in liver tissues analyzed using western blotting.
(I) Immunofluorescence double staining of α-SMA and HIF-1α in the liver sections of mice (×100 magnification). The arrow heads represent colocalization of staining.
(J) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin and eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, interleukin 6; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-13020_2025_1109_fig7_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyQG promotes ferroptosis of HSCs and inhibits HSCs activation through MARCHF8 mediated ubiquitination of GPX4. (A-C) Primary mouse HSCs were divided into control + shNC, control + shMARCHF8, QG + shNC, and QG + shMARCHF8 groups. A MFI of intracellular C-AM was determined by flow cytometry. B Lipid ROS was detected by flow cytometry. C LDH activity was detected. * P < 0.05, ** P < 0.01, *** P < 0.001. D–E TGF-β1-treated primary mouse HSCs were divided into control + shNC, control + shMARCHF8, QG + shNC, and QG + shMARCHF8 groups. D Positive expression of α-SMA was detected by immunofluorescence staining (scale bar, 40 μm). E The mRNA levels of ACTA2, LAMA1, COLlA1, and FN1 were detected by qRT-PCR. * P < 0.05, ** P < 0.01 vs shNC + Control. # P < 0.05 vs shMARCHF8 + Control Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-025-01109-x'>40524220</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-if.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyImmunofluorescent analysis of A431 cells, using alpha smooth muscle Actin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-13020_2025_1109_fig3_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyQG inhibits TGF-β1-induced HSC activation and promotes HSC death in vitro. A The positive expressions of α-SMA and desmin in liver tissues of control, QG, CCl 4 , CCl 4 + QG group mice or NCD, NCD + QG, HFHCD, HFHCD + QG group mice were detected by immunohistochemical staining (scale bar, 100 μm). B–C Primary mouse HSCs or LX-2 cells were divided into control, TGF-β1, TGF-β1 + QG-L, TGF-β1 + QG-M, and TGF-β1 + QG-H groups. B Positive expression of α-SMA was detected by immunofluorescence staining (scale bar, 40 μm). C The mRNA levels of ACTA2, LAMA1, COLlA1, and FN1 were detected by qRT-PCR. * P < 0.05, ** P < 0.01, *** P < 0.001 vs control; # P < 0.05, ## P < 0.01 vs TGF-β1. D Primary mouse HSCs or LX-2 cells were divided into control and QG groups. The LDH activity was detected. * P < 0.05 vs control Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-025-01109-x'>40524220</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-ijmsv17p0137g003.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyEnhanced expression of α-SMA, CTGF and Col1 by TGF-β1 . RT-qPCR revealing the enhanced transcription of α-SMA ( A ), CTGF ( B ) and Col1A1 mRNAs ( C ) in PSCs and HP-1 cells by TGF-β1 but not PDGF; Western blot showing the increased expression of α-SMA, CTGF and Col1 proteins in PSCs and HP-2 cells consistent with their mRNA expression ( D ).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6945563/&orig_host=www.ncbi.nlm.nih.gov'>31929747</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-41598_2022_6848_fig4_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyFer-1 ameliorated MCT-induced haemodynamics, RV hypertrophy and pulmonary vascular remodelling in rats. ( A ) Representative RV pressure curves in the sham, sham + Fer-1, MCT, and MCT + Fer-1 groups. The MCT + Fer-1 group was pretreated with Fer-1 (2 mg/kg/d). ( B ) Bar graph comparing RVSPs in the different groups of rats. ( C ) Fer-1 pretreatment reduced the RV/LV + S ratio of MCT-induced rats. ( D ) Representative image of haematoxylin–eosin (HE) staining showing the expression of α-SMA to compare arteriole wall thickness in the sham, sham + Fer-1, MCT, and MCT + Fer-1 pretreatment groups. ( E ) Quantification of arteriole percent medial thickness. ( F ) The percentage of muscularization is shown by staining for α-SMA. The data represent the means ± SD. # P > 0.05 versus the sham group, * P < 0.05 versus the sham group, ** P < 0.05 versus the MCT group. n = 8–12/group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-022-06848-7'>35197507</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12929_2024_1040_fig3_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyPDGFRB somatic mutation induce phenotypic modulation in SMCs. Immunostaining reveals the expression levels of smooth muscle markers (a-SMA and SM22a) and inflammatory markers (VCAM1, ICAM1, MMP1 and MMP9) in HBVSMCs transfected with different viruses (Control: vector; Wild Type: PDGFRB; Y562D: PDGFRB Y562D ) ( a ). The relative density of immunoblot bands about markers shown in ( A ) were display ( B ) (normalized to those in cells transfected with vector viruses). RT-qPCR ( C ) of SMCs markers (α-SMA and SM22α) and inflammatory markers (VCAM-1, ICAM1, MMP-9 and MMP-1) in HBVSMCs underwent different treatments. Student's t-test and Benjamini–Hochberg correction are employed to assess the statistical significance. Edu assay exhibit the proliferation ability of HBVSMCs under different treatment conditions ( D ). Statistical analysis of the proportion of Edu-positive cells in the different groups from 5 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is used for statistical differences ( E ). Scratch assay displays migratory ability of HBVSMCs underwent different treatment ( F ). Statistical analysis of the rate of wound healing (reduced area at 4H /area at 0H) in the different groups from 9 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is utilized to evaluate the statistical significance. * p adj < 0.05, ** p adj < 0.01, *** p adj < 0.001, **** p adj < 0.0001 ( G ). The above experiments are all repeated three times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12929_2024_1040_fig1_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodySingle-cell transcriptional profiling of intracranial fusiform aneurysmal cells ( A - K ) and multi-color immunofluorescence (mIF) of smooth muscle cells (SMCs) markers and inflammatory markers between intracranial fusiform aneurysms (IFAs) and normal cerebral arteries (NCAs) ( L - M ). T-SNE visualization of intracranial fusiform aneurysmal cells type. Colored according to cell type ( A ). Visualization of specific gene expression patterns related to cell subsets identified in ( A ) using a bubble plot ( B ). T-SNE visualization of VSMC cell clusters. Colored according to clusters ( C ). Visualization of structural protein and inflammation-related genes expression patterns within the subsets of smooth muscle cells identified in ( C ) using a bubble plot ( D ). The violin plots show the expression differences of structural protein genes and inflammatory genes between the contraction subgroup (VSMC5) and the inflammatory subgroup (VSMC6) ( E ). The volcano plot specifically shows the gene expression differences between the two cell groups ( F ). The petal plot displays the GO enrichment analysis results of differential genes between the VSMC5 and VSMC6 ( G ). The bar graph shows the KEGG enrichment analysis results of differential genes between these two cell subsets ( H ). The GSEA enrichment analysis results of differential genes between the two groups. The enrichment results of differential genes related to signaling pathways ( I ). The enrichment results of differential genes related to structural protein genes ( J ). The enrichment results of differential genes related to the process of inflammatory factor secretion ( K ). α-SMA (green, SMCs marker), MMP-9 (blue, inflammatory marker) and ICAM-1 (red, inflammatory marker) in FIAs and NCAs are detected using mIF. Scale bar, 100 μm ( L ). Statistical analysis of mean fluorescence intensity about SMCs marker (α-SMA) and inflammatory markers (ICAM-1 and MMP-9) between NCAs ( n = 4) and FIAs ( n = 5). 'n' represented the number of samples. Three random fields were selected for statistical analysis in each sample, and the average value represented the detection value of this marker in this sample. The Student's t-test is utilized to examine the statistical differences among each marker. ns, no significant; ** p < 0.01, *** p < 0.01 (M). n values indicate number of independent experiments performed <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12964_2024_1481_fig3_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyMacrophage removal alleviated succinate-induced kidney interstitial fibrosis. A F4/80 immunohistochemistry staining showed clodronate liposomes effectively removed kidney interstitial macrophages of mice. B Clodronate liposomes markedly prevented succinate-mediated upregulation of M2-related profibrotic factors in the kidney. *** P < 0.001, versus control group; &&& P < 0.001, versus succinate group, n = 10 in the control group, n = 9 in succinate group and n = 7 in clodronate liposomes group. C Masson and Sirius Red staining ( D ) revealed succinate-induced interstitial fibrosis was alleviated by clodronate liposomes. *** P < 0.001, versus control group; &&& P < 0.001, versus succinate group, n = 10 in control group, n = 9 in succinate group and n = 7 in clodronate liposomes group. E The elevation of protein levels of renal fibronectin and α-SMA was revised by clodronate liposomes. *** P < 0.001, versus control group; &&& P < 0.001, & P < 0.05, versus succinate group, n = 10 in control group, n = 9 in succinate group and n = 7 in clodronate liposomes group <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01481-5'>38291510</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12964_2024_1481_fig1_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodySuccinate induced renal interstitial fibrosis in mice. Male C57 BL/6 mice were fed with special water (containing 4% succinate) for 12w. A Masson and Sirius red. B staining showed succinate induced renal interstitial fibrosis in mice.*** P < 0.001 versus control group, n = 5. C Immunoblotting showed succinate increased renal protein levels of fibronectin and α-SMA. *** P < 0.001 versus control group, n = 5 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01481-5'>38291510</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-fphar-16-1565569-g007.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyEffects of DBT on the expression of α-SMA, FN1, p-SMAD3 and TGF-β1 in rat lung tissue. α-SMA protein expression after (A) 28 and (B) 42 days of DBT administration. FN1 protein expression after (C) 28 and (D) 42 days of DBT administration; n = 4. (E) TGF-β1 and (F) p-SMAD3, n = 5. TGF-β1 protein expression after (G) 28 and (H) 42 days of DBT administration; n = 4 (G, H) , * P < 0.05 or ** P < 0.01; N.S. , not statistically significant, compared with the silica group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2025.1565569/full'>40206091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-13048_2025_1679_fig4_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyYJD affected angiogenesis and oxidative stress in POF rats. ( A ) IHC was performed to detect the expression of CD31 and α-SMA, which is located around growing follicles in the ovaries; Black arrows point to areas of positive staining. ( B ) Average optical density of CD31. ( C ) The average optical density of α-SMA. ( D – H ) Serum levels of the hormones P, E2, FSH, LH, and AMH were examined by ELISA. ( I – J ) Serum levels of indicators of oxidative stress, MDA and SOD, were assessed by ELISA. *** P < 0.001 vs. Control; # P < 0.05, ## P < 0.01, ### P < 0.001 vs. TP; & P < 0.05, && P < 0.01, &&& P < 0.001 vs. TP + M-YJD <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-fphar-13-911945-g006.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyOverexpression of TRIB3 activates lung fibroblasts. (A) Representative images and quantification of the invasion experiment results for mouse lung fibroblasts with or without TRIB3 overexpression. Scale bars, 100 μm. (B) mRNA expression of fibrosis genes in mouse lung fibroblasts with or without TRIB3 overexpression. (C) Representative images and quantification of α-SMA immunostaining in mouse lung fibroblasts with or without TRIB3 overexpression. Scale bars, 50 μm. Data are representative of 3 independent experiments. Data represent means ± SEM Statistical significance: * p < 0.05, ** p < 0.01 or *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9163739/&orig_host=www.ncbi.nlm.nih.gov'>35668944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-sma-primary-antibodies-wb-testing-2_1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody Western blot analysis of ACTA2 using anti-ACTA2 antibody (M01072-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: rat brain tissue lysates,<br>
Lane 4: mouse heart tissue lysates,<br>
Lane 5: mouse lung tissue lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACTA2 antigen affinity purified monoclonal antibody (Catalog # M01072-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACTA2 at approximately 42 kDa. The expected band size for ACTA2 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12964_2024_1481_fig4_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyConditioned medium of macrophages following succinate treatment triggered renal fibroblast proliferation and activation. 500 μM succinate was used to stimulate RAW 264.7 cells for 48 h, and the conditioned medium was collected, centrifuged, and incubated with NRK-49F. A The results of the CCK8 assay and EdU staining displayed that the conditioned medium of the succinate group enhanced NRK-49F proliferation. *** P < 0.001, versus control group, n = 6 in CCK8 and n = 3 in EdU staining, biologically repeated 3 times. B Protein levels of fibronectin and α-SMA were increased by the conditioned medium of the succinate group. *** P < 0.001, versus control group, n = 3, biologically repeated 3 times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01481-5'>38291510</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-ijmsv17p0137g001.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyKey characteristics of the immortalized HP-1 human PSC cell line. Phase contrast microscopy in HP-1 cells after seeding for 12 h ( A ); Double-immunofluorescence labelling using antibodies for SV40 antigen and GFAP, green, localization of SV40 antigen, red, localization of GFAP (B); Immunofluorescence showing the presence of α-SMA ( C ); Double-immunofluorescence labelling for vimentin and desmin. Green, localization of vimentin (D), red, localization of desmin (E), yellow, colocalization of vimentin and desmin (F). (Original magnification × 200 in A ; × 400 in B-F ).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6945563/&orig_host=www.ncbi.nlm.nih.gov'>31929747</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12964_2024_1481_fig5_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodySUCNR1 was required for the effects of succinate on M2 polarization, upregulation of profibrotic factors, and paracrine actions on fibroblasts. RAW 264.7 was transfected with SUCNR1 siRNA for 36 h, and 500 μM succinate was stimulated for 24 h. A SUCNR1 mRNA levels were significantly reduced by SUCNR1 siRNA. &&& P < 0.001, versus succinate group, n = 3, biologically repeated 3 times. B Knockdown of SUCNR1 inhibited the downregulation of proinflammatory M1 cytokines (iNOS and IL6) and upregulation of anti-inflammatory M2 cytokines (Arg1, Fizz1, Mgl2, IL10) ( C ) induced by succinate. *** P < 0.001, versus the control group, &&& P < 0.001, versus the succinate group, n = 3, biologically repeated 3 times. D The elevated profibrotic factors were also restored by SUCNR1 siRNA. *** P < 0.001, versus the control group, &&& P < 0.001, versus the succinate group, n = 3, biologically repeated 3 times. E The proliferative effects of the conditioned medium in the succinate group were abolished by SUCNR1 siRNA. *** P < 0.001, versus the control group, &&& P < 0.001, versus the succinate group, n = 6, biologically repeated 3 times. F The enhanced protein expressions of fibronectin and α-SMA were reduced by SUCNR1 siRNA. *** P < 0.001, versus the control group, &&& P < 0.001, versus the succinate group, n = 3, biologically repeated 3 times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01481-5'>38291510</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-ajtr0011-0641-f1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyGRP78 is upregulated in hypoxic rat PASMCs. A. The purity of PASMCs was identified by αSMA immunofluorescence staining (magnification, × 200). B. GRP78 protein expression in PASMCs treated with different oxygen concentrations. C. GRP78 protein expression in PASMCs treated with the indicated times of hypoxia. D. Immunofluorescence staining of GRP78 visually verified ERS changes under hypoxia and normoxia. Data are shown as the mean ± SEM; n = 3. *P < 0.05, **P < 0.01. *compared with the normoxia group or 0 h time point; 0 h was considered to be a control point, which was compared with all of the other time points.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6413268/&orig_host=www.ncbi.nlm.nih.gov'>30899368</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-12964_2024_1481_fig6_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyCTGF neutralizing antibody inhibited the stimulation of fibroblasts by macrophage-conditioned medium. A CTGF antibody prevented the proliferative effects of CM on NRK-49F, indicated by the results of the CCK8 assay. *** P < 0.001, versus control group, n = 6 in CCK8, biologically repeated 3 times. B Also, the CTGF antibody suppressed the activation effects of CM on NRK-49F, as indicated by the results of the protein quantitative analysis of fibronectin and α-SMA. *** P < 0.001, versus control group, &&& P < 0.001, versus the succinate group, n = 3, biologically repeated 3 times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01481-5'>38291510</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-13020_2025_1109_fig4_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyQG promotes ferroptosis of HSCs and inhibits HSC activation in vitro. A, B Primary mouse HSCs or Hpys were divided into control and QG groups. A MFI of intracellular C-AM was determined by flow cytometry. B Lipid ROS were detected by flow cytometry. ** P < 0.01 vs control. C Primary mouse HSCs were divided into control, QG, QG + Fer-1, QG + zVAD, and QG + Nec-1 groups. LDH activity was detected. ** P < 0.01 vs control or QG. D–F Mouse primary HSCs were divided into control, TGF-β1, TGF-β1 + QG, and TGF-β1 + QG + Fer-1 groups. The QG-induced ferroptosis was confirmed by utilizing FerroOrange staining ( D ) and BODIPY C11 staining ( E ). F The mRNA levels of ACTA2, LAMA1, COLlA1 and FN1 were detected by qRT-PCR. ** P < 0.01, *** P < 0.001 vs control; ## P < 0.01, ### P < 0.001 vs TGF-β1; & P < 0.05 vs TGF-β1 + QG Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-025-01109-x'>40524220</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-fphar-13-911945-g001.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyTRAF6 expression in lung fibroblasts is negatively correlated with PF progression. (A) Western blot analysis of TRAF6 expression in the lungs of mice following BLM induction. (B) Correlation analysis between TRAF6 expression in the lungs of PF mice and respiratory system compliance (Crs) in mice. Each point represents the value of one mouse. Spearman’s rank correlation test was employed to determine statistical significance. (C) Correlation analysis between TRAF6 expression and Acta2 expression in the lungs of PF mice. Each point represents the value of one mouse. Spearman’s rank correlation test was employed to determine statistical significance. (D) Western blot analysis of TRAF6 expression in lung fibroblasts isolated from the lungs of mice following BLM induction. (E) Masson staining was performed to evaluate fibrotic changes in the indicated mice (Group 1: BLM + Lenti-Ctrl, Group 2: BLM + Lenti-Traf6; n = 5 per group). Scale bars, 100 μm. Crs (F) and hydroxyproline content in the right lung (G) were assessed to evaluate pulmonary fibrosis and lung function (Group 1: BLM + Lenti-Ctrl, Group 2: BLM + Lenti-Traf6; n = 5 per group). Data are representative of 3 independent experiments. Data represent means ± SEM Statistical significance: * p < 0.05 or ** p < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9163739/&orig_host=www.ncbi.nlm.nih.gov'>35668944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(A) Images of H&E, Masson’s trichrome, Sirius red, and immunohistochemistry of α-SMA, vimentin, and p-4EBP1 staining of representative liver sections (×200 magnification).
(B) Representative Masson and Sirius red staining of liver tissues and positive content (%) of α-SMA, vimentin, and p-4EBP1 staining (n = 5).
(C) The protein expression of α-SMA, COL1α1, vimentin, p-4EBP1, and 4EBP1 in liver tissues was analyzed using western blotting.
(D) The protein expression of α-SMA, vimentin, p-4EBP1, and 4EBP1 in TGF-β1-activated LX-2 cells for 0, 6, 12, 24, and 48 h.
(E and F) Immunofluorescence double staining of α-SMA and p-4EBP1 in TGF-β1-stimulated LX-2 cells for 0, 6, 12, 24, and 48 h (×400 magnification). Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001. α-SMA, alpha-smooth muscle actin; BDL, bile duct ligation; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin and eosin; TGF-β1, transforming growth factor β1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-41467_2023_41529_fig1_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodySchematic illustration showing the strategy of using a joint-engineered mesenchymal stem cell (Pg-Fe-hMSC) to enable a powerful and sustained intercellular mitochondrial delivery specialized to injured lung epithelial cells (LECs) for the potent intervention of pulmonary fibrosis (PF). These joint-engineered hMSC using iron oxide nanoparticles (IONPs) and pioglitazone realized powerful intercellular mitochondrial transfer, which is mainly due to the promoted mitochondrial biogenesis through the PGC-1 α pathway and augmented mitochondrial transfer through the gap junction facilitated trafficking (e.g. annular gap junction mediated internalization). The Pg-Fe-hMSC can be used as both a mitochondrial generation factory and a smart vehicle for selective mitochondrial transfer to injured lung cells, showing the advantages of enabling efficient and sustained mitochondrial transfer. Consequently, Pg-Fe-hMSC achieves efficient intervention treatment for PF. This demonstrated strategy provides a potential approach to prepare mitochondria donor cells and mitochondria vehicles for workable mitochondrial replenishment treatments. Cx43 connexin 43, NRF1 nuclear respiratory factor 1, TFAM mitochondrial transcription factor A, JNK c-Jun N-terminal kinase, TCA tricarboxylic acid cycle, ROS reactive oxygen species, TGF- β transforming growth factor- β . Figure was partially created with BioRender.com. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-023-41529-7'>37723135</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-4.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(H) Relative quantification of α-SMA, cleaved caspase-3, and colocalization of α-SMA and cleaved caspase-3. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; BDL, bile duct ligation; BP, biological process; CC, cellular component; DAPI, 4′,6-diamidino-2-phenylindole; ECM, extracellular matrix; LV, lentivirus; MF, molecular function.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-fphar-13-911945-g002.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyOverexpression of TRAF6 suppresses fibroblast activation. (A) IHC staining showing the expression of α-SMA in lung tissues. Representative data and quantified results are shown (Group 1: BLM + Lenti- Ctrl , Group 2: BLM + Lenti- Traf6 ; n = 5 per group). Scale bar, 100 μm. (B) mRNA expression of fibrosis genes in mouse PF lung fibroblasts with or without TRAF6 overexpression. (C) Representative images and quantification of the invasion experiment results for mouse PF lung fibroblasts with or without TRAF6 overexpression. Scale bars, 100 μm. (D) Representative images and quantification of α-SMA immunostaining in mouse PF fibroblasts with or without TRAF6 overexpression. Scale bars, 50 μm. Data are representative of 3 independent experiments. Data represent means ± SEM Statistical significance: * p < 0.05, ** p < 0.01 or *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9163739/&orig_host=www.ncbi.nlm.nih.gov'>35668944</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-40752108-figure-5.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody(I) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in LX-2 cells analyzed using western blotting.
(J) Immunofluorescence double staining of α-SMA and HIF-1α in vehicle or TGF-β1-stimulated LX-2 cells transducted with LV-empty or LV-4EBP1-4A-3xflag (×400 magnification).
(M and N) (M) The apoptosis of vehicle or TGF-β1-stimulated LX-2 cells transducted with LV-empty or LV-4EBP1-4A-3xflag determined using flow cytometry and (N) percentages of apoptotic cells (early and late apoptotic cells). EV, LV-empty; OE, LV-4EBP1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1.<br><b>Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-41467_2023_41529_fig5_html.pngAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyTherapeutic potentials of Pg-Fe-hMSC in both monocellular and multicellular humanized fibrotic models. a Schematic illustration and representative image of EpCAM immunostaining in primary human lung epithelial cells (hLECs). Scale bar, 50 μm. b Mitochondrial transfer rates from the indicated hMSC to the primary hLEC ( n = 3 biologically independent cells). c Relative intracellular ROS levels ( n = 3 biologically independent cells), d TGF- β expression levels ( n = 4 biologically independent cells), and e Viability of BLM-treated hLEC after the indicated treatment using different engineered hMSCs ( n = 3 biologically independent cells). f Schematic illustration showing the preparation of the 3D multicellular human fibrotic model. g Representative immunostaining images showing the expression of α -smooth muscle actin ( α -SMA), vimentin, collagen-I, and Ki-67 in the healthy and fibrotic multicellular human spheroid models. Blue fluorescent signals indicate the cell nuclei and green signals indicate the biomarkers. Scale bar, 20 μm. h Mitochondrial transfer rates of different engineered hMSC in fibrotic human lung spheroids ( n = 3 biologically independent experiments). i Relative intracellular ROS levels ( n = 3 biologically independent experiments) and j TGF- β expression levels of fibrotic human lung spheroids after the indicated treatment using different engineered hMSCs ( n = 4 biologically independent experiments). k Viability of fibrotic human lung spheroids after the indicated treatment using different engineered hMSCs ( n = 3 biologically independent experiments). Data are presented as means ± SD. Statistical significance was analyzed using ordinary one-way ANOVA. ECs epithelial cells. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-023-41529-7'>37723135</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-1-fphar-13-911945-g007.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyTRIB3 activates lung fibroblasts by reducing TRAF6 expression. (A) Transwell assay for the evaluation of invasion of TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. (B) mRNA expression of fibrosis genes in TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. (C) Representative images of α-SMA immunostaining in TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. Scale bars, 50 μm. (D) mRNA expression of Wnt3a in TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. (E) mRNA expression of the β-catenin target genes in TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. (F) Wnt-reporter luciferase activity in TRIB3-silenced PF lung fibroblasts with or without TRAF6 knockdown. Data are representative of 3 independent experiments. Data represent means ± SEM Statistical significance: * p < 0.05, ** p < 0.01 or *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC9163739/&orig_host=www.ncbi.nlm.nih.gov'>35668944</a></b>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-methyl-histone-h3-di-k4-rabbit-monoclonal-antibody-m12477-1-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-1-h3c1-primary-antibodies-wb-testing-1.jpgAnti-Methyl-Histone H3 (di K4) HIST1H3A Rabbit Monoclonal Antibody Western blot analysis of Methyl-Histone H3 (di K4) using anti-Methyl-Histone H3 (di K4) antibody (M12477-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse RAW264.7 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Methyl-Histone H3 (di K4) antigen affinity purified monoclonal antibody (Catalog # M12477-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Methyl-Histone H3 (di K4) at approximately 15 kDa. The expected band size for Methyl-Histone H3 (di K4) is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/1/M12477-1-HIST1H3A-primary-antibodies-IHC-testing-1.jpgAnti-Methyl-Histone H3 (di K4) HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human liver, using Methyl-Histone H3 (di K4) Antibody(M12477-1)<br>HIST1H3A was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-HIST1H3A Antibody (M12477-1)overnight at 4℃. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37℃. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. <br>
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-smooth-muscle-actin-rabbit-monoclonal-antibody-m01072-3-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-3-alpha-sma-primary-antibodies-wb-testing-1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal Antibody Western blot analysis of alpha-SMA using anti-alpha-SMA antibody (M01072-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates.<br>
Lane 4: rat C6 whole cell lysates.<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-alpha-SMA antigen affinity purified monoclonal antibody (Catalog # M01072-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for alpha-SMA at approximately 42 kDa. The expected band size for alpha-SMA is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/M/0/M01072-3-ACTA2-primary-antibodies-IHC-testing-1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human breast carcinoma, using alpha smooth muscle Actin Antibody(M01072-3)<br>ACTA2 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-ACTA2 Antibody (M01072-3)overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-3-alpha-sma-primary-antibodies-if-testing-1.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyIF analysis of alpha-SMAusing anti-alpha-SMA antibody (M01072-3).<br>
alpha-SMA was detected in a paraffin-embedded section of human tosil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated at 1:50 rabbit anti-alpha-SMA Antibody (M01072-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01072-3-alpha-sma-primary-antibodies-if-testing-2.jpgAnti-alpha smooth muscle Actin ACTA2 Rabbit Monoclonal AntibodyIF analysis of alpha-SMAusing anti-alpha-SMA antibody (M01072-3).<br>
alpha-SMA was detected in a paraffin-embedded section of rat brain vessel tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated at 1:50 rabbit anti-alpha-SMA Antibody (M01072-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myosin-light-chain-kinase-rabbit-monoclonal-antibody-m01697-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01697-wb.jpgAnti-Myosin light chain kinase MYLK Rabbit Monoclonal AntibodyWestern blot analysis of myosin light chain kinase expression in HUVEC cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01697-fcell-08-613061-g006.jpgAnti-Myosin light chain kinase MYLK Rabbit Monoclonal AntibodyThe co-expression of EspF and ANXA6 protein in Caco-2 cells activates the MLCK-MLC pathway. The WB strips of MLCK-MLC pathway proteins in different plasmid-transfection groups, as indicated, are shown. Increased expression of MLCK, phosphorylated expression of MLC and PKCα, and decreased expression of Calmodulin in the EspF-ANXA6 transfected group, suggesting that EspF-ANXA6 activates the MLCK-MLC pathway, which may perturb TJ function. NC, non-transfected cells; EY, cells transfected with pEYFP; EYEA, cells transfected with pEYFP-EspF-T2A-ANXA6; EE, cells transfected with pEGFP-EspF. *Statistically significant difference. * p < 0.05. ** p < 0.01.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.613061/full'>33425920</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01697-ihc.jpgAnti-Myosin light chain kinase MYLK Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human colon, using Myosin light chain kinase Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-di-methyl-k9-rabbit-monoclonal-antibody-m12477-2-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-2-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (di methyl K9) HIST1H3A Rabbit Monoclonal Antibody Western blot analysis of Histone H3 using anti-Histone H3 antibody (M12477-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 antigen affinity purified monoclonal antibody (Catalog # M12477-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Histone H3 at approximately 15 kDa. The expected band size for Histone H3 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-2-wb7.jpgAnti-Histone H3 (di methyl K9) HIST1H3A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-interferon-receptor-alpha-rabbit-monoclonal-antibody-m00306-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-wb.jpgAnti-Interferon Receptor alpha IFNAR1 Rabbit Monoclonal AntibodyWestern blot analysis of Interferon Receptor alpha expression in SH-SY5Y cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2a-hydroxyl-y39-rabbit-monoclonal-antibody-m16777-1-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-1-wb.jpgAnti-Histone H2A (hydroxyl Y39) HIST1H2AB Rabbit Monoclonal AntibodyWestern blot analysis of Calreticulin expression in (1) NIH/3T3 cell lysate; (2) A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-1-ihc.jpgAnti-Histone H2A (hydroxyl Y39) HIST1H2AB Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded mouse colon, using Histone H2A (hydroxyl Y39) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-beta-2-adrenergic-receptor-rabbit-monoclonal-antibody-m00072-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00072-wb.jpgAnti-beta 2 Adrenergic Receptor ADRB2 Rabbit Monoclonal AntibodyWestern blot analysis of beta 2 Adrenergic Receptor expression in A431 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-r2-rabbit-monoclonal-antibody-m12477-3-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-3-icc1.jpgAnti-Histone H3 (mono methyl R2) HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-3-icc2.jpgAnti-Histone H3 (mono methyl R2) HIST1H3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-3-wb.jpgAnti-Histone H3 (mono methyl R2) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono methyl R2) expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h4-tri-methyl-k20-rabbit-monoclonal-antibody-m14495-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-wb.jpgAnti-Histone H4 (tri methyl K20) HIST1H4A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H4 (tri methyl K20) expression in HeLa cell lysate. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-ihc.jpgAnti-Histone H4 (tri methyl K20) HIST1H4A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human stomach, using Histone H4 (tri methyl K20) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-transferrin-receptor-cd71-rabbit-monoclonal-antibody-m00591-1-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00591-1-cd71-primary-antibodies-wb-testing-1.jpgAnti-Transferrin Receptor (CD71) TFRC Rabbit Monoclonal Antibody Western blot analysis of CD71 using anti-CD71 antibody (M00591-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human U-87MG whole cell lysates,<br>
Lane 3: rat liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD71 antigen affinity purified monoclonal antibody (Catalog # M00591-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD71 at approximately 95 kDa. The expected band size for CD71 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00591-1-tfrc-primary-antibodies-ihc-testing-2.jpgAnti-Transferrin Receptor (CD71) TFRC Rabbit Monoclonal Antibody IHC analysis of CD71 using anti-CD71 antibody (M00591-1). <br>
CD71 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CD71 Antibody (M00591-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-delta-1-catenin-p120-catenin-rabbit-monoclonal-antibody-m02333-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02333-wb7.jpgAnti-delta 1 Catenin/p120 Catenin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02333-if.jpgAnti-delta 1 Catenin/p120 Catenin Rabbit Monoclonal AntibodyImmunofluorescent analysis of MCF-7 cells, using delta 1 Catenin/p120 Catenin Antibody .https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02333-wb8.jpgAnti-delta 1 Catenin/p120 Catenin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02333-wb.jpgAnti-delta 1 Catenin/p120 Catenin Rabbit Monoclonal AntibodyWestern blot analysis of delta1 Catenin expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-r17-rabbit-monoclonal-antibody-m12477-4-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: rat C6 whole cell lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 antigen affinity purified monoclonal antibody (M12477-4) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H3 at approximately 17 kDa. The expected band size for Histone H3 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-1.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-3.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-4.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-5.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-6.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-7.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-8.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-4-histone-h3-primary-antibodies-ihc-testing-9.jpgAnti-Histone H3 (mono methyl R17) HIST1H3A Rabbit Monoclonal AntibodyIHC analysis of Histone H3 using anti-Histone H3 antibody (M12477-4). <br>Histone H3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 Antibody (M12477-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h4-mono-methyl-k16-rabbit-monoclonal-antibody-m14495-1-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-1-wb.jpgAnti-Histone H4 (mono methyl K16) HIST1H4A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H4 (mono methyl K16) expression in (1) NIH/3T3 cell lysate; (2) A549 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-k36-rabbit-monoclonal-antibody-m12477-5-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-5_41467_2025_61236_fig1_html.pngAnti-Histone H3 (mono methyl K36) HIST1H3A Rabbit Monoclonal AntibodyRelative sEVs and dsDNA levels in RIM patients. a The NTA and TEM images of sEVs isolated from nasal secretions of RIM patients before and after RT. Scale bars: 200 nm. b The relative sEVs amount and dsDNA level in nasal secretions. Data represent the mean ± S.D. ( n = 20 samples). c The correlations of IL-6 and TNF-α with relative sEVs amount and cfDNA level in nasal secretions from RIM patients. d Representative NET images of neutrophils treated with post-radiation sEVs and sEVs+C-178. Scale bars: 20 µm. e Representative CD11b + /F4/80 + /CD86 + in the RAW 264.7 cells treated with sEVs and sEVs+C-178. f Quantification of the percentage of CitH3 positive area, MPO positive area in NET images, and the percentage of macrophages with M1 phenotype. Data represent the mean ± S.D. ( n = 3 independent experiments). Statistical significances were assessed by paired two-tailed Student’s t -test ( b for sEVs), Wilcoxon test ( b for dsDNA), or one-way ANOVA ( f ), and multiple comparisons post hoc tests were performed via the Prism recommendation (Tukey or Dunnett) method. Abbreviations: RT: radiotherapy; sEVs: small extracellular vesicles; CitH3: citrullinated histone H3; MPO: myeloperoxidase. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41467-025-61236-9'>40610425</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-5-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (mono methyl K36) HIST1H3A Rabbit Monoclonal Antibody Western blot analysis of Histone H3 using anti-Histone H3 antibody (M12477-5). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates,<br>
Lane 5: rat heart tissue lysates,<br>
Lane 6: rat RH35 whole cell lysates,<br>
Lane 7: mouse heart tissue lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 antigen affinity purified monoclonal antibody (Catalog # M12477-5) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Histone H3 at approximately 15-17 kDa. The expected band size for Histone H3 is at 15 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-k18-rabbit-monoclonal-antibody-m12477-6-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-6-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (mono methyl K18) HIST1H3A Rabbit Monoclonal Antibody Western blot analysis of Histone H3 (mono methyl K18) using anti-Histone H3 (mono methyl K18) antibody (M12477-6). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates,<br>
Lane 5: human PC-12 whole cell lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse RAW264.7 whole cell lysates,<br>
Lane 8: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 (mono methyl K18) antigen affinity purified monoclonal antibody (Catalog # M12477-6) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Histone H3 (mono methyl K18) at approximately 17 kDa. The expected band size for Histone H3 (mono methyl K18) is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-6-histone-h3-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3 (mono methyl K18) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (mono methyl K18) using anti-Histone H3 (mono methyl K18) antibody (M12477-6). <br>
Histone H3 (mono methyl K18) was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:500 rabbit anti-Histone H3 (mono methyl K18) Antibody (M12477-6) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-6-histone-h3-primary-antibodies-ihc-testing-3.jpgAnti-Histone H3 (mono methyl K18) HIST1H3A Rabbit Monoclonal Antibody IHC analysis of Histone H3 (mono methyl K18) using anti-Histone H3 (mono methyl K18) antibody (M12477-6). <br>
Histone H3 (mono methyl K18) was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:500 rabbit anti-Histone H3 (mono methyl K18) Antibody (M12477-6) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-6-histone-h3-primary-antibodies-if-testing-4.jpgAnti-Histone H3 (mono methyl K18) HIST1H3A Rabbit Monoclonal Antibody IF analysis of Histone H3 (mono methyl K18) using anti-Histone H3 (mono methyl K18) antibody (M12477-6) and anti-Beta Tubulin antibody (M01857-3).<br>
Histone H3 (mono methyl K18) was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:100 with rabbit anti-Histone H3 (mono methyl K18) Antibody (M12477-6) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-retinoic-acid-receptor-alpha-rabbit-monoclonal-antibody-m00392-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00392-wb.jpgAnti-Retinoic Acid Receptor alpha RARA Rabbit Monoclonal AntibodyWestern blot analysis of Retinoic Acid Receptor alpha expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00392-kd1.jpgAnti-Retinoic Acid Receptor alpha RARA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1000 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00392-wb10.jpgAnti-Retinoic Acid Receptor alpha RARA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1000 dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-r128-rabbit-monoclonal-antibody-m12477-7-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-7-wb.jpgAnti-Histone H3 (mono methyl R128) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono methyl R128) expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-mono-methyl-r79-rabbit-monoclonal-antibody-m07286-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-wb.jpgAnti-Histone H2B (mono methyl R79) HIST2H2BE Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B (mono methyl R79) expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-stromal-interaction-molecule-1-rabbit-monoclonal-antibody-m00312-boster.html2026-03-24T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00312-stim1-primary-antibodies-wb-testing-1.jpgAnti-Stromal interaction molecule 1 STIM1 Rabbit Monoclonal Antibody Western blot analysis of STIM1 using anti-STIM1 antibody (M00312). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human HUH-7 whole cell lysates,<br>
Lane 5: rat RH35 whole cell lysates,<br>
Lane 6: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STIM1 antigen affinity purified monoclonal antibody (Catalog # M00312) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STIM1 at approximately 85 kDa. The expected band size for STIM1 is at 77 kDa.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-androgen-receptor-ar-v7-specific-rabbit-monoclonal-antibody-m00542-3-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-3-wb.jpgAnti-Androgen Receptor (AR-V7 specific) Rabbit Monoclonal AntibodyWestern blot analysis of Androgen Receptor expression in 22Rv1 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-3-ihc.jpgAnti-Androgen Receptor (AR-V7 specific) Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded human prostate carcinoma, using Androgen Receptor(AR-V7 specific) Antibody.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00542-3-wb7.jpgAnti-Androgen Receptor (AR-V7 specific) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-di-tri-methyl-k79-rabbit-monoclonal-antibody-m12477-8-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-8-wb.jpgAnti-Histone H3 (mono+di+tri methyl K79) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono+di+tri methyl K79) expression in (1) NIH/3T3 cell lysate; (2) A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-8-ihc.jpgAnti-Histone H3 (mono+di+tri methyl K79) HIST1H3A Rabbit Monoclonal AntibodyImmunohistochemical analysis of paraffin-embedded rat colon, using Histone H3 (mono+di+tri methyl K79) Antibody.
https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-di-tri-methyl-k14-rabbit-monoclonal-antibody-m12477-9-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-9-wb.jpgAnti-Histone H3 (mono+di+tri methyl K14) HIST1H3A Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono+di+tri methyl K14) expression in HeLa cell lysate.
https://www.bosterbio.com/products/primary-antibodies/anti-laminin-picoband-trade-antibody-a03522-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-1-43556_2023_159_fig6_html.pngAnti-Laminin Antibody Picoband®The effect of MSCs/GDNF transplantation on blood vessels and associated proteins. a - c The images of laminin, CD31, VEGF IHC staining in ipsilateral striata of rats. d - f The numbers of blood vessels, CD31- and VEGF-positive cells in the striata of the different groups ( n = 5 per group). g Representative electron micrographs of brain capillaries in the different groups. The arrowhead indicates a tight junction between two endothelial cells. Asterisks show the basement membrane of the brain capillary. NCe, the nucleus of the endothelial cell; ery, erythrocyte; e, endothelial cell; p, pericyte; a, foot of astrocyte; m, mitochondrion. h Quantitative analysis of the thickness of capillary basement membrane. Scale bar, 100 μm ( a-c ) and 1 μm ( g ). * P < 0.05, *** P < 0.001, and **** P < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s43556-023-00159-7'>38008847</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-1-laminin-primary-antibodies-wb-testing-1.jpgAnti-Laminin Antibody Picoband® Western blot analysis of Laminin using anti-Laminin antibody (A03522-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human placenta tissue lysates, <br>
Lane 2: human HCCT tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Laminin antigen affinity purified polyclonal antibody (Catalog # A03522-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Laminin at approximately 200 kDa. The expected band size for Laminin is at 177-200 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03522-1-laminin-primary-antibodies-ihc-testing-2.jpgAnti-Laminin Antibody Picoband® IHC analysis of Laminin using anti-Laminin antibody (A03522-1). <br>
Laminin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Laminin Antibody (A03522-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-galectin-1-picoband-trade-antibody-a00470-2-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00470-2-galectin-1-primary-antibodies-elisa-testing-1.jpgAnti-Galectin 1 Lgals1 Antibody Sandwich ELISA - Recombinant mouse Galectin 1 protein standard curve.<br>
Use in combination with reagents from Mouse Galectin 1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0763).
https://www.bosterbio.com/products/primary-antibodies/anti-tff1-picoband-trade-antibody-a01391-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01391-1-tff1-primary-antibodies-elisa-testing-1.jpgAnti-Tff1 Antibody Sandwich ELISA - Recombinant mouse Tff1 protein standard curve.<br>
Use in combination with reagents from Mouse Tff1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1620).
https://www.bosterbio.com/products/primary-antibodies/anti-pon1-picoband-trade-antibody-a00516-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00516-pon1-primary-antibodies-wb-testing-1_2.jpgAnti-PON1 Antibody Picoband® Western blot analysis of PON1 using anti-PON1 antibody (A00516). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: mouse liver tissue lysates,<br>
Lane 3: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PON1 antigen affinity purified polyclonal antibody (Catalog # A00516) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PON1 at approximately 40 kDa. The expected band size for PON1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00516-pon1-primary-antibodies-ihc-testing-2.jpgAnti-PON1 Antibody Picoband®IHC analysis of PON1 using anti-PON1 antibody (A00516). PON1 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PON1 Antibody (A00516) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00516-pon1-primary-antibodies-ihc-testing-3.jpgAnti-PON1 Antibody Picoband®IHC analysis of PON1 using anti-PON1 antibody (A00516). PON1 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PON1 Antibody (A00516) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00516-pon1-primary-antibodies-ihc-testing-4.jpgAnti-PON1 Antibody Picoband®IHC analysis of PON1 using anti-PON1 antibody (A00516). PON1 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PON1 Antibody (A00516) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-trem1-picoband-trade-antibody-a02135-3-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box.pngAnti-TREM1 AntibodyBoster Kit Box
https://www.bosterbio.com/products/primary-antibodies/anti-sur1-picoband-trade-antibody-a00895-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00895-1-sur1-primary-antibodies-wb-testing-1.jpgAnti-SUR1/ABCC8 Antibody Picoband® Western blot analysis of SUR1 using anti-SUR1 antibody (A00895-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: rat brain tissue lysates,<br>Lane 3: mouse brain tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SUR1 antigen affinity purified polyclonal antibody (Catalog # A00895-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SUR1 at approximately 177KD. The expected band size for SUR1 is at 177KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00895-1-abcc8-primary-antibodies-fc-testing-2.jpgAnti-SUR1/ABCC8 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-ABCC8 antibody (A00895-1).<br>Overlay histogram showing A431 cells stained with A00895-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABCC8 Antibody (A00895-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ace-picoband-trade-antibody-a00251-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-ace-primary-antibodies-wb-testing-1.jpgAnti-Angiotensin Converting Enzyme 1/Ace Antibody Picoband®Western blot analysis of ACE using anti-ACE antibody (A00251). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat lung tissue lysates, <br>
Lane 2: mouse lung tissue lysates, <br>
Lane 3: mouse kidney tissue lysates, <br>
Lane 4: mouse heart tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACE antigen affinity purified polyclonal antibody (A00251) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ACE at approximately 150-180 kDa. The expected band size for ACE is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-ace-primary-antibodies-ihc-testing-1.jpgAnti-Angiotensin Converting Enzyme 1/Ace Antibody Picoband®IHC analysis of ACE using anti-ACE antibody (A00251). <br>
ACE was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-ace-primary-antibodies-ihc-testing-2.jpgAnti-Angiotensin Converting Enzyme 1/Ace Antibody Picoband®IHC analysis of ACE using anti-ACE antibody (A00251). <br>
ACE was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-ace-primary-antibodies-ihc-testing-3.jpgAnti-Angiotensin Converting Enzyme 1/Ace Antibody Picoband®IHC analysis of ACE using anti-ACE antibody (A00251). <br>
ACE was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-ace-primary-antibodies-fcm-testing-1.jpgAnti-Angiotensin Converting Enzyme 1/Ace Antibody Picoband®Flow Cytometry analysis of RAW264.7 cells using anti-ACE antibody (A00251). <br>
Overlay histogram showing RAW264.7 cells stained with A00251 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ACE Antibody (A00251, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-ada-picoband-trade-antibody-a00866-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00866-1-ada-primary-antibodies-wb-testing-1_1.jpgAnti-ADA Antibody Picoband® Western blot analysis of ADA using anti-ADA antibody (A00866-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat stomach tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: mouse small intestine tissue lysates,<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADA antigen affinity purified polyclonal antibody (Catalog # A00866-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADA at approximately 45KD. The expected band size for ADA is at 40KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-1-ADA-primary-antibodies-IHC-testing-2.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-1).
ADA was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-1-ADA-primary-antibodies-IHC-testing-3.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-1).
ADA was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-1-ADA-primary-antibodies-IHC-testing-4.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-1).
<br>ADA was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-1-ADA-primary-antibodies-IHC-testing-5.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-1).
<br>ADA was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-1-ADA-primary-antibodies-IHC-testing-6.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-1).
<br>ADA was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-ada-picoband-trade-antibody-a00866-2-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00866-2-ada-primary-antibodies-wb-testing-1_1.jpgAnti-ADA Antibody Picoband® Western blot analysis of ADA using anti-ADA antibody (A00866-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: rat liver tissue lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse spleen tissue lysates,<br>
Lane 6: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADA antigen affinity purified polyclonal antibody (Catalog # A00866-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADA at approximately 41 kDa. The expected band size for ADA is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-2-ADA-primary-antibodies-IHC-testing-2.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-2).
ADA was detected in paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-2-ADA-primary-antibodies-IHC-testing-3.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-2).
ADA was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00866-2-ADA-primary-antibodies-IHC-testing-4.jpgAnti-ADA Antibody Picoband® IHC analysis of ADA using anti-ADA antibody (A00866-2).
<br>ADA was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ADA Antibody (A00866-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-adam10-picoband-trade-antibody-a00566-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00566-1-ADAM10-primary-antibodies-WB-testing-1.jpgAnti-ADAM10 Antibody Picoband® Western blot analysis of ADAM10 using anti-ADAM10 antibody (A00566-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat thymus tissue lysates,<br>Lane 2: rat stomach tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM10 antigen affinity purified polyclonal antibody (Catalog # A00566-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM10 at approximately 72KD. The expected band size for ADAM10 is at 84KD.
https://www.bosterbio.com/products/primary-antibodies/anti-grk2-picoband-trade-antibody-a01473-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-wb-testing-1.jpgAnti-GRK2/GRK2 Antibody Picoband® Western blot analysis of GRK2 using anti-GRK2 antibody (A01473-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysates,<br>Lane 2: rat stomach tissue lysates,<br>Lane 3: mouse lung tissue lysates,<br>Lane 4: mouse liver tissue lysates,<br>Lane 5: mouse pancreas tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GRK2 antigen affinity purified polyclonal antibody (Catalog # A01473-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GRK2 at approximately 79KD. The expected band size for GRK2 is at 79KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-ihc-testing-2.jpgAnti-GRK2/GRK2 Antibody Picoband® IHC analysis of GRK2 using anti-GRK2 antibody (A01473-1). <br> GRK2 was detected in paraffin-embedded section of human Lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GRK2 Antibody (A01473-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-ihc-testing-3.jpgAnti-GRK2/GRK2 Antibody Picoband® IHC analysis of GRK2 using anti-GRK2 antibody (A01473-1). <br> GRK2 was detected in paraffin-embedded section of mouse spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GRK2 Antibody (A01473-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-ihc-testing-4.jpgAnti-GRK2/GRK2 Antibody Picoband® IHC analysis of GRK2 using anti-GRK2 antibody (A01473-1). <br> GRK2 was detected in paraffin-embedded section of rat spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GRK2 Antibody (A01473-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-if-testing-5.jpgAnti-GRK2/GRK2 Antibody Picoband® IF analysis of GRK2 using anti-GRK2 antibody (A01473-1). <br>
GRK2 was detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-GRK2 Antibody (A01473-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01473-1-grk2-primary-antibodies-fcm-testing-6.jpgAnti-GRK2/GRK2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-GRK2 antibody (A01473-1).<br>Overlay histogram showing U87 cells stained with A01473-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GRK2 Antibody (A01473-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-alpha-1-fetoprotein-picoband-trade-antibody-a00522-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00522-alpha_1_fetoprotein-primary-antibodies-wb-testing-1_1.jpgAnti-Alpha 1 Fetoprotein/Afp Antibody Picoband® Western blot analysis of Alpha 1 Fetoprotein using anti-Alpha 1 Fetoprotein antibody (A00522). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse HEPA1-6 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha 1 Fetoprotein antigen affinity purified polyclonal antibody (Catalog # A00522) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha 1 Fetoprotein at approximately 69KD. The expected band size for Alpha 1 Fetoprotein is at 69KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00522-alpha_1_fetoprotein-primary-antibodies-wb-testing-2.jpgAnti-Alpha 1 Fetoprotein/Afp Antibody Picoband® Western blot analysis of Alpha 1 Fetoprotein using anti-Alpha 1 Fetoprotein antibody (A00522). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: rat RH35 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha 1 Fetoprotein antigen affinity purified polyclonal antibody (Catalog # A00522) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha 1 Fetoprotein at approximately 69KD. The expected band size for Alpha 1 Fetoprotein is at 69KD.
https://www.bosterbio.com/products/primary-antibodies/anti-agrp-picoband-trade-antibody-a00272-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00272-1-AGRP-primary-antibodies-IHC-testing-1.jpgAnti-AGRP Antibody IHC analysis of AGRP using anti-AGRP antibody (A00272-1).
<br>AGRP was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-AGRP Antibody (A00272-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00272-1-fendo-09-00476-g005.jpgAnti-AGRP AntibodyEffects of long-term L -serine administration on orexigenic neuropeptide expression in aging mice. NPY (A–E) and AGRP (F–J) expression as determined by immunohistochemistry; relative NPY (K) and AGRP (L) mRNA expression. Aged, untreated control mice; Low-ser, mice supplemented with 0.1% (wt/vol) L -serine dissolved in the drinking water; Middle-ser, mice supplemented with 0.2% (wt/vol) L -serine dissolved in the drinking water; High-ser, mice supplemented with 0.5% (wt/vol) L -serine dissolved in the drinking water. Young, adult male mice at the age of 18 months. Arrow (yellow), expression of target proteins; NPY, neuropeptide Y; AGRP, agouti-related protein. Values are expressed as mean ± SEM, n = 8; a, b Means of the bars with different letters were significantly different among groups ( P < 0.05).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2018.00476/full'>30190704</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00272-1-AGRP-primary-antibodies-IHC-testing-2.jpgAnti-AGRP Antibody IHC analysis of AGRP using anti-AGRP antibody (A00272-1).
<br>AGRP was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-AGRP Antibody (A00272-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00272-1-AGRP-primary-antibodies-IHC-testing-3.jpgAnti-AGRP Antibody IHC analysis of AGRP using anti-AGRP antibody (A00272-1).<br>
AGRP was detected in paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-AGRP Antibody (A00272-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-amotl2-picoband-trade-antibody-a06852-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06852-13020_2023_769_fig8_html.pngAnti-AMOTL2 Antibody Picoband®Validation of drug targets of proteomics and network pharmacology with western blot. A Western blot images of PIKfyve, AFF4, Amotl2, and GLP1R in the lung tissue. B – E Data were expressed as the expression ratio of PIKfyve/β-actin, AFF4/β-actin, Amotl2/β-actin, and GLP1R/β-actin (n = 3 per group). F Western blot images of HSP90AA1, MMP1, TGF-β1, JUN, P53, p-Akt, Akt, p-STAT3 and STAT3 in the lung tissue. G – M : Data were expressed as the expression ratio of HSP90AA1/β-actin, MMP1/β-actin, TGF-β1/β-actin, JUN/β-actin, P53/β-actin, p-Akt/Akt, and p-STAT3/STAT3 (n = 3 per group). * P < 0.05, ** P < 0.01 compared with CC group; # P < 0.05, ## P < 0.01 compared with PF group. C C: control group, PF bleomycin-induced PF group, GH GHSPT treated bleomycin-induced PF group, GHSPT ginseng honeysuckle superfine powdered tea, PF pulmonary fibrosis <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-023-00769-x'>37221600</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06852-amotl2-primary-antibodies-wb-testing-1.jpgAnti-AMOTL2 Antibody Picoband®Western blot analysis of AMOTL2 using anti-AMOTL2 antibody (A06852). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AMOTL2 antigen affinity purified polyclonal antibody (A06852) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AMOTL2 at approximately 130-150 kDa. The expected band size for AMOTL2 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06852-amotl2-primary-antibodies-if-testing-1.jpgAnti-AMOTL2 Antibody Picoband®IF analysis of AMOTL2 using anti-AMOTL2 antibody (A06852). <br>
AMOTL2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AMOTL2 Antibody (A06852) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-complement-c7-picoband-trade-antibody-a00844-1-boster.html2026-03-24T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00844-1-Complement_C7-primary-antibodies-WB-testing-1.jpgAnti-Complement C7 Antibody Picoband® Western blot analysis of Complement C7 using anti-Complement C7 antibody (A00844-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human 293T cell lysates, <br>Lane 2: human HepG2 cell lysates, <br>Lane 3: human A549 cell lysates, <br>Lane 4: rat liver tissue lysates,<br>Lane 5: mouse small intestine tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Complement C7 antigen affinity purified polyclonal antibody (Catalog # A00844-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Complement C7 at approximately 93KD. The expected band size for Complement C7 is at 93KD.
https://www.bosterbio.com/products/primary-antibodies/anti-complement-c9-picoband-trade-antibody-a01010-2-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01010-2-complement_c9-primary-antibodies-wb-testing-1.jpgAnti-Complement C9 Antibody Picoband® Western blot analysis of Complement C9 using anti-Complement C9 antibody (A01010-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human placenta tissue lysates.<br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Complement C9 antigen affinity purified polyclonal antibody (Catalog # A01010-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Complement C9 at approximately 80KD. The expected band size for Complement C9 is at 63KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01010-2-complement_c9-primary-antibodies-wb-testing-2.jpgAnti-Complement C9 Antibody Picoband® Western blot analysis of Complement C9 using anti-Complement C9 antibody (A01010-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: mouse liver tissue lysates, <br> Lane 2: mouse lung tissue lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Complement C9 antigen affinity purified polyclonal antibody (Catalog # A01010-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Complement C9 at approximately 80KD. The expected band size for Complement C9 is at 63KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cad-antibody-a00463-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00463-1-cad-primary-antibodies-wb-testing-1.jpgAnti-CAD/CAD Antibody Picoband® Western blot analysis of CAD using anti-CAD antibody (A00463-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse pancreas tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAD antigen affinity purified polyclonal antibody (Catalog # A00463-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CAD at approximately 270KD. The expected band size for CAD is at 243KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cars-picoband-trade-antibody-a00259-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00259-1-CARS-primary-antibodies-WB-testing-1.jpgAnti-CARS Antibody Picoband® Western blot analysis of CARS using anti-CARS antibody (A00259-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysates, <br>Lane 2: human COLO-320 cell lysates, <br>Lane 3: human A549 cell lysates, <br>Lane 4: human PANC-1 cell lysates, <br>Lane 5: human 22RV1 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CARS antigen affinity purified polyclonal antibody (Catalog # A00259-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CARS at approximately 85KD. The expected band size for CARS is at 85KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00259-1-cars-primary-antibodies-if-testing-2.jpgAnti-CARS Antibody Picoband® IF analysis of CARS using anti-CARS antibody (A00259-1) <br> CARS was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-CARS Antibody (A00259-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00259-1-cars-primary-antibodies-fc-testing-3.pngAnti-CARS Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-CARS antibody (A00259-1). <br> Overlay histogram showing A431 cells stained with A00259-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CARS Antibody (A00259-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00259-1-4.jpgAnti-CARS Antibody Picoband® IHC analysis of CARS using anti-CARS antibody (A00259-1). <br> CARS was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CARS Antibody (A00259-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cp110-picoband-trade-antibody-a05058-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05058-1-cp110-primary-antibodies-wb-testing-1.jpgAnti-CP110/CCP110 Antibody Picoband® Western blot analysis of CP110 using anti-CP110 antibody (A05058-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MOLT4 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human PANC-1 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CP110 antigen affinity purified polyclonal antibody (Catalog # A05058-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CP110 at approximately 113 kDa. The expected band size for CP110 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05058-1-cp110-primary-antibodies-ihc-testing-2.jpgAnti-CP110/CCP110 Antibody Picoband® IHC analysis of CP110 using anti-CP110 antibody (A05058-1). <br>
CP110 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CP110 Antibody (A05058-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05058-1-cp110-primary-antibodies-ihc-testing-3.jpgAnti-CP110/CCP110 Antibody Picoband® IHC analysis of CP110 using anti-CP110 antibody (A05058-1). <br>
CP110 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CP110 Antibody (A05058-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05058-1-cp110-primary-antibodies-ihc-testing-4.jpgAnti-CP110/CCP110 Antibody Picoband® IHC analysis of CP110 using anti-CP110 antibody (A05058-1). <br>
CP110 was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CP110 Antibody (A05058-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05058-1-cp110-primary-antibodies-if-testing-5.jpgAnti-CP110/CCP110 Antibody Picoband® IF analysis of CP110 using anti-CP110 antibody (A05058-1). <br>
CP110 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CP110 Antibody (A05058-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-ccr5-picoband-trade-antibody-a00061-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00061-CCR5-primary-antibodies-WB-testing-1.jpgAnti-CCR5 Antibody Picoband® Western blot analysis of CCR5 using anti-CCR5 antibody (A00061).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Jurkat cell lysates, <br>Lane 2: human MCF-7 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR5 antigen affinity purified polyclonal antibody (Catalog # A00061) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCR5 at approximately 40KD. The expected band size for CCR5 is at 40KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd1c-picoband-trade-antibody-a01188-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01188-1-CD1c-primary-antibodies-WB-testing-1.jpgAnti-CD1c Antibody Picoband® Western blot analysis of CD1c using anti-CD1c antibody (A01188-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD1c antigen affinity purified polyclonal antibody (Catalog # A01188-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD1c at approximately 62KD. The expected band size for CD1c is at 38KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd5-picoband-trade-antibody-a00480-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00480-1-cd5-primary-antibodies-wb-testing-1.jpgAnti-CD5 Antibody Picoband® Western blot analysis of CD5 using anti-CD5 antibody (A00480-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human CCRF-CEM whole cell lysates, <br>
Lane 3: human MOLT-4 whole cell lysates, <br>
Lane 4: rat thymus tissue lysates, <br>
Lane 5: mouse thymus tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD5 antigen affinity purified polyclonal antibody (Catalog # A00480-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD5 at approximately 67 kDa. The expected band size for CD5 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00480-1-cd5-primary-antibodies-fcm-testing-2.jpgAnti-CD5 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-CD54 antibody (A00480-1). <br>
Overlay histogram showing Jurkat cells stained with A00480-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD5 Antibody (A00480-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd40-picoband-trade-antibody-a00068-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00068-1-cd40-primary-antibodies-wb-testing-1.jpgAnti-CD40/Cd40 Antibody Picoband® Western blot analysis of CD40 using anti-CD40 antibody (A00068-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat PC-12 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD40 antigen affinity purified polyclonal antibody (Catalog # A00068-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD40 at approximately 36KD. The expected band size for CD40 is at 30KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd40l-picoband-trade-antibody-a01114-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01114-1-CD40L-primary-antibodies-WB-testing-1.jpgAnti-CD40L/CD40LG Antibody Picoband® Western blot analysis of CD40L using anti-CD40L antibody (A01114-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human HepG2 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD40L antigen affinity purified polyclonal antibody (Catalog # A01114-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD40L at approximately 19KD. The expected band size for CD40L is at 29KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd40l-picoband-trade-antibody-a01114-2-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01114-2-CD40L-primary-antibodies-WB-testing-1.jpgAnti-CD40L/Cd40lg Antibody Picoband® Western blot analysis of CD40L using anti-CD40L antibody (A01114-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat spleen tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD40L antigen affinity purified polyclonal antibody (Catalog # A01114-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD40L at approximately 36KD. The expected band size for CD40L is at 29KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01114-2-cd40lg-primary-antibodies-ihc-testing-4.jpgAnti-CD40L/Cd40lg Antibody Picoband®IHC analysis of CD154/CD40LG using anti-CD154/CD40LG antibody (A01114-2). <br>CD154/CD40LG was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD154/CD40LG Antibody (A01114-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01114-2-CD40L-primary-antibodies-IHC-testing-2.jpgAnti-CD40L/Cd40lg Antibody Picoband® IHC analysis of CD40L using anti-CD40L antibody (A01114-2).<br>
CD40L was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD40L Antibody (A01114-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01114-2-CD40L-primary-antibodies-IHC-testing-3.jpgAnti-CD40L/Cd40lg Antibody Picoband® IHC analysis of CD40L using anti-CD40L antibody (A01114-2).<br>
CD40L was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD40L Antibody (A01114-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01114-2-cd40l-primary-antibodies-wb-testing-4.jpgAnti-CD40L/Cd40lg Antibody Picoband® Western blot analysis of CD40L using anti-CD40L antibody (A01114-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human MCF-7 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD40L antigen affinity purified polyclonal antibody (Catalog # A01114-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD40L at approximately 36KD. The expected band size for CD40L is at 29KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd59-picoband-trade-antibody-a00914-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00914-cd59-primary-antibodies-wb-testing-1.jpgAnti-CD59/Cd59a Antibody Picoband® Western blot analysis of CD59 using anti-CD59 antibody (A00914). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: rat spleen tissue lysates,<br>Lane 4: rat brain tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD59 antigen affinity purified polyclonal antibody (Catalog # A00914) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD59 at approximately 20KD. The expected band size for CD59 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00914-CD59-primary-antibodies-IHC-testing-2.jpgAnti-CD59/Cd59a Antibody Picoband® IHC analysis of CD59 using anti-CD59 antibody (A00914).<br>
CD59 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD59 Antibody (A00914) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00914-CD59-primary-antibodies-IHC-testing-3.jpgAnti-CD59/Cd59a Antibody Picoband® IHC analysis of CD59 using anti-CD59 antibody (A00914).<br>
CD59 was detected in paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD59 Antibody (A00914) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ve-cadherin-picoband-trade-antibody-a02632-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-wb-testing-1.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® Western blot analysis of VE Cadherin using anti-VE Cadherin antibody (A02632-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VE Cadherin antigen affinity purified polyclonal antibody (Catalog # A02632-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VE Cadherin at approximately 120 kDa. The expected band size for VE Cadherin is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-ihc-testing-2.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® IHC analysis of VE Cadherin using anti-VE Cadherin antibody (A02632-1). <br>
VE Cadherin was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VE Cadherin Antibody (A02632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-ihc-testing-3.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® IHC analysis of VE Cadherin using anti-VE Cadherin antibody (A02632-1). <br>
VE Cadherin was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VE Cadherin Antibody (A02632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-ihc-testing-4.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® IHC analysis of VE Cadherin using anti-VE Cadherin antibody (A02632-1). <br>
VE Cadherin was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VE Cadherin Antibody (A02632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-if-testing-5.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® IF analysis of VE Cadherin using anti-VE Cadherin antibody (A02632-1). <br>
VE Cadherin was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-VE Cadherin Antibody (A02632-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02632-1-cdh5-primary-antibodies-fcm-testing-6.jpgAnti-VE-Cadherin CDH5 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-VE Cadherin antibody (A02632-1). <br>
Overlay histogram showing HepG2 cells stained with A02632-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-VE Cadherin Antibody (A02632-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-factor-d-picoband-trade-antibody-a01134-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-1-cfd-primary-antibodies-wb-testing-1.jpgAnti-Factor D/CFD Antibody Picoband® Western blot analysis of CFD using anti-CFD antibody (A01134-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: rat lung tissue lysates,<br>
Lane 4: mouse lung tissue lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CFD antigen affinity purified polyclonal antibody (Catalog # A01134-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CFD at approximately 45 kDa. The expected band size for CFD is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-1-cfd-primary-antibodies-ihc-testing-2.jpgAnti-Factor D/CFD Antibody Picoband® IHC analysis of CFD using anti-CFD antibody (A01134-1). <br>
CFD was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CFD Antibody (A01134-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-1-cfd-primary-antibodies-ihc-testing-3.jpgAnti-Factor D/CFD Antibody Picoband® IHC analysis of CFD using anti-CFD antibody (A01134-1). <br>
CFD was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CFD Antibody (A01134-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-1-cfd-primary-antibodies-ihc-testing-4.jpgAnti-Factor D/CFD Antibody Picoband® IHC analysis of CFD using anti-CFD antibody (A01134-1). <br>
CFD was detected in a paraffin-embedded section of mouse adipose tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CFD Antibody (A01134-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-1-cfd-primary-antibodies-ihc-testing-5.jpgAnti-Factor D/CFD Antibody Picoband® IHC analysis of CFD using anti-CFD antibody (A01134-1). <br>
CFD was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CFD Antibody (A01134-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-factor-d-picoband-trade-antibody-a01134-2-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01134-2-factor_d-primary-antibodies-wb-testing-1.jpgAnti-Factor D/Cfd Antibody Picoband® Western blot analysis of Factor D using anti-Factor D antibody (A01134-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat RH35 cell lysates, <br>Lane 2: rat PC-12 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Factor D antigen affinity purified polyclonal antibody (Catalog # A01134-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Factor D at approximately 27KD. The expected band size for Factor D is at 27KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01134-2-Factor_D-primary-antibodies-IHC-testing-2.jpgAnti-Factor D/Cfd Antibody Picoband® IHC analysis of Factor D using anti-Factor D antibody (A01134-2).<br>
Factor D was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Factor D Antibody (A01134-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01134-2-Factor_D-primary-antibodies-IHC-testing-3.jpgAnti-Factor D/Cfd Antibody Picoband® IHC analysis of Factor D using anti-Factor D antibody (A01134-2).<br>
Factor D was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Factor D Antibody (A01134-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01134-2-Factor_D-primary-antibodies-IHC-testing-4_1.jpgAnti-Factor D/Cfd Antibody Picoband® IHC analysis of Factor D using anti-Factor D antibody (A01134-2).
<br>Factor D was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Factor D Antibody (A01134-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-carboxypeptidase-a-picoband-trade-antibody-a05985-1-boster.html2026-03-24T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05985-1-cpa1-primary-antibodies-wb-testing-1.jpgAnti-Carboxypeptidase A/CPA1 Antibody Picoband® Western blot analysis of Carboxypeptidase A/CPA1 using anti-Carboxypeptidase A/CPA1 antibody (A05985-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat pancreas tissue lysates, <br>
Lane 2: mouse pancreas tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Carboxypeptidase A/CPA1 antigen affinity purified polyclonal antibody (Catalog # A05985-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Carboxypeptidase A/CPA1 at approximately 47 kDa. The expected band size for Carboxypeptidase A/CPA1 is at 47 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-dnmt1-picoband-trade-antibody-a00172-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-dnmt1-primary-antibodies-wb-testing-1.jpgAnti-Dnmt1 Antibody Picoband® Western blot analysis of DNMT1 using anti-DNMT1 antibody (A00172-1). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human SH-SY5Y whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNMT1 antigen affinity purified polyclonal antibody (A00172-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNMT1 at approximately 200 kDa. The expected band size for DNMT1 is at 183 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-dnmt1-primary-antibodies-ihc-testing-1.jpgAnti-Dnmt1 Antibody Picoband®IHC analysis of DNMT1 using anti-DNMT1 antibody (A00172-1). <br>
DNMT1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNMT1 Antibody (A00172-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-fonc-10-524922-g005.jpgAnti-Dnmt1 Antibody Picoband®Decreased DNA methylation in apoptosis-related genes in MDA-MB-231 cells. (A) Immunofluorescence staining of DNMT1 in MDA-MB-231 cells. The nuclei (blue) were stained with DAPI. (***p < 0.001). (B) Western blotting analysis of DNMT1 protein (***p < 0.001). (C) The DNA methylation levels of genes involved in apoptosis and the PI3K–AKT pathway. (D) The top five pathways of downregulated DNA methylation genes were enriched. (E) Network of genes with downregulated methylation genes and genes (red) of the PI3K–AKT pathway. (F) Survival curves of the DNA methylation level of TSC1, FADD , and TRADD were analyzed by MethSurv. (All values from three independent experiments are quantified as mean ± SD, ***p < 0.001).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.524922/full'>33194583</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-fonc-10-524922-g006.jpgAnti-Dnmt1 Antibody Picoband®6-TG treatment retarded tumor growth in vivo . (A) Drug-response curves of the MDA-MB-231 tumors. The data points represent the mean values ± SD of five independent experiments. The blue, red, and violet lines represent the control group, 6-TG group and docetaxel group,respectively. (B) Tumor morphology of the control group (top), 6-TG group (middle) and docetaxel group (bottom). (C) Weights of the final tumors. (D) Weight of mice during the treatment. X-axis indicated the days after implantation; Y-axis indicated the average weights of every groups. (E) The tumor sections were stained with HE. The positions indicated by the red arrow are pathological mitotic events. (Scale bar: 200 μm) (F) Immunohistochemical staining of DNMT1 and caspase-3 antibodies in tumors. (Scale bar: 200 μm). (G) The livers and kidneys from tumor bearing mice in control group and 6-TG group were stained with HE (Scale bar: 400 μm). The red arrows pointed the central veins in livers. The black arrows pointed the renal corpuscles, and the black boxes pointed the proximal convoluted tubules. (All values from three independent experiments are quantified as mean ± SD, *p < 0.05, ***p < 0.001, ns indicates no significant).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.524922/full'>33194583</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-dnmt1-primary-antibodies-ihc-testing-2.jpgAnti-Dnmt1 Antibody Picoband®IHC analysis of DNMT1 using anti-DNMT1 antibody (A00172-1). <br>
DNMT1 was detected in a paraffin-embedded section of human pancrease cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNMT1 Antibody (A00172-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-dnmt1-primary-antibodies-if-testing-2.jpgAnti-Dnmt1 Antibody Picoband® IF analysis of DNMT1 using anti-DNMT1 antibody (A00172-1) and anti-Tubulin Alpha antibody (M03989-3).<br>
DNMT1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DNMT1 Antibody (A00172-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1127) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00172-1-dnmt1-primary-antibodies-fcm-testing-3.jpgAnti-Dnmt1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-DNMT1 antibody (A00172-1). <br>
Overlay histogram showing 293T cells stained with A00172-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DNMT1 Antibody (A00172-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-dynlt1-picoband-trade-antibody-a05556-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-wb-testing-1_1.jpgAnti-DYNLT1 Antibody Picoband®Western blot analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
Electrophoresis was performed on a 13% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates, <br>
Lane 2: human U251 whole cell lysates, <br>
Lane 3: human SH-SY5Y whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DYNLT1 antigen affinity purified polyclonal antibody (Catalog # A05556) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DYNLT1 at approximately 16 kDa. The expected band size for DYNLT1 is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-1.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-2_1.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human esophageal keratinizing squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-3_1.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-4_1.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-5.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of mouse epididymis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-6.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-ihc-testing-7.jpgAnti-DYNLT1 Antibody Picoband®IHC analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-if-testing-1.jpgAnti-DYNLT1 Antibody Picoband®IF analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Cy2 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-if-testing-2.jpgAnti-DYNLT1 Antibody Picoband®IF analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of human testicular cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Cy2 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05556-dynlt1-primary-antibodies-if-testing-3.jpgAnti-DYNLT1 Antibody Picoband®IF analysis of DYNLT1 using anti-DYNLT1 antibody (A05556). <br>
DYNLT1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-DYNLT1 Antibody (A05556) overnight at 4°C. Cy2 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-epo-receptor-picoband-trade-antibody-a00427-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00427-1-epo_receptor-primary-antibodies-wb-testing-1.jpgAnti-EPO Receptor/EPOR Antibody Picoband® Western blot analysis of EPO Receptor using anti-EPO Receptor antibody (A00427-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat lung tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EPO Receptor antigen affinity purified polyclonal antibody (Catalog # A00427-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EPO Receptor at approximately 55KD. The expected band size for EPO Receptor is at 55KD.
https://www.bosterbio.com/products/primary-antibodies/anti-epo-receptor-picoband-trade-antibody-a00427-2-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00427-2-epo_receptor-primary-antibodies-wb-testing-1.jpgAnti-EPO Receptor/Epor Antibody Picoband® Western blot analysis of EPO Receptor using anti-EPO Receptor antibody (A00427-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat lung tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EPO Receptor antigen affinity purified polyclonal antibody (Catalog # A00427-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EPO Receptor at approximately 55KD. The expected band size for EPO Receptor is at 55KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00427-2-epo_receptor-primary-antibodies-wb-testing-2.jpgAnti-EPO Receptor/Epor Antibody Picoband® Western blot analysis of EPO Receptor using anti-EPO Receptor antibody (A00427-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human U87-MG whole cell lysates, <br> Lane 2: human A431 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EPO Receptor antigen affinity purified polyclonal antibody (Catalog # A00427-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EPO Receptor at approximately 55KD. The expected band size for EPO Receptor is at 55KD.
https://www.bosterbio.com/products/primary-antibodies/anti-erbb-4-picoband-trade-antibody-a00296-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-erbb-4-primary-antibodies-wb-testing-1.jpgAnti-ErbB 4/ERBB4 Antibody Picoband® Western blot analysis of ErbB 4 using anti-ErbB 4 antibody (A00296). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human 293T whole cell lysates, <br>
Lane 3: human Hela whole cell lysates, <br>
Lane 4: rat brain tissue lysates, <br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ErbB 4 antigen affinity purified polyclonal antibody (Catalog # A00296) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ErbB 4 at approximately 180 kDa. The expected band size for ErbB 4 is at 148 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00296-ErbB_4-primary-antibodies-IHC-testing-2.jpgAnti-ErbB 4/ERBB4 Antibody Picoband® IHC analysis of ErbB 4 using anti-ErbB 4 antibody (A00296).
<br>ErbB 4 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ErbB 4 Antibody (A00296) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00296-ErbB_4-primary-antibodies-IHC-testing-3.jpgAnti-ErbB 4/ERBB4 Antibody Picoband® IHC analysis of ErbB 4 using anti-ErbB 4 antibody (A00296).
ErbB 4 was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ErbB 4 Antibody (A00296) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00296-ErbB_4-primary-antibodies-IHC-testing-4.jpgAnti-ErbB 4/ERBB4 Antibody Picoband® IHC analysis of ErbB 4 using anti-ErbB 4 antibody (A00296).
<br>ErbB 4 was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ErbB 4 Antibody (A00296) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00296-ErbB_4-primary-antibodies-IHC-testing-5.jpgAnti-ErbB 4/ERBB4 Antibody Picoband® IHC analysis of ErbB 4 using anti-ErbB 4 antibody (A00296).
<br>ErbB 4 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ErbB 4 Antibody (A00296) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
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https://www.bosterbio.com/products/primary-antibodies/anti-ercc1-picoband-trade-antibody-a00388-2-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00388-2-ercc1-primary-antibodies-wb-testing-1.jpgAnti-ERCC1 Antibody Picoband® Western blot analysis of ERCC1 using anti-ERCC1 antibody (A00388-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat stomach tissue lysates,<br>Lane 2: mouse stomach tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERCC1 antigen affinity purified polyclonal antibody (Catalog # A00388-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ERCC1 at approximately 33KD. The expected band size for ERCC1 is at 33KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00388-2-ercc1-primary-antibodies-wb-testing-2.jpgAnti-ERCC1 Antibody Picoband® Western blot analysis of ERCC1 using anti-ERCC1 antibody (A00388-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human Hela whole cell lysates, <br> Lane 2: human MCF-7 whole cell lysates, <br> Lane 3: human COLO-320 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERCC1 antigen affinity purified polyclonal antibody (Catalog # A00388-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ERCC1 at approximately 33KD. The expected band size for ERCC1 is at 33KD.
https://www.bosterbio.com/products/primary-antibodies/anti-etv6-tel-picoband-trade-antibody-a00361-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6-primary-antibodies-wb-testing-1_1.jpgAnti-ETV6/Tel Antibody Picoband® Western blot analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: human Hela cell lysates, <br>Lane 3: human 22RV1 cell lysates, <br>Lane 4: human SKOV cell lysates, <br>Lane 5: human A549 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ETV6/Tel antigen affinity purified polyclonal antibody (Catalog # A00361-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ETV6/Tel at approximately 59KD. The expected band size for ETV6/Tel is at 53KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6-primary-antibodies-ihc-testing-2.jpgAnti-ETV6/Tel Antibody Picoband® IHC analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1).<br>
ETV6/Tel was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ETV6/Tel Antibody (A00361-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6-primary-antibodies-ihc-testing-3.jpgAnti-ETV6/Tel Antibody Picoband® IHC analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1).<br>
ETV6/Tel was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ETV6/Tel Antibody (A00361-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6-primary-antibodies-ihc-testing-4.jpgAnti-ETV6/Tel Antibody Picoband® IHC analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1).<br>
ETV6/Tel was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ETV6/Tel Antibody (A00361-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6-primary-antibodies-ihc-testing-5.jpgAnti-ETV6/Tel Antibody Picoband® IHC analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1).<br>
ETV6/Tel was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ETV6/Tel Antibody (A00361-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00361-1-etv6tel-primary-antibodies-wb-testing-6.jpgAnti-ETV6/Tel Antibody Picoband® Western blot analysis of ETV6/Tel using anti-ETV6/Tel antibody (A00361-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: rat testis tissue lysates, <br> Lane 2: mouse NIIH3T3 whole cell lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ETV6/Tel antigen affinity purified polyclonal antibody (Catalog # A00361-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ETV6/Tel at approximately 59KD. The expected band size for ETV6/Tel is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-3-picoband-trade-antibody-a01276-3-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-WB-testing-1.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® Western blot analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat liver tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF Receptor 3 antigen affinity purified polyclonal antibody (Catalog # A01276-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF Receptor 3 at approximately 153KD. The expected band size for VEGF Receptor 3 is at 153KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-vegf_receptor_3-primary-antibodies-fcm-testing-10.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-VEGF Receptor 3 antibody (A01276-3).<br>
Overlay histogram showing U20S cells stained with A01276-3 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VEGF Receptor 3 Antibody (A01276-3,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-100194-g001.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband®Trends in the number of rat lymphatic vessels at 2 weeks and 4 weeks after bile duct ligation. A: Representative immunohistochemistry images of Masson’s trichrome, lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1), vascular endothelial growth factor C (VEGF-C) and VEGF receptor 3 (VEGFR-3) staining in the livers of the different groups; B: Quantitative analysis of Masson’s trichrome; C: Quantitative analysis of LYVE-1; D: Quantitative analysis of VEGF-C; E: Quantitative analysis of VEGFR-3 staining; F: Luminal area of lymphatic vessels were also measured; G: The number of lymphatic vessels was also measured. The data represent the mean ± SD. a P < 0.05. b P < 0.01. c P < 0.001. BDL: Bile duct ligation; W: Week.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11886527/'>40093669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-100194-g002.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband®Intervention with adeno-associated virus-vascular endothelial growth factor C relieves liver fibrosis and portal hypertension by increasing the number of lymphatic vessels involved in bile duct ligation. A: Representative immunohistochemistry images of Masson’s trichrome, virus-vascular endothelial growth factor C (VEGF-C), vascular endothelial growth factor receptor 3 (VEGFR-3) and transforming growth factor beta (TGF-β) staining in the livers of the different groups; Quantitative analysis of B: Masson’s trichrome; C: VEGF-C; D: VEGFR-3; E: TGF-β staining; F: The levels of portal pressure were also measured. The data represent the mean ± SD. a P < 0.05. b P < 0.01. c P < 0.001. AAV: Adeno-associated virus; BDL: Bile duct ligation; PP: Portal pressure; TGF-β: Transforming growth factor beta; VEGF-C: Vascular endothelial growth factor C; VEGFR-3: Vascular endothelial growth factor receptor 3; VEH: Vehicle.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11886527/'>40093669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-100194-g005.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband®Platelet-rich plasma-induced platelets increase intrahepatic lymphatic vessels via the vascular endothelial growth factor C/vascular endothelial growth factor receptor 3 pathway. A: Representative immunohistochemistry images of lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1), vascular endothelial growth factor C (VEGF-C) and vascular endothelial growth factor receptor 3 (VEGFR-3), fibronectin (FN) and cluster of differentiation 41 (CD41) in the livers of the different groups; Quantitative analysis of B: LYVE-1; C: VEGF-C; D: VEGFR-3; E: The luminal area; F: The number of lymphatic vessels were also measured; G: FN; H: CD41 expression. The data represent the mean ± SD. a P < 0.05. b P < 0.01. c P < 0.001. BDL: Bile duct ligation; PRP: Platelet-rich plasma; VEH: Vehicle.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11886527/'>40093669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-100194-g008.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband®Inhibition of vascular endothelial growth factor C/vascular endothelial growth factor receptor 3 reverses the amelioration of mesenteric angiogenesis and inflammation by platelet-rich plasma-induced platelets. A: Representative immunohistochemistry images of hematoxylin and eosin, lymphatic vessel endothelial hyaluronan receptor-1 (LYVE-1), vascular endothelial growth factor C (VEGF-C) and vascular endothelial growth factor receptor 3 (VEGFR-3) and cluster of differentiation 68 (CD68) in the mesentery of the different groups; Quantitative analysis of B: Wall thickness; C: LYVE-1; D: VEGF-C; E: VEGFR-3; F: CD68. The data represent the mean ± SD. a P < 0.05. b P < 0.01. c P < 0.001. BDL: Bile duct ligation; PRP: Platelet-rich plasma; SO-VEH: Sham-operated-vehicle; VEH: Vehicle.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11886527/'>40093669</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-2.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).<br>
VEGF Receptor 3 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-3.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).<br>
VEGF Receptor 3 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-4.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).
<br>VEGF Receptor 3 was detected in paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-5.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).
<br>VEGF Receptor 3 was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-6.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).
<br>VEGF Receptor 3 was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01276-3-VEGF_Receptor_3-primary-antibodies-IHC-testing-7.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3).
<br>VEGF Receptor 3 was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-vegf_receptor_3-primary-antibodies-ihc-testing-8.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IHC analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3). <br>
VEGF Receptor 3 was detected in frozen section of human placenta tissue. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-vegf_receptor_3-primary-antibodies-ihc-testing-9.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IF analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3). <br>
VEGF Receptor 3 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01276-3-vegf_receptor_3-primary-antibodies-if-testing-11.jpgAnti-VEGF Receptor 3/FLT4 Antibody Picoband® IF analysis of VEGF Receptor 3 using anti-VEGF Receptor 3 antibody (A01276-3). <br>
VEGF Receptor 3 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-VEGF Receptor 3 Antibody (A01276-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-fzd3-antibody-a04680-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04680-1-FZD3-primary-antibodies-WB-testing-1.jpgAnti-FZD3 Antibody Picoband® Western blot analysis of FZD3 using anti-FZD3 antibody (A04680-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human SK-OV-3 cell lysates, <br>Lane 2: human Jurkat cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FZD3 antigen affinity purified polyclonal antibody (Catalog # A04680-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FZD3 at approximately 76KD. The expected band size for FZD3 is at 76KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04680-1-FZD3-primary-antibodies-IHC-testing-2.jpgAnti-FZD3 Antibody Picoband® IHC analysis of FZD3 using anti-FZD3 antibody (A04680-1).<br>
FZD3 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FZD3 Antibody (A04680-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04680-1-FZD3-primary-antibodies-IHC-testing-3.jpgAnti-FZD3 Antibody Picoband® IHC analysis of FZD3 using anti-FZD3 antibody (A04680-1).<br>
FZD3 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FZD3 Antibody (A04680-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04680-1-FZD3-primary-antibodies-IHC-testing-4.jpgAnti-FZD3 Antibody Picoband® IHC analysis of FZD3 using anti-FZD3 antibody (A04680-1).
<br>FZD3 was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FZD3 Antibody (A04680-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04680-1-FZD3-primary-antibodies-IHC-testing-5.jpgAnti-FZD3 Antibody Picoband® IHC analysis of FZD3 using anti-FZD3 antibody (A04680-1).
<br>FZD3 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-FZD3 Antibody (A04680-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-frizzled-4-picoband-trade-antibody-a02191-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02191-1-Frizzled_4-primary-antibodies-WB-testing-1.jpgAnti-Frizzled 4/FZD4 Antibody Picoband® Western blot analysis of Frizzled 4 using anti-Frizzled 4 antibody (A02191-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysates,<br>Lane 2: human MCF-7 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Frizzled 4 antigen affinity purified polyclonal antibody (Catalog # A02191-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Frizzled 4 at approximately 65KD. The expected band size for Frizzled 4 is at 60KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02191-1-Frizzled_4-primary-antibodies-IHC-testing-2.jpgAnti-Frizzled 4/FZD4 Antibody Picoband® IHC analysis of Frizzled 4 using anti-Frizzled 4 antibody (A02191-1).
Frizzled 4 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Frizzled 4 Antibody (A02191-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02191-1-Frizzled_4-primary-antibodies-IHC-testing-3.jpgAnti-Frizzled 4/FZD4 Antibody Picoband® IHC analysis of Frizzled 4 using anti-Frizzled 4 antibody (A02191-1).
Frizzled 4 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Frizzled 4 Antibody (A02191-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02191-1-Frizzled_4-primary-antibodies-IHC-testing-4.jpgAnti-Frizzled 4/FZD4 Antibody Picoband® IHC analysis of Frizzled 4 using anti-Frizzled 4 antibody (A02191-1).
<br>Frizzled 4 was detected in paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Frizzled 4 Antibody (A02191-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02191-1-Frizzled_4-primary-antibodies-IHC-testing-5.jpgAnti-Frizzled 4/FZD4 Antibody Picoband® IHC analysis of Frizzled 4 using anti-Frizzled 4 antibody (A02191-1).
<br>Frizzled 4 was detected in paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Frizzled 4 Antibody (A02191-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
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https://www.bosterbio.com/products/primary-antibodies/anti-gad65-picoband-trade-antibody-a03142-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03142-1-gad65-primary-antibodies-wb-testing-1.jpgAnti-GAD65/GAD2 Antibody Picoband® Western blot analysis of GAD65 using anti-GAD65 antibody (A03142-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAD65 antigen affinity purified polyclonal antibody (Catalog # A03142-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAD65 at approximately 65 kDa. The expected band size for GAD65 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03142-1-GAD65-primary-antibodies-IHC-testing-2.jpgAnti-GAD65/GAD2 Antibody Picoband® IHC analysis of GAD65 using anti-GAD65 antibody (A03142-1).<br>
GAD65 was detected in paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAD65 Antibody (A03142-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03142-1-GAD65-primary-antibodies-IHC-testing-3.jpgAnti-GAD65/GAD2 Antibody Picoband® IHC analysis of GAD65 using anti-GAD65 antibody (A03142-1).<br>
GAD65 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GAD65 Antibody (A03142-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-gale-picoband-trade-antibody-a00551-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00551-1-gale-primary-antibodies-wb-testing-1.jpgAnti-GALE Antibody Picoband® Western blot analysis of GALE using anti-GALE antibody (A00551-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates,<br>
Lane 3: human HEL whole cell lysates,<br>
Lane 4: human Caco-2 whole cell lysates,<br>
Lane 5: human A549 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALE antigen affinity purified polyclonal antibody (Catalog # A00551-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALE at approximately 38 kDa. The expected band size for GALE is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00551-1-gale-primary-antibodies-wb-testing-2.jpgAnti-GALE Antibody Picoband® Western blot analysis of GALE using anti-GALE antibody (A00551-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat PC-12 whole cell lysates,<br>
Lane 3: mouse stomach tissue lysates,<br>
Lane 4: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALE antigen affinity purified polyclonal antibody (Catalog # A00551-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALE at approximately 38 kDa. The expected band size for GALE is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00551-1-GALE-primary-antibodies-IHC-testing-2.jpgAnti-GALE Antibody Picoband® IHC analysis of GALE using anti-GALE antibody (A00551-1).
<br>GALE was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALE Antibody (A00551-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00551-1-GALE-primary-antibodies-IHC-testing-3.jpgAnti-GALE Antibody Picoband® IHC analysis of GALE using anti-GALE antibody (A00551-1).<br>
GALE was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALE Antibody (A00551-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00551-1-GALE-primary-antibodies-IHC-testing-4.jpgAnti-GALE Antibody Picoband® IHC analysis of GALE using anti-GALE antibody (A00551-1).
<br>GALE was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALE Antibody (A00551-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00551-1-GALE-primary-antibodies-IHC-testing-5_1.jpgAnti-GALE Antibody Picoband® IHC analysis of GALE using anti-GALE antibody (A00551-1).
<br>GALE was detected in paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALE Antibody (A00551-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00551-1-GALE-primary-antibodies-IHC-testing-6_1.jpgAnti-GALE Antibody Picoband® IHC analysis of GALE using anti-GALE antibody (A00551-1).
<br>GALE was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALE Antibody (A00551-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-galns-picoband-trade-antibody-a02954-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02954-1-galns-primary-antibodies-wb-testing-1.jpgAnti-GALNS Antibody Picoband® Western blot analysis of GALNS using anti-GALNS antibody (A02954-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U87 whole cell lysates,<br>
Lane 2: human A549 whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: rat kidney tissue lysates,<br>
Lane 5: rat spleen tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNS antigen affinity purified polyclonal antibody (Catalog # A02954-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALNS at approximately 58 kDa. The expected band size for GALNS is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-2.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).<br>
GALNS was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-3.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).<br>
GALNS was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-4.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).
<br>GALNS was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-5.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).
<br>GALNS was detected in paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-6.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).
<br>GALNS was detected in paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02954-1-GALNS-primary-antibodies-IHC-testing-7.jpgAnti-GALNS Antibody Picoband® IHC analysis of GALNS using anti-GALNS antibody (A02954-1).
<br>GALNS was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GALNS Antibody (A02954-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-galt-picoband-trade-antibody-a01460-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01460-1-galt-primary-antibodies-wb-testing-1.jpgAnti-GALT Antibody Picoband® Western blot analysis of GALT using anti-GALT antibody (A01460-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human 293T whole cell lysates, <br>
Lane 2: human THP-1 whole cell lysates, <br>
Lane 3: human HepG2 whole cell lysates, <br>
Lane 4: human Hela whole cell lysates, <br>
Lane 5: rat lung tissue lysates, <br>
Lane 6: rat kidney tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALT antigen affinity purified polyclonal antibody (A01460-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALT at approximately 43 kDa. The expected band size for GALT is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01460-1-galt-primary-antibodies-ihc-testing-2.jpgAnti-GALT Antibody Picoband® IHC analysis of GALT using anti-GALT antibody (A01460-1). <br>GALT was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GALT Antibody (A01460-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01460-1-galt-primary-antibodies-fcm-testing-3.jpgAnti-GALT Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GALT antibody (A01460-1). <br>
Overlay histogram showing HepG2 cells stained with A01460-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GALT Antibody (A01460-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01460-1-galt-primary-antibodies-ip-testing-4.jpgAnti-GALT Antibody Picoband® Immunoprecipitating GALT in THP-1 whole cell lysate.<br>
Western blot analysis of GALT using anti-GALT antibody (A01460-1); <br>
Lane 1: THP-1 whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-GALT antibody in THP-1 whole cell lysate;<br>
Lane 3: anti-GALT antibody (2μg) + THP-1 whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GALT antigen affinity purified polyclonal antibody (A01460-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GALT at approximately 43 kDa. The expected band size for GALT is at 43 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-glucokinase-picoband-trade-antibody-a00884-1-boster.html2026-03-24T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00884-1-glucokinase-primary-antibodies-wb-testing-1.jpgAnti-Glucokinase/GCK Antibody Picoband®Western blot analysis of Glucokinase using anti-Glucokinase antibody (A00884-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates, <br>
Lane 2: human Jurkat whole cell lysates, <br>
Lane 3: rat liver tissue lysates, <br>
Lane 4: rat RH35 whole cell lysates, <br>
Lane 5: mouse HEPA6/1 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Glucokinase antigen affinity purified polyclonal antibody (A00884-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Glucokinase at approximately 52 kDa. The expected band size for Glucokinase is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00884-1-glucokinase-primary-antibodies-if-testing-1.jpgAnti-Glucokinase/GCK Antibody Picoband®IF analysis of Glucokinase using anti-Glucokinase antibody (A00884-1). <br>
Glucokinase was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Glucokinase Antibody (A00884-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-glycerol-kinase-picoband-trade-antibody-a02884-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02884-1-glycerol_kinase-primary-antibodies-wb-testing-1.jpgAnti-Glycerol kinase/GK Antibody Picoband® Western blot analysis of Glycerol kinase using anti-Glycerol kinase antibody (A02884-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysates,<br>Lane 2: human HepG2 whole cell lysates,<br>Lane 3: human SW579 whole cell lysates,<br>Lane 4: human SK-OV-3 whole cell lysates,<br>Lane 5: human U-87MG whole cell lysates,<br>Lane 6: rat testis tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Glycerol kinase antigen affinity purified polyclonal antibody (Catalog # A02884-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Glycerol kinase at approximately 61KD. The expected band size for Glycerol kinase is at 61KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02884-1-gk-primary-antibodies-ihc-testing-4.jpgAnti-Glycerol kinase/GK Antibody Picoband®IHC analysis of Glycerokinase/GK using anti-Glycerokinase/GK antibody (A02884-1). <br>Glycerokinase/GK was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Glycerokinase/GK Antibody (A02884-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02884-1-Glycerol_kinase-primary-antibodies-IHC-testing-2.jpgAnti-Glycerol kinase/GK Antibody Picoband® IHC analysis of Glycerol kinase using anti-Glycerol kinase antibody (A02884-1).
<br>Glycerol kinase was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Glycerol kinase Antibody (A02884-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02884-1-Glycerol_kinase-primary-antibodies-IHC-testing-3.jpgAnti-Glycerol kinase/GK Antibody Picoband® IHC analysis of Glycerol kinase using anti-Glycerol kinase antibody (A02884-1).
<br>Glycerol kinase was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Glycerol kinase Antibody (A02884-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-gstm1-picoband-trade-antibody-a00569-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00569-1-GSTM1-primary-antibodies-WB-testing-1.jpgAnti-GSTM1 Antibody Picoband® Western blot analysis of GSTM1 using anti-GSTM1 antibody (A00569-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat lung tissue lysates,<br>Lane 3: mouse stomach tissue lysates,<br>Lane 4: mouse kidney tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTM1 antigen affinity purified polyclonal antibody (Catalog # A00569-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GSTM1 at approximately 26KD. The expected band size for GSTM1 is at 26KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00569-1-gstm1-primary-antibodies-fc-testing-2.pngAnti-GSTM1 Antibody Picoband® Flow Cytometry analysis of HeLa cells using anti-GSTM1 antibody (A00569-1). <br> Overlay histogram showing HeLa cells stained with A00569-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GSTM1 Antibody (A00569-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00569-1-primary-antibodies-if-testing-3.jpgAnti-GSTM1 Antibody Picoband® IF analysis of GSTM1 using anti-GSTM1 antibody (A00569-1). <br>
GSTM1 was detected in an immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GSTM1 Antibody (A00569-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-hoxa5-picoband-trade-antibody-a04018-2-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04018-2-HOXA5-primary-antibodies-WB-testing-1.jpgAnti-HOXA5 Antibody Picoband® Western blot analysis of HOXA5 using anti-HOXA5 antibody (A04018-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysates,<br>Lane 2: human Hela cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HOXA5 antigen affinity purified polyclonal antibody (Catalog # A04018-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HOXA5 at approximately 29KD. The expected band size for HOXA5 is at 29KD.
https://www.bosterbio.com/products/primary-antibodies/anti-icos-picoband-trade-antibody-a00291-2-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00291-2-icos-primary-antibodies-wb-testing-1.jpgAnti-ICOS Antibody Picoband® Western blot analysis of ICOS using anti-ICOS antibody (A00291-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse stomach tissue lysates,<br>Lane 2: mouse spleen tissue lysates,<br>Lane 3: mouse thymus tissue lysates,<br>Lane 4: mouse small intestine tissue lysates,<br>Lane 5: rat thymus tissue lysates,<br>Lane 6: human placenta tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICOS antigen affinity purified polyclonal antibody (Catalog # A00291-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ICOS at approximately 20KD. The expected band size for ICOS is at 22KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00291-2-41598_2025_88671_fig9_html.pngAnti-ICOS Antibody Picoband®Relative expression of genes expression in GBM tissues. Expression levels of WTAP and ZC3H13 genes were compared with those of the control group on GBM tissues, 10 GBM and adjacent tissues, respectively ( A ). The expression levels of siRNA WTAP and overexpression ZC3H13 genes ( B and C ). The expression levels of CD27, CD70, CD80, CD86, ICOS, CTLA4, and LAG3 in siRNA WTAP and overexpression ZC3H13 were demonstrated in Fig. D and F, respectively. The result were determined by qRT-PCR. The data are mean ± standard deviation of six replicate experiments. * P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00291-2-ICOS-primary-antibodies-IHC-testing-2.jpgAnti-ICOS Antibody Picoband® IHC analysis of ICOS using anti-ICOS antibody (A00291-2).<br>
<br>ICOS was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICOS Antibody (A00291-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00291-2-ICOS-primary-antibodies-IHC-testing-3.jpgAnti-ICOS Antibody Picoband® IHC analysis of ICOS using anti-ICOS antibody (A00291-2).<br>
ICOS was detected in paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICOS Antibody (A00291-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00291-2-ICOS-primary-antibodies-IHC-testing-4.jpgAnti-ICOS Antibody Picoband® IHC analysis of ICOS using anti-ICOS antibody (A00291-2).
<br>ICOS was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICOS Antibody (A00291-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-il1f10-picoband-trade-antibody-a09268-2-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A09268-2-IL1F10-primary-antibodies-WB-testing-1.jpgAnti-IL1F10 Antibody Picoband® Western blot analysis of IL1F10 using anti-IL1F10 antibody (A09268-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat lung tissue lysates,<br>Lane 3: rat RH35 cell lysates, <br>Lane 4: mouse lung tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL1F10 antigen affinity purified polyclonal antibody (Catalog # A09268-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL1F10 at approximately 17KD. The expected band size for IL1F10 is at 17KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il12a-picoband-trade-antibody-a00918-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00918-1-IL12A-primary-antibodies-WB-testing-1.jpgAnti-IL12A Antibody Picoband® Western blot analysis of IL12A using anti-IL12A antibody (A00918-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysates, <br>Lane 2: human SW620 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL12A antigen affinity purified polyclonal antibody (Catalog # A00918-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL12A at approximately 35KD. The expected band size for IL12A is at 25KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-1-12931_2023_2557_fig3_html.pngAnti-IL12A Antibody Picoband®IL-25 inhibited the production of IL-12, IL-23 in amodel of of neutrophilia-dominant airway inflammation. ( A - D ) Measurement of Il12a , Il12b , Il23a and Il25 mRNA levels in lung tissue using RT-PCR. ( E ) Representative images of IL-12B and CD80 immunofluorescence staining in lung sections. Scale bar, 50 μm. ( F ) The proportion of CD80 staining-positive cells in lung sections in different groups. ( G ) The proportion of IL-12B staining-positive cells in lung sections in different groups. ( H ) The proportion of CD80 and IL-12B staining-positive cells in lung sections in different groups. There were 4–6 mice in each group. One-way ANOVA was used for statistical analysis (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-1-12931_2023_2557_fig4_html.pngAnti-IL12A Antibody Picoband®Exogenous IL-25 inhibited LPS-induced M1 polarization and the expression of IL-12 and IL-23 in mouse pulmonary cells. ( A ) Representative Western blots showing IL-12 A and β-Tubulin protein in primary culture of mouse pulmonary macrophages. ( B ) Quantitative analysis of IL-12 A in mouse pulmonary macrophages using ImageJ. Values are expressed in arbitrary units (a.u.). ( C ) Representative Western blots showing IL-12B, IL-23 A, and β-Tubulin protein in mouse pulmonary macrophages. ( D - E ) Quantitative analysis IL-12B, and IL-23A in mouse pulmonary macrophages using ImageJ. ( F - J ) Detection of Il12a, Il12b, Il23a, Cd80 , and Il-1β mRNA level in mouse pulmonary macrophages using RT-PCR. The experiment was repeated 3 times independently, and a similar trend was obtained. One-way ANOVA was used for statistical analysis (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-1-12931_2023_2557_fig5_html.pngAnti-IL12A Antibody Picoband®IL-25 inhibited LPS-induced translocation of c-Rel in STAT3-dependent manner in pulmonary macrophages. ( A ) The level of STAT3 phosphorylation was detected using Western blot. ( B ) Quantitative analysis of STAT3 phosphorylation in primary culture of pulmonary macrophages using ImageJ. Values are expressed in arbitrary units (a.u.). ( C - D ) Western blot was performed to measure the protein levels of c-Rel in the cytoplasm ( C ) and nucleus ( D ) of pulmonary macrophages. ( E - F ) Quantitative analysis of c-Rel expresion in cytoplasm ( E ) and nucleus ( F ) of pulmonary macrophages using ImageJ. ( G ) Representative images of c-Rel immunofluorescence staining in primary culture of macrophage from lung. Scale bar, 50 μm. ( H ) The protein levels of IL-12 A and IL-23 A of pulmonary macrophages was measured using Western blot. ( I - J ) Quantitative analysis of IL-12 A and IL-23 A in pulmonary macrophages using ImageJ. Values are expressed in arbitrary units (a.u.). ( K ) The graphical abstract of this study, which was drawn by Figdraw. The experiment was repeated 3 times independently, and the similar trend was obtained. One way ANOVA was used for statistical analysis (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00918-1-12931_2023_2557_fig6_html.pngAnti-IL12A Antibody Picoband®The expression of IL-25 was decreased whereas IL-12, IL-23, and M1 macrophage markers were increased in severe of non-eosinophilic asthmatics. ( A ) IL-25 protein levels were decreased in sputum from a cohort of non-smoker severe asthma in the U-BIOPRED study. Based on the analysis of the data provided by Takahashi et al. [ ], 158 downregulated and 187 upregulated proteins were identified in the supernatant of induced sputum from non-smoker severe asthma patients (n = 37) compared to controls (n = 18) by proteomic assay and were shown in the volcano plot. The protein level of IL-25 (indicated by the red arrow) was decreased in the supernatant of induced sputum from non-smoker severe asthma patients compared to controls (log2 of fold change = -0.274, P = 0.019). ( B ) Detection of IL-25 mRNA level in airway brushings of eosinophilic asthma (n = 20) and non-eosinophilic asthma (n = 14) by RT-PCR. ( C - E ) Detection of IL-12 A, IL-12B and IL-23 A mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. ( F - J ) Detection of I L-1β, IFN-γ, CD80, iNOS , and CD206 mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. ( K ) Representative images of IL-12B and CD80 immunofluorescence staining in BALF cells of control, eosinophilic asthma, and non-eosinophilic asthma. Scale bar, 5 μm. ( L ) Detection of IL-25 mRNA level in induced sputum of eosinophilic asthma (n = 17) and non-eosinophilic asthma (n = 12) by RT-PCR. One way ANOVA was used for statistical analysis. (* P < 0.05; ** P < 0.01; *** P < 0.001) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-023-02557-5'>37898756</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00918-1-IL12A-primary-antibodies-IHC-testing-2.jpgAnti-IL12A Antibody Picoband® IHC analysis of IL12A using anti-IL12A antibody (A00918-1).<br>
IL12A was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL12A Antibody (A00918-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00918-1-IL12A-primary-antibodies-IHC-testing-3.jpgAnti-IL12A Antibody Picoband® IHC analysis of IL12A using anti-IL12A antibody (A00918-1).<br>
IL12A was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL12A Antibody (A00918-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-il12b-picoband-trade-antibody-a01152-4-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01152-4-IL12B-primary-antibodies-WB-testing-1.jpgAnti-IL12B Antibody Picoband® Western blot analysis of IL12B using anti-IL12B antibody (A01152-4).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse NIH3T3 cell lysates, <br>Lane 2: human A549 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL12B antigen affinity purified polyclonal antibody (Catalog # A01152-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL12B at approximately 37KD. The expected band size for IL12B is at 37KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il17-picoband-trade-antibody-a00421-2-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00421-2-il17-primary-antibodies-wb-testing-1.jpgAnti-IL17/Il17a Antibody Picoband® Western blot analysis of IL17 using anti-IL17 antibody (A00421-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Jurkat cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17 antigen affinity purified polyclonal antibody (Catalog # A00421-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17 at approximately 27KD. The expected band size for IL17 is at 17KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00421-2-fphar-15-1485255-g007.jpgAnti-IL17/Il17a Antibody Picoband®Que decreases the protein expression level of IL-17A and NF-κB. (A–C) Protein expression of IL-17A and NF-κB in colon of mice (n = 4). * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1485255/full'>39717557</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00421-2-fphar-15-1485255-g008.jpgAnti-IL17/Il17a Antibody Picoband®Workflow for analyzing Que’s mechanisms in UC treatment. Network pharmacology, in conjunction with transcriptomic methodologies and experimental validation, demonstrated that quercetin alleviated the symptoms associated with DSS-induced colitis. It attenuates the inflammatory response, promotes the repair of colonic mucosal tissues, and elevates the levels of colonic tight junction proteins in mice with ulcerative colitis. These effects may enhance tight junction integrity and restore intestinal barrier function by modulating the IL-17A signaling pathway while simultaneously inhibiting the CXCL8-CXCR1/2 axis.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1485255/full'>39717557</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00421-2-41598_2017_15533_fig2_html.jpgAnti-IL17/Il17a Antibody Picoband®Th1/Th2 imbalance and Th17 immune response. ( A ) Immunohistochemistry and average optical density for IFN-γ, F DBP = 5.596 (p = 0.002), F TG = 142.67 (p = 0.000), F DBP*TG = 1.114 (p = 0.351). ( B ) Immunohistochemistry and average optical density for IL-4, F DBP = 0.537 (p = 0.659), F TG = 1.419 (p = 0.24), F DBP*TG = 0.168 (p = 0.917). ( C ) Immunohistochemistry and average optical density for IL-17 F DBP = 6.966 (p = 0.001), F TG = 93.46 (p = 0.000), F DBP*TG = 4.136 (p = 0.011). Magnification = ×40. *p < 0.05, **p < 0.01, compared with the saline group; # p < 0.05, ## p < 0.01, compared with the TG group; & p < 0.05, && p < 0.01, compared with the DBP50 + TG group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-017-15533-z'>29133889</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00421-2-IL17-primary-antibodies-IHC-testing-2.jpgAnti-IL17/Il17a Antibody Picoband® IHC analysis of IL17 using anti-IL17 antibody (A00421-2).
<br>IL17 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL17 Antibody (A00421-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00421-2-IL17-primary-antibodies-IHC-testing-3.jpgAnti-IL17/Il17a Antibody Picoband® IHC analysis of IL17 using anti-IL17 antibody (A00421-2).<br>
IL17 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL17 Antibody (A00421-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00421-2-IL17-primary-antibodies-IHC-testing-4.jpgAnti-IL17/Il17a Antibody Picoband® IHC analysis of IL17 using anti-IL17 antibody (A00421-2).
<br>IL17 was detected in paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IL17 Antibody (A00421-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00421-2-il17-primary-antibodies-elisa-testing-5.jpgAnti-IL17/Il17a Antibody Picoband® Sandwich ELISA - Recombinant mouse IL17/Il17a protein standard curve.<br>
Use in combination with reagents from Mouse IL17/Il17a ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0431).
https://www.bosterbio.com/products/primary-antibodies/anti-il23-picoband-trade-antibody-a01097-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01097-1-il23-primary-antibodies-wb-testing-1.jpgAnti-IL23/IL23A Antibody Picoband® Western blot analysis of IL23 using anti-IL23 antibody (A01097-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human placenta tissue lysates,<br>Lane 2: human PANC-1 cell lysates, <br>Lane 3: rat lymph tissue lysates,<br>Lane 4: rat small intestine tissue lysates,<br>Lane 5: rat testis tissue lysates,<br>Lane 6: rat ovary tissue lysates,<br>Lane 7: mouse testis tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL23 antigen affinity purified polyclonal antibody (Catalog # A01097-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL23 at approximately 19KD. The expected band size for IL23 is at 21KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01097-1-fimmu-12-811803-g001.jpgAnti-IL23/IL23A Antibody Picoband®Neutrophils, lung function and BALF IL-23/IL-17A levels between patients with stable COPD (con-COPD, n = 33) and patients with P. aeruginosa -infected COPD (PA-COPD, n = 34). PA-COPD patients had higher absolute and percent numbers of neutrophils in BALF, but not in blood (A, B) . Forced expiratory volums (C) , expiratory flows (D) and forced oscillation tests (E) were compared between con-COPD and PA-COPD patients. IL-23 and IL-17A levels were significantly elevated in patients with PA-COPD (F) . Data were presented as mean ± SD. *P < 0.05, ** P < 0.01, ns, non-significant. Correlation analysis showed that there was a notably positive correlation between the two cytokines (G) , and further regression analysis revealed that IL-23 might be an important factor contributing to elevation of IL-17A (H) . There was also a significantly positive correlation between IL-17A levels and absolute neutrophil numbers in BALF (I) . The spirometry results, including FEV 1.0 % predicted (J) , FEV 1.0 /FVC% (K) and MMEF (L) were negatively correlated with the levels of IL-17A. BALF, bronchoalveolar lavage fluid; COPD, chronic obstructive pulmonary disease; IL, interleukin; FEV 1.0 , forced expiratory volume in one second; FVC, forced vital capacity; MMEF, maximal mid-expiratory flow.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.811803/full'>35095906</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01097-1-fimmu-12-811803-g002.jpgAnti-IL23/IL23A Antibody Picoband®P. aeruginosa infection increased IL-23/IL-17 axis signaling in the lungs of COPD mouse models. C57BL/6 mice were exposed to ozone twice a week for 6 weeks to establish COPD models, and then were intrabronchially inoculated with sterile agar beads (con-COPD) or 1.0 × 10 5 CFU agar-entrapped P. aeruginosa (PA-COPD). Lungs were excised at one day post inoculation, and were sectioned and stained with masson trichrome to measure tissue fibrosis ( A , upper row), and PAS to quantify glycogen [ (A) , bottom row]. Blue areas around airways were identified as collagen deposition (indicated by black arrows), and purple areas within tracheal cavity were identified as mucus production and goblet cell hyperpasia (indicated by blue arrows). Internal scale bar = 100 μm. Quantitative real-time PCR, semiquantitative RT-PCR, and western-blot analysis of IL-23 and its receptor (B) , and IL-17A and its receptor (C) were performed using lung tissues. β-actin serves as the loading control. Data were presented as mean ± SD ( n = 5 per group). ** P < 0.01. The lungs were processed for immunofluorescent analysis (D) , and the sections were stained with anti-IL-17RA (red) and anti-Ly6G (green), and DAPI (blue) for nuclei. Internal scale bar = 100 μm. Two independent experiments were performed. Correlation analysis showed that there was a significantly negative correlation between the numbers of Ly6G + IL-17RA + cells and the spirometry results (E) . COPD, chronic obstructive pulmonary disease; CFU, colony-forming units; IL, interleukin; FVC, forced vital capacity; FEV 50 , volume expired in the first 50 ms of fast expiration.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.811803/full'>35095906</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01097-1-fimmu-12-811803-g007.jpgAnti-IL23/IL23A Antibody Picoband®Adjunctive therapy of IL-17A–neutralizing antibody to antibiotic improved the outcome of P. aeruginosa infection in COPD mouse models. COPD mouse models were intrabronchially inoculated with 1.0 × 10 5 CFU agar-entrapped P. aeruginosa . Oral ciprofloxacin (5 mg/kg, every 12 h) was applied concurrently with intraperitoneally administered IL-17A–neutralizing antibody (2 mg/kg, every 4 h) or IgG starting at 16 h post inoculation. Mouse lungs were excised, sectioned and stained with hematoxylin and eosin (internal scale bar = 100 μm) after treatment (A) , and the infiltrate scores (B) and MPO activity (C) were determined on each day. Bacterial plate counting (D) , protein levels of IL-17A (E) , IL-23 (F) , and RBP4 (G) , and spirometry tests, including FVC (H) , FEV 50 (I) , MMEF (J) , FEF 50 (K) , and FEF 75 (L) , were performed and compared between groups treated with and without IL-17A block. Data are representative of three independent experiments, and are presented as mean ± SD ( n = 3 per group). * P < 0.05. COPD, chronic obstructive pulmonary disease; Cip, ciprofloxacin; CFU, colony-forming units; MPO, myeloperoxidase; FVC, forced vital capacity; FEV50, volume expired in the first 50 ms of fast expiration; MMEF, maximal mid-expiratory flow; FEF 50 , forced expiratory flow at 50% FVC; FEF 75 , forced expiratory flow at 75% FVC.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.811803/full'>35095906</a></b>
https://www.bosterbio.com/products/primary-antibodies/anti-il33-picoband-trade-antibody-a00113-2-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-2-il33-primary-antibodies-wb-testing-1_1.jpgAnti-IL33 Antibody Picoband®Western blot analysis of IL33 using anti-IL33 antibody (A00113-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat lung tissue lysates, <br>
Lane 2: mouse lung tissue lysates, <br>
Lane 3: mouse RAW264.7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL33 antigen affinity purified polyclonal antibody (A00113-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IL33 at approximately 35 kDa. The expected band size for IL33 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-2-il33-primary-antibodies-ihc-testing-1.jpgAnti-IL33 Antibody Picoband®IHC analysis of IL33 using anti-IL33 antibody (A00113-2). <br>
IL33 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL33 Antibody (A00113-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00113-2-il33-primary-antibodies-ihc-testing-2.jpgAnti-IL33 Antibody Picoband®IHC analysis of IL33 using anti-IL33 antibody (A00113-2). <br>
IL33 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IL33 Antibody (A00113-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-iqgap2-picoband-trade-antibody-a04787-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04787-1-IQGAP2-primary-antibodies-WB-testing-1.jpgAnti-IQGAP2 Antibody Picoband® Western blot analysis of IQGAP2 using anti-IQGAP2 antibody (A04787-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysates, <br>Lane 2: human placenta tissue lysates,<br>Lane 3: human HepG2 cell lysates, <br>Lane 4: mouse stomach tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IQGAP2 antigen affinity purified polyclonal antibody (Catalog # A04787-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IQGAP2 at approximately 181KD. The expected band size for IQGAP2 is at 181KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04787-1-iqgap2-primary-antibodies-fc-testing-2.pngAnti-IQGAP2 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-IQGAP2 antibody (A04787-1). <br> Overlay histogram showing U20S cells stained with A04787-1 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IQGAP2 Antibody (A04787-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04787-1-iqgap2-primary-antibodies-ihc-testing-3.jpgAnti-IQGAP2 Antibody Picoband® IHC analysis of IQGAP2 using antiIQGAP2 antibody (A04787-1). <br>
IQGAP2 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IQGAP2 Antibody (A04787-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04787-1-iqgap2-primary-antibodies-ihc-testing-4.jpgAnti-IQGAP2 Antibody Picoband® IHC analysis of IQGAP2 using antiIQGAP2 antibody (A04787-1). <br>
IQGAP2 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-IQGAP2 Antibody (A04787-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04787-1-iqgap2-primary-antibodies-if-testing-5.jpgAnti-IQGAP2 Antibody Picoband® IF analysis of IQGAP2 using anti-IQGAP2 antibody (A04787-1). <br>
IQGAP2 was detected in immunocytochemical section of MCF7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-IQGAP2 Antibody (A04787-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04787-1-iqgap2-primary-antibodies-fcm-testing-6.jpgAnti-IQGAP2 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-IQGAP2 antibody (A04787-1).<br>Overlay histogram showing SiHa cells stained with A04787-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IQGAP2 Antibody (A04787-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-irak-picoband-trade-antibody-a01021-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01021-irak-primary-antibodies-wb-testing-1.jpgAnti-IRAK/IRAK1 Antibody Picoband® Western blot analysis of IRAK1 using anti-IRAK1 antibody (A01021). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: rat kidney tissue lysates,<br>
Lane 4: mouse liver tissue lysates,<br>
Lane 5: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRAK1 antigen affinity purified polyclonal antibody (Catalog # A01021) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRAK1 at approximately 77 kDa. The expected band size for IRAK1 is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01021-irak-primary-antibodies-if-testing-2.jpgAnti-IRAK/IRAK1 Antibody Picoband® IF analysis of IRAK using anti-IRAK antibody (A01021). <br>
IRAK was detected in immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-IRAK Antibody (A01021) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01021-irak-primary-antibodies-fcm-testing-3.jpgAnti-IRAK/IRAK1 Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-IRAK antibody (A01021).<br>Overlay histogram showing U937 cells stained with A01021 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRAK Antibody (A01021,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-fbxl11-picoband-trade-antibody-a03027-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03027-1-FBXL11-primary-antibodies-WB-testing-1.jpgAnti-FBXL11/KDM2A Antibody Picoband® Western blot analysis of FBXL11 using anti-FBXL11 antibody (A03027-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse liver tissue lysates,<br>Lane 2: human A431 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXL11 antigen affinity purified polyclonal antibody (Catalog # A03027-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FBXL11 at approximately 150KD. The expected band size for FBXL11 is at 133KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-2-picoband-trade-antibody-a00901-3-boster.html2026-04-03T05:00:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-vegf_receptor_2-primary-antibodies-wb-testing-1_1.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® Western blot analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3). <br>
The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: Marker<br>
Lane 2: mouse heart tissue lysates, <br>
Lane 3: mouse thymus tissue lysates, <br>
Lane 4: mouse spleen tissue lysates, <br>
Lane 5: mouse kidney tissue lysates. <br>
Lane 6: mouse brain tissue lysates, <br>
Lane 5: mouse lung tissue lysates. <br>
Lane 7: mouse HEPA1-6 whole cell lysates,<br>
Lane 8: mouse NIH3T3 whole cell lysates.<br>
The membrane was incubated with rabbit anti-VEGF Receptor 2 antigen affinity purified polyclonal antibody (Catalog # A00901-3) at 1.0 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-13048_2025_1679_fig5_html.pngAnti-VEGF Receptor 2/Kdr Antibody Picoband®YJD affected the VEGF/VEGFR-2/FAK pathway in vivo. ( A – B ) Germ cell markers MVH and Oct4 were detected by IF. ( C ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( D ) VEGF, VEGFR-2, FAK expression in the ovaries was examined by IHC; Black arrows point to areas of positive staining. ( E - F ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ** P < 0.01, *** P < 0.001 vs. Control; # P < 0.05, ## P < 0.01, ### P < 0.001 vs. TP; & P < 0.05, && P < 0.01 vs. TP + M-YJD <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-13048_2025_1679_fig6_html.pngAnti-VEGF Receptor 2/Kdr Antibody Picoband®YJD affected the VEGF/VEGFR-2/FAK pathway and KGN cell injury in vitro. ( A ) Screening of YJD for medicated serum concentrations utilized the CCK-8 assay. ( B ) The cell viability of each group was measured by CCK-8. ( C – G ) Serum levels of the hormones P, E2, FSH, LH, and AMH were examined by ELISA. ( H ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( I - J ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ( K ) Apoptosis index was detected by Annexin V-FITC flow cytometry. ( L ) The expression of Bcl-2, pro-Caspase-3, Caspase-3 and AIF were assessed by WB. ** P < 0.01, *** P < 0.001 vs. Control; # P < 0.05, ## P < 0.01, ### P < 0.001 vs. TP <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-13048_2025_1679_fig7_html.pngAnti-VEGF Receptor 2/Kdr Antibody Picoband®YJD affected POF by regulating the VEGF/VEGFR-2/FAK signaling pathway. ( A – E ) Serum levels of the hormones P, E2, FSH, LH, and AMH were examined by ELISA. Control and TP groups were set up, and the remaining groups were co-treated with TP and 15% medicated serum, along with VEGF inhibitor (Avastin), VEGFR-2 inhibitor (SU5408), or FAK inhibitor (Y15). ( F - G ) Serum levels of indicators of oxidative stress, MDA and SOD were assessed by ELISA. ( H - J ) The expression of VEGF, VEGFR-2, and FAK was detected by qRT-PCR. ( K - L ) The expression of VEGF, VEGFR-2, FAK, p-VEGFR-2 and p-FAK were assessed by WB. ( M ) Apoptosis rate was detected by Annexin V-FITC flow cytometry. ( N ) The expression of Bcl-2, pro-Caspase-3, Caspase-3 and AIF were assessed by western blotting. ** P < 0.01, *** P < 0.001 vs. Control; ## P < 0.01, ### P < 0.001 vs. TP; & P < 0.05, && P < 0.01, &&& P < 0.001 vs. TP + 15% medicated serum <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13048-025-01679-2'>40287776</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-3-VEGF_Receptor_2-primary-antibodies-IHC-testing-2.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).<br>
VEGF Receptor 2 was detected in paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00901-3-VEGF_Receptor_2-primary-antibodies-IHC-testing-3.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® IHC analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3).<br>
VEGF Receptor 2 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGF Receptor 2 Antibody (A00901-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-vegf_receptor_2-primary-antibodies-if-testing-4.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® IF analysis of VEGF Receptor 2 using anti-VEGF Receptor 2 antibody (A00901-3). <br>
VEGF Receptor 2 was detected in immunocytochemical section of NIH3T3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-VEGF Receptor 2 Antibody (A00901-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-vegf_receptor_2-primary-antibodies-fcm-testing-5.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® Flow Cytometry analysis of MFC cells using anti-VEGF Receptor 2 antibody (A00901-3).<br>Overlay histogram showing MFC cells stained with A00901-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VEGF Receptor 2 Antibody (A00901-3,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00901-3-vegf_receptor_2-primary-antibodies-fcm-testing-6.jpgAnti-VEGF Receptor 2/Kdr Antibody Picoband® Flow Cytometry analysis of LLC cells using anti-VEGF Receptor 2 antibody (A00901-3).<br>Overlay histogram showing LLC cells stained with A00901-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VEGF Receptor 2 Antibody (A00901-3,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-kallikrein-6-picoband-trade-antibody-a01882-2-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01882-2-klk6-primary-antibodies-wb-testing-1.jpgAnti-Kallikrein 6/KLK6 Antibody Picoband® Western blot analysis of Kallikrein 6/KLK6 using anti-Kallikrein 6/KLK6 antibody (A01882-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Kallikrein 6/KLK6 antigen affinity purified polyclonal antibody (Catalog # A01882-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Kallikrein 6/KLK6 at approximately 29 kDa. The expected band size for Kallikrein 6/KLK6 is at 27 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-nkg2d-picoband-trade-antibody-a00661-1-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00661-1-nkg2d-primary-antibodies-wb-testing-1.jpgAnti-NKG2D/KLRK1 Antibody Picoband® Western blot analysis of NKG2D using anti-NKG2D antibody (A00661-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat lymph tissue lysates,<br>Lane 2: rat spleen tissue lysates,<br>Lane 3: mouse thymus tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NKG2D antigen affinity purified polyclonal antibody (Catalog # A00661-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NKG2D at approximately 35KD. The expected band size for NKG2D is at 25KD.
https://www.bosterbio.com/products/primary-antibodies/anti-leptin-picoband-trade-antibody-a00479-3-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00479-3-Leptin-primary-antibodies-WB-testing-1.jpgAnti-Leptin Antibody Picoband® Western blot analysis of Leptin using anti-Leptin antibody (A00479-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant human Leptin protein 1ng.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Leptin antigen affinity purified polyclonal antibody (Catalog # A00479-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Leptin at approximately 16KD. The expected band size for Leptin is at 16KD.
https://www.bosterbio.com/products/primary-antibodies/anti-lif-picoband-trade-antibody-a01400-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01400-LIF-primary-antibodies-WB-testing-1.jpgAnti-LIF Antibody Picoband® Western blot analysis of LIF using anti-LIF antibody (A01400).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat heart tissue lysates,<br>Lane 3: rat liver tissue lysates,<br>Lane 4: rat kidney tissue lysates,<br>Lane 5: human Hela cell lysates, <br>Lane 6: human placenta tissue lysates,<br>Lane 7: human Jurkat cell lysates, <br>Lane 8: mouse liver tissue lysates.<br>Lane 9: mouse kidney tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIF antigen affinity purified polyclonal antibody (Catalog # A01400) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIF at approximately 18KD. The expected band size for LIF is at 22KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mmp13-picoband-trade-antibody-a00420-2-boster.html2026-03-24T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00420-2-mmp13-primary-antibodies-wb-testing-1_1_2.jpgAnti-MMP13 Antibody Picoband® Western blot analysis of MMP13 using anti-MMP13 antibody (A00420-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human A549 whole cell lysates<br> Lane 2: human PC-3 whole cell lysates<br> Lane 3: human U2OS whole cell lysates<br> Lane 4: human HEK293 whole cell lysates<br> Lane 5: rat testicular tissue lysates<br> Lane 6: mouse testicular tissue lysates <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP13 antigen affinity purified polyclonal antibody (Catalog # A00420-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP13 at approximately 54KD. The expected band size for MMP13 is at 54KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00420-2-thnov15p6553g008.jpgAnti-MMP13 Antibody Picoband®Therapeutic effectiveness evaluated after administering AE@SiO 2 -MTX. (A) Knee joints were stained with HE and safranin O. Scale bar: 100 μm. (B) TNF-α, IL-6, MMP3 and MMP13 and DAPI staining applied to knee sections. (C) Line profile analysis verified the co-expression and co-localization of TNF-α and IL-6, MMP3 and MMP13. Scale bar: 50 μm.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12160022/'>40521182</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00420-2-fbioe-13-1639117-g009.jpgAnti-MMP13 Antibody Picoband®(A) Representative immunohistochemistry images of ColII and MMP-13 staining across all groups. (B, C) Quantitative analysis of ColII and MMP-13 protein expression levels in the NP. Immunohistological analysis showing that the protein expression level of ColII in the ILS+STZ+ IP group was higher and this of MMP-13 was lower than those in the ILS+STZ group. Note: *P < 0.05, **P < 0.01; scale bars = 200 μm as indicated.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/bioengineering-and-biotechnology/articles/10.3389/fbioe.2025.1639117/full'>40837020</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00420-2-MMP13-primary-antibodies-IHC-testing-2.jpgAnti-MMP13 Antibody Picoband® IHC analysis of MMP13 using anti-MMP13 antibody (A00420-2).
<br>MMP13 was detected in paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP13 Antibody (A00420-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00420-2-MMP13-primary-antibodies-IHC-testing-3.jpgAnti-MMP13 Antibody Picoband® IHC analysis of MMP13 using anti-MMP13 antibody (A00420-2).<br>
MMP13 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP13 Antibody (A00420-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00420-2-MMP13-primary-antibodies-IHC-testing-4.jpgAnti-MMP13 Antibody Picoband® IHC analysis of MMP13 using anti-MMP13 antibody (A00420-2).
<br>MMP13 was detected in paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP13 Antibody (A00420-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00420-2-MMP13-primary-antibodies-IHC-testing-5.jpgAnti-MMP13 Antibody Picoband® IHC analysis of MMP13 using anti-MMP13 antibody (A00420-2).
<br>MMP13 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MMP13 Antibody (A00420-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-muc1-picoband-trade-antibody-a00187-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00187-muc1-primary-antibodies-wb-testing-1_2.jpgAnti-MUC1 Antibody Picoband®Western blot analysis of MUC1 using anti-MUC1 antibody (A00187). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUC1 antigen affinity purified polyclonal antibody (A00187) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MUC1 at approximately 120, 200 kDa. The expected band size for MUC1 is at 122 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00187-muc1-primary-antibodies-ihc-testing-1.jpgAnti-MUC1 Antibody Picoband®IHC analysis of MUC1 using anti-MUC1 antibody (A00187). <br>MUC1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC1 Antibody (A00187) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00187-muc1-primary-antibodies-ihc-testing-2.jpgAnti-MUC1 Antibody Picoband®IHC analysis of MUC1 using anti-MUC1 antibody (A00187). <br>MUC1 was detected in a paraffin-embedded section of human ovarican cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC1 Antibody (A00187) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00187-muc1-primary-antibodies-ihc-testing-3.jpgAnti-MUC1 Antibody Picoband®IHC analysis of MUC1 using anti-MUC1 antibody (A00187). <br>MUC1 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC1 Antibody (A00187) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00187-muc1-primary-antibodies-ihc-testing-4.jpgAnti-MUC1 Antibody Picoband®IHC analysis of MUC1 using anti-MUC1 antibody (A00187). <br>MUC1 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC1 Antibody (A00187) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-muc2-antibody-a01212-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-ihc-testing-1_1_1.jpgAnti-MUC2 Antibody IHC analysis of MUC2 using anti-MUC2 antibody (A01212). <br>
MUC2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-ihc-testing-2_1_1.jpgAnti-MUC2 Antibody IHC analysis of MUC2 using anti-MUC2 antibody (A01212). <br>
MUC2 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-fimmu-16-1582688-g002.jpgAnti-MUC2 AntibodyIL-22 is the key cytokine underlying the effects of the human infant Th17-conditioned media. (A) Experimental design for enteroid stimulation. (B) Representative immunofluorescent staining of Ki67 (red), E-cadherin (green), and DAPI (blue) in infant enteroids cultured in control media (left), control media supplemented with infant Th17-conditioned media (middle), or control media plus Th17-conditioned media plus neutralizing anti-IL-22 (right) (Scale bars, 50 μm). (C, E) Fluorescence intensity of Ki67 and MUC2 per enteroid relative to DAPI following exposure to Th17-conditioned media. (technical replicates n=5; N= 4 individuals, statistical difference calculated by one-way ANOVA). Enteroids exposed to infant Th17-conditioned media showed more goblet cell (MUC2) staining as compared to control, and Th17-conditioned media plus neutralizing IL-22 groups (Scale bar, 50 μm). (D) Infant enteroids stimulated by neonatal Th17-conditioned media display increased goblet cell numbers/size as indicated by increased MUC2 intensity per enteroid. MUC2 intensity was normalized to DAPI (technical replicates n=5; N= 4 individuals, statistical differences calculated by t-test **P < 0.01, *** P <0.001, **** P <0.0001) (Scale bar, 50 μm). Enteroid samples used N001, N002, N011 and N012.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1582688/full'>40375988</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-ihc-testing-3_1_1.jpgAnti-MUC2 Antibody IHC analysis of MUC2 using anti-MUC2 antibody (A01212). <br>
MUC2 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-4.jpgAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212).<br>
MUC2 was detected in paraffin-embedded section of human intestine cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-5.pngAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212). <br> MUC2 was detected in paraffin-embedded section of human ileum tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-6.pngAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212). <br> MUC2 was detected in paraffin-embedded section of human colon organoid tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-7.pngAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212). <br> MUC2 was detected in paraffin-embedded section of mouse ileum tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-8.pngAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212). <br> MUC2 was detected in paraffin-embedded section of mouse ileum organoid tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01212-muc2-primary-antibodies-if-testing-9.jpgAnti-MUC2 Antibody IF analysis of MUC2 using anti-MUC2 antibody (A01212).<br>
MUC2 was detected in paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MUC2 Antibody (A01212) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-myf5-picoband-trade-antibody-a04040-1-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04040-1-Myf5-primary-antibodies-WB-testing-1.jpgAnti-Myf5 Antibody Picoband® Western blot analysis of Myf5 using anti-Myf5 antibody (A04040-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human SW620 cell lysates, <br>Lane 2: mouse testis tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Myf5 antigen affinity purified polyclonal antibody (Catalog # A04040-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Myf5 at approximately 28KD. The expected band size for Myf5 is at 28KD.
https://www.bosterbio.com/products/primary-antibodies/anti-nmu-picoband-trade-antibody-a01919-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-1-nmu-primary-antibodies-wb-testing-1.jpgAnti-NMU Antibody Picoband®Western blot analysis of NMU using anti-NMU antibody (A01919-1). <br>
Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat PC-12 whole cell lysates, <br>
Lane 2: mouse kidney tissue lysates, <br>
Lane 3: mouse Neuro-2a whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NMU antigen affinity purified polyclonal antibody (A01919-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NMU at approximately 26 kDa. The expected band size for NMU is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-1-nmu-primary-antibodies-ihc-testing-1.jpgAnti-NMU Antibody Picoband®IHC analysis of NMU using anti-NMU antibody (A01919-1). <br>NMU was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NMU Antibody (A01919-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01919-1-nmu-primary-antibodies-ihc-testing-2.jpgAnti-NMU Antibody Picoband®IHC analysis of NMU using anti-NMU antibody (A01919-1). <br>NMU was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NMU Antibody (A01919-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-nsf-picoband-trade-antibody-a00585-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00585-nsf-primary-antibodies-wb-testing-1.jpgAnti-NSF Antibody Picoband® Western blot analysis of NSF using anti-NSF antibody (A00585). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: mouse brain tissue lysates,<br>Lane 3: human HepG2 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSF antigen affinity purified polyclonal antibody (Catalog # A00585) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSF at approximately 82KD. The expected band size for NSF is at 82KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00585-NSF-primary-antibodies-IHC-testing-2.jpgAnti-NSF Antibody Picoband® IHC analysis of NSF using anti-NSF antibody (A00585).
<br>NSF was detected in paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NSF Antibody (A00585) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00585-NSF-primary-antibodies-IHC-testing-3.jpgAnti-NSF Antibody Picoband® IHC analysis of NSF using anti-NSF antibody (A00585).<br>
NSF was detected in paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NSF Antibody (A00585) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00585-NSF-primary-antibodies-IHC-testing-4.jpgAnti-NSF Antibody Picoband® IHC analysis of NSF using anti-NSF antibody (A00585).
<br>NSF was detected in paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NSF Antibody (A00585) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00585-NSF-primary-antibodies-IHC-testing-5.jpgAnti-NSF Antibody Picoband® IHC analysis of NSF using anti-NSF antibody (A00585).
<br>NSF was detected in paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NSF Antibody (A00585) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00585-NSF-primary-antibodies-IHC-testing-6.jpgAnti-NSF Antibody Picoband® IHC analysis of NSF using anti-NSF antibody (A00585).
<br>NSF was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NSF Antibody (A00585) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-pax5-picoband-trade-antibody-a00669-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00669-1-pax5-primary-antibodies-wb-testing-1.jpgAnti-PAX5 Antibody Picoband® Western blot analysis of PAX5 using anti-PAX5 antibody (A00669-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates, <br>
Lane 2: human Ramos whole cell lysates, <br>
Lane 3: human Daudi whole cell lysates, <br>
Lane 4: human Jurkat whole cell lysates, <br>
Lane 5: mouse spleen tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX5 antigen affinity purified polyclonal antibody (Catalog # A00669-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAX5 at approximately 45 kDa. The expected band size for PAX5 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00669-1-PAX5-primary-antibodies-IHC-testing-2.jpgAnti-PAX5 Antibody Picoband® IHC analysis of PAX5 using anti-PAX5 antibody (A00669-1).
<br>PAX5 was detected in paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PAX5 Antibody (A00669-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00669-1-PAX5-primary-antibodies-IHC-testing-3.jpgAnti-PAX5 Antibody Picoband® IHC analysis of PAX5 using anti-PAX5 antibody (A00669-1).<br>
PAX5 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PAX5 Antibody (A00669-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00669-1-PAX5-primary-antibodies-IHC-testing-4.jpgAnti-PAX5 Antibody Picoband® IHC analysis of PAX5 using anti-PAX5 antibody (A00669-1).
<br>PAX5 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PAX5 Antibody (A00669-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00669-1-pax5-primary-antibodies-if-testing-5.jpgAnti-PAX5 Antibody Picoband® IF analysis of PAX5 using anti-PAX5 antibody (A00669-1).<br> PAX5 was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-PAX5 Antibody (A00669-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00669-1-pax5-primary-antibodies-if-testing-6.jpgAnti-PAX5 Antibody Picoband® IF analysis of PAX5 using anti-PAX5 antibody (A00669-1).<br> PAX5 was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-PAX5 Antibody (A00669-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-pdk2-picoband-trade-antibody-a03261-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-wb-testing-1.jpgAnti-PDK2 Antibody Picoband®Western blot analysis of PDK2 using anti-PDK2 antibody (A03261). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: rat heart tissue lysates,<br>
Lane 3: rat skeletal muscle tissue lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse heart tissue lysates,<br>
Lane 6: mouse skeletal muscle tissue lysates,<br>
Lane 7: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDK2 antigen affinity purified polyclonal antibody (A03261) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDK2 at approximately 46 kDa. The expected band size for PDK2 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-ihc-testing-1.jpgAnti-PDK2 Antibody Picoband®IHC analysis of PDK2 using anti-PDK2 antibody (A03261). <br>PDK2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK2 Antibody (A03261) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-ihc-testing-2.jpgAnti-PDK2 Antibody Picoband®IHC analysis of PDK2 using anti-PDK2 antibody (A03261). <br>PDK2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK2 Antibody (A03261) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-if-testing-1.jpgAnti-PDK2 Antibody Picoband®IF analysis of PDK2 using anti-PDK2 antibody (A03261) and anti-Tubulin Alpha antibody (M03989-3).<br>
PDK2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PDK2 Antibody (A03261) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-if-testing-2.jpgAnti-PDK2 Antibody Picoband®IF analysis of PDK2 using anti-PDK2 antibody (A03261). <br>
PDK2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PDK2 Antibody (A03261) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03261-pdk2-primary-antibodies-fcm-testing-1.jpgAnti-PDK2 Antibody Picoband®Flow Cytometry analysis of JK cells using anti-PDK2 antibody (A03261). <br>
Overlay histogram showing JK cells stained with A03261 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDK2 Antibody (A03261, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd31-picoband-trade-antibody-a01513-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-wb-testing-1_1.jpgAnti-CD31/Pecam1 Antibody Picoband® Western blot analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD31 antigen affinity purified polyclonal antibody (Catalog # A01513-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD31 at approximately 120-130 kDa. The expected band size for CD31 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-2.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-3.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-4.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-5.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse epididymis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-6.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-7.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-8.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse pancrease tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-9.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01513-1-cd31-primary-antibodies-ihc-testing-10.jpgAnti-CD31/Pecam1 Antibody Picoband® IHC analysis of CD31 using anti-CD31 antibody (A01513-1). <br>
CD31 was detected in a paraffin-embedded section of mouse thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD31 Antibody (A01513-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-pf4-picoband-trade-antibody-a00871-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00871-pf4-primary-antibodies-wb-testing-1.jpgAnti-PF4 Antibody Picoband® Western blot analysis of PF4 using anti-PF4 antibody (A00871). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PF4 antigen affinity purified polyclonal antibody (Catalog # A00871) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PF4 at approximately 11KD. The expected band size for PF4 is at 11KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00871-PF4-primary-antibodies-IHC-testing-2.jpgAnti-PF4 Antibody Picoband® IHC analysis of PF4 using anti-PF4 antibody (A00871).<br>
PF4 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PF4 Antibody (A00871) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00871-PF4-primary-antibodies-IHC-testing-3.jpgAnti-PF4 Antibody Picoband® IHC analysis of PF4 using anti-PF4 antibody (A00871).<br>
PF4 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PF4 Antibody (A00871) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-nap2-picoband-trade-antibody-a02736-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02736-NAP2-primary-antibodies-WB-testing-1.jpgAnti-NAP2/Ppbp Antibody Picoband® Western blot analysis of NAP2 using anti-NAP2 antibody (A02736).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse bone tissue lysates,<br>Lane 2: mouse lung tissue lysates,<br>Lane 3: mouse spleen tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAP2 antigen affinity purified polyclonal antibody (Catalog # A02736) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAP2 at approximately 11KD. The expected band size for NAP2 is at 14KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02736-NAP2-primary-antibodies-IHC-testing-2.jpgAnti-NAP2/Ppbp Antibody Picoband® IHC analysis of NAP2 using anti-NAP2 antibody (A02736).<br>
NAP2 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-NAP2 Antibody (A02736) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ppid-picoband-trade-antibody-a02424-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02424-ppid-primary-antibodies-wb-testing-1.jpgAnti-PPID Antibody Picoband® Western blot analysis of PPID using anti-PPID antibody (A02424). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U87 whole cell lysates,<br>
Lane 2: rat brain tissue lysates,<br>
Lane 3: rat liver tissue lysates,<br>
Lane 4: mouse brain tissue lysates,<br>
Lane 5: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPID antigen affinity purified polyclonal antibody (Catalog # A02424) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPID at approximately 38 kDa. The expected band size for PPID is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02424-PPID-primary-antibodies-IHC-testing-2.jpgAnti-PPID Antibody Picoband® IHC analysis of PPID using anti-PPID antibody (A02424).<br>
PPID was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PPID Antibody (A02424) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02424-PPID-primary-antibodies-IHC-testing-3.jpgAnti-PPID Antibody Picoband® IHC analysis of PPID using anti-PPID antibody (A02424).<br>
PPID was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PPID Antibody (A02424) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02424-PPID-primary-antibodies-IHC-testing-4.jpgAnti-PPID Antibody Picoband® IHC analysis of PPID using anti-PPID antibody (A02424).
<br>PPID was detected in paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PPID Antibody (A02424) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02424-ppid-primary-antibodies-fc-testing-5.jpgAnti-PPID Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PPID antibody (A02424).<br>Overlay histogram showing U251 cells stained with A02424 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPID Antibody (A02424,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02424-ppid-primary-antibodies-fc-testing-6.jpgAnti-PPID Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-PPID antibody (A02424).<br>Overlay histogram showing U20S cells stained with A02424 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPID Antibody (A02424,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02424-ppid-primary-antibodies-if-testing-7.jpgAnti-PPID Antibody Picoband® IF analysis of PPID using anti-PPID antibody (A02424). <br>
PPID was detected in immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-PPID Antibody (A02424) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-ptpn22-picoband-trade-antibody-a00581-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00581-1-PTPN22-primary-antibodies-WB-testing-1.jpgAnti-PTPN22 Antibody Picoband® Western blot analysis of PTPN22 using anti-PTPN22 antibody (A00581-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat thymus tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTPN22 antigen affinity purified polyclonal antibody (Catalog # A00581-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTPN22 at approximately 92KD. The expected band size for PTPN22 is at 92KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00581-1-PTPN22-primary-antibodies-IHC-testing-2.jpgAnti-PTPN22 Antibody Picoband® IHC analysis of PTPN22 using anti-PTPN22 antibody (A00581-1).
<br>PTPN22 was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PTPN22 Antibody (A00581-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00581-1-PTPN22-primary-antibodies-IHC-testing-3.jpgAnti-PTPN22 Antibody Picoband® IHC analysis of PTPN22 using anti-PTPN22 antibody (A00581-1).<br>
PTPN22 was detected in paraffin-embedded section of rat lymphaden tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PTPN22 Antibody (A00581-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00581-1-ptpn22-primary-antibodies-wb-testing-4.jpgAnti-PTPN22 Antibody Picoband® Western blot analysis of PTPN22 using anti-PTPN22 antibody (A00581-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human SW579 whole cell lysates, <br> Lane 2: human HepG2 whole cell lysates, <br> Lane 3: human placenta tissue lysates, <br> Lane 4: human Hela whole cell lysates, <br> Lane 5: human SW620 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTPN22 antigen affinity purified polyclonal antibody (Catalog # A00581-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTPN22 at approximately 92KD. The expected band size for PTPN22 is at 92KD.
https://www.bosterbio.com/products/primary-antibodies/anti-reck-picoband-trade-antibody-a06439-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-1-reck-primary-antibodies-wb-testing-1.jpgAnti-RECK Antibody Picoband® Western blot analysis of RECK using anti-RECK antibody (A06439-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MOLT-4 whole cell lysates, <br>
Lane 2: human U87 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RECK antigen affinity purified polyclonal antibody (Catalog # A06439-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RECK at approximately 110 kDa. The expected band size for RECK is at 110 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-rnf186-picoband-trade-antibody-a15259-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A15259-1-RNF186-primary-antibodies-WB-testing-1.jpgAnti-RNF186 Antibody Picoband® Western blot analysis of RNF186 using anti-RNF186 antibody (A15259-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human SW620 cell lysates, <br>Lane 2: human HepG2 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RNF186 antigen affinity purified polyclonal antibody (Catalog # A15259-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RNF186 at approximately 28KD. The expected band size for RNF186 is at 24KD.
https://www.bosterbio.com/products/primary-antibodies/anti-psoriasin-picoband-trade-antibody-a02369-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02369-1-Psoriasin-primary-antibodies-WB-testing-1.jpgAnti-Psoriasin/S100A7 Antibody Picoband® Western blot analysis of Psoriasin using anti-Psoriasin antibody (A02369-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human placenta tissue lysates,<br>Lane 2: human Hela cell lysates, <br>Lane 3: rat spleen tissue lysates,<br>Lane 4: rat RH35 cell lysates, <br>Lane 5: mouse spleen tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Psoriasin antigen affinity purified polyclonal antibody (Catalog # A02369-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Psoriasin at approximately 17KD. The expected band size for Psoriasin is at 11KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02369-1-Psoriasin-primary-antibodies-IHC-testing-2.jpgAnti-Psoriasin/S100A7 Antibody Picoband® IHC analysis of Psoriasin using anti-Psoriasin antibody (A02369-1).<br>
Psoriasin was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Psoriasin Antibody (A02369-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02369-1-Psoriasin-primary-antibodies-IHC-testing-3.jpgAnti-Psoriasin/S100A7 Antibody Picoband® IHC analysis of Psoriasin using anti-Psoriasin antibody (A02369-1).<br>
Psoriasin was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Psoriasin Antibody (A02369-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02369-1-psoriasin-primary-antibodies-if-testing-4.jpgAnti-Psoriasin/S100A7 Antibody Picoband® IF analysis of Psoriasin using anti-Psoriasin antibody (A02369-1). <br>
Psoriasin was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-Psoriasin Antibody (A02369-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02369-1-psoriasin-primary-antibodies-fcm-testing-5.jpgAnti-Psoriasin/S100A7 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-Psoriasin antibody (A02369-1).<br>Overlay histogram showing A431 cells stained with A02369-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Psoriasin Antibody (A02369-1,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-sacsin-picoband-trade-antibody-a00519-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00519-sacs-primary-antibodies-ihc-testing-4.jpgAnti-Sacsin AntibodyIHC analysis of SACS using anti-SACS antibody (A00519). <br>SACS was detected in a paraffin-embedded section of human cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SACS Antibody (A00519) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00519-sacsin-primary-antibodies-ihc-testing-1.jpgAnti-Sacsin AntibodyIHC analysis of Sacsin using anti-Sacsin antibody (A00519). <br>Sacsin was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Sacsin Antibody (A00519) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00519-sacsin-primary-antibodies-ihc-testing-2.jpgAnti-Sacsin AntibodyIHC analysis of Sacsin using anti-Sacsin antibody (A00519). <br>Sacsin was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Sacsin Antibody (A00519) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00519-sacsin-primary-antibodies-ihc-testing-3.jpgAnti-Sacsin AntibodyIHC analysis of Sacsin using anti-Sacsin antibody (A00519). <br>Sacsin was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Sacsin Antibody (A00519) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-pai1-picoband-trade-antibody-a00637-2-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00637-2-PAI1-primary-antibodies-WB-testing-1.jpgAnti-PAI1/Serpine1 Antibody Picoband® Western blot analysis of PAI1 using anti-PAI1 antibody (A00637-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat small intestine tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: mouse kidney tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAI1 antigen affinity purified polyclonal antibody (Catalog # A00637-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAI1 at approximately 45-50KD. The expected band size for PAI1 is at 45KD.
https://www.bosterbio.com/products/primary-antibodies/anti-sod3-picoband-trade-antibody-a01784-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01784-1-SOD3-primary-antibodies-IHC-testing-1.jpgAnti-Superoxide Dismutase 3/SOD3 Antibody Picoband® IHC analysis of SOD3 using anti-SOD3 antibody (A01784-1).
<br>SOD3 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-SOD3 Antibody (A01784-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01784-1-SOD3-primary-antibodies-IHC-testing-2.jpgAnti-Superoxide Dismutase 3/SOD3 Antibody Picoband® IHC analysis of SOD3 using anti-SOD3 antibody (A01784-1).
SOD3 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-SOD3 Antibody (A01784-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01784-1-sod3-primary-antibodies-wb-testing-3.jpgAnti-Superoxide Dismutase 3/SOD3 Antibody Picoband® Western blot analysis of SOD3 using anti-SOD3 antibody (A01784-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human PC-3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOD3 antigen affinity purified polyclonal antibody (Catalog # A01784-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOD3 at approximately 33 kDa. The expected band size for SOD3 is at 27 kDa.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01784-1-sod3-primary-antibodies-if-testing-4.jpgAnti-Superoxide Dismutase 3/SOD3 Antibody Picoband® IF analysis of SOD3 using anti-SOD3 antibody (A01784-1). <br>
SOD3 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SOD3 Antibody (A01784-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-sp6-picoband-trade-antibody-a08730-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-wb-testing-1_1.jpgAnti-SP6 Antibody Picoband® Western blot analysis of SP6 using anti-SP6 antibody (A08730-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human CACO-2 whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human A431 whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SP6 antigen affinity purified polyclonal antibody (Catalog # A08730-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SP6 at approximately 40 kDa. The expected band size for SP6 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-ihc-testing-2.jpgAnti-SP6 Antibody Picoband® IHC analysis of SP6 using anti-SP6 antibody (A08730-1). <br>
SP6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SP6 Antibody (A08730-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-ihc-testing-3.jpgAnti-SP6 Antibody Picoband® IHC analysis of SP6 using anti-SP6 antibody (A08730-1). <br>
SP6 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SP6 Antibody (A08730-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-ihc-testing-4.jpgAnti-SP6 Antibody Picoband® IHC analysis of SP6 using anti-SP6 antibody (A08730-1). <br>
SP6 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SP6 Antibody (A08730-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-ihc-testing-5.jpgAnti-SP6 Antibody Picoband® IHC analysis of SP6 using anti-SP6 antibody (A08730-1). <br>
SP6 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SP6 Antibody (A08730-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08730-1-sp6-primary-antibodies-if-testing-6.jpgAnti-SP6 Antibody Picoband® IF analysis of SP6 using anti-SP6 antibody (A08730-1) and anti-Beta Tubulin antibody (M01857-3).<br>
SP6 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SP6 Antibody (A08730-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Donkey Anti-Rabbit IgG (BA1144) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-tal1-picoband-trade-antibody-a00944-2-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00944-2-Tal1-primary-antibodies-WB-testing-1.jpgAnti-Tal1 Antibody Picoband® Western blot analysis of Tal1 using anti-Tal1 antibody (A00944-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human U20S cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tal1 antigen affinity purified polyclonal antibody (Catalog # A00944-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tal1 at approximately 39KD. The expected band size for Tal1 is at 34KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tff3-picoband-trade-antibody-a01738-3-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01738-3-TFF3-primary-antibodies-WB-testing-1.jpgAnti-TFF3 Antibody Picoband® Western blot analysis of TFF3 using anti-TFF3 antibody (A01738-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse small intestine tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFF3 antigen affinity purified polyclonal antibody (Catalog # A01738-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFF3 at approximately 12KD. The expected band size for TFF3 is at 9KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01738-3-tff3-primary-antibodies-ihc-testing-2.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-3). <br>
TFF3 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TFF3 Antibody (A01738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01738-3-tff3-primary-antibodies-ihc-testing-3.jpgAnti-TFF3 Antibody Picoband® IHC analysis of TFF3 using anti-TFF3 antibody (A01738-3). <br>
TFF3 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TFF3 Antibody (A01738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01738-3-tff3-primary-antibodies-if-testing-4.jpgAnti-TFF3 Antibody Picoband® IF analysis of TFF3 using anti-TFF3 antibody (A01738-3). <br>
TFF3 was detected in a paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TFF3 Antibody (A01738-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01738-3-tff3-primary-antibodies-if-testing-5.jpgAnti-TFF3 Antibody Picoband® IF analysis of TFF3 using anti-TFF3 antibody (A01738-3). <br>
TFF3 was detected in a paraffin-embedded section of rat intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TFF3 Antibody (A01738-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-cd252-picoband-trade-antibody-a02554-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02554-1-CD252-primary-antibodies-WB-testing-1.jpgAnti-CD252/Tnfsf4 Antibody Picoband® Western blot analysis of CD252 using anti-CD252 antibody (A02554-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. <br>Lane 1: recombinant mouse CD252 protein 1ng.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD252 antigen affinity purified polyclonal antibody (Catalog # A02554-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD252 at approximately 21-25KD. The expected band size for CD252 is at 18KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02554-1-CD252-primary-antibodies-IHC-testing-2.jpgAnti-CD252/Tnfsf4 Antibody Picoband® IHC analysis of CD252 using anti-CD252 antibody (A02554-1).<br>
CD252 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD252 Antibody (A02554-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tl1a-picoband-trade-antibody-a02402-1-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02402-1-TL1A-primary-antibodies-WB-testing-1.jpgAnti-TL1A/TNFSF15 Antibody Picoband® Western blot analysis of TL1A using anti-TL1A antibody (A02402-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat liver tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: mouse kidney tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TL1A antigen affinity purified polyclonal antibody (Catalog # A02402-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TL1A at approximately 28KD. The expected band size for TL1A is at 28KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02402-1-tl1a-primary-antibodies-ihc-testing-2.jpg.jpgAnti-TL1A/TNFSF15 Antibody Picoband® IHC analysis of TL1A using anti-TL1A antibody (A02402-1).<br> TL1A was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TL1A Antibody (A02402-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02402-1-tl1a-primary-antibodies-ihc-testing-3.jpg.jpgAnti-TL1A/TNFSF15 Antibody Picoband® IHC analysis of TL1A using anti-TL1A antibody (A02402-1).<br> TL1A was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TL1A Antibody (A02402-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02402-1-tl1a-primary-antibodies-ihc-testing-4.jpg.jpgAnti-TL1A/TNFSF15 Antibody Picoband® IHC analysis of TL1A using anti-TL1A antibody (A02402-1).<br> TL1A was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TL1A Antibody (A02402-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02402-1-tl1a-primary-antibodies-ihc-testing-5.jpg.jpgAnti-TL1A/TNFSF15 Antibody Picoband® IHC analysis of TL1A using anti-TL1A antibody (A02402-1).<br> TL1A was detected in paraffin-embedded section of human prostatic cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TL1A Antibody (A02402-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-traf3-picoband-trade-antibody-a00424-boster.html2026-03-24T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00424-traf3-primary-antibodies-wb-testing-1.jpgAnti-TRAF3 Antibody Picoband® Western blot analysis of TRAF3 using anti-TRAF3 antibody (A00424). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human K562 cell lysates, <br>Lane 2: rat brain tissue lysates,<br>Lane 3: rat PC-12 cell lysates, <br>Lane 4: mouse brain tissue lysates,<br>Lane 5: mouse HEPA1-6 cell lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAF3 antigen affinity purified polyclonal antibody (Catalog # A00424) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRAF3 at approximately 60,64KD. The expected band size for TRAF3 is at 64KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tspan12-picoband-trade-antibody-a05472-1-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05472-1-tspan12-primary-antibodies-wb-testing-1_1.jpgAnti-TSPAN12 Antibody Picoband® Western blot analysis of TSPAN12 using anti-TSPAN12 antibody (A05472-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HepG2 whole cell lysates, <br>
Lane 2: rat kidney tissue lysates, <br>
Lane 3: rat NRK whole cell lysates, <br>
Lane 4: mouse kidney tissue lysates, <br>
Lane 5: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSPAN12 antigen affinity purified polyclonal antibody (A05472-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TSPAN12 at approximately 40 kDa. The expected band size for TSPAN12 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05472-1-tspan12-primary-antibodies-ihc-testing-2.jpgAnti-TSPAN12 Antibody Picoband® IHC analysis of TSPAN12 using anti-TSPAN12 antibody (A05472-1). <br>
TSPAN12 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TSPAN12 Antibody (A05472-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05472-1-tspan12-primary-antibodies-ihc-testing-3.jpgAnti-TSPAN12 Antibody Picoband® IHC analysis of TSPAN12 using anti-TSPAN12 antibody (A05472-1). <br>
TSPAN12 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TSPAN12 Antibody (A05472-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-ugt1a1-picoband-trade-antibody-a01865-1-boster.html2026-04-01T05:01:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01865-1-ugt1a1-primary-antibodies-wb-testing-1.jpgAnti-UGT1A1 Antibody Picoband®Western blot analysis of UGT1A1 using anti-UGT1A1 antibody (A01865-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: rat liver tissue lysates,<br>
Lane 4: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UGT1A1 antigen affinity purified polyclonal antibody (A01865-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UGT1A1 at approximately 55 kDa. The expected band size for UGT1A1 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01865-1-ugt1a1-primary-antibodies-ihc-testing-1.jpgAnti-UGT1A1 Antibody Picoband®IHC analysis of UGT1A1 using anti-UGT1A1 antibody (A01865-1). <br>UGT1A1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UGT1A1 Antibody (A01865-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01865-1-ugt1a1-primary-antibodies-if-testing-1.jpgAnti-UGT1A1 Antibody Picoband®IF analysis of UGT1A1 using anti-UGT1A1 antibody (A01865-1). <br>
UGT1A1 was detected in an immunocytochemical section of CACO-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-UGT1A1 Antibody (A01865-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01865-1-ugt1a1-primary-antibodies-fcm-testing-1.jpgAnti-UGT1A1 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-UGT1A1 antibody (A01865-1). <br>
Overlay histogram showing HepG2 cells stained with A01865-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UGT1A1 Antibody (A01865-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-vegfb-picoband-trade-antibody-a04494-2-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04494-2-vegfb-primary-antibodies-wb-testing-1.jpgAnti-VEGFB Antibody Picoband® Western blot analysis of VEGFB using anti-VEGFB antibody (A04494-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat heart tissue lysates.<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGFB antigen affinity purified polyclonal antibody (Catalog # A04494-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGFB at approximately 29KD. The expected band size for VEGFB is at 22KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04494-2-VEGFB-primary-antibodies-IHC-testing-2.jpgAnti-VEGFB Antibody Picoband® IHC analysis of VEGFB using anti-VEGFB antibody (A04494-2).<br>
VEGFB was detected in paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGFB Antibody (A04494-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04494-2-VEGFB-primary-antibodies-IHC-testing-3.jpgAnti-VEGFB Antibody Picoband® IHC analysis of VEGFB using anti-VEGFB antibody (A04494-2).<br>
VEGFB was detected in paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGFB Antibody (A04494-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04494-2-VEGFB-primary-antibodies-IHC-testing-4.jpgAnti-VEGFB Antibody Picoband® IHC analysis of VEGFB using anti-VEGFB antibody (A04494-2).
<br>VEGFB was detected in paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGFB Antibody (A04494-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04494-2-VEGFB-primary-antibodies-IHC-testing-5.jpgAnti-VEGFB Antibody Picoband® IHC analysis of VEGFB using anti-VEGFB antibody (A04494-2).
<br>VEGFB was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-VEGFB Antibody (A04494-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-vip-receptor-1-picoband-trade-antibody-a04345-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04345-vip_receptor_1-primary-antibodies-wb-testing-1.jpgAnti-VIP Receptor 1/VIPR1 Antibody Picoband® Western blot analysis of VIP Receptor 1 using anti-VIP Receptor 1 antibody (A04345). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human A431 cell lysates, <br> Lane 2: human PANC-1 cell lysates.<br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VIP Receptor 1 antigen affinity purified polyclonal antibody (Catalog # A04345) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VIP Receptor 1 at approximately 52KD. The expected band size for VIP Receptor 1 is at 52KD.
https://www.bosterbio.com/products/primary-antibodies/anti-xrcc1-picoband-trade-antibody-a00571-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-wb-testing-1_1.jpgAnti-XRCC1 Antibody Picoband® Western blot analysis of XRCC1 using anti-XRCC1 antibody (A00571). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human K562 whole cell lysates,<br>
Lane 4: human Jurkat whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat liver tissue lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-XRCC1 antigen affinity purified polyclonal antibody (Catalog # A00571) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for XRCC1 at approximately 90 kDa. The expected band size for XRCC1 is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00571-XRCC1-primary-antibodies-IHC-testing-2.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571).
<br>XRCC1 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00571-XRCC1-primary-antibodies-IHC-testing-3.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571).<br>
XRCC1 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00571-XRCC1-primary-antibodies-IHC-testing-4.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571).
<br>XRCC1 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00571-XRCC1-primary-antibodies-IHC-testing-5.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571).
<br>XRCC1 was detected in paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-if-testing-6.jpgAnti-XRCC1 Antibody Picoband® IF analysis of XRCC1 using anti-XRCC1 antibody (A00571). <br> XRCC1 was detected in immunocytochemical section of NIH3T3 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-fc-testing-7.pngAnti-XRCC1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-XRCC1 antibody (A00571). <br> Overlay histogram showing THP-1 cells stained with A00571 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-XRCC1 Antibody (A00571,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-ihc-testing-8.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571). <br> XRCC1 was detected in frozen section of human placenta tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-ihc-testing-9.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571). <br> XRCC1 was detected in frozen section of rat intestine tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00571-xrcc1-primary-antibodies-ihc-testing-10.jpgAnti-XRCC1 Antibody Picoband® IHC analysis of XRCC1 using anti-XRCC1 antibody (A00571). <br> XRCC1 was detected in frozen section of mouse intestine tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-XRCC1 Antibody (A00571) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-med6-picoband-trade-antibody-a09224-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09224-med6-primary-antibodies-wb-testing-1_1.jpgAnti-MED6 Antibody Picoband® Western blot analysis of MED6 using anti-MED6 antibody (A09224). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Jurkat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human PC-3 whole cell lysates,<br>
Lane 5: human U2OS whole cell lysates,<br>
Lane 6: human A549 whole cell lysates,<br>
Lane 7: human MCF-7 whole cell lysates,<br>
Lane 8: rat C6 whole cell lysates.<br>
Lane 9: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED6 antigen affinity purified polyclonal antibody (Catalog # A09224) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED6 at approximately 34 kDa. The expected band size for MED6 is at 28 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-aha1-picoband-trade-antibody-a05733-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05733-aha1-primary-antibodies-wb-testing-1.jpgAnti-AHA1/AHSA1 Antibody Picoband® Western blot analysis of AHA1 using anti-AHA1 antibody (A05733). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human PC-3 whole cell lysates, <br>
Lane 3: human A549 whole cell lysates, <br>
Lane 4: monkey COS-7 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AHA1 antigen affinity purified polyclonal antibody (Catalog # A05733) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AHA1 at approximately 40 kDa. The expected band size for AHA1 is at 38 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-angptl3-picoband-trade-antibody-a02929-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02929-ANGPTL3-primary-antibodies-WB-testing-1.jpgAnti-ANGPTL3 Antibody Picoband® Western blot analysis of ANGPTL3 using anti-ANGPTL3 antibody (A02929).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse HEPA1-6 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANGPTL3 antigen affinity purified polyclonal antibody (Catalog # A02929) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANGPTL3 at approximately 54KD. The expected band size for ANGPTL3 is at 54KD.
https://www.bosterbio.com/products/primary-antibodies/anti-bcl-2-picoband-trade-antibody-a00040-2-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-nrr-12-96-g005.jpgAnti-Bcl-2/BCL2 Antibody Picoband®Nicotiflorin effect on Bcl-2 and Bax immunreactivity in the ischemic cerebral cortex of I/R rats (immunohistochemical staining). (A) High-magnification images of Bcl-2 and Bax immunohistochemical staining (arrows show immunoreactive cells). Scale bar: 25 μm. (B) For each antibody staining, immunoreactive cells in a 1 mm width were counted under optical microscopy. The average count number was used for quantitation and comparison between groups. Respective numbers of Bcl-2- and Bax-positive cells show that nicotiflorin decreases Bax immunoreactivity and increases Bcl-2 immunoreactivity. * P < 0.05, ** P < 0.01, vs . I/R group (mean ± SEM, n = 3, one-way analysis of variance followed by post hoc Tukey test). I/R: Ischemia/reperfusion.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5319249/&orig_host=www.ncbi.nlm.nih.gov'>28250754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41598_2018_34156_fig5_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®Protective effects of maltol on cisplatin-induced injury in HEK293 cells. ( A ) The cytotoxic effects of cisplatin on HEK293 cells. ( B ) Effect of maltol on the activity of normal cells. ( C ) The viability of HEK293 cells incubated with maltol after cisplatin exposure. Effects of maltol on the protein expression levels of Bcl-2, Bax and caspase 3, 8, 9 as well as GAPDH protein was used as a loading control. ( D ) Cells were used for western blot analysis of indicated proteins (upper panel). Column chart represents relative protein levels compared with the control group after normalization to GAPDH levels (lower panel) Values are expressed as mean ± S.D. n = 8. ** p < 0.01 vs . normal group; # p < 0.05, ## p < 0.01 vs . cisplatin group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-34156-6'>30374107</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41467_2025_64480_fig2_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®RTECs-specific knockout of PGK1 protected against I/R-induced AKI. After adaptation for one week, eight-week-old PGK1 flox/flox and PGK1 CKO mice underwent renal ischemia for 30 min, followed by renal reperfusion for 24 h. The blood and kidneys were then collected for serological testing and histological examination. a BUN levels ( n = 6 per group). b Scr levels ( n = 6 per group). c Serum cystatin C levels ( n = 6 per group). d Tubular injury score ( n = 6 per group). e Quantitative analysis of DHE oxidation ( n = 6 per group). f HE staining, DHE oxidation, Nox2 immunofluorescence, TUNEL analysis, F4/80 immunofluorescence, and IL-1β immunofluorescence of renal sections ( n = 6 per group). g Quantitative analysis of Nox2 immunofluorescence ( n = 6 per group). h Quantitative analysis of TUNEL analysis ( n = 6 per group). i Quantitative analysis of F4/80 immunofluorescence ( n = 6 per group). j Quantitative analysis of IL-1β immunofluorescence ( n = 6 per group). k Relative mRNA level of IL-1β ( n = 6 per group). l Relative mRNA level of IL-6 ( n = 6 per group). m Relative mRNA level of IL-10 ( n = 6 per group). n Relative mRNA level of TNF-α ( n = 6 per group). o Relative mRNA level of 12-Lox ( n = 6 per group). p Relative mRNA level of Rac-1 ( n = 6 per group). q Quantitative analysis of NGAL ( n = 6 per group). r Representative blots of NGAL, Bax, and Bcl-2 ( n = 6 per group). s Quantitative analysis of Bax ( n = 6 per group). t Quantitative analysis of Bcl-2 ( n = 6 per group). Data are represented as the Mean ± SEM. Statistical differences for ( a – t ) were performed using one-sided ANOVA/Bonferroni test. Source data are provided as a Source Data file. RTECs renal tubular epithelial cells, BUN blood urea nitrogen, Scr serum creatinine, DHE dihydroethidium, I/R ischemic/reperfusion, HE hematoxylin-Eosin, NOX2 reduced nicotinamide adenine dinucleotide phosphate oxidase 2, TUNEL terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling, IL-1β interleukin-1β, IL-6 interleukin-6, IL-10 interleukin-10, TNF-α tumor necrosis factor α, 12-Lox 12-lipoxygenase, Rac-1 Ras-related C3 botulinum toxin substrate 1, NGAL neutrophil gelatinase-associated lipocalin, Bax Bcl-2-associated X protein, Bcl-2, B-cell lymphoma/leukemia-2 gene, CKO conditional knockout. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-64480-1'>41136411</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41467_2025_64480_fig3_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®3-PG infusion worsened I/R-induced AKI. After adaptation for one week, eight-week-old C57BL/6J mice were intraperitoneally injected with 3-PG (30 mg/kg) for 2 consecutive weeks before undergoing renal I/R surgery. After renal reperfusion for 24 h, the blood and kidneys were then collected for serological testing and histological examination. a BUN levels ( n = 6 per group). b Scr levels ( n = 6 per group). c Serum cystatin C levels ( n = 6 per group). d Tubular injury score ( n = 6 per group). e Quantitative analysis of DHE oxidation ( n = 6 per group). f HE staining, DHE oxidation, Nox2 immunofluorescence, TUNEL analysis, F4/80 immunofluorescence, IL-1β immunofluorescence of renal sections ( n = 6 per group). g Quantitative analysis of Nox2 immunofluorescence ( n = 6 per group). h Quantitative analysis of TUNEL analysis ( n = 6 per group). i Quantitative analysis of F4/80 immunofluorescence ( n = 6 per group). j Quantitative analysis of IL-1β immunofluorescence ( n = 6 per group). k Relative mRNA level of IL-1β ( n = 6 per group). l Relative mRNA level of IL-6 ( n = 6 per group). m Relative mRNA level of IL-10 ( n = 6 per group). n Relative mRNA level of TNF-α ( n = 6 per group). o Relative mRNA level of 12-Lox ( n = 6 per group). p Relative mRNA level of Rac-1 ( n = 6 per group). q Quantitative analysis of NGAL ( n = 6 per group). r Quantitative analysis of Bax ( n = 6 per group). s Quantitative analysis of Bcl-2 ( n = 6 per group). t Representative blots of NGAL, Bax, and Bcl-2 ( n = 6 per group). Data are represented as the Mean ± SEM. Statistical differences for ( a – t ) were performed using one-sided ANOVA/Bonferroni test. Source data are provided as a Source Data file. 3-PG 3-phosphoglycerate, I/R ischemic/reperfusion, BUN blood urea nitrogen, Scr serum creatinine, DHE dihydroethidium, HE hematoxylin-Eosin, NOX2 reduced nicotinamide adenine dinucleotide phosphate oxidase 2, TUNEL terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling, IL-1β interleukin-1β, IL-6 interleukin-6, IL-10 interleukin-10, TNF-α tumor necrosis factor α, 12-Lox 12-lipoxygenase, Rac-1 Ras-related C3 botulinum toxin substrate 1, NGAL neutrophil gelatinase-associated lipocalin, Bax Bcl-2-associated X protein, Bcl-2 B-cell lymphoma/leukemia-2 gene. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-025-64480-1'>41136411</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-fphar-08-00044-g007.jpgAnti-Bcl-2/BCL2 Antibody Picoband®Celastrol attenuates ganglion cells apoptosis in the retina of EAE rats. Treatment of celastrol decreased the number of TUNEL-positive cells (A) , upregulated expression of Bcl-2 (B) and downregulated expression of Bax, cleaved-caspase 3 and cleaved-PARP. Scale bar: 100 μm. Data were shown as mean ± SD, n = 5. ∗∗ P < 0.01 versus control group, ## P < 0.01 versus EAE group, †† P < 0.01 versus low dosage of celastrol group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00044/full'>28239352</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-bcl2-primary-antibodies-wb-testing-1.jpgAnti-Bcl-2/BCL2 Antibody Picoband® Western blot analysis of BCL2 using anti-BCL2 antibody (A00040-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human HL-60 whole cell lysates, <br>
Lane 3: human THP-1 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL2 antigen affinity purified polyclonal antibody (Catalog # A00040-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL2 at approximately 26 kDa. The expected band size for BCL2 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-fphar-10-00175-g006.jpgAnti-Bcl-2/BCL2 Antibody Picoband®Trimetazidine inhibited EE-induced apoptosis of myocardial cells. (A) The apoptosis in myocardial tissues was evaluated by TUNEL staining. Scale bar is 50 μm. Western blot analysis of the levels of apoptosis-related proteins B-cell lymphoma 2 (Bcl-2) (B) , Bcl-2-associated X protein (Bax) (C) , cleaved caspase-3 (D) , cleaved PARP (E) , and cytoplasmic cytochrome complex (Cytochrome c, Cyto-C) (F) in myocardial tissues. GAPDH was used as a loading control. Each value is shown as mean ± SD ( n = 6). ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, versus the indicated group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00175/full'>30890937</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-bcl2-primary-antibodies-if-testing-2.jpgAnti-Bcl-2/BCL2 Antibody Picoband® IF analysis of BCL2 and Tubulin alpha using anti-BCL2 antibody (A00040-2) and anti-Tubulin alpha antibody (M03989-3).<br>
BCL2 and Tubulin alpha were detected in immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-BCL2 antibody (A00040-2) and mouse anti-Tubulin alpha Antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41598_2018_34156_fig4_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®Effects of maltol on the levels of inflammation cytokines in cisplatin-induced renal toxicity. ( A ) Effects of maltol on the positive expressions of Bax, Bcl-2, iNOS and COX-2 in renal tissues were examined by IHC in renal tissues (magnification × 200), And the column chart shows stained area, semiquantitative analysis of Bax, Bcl-2, iNOS and COX-2 expression in kidneys to IHC. ( B ) Inflammation cytokines level of TNF-α, IL-1β, iNOS and NF-κB in serum of mice were measured by ELISA kits. All values were expressed as mean ± S.D. * p < 0.05, ** p < 0.01 vs . normal group; # p < 0.05, ## p < 0.01 vs . cisplatin group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-34156-6'>30374107</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-medscimonit-25-5482-g006.jpgAnti-Bcl-2/BCL2 Antibody Picoband®AKT antagonist and AKT agonist contributed to upregulating p-AKT, PI3K, and apoptosis-associated proteins expression in HGC cells after infection. ( A ) For AKT inhibitor. ( B ) For AKT agonist. When the groups were pretreated with AKT antagonist MK-2206, the expression of the Bax/Bcl-2 and cleaved caspase 3 proteins increased in HGC cells compared with cells without AKT antagonist (** P<0.01). The expression of the Bax/Bcl-2 and cleaved caspase 3 proteins decreased significantly (** P<0.01) in cells with AKT agonist IGF-1 treatment compared with cells without pretreatment. On the other hand, the expression of PI3K and p-AKT proteins decreased in AKT antagonist-pretreated groups (** P<0.01), but increased in AKT agonist-pretreated groups (** P<0.01).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6671559/&orig_host=www.ncbi.nlm.nih.gov'>31337746</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-12931_2021_1908_fig5_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®Inhibitors of ERK, JNK, and p38 MAPK reversed the effect of TRB3 overexpression on PASMC biological behavior. A The CCK-8 assay was used to evaluated the proliferation of TRB3-overexpressing cells after treating with U0126, SP600125, and SB203580. B – D Western blot analysis of PCNA expression in TRB3 overexpressing cells incubated with U0126, SP600125, or SB203580 for 12 h. E Cell apoptosis induced by U0126, SP600125 and SB203580 in TRB3-overexpressing cells was evaluated using flow cytometry, and the percentage of early apoptotic (Annexin V+/PI−) and late apoptotic (Annexin V+ /PI+) cells was analyzed. F – H Western blot analysis of the protein expression of PARP, BAX, and Bcl2 in TRB3-overexpressing cells incubated with U0126, SP600125, and SB203580 for 12 h. I Crystal violet staining is presented at × 200 magnification for the Transwell assay and the migrated cells were counted and analyzed. J – L Western blot analysis of MMP9 expression in TRB3-overexpressing cells incubated with U0126, SP600125, and SB203580 for 12 h. Data represent the mean ± SEM (n = 4). *P < 0.05 compared to normoxic PASMCs transfected with lv-NC. # P < 0.05 and ## P < 0.01 compared to PASMCs transfected with lv-TRB3. U0126, an ERK signaling inhibitor; SP600125, an JNK signaling inhibitor; SB203580, an p38 MAPK signaling inhibitor <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-021-01908-4'>34906150</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-12935_2020_1454_fig7_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®TPX2 regulated proliferation, apoptosis, and aerobic glycolysis in glioma cells. a – l LN229 and U251 cells were introduced with si-NC or si-TPX2. a The transfection efficiency of si-TPX2 was checked with RT-qPCR assay in LN229 and U251 cells. b , c The cell viability of LN229 and U251 cells was determined with MTT assay. d The apoptosis rate of transfected LN229 and U251 cells was represented by flow cytometry assay. e The western blot assay was used to assay the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The activity of caspase-3 was detected with a caspase-3 assay kit. g – i The glucose, lactate, and ATP production levels were shown. j The protein expression levels of HK2 and LDHA were estimated by western blot assay in LN229 and U251 cells. k , l LDHA enzyme activity and ROS content were evaluated in LN229 and U251 cells post-transfection. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-medscimonit-25-5482-g005.jpgAnti-Bcl-2/BCL2 Antibody Picoband®The contribution of rL-RVG, α7-nAChR antagonist MLA, agonist ACB, or siRNA downregulation to the expression of α7-nAChR, p-AKT, PI3K, and apoptosis-associated proteins in HGC cells after infection. ( A ) For α7-nAChR antagonist. ( B ) For α7-nAChR agonist. ( C ) For α7-nAChR siRNA. When the groups were pretreated with α7-nAChR antagonist MLA, the expression of Bax/Bcl-2 and cleaved caspase 3 proteins increased in HGC cells compared to cells without MLA or α7-nAChR siRNA treatment (** P<0.01), except for the rL-RVG +MLA group and the rL-RVG group. The expression of the Bax/Bcl-2 and cleaved caspase 3 proteins decreased significantly (** P<0.01) in cells with α7-nAChR agonist ACB treatment compared with cells without pretreatment. The expression of α7-nAChR proteins decreased in MLA-pretreated groups (** P<0.01), but increased in ACB-pretreated groups (** P<0.01). The expression of p-AKT and PI3K proteins decreased in MLA and α7-nAChR siRNA-pretreated groups (** P<0.01), except for the rL-RVG group and the pretreated groups, but increased in the ACB-pretreated groups (** P<0.01). * P<0.05.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC6671559/&orig_host=www.ncbi.nlm.nih.gov'>31337746</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-12935_2020_1454_fig2_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®The influences of circPOSTN silencing on proliferation, apoptosis and aerobic glycolysis of glioma cells. a – l LN229 and U251 cells were transfected with si-circPOSTN or si-NC. a The interference efficiency of si-circPOSTN was analyzed with RT-qPCR assay in LN229 and U251 cells. b , c Effect of circPOSTN silencing on the cell viability of LN229 and U251 cells was assessed with MTT assay. d The apoptosis rate was computed with flow cytometry assay in transfected LN229 and U251 cells. e The western blot assay showed the expression levels of Bcl-2 and Bax in LN229 and U251 cells. f The caspase-3 activity was measured with a caspase-3 assay kit. g – i The concentration of glucose and lactate in the culture medium, as well as ATP production level were measured with a series of kits, respectively. j The protein expression levels of HK2 and LDHA were determined with western blot assay in transfected LN229 and U251 cells. k – l LDHA enzyme activity and ROS accumulation were evaluated in LN229 and U251 cells post-transfection with lactate dehydrogenase activity detection kit and reactive oxygen species assay kit, respectively. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-12935_2020_1454_fig4_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®Knockdown of circPOSTN mediated-effects on proliferation and apoptosis of glioma cells could be eliminated by silencing miR-361-5p. a – j LN229 and U251 cells were transfected with si-NC, si-circPOSTN, si-circPOSTN + anti-miR-NC, or si-circPOSTN + anti-miR-361-5p. a , b The relativity expression level of miR-361-5p was analyzed with RT-qPCR assay in LN229 and U251 cells. c , d MTT assay was administrated to assess cell viability of LN229 and U251 cells after transfection. e , f The apoptosis of transfected LN229 and U251 cells was monitored by flow cytometry. g , h The western blot assay was employed to show the expression levels of Bcl-2 and Bax in LN229 and U251 cells. i , j The caspase-3 activity was examined by caspase-3 assay kit. * P < 0.05 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12935-020-01454-x'>32774168</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41420_2021_448_fig5_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®CircHIPK3 regulates autophagy and apoptosis via the CircHIPK3/miR-20b-5p/ATG7 axis. A Luciferase reporter assay showed that miR-20b-5p mimics directly binds to the 3′-UTR of ATG7 and inhibits luciferase activity. * P < 0.05 compared with the NC-mimics group. B ATG7 protein expression was detected by western blotting. n = 3. * P < 0.05 compared with the MNC group. # P < 0.05 compared with the INC group. C The protein expression levels of LC3-II, P62, and ATG7 were measured by western blotting. n = 3. D The intracellular ROS level was detected by flow cytometry. n = 3. E Annexin V-FITC/PI flow cytometry was used to evaluate apoptosis under different treatment conditions. n = 3. F Apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2, were detected by western blotting. n = 3. * P < 0.05 compared with the H/R group. # P < 0.05 compared with the H/R + sicircHIPK3 group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41420_2021_448_fig4_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®MiR-20b-5p inhibits autophagy and apoptosis of cardiomyocytes under H/R conditions. A Transfection efficacy of miR-20b-5p mimics and miR-20b-5p inhibitors in cardiomyocytes. B Western blot showed the effect of transfection of miR-20b-5p mimics and miR-20b-5p inhibitors on the expression of LC3II and P62 in normal cardiomyocytes. n = 3. C Western blot showed the effect of transfection of miR-20b-5p mimics and miR-20b-5p inhibitors on the expression of apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2 in normal cardiomyocytes. n = 3. D Western blot showed the effects of miR-20b-5p mimics and miR-20b-5p inhibitor transfection on the expression of LC3II and P62 in cardiomyocytes under H/R conditions. n = 3. E Annexin V-FITC/PI flow cytometry was used to evaluate the effect of miR-20b-5p mimics and miR-20b-5p inhibitors on cardiomyocyte apoptosis under H/R conditions. n = 3. F Western blot analyzed the expression of apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2 in cardiomyocytes under H/R conditions by miR-20b-5p mimics and miR-20b-5p inhibitors transfection. n = 3. * P < 0.05 compared with the mimics-NC (MNC) group. # P < 0.05 compared with the inhibitors-NC (INC) group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-41420_2021_448_fig2_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®CircHIPK3 promotes H/R-induced cardiomyocyte apoptosis. A The intracellular ROS level was detected by flow cytometry. n = 3. B Annexin V-FITC/PI flow cytometry was used to evaluate the effect of circHIPK3 on cardiomyocyte apoptosis. n = 3. C Apoptosis-related proteins, including procaspase-3, cleaved caspase-3, Bax, and Bcl-2, were detected by western blotting. n = 3. * P < 0.05 compared with the normal group. # P < 0.05 compared with the H/R group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41420-021-00448-6'>33824287</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-nrr-12-96-g006.jpgAnti-Bcl-2/BCL2 Antibody Picoband®Nicotiflorin effect on Bcl-2, Bax, and caspase-3 expression in the ischemic cerebral cortex of I/R rats (western blot assay). (A, C, E) Western blot images of Bax, Bcl-2, and caspases-3 protein; (B, D, F) Western blot assay shows up-regulation of caspase-3 and Bax expreesssion and down-regulation of Bcl-2 expression in the I/R group (* P < 0.05, ** P < 0.01, vs . I/R group). Both Bax and caspase-3 expression were decreased and Bcl-2 expreesssion increased in the nicotiflorin group. Data are expressed as the mean ± SEM, n = 3, one-way analysis of variance followed by post hoc Tukey test. I/R: Ischemia/reperfusion.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5319249/&orig_host=www.ncbi.nlm.nih.gov'>28250754</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-fphar-10-00285-g005.jpgAnti-Bcl-2/BCL2 Antibody Picoband®The effect of the combination of alteronol and ADM on protein levels of apoptosis-related molecules in 4T1 cells. (A) The protein levels of Bax and Bcl-2 were measured by western blot. (B) Quantitative analysis of Bax and Bcl-2 protein levels in 4T1 cells after treatment with alteronol and/or ADM. (C) The protein levels of cleaved PARP, cleaved caspase-9, and cleaved caspase-3 were examined by western blot. (D) Quantitative analysis of cleaved PARP, cleaved caspase-9, and cleaved caspase-3 protein levels after the indicated treatments. ∗ P < 0.05, ∗∗ P < 0.01 vs. control group. # P < 0.05, ## P < 0.01 vs. alteronol group. & P < 0.05, && P < 0.01 vs. ADM group. All data are expressed as mean ± SD of three independent experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00285/full'>31001113</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-12931_2021_1908_fig2_html.pngAnti-Bcl-2/BCL2 Antibody Picoband®Effect of TRB3 knockdown on proliferation, migration, and apoptosis of hypoxic PASMCs. PASMCs were transfected with lentiviral vectors encoding short hairpin RNAs targeting against rat TRB3(si-TRB3) or negative control(si-NC) for further analysis. A CCK-8 assays were performed to test cell viability after TRB3 knockdown in hypoxic PASMCs. B The EdU proliferation assay was used to measure cell proliferation. All images are × 400 magnification. C EdU‐positive cells were analyzed. D and E The expression of PCNA and Survivin was examined by western blot, and the gray value was quantified by ImageJ software. F Cell apoptosis was evaluated by Hoechst 33342 staining, and the percentage of apoptosis was quantified. G Crystal violet staining of PASMCs is presented at × 200 magnification for the Transwell assay, and the migrated cells were counted manually. H Apoptosis-related protein expression was evaluated and quantification of the analysis is shown. I The expression of MMP9 was evaluated. Data represent the mean ± SEM (n = 4). *P < 0.05 and **P < 0.01 compared to normoxic PASMCs transfected with si-NC. # P < 0.05 and ## P < 0.01 compared to hypoxic PASMCs transfected with si-TRB3. si-NC, lentiviral vectors encoding the negative control sequence; si-TRB3, lentiviral vectors encoding the short-hairpin RNAs against rat TRB3; PCNA, proliferating cell nuclear antigen; TRB3, Tribbles homolog 3; BAX, BCL2 associated X; Bcl2, B cell leukemia/lymphoma 2; MMP9, matrix metallopeptidase 9 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12931-021-01908-4'>34906150</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-bcl2-primary-antibodies-fcm-testing-3.jpgAnti-Bcl-2/BCL2 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-BCL2 antibody (A00040-2). <br>Overlay histogram showing U20S cells stained with A00040-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BCL2 Antibody (A00040-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00040-2-bcl2-primary-antibodies-wb-testing-2.pngAnti-Bcl-2/BCL2 Antibody Picoband®Western blot analysis of Bcl-2 using anti-Bcl-2 antibody (A00040-2).<br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions.<br>
Lane 1: huamn OE19 whole cell lysates,<br>
Lane 2: human OE19 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bcl-2 antigen affinity purified monoclonal antibody (A00040-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Bcl-2 at approximately ~30 kDa. The expected band size for Bcl-2 is at ~26 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bmpr2-picoband-trade-antibody-a00324-1-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00324-1-BMPR2-primary-antibodies-WB-testing-1.jpgAnti-BMPR2 Antibody Picoband® Western blot analysis of BMPR2 using anti-BMPR2 antibody (A00324-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: mouse brain tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMPR2 antigen affinity purified polyclonal antibody (Catalog # A00324-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BMPR2 at approximately 130KD. The expected band size for BMPR2 is at 115KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hp1-gamma-picoband-trade-antibody-a01142-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1-gamma-primary-antibodies-wb-testing-1.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® Western blot analysis of HP1 gamma using anti-HP1 gamma antibody (A01142). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: rat spleen tissue lysate, <br>
Lane 3: rat testis tissue lysate, <br>
Lane 4: rat PC-12 whole cell lysate, <br>
Lane 5: mouse brain tissue lysate, <br>
Lane 6: mouse brain tissue lysate, <br>
Lane 7: mouse testis tissue lysate, <br>
Lane 8: mouse HEPA1-6 whole cell lysate, <br>
Lane 9: mouse NIH/3T3 whole cell lysate. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HP1 gamma antigen affinity purified polyclonal antibody (Catalog # A01142) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HP1 gamma at approximately 21KD. The expected band size for HP1 gamma is at 21KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1-gamma-primary-antibodies-wb-testing-2.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® Western blot analysis of HP1 gamma using anti-HP1 gamma antibody (A01142). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysate, <br>
Lane 2: human MCF-7 whole cell lysate, <br>
Lane 3: human COLO320 whole cell lysate, <br>
Lane 4: human HepG2 whole cell lysate, <br>
Lane 5: human placenta tissue lysate, <br>
Lane 6: human A549 whole cell lysate, <br>
Lane 7: human SKOV-3 whole cell lysate, <br>
Lane 8: human PANC-1 whole cell lysate. <br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HP1 gamma antigen affinity purified polyclonal antibody (Catalog # A01142) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HP1 gamma at approximately 21KD. The expected band size for HP1 gamma is at 21KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01142-HP1_gamma-primary-antibodies-IHC-testing-3.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).
<br>HP1 gamma was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01142-HP1_gamma-primary-antibodies-IHC-testing-4.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).
<br>HP1 gamma was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01142-HP1_gamma-primary-antibodies-IHC-testing-5.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).
<br>HP1 gamma was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01142-HP1_gamma-primary-antibodies-IHC-testing-6.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).
<br>HP1 gamma was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1_gamma-primary-antibodies-if-testing-7.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IF analysis of HP1 gamma using anti-HP1 gamma antibody (A01142). <br> HP1 gamma was detected in immunocytochemical section of U20S cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1_gamma-primary-antibodies-fc-testing-8.pngAnti-HP1 gamma/CBX3 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-HP1 gamma antibody (A01142). <br> Overlay histogram showing A431 cells stained with A01142 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HP1 gamma Antibody (A01142,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1_gamma-primary-antibodies-ihc-f-testing-9.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).<br> HP1 gamma was detected in frozen section of rat spleen tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1_gamma-primary-antibodies-ihc-f-testing-10.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).<br> HP1 gamma was detected in frozen section of human placenta tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01142-hp1_gamma-primary-antibodies-ihc-f-testing-11.jpgAnti-HP1 gamma/CBX3 Antibody Picoband® IHC analysis of HP1 gamma using anti-HP1 gamma antibody (A01142).<br> HP1 gamma was detected in frozen section of mouse spleen tissues. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HP1 gamma Antibody (A01142) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd7-picoband-trade-antibody-a01974-2-boster.html2026-03-24T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01974-2-CD7-primary-antibodies-IHC-testing-1.jpgAnti-CD7 Antibody Picoband® IHC analysis of CD7 using anti-CD7 antibody (A01974-2).
<br>CD7 was detected in paraffin-embedded section of human tonsil tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD7 Antibody (A01974-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01974-2-CD7-primary-antibodies-FC-testing-2.jpgAnti-CD7 Antibody Picoband® Flow Cytometry analysis of PBMC cells using anti-CD7 antibody (A01974-2).<br>Overlay histogram showing PBMC cells stained with A01974-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD7 Antibody (A01974-2,1μg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01974-2-CD7-primary-antibodies-WB-testing-1.jpgAnti-CD7 Antibody Picoband® Western blot analysis of CD7 using anti-CD7 antibody (A01974-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.
<br>Lane 1: recombinant human CD7 protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD7 antigen affinity purified polyclonal antibody (Catalog # A01974-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD7 at approximately 30-40KD. The expected band size for CD7 is at 18KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd8-alpha-picoband-trade-antibody-a02236-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02236-1-CD8_alpha-primary-antibodies-WB-testing-1.jpgAnti-CD8 alpha/Cd8a Antibody Picoband® Western blot analysis of CD8 alpha using anti-CD8 alpha antibody (A02236-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat spleen tissue lysate,<br>Lane 2: rat thymus tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD8 alpha antigen affinity purified polyclonal antibody (Catalog # A02236-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD8 alpha at approximately 36KD. The expected band size for CD8 alpha is at 26KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-2186-3326-86-0392-g003.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Immunohistochemical analysis of the CD8a-positive area in the injured spinal region 7 days after SCI. Bar: 40 µm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml'>39355370</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-fimmu-12-616074-g003.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Effect of berberine treatment on the T cell immune responses to cardiac allografts. (A) MLR responses. Recipient SPCs were isolated at POD 7 (responders) and mitomycin C-treated naïve BALB/c SPCs (stimulators) were co-cultured for 3 days (n = 3 mice/group). Total SPCs were isolated at PDO 7, and the absolute numbers of (B) SPCs were determined by flow cytometry. (C) The percentage of CD4 + Foxp3 + Treg cells was determined by flow cytometry. Syngeneic recipients are shown for comparison (n = 3 mice/group). (D) The spleens of recipient mice were harvested and weighed at POD 7 (n = 5 mice/group). (E) The absolute numbers of CD4 + and CD8 + T cells SPCs (n = 3 mice/group). (F) SPCs and (G) LNCs were isolated at POD 7, and the percentage of CD4 + and CD8 + T cells was determined by flow cytometry. Syngeneic recipients are shown for comparison (n = 3 mice/group). (H) CD44 + CD69 + T cell activation assays. SPCs were isolated at POD 7, and the percentages of (i) CD4 + CD44 + CD69 + and (ii) CD8 + CD44 + CD69 + T cells were determined by flow cytometry (n = 3 mice/group). (I) LNCs were isolated at POD 7, and the percentages of (i) CD4 + CD44 + CD69 + and (ii) CD8 + CD44 + CD69 + T cells were determined by flow cytometry (n = 3 mice/group). (J) Serum plasma levels of proinflammatory cytokines. Peripheral blood was collected at POD 7, and (i) IFN-γ, (ii) IL-6, and (iii) TNF-α plasma levels were measured by ELISA (n = 3 mice/group). SPCs, spleen cells; LNCs, lymph node cells; MLR, mixed lymphocyte reaction; POD, post-operative day. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the normal saline-treated group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.616074/full'>33732240</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-fimmu-12-616074-g004.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Phenotypic and functional characteristics of allograft-infiltrating CD4 + or CD8 + T cells. Allografts were recovered at POD 7, and POD 100 syngeneic grafts are shown for comparison. (A) (i) Immunofluorescent staining of CD4 (red), KI67 (green), and 4′,6-diamidino-2-phenylindole (DAPI, blue) in grafts. (ii) Immunofluorescent staining of CD8 (red), KI67 (green), and DAPI in grafts (Scale bar = 200 μm; original magnification: ×200). (B) Proportion and absolute number of graft-infiltrating (i) CD4 + T cells and their expression of (ii) KI67, and proportion and absolute number of graft-infiltrating (iii) CD8 + T cells and their expression of (iv) KI67 (n = 3 mice/group). (C) Proportion of (i) IFN-γ and (ii) cleaved-caspase-3 in graft-infiltrating CD3 + T cells (n = 3 mice/group). (D) (i) Cleaved-caspase-3 and cleaved-PARP protein expression in grafts. Myocardial cell apoptosis co-immunofluorescence staining and expression of (ii) cleaved-caspase-3 and (iii) cleaved-PARP (n = 3 mice/group). (E) Relative mRNA expression of IFN-γ , IL-6, IL-10 , Foxp3 , and FasL in grafts measured by qPCR (n = 3 mice/group). SPCs, spleen cells; LNCs, lymph node cells; POD, post-operative day. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the normal saline-treated group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.616074/full'>33732240</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-fimmu-12-616074-g006.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®The effects of berberine on CD4 + and CD8 + T cell apoptosis, activation, and proliferation in vitro . (A) T cell activation assay. The percentages of (i) CD4 + CD44 + and (ii) CD8 + CD44 + T cells were determined by flow cytometry. (B) T cell proliferation assay. T cells from naïve C57BL/6 mice were labeled with CFSE and then co-stimulated with anti-CD3/CD28 Abs in the absence or presence of berberine. After 3 days of co-culture, (i) CD4 + and (ii) CD8 + T cell division was determined by flow cytometry. (C) (i) Supernatant levels of IFN-γ measured by ELISA, and (ii) mRNA expression of IFN-γ in T cells measured by qPCR. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the (Positive Control) PC group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.616074/full'>33732240</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-thnov10p9332g002.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Targeting USP7 inhibits murine M2 phenotype and function in vitro . (A) The mRNA expression of common genes related to DUBs was detected by RT-PCR in M0, M1 (LPS/IFN-γ M1), and M2 (IL-4/13 M2 and IL-10 M2) induced from ANA-1. ( B ) The mRNA expression of USP7 in MΦs, M1, and M2 induced from BMDMs was detected by RT-PCR. ( C ) Western blotting showing the expression of USP7 in MΦ, M1, and M2 induced from BMDMs. ( D-E ) Flow cytometry analyses of the expression of CD206 in IL-4/13-induced BMDM M2 cells, which had been treated with P5091 (5 μM or 10 μM) for 24 h. Data are presented as the mean ± SEM (n = 3). ( F ) Detection of the expression of USP7 in BMDMs, which were transfected with either NC- or USP7-siRNA by western blotting. ( G ) The expression of CD206 in BMDMs of NC-siRNA and USP7-siRNA group was detected by flow cytometry. ( H-I ) Flow cytometry analyses of CFSE expression on the surface of CD8 + T cells in the presence of conditioned medium from either DMSO- or P5091- (5 μM or 10 μM) treated IL-4/13-induced BMDM M2 cells. Data are presented as the mean ± SEM (n = 3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7415808/&orig_host=www.ncbi.nlm.nih.gov'>32802195</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-fimmu-12-616074-g005.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Berberine induces T cell apoptosis via the mitochondrial apoptosis pathway. (A) (i) KEGG functional categories of differentially expressed genes following berberine and saline treatment. The Y-axis represents the KEGG functional categories. (ii) KEGG analysis of the significantly altered signaling pathways in cell growth- and death-associated genes. The X-axis represents the rich ratio of the number of differentially expressed genes and the Y-axis represents the KEGG pathways. (iii) qPCR analysis of Bcl-2 and TNF-α mRNA expression in SPCs collected from heart transplant recipients treated with berberine or not. (B) T cell apoptosis assays in vivo . (i) SPCs and (ii) LNCs were collected at POD 7. The percentages of apoptotic CD4 + and CD8 + T cells were determined by flow cytometry (n = 3 mice/group). (C) T cell apoptosis assay in vitro . T cells from naïve C57BL/6 mice were co-stimulated with anti-CD3/CD28 Abs in the absence or presence of berberine. The percentages of apoptotic (i) CD4 + and (ii) CD8 + T cells were determined by flow cytometry. (D) Berberine activates the mitochondrial apoptosis pathway in vivo . (i) Relative protein expression of Bcl-2, Bax, cytochrome c, cleaved-caspase-3, and cleaved-PARP in SPC. (ii) β-actin was used as a loading control (n = 3 mice/group), and OD values (relative to β-actin) are presented as means ± SEMs. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the normal saline-treated group. (E) Berberine activates the mitochondrial apoptosis pathway in vitro . Relative protein expression of Bcl-2, Bax, cytochrome c, cleaved-caspase-3, and cleaved-PARP expression in CD3 + T cells. (ii) β-actin was used as a loading control; OD values (relative to β-actin) are presented as means ± SEMs. SPCs, spleen cells; LNCs, lymph node cells; POD, post-operative day. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the PC group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.616074/full'>33732240</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-thnov10p9332g003.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Targeting USP7 inhibits tumor growth and induces local anti-tumor immunity in vivo . ( A ) Harvested and photographed tumors in the P5091 and the Control group. ( B ) Lewis tumor growth following P5091 or Vehicle treatment in vivo. Data are presented as the mean ± SEM (n = 6 per group). ( C ) Spider diagram of the tumor volume growth in each mouse from the P5091 group and the Control group. ( D ) Gating strategy for detection of the TAMs by flow cytometry. ( E-G ) Proportions of M1 ( E ) and M2 ( F ), and M1/M2 ratio ( G ) in the TME of the P5091 group and the Control group. ( H-M ) Percentages of MDSC ( H ), Treg ( I ), CD4 + T ( J ), CD8 + T ( K ), Th1 ( L ), and CTLs ( M ) within the TME in each group. Data are presented as the mean ± SEM (n = 7) for ( E-M ).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7415808/&orig_host=www.ncbi.nlm.nih.gov'>32802195</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-thnov10p9332g004.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Targeting USP7 activates local and systemic anti-tumor immunity. ( A ) Multicolor immunofluorescence detection of TAMs and CTLs in the TME of the P5091 group and the Control group. ( B-F ) Cytokines IFN-γ ( B ), TNF-α ( C ), IL-2 ( D ), IL-5 ( E ), and IL-6 ( F ) in the TME of each group were detected by Mul-Analyte Flow Assay Kit. ( G-K ) Proportion of Treg ( G ), CD4 + T ( H ), CD8 + T ( I ), Th1 ( J ), and CTLs ( K ) in the spleen of each group. Data are presented as the mean ± SEM (n = 7) for ( B-K ).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7415808/&orig_host=www.ncbi.nlm.nih.gov'>32802195</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-thnov10p9332g006.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®Targeting USP7 can activate the p38 MAPK pathway to reprogram TAMs. ( A ) The strategy for sorting TAMs in TME by flow cytometry. ( B ) Heat maps illustrating the differentially expressed M1- and M2-related genes in TAMs between the P5091 group and the Control group based on the results of RNA sequencing. ( C ) RT-PCR further verifying the differentially expressed genes of sorted TAMs in each group. Data are presented as the mean ± SEM (n = 3). ( D ) KEGG analysis identifying 20 most obviously enriched pathways based on the differentially expressed genes of the two groups. ( E ) Western blotting detection of the expression of JNK, p-JNK, ERK1/2, p-ERK1/2, p38, p-p38, and β-actin in IL-4/13-BMDM M2 cells treated with P5091 (10 µM) at the indicated time points. ( F ) Flow cytometry analysis of CFSE expression on the surface of CD8 + T cells in the presence of conditioned medium of IL-4/13-induced BMDM M2 cells from various indicated treatments. Treatments indicated: DMSO stimulation, P5091 (10 µM) stimulation, P5091 (10 µM) stimulation in the presence of inhibitors of p38 (SB203580, 10 µM), JNK (SP600125, 10 µM), Erk1/2 (U0126-EtOH, 10 µM). Data are presented as the mean ± SEM (n = 4).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC7415808/&orig_host=www.ncbi.nlm.nih.gov'>32802195</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-41208878-figure-5.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®ASNS shapes the immune landscapes in metastatic TdLN and primary tumor site. Figure 5A-C. LN metastasis model was conducted on C57BL/6 mice with LLC-ASNS WT(n=6), ASNSC2A overexpression cells(n=6) and control group(n=6), primary tumor and popliteal lymph nodes were isolated at the end of the experiment, and primary tumor volume(B) and TdLN volume/tumor volume(C) was measured and analyzed. 5D-F. (D) Representative FACS profiles of CD8+T cells are shown. The percentage(E) and number(F) of CD8+ subset in TIL cells isolated from primary tumor is shown. 5G-I. (G) Representative FACS profiles of the co-expression pattern of CD44 and CD62L, or the co-expression pattern of TCF-1and TOX in CD8+ T cells are shown. The number(H) and percentage(I) of CD44+, CD44+CD62L+, CD44+CD62L-, Tsl and TTSM subset in CD8+T cells isolated from TdLN is shown. 5J-L. (J) Representative FACS profiles of the co-expression pattern of CD44 and CD62L, or the co-expression pattern of TCF-1and TOX in CD8+ T cells are shown. The number(K) and percentage(L) of CD44+, CD44+CD62L+, CD44+CD62L-, Tsl and TTSM subset in CD8+T cells isolated from primary tumor is shown.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ijbs.com/v21p6501.htm'>41208878</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-41208878-figure-6.jpgAnti-CD8 alpha/Cd8a Antibody Picoband®ASNS-high-expression metastases generated lymphocyte niches enriched with activated T cells, memory T cells, Tsl and TTSM. Figure 6A-C. Representative immunofluorescence staining images of metastatic TdLNs from LN metastasis model. 6D. The number of CD8+ T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6E-F. The number(E) and percentage(F) of CD44+CD8+T cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6G-H. The number(G) and percentage(H) of Tsl cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6I-J. The number(I) and percentage(J) of TTSM cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=5, ASNSC2A, n=4, and EV, n=3). 6K. Quantitative estimates of the distance from ova+ to CD8+CD44+CD62L+TCF+(TTSM) (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6L-M. Representative immunofluorescence staining images of metastatic TdLNs from NSCLC patients. 6N-O. The number(C) and percentage(D) of CD8+ T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6P-Q. The number (E) and percentage(F) of CD45RO+CD8+ T cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6R-S. The number (G) and percentage(H) of Tsl cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6T-U. The number (I) and percentage(J) of TTSM cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ijbs.com/v21p6501.htm'>41208878</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02236-1-CD8_alpha-primary-antibodies-IHC-testing-2.jpgAnti-CD8 alpha/Cd8a Antibody Picoband® IHC analysis of CD8 alpha using anti-CD8 alpha antibody (A02236-1).
<br>CD8 alpha was detected in paraffin-embedded section of mouse spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD8 alpha Antibody (A02236-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02236-1-CD8_alpha-primary-antibodies-IHC-testing-3.jpgAnti-CD8 alpha/Cd8a Antibody Picoband® IHC analysis of CD8 alpha using anti-CD8 alpha antibody (A02236-1).
<br>CD8 alpha was detected in paraffin-embedded section of rat spleen tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD8 alpha Antibody (A02236-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02236-1-cd8-alpha-primary-antibodies-fcm-testing-4.jpgAnti-CD8 alpha/Cd8a Antibody Picoband® Flow Cytometry analysis of mouse spleen tissues using anti-CD8 alpha antibody (A02236-1). <br>
Overlay histogram showing mouse spleen tissues stained with A02236-1 (Blue line). The tissues were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD8 alpha Antibody (A02236-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd44-picoband-trade-antibody-a00052-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13045_2025_1693_fig8_html.pngAnti-CD44 Antibody Picoband®R-RAS2 is downstream of CD44 promoting migratory, invasive and metastatic behavior of breast cancer cells. a , Box and whiskers plot showing all experimental points of a migration assay in Boyden chambers separated by a 8 μm-diameter pore membrane. Cells were incubated overnight (~16 h). Each point represents the mean of cells per surface unit (mm 2 ) of membrane counted. A number of 18 areas of the membrane were counted per experimental condition. Statistical significance was assessed by carrying out a Mann-Whitney test. b , Box and whiskers plot showing all experimental points of a migration assay in Boyden chambers separated by a 8 μm-diameter pore membrane and layered on the upper chamber with 100 μL of Matrigel. Cells were incubated overnight (~16 h). Each point represents the mean of cells per surface unit (mm 2 ) of membrane counted. A number of 18 areas of the membrane were counted per experimental condition. Statistical significance was assessed by carrying out a Mann-Whitney test. c , Light field microscopy of the bottom part of the membrane with 8-μm diameter pores separating an upper Boyden chamber in which CBM-MBC21 control of knockdown cells were seeded in serum-free medium and a lower chamber containing medium with 20% feta bovine serum. In addition, the upper chamber had a layer or either Matrigel or Matrigel + hyaluronic acid directly on top of the membrane. Cells were allowed to migrate for 8 h from the top to the bottom chambers and through the Matrigel or Matrigel + HA layers. The bottom part of the membrane was stained with crystal violet to count the number of migrated cells. d , Box and whiskers plot showing all experimental points of the experiment illustrated in Fig. c. Each point represents the mean of cells per surface unit (mm 2 ) of membrane counted. A number of 14 areas of the membrane were counted per experimental condition. Statistical significance was assessed using unpaired t-tests. e , An invasion assay as this of Fig. 8 b and d, was carried out in Boyden chambers coated in the upper chamber with a layer of Matrigel + hyaluronic acid. Control and knockdown CBM-MBC21 cells were incubated or not (no Ab) with 5 μg/mL of blocking anti-CD44 antibody in the upper chamber for 8 h. Box and whiskers plot showing all experimental points that represent the mean of cells per surface unit (mm 2 ) of membrane counted. A number of 13–14 areas of the membrane were counted per experimental condition. Statistical significance was assessed using a one-way ANOVA Tukey’s multiple comparison test. f , The metastatic capacity of control and knockdown CBM-MBC21 cells 25 days after orthotopic inoculation in the left inguinal mammary gland of female C57BL/6 mice was assessed by flow cytometry of the lungs and liver. The pseudocolor plot shows the identification of metastatic breast cancer cells in the lungs according to the expression of GFP and CD44. g , Box and whiskers plot showing all experimental points calculated as illustrated in Fig. f and Suppl Fig. f referring to BC cell infiltration of lungs and liver, respectively. Each point represents a single mouse. Statistical significance was assessed by carrying out Mann-Whitney tests. h , Box and whiskers plot showing all experimental points indicating primary tumor weight in mice inoculated with BT-549 human BC cells at the day of sacrifice (day 39). Statistical significance was assessed by carrying out a Mann-Whitney test. i , Photograph of the entire liver taken from a mouse inoculated with wild type BT-549, control, BC cells. The blue arrow points at the presence of a green fluorescent BC tumor nodule. j , The metastatic capacity of control and knockdown BT-549 cells 39 days after orthotopic inoculation in the left inguinal mammary gland of female Rag2 −/− γc −/− mice was assessed by flow cytometry of the lungs and liver. The two-color plot shows the identification of metastatic breast cancer cells in the lungs according to the expression of GFP and human EGFR. k , Box and whiskers plot showing all experimental points calculated as illustrated in Fig. j referring to BC cell infiltration of lungs and liver. One out of four liver lobules per animal were processed for flow cytometry analysis. Each point represents a single mouse. Statistical significance was assessed by carrying out Mann-Whitney tests <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13045-025-01693-3'>40221767</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cd44-primary-antibodies-wb-testing-1.jpgAnti-CD44 Antibody Picoband® Western blot analysis of CD44 using anti-CD44 antibody (A00052). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human U251 whole cell lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: rat small intestine tissue lysates,<br>
Lane 4: mouse lung tissue tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD44 antigen affinity purified polyclonal antibody (Catalog # A00052) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD44 at approximately 82 kDa. The expected band size for CD44 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13045_2025_1693_fig4_html.pngAnti-CD44 Antibody Picoband®R-RAS2 controls PI3K/Akt, ERK/MAPK and mTORC1 pathway activation in murine RRAS2-overexpressing breast cancer cells. a , Cartoon illustrating RAS/ERK/MAPK, PI3K/Akt and mTORC1 pathway activation by Receptor Tyrosine Kinases (RTKs) like EphaA2, EGFR or HER2, and by amino acid transporters like the CD98hc/CD98lc(LAT1) complex, and by CD44. The positions of some relevant phosphorylated residues are indicated, as well as the putative position of R-RAS2 downstream of the RTKs, CD44 and CD98. b , Western blot analysis of signaling pathway activity based on the phosphorylation of key residues in the elements indicated. Post-nuclear cell lysates of wild type CBM-MBC21 cells and a shRNA-generated RRAS2 knockdown of that cell line were analyzed in the blots. c , Summary of the results generated by Western blot. The inhibitory effect of R-RAS2 depletion is indicated by the number of arrows pointing downwards <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13045-025-01693-3'>40221767</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-fonc-14-1463656-g004.jpgAnti-CD44 Antibody Picoband®Representative images of the expression of caspase-3, Bax, Bcl-2, Ki67, VEGFA, VEGFR-2, MDA, CD24, CD44, ALDH1A1, EpCam, H3K4m3, H3K9m3, H4K20m3, H4K16ac in rat carcinoma tissue of mammary gland. For detection, polyclonal caspase-3 antibody (Bioss, Woburn, USA), polyclonal Bax and Bcl-2 antibodies (Santa Cruz Biotechnology, Paso Robles, CA, USA), monoclonal Ki67 antibody (Dako, Glostrup, Denmark), monoclonal VEGFA and VEGFR-2 antibodies (Santa Cruz Biotechnology, Paso Robles, CA, USA), polyclonal CD24 antibody (GeneTex, Irvine, CA, USA), polyclonal CD44 antibody (Boster, Pleasanton, CA, USA), polyclonal ALDH1A1 antibody (ThermoFisher, Rockford, IL, USA), polyclonal MDA, EpCAM, H3K4m, H3K9m3, and H4K20m3 antibodies (Abcam, Cambridge, MA, USA), and monoclonal H4K16ac antibody (Abcam, Cambridge, MA, USA) were applied; final magnification: ×400.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11491292/'>39435289</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13045_2025_1693_fig3_html.pngAnti-CD44 Antibody Picoband®R-RAS2 interacts with plasma membrane receptors known to be important for breast cancer. a , Selected list of plasma membrane proteins that interact with R-RAS2 in a murine breast cancer tumor isolated from a Rosa26- RRAS2 fl/fl x Wap-Cre female mouse. Full data can be found in Extended Data Table . The known involvement of these proteins in cancer and breast cancer is briefly summarized, and the Mascot Score for the specific affinity column with anti-hemagglutinin (for hemagglutinin-tagged R-RAS2) and a control isotypic immunoglobulin column is also shown. Protein function and association with cancer data have been retrieved from The Human Protein Atlas: . b , Biological processes and pathways found to be significantly altered after KEGG analysis of the R-RAS2 plasma membrane interactome of Extended Data Table . The x-axis shows the percentage or proteins in the pathway found associated to R-RAS2 and the y-axis the–Log10 of the P adjusted value. Full data is provided in Extended Data Table . c , STRING network of physical and functional interactions among the indicated proteins from Fig. a. Pink lines indicate experimentally-determined interactions; blue lines indicated interactions found in curated databases; green lines indicate interactions found by textmining and black lines indicate co-expression. d , Co-immunoprecipitation of CD44, Epha2 and Slc3a2 (CD98hc) with R-RRAS2 (IP anti-Hag) was studied in detergent lysates of the CBM-MBC21 mouse cell line. The membranes were re-probed with anti-Hag as a control for loading of R-RAS2, and the arrows indicate the positions of the co-immunoprecipitated proteins and those in the whole cell lysate (WCL). The molecular weight markers are shown on the left. e , Co-immunoprecipitation of CD44, Epha2 and Slc3a2 (CD98hc) with R-RRAS2 in detergent lysates of the human breast cancer cell line BT-549 transfected with a Hag-tagged R-RAS2 construct. Legend as in panel d . f , Mid-plane confocal microscopy sections of CBM-MBC21 cells fixed and stained with R-RAS2 (anti-Hag) and anti-CD44 antibodies to show their co-localization at the plasma membrane. The nucleus of the cells is stained with DAPI (blue). Details of 4 areas of the plasma membranes are shown to the right to show the co-localization of R-RAS2 with CD44 in cell protrusions. g , Co-localization of R-RAS2 and CD44 was measured by analysis of all pixels in 23 cell protusions as in the inset of Fig. f and calculating the Pearson’s correlation coefficient. The violin plot shows all data points, the median (= 0.70) and the 75% and 25% percentiles. h , Mid-plane confocal microscopy sections of CBM-MBC21 cells fixed and stained with R-RAS2 (anti-Hag) and anti-CD98hc antibodies to show their co-localization at the plasma membrane. The nucleus of the cells is stained with DAPI (blue). Details of 4 areas of the plasma membranes are shown to the right to show the co-localization of R-RAS2 with CD98hc at the external (apical) plasma membrane of the cell aggregate. i , Co-localization of R-RAS2 and CD98hc was measured by analysis of all pixels in 25 membrane regions as in the inset of Fig. h and calculating the Pearson’s correlation coefficient. The violin plot shows all data points, the median (= 0.69) and the 75% and 25% percentiles <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13045-025-01693-3'>40221767</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13045_2025_1693_fig6_html.pngAnti-CD44 Antibody Picoband®R-RAS2 co-localizes with CD44 in F-actin-rich cell protrusions of breast cancer cells. a , Confocal microscopy sections at the plane of contact with the coverslips of CBM-MBC21 control and knockdown cells plated on coverslips coated with poly-L-lysine alone or with poly-L-lysine plus hyaluronic acid (HA). Cells were plated in the presence or absence of a blocking anti-CD44 antibody. After incubation, cells were fixed and stained with R-RAS2 (anti-Hag) and phalloidin to show their co-localization at sites rich in F-actin. The nucleus of the cells is stained with DAPI (blue). b , Co-localization of R-RAS2 and F-actin at cell protrusions was measured by analysis of all pixels in 17–33 cell protrusions and calculating the Pearson’s correlation coefficient. The violin plot shows all data points, the median and the 75% and 25% percentiles for each condition. Statistical significance was assessed using a one-way ANOVA Tukey’s multiple comparison test. ***, p < 0.001, ****, p < 0.0001. c , Cell area at the contact site with the coverslip in the experiment of Fig. a-b, was calculated for 7–28 cells per condition. The violin plot shows all data points, the median and the 75% and 25% percentiles for each condition. Statistical significance was assessed using a one-way ANOVA Tukey’s multiple comparison test. *, p = 0.03; **, p = 0.008; ***, p = 0.0003; ****, p < 0.0001. d , The number and distance to the center of cell protrusions were measured in phalloidin stains by calculating the center of mass and drawing lines (yellow) from the center to the tip of cell protrusions. e , The number of protrusions was calculated as in Fig. d for a minimum of 15 cells per culture condition. The violin plot shows all data points, the median and the 75% and 25% percentiles for each condition. Statistical significance was assessed using a one-way ANOVA Tukey’s multiple comparison test. *, p < 0.05; **, p = 0.002; ****, p < 0.0001. f , The distance to the cell center of mass of protrusions was calculated as in Fig. d for a minimum of 100 cell protrusions per culture condition. The violin plot shows all data points, the median and the 75% and 25% percentiles for each condition. Statistical significance was assessed using a one-way ANOVA Tukey’s multiple comparison test. *, p < 0.05; ****, p < 0.0001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13045-025-01693-3'>40221767</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig1_html.pngAnti-CD44 Antibody Picoband®CD44 is upregulated in TECs and associated with mitochondrial dysfunction and apoptosis. A UMAP shows cell population in kidneys of sham and IRI at 6 h and day 2. PT proximal tubule, PT-Inj injured PT, PT-R repairing PT, FR-PTC failed repair PT cell, PT-AcInj acute injury PT, DTL descending limb of loop of Henle (LoH), ATL thin ascending limb of LoH, TAL thick ascending limb of LoH, DCT distal convoluted tubule, CNT connecting tubule, PC principal cell of collecting duct, ICA type A intercalated cell of collecting duct, ICB type B intercalated cell of collecting duct, Pod podocyte, EC endothelial cell, Fib fibroblast, Myofib myofibroblast, Ma macrophage (Mφ), B/T immune cell, Uro urothelium. Data from PMID: 36265491. B Graphic presentation of single-cell sequencing analysis shows the expression of CD44 in different cell populations. C Graphic presentation of single-cell sequencing analysis shows the expression of CD44 at different time point. D and E Representative western blot of CD44 ( D ) and graphical presentations ( E ) of protein expressional levels are shown. ** P < 0.01 versus sham group ( n = 5). F Representative micrographs show the expression of CD44 in sham and IRI groups, as indicated. Frozen kidney sections were stained with an antibody against CD44. Arrow indicates positive staining. Scale bar, 50 μm. G Co-localization staining of CD44 and various segment-specific tubular markers in the kidneys of the IRI model. Frozen kidney sections were collected from the mice 1 day after IRI. CD44 (red) and various segment-specific tubular markers (green), including LTL, PNA, and DBA, were detected by immunofluorescence. Arrows indicate positive staining. Scale bar, 50 μm. H GO analysis of CD44-related pathway through STRING ( ). I Co-localization of CD44 and TOMM20 in tubules. Frozen renal sections were subjected to immunostaining of CD44 (red) and TOMM20 (green). Scale bar, 50 μm. J Co-localization of CD44 and cleaved caspase 3 in IRI group. Frozen kidney sections were subjected to immunostaining of CD44 (red) and cleaved caspase 3 (green). Scale bar, 50 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig6_html.pngAnti-CD44 Antibody Picoband®The anti-leukemic effect of Ara-C@HSPC-Lipo in Ka539 leukemia model. a Schematic illustration of animal experiment design. Cell membranes were derived from primary isolated HSPCs. Each received approximately 20 μg of liposomes and 10 μg of cell membrane. b Representative flow cytometry plots of leukemia cells (GFP positive cells) in bone marrow. Leukemic mice were euthanized at day 28 to collect bone marrow cells for analysis. c Quantitative analysis of leukemia cells in bone marrow. Data were presented as mean ± s.d. ( n = 5 mice). d Quantitative analysis of leukemia cells in spleen. Data were presented as mean ± s.d. ( n = 5 mice). e Weight of Spleen. Data were presented as mean ± s.d. ( n = 5 mice). f Survival curves of the leukemic mice received different treatments. The statistics and P -values were calculated using the Log-rank (Mantel-Cox) test. ( n = 6 mice for control, HSPC-Lipo and Ara-C group, and n = 8 mice for Ara-C@Lipo, and n = 12 mice for Ara-C@HSPC-Lipo group). Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig2_html.pngAnti-CD44 Antibody Picoband®Gene ablation of CD44 attenuates renal tubular cell apoptosis and kidney injury upon IRI. A Experimental design: Wild-type mice and CD44 conventional knockout mice were subjected to IRI or sham, respectively, and euthanized 24 h after IRI. B Scr levels in four groups, as indicated. Scr was expressed as milligrams per deciliter. ** P < 0.01 versus wild-type mice upon sham group; ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). C BUN levels in four groups, as indicated. BUN was expressed as milligrams per deciliter. *** P < 0.001 versus wild-type mice upon sham group; ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). D and E Representative western blot of CD44 ( D ) and graphical presentations ( E ) of protein expressional levels are shown. ** P < 0.01 versus wild-type mice upon sham group; ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). F Representative micrographs show the expression of CD44 in different groups, as indicated. Frozen kidney sections were stained with an antibody against CD44. Arrow indicates positive staining. Scale bar, 50 μm. G GO analysis shows CD44 is involved with several important pathways, including MAPK, NF-κB, apoptosis, mitochondria and FAO. H GSEA shows that negative regulation of apoptosis was enriched in CD44 knockout mice versus wild-type mice upon IRI. NES, normalized enrichment score; FDR q-value < 0.25. I–L Representative western blot ( I ) and graphical presentations of J BAX, K BCL2, and L cleaved caspase 3 protein expressional levels are shown. * P < 0.05, *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05, ## P < 0.01, ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). M Representative micrographs show TUNEL assay in different groups, as indicated. Frozen kidney sections were subjected to TUNEL assay. Parrafin sections were performed by immunohistochemistry staining of NGAL. Arrow indicates positive staining. Scale bar, 50 μm. N and O Representative western blot of NGAL ( N ) and graphical presentations ( O ) of protein expressional levels are shown. *** P < 0.001 versus wild-type mice upon sham group; ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig3_html.pngAnti-CD44 Antibody Picoband®CD44 knockout ameliorates mitochondrial dysfunction and FAO deficiency in IRI mice. A GSEA shows that positive regulation of mitochondrial function and FAO was enriched in CD44 knockout mice versus wild-type mice upon IRI. NES, normalized enrichment score; FDR q -value < 0.25. B Graphic presentation shows the relative levels of renal expression of PGC-1α mRNA in different groups as indicated. *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05 versus wild-type mice upon IRI group ( n = 5). C Graphic presentation shows the relative levels of ATP production in 2 groups as indicated. ** P < 0.01 versus wild-type upon IRI group ( n = 5). D and E Representative western blot ( D ) and graphical presentations of PGC-1α and TOMM20 protein expression levels are shown. ** P < 0.01, *** P < 0.001 versus wild-type mice upon sham group; ## P < 0.01, ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). F Co-localization of CD44 and PGC-1α in CD44 gene ablation mice upon IRI. Frozen kidney sections were subjected to immunostaining of CD44 (red) and PGC-1α (green). Scale bar, 50 μm. G Representative micrographs show the expression of PGC-1α, TOMM20, mitochondrial morphology via TEM, and mitochondrial ROS via MitoSox staining in different groups, as indicated. Arrows indicate positive staining or impaired mitochondria. Scale bar, 50 or 1 μm, as indicated. H Graphic presentation shows the relative mRNA levels of renal expression of PPARα, CPT1, CPT2, and ACOX1 mRNA in different groups as indicated. ** P < 0.01, *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05, ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). I Representative micrographs show the abundance of LDs via TEM in 2 groups, as indicated. Arrows indicate LDs. Scale bar, 1 μm. J and K Representative western blot ( J ) and graphical presentations of CPT1a and PPARα protein expression levels are shown. * P < 0.05, ** P < 0.01 versus wild-type mice upon sham group; # P < 0.05, ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). L Representative micrographs show the expression of PPARα, CPT1a, perilipin 2, and LDs via Oil Red O staining in different groups, as indicated. Arrows indicate positive staining. Frozen kidney sections were subjected to Oil Red O staining or stained with antibodies against PPARα, CPT1a, and perilipin 2. Scale bar, 50 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig4_html.pngAnti-CD44 Antibody Picoband®CD44 promotes AKI progression through inducing MAPK and NF-κB p65 signaling. A Representative heatmap gene expression of RNA sequencing analysis shows that CD44 is involved with MAPK and NF-κB signaling pathway. B and C GSEA shows that negative regulation of MAPK and NF-κB pathway was enriched in CD44 knockout mice versus wild-type mice upon IRI. NES, normalized enrichment score; FDR q -value < 0.25. D Representative micrographs show the expression of p-ERK1/2 and p-p38 in different groups, as indicated. Paraffin sections were stained with antibodies against p-ERK1/2 and p-p38. Arrows indicate positive staining. Scale bar, 50 μm. E and F Representative western blot ( E ) and graphical presentations of p-p38/p38 and p-ERK1/2/ERK1/2 protein levels are shown. ** P < 0.01, *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05, ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). G Co-localization of CD44 and p65 in 2 groups, as indicated. Frozen kidney sections were subjected to immunostaining of CD44 (red) and p65 (green). Scale bar, 50 μm. H and I Representative western blot ( H ) and graphical presentations of p-p65, p65, and p-p65/p65 protein levels are shown. ** P < 0.01, *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05, ## P < 0.01, ### P < 0.001 versus wild-type mice upon IRI group ( n = 5). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig7_html.pngAnti-CD44 Antibody Picoband®Transcriptome analysis reveals mechanisms of Ara-C@HSPC-Lipo treatment. a Volcano plot of differential gene expression in Ka539 cells. b Heat map of clustering analysis of differential gene in Ka539 cells. c Volcano plot of differential gene expression in C1498 cells. d Heat map of clustering analysis of differential gene in C1498 cells. e GO pathway enrichment analysis in Ka539 cells. f GO pathway enrichment analysis in C1498 cells. g KEGG enrichment analysis in Ka539 cells. h KEGG enrichment analysis in C1498 cells. i Enrichment analysis of GSEA gene set in C1498 cells. The statistical analyzes of P values were derived from a two-sided statistical test ( a, c ) or one-sided statistical test ( e – i ) and without adjustment for multiple comparisons. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig5_html.pngAnti-CD44 Antibody Picoband®Ectopic CD44 aggravates tubular cell apoptosis and kidney injury in IRI mice. A Experimental design: Green arrow indicated the injection of pcDNA3 plasmid or p-HA-CD44 overexpression plasmid. Mice were subjected to IRI surgery or sham surgery, respectively, as shown in the red arrow. Mice are euthanized 24 h after surgery. B Scr levels in three groups, as indicated. Scr was expressed as milligrams per deciliter. * P < 0.05 versus sham group; # P < 0.05 versus IRI group injected with pcDNA3 ( n = 5). C BUN levels in three groups, as indicated. BUN was expressed as milligrams per deciliter. ** P < 0.01 versus sham group; # P < 0.05 versus IRI group injected with pcDNA3 ( n = 5). D and E Representative western blot of CD44 ( D ) and graphical presentations ( E ) of protein levels are shown. ** P < 0.01 versus sham group; # P < 0.05 versus IRI group injected with pcDNA3 ( n = 5). F Representative micrographs show the expression of CD44, and TUNEL assay in different groups, as indicated. Arrows indicate positive staining. Frozen kidney sections were subjected to TUNEL assay or stained with an antibody against CD44. Scale bar, 50 μm. G–J Representative western blot ( G ) and graphical presentations of H BCL2, I BAX, and J cleaved caspase 3 protein expression levels are shown. * P < 0.05, ** P < 0.01 versus sham group; # P < 0.05, ### P < 0.001 versus IRI group injected with pcDNA3 ( n = 5). K and L Representative western blot of NGAL ( K ) and graphical presentations ( L ) of protein levels are shown. ** P < 0.01 versus sham group; ## P < 0.01 versus IRI group injected with pcDNA3 ( n = 5). M Representative micrographs show renal tubular morphologic injury and the expression of KIM-1 in different groups, as indicated. Paraffin sections were subjected to PAS staining, and were stained with an antibody against KIM-1. Arrows indicate positive staining. Scale bar, 50 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig8_html.pngAnti-CD44 Antibody Picoband®Safety evaluation and analysis of HSPC-Lipo. a Schematic illustration of animal experiment design. b Body weight of mice in different treatment groups. Data represent the mean ± s.d. ( n = 6 mice). c Quantitative analysis of hematopoietic stem progenitor cells in total mononuclear cells. d Quantitative analysis of progenitor cells in total mononuclear cells. e Quantitative analysis of lineage cells in total mononuclear cells. f Quantitative analysis of absolute number of hematopoietic stem progenitor cells per legs of tibia and femur. g Quantitative analysis of absolute number of progenitor cells per legs of tibia and femur. h Quantitative analysis of absolute number of lineage cells per legs of tibia and femur. n = 6 mice ( c - h ). The data represent the mean ± s.d ( c – h ). Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig6_html.pngAnti-CD44 Antibody Picoband®Ectopic expression of CD44 impairs mitochondrial function and FAO through activating MAPK and NF-κB p65 signaling. A Representative micrographs show the expression of p-ERK1/2 and p-p38 in different groups, as indicated. Paraffin sections were stained with antibodies against p-ERK1/2 and p-p38. Arrows indicate positive staining. Scale bar, 50 μm. B and C Representative western blot ( B ) and graphical presentations of p-ERK1/2/ERK1/2 and p-p38/p38 protein levels are shown. ** P < 0.01, *** P < 0.001 versus sham group; ## P < 0.01, ### P < 0.001 versus IRI group injected with pcDNA3 ( n = 5). D Co-localization of CD44 and p65 in CD44 overexpression mice upon IRI. Frozen renal sections were subjected to immunostaining of CD44 (red) and p65 (green). Scale bar, 50 μm. E and F Representative western blot ( E ) and graphical presentations of p-p65, p65, and p-p65/p65 protein levels are shown. ** P < 0.01, *** P < 0.001 versus sham group; ## P < 0.01, ### P < 0.001 versus IRI group injected with pcDNA3 ( n = 5). G Co-localization of CD44 and PGC-1α in CD44 overexpression mice upon IRI. Frozen renal sections were subjected to immunostaining of CD44 (red) and PGC-1α (green). Scale bar, 50 μm. H and I Representative western blot ( H ) and graphical presentations of PGC-1α, TOMM20, PPARα, and CPT1a protein expression levels are shown. ** P < 0.01, *** P < 0.001 versus sham group; # P < 0.05, ## P < 0.01 versus IRI group injected with pcDNA3 ( n = 5). J Representative micrographs show the expression of perilipin 2, and LDs via Oil Red O staining in different groups, as indicated. Frozen kidney sections were subjected to Oil Red O staining or stained with an antibody against perilipin 2. Arrows indicate positive staining. Scale bar, 50 or 100 μm. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-nrr-8-427-g001.jpgAnti-CD44 Antibody Picoband®Morphology of neuron-like cells derived from rat bone marrow mesenchymal stem cells. (A, D–F) Inverted phase-contrast microscope, × 100; (B, C) immunocytochemical staining, × 400. (A) Passage 3 bone marrow mesenchymal stem cells. (B) Bone marrow mesenchymal stem cells were positive for CD44 (arrow, cytoplasmic staining was brown-yellow). (C) Bone marrow mesenchymal stem cells were negative for CD34. (D) Neuron-like cells (arrow) derived from rat bone marrow mesenchymal stem cell induced by basic fibroblast growth factor 8 and Xiangdan injection for 3 hours. (E) Neuron-like cells (arrow) derived from rat bone marrow mesenchymal stem cells induced by basic fibroblast growth factor 8, all-trans retinoic acid and glial cell line-derived neurotrophic factor for 6 days. (F) Neuron-like cells (arrow) derived from rat bone marrow mesenchymal stem cells induced by basic fibroblast growth factor, sonic hedgehog and fibroblast growth factor 8 for 12 days.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4146134/&orig_host=www.ncbi.nlm.nih.gov'>25206684</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig7_html.pngAnti-CD44 Antibody Picoband®CD44 aggravates mitochondrial and FAO dysfunction and drives cell apoptosis through MAPK and NF-κB p65 signaling in vitro. A and B HKC-8 was transfected with Ctrl-shR or CD44-shR and then were incubated in basal culture medium in a 1% O 2 environment for 24 h and then were reoxygenated in normal O 2 for 6 h. Representative western blot ( A ) and graphical presentations of p-p38/p38, p-ERK1/2/ERK1/2, and p-p65 protein expression levels are shown. ** P < 0.01 versus Crtl-shR group; ## P < 0.01, ### P < 0.001 versus H/R with Crtl-shR group ( n = 3). C Representative micrographs show the expression of p-p65 and MitoSox staining in different groups, as indicated. Arrows indicate positive staining. Cells cultured on coverslips were stained with an antibody against p-p65 or were stained with MitoSox. Scale bar, 25 or 50 μm. D Graphic presentation shows the relative mRNA levels of PGC-1α in different groups as indicated. ** P < 0.01 versus Crtl-shR group; ## P < 0.01 versus H/R with Crtl-shR group ( n = 3). E and F Representative western blot ( E ) and graphical representations of PGC-1α, TOMM20, CPT1a, and PPARα protein expression levels are shown. * P < 0.05, ** P < 0.01 versus Crtl-shR group; # P < 0.05, ## P < 0.01 versus H/R with Crtl-shR group ( n = 3). G Representative micrographs show Nile Red staining and TUNEL assay in different groups, as indicated. Arrows indicate positive staining. Cells cultured on coverships were stained with Nile Red or TUNEL assay. Scale bar, 25 or 50 μm. H Co-localization of CD44 and cleaved caspase 3 in HKC-8 after H/R treatment. Cells cultured on coverships were subjected to immunostaining of CD44 (red) and cleaved caspase 3 (green). Scale bar, 50 μm. I and J Representative western blot ( I ) and graphical representations of BCL2, BAX, and cleaved caspase 3 protein expression levels are shown. ** P < 0.01 versus Crtl-shR group; # P < 0.05 versus H/R with Crtl-shR group ( n = 3). K and L HKC-8 was transfected with pcDNA3 or p-HA-CD44 overexpression plasmid and then were incubated in basal culture medium in a 1% O 2 environment for 24 h and then were reoxygenated in normal O 2 for 6 h. Representative western blot ( K ) and graphical representations of CD44, p-ERK1/2/ERK1/2, p-p38/p38 and p-p65 protein expression levels are shown. * P < 0.05, ** P < 0.01, *** P < 0.001 versus pcDNA3 group; # P < 0.05, ## P < 0.01 versus H/R with pcDNA3 group ( n = 3). M and N Representative western blot ( M ) and graphical presentations of PGC-1α, CPT1a, and PPARα protein expression levels are shown. * P < 0.05, *** P < 0.001 versus pcDNA3 group; # P < 0.05 versus H/R with pcDNA3 group ( n = 3). O Representative micrographs show MitoSox staining in different groups, as indicated. Arrow indicates positive staining. Cells cultured on coverships were stained with MitoSox. Scale bar, 25 μm. P and Q Representative western blot ( P ) and graphical representations of BCL2, BAX, and cleaved caspase 3 protein expression levels are shown. * P < 0.05, ** P < 0.01 versus pcDNA3 group; # P < 0.05; ## P < 0.01 versus H/R with pcDNA3 group ( n = 3). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig8_html.pngAnti-CD44 Antibody Picoband®CD44 induces tubular cell injury through MAPK-NF-κB p65-silenced PGC-1α signaling. A and B HKC-8 was transfected with pcDNA3 or p-Flag-p65 overexpression plasmid for 24 h. Representative western blot ( A ) and graphical presentations of PGC-1α, CPT1a, BCL2, and cleaved caspase 3 protein expression levels are shown. * P < 0.05, ** P < 0.01, *** P < 0.001 versus pcDNA3 groups ( n = 3). C Quantitative PCR result showing relative mRNA level of PGC-1α. * P < 0.05 versus pcDNA3 groups ( n = 3). D Representative ChIP assay results showing the binding of p65 to PGC-1α gene promoter region. HKC-8 cells were transfected with pcDNA3 or p-Flag-p65 for 24 h. Cell lysates were precipitated with an antibody against p65, histone H3, or nonimmune IgG, and ChIP assay was performed for PGC-1α gene promoters. Total diluted lysate was used as total genomic input DNA. E–I HKC-8 was pre-treated with SB203580, PD98059 or PDTC at 1 h before transfection with pcDNA3 or p-HA-CD44 plasmid for 24 h. Representative western blot ( E ) and graphical presentations of F p-p38/p38, G p-ERK1/2/ERK1/2, H p-p65, and I PGC-1α protein expression levels are shown. ** P < 0.01, *** P < 0.001 versus pcDNA3 group; # P < 0.05, ## P < 0.01 versus pHA-CD44 group; †† P < 0.01, ††† P < 0.001 versus pHA-CD44 group; φφφ P < 0.001 versus pHA-CD44 group ( n = 3). J The heatmap exhibiting differentiated lipids of lipidomics sequencing between H/R with Crtl-shR group and H/R with CD44-shR group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13046_2011_article_437_fig1_html.jpgAnti-CD44 Antibody Picoband®The expression of CD44 in RMG-I and RMG-I-H cells detected by immunocytochemistry (×400) . Panels 1 and 5 are negative controls; panels 2 and 6 are Lewis y antibody-untreated cells; panels 3 and 7 are Lewis y antibody-treated cells; panels 4 and 8 are cells treated by irrelevant isotype-matched control. The expression of CD44 was detected by SABC methods in RMG-I and RMG-I-H cells, and brown color degree by DAB staining indicated the expression level of CD44. It can be seen from the figure that the expression of CD44 in the RMG-I-H cells was stronger than that in RMG-I cells, which was decreased after Lewis y antibody blocking. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1756-9966-30-15'>21294926</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41419_2025_7438_fig9_html.pngAnti-CD44 Antibody Picoband®CD44 promotes tubular cell injury and AKI partially through ferroptosis. A HKC-8 was transfected with Ctrl-shR or CD44-shR plasmid and then treated with 5 μM erastin for 24 h. Representative micrographs show the Fe 2+ content via FerroOrange staining in different groups, as indicated. Scale bar, 25 μm. B and C Quantitative results of QPCR showing relative ( B ) GPX4 and ( C ) ACSL4 mRNA levels among different groups. ** P < 0.01 versus Ctrl-shR group; # P < 0.05 versus erastin with ctrl-shR ( n = 3). D HKC-8 was transfected with pcDNA3 or pHA-CD44 overexpression plasmid and then treated with 5 μM erastin for 24 h. Representative micrographs show the Fe 2+ content via FerroOrange staining in different groups, as indicated. Scale bar, 25 μm. E and F Quantitative result of QPCR showing relative ( E ) GPX4 and ( F ) ACSL4 mRNA levels among different groups. *** P < 0.001 versus pcDNA3 group; # P < 0.05 versus erastin with pcDNA3 ( n = 3). G Representative micrographs show the Fe 2+ content via FerroOrange staining in different groups, as indicated. Scale bar, 25 μm. H and I Quantitative result of QPCR showing relative H GPX4 and I ACSL4 mRNA level among different groups. *** P < 0.001 versus Ctrl-shR group; ## P < 0.01, ### P < 0.001 versus H/R with ctrl-shR ( n = 3). J Quantitative result showing MDA content among different groups. *** P < 0.001 versus Ctrl-shR group; # P < 0.05 versus H/R with ctrl-shR ( n = 3). K and L Quantitative result of QPCR showing relative ( K ) GPX4 and ( L ) ACSL4 mRNA levels among different groups. *** P < 0.001 versus pcDNA3 group; # P < 0.05 versus H/R with pcDNA3 ( n = 3). M Quantitative result showing MDA content among different groups. *** P < 0.001 versus pcDNA3 group; # P < 0.05 versus H/R with pcDNA3 ( n = 3). N Representative micrographs show the Fe 2+ content via FerroOrange staining in different groups, as indicated. Scale bar, 25 μm. O Quantitative result showing total iron content in kidney tissue among different groups. *** P < 0.001 versus wild-type mice upon sham group; ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). P and Q Quantitative result of QPCR showing relative P GPX4 and Q ACSL4 mRNA levels among different groups. ** P < 0.01, *** P < 0.001 versus wild-type mice upon sham group; # P < 0.05, ## P < 0.01 versus wild-type mice upon IRI group ( n = 5). R Quantitative result showing MDA content in kidney tissue among different groups. ** P < 0.01 versus wild-type mice upon sham group; # P < 0.05 versus wild-type mice upon IRI group ( n = 5). S Quantitative result showing total iron content in kidney tissue among different groups. *** P < 0.001 versus sham group; ## P < 0.01 versus IRI group injected with pcDNA3 ( n = 5). T and U Quantitative result of QPCR showing relative S GPX4 and T ACSL4 mRNA level among different groups. *** P < 0.001 versus sham group; # P < 0.05 versus IRI group injected with pcDNA3 ( n = 5). V Quantitative result showing MDA content in kidney tissue among different groups. *** P < 0.001 versus sham group; ### P < 0.001 versus IRI group injected with pcDNA3 ( n = 5). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41419-025-07438-x'>39979265</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig2_html.pngAnti-CD44 Antibody Picoband®Characterization and bone marrow targeting of HSPC-Lipo. a The representative TEM images of HSPC-Lipo. Scale bar, 100 nm. b The average particle size distribution of HSPC-Lipo. Measured by Dynamic Light Scattering. c The representative immunofluorescence confocal images of co-localization of HSPC cell membrane and liposome. HSPC cell membrane was labeled with DiO (green), liposome was labeled with DiD (red). Scale bar, 5 μm. d Representative fluorescence images of ICG fluorescent labeled different leukocyte membrane-coated liposomes in leukemic mice (Ka539 model). Mice were subjected to in vivo imaging detection at different time intervals (2, 6, 12, 24 hours) after tail vein injection of different liposomes. Each received approximately 20 μg of liposomes and 10 μg of cell membrane (indicated by total cell membrane protein weight). n = 3 mice. e Representative fluorescence images of different leukocyte membrane-coated liposomes in the tibia and femur of mice. Mice were sacrificed at 24 h after tail vein injection of different liposomes, the tibia and femur were taken for in vivo imaging detection. n = 3 mice. f Quantitative analysis of different liposomes in tibia and femur. Data were presented as mean ± s.d. ( n = 3 mice). g Representative immunofluorescence images of HSPC-Lipo in bone marrow. Scale bar, 20 μm. h Quantitative analysis of immunofluorescence results. The data were presented as mean ± s.d. ( n = 3 mice). Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13046_2011_article_437_fig2_html.jpgAnti-CD44 Antibody Picoband®Co-location of CD44 and Lewis y antigen on RMG-I-H cells observed under confocal laser scanning microscope . Red fluoscence on the upper left panel indicates CD44 expression; green fluoscence on the upper right panel indicates Lewis y antigen expression; blue fluoscence on the upper right panel indicates cell nuclear location; the lower right panel is a merged image of the other three panels. Lewis y antigen CD44 mainly expressed in the cell membrane observed under the confocal laser scanning microscope, and it were seen as yellow fluorescence after the two overlap, suggesting that Lewis y antigen and CD44 co-localizated in the cell membrane. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1756-9966-30-15'>21294926</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig3_html.pngAnti-CD44 Antibody Picoband®HSPC-Lipo exhibits higher affinity to leukemic cells. a Schematic illustration of Liquid chromatography tandem mass spectrometry (LC-MS/MS) sequencing design of HSPC cell membrane and HSPC-Lipo. The HSPCs cells were isolated from C57BL/6 mice. b Protein type analysis diagram. c Protein pathway enrichment analysis. d Proteins that coexist in HSPC cell membrane and HSPC-Lipo. e Western blot analysis of CD44 and ITGB2. f Determination of hyaluronic acid content in mouse bone marrow. Data were presented as mean ± s.d. ( n = 3 mice). g Representative immunofluorescence images of co-localization of hyaluronic acid and HSPC-Lipo. Scale bar, 10 μm. h Representative fluorescence images of CD44 knockdown HSPC-Lipo at 24 hours after tail vein injection (cell membrane derived from progenitor cell line 32D cells). ( n = 3 mice). i Quantitative analysis of fluorescence images of CD44 knockdown HSPC-Lipo. Data were presented as mean ± s.d. ( n = 3 mice). j Flow cytometry detection of leukemic cell targeting ability of different leukocyte membrane-coated liposomes. Leukemia cells were harvested for detection at 0.5 hours after incubation with different liposomes. n = 3 experimental replicates. k Representative flow cytometry histograms and cytometry plots of ICAM-1 expression on mouse leukemia cells and mouse progenitor cell line (32D). l Quantitative analysis of ICAM-1 expression. n = 3 experimental replicates. m Representative immunofluorescence images of co-localization of ICAM-1 and HSPC-Lipo. Scale bar, 10 μm. n Representative flow cytometry plots of the leukemic cells targeting ability of ITGB2 knockdown HSPC-Lipo (cell membrane derived from mouse progenitor cell line 32D). Leukemic cells were harvested for detection 0.5 hours after incubation with different liposomes. o Quantitative analysis of the leukemic cells targeting ability of ITGB2 knockdown HSPC-Lipo. n = 3 experimental replicates. The data were presented as mean ± s.d. Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig4_html.pngAnti-CD44 Antibody Picoband®Drug loading and in vitro toxicity against leukemia cells. a Drug release kinetics of HSPC-Lipo. Data were presented as mean ± s.d. ( n = 3 experimental replicates). b Cell viability assay of leukemic cells after different treatments at 48 hours in vitro. Data were presented as mean ± s.d. ( n = 3 experimental replicates). c Representative flow cytometry plots and quantitative analysis of Annexin V positive cells after 48 hours of different treatment in Ka539 leukemia cells. Data were presented as mean ± s.d. ( n = 3 experimental replicates). d Representative flow cytometry plots and quantitative analysis of Annexin V positive cells after 48 hours of different treatment by in C1498 leukemia cells. The leukemia cells were harvested at 48 h after different treatments and displays the same number of cells in each flow cytometry result. Data were presented as mean ± s.d. ( n = 3 experimental replicates). e Representative flow cytometry plots of leukemia stem cells (Sca-1+c-Kit + ) after 48 hours of different treatment in C1498 cells. f Quantitative analysis of LSC in C1498 cells. Data were presented as mean ± s.d. ( n = 3 experimental replicates). g Representative flow cytometry plots of mature cells after 48 hours of different treatment in C1498 cells. h Quantitative analysis of mature cells in C1498 cells. n = 3 experimental replicates. The data were presented as mean ± s.d. Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13046_2011_article_437_fig3_html.jpgAnti-CD44 Antibody Picoband®The expression of CD44 and Lewis y antigen in RMG-I and RMG-I-H cells . Panel A shows the expression of Lewis y antigen in RMG-I-H cells was higher than that in RMG-I; panel B shows the expression of CD44 in RMG-I-H cells was higher than that in RMG-I; panel C shows that Lewis y antigen, which in RMG-I-H cells was higher than that in RMG-I, was expressed both in RMG-I and RMG-I-H cells after CD44 immunoprecipitation; panel D Quantitative data were expressed as the intensity ratio target genes to beta-actin. ( P < 0.01) <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1756-9966-30-15'>21294926</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41467_2024_50021_fig5_html.pngAnti-CD44 Antibody Picoband®The anti-leukemic effect of Ara-C@HSPC-Lipo in MLL-AF9 leukemia model. a Schematic illustration of animal experiment design. Cell membranes were derived from primary isolated HSPCs. Each received approximately 20 μg of liposomes and 10 μg of cell membrane. b Survival curves of the leukemic mice received different treatments. The statistics and P -values were calculated using the Log-rank (Mantel-Cox) test. ( n = 6 mice for control, HSPC-Lipo and Ara-C group, and n = 7 mice for Ara-C@Lipo group, and n = 11 mice for Ara-C@HSPC-Lipo group). c Representative flow cytometry plots of leukemia cells (GFP positive cells) in bone marrow. Leukemic mice were euthanized on the day 21 to collect bone marrow cells for flow cytometry analysis. d Quantitative analysis of leukemia cells in bone marrow. Data were presented as mean ± s.d. ( n = 5 mice). e Representative flow cytometry plots of leukemia stem cells (CD34 + CD16/32 + ) in bone marrow after different treatments. f Quantitative analysis of leukemia stem cells in BM. Data were presented as mean ± s.d. ( n = 5 mice). g Representative flow cytometry plots of leukemic cells (GFP positive cells) in spleen. h Quantitative analysis of leukemia cells in spleen. Data were presented as mean ± s.d. ( n = 5 mice). i Quantitative analysis of leukemic cells (GFP positive cells) in peripheral blood. Data were presented as mean ± s.d. ( n = 5 mice). j Representative spleen images in leukemic mice after different treatment. k Weight of Spleen. n = 5 mice. The data were presented as mean ± s.d. Statistical significance of P values was calculated via a two-tailed, unpaired Student’s t test and were indicated as * P < 0.05, ** P < 0.01 and *** P < 0.001. Source data are provided as a Source Data file. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41467-024-50021-9'>38971796</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-13046_2011_article_437_fig4_html.jpgAnti-CD44 Antibody Picoband®The mRNA expression of CD44 and α1, 2-FT in RMG-I and RMG-I-H cells were tested by quantitative Real-Time RT-PCR . The mRNA level of α1, 2-FT was significantly increased, but the mRNA level of CD44 was almost the same in RMG-1-hFUT cells and RMG-1 cells. (** P < 0.01, * P > 0.05). <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1756-9966-30-15'>21294926</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-oncotarget-07-8043-g003.jpgAnti-CD44 Antibody Picoband®Depletion of PLCγ1 suppresses growth and metastasis of gastric adenocarcinoma in a nude mouse tumor xenograft model. ( A ) Volume and weight of tumor samples from nude mice. ( B ) The protein levels of PCNA, cleaved-PARP, PARP, and Bcl-2 in the tumor samples were detected by Immunohistochemistry (Magnificationx100, x400) and Western blotting analyses as described in Materials and Methods. ( C ) The levels of MMP2 and MMP9 in the tumor samples were detected by Immunohistochemistry analysis as described in Materials and Methods (Magnificationx100, x400). The protein and mRNA levels of MMP2, MMP9, E-cadherin(CDH1), N-cadherin(CDH2), snail(SNAIL), and slug(SLUG) in the tumor samples were detected by Western Blotting and Real-time PCR analyses as described in Materials and Methods. ( D ) The protein levels of VEGF and CD34 and the mRNA level of VEGF in tumor samples were detected by Immunohistochemistry and Real-time PCR analysis as described in Materials and Methods. The number of microvessels was accounted under OLYPUS x41 microscope (Magnification x100, x400). ( E ) The lymphoid follicles in inguinal lymph nodes of nude mice were observed under OLYPUS x41microscope, and the protein levels of CD44 and GFP in inguinal lymph nodes of nude mice was detected by Immunohistochemistry analysis as described in Materials and Methods (Magnificationx40, x400). Data are reported as means ± S.D. of three independent experiments (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, vs respective control).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC4884974/&orig_host=www.ncbi.nlm.nih.gov'>26811493</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cam4-14-e70993-g004_1.jpgAnti-CD44 Antibody Picoband®MSH2 knockdown increase the sensitivity of glioma cells to cisplatin. (A, B) The expression of stemness‐related proteins including CD44 and SOX2 was detected in shCtrl and shMSH2 groups of U251 (A) and SHG‐44 (B) cells. (C, D) The sphere‐forming abilities of U251 (C) and SHG‐44 (D) cells were assessed by a 3D sphere formation assay. (E, F) The effects of MSH2 on cisplatin IC50 and cisplatin‐induced cell apoptosis were evaluated in U251 (E) and SHG‐44 (F) cells. Data were shown as mean with standard deviation (SD) ( n ≥ 3). p < 0.05 was considered to be statistically significant. * p < 0.05, ** p < 0.01, *** p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12209330//'>40589077</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41208878-figure-5.jpgAnti-CD44 Antibody Picoband®ASNS shapes the immune landscapes in metastatic TdLN and primary tumor site. Figure 5A-C. LN metastasis model was conducted on C57BL/6 mice with LLC-ASNS WT(n=6), ASNSC2A overexpression cells(n=6) and control group(n=6), primary tumor and popliteal lymph nodes were isolated at the end of the experiment, and primary tumor volume(B) and TdLN volume/tumor volume(C) was measured and analyzed. 5D-F. (D) Representative FACS profiles of CD8+T cells are shown. The percentage(E) and number(F) of CD8+ subset in TIL cells isolated from primary tumor is shown. 5G-I. (G) Representative FACS profiles of the co-expression pattern of CD44 and CD62L, or the co-expression pattern of TCF-1and TOX in CD8+ T cells are shown. The number(H) and percentage(I) of CD44+, CD44+CD62L+, CD44+CD62L-, Tsl and TTSM subset in CD8+T cells isolated from TdLN is shown. 5J-L. (J) Representative FACS profiles of the co-expression pattern of CD44 and CD62L, or the co-expression pattern of TCF-1and TOX in CD8+ T cells are shown. The number(K) and percentage(L) of CD44+, CD44+CD62L+, CD44+CD62L-, Tsl and TTSM subset in CD8+T cells isolated from primary tumor is shown.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ijbs.com/v21p6501.htm'>41208878</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-41208878-figure-6.jpgAnti-CD44 Antibody Picoband®ASNS-high-expression metastases generated lymphocyte niches enriched with activated T cells, memory T cells, Tsl and TTSM. Figure 6A-C. Representative immunofluorescence staining images of metastatic TdLNs from LN metastasis model. 6D. The number of CD8+ T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6E-F. The number(E) and percentage(F) of CD44+CD8+T cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6G-H. The number(G) and percentage(H) of Tsl cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6I-J. The number(I) and percentage(J) of TTSM cells among all CD8 T cells in the metastasis locations within TdLNs (ASNSWT, n=5, ASNSC2A, n=4, and EV, n=3). 6K. Quantitative estimates of the distance from ova+ to CD8+CD44+CD62L+TCF+(TTSM) (ASNSWT, n=6, ASNSC2A, n=5, and EV, n=4). 6L-M. Representative immunofluorescence staining images of metastatic TdLNs from NSCLC patients. 6N-O. The number(C) and percentage(D) of CD8+ T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6P-Q. The number (E) and percentage(F) of CD45RO+CD8+ T cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6R-S. The number (G) and percentage(H) of Tsl cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6). 6T-U. The number (I) and percentage(J) of TTSM cells in CD8+T cells in the metastasis locations within TdLNs(ASNS high group, n=7, and ASNS low group, n=6).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ijbs.com/v21p6501.htm'>41208878</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-ijbsv21p6501s1_03.jpgAnti-CD44 Antibody Picoband®Representative IHC images showing the expression of B2M in primary tumor and LN metastasis
from intrapulmonary implantation mouse model performed on C57BL/6 mice (upper, n=3) and
popliteal lymph node implantation mouse model performed on C57BL/6 mice (below, n=4). 3B.
A549 cells were treated with low asparagine medium for 48 h. The expression of HLA was
determined by western blotting. 3C-E. A549 cells were treated with asparagine (C), creatine (D)
or creatinine (E) for 48 h. The expression of HLA was determined by western blotting. 3F.
Representative FACS profiles are shown. OT-I CD8+T cells were treated with Asn, AABA or both
for 48 h, and of the expression level of CD44 and CD62L was evaluated (n=3).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.ijbs.com/v21p6501.htm'>41208878</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00052-CD44-primary-antibodies-IHC-testing-2.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052).
<br>CD44 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD44 Antibody (A00052) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00052-CD44-primary-antibodies-IHC-testing-3.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052).
<br>CD44 was detected in paraffin-embedded section of human placenta tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD44 Antibody (A00052) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00052-CD44-primary-antibodies-IHC-testing-4.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052).
<br>CD44 was detected in paraffin-embedded section of mouse kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD44 Antibody (A00052) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00052-CD44-primary-antibodies-IHC-testing-5.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052).
<br>CD44 was detected in paraffin-embedded section of rat kidney tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD44 Antibody (A00052) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cd44-primary-antibodies-fc-testing-6.pngAnti-CD44 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-CD44 antibody (A00052). <br> Overlay histogram showing Jurkat cells stained with A00052 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD44 Antibody (A00052,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cd44-primary-antibodies-if-testing-7.jpgAnti-CD44 Antibody Picoband® IF analysis of CD44 using anti-CD44 antibody (A00052) <br> CD44 was detected in paraffin-embedded section of mouse lymphaden tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-CD44 Antibody (A00052) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cd44-primary-antibodies-if-testing-8.jpgAnti-CD44 Antibody Picoband® IF analysis of CD44 using anti-CD44 antibody (A00052) <br> CD44 was detected in paraffin-embedded section of mouse lymphaden tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-CD44 Antibody (A00052) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cam4-14-e70993-g004.jpgAnti-CD44 Antibody Picoband®MSH2 knockdown increase the sensitivity of glioma cells to cisplatin. (A, B) The expression of stemness‐related proteins including CD44 and SOX2 was detected in shCtrl and shMSH2 groups of U251 (A) and SHG‐44 (B) cells. (C, D) The sphere‐forming abilities of U251 (C) and SHG‐44 (D) cells were assessed by a 3D sphere formation assay. (E, F) The effects of MSH2 on cisplatin IC50 and cisplatin‐induced cell apoptosis were evaluated in U251 (E) and SHG‐44 (F) cells. Data were shown as mean with standard deviation (SD) ( n ≥ 3). p < 0.05 was considered to be statistically significant. * p < 0.05, ** p < 0.01, *** p < 0.001. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12209330/'>40589077</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-cd44-primary-antibodies-wb-testing-2.pngAnti-CD44 Antibody Picoband® Western blot analysis of CD44 using anti-CD44 antibody (A00052). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: Normal group-rat colon tissue lysates, <br>
Lane 2: Triditional Chinese medicine treatment (low dose)-rat colon tissue lysates, <br>
Lane 3: Model group-rat colon tissue lysates, <br>
Lane 4: Triditional Chinese medicine treatment (medium dose)-rat colon tissue lysates, <br>
Lane 5: Triditional Chinese medicine treatment(high dose)-rat colon tissue lysates, <br>
Lane 6: Western medicine treatment-rat colon tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD44 antigen affinity purified polyclonal antibody (Catalog # A00052) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for CD44 at approximately 82 kDa. The expected band size for CD44 is at 82 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-tapa1-picoband-trade-antibody-a01281-2-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-tapa1-primary-antibodies-wb-testing-1.jpgAnti-TAPA1/CD81 Antibody Picoband® Western blot analysis of TAPA1 using anti-TAPA1 antibody (A01281-2). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: mouse raw264.7 whole cell lysates, <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TAPA1 antigen affinity purified polyclonal antibody (Catalog # A01281-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TAPA1 at approximately 22KD. The expected band size for TAPA1 is at 22KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-tapa1-primary-antibodies-ihc-testing-2.jpgAnti-TAPA1/CD81 Antibody Picoband® IHC analysis of TAPA1 using anti-TAPA1 antibody (A01281-2).
<br>TAPA1 was detected in paraffin-embedded section of human tonsil tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-TAPA1 Antibody (A01281-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-10020_2025_1192_fig6_html.pngAnti-TAPA1/CD81 Antibody Picoband®Identification of hAMSC-Exos ( A ) The morphology of hAMSC-Exos was observed using transmission electron microscopy. Scale bar = 100 nm. ( B ) The hAMSC-Exos particle size distribution was detected using NTA. ( C ) Western blot was used to detect the expression of hAMSC-Exos surface proteins CD9, CD63 and CD81 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s10020-025-01192-8'>40329179</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-12886_2022_2592_fig7_html.pngAnti-TAPA1/CD81 Antibody Picoband®Western blot analysis of specific protein expression ( n = 3). ( A ) Colored bands of GFAP, LRP6, THBS1 and CD81; ( B ) Expression levels of LRP6, THBS1 and CD81 gradually decreased with the increase of the stretch amplitude, while the expression level of GFAP gradually increased with the increase of the stretch amplitude. Error bars indicate standard error of the mean (SEM); * P < 0.05 and ** P < 0.01 indicate statistical significance <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12886-022-02592-8'>36114477</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-tapa1-primary-antibodies-fcm-testing-3.jpgAnti-TAPA1/CD81 Antibody Picoband® Flow Cytometry analysis of HL-60 cells using anti-TAPA1 antibody (A01281-2). <br>
Overlay histogram showing HL-60 cells stained with A01281-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TAPA1 Antibody (A01281-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-2-tapa1-primary-antibodies-fcm-testing-4_1.jpgAnti-TAPA1/CD81 Antibody Picoband® Flow Cytometry analysis of U2OS cells using anti-TAPA1 antibody (A01281-2). <br>
Overlay histogram showing U2OS cells stained with A01281-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TAPA1 Antibody (A01281-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-tapa1-picoband-trade-antibody-a01281-3-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-3-tapa1-primary-antibodies-wb-testing-1_1.jpgAnti-TAPA1/Cd81 Antibody Picoband® Western blot analysis of TAPA1/CD81 using anti-TAPA1/CD81 antibody (A01281-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates, <br>
Lane 2: mouse ovary tissue lysates, <br>
Lane 3: mouse brain tissue lysates, <br>
Lane 4: mouse NIH/3T3 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TAPA1/CD81 antigen affinity purified polyclonal antibody (Catalog # A01281-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TAPA1/CD81 at approximately 22 kDa. The expected band size for TAPA1/CD81 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-3-tapa1-primary-antibodies-ihc-testing-2.jpgAnti-TAPA1/Cd81 Antibody Picoband® IHC analysis of TAPA1/CD81 using anti-TAPA1/CD81 antibody (A01281-3). <br>
TAPA1/CD81 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TAPA1/CD81 Antibody (A01281-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-3-tapa1-primary-antibodies-if-testing-3.jpgAnti-TAPA1/Cd81 Antibody Picoband® IF analysis of TAPA1/CD81 using anti-TAPA1/CD81 antibody (A01281-3). <br>
TAPA1/CD81 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TAPA1/CD81 Antibody (A01281-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01281-3-tapa1-primary-antibodies-if-testing-4.jpgAnti-TAPA1/Cd81 Antibody Picoband® IF analysis of TAPA1/CD81 using anti-TAPA1/CD81 antibody (A01281-3). <br>
TAPA1/CD81 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TAPA1/CD81 Antibody (A01281-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-gro-alpha-picoband-trade-antibody-a00533-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-cxcl1-primary-antibodies-wb-testing-1.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband® Western blot analysis of GRO alpha using anti-GRO alpha antibody (A00533). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.<br>
Lane 1: recombinant rat CXCL1 protein 10 ng.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GRO alpha antigen affinity purified polyclonal antibody (Catalog # A00533) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GRO alpha at approximately 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2019_1584_fig1_html.pngAnti-GRO alpha/Cxcl1 Antibody Picoband®Experimental time flow. Pain threshold measurement, using a series of von Frey hairs with logarithmically increasing stiffness (0.02–2.56 g, Stoelting), was performed day − 2 and day − 1 prior to, as well as on day 14, day 21, day 28, and day 35 upon surgery (intraprostatic injection of 1% carrageenan (20 μl), day 0). The effects of intrathecal injection of different reagents on pain threshold were measured on day 14 or 35 after surgery. Some of sham and CP/CPPS mice were sacrificed for spinal cord slices for immunostaining on day 14. Others were sacrificed for prostate sampling for histology examination (H&E), spinal cord slices for immunostaining, spinal cord dorsal horn structures isolation for CXCL1 measurement by ELISA, and for pERK and ERK expression measurement by Western blot on day 35 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12974-019-1584-3'>31653262</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2019_1584_fig7_html.pngAnti-GRO alpha/Cxcl1 Antibody Picoband®Prostatitis induced CXCL1 expression in spinal cord dorsal horn and contributed to mechanical allodynia. a ELISA analysis showing CXCL1 expression was increased in spinal cord dorsal horn 5 weeks after carrageenan injection. * P < 0.05, vs. control (con, saline-treated group), Student’s t test. n = 4 mice per group. b ELISA analysis shows decreased CXCL1 release in the CSF in the carrageenan-injected group at 3 h after the intrathecal injection of CBX (5 μg). * P < 0.05, vs. control (con, saline-treated group); # P < 0.05, vs. the vehicle group. One-way ANOVA, followed by post hoc Bonferroni test. n = 4 mice/group. c Prostatitis-induced mechanical allodynia in the lower abdominal area were partially reversed by intrathecal injection of the CXCL1 neutralizing antibody (5 μg) at 5 weeks after carrageenan injection. d Prostatitis-induced mechanical allodynia in the lower abdominal area was partially reversed by intrathecal injection of the CXCR2 antagonist SB225002 (20 μg) at 5 weeks after carrageenan injection. BL, baseline. * P < 0.05, vs. Carr 5w, two-way ANOVA, followed by post-hoc Bonferroni test. n = 6 mice/group. All data are expressed as mean ± S.E.M. Arrows indicate drug injection <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12974-019-1584-3'>31653262</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g001.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The number of MCs and percentage of MCs degranulation in CLN or skin from PbANKA-infected mice with C48/80 or DSCG treatment. (A,B) MCs were evaluated by toluidine blue staining in CLN (magnification, x400) or skin (magnification, x400) from the uninfected mice treated with saline (a), C48/80 (d), or DSCG (g), and the infected mice treated with saline (b), C48/80 (e), or DSCG (h) at 4 days p.i, respectively; infected mice treated with saline (c), C48/80 (f), or DSCG (i) at 9 days p.i., respectively; Intact MCs (arrowheads); Degranulated MCs (arrows). (C) The density of MCs in CLN or skin tissue were analyzed from different groups by using Student's t -test. * P < 0.05 and ** P < 0.01 vs. the Naive mice, # P < 0.05 and ## P < 0.01 vs. the infected controls at 4 days p.i., & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i.; (D) the level of degranulated MCs in CLN or skin tissue were analyzed from different groups by using Student's t -test. § P < 0.05 and §§ P < 0.01 vs. the Naive mice, $ P < 0.05 and $$ P < 0.01 vs. the C48/80 group, P < 0.05 and P < 0.01 vs. the DSCG group. There were four to six mice per group, and the data were representative of three experiments.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g004.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The changes of vascular permeability in liver or lung from PbANKA-infected mice with C48/80 or DSCG treatment. Mice were infected i.p. with 10 6 iRBCs, and treated with saline, C48/80 or DSCG. At 4 and 9 days p.i., different group of mice ( n = 4–6/group) were injected 100 μl of 1.0% Evans blue dye via tail veins, and the degree of vascular permeability in liver or lung was expressed as ng/mg of tissue weight. The experiment was repeated three times, and data were presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. the Naive mice, # P < 0.05 and ## P < 0.01 vs. the infected controls at 4 days p.i., & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i. by using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g005.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The changes of vascular permeability in brain from ECM mice caused by PbANKA infection with C48/80 or DSCG treatment. ECM mice were randomly selected from PbANKA-infected mice treated with saline (Pb group), C48/80 (Pb+C48/80 group), or DSCG (Pb+DSCG group). Different group of ECM mice ( n = 4–6/group) were injected 100 μl of 1.0% Evans blue dye via tail veins, (A) representative optical image of the brain was captured, and (B) the degree of vascular permeability in brain was expressed as ng/mg of tissue weight. The experiment was repeated three times, and data were presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. ECM mice in Pb group. The statistical analysis of vascular permeability in brain of ECM mice was performed by Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g003.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®Histopathological examination in CLN or liver tissue from PbANKA-infected mice with C48/80 or DSCG treatment. (A,B) Infected mice i.p. inoculated with 10 6 iRBCs from different groups were killed at 4 and 9 days p.i., and histopathology in CLN or liver was evaluated by H&E staining (magnification, x400). Naive mice (a); infected mice treated with saline at 4 days p.i. (b) and 9 days p.i. (c); uninfected mice treated with C48/80 (d); infected mice with C48/80 treatment at 4 days p.i. (e) and 9 days p.i. (f); uninfected mice treated with DSCG (g); infected mice with DSCG treatment at 4 days p.i. (h); and 9 days p.i. (i); Hyperplasia of germinal center (arrows); Inflammatory foci (arrowheads); (C) Liver damage was determined by measuring inflammatory foci counts per field, as well as the protein levels of AST and ALT in sera. There were four mice per group. The experiment was repeated three times, and the data were represented as mean ± SD. Statistically significant differences in liver histopathological score for comparison with the infected controls at 4 days p.i. ( # P < 0.05; and ## P < 0.01) and 9 days p.i. ( & P < 0.05; and && P < 0.01) by using Kruskal-Wallis rank sum test. Statistically significant differences in protein levels of AST or ALT in sera for comparison with Naive mice (* P < 0.05; and ** P < 0.01), with the infected controls at 4 days p.i. ( $ P < 0.05; and $$ P < 0.01) and 9 days p.i. ( P < 0.05; and P < 0.01) using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g006.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The changes of leukocyte number from PbANKA-infected mice with C48/80 or DSCG treatment. Mice were infected i.p. with 10 6 iRBCs, and treated with saline, C48/80 or DSCG. At 4 and 9 days p.i., blood from different group of mice ( n = 4–6/group) was analyzed for the kind and numbers of leukocyte using hemocytometer. The experiment was repeated three times, and data were presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. the Naive mice, # P < 0.05 and ## P < 0.01 vs. the infected controls at 4 days p.i., & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i. by using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g007.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The changes of CCL2, CXCL1, MMP-9, and IgE in sera from PbANKA-infected mice with C48/80 or DSCG treatment. Mice were infected i.p. with 10 6 iRBCs, and treated with saline, C48/80 or DSCG. At 4 and 9 days p.i., sera were collected from different group of mice ( n = 4–6/group) and assessed for CCL2, CXCL1, MMP-9, and IgE by ELISA assay. The experiment was repeated three times, and data were presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. the Naive mice, # P < 0.05 and ## P < 0.01 vs. the infected controls at 4 days p.i., & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i. by using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g008.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®Cytokine and chemokine receptor mRNA expressions in CLN or skin from PbANKA-infected mice with C48/80 or DSCG treatment using qPCR method. (A) mRNA levels of TNF-α, IFN-γ, IL-4, IL-10, CCR2, and CXCR2 in CLN tissue; (B) mRNA levels of TNF-α, IFN-γ, IL-4, IL-10, CCR2, and CXCR2 in skin tissue. There were 4 to 6 mice per group. The data were representative of three experiments, and presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. the Naive mice, # P < 0.05 and ## P < 0.01 vs. the infected controls at 4 days p.i., & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i. by using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-fcimb-09-00322-g009.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®The density of MCs tryptase-CCL2, -CXCL1, and -MMP-9 in CLN or skin from PbANKA-infected mice with C48/80 or DSCG treatment by immunofluorescence staining. (A,B) MCs tryptase-CCL2, -CXCL1, and -MMP-9 were evaluated in CLN or skin from uninfected control mice (Naive group), infected mice treated with saline (Pb group), C48/80 (Pb+C48/80 group), or DSCG (Pb+DSCG group) at 9 days p.i. Immunofluorescence positive signals would appear as yellow fluorescence once MCs tryptase and CCL2 (or CXCL1, MMP-9) were superimposed in one vision (magnification, x400). MCs were seen to release CCL2, CXCL1, or MMP-9 when CCL2, CXCL1, or MMP-9 was found outside the MCs cell membrane (arrows). (C,D) The density of MCs with CCL2, -CXCL1, or -MMP-9 outside cell membrane in CLN or skin tissue were analyzed from the uninfected control mice, infected mice treated with C48/80 or DSCG at 9 days p.i. The experiment was repeated three times, and data were presented as means ± SD. * P < 0.05 and ** P < 0.01 vs. the Naive mice, & P < 0.05 and && P < 0.01 vs. the infected controls at 9 days p.i. by using Student's t -test.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2019.00322/full'>31552201</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2014_article_955_fig2_html.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®RM-1 cell inoculation induces CXCL1 upregulation in spinal astrocytes. (A) Real-time PCR results show the increase of CXCL1 mRNA expression in the spinal cord after inoculation. CXCL1 mRNA upregulation was gradually increased from 7 days to 21 days. * P <0.05 vs . sham control. n = 4 mice per group. (B-F) Immunostaining shows the CXCL1-IR was increased in the spinal cord at 7 days (D) , 14 days (E) , and 21 days (F) . *** P <0.001 vs . naive. n = 4 mice per group. (G-I) Double staining shows CXCL1 was colocalized with astrocytic marker, GFAP (G) , but not with microglial marker CD11b (H) or neuronal marker NeuN (I) . <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1742-2094-11-38'>24580964</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2014_article_955_fig3_html.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®Intrathecal injection of CXCL1 neutralizing antibody attenuates bone cancer pain. CXCL1 neutralizing antibody at a lower dose (4 μg) had mild effect on RM-1 cell inoculation-induced pain hypersensitivity (A, B) , whereas the neutralizing antibody at a higher dose (8 μg) reversed inoculation-induced mechanical allodynia (A) and heat hyperalgesia (B) for more than 6 h. * P <0.05, ** P <0.01, *** P <0.001 vs . control serum. n = 6 mice per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1742-2094-11-38'>24580964</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2014_article_955_fig5_html.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®TNF-α induces NFκB-dependent CXCL1 increase in cultured astrocytes. (A-D) CXCL1 was expressed in control astrocytes (A) and increased at 1 h after TNF-α incubation (B) . Double staining of CXCL1 (B) with GFAP (C) shows the expression of CXCL1 by astrocytes (D) . (E) ELISA results show TNF-α-induced CXCL1 upregulation was decreased by pretreatment with NFκB inhibitor, BAY11-7082. *** P <0.001 vs . control. # P <0.05, ### P <0.001 vs . TNF-α treatment. (F) Quantitative PCR shows TNF-α-induced CXCL1 mRNA increase was decreased by BAY11-7082. *** P <0.001 vs . control. ## P <0.01, ### P <0.001 vs. TNF-α treatment. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1742-2094-11-38'>24580964</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-12974_2014_article_955_fig7_html.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband®NFκB inhibitor attenuated RM-1 cell inoculation-induced pain hypersensitivity and upregulation of CXCL1 in the spinal cord. (A, B) Intrathecal injection of NFκB inhibitor, BAY11-7082 at the dose of 0.4 μg had no effect on mechanical allodynia or heat hyperalgesia, whereas at the dose of 4 μg attenuated mechanical allodynia (A) and heat hyperalgesia (B) at 1 h and 3 h. * P <0.05, ** P <0.01, *** P <0.001 vs. vehicle. One-way ANOVA followed by Newman-Keuls test. (C, D) Immunostaining of CXCL1 in the spinal cord in vehicle and BAY11-7082-treated animals. (E) The CXCL1-IF intensity was decreased by BAY11-7082. *** P <0.001 vs . vehicle. n = 4 mice per group. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/1742-2094-11-38'>24580964</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-gro_alpha-primary-antibodies-elisa-testing-2.jpgAnti-GRO alpha/Cxcl1 Antibody Picoband® Sandwich ELISA - Recombinant rat GRO alpha/Cxcl1 protein standard curve.<br>
Use in combination with reagents from Rat GRO alpha/Cxcl1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0724).
https://www.bosterbio.com/products/primary-antibodies/anti-nox2-gp91phox-antibody-a00328-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00328-nox2-primary-antibodies-wb-testing-1_1.jpgAnti-NOX2/gp91phox/CYBB Antibody Picoband® Western blot analysis of NOX2 using anti-NOX2 antibody (A00328).<br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human U-87MG cell lysate,<br> Lane 2: human Hela cell lysate,<br> Lane 3: human HepG2 cell lysate. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOX2 antigen affinity purified polyclonal antibody (Catalog # A00328) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOX2 at approximately 65KD. The expected band size for NOX2 is at 65KD.
https://www.bosterbio.com/products/primary-antibodies/anti-eea1-picoband-trade-antibody-a02296-3-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02296-3-eea1-primary-antibodies-wb-testing-1.jpgAnti-EEA1 Antibody Picoband® Western blot analysis of EEA1 using anti-EEA1 antibody (A02296-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human RT4 whole cell lysates,<br>
Lane 2: human Hacat whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human SiHa whole cell lysates,<br>
Lane 5: humna K562 whole cell lysates,<br>
Lane 6: humna MCF-7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EEA1 antigen affinity purified polyclonal antibody (Catalog # A02296-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EEA1 at approximately 162 kDa. The expected band size for EEA1 is at 162 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02296-3-eea1-primary-antibodies-wb-testing-2.jpgAnti-EEA1 Antibody Picoband® Western blot analysis of EEA1 using anti-EEA1 antibody (A02296-3). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat lung tissue lysates,<br>
Lane 3: mouse brain tissue lysates,<br>
Lane 4: mouse kidney tissue lysates,<br>
Lane 5: mouse lung tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EEA1 antigen affinity purified polyclonal antibody (Catalog # A02296-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EEA1 at approximately 162 kDa. The expected band size for EEA1 is at 162 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02296-3-eea1-primary-antibodies-ihc-testing-3.jpgAnti-EEA1 Antibody Picoband® IHC analysis of EEA1 using anti-EEA1 antibody (A02296-3). <br>
EEA1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EEA1 Antibody (A02296-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02296-3-eea1-primary-antibodies-ihc-testing-4.jpgAnti-EEA1 Antibody Picoband® IHC analysis of EEA1 using anti-EEA1 antibody (A02296-3). <br>
EEA1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EEA1 Antibody (A02296-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02296-3-eea1-primary-antibodies-if-testing-5.jpgAnti-EEA1 Antibody Picoband® IF analysis of EEA1 using anti- EEA1 antibody (A02296-3). <br>
EEA1 was detected in immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti- EEA1 Antibody (A02296-3) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-eph-receptor-a2-picoband-trade-antibody-a00578-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00578-Eph_receptor_A2_-primary-antibodies-WB-testing-1.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband® Western blot analysis of Eph receptor A2 using anti-Eph receptor A2 antibody (A00578).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysate,<br>Lane 2: human U-87MG cell lysate,<br>Lane 3: human SHG-44 cell lysate,<br>Lane 4: human COLO-320 cell lysate,<br>Lane 5: human SK-OV-3 cell lysate,<br>Lane 6: human A549 cell lysate,<br>Lane 7: mouse HEPA1-6 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Eph receptor A2 antigen affinity purified polyclonal antibody (Catalog # A00578) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Eph receptor A2 at approximately 125KD. The expected band size for Eph receptor A2 is at 108KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g001.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®Analysis of EPHA2 expression (A) High EPHA2 were associated with shorter relapse-free survival (RFS) in TNBC (Logrank p = 0.037) as demonstrated by Kaplan-Meier analysis. (B) According to the results of UCSC Xena in different BRCA subtypes, the expression level of EPHA2 was higher in TNBC than that in Luminal A ( p = 0.034), Luminal B ( p = 0.019) and normal-like ( p = 0.031) (Mann–Whitney test). (C) Relative protein expression of EPHA2 in different BRCA cell lines derived from metastatic tumors and primary tumors using DepMap portal. (D) The confirmation of relative protein expression of EPHA2 in different BRCA cell lines using western blot. *p < 0.05, **p < 0.01, ****p < 0.0001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g002.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®Spatial distribution of cell types expressing EPHA2. (A) UMAP plots of stromal cells. (B) UMAP plots of epithelial cells. (C) EPHA2 expression distribution in stromal cells by subtype and celltype_subset. (D) EPHA2 expression distribution in epithelial cells by celltype_subset and subtype. (E) EPHA2 expression in different stromal cells. (F) EPHA2 expression in different epithelial cells. All these were analyzed using Single Cell Portal ( ). * p < 0.05, ns indicates no significant difference (Mann–Whitney test).<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g003.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®EPHA2 knockdown affected MDA-MB-231 proliferation and invasion. (A) The verification of the knockdown efficiency of three EPHA2 shRNAs. (B) The transduction efficiency of EPHA2 shRNA was confirmed using Fluorescence microscopy. (C) Relative proliferation of MDA-MB-231 cells was decreased in EPHA2 shRNA group, compared to the control shRNA group ( p = 0.0007, t -test). (D) Knockdown of EPHA2 inhibited invasion of MDA-MB-231 as assessed by crystal violet staining ( p = 0.0003, t -test). Bars represent the mean ± SD. ***p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g004.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®EPHA2 knockdown induced MDA-MB-231 pyroptosis. (A) Volcano plot demonstrating an overview of the differential expression of all genes. (B) Enrichment ratio and enriched function of these DEGs was analyzed using KOBAS online server. C1-C5 represent different clusters. (C) STRING protein-protein interaction network. Proteins are represented as nodes while interactions appear as edges. Relative NLRP3 expression (D) and IL1β expression (E) in EPHA2 shRNA groups were all lower than in control shRNA groups ( p = 0.0006 and p = 0.0001, respectively, t -test). (F) The electron microscopy images of control shRNA and EPHA2 shRNA, red arrows indicating the apoptotic bodies for pyroptotic morphology. Bars represent the mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g005.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®EPHA2 knockdown induced pyroptosis pathway activation and inhibits PI3K/AKT/mTOR signal pathway activation. (A) Western blot analysis of NLRP3, GSDMD, caspase-1, AKT, p-AKT, PI3K, p-PI3K, mTOR and p-mTOR expression. * p <0.05, ** p < 0.01, *** p < 0.001. Statistical analysis of the two groups were performed using two-tailed Student’s t test. (B) Analysis of pathways and co-expression data for pyroptosis and genes related to the PI3K/AKT/mTOR signaling pathway using GeneMANIA. (C) Correlation of EPHA2 and IL18 expression in epithelial cells by subtype was analyzed based on Single Cell Portal. (D) The concentration of IL18 in cell culture supernatant of shEPHA2–1 was lower than in shControl RNA group ( p =0.0174, t -test). (E) Correlation of EPHA2 and IL1β expression in epithelial cells by celltype_subset was analyzed based on Single Cell Portal. (F) The concentration of IL1β in cell culture supernatant of shEPHA2–1 was lower than in shControl RNA group ( p =0.0259, t -test). Bars represent the mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-fonc-15-1620122-g006.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband®AKT inhibition induced MDA-MB-231 pyroptosis and decrease SLC7A11 expression. (A) Western blot analysis of NLRP3, GSDMD, caspase-1, AKT, p-AKT, PI3K, p-PI3K, mTOR and p-mTOR expression in MDA-MB-231 cells treated with AKT inhibitor or control buffer. * p <0.05, ** p < 0.01. Statistical analysis of the two groups were performed using two-tailed Student’s t test. The concentration of IL1β (B) and IL18 (C) in cell culture supernatant were all significantly elevated in the MK-2206-treated group, compared to the control group ( p = 0.0134 and p = 0.0015, respectively, t -test). (D) Analysis of pathways and co-expression data of SLC7A11, EHPA2, pyroptosis related genes and AKT/PI3K/mTOR related genes. Relative mRNA expression levels ( p = 0.0002, t -test) (E) and protein expression levels (F) of ferroptosis-associated gene SLC7A11 were all decreased in shEPHA2–1 group. Bars represent the mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12411449/'>40919148</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-eph-receptor-a2-primary-antibodies-fc-testing-2.pngAnti-Eph receptor A2/EPHA2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-Eph receptor A2 antibody (A00578). <br> Overlay histogram showing A549 cells stained with A00578 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Eph receptor A2 Antibody (A00578,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-eph-receptor-a2-primary-antibodies-fc-testing-3.pngAnti-Eph receptor A2/EPHA2 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Eph receptor A2 antibody (A00578). <br> Overlay histogram showing U20S cells stained with A00578 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Eph receptor A2 Antibody (A00578,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00578-eph_receptor_a2-primary-antibodies-if-testing-4.jpg.jpgAnti-Eph receptor A2/EPHA2 Antibody Picoband® IF analysis of Eph receptor A2 using anti-Eph receptor A2 antibody (A00578). <br>
Eph receptor A2 was detected in immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-Eph receptor A2 Antibody (A00578) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-prothrombin-picoband-trade-antibody-a00044-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00044-prothrombin_-primary-antibodies-wb-testing-1.jpgAnti-Prothrombin/F2 Antibody Picoband® Western blot analysis of Prothrombin using anti-Prothrombin antibody (A00044). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human plasma lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Prothrombin antigen affinity purified polyclonal antibody (Catalog # A00044) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Prothrombin at approximately 85KD. The expected band size for Prothrombin is at 70KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00044-fonc-11-621806-g007.jpgAnti-Prothrombin/F2 Antibody Picoband®Immunohistochemistry of FGA, F2, CFH, PIPOX, ITIH4, GNMT, MAT1A, MTHFD1, HPX, CTH, CFHR3, ENNP1, and NAT2 in clinical GBC and control specimens.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.621806/full'>33718182</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00044-Prothrombin_-primary-antibodies-IHC-testing-2.jpgAnti-Prothrombin/F2 Antibody Picoband® IHC analysis of Prothrombin using anti-Prothrombin antibody (A00044).
<br>Prothrombin was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Prothrombin Antibody (A00044) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00044-Prothrombin_-primary-antibodies-IHC-testing-3.jpgAnti-Prothrombin/F2 Antibody Picoband® IHC analysis of Prothrombin using anti-Prothrombin antibody (A00044).
<br>Prothrombin was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Prothrombin Antibody (A00044) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00044-prothrombin-primary-antibodies-fc-testing-4.pngAnti-Prothrombin/F2 Antibody Picoband®4. Flow Cytometry analysis of H-PBMC cells using anti-Prothrombin antibody (A00044). <br> Overlay histogram showing H-PBMC cells stained with A00044 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Prothrombin Antibody (A00044,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-fcgr1a-picoband-trade-antibody-a02428-1-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02428-1-fcgr1a-primary-antibodies-wb-testing-1.jpgAnti-FCGR1A Antibody Picoband® Western blot analysis of FCGR1A using anti-FCGR1A antibody (A02428-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SiHa whole cell lysates, <br>
Lane 2: human A431 whole cell lysates, <br>
Lane 3: human HCCT tissue lysates, <br>
Lane 4: human Hela whole cell lysates, <br>
Lane 5: rat PC-12 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FCGR1A antigen affinity purified polyclonal antibody (Catalog # A02428-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FCGR1A at approximately 70 kDa. The expected band size for FCGR1A is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02428-1-fcgr1a-primary-antibodies-fcm-testing-2.jpgAnti-FCGR1A Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-FCGR1A antibody (A02428-1). <br>Overlay histogram showing U937 cells stained with A02428-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FCGR1A Antibody (A02428-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-fes-picoband-trade-antibody-a01453-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01453-FES-primary-antibodies-WB-testing-1.jpgAnti-FES Antibody Picoband® Western blot analysis of FES using anti-FES antibody (A01453).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysate,<br>Lane 2: human 293T cell lysate,<br>Lane 3: human SK-OV-3 cell lysate,<br>Lane 4: human A549 cell lysate,<br>Lane 5: human MCF-7 cell lysate,<br>Lane 6: human placenta tissue lysate,<br>Lane 7: human PANC-1 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FES antigen affinity purified polyclonal antibody (Catalog # A01453) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FES at approximately 93KD. The expected band size for FES is at 93KD.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-1-antibody-a00534-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00534-VEGF_Receptor_1_-primary-antibodies-WB-testing-1.jpgAnti-VEGF Receptor 1/FLT1 Antibody Picoband® Western blot analysis of VEGF Receptor 1 using anti-VEGF Receptor 1 antibody (A00534).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysate,<br>Lane 2: human placenta tissue lysate,<br>Lane 3: human A549 cell lysate,<br>Lane 4: human COLO-320 cell lysate,<br>Lane 5: Human A431 cell lysate,<br>Lane 6: human SK-OV-3 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF Receptor 1 antigen affinity purified polyclonal antibody (Catalog # A00534) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF Receptor 1 at approximately 125KD. The expected band size for VEGF Receptor 1 is at 150KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00534-vegf_receptor_1-primary-antibodies-icc-testing-2.jpgAnti-VEGF Receptor 1/FLT1 Antibody Picoband® IF analysis of VEGF Receptor 1/FLT1 using anti-VEGF Receptor 1/FLT1 antibody (A00534). <br>
VEGF Receptor 1/FLT1 was detected in immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-VEGF Receptor 1/FLT1 Antibody (A00534) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00534-vegf_receptor_1-primary-antibodies-fcm-testing-3_1.pngAnti-VEGF Receptor 1/FLT1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-VEGF Receptor 1/FLT1 antibody (A00534). <br>Overlay histogram showing A549 cells stained with A00534 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VEGF RECEPTOR 1/FLT1 Antibody (A00534, 1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-vegf-receptor-1-picoband-trade-antibody-a00534-1-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00534-1-VEGF_Receptor_1_-primary-antibodies-WB-testing-1.jpgAnti-VEGF Receptor 1/FLT1 Antibody Picoband® Western blot analysis of VEGF Receptor 1 using anti-VEGF Receptor 1 antibody (A00534-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat kidney tissue lysate,<br>Lane 2: mouse liver tissue lysate,<br>Lane 3: mouse HEPA1-6 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGF Receptor 1 antigen affinity purified polyclonal antibody (Catalog # A00534-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGF Receptor 1 at approximately 150KD. The expected band size for VEGF Receptor 1 is at 150KD.
https://www.bosterbio.com/products/primary-antibodies/anti-foxa1-picoband-trade-antibody-a00266-1-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00266-1-foxa1-primary-antibodies-wb-testing-1.jpgAnti-FOXA1 Antibody Picoband® Western blot analysis of FOXA1 using anti-FOXA1 antibody (A00266-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human MCF-7 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human RT4 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXA1 antigen affinity purified polyclonal antibody (A00266-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXA1 at approximately 49 kDa. The expected band size for FOXA1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00266-1-foxa1-primary-antibodies-fcm-testing-2.jpgAnti-FOXA1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-FOXA1 antibody (A00266-1). <br>
Overlay histogram showing RT4 cells stained with A00266-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FOXA1 Antibody (A00266-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-gc-picoband-trade-antibody-a03364-2-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03364-2-gc-primary-antibodies-wb-testing-1.jpgAnti-Vitamin D Binding protein/Gc Antibody Picoband® Western blot analysis of Gc using anti-Gc antibody (A03364-2). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat liver tissue lysate,<br>Lane 2: rat liver tissue lysate,<br>Lane 3: mouse liver tissue lysate,<br>Lane 4: mouse liver tissue lysate,<br>Lane 5: human placenta tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Gc antigen affinity purified polyclonal antibody (Catalog # A03364-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Gc at approximately 53KD. The expected band size for Gc is at 53KD.
https://www.bosterbio.com/products/primary-antibodies/anti-nmdar1-picoband-trade-antibody-a01808-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01808-NMDAR1-primary-antibodies-WB-testing-1.jpgAnti-NMDAR1/GRIN1 Antibody Picoband® Western blot analysis of NMDAR1 using anti-NMDAR1 antibody (A01808).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NMDAR1 antigen affinity purified polyclonal antibody (Catalog # A01808) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NMDAR1 at approximately 120KD. The expected band size for NMDAR1 is at 105KD.
https://www.bosterbio.com/products/primary-antibodies/anti-gsk3-alpha-picoband-trade-antibody-a03152-2-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03152-2-GSK3_alpha-primary-antibodies-WB-testing-1.jpgAnti-GSK3 alpha/GSK3A Antibody Picoband® Western blot analysis of GSK3 alpha using anti-GSK3 alpha antibody (A03152-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysate,<br>Lane 2: rat testis tissue lysate,<br>Lane 3: mouse testis tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSK3 alpha antigen affinity purified polyclonal antibody (Catalog # A03152-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GSK3 alpha at approximately 51KD. The expected band size for GSK3 alpha is at 51KD.
https://www.bosterbio.com/products/primary-antibodies/anti-gstm3-picoband-trade-antibody-a03298-1-boster.html2026-03-24T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03298-1-gstm3-primary-antibodies-wb-testing-1.jpgAnti-GSTM3 Antibody Picoband®Western blot analysis of GSTM3 using anti-GSTM3 antibody (A03298-1). <br>Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human SiHa whole cell lysates,<br>
Lane 4: human THP-1 whole cell lysates,<br>
Lane 5: mouse testis tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTM3 antigen affinity purified polyclonal antibody (A03298-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSTM3 at approximately 27 kDa. The expected band size for GSTM3 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03298-1-gstm3-primary-antibodies-ihc-testing-1.jpgAnti-GSTM3 Antibody Picoband®IHC analysis of GSTM3 using anti-GSTM3 antibody (A03298-1). <br>GSTM3 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GSTM3 Antibody (A03298-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-hsf2-picoband-trade-antibody-a04692-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04692-hsf2-primary-antibodies-wb-testing-1.jpgAnti-HSF2 Antibody Picoband® Western blot analysis of HSF2 using anti-HSF2 antibody (A04692). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human Raji whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSF2 antigen affinity purified polyclonal antibody (Catalog # A04692) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSF2 at approximately 60 kDa. The expected band size for HSF2 is at 60 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-icam1-picoband-trade-antibody-a00171-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-wb-testing-1_1.jpgAnti-ICAM1 Antibody Picoband® Western blot analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>Lane 1: rat spleen tissue lysate,<br>Lane 2: rat thymus tissue lysate,<br>Lane 3: rat RH35 cell lysate,<br>Lane 4: mouse spleen tissue lysate,<br>Lane 5: mouse thymus tissue lysate,<br>Lane 6: mouse HEPA1-6 cell lysate,<br>Lane 7: mouse heart tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM1 antigen affinity purified polyclonal antibody (Catalog # A00171) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ICAM1 at approximately 90 kDa. The expected band size for ICAM1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-12964_2024_1841_fig2_html.pngAnti-ICAM1 Antibody Picoband®STAT3 inhibitor attenuates L-AKI and restores kidney function. A Schematic diagram of the animal model. B BUN and serum creatinine were measured to assess kidney function. Groups: Control, LPS, LPS + Stattic (5 mg/kg) and LPS + Stattic (10 mg/kg) ( n = 6 in each group). C Flow cytometric comparison of pSTAT3 levels was conducted between two populations (kidney macrophages, CD11b high F4/80 low and CD11b low F4/80 high ) in LPS-induced kidneys. D Western blotting representative image (left) and quantification (right) of pSTAT3, STAT3 and ICAM-1. Each band shows a typical group, as indicated. E Changes in the proportion of two macrophage subpopulations between each group were observed with FACS analysis, and the frequency and ratio of individual populations were quantified using GraphPad Prism. F Upregulated expression of ICAM-1, NGAL, and pSTAT3 by LPS induction in IHC analysis ( n = 6 in each group) decreased with Stattic treatment. Scale bars, 100 μm (100X) and 50 μm (400X). All experiments were independently replicated at least three times, and the data are presented as mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001 <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12964-024-01841-1'>39367511</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-12929_2024_1040_fig1_html.pngAnti-ICAM1 Antibody Picoband®Single-cell transcriptional profiling of intracranial fusiform aneurysmal cells ( A - K ) and multi-color immunofluorescence (mIF) of smooth muscle cells (SMCs) markers and inflammatory markers between intracranial fusiform aneurysms (IFAs) and normal cerebral arteries (NCAs) ( L - M ). T-SNE visualization of intracranial fusiform aneurysmal cells type. Colored according to cell type ( A ). Visualization of specific gene expression patterns related to cell subsets identified in ( A ) using a bubble plot ( B ). T-SNE visualization of VSMC cell clusters. Colored according to clusters ( C ). Visualization of structural protein and inflammation-related genes expression patterns within the subsets of smooth muscle cells identified in ( C ) using a bubble plot ( D ). The violin plots show the expression differences of structural protein genes and inflammatory genes between the contraction subgroup (VSMC5) and the inflammatory subgroup (VSMC6) ( E ). The volcano plot specifically shows the gene expression differences between the two cell groups ( F ). The petal plot displays the GO enrichment analysis results of differential genes between the VSMC5 and VSMC6 ( G ). The bar graph shows the KEGG enrichment analysis results of differential genes between these two cell subsets ( H ). The GSEA enrichment analysis results of differential genes between the two groups. The enrichment results of differential genes related to signaling pathways ( I ). The enrichment results of differential genes related to structural protein genes ( J ). The enrichment results of differential genes related to the process of inflammatory factor secretion ( K ). α-SMA (green, SMCs marker), MMP-9 (blue, inflammatory marker) and ICAM-1 (red, inflammatory marker) in FIAs and NCAs are detected using mIF. Scale bar, 100 μm ( L ). Statistical analysis of mean fluorescence intensity about SMCs marker (α-SMA) and inflammatory markers (ICAM-1 and MMP-9) between NCAs ( n = 4) and FIAs ( n = 5). 'n' represented the number of samples. Three random fields were selected for statistical analysis in each sample, and the average value represented the detection value of this marker in this sample. The Student's t-test is utilized to examine the statistical differences among each marker. ns, no significant; ** p < 0.01, *** p < 0.01 (M). n values indicate number of independent experiments performed <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-12929_2024_1040_fig3_html.pngAnti-ICAM1 Antibody Picoband®PDGFRB somatic mutation induce phenotypic modulation in SMCs. Immunostaining reveals the expression levels of smooth muscle markers (a-SMA and SM22a) and inflammatory markers (VCAM1, ICAM1, MMP1 and MMP9) in HBVSMCs transfected with different viruses (Control: vector; Wild Type: PDGFRB; Y562D: PDGFRB Y562D ) ( a ). The relative density of immunoblot bands about markers shown in ( A ) were display ( B ) (normalized to those in cells transfected with vector viruses). RT-qPCR ( C ) of SMCs markers (α-SMA and SM22α) and inflammatory markers (VCAM-1, ICAM1, MMP-9 and MMP-1) in HBVSMCs underwent different treatments. Student's t-test and Benjamini–Hochberg correction are employed to assess the statistical significance. Edu assay exhibit the proliferation ability of HBVSMCs under different treatment conditions ( D ). Statistical analysis of the proportion of Edu-positive cells in the different groups from 5 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is used for statistical differences ( E ). Scratch assay displays migratory ability of HBVSMCs underwent different treatment ( F ). Statistical analysis of the rate of wound healing (reduced area at 4H /area at 0H) in the different groups from 9 different fields of each group at × 200 magnification. Tukey's multiple comparisons test is utilized to evaluate the statistical significance. * p adj < 0.05, ** p adj < 0.01, *** p adj < 0.001, **** p adj < 0.0001 ( G ). The above experiments are all repeated three times <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12929-024-01040-7'>38741091</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-fimmu-15-1375943-g011.jpgAnti-ICAM1 Antibody Picoband®Protein (A) (immunohistochemistry) and gene (B) expression of ICAM-1. Sham, false-operated rats; BD, rats submitted to brain death; MP, rats treated with methylprednisolone (MP) after 3h of confirmation of BD and MP/E2, rats treated with 17β-estradiol (E2) and methylprednisolone after 3h of confirmation of BD. Data expressed as mean ± SEM from 5-8 animals per group (A) . Data expressed as median and 95th percentile from 6-8 animals (B) . 1 section per animal and 10 areas per section were analyzed. The photomicrographs (x20) are representative of protein expression on each group. (A) p (Kruskal Wallis) =0.6009; (B) p (Kruskal Wallis) =0.7960.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1375943/full'>38765005</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-13054_2012_article_1742_fig3_html.jpgAnti-ICAM1 Antibody Picoband®mRNA expression of ICAM-1, VCAM-1 and PBEF and protein expression of ICAM-1 and VCAM-1 in lung . A ) Real-time PCR showed that the expression levels of ICAM-1, VCAM-1 and PBEF mRNA decreased significantly in the EP and GL groups compared to the control group. B ) Western-blot showed that the expression levels of ICAM-1 and VCAM-1 protein decreased significantly in the EP and GL groups compared to the control group. C ) Quantitative assessment of protein relative to β-actin showed that the expression levels of ICAM-1 and VCAM-1 protein decreased significantly in the EP and GL groups compared to the control group. * P < 0.05 versus the control group. EP, ethyl pyruvate; GL, glycyrrhizin; ICAM-1, intercellular adhesion molecule-1; PBEF, pre-B-cell colony-enhancing factor; VCAM-1, vascular cell adhesion molecule 1. <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/cc12558'>23497622</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-wb-testing-2_1.jpgAnti-ICAM1 Antibody Picoband® Western blot analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Raji whole cell lysates,<br>
Lane 2: human K562 whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: human 293T whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM1 antigen affinity purified polyclonal antibody (Catalog # A00171) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ICAM1 at approximately 90 kDa. The expected band size for ICAM1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-ihc-testing-3_1.jpgAnti-ICAM1 Antibody Picoband® IHC analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-fc-testing-9.pngAnti-ICAM1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ICAM1 antibody (A00171). <br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-ihc-testing-4_1.jpgAnti-ICAM1 Antibody Picoband® IHC analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-ihc-testing-5.jpgAnti-ICAM1 Antibody Picoband® IHC analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-ihc-testing-6.jpgAnti-ICAM1 Antibody Picoband® IHC analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-ihc-testing-7.jpgAnti-ICAM1 Antibody Picoband® IHC analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00171-icam1-primary-antibodies-icc-testing-8.jpgAnti-ICAM1 Antibody Picoband® IF analysis of ICAM1 using anti-ICAM1 antibody (A00171). <br>
ICAM1 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-ICAM1 Antibody (A00171) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-icam2-picoband-trade-antibody-a03965-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03965-icam2-primary-antibodies-wb-testing-1.jpgAnti-ICAM2 Antibody Picoband®Western blot analysis of ICAM2 using anti-ICAM2 antibody (A03965). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates, <br>
Lane 2: human HEL whole cell lysates, <br>
Lane 3: human K562 whole cell lysates, <br>
Lane 4: mouse spleen tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM2 antigen affinity purified polyclonal antibody (A03965) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ICAM2 at approximately 60 kDa. The expected band size for ICAM2 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03965-icam2-primary-antibodies-fcm-testing-1.jpgAnti-ICAM2 Antibody Picoband®Flow Cytometry analysis of HEL cells using anti-ICAM2 antibody (A03965). <br>
Overlay histogram showing HEL cells stained with A03965 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ICAM2 Antibody (A03965, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-il6-picoband-trade-antibody-a00102-2-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-djir_a_12469678_f0001_c.jpgAnti-IL6 Antibody Picoband® (A) Cell viability values after stimulation of chondrocytes using IL-1β, detected by CCK8 assay after 12h, 24h and 48h, respectively. (B) Results of Hoechst 33342 staining of chondrocytes after IL-1β stimulation. (C) Quantitative results of quantitative polymerase chain reaction analysis of IL-6. (D) Protein blotting images of IL-6 and BCL-2. (E) Results of quantification of protein blotting of IL-6 and BCL-2. (F) Lectin blot images of LTL and AAL, and locations of differential bands. (n=3). *P < 0.05, **P < 0.01.
<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S520179'>40860947</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-djir_a_12469678_f0006_c.jpgAnti-IL6 Antibody Picoband®(A–C) Protein blotting images and quantitative results of Nocth1 and JAG1. (D–G) Protein blotting images and quantitative results of NICD, RBPJK and HES1. (H–K) Protein blotting images and quantitative results of MMP-9, IL-6 and Caspase-3. (n=3). *p < 0.05, **p < 0.01,***p < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S520179'>40860947</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-djir_a_12469678_f0007_c.jpgAnti-IL6 Antibody Picoband®(A) HE, SO and TB staining results of rat knee cartilage from different experimental groupings (control, OA, OA+2FF LOW, OA+2FF HIGH groups) (Concentration 2μM/5μM). (B) OARSI scores of cartilage in different experimental groups. (C) Expression levels of TNF-α and IL-6 in rat serum, quantitative analysis of ELISA results. (n=3). *P < 0.05, **P < 0.01,***P < 0.001.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S520179'>40860947</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-djir_a_12469679_f0005_c.jpgAnti-IL6 Antibody Picoband®1 Hz rTSMS reduces astrocyte activation and neuroinflammation. (A) Representative immunofluorescence images showing GFAP (red) and Dapi (blue) staining in the injured spinal cord across groups. (B) Quantification of mean GFAP fluorescence intensity. (C) Western blot analysis of GFAP and BDNF expression. (D and E) Quantification of GFAP and BDNF relative to β-actin. (F) Western blot analysis of pro-inflammatory cytokines (TNF-α, IFN-γ and IL-6) and anti-inflammatory cytokines (IL-4 and IL-10). (G–K) Corresponding quantification of cytokine expression. n=5. Scale bar=20 μm. aP < 0.05, bP< 0.01, cP < 0.001, vs Sham group. dP < 0.05, eP < 0.01, fP < 0.001, vs SCI group. gP < 0.05, hP <0.01, vs 1 Hz group. The data are expressed as the mean ± SD.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S516006'>40873779</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-djir_a_12469679_f0008_c.jpgAnti-IL6 Antibody Picoband®1Hz MS reduced the release of pro-inflammatory cytokines and enhanced the release of anti-inflammatory cytokines in the BV2 injury model. (A-C) Statistical graphs of ELISA assays showing the release of pro-inflammatory cytokines TNF-α (A), IL-6 (B), and IL-1β (C) from BV2 cells. (D–F) Statistical graphs of ELISA assays showing the release of pro-inflammatory cytokines TGF-β1 (D), IL-4 (E), and IL-10 (F) from BV2 cells. n=5. aP<0.01, bP<0.001, vs Con group. cP<0.05, dP<0.01, eP<0.001, vs LPS group. fP<0.05, gP<0.01, vs LPS+MS group. The data are expressed as the mean ± SD.
<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.tandfonline.com/doi/abs/10.2147/JIR.S516006'>40873779</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00102-2-il6-primary-antibodies-wb-testing-1.jpgAnti-IL6 Antibody Picoband® Western blot analysis of IL6 using anti-IL6 antibody (A00102-2). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat spleen tissue lysates, <br>
Lane 2: mouse spleen tissue lysates, <br>
Lane 3: mouse Ana-1 whole cell lysates, <br>
Lane 4: mouse RAW264.7 whole cell lysates, <br>
Lane 5: mouse EL-4 whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL6 antigen affinity purified polyclonal antibody (Catalog # A00102-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL6 at approximately 30 kDa. The expected band size for IL6 is at 24 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-il17b-picoband-trade-antibody-a10846-3-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/1/A10846-3-IL17B_-primary-antibodies-WB-testing-1.jpgAnti-IL17B Antibody Picoband® Western blot analysis of IL17B using anti-IL17B antibody (A10846-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse NIH3T3 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17B antigen affinity purified polyclonal antibody (Catalog # A10846-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17B at approximately 20KD. The expected band size for IL17B is at 20KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il18-binding-protein-antibody-a07261-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07261-1-il18_binding_protein-primary-antibodies-wb-testing-1.jpgAnti-IL18 binding protein/Il18bp Antibody Picoband® Western blot analysis of IL18 binding protein using anti-IL18 binding protein antibody (A07261-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse heart tissue lysate,<br>Lane 2: mouse brain tissue lysate,<br>Lane 3: rat heart tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL18 binding protein antigen affinity purified polyclonal antibody (Catalog # A07261-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL18 binding protein at approximately 43KD. The expected band size for IL18 binding protein is at 21KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il22-picoband-trade-antibody-a00963-3-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00963-3-IL22_-primary-antibodies-WB-testing-1.jpgAnti-IL22 Antibody Picoband® Western blot analysis of IL22 using anti-IL22 antibody (A00963-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse kidney tissue lysate,<br>Lane 2: mouse brain tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL22 antigen affinity purified polyclonal antibody (Catalog # A00963-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL22 at approximately 20KD. The expected band size for IL22 is at 20KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il17e-picoband-trade-antibody-a04429-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04429-1-IL17E-primary-antibodies-WB-testing-1.jpgAnti-IL17E/IL25 Antibody Picoband® Western blot analysis of IL17E using anti-IL17E antibody (A04429-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.
<br>Lane 1: recombinant human IL25 protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17E antigen affinity purified polyclonal antibody (Catalog # A04429-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17E at approximately 17KD. The expected band size for IL17E is at 17KD.
https://www.bosterbio.com/products/primary-antibodies/anti-integrin-alpha-5-picoband-trade-antibody-a01911-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01911-itga5-primary-antibodies-wb-testing-1.jpgAnti-Integrin alpha 5/ITGA5 Antibody Picoband® Western blot analysis of ITGA5 using anti-ITGA5 antibody (A01911). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human placenta tissue lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: rat PC-12 whole cell lysates,<br>
Lane 6: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITGA5 antigen affinity purified polyclonal antibody (Catalog # A01911) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITGA5 at approximately 130 kDa. The expected band size for ITGA5 is at 115 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01911-itga5-primary-antibodies-ihc-testing-2.jpgAnti-Integrin alpha 5/ITGA5 Antibody Picoband® IHC analysis of ITGA5 using anti-ITGA5 antibody (A01911). <br>
ITGA5 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITGA5 Antibody (A01911) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01911-itga5-primary-antibodies-ihc-testing-3.jpgAnti-Integrin alpha 5/ITGA5 Antibody Picoband® IHC analysis of ITGA5 using anti-ITGA5 antibody (A01911). <br>
ITGA5 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITGA5 Antibody (A01911) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-cd11c-picoband-trade-antibody-a00357-1-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00357-1-CD11c-primary-antibodies-WB-testing-1.jpgAnti-CD11c/ITGAX Antibody Picoband® Western blot analysis of CD11c using anti-CD11c antibody (A00357-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse spleen tissue lysate,<br>Lane 2: mouse thymus tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD11c antigen affinity purified polyclonal antibody (Catalog # A00357-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD11c at approximately 150KD. The expected band size for CD11c is at 128KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00357-1-CD11c-primary-antibodies-IHC-testing-2.jpgAnti-CD11c/ITGAX Antibody Picoband® IHC analysis of CD11c using anti-CD11c antibody (A00357-1).
<br>CD11c was detected in paraffin-embedded section of human tonsil tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-CD11c Antibody (A00357-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-kcnh1-picoband-trade-antibody-a01036-2-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01036-2-KCNH1-primary-antibodies-WB-testing-1.jpgAnti-KCNH1 Antibody Picoband® Western blot analysis of KCNH1 using anti-KCNH1 antibody (A01036-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human COLO-320 cell lysate,<br>Lane 2: human HepG2 cell lysate,<br>Lane 3: human A549 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KCNH1 antigen affinity purified polyclonal antibody (Catalog # A01036-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KCNH1 at approximately 150KD. The expected band size for KCNH1 is at 111KD.
https://www.bosterbio.com/products/primary-antibodies/anti-kallikrein-1-antibody-a02789-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02789-Kallikrein_1_-primary-antibodies-WB-testing-1.jpgAnti-Kallikrein 1/KLK1 Antibody Picoband® Western blot analysis of Kallikrein 1 using anti-Kallikrein 1 antibody (A02789).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.
<br>Lane 1: recombinant human KLK1 protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Kallikrein 1 antigen affinity purified polyclonal antibody (Catalog # A02789) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Kallikrein 1 at approximately 32KD. The expected band size for Kallikrein 1 is at 29KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02789-kallikrein_1_-primary-antibodies-elisa-testing-2.jpgAnti-Kallikrein 1/KLK1 Antibody Picoband® Sandwich ELISA - Recombinant human Kallikrein 1/KLK1 protein standard curve.<br>
Use in combination with reagents from Human Kallikrein 1/KLK1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ0903).
https://www.bosterbio.com/products/primary-antibodies/anti-kallikrein-2-picoband-trade-antibody-a03879-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03879-Kallikrein_2_-primary-antibodies-WB-testing-1.jpgAnti-Kallikrein 2/KLK2 Antibody Picoband® Western blot analysis of Kallikrein 2 using anti-Kallikrein 2 antibody (A03879).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human MCF-7 cell lysate,<br>Lane 2: human COLO-320 cell lysate,<br>Lane 3: human SK-OV-3 cell lysate,<br>Lane 4: human HepG2 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Kallikrein 2 antigen affinity purified polyclonal antibody (Catalog # A03879) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Kallikrein 2 at approximately 21KD. The expected band size for Kallikrein 2 is at 28KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03879-Kallikrein_2_-primary-antibodies-IHC-testing-2.jpgAnti-Kallikrein 2/KLK2 Antibody Picoband® IHC analysis of Kallikrein 2 using anti-Kallikrein 2 antibody (A03879).
<br>Kallikrein 2 was detected in paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Kallikrein 2 Antibody (A03879) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-map3k20-picoband-trade-antibody-a00902-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00902-1-map3k20-primary-antibodies-wb-testing-1.jpgAnti-MAP3K20 Antibody Picoband® Western blot analysis of MAP3K20 using anti-MAP3K20 antibody (A00902-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: mouse thymus tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP3K20 antigen affinity purified polyclonal antibody (Catalog # A00902-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP3K20 at approximately 91KD. The expected band size for MAP3K20 is at 91KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00902-1-map3k20-primary-antibodies-wb-testing-2.jpgAnti-MAP3K20 Antibody Picoband® Western blot analysis of MAP3K20 using anti-MAP3K20 antibody (A00902-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: human PANC-1 whole cell lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP3K20 antigen affinity purified polyclonal antibody (Catalog # A00902-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP3K20 at approximately 91KD. The expected band size for MAP3K20 is at 91KD.
https://www.bosterbio.com/products/primary-antibodies/anti-max-picoband-trade-antibody-a03239-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03239-max-primary-antibodies-wb-testing-1_1.jpgAnti-MAX Antibody Picoband® Western blot analysis of MAX using anti-MAX antibody (A03239). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,<br>
Lane 2: human PC-3 whole cell lysates,<br>
Lane 3: mouse lung tissue lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAX antigen affinity purified polyclonal antibody (Catalog # A03239) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAX at approximately 19-21 kDa. The expected band size for MAX is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03239-max-primary-antibodies-if-testing-2.jpgAnti-MAX Antibody Picoband® IF analysis of MAX using anti-MAX antibody (A03239). <br>
MAX was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAX Antibody (A03239) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03239-max-primary-antibodies-fcm-testing-3.jpgAnti-MAX Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-MAX antibody (A03239). <br>
Overlay histogram showing THP-1 cells stained with A03239 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAX Antibody (A03239, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-mst1-picoband-trade-antibody-a01069-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01069-1-mst1-primary-antibodies-wb-testing-1.jpgAnti-MST1 Antibody Picoband® Western blot analysis of MST1 using anti-MST1 antibody (A01069-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela cell lysate,<br>Lane 2: human MCF-7 cell lysate,<br>Lane 3: human HepG2 cell lysate,<br>Lane 4: human SK-OV-3 cell lysate,<br>Lane 5: human A549 cell lysate,<br>Lane 6: rat kidney tissue lysate,<br>Lane 7: mouse kidney tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MST1 antigen affinity purified polyclonal antibody (Catalog # A01069-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MST1 at approximately 80KD. The expected band size for MST1 is at 80KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mvd-picoband-trade-antibody-a01631-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01631-1-MVD-primary-antibodies-WB-testing-1.jpgAnti-MVD Antibody Picoband® Western blot analysis of MVD using anti-MVD antibody (A01631-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human HepG2 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MVD antigen affinity purified polyclonal antibody (Catalog # A01631-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MVD at approximately 45KD. The expected band size for MVD is at 43KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01631-1-mvd-primary-antibodies-wb-testing-2.jpgAnti-MVD Antibody Picoband® Western blot analysis of MVD using anti-MVD antibody (A01631-1). <br> Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br> Lane 1: rat liver tissue lysates. <br> After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MVD antigen affinity purified polyclonal antibody (Catalog # A01631-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MVD at approximately 45KD. The expected band size for MVD is at 43KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ogg1-picoband-trade-antibody-a00768-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00768-1-ogg1-primary-antibodies-wb-testing-1.jpgAnti-Ogg1 Antibody Picoband®Western blot analysis of Ogg1 using anti-Ogg1 antibody (A00768-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates, <br>
Lane 2: human HepG2 whole cell lysates, <br>
Lane 3: human Hela whole cell lysates, <br>
Lane 4: human 293T whole cell lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ogg1 antigen affinity purified polyclonal antibody (A00768-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Ogg1 at approximately 39 kDa. The expected band size for Ogg1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00768-1-ogg1-primary-antibodies-ihc-testing-1.jpgAnti-Ogg1 Antibody Picoband®IHC analysis of Ogg1 using anti-Ogg1 antibody (A00768-1). <br>
Ogg1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Ogg1 Antibody (A00768-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00768-1-ogg1-primary-antibodies-ihc-testing-2.jpgAnti-Ogg1 Antibody Picoband®IHC analysis of Ogg1 using anti-Ogg1 antibody (A00768-1). <br>
Ogg1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Ogg1 Antibody (A00768-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00768-1-ogg1-primary-antibodies-if-testing-1.jpgAnti-Ogg1 Antibody Picoband®IF analysis of Ogg1 using anti-Ogg1 antibody (A00768-1) and anti-Tubulin Alpha antibody (M03989-3).<br>
Ogg1 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Ogg1 Antibody (A00768-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00768-1-ogg1-primary-antibodies-ip-testing-1.jpgAnti-Ogg1 Antibody Picoband®Immunoprecipitating (IP) Ogg1 in 293T whole cell lysate.<br>
Western blot analysis of Ogg1 using anti-Ogg1 antibody (A00768-1); <br>
Lane 1: 293T whole cell lysates (30ug);<br>
Lane 2: Rabbit control IgG instead of anti-Ogg1 antibody in 293T whole cell lysate;<br>
Lane 3: anti-Ogg1 antibody (2μg) + 293T whole cell lysate (500μg).<br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Ogg1 antigen affinity purified polyclonal antibody (A00768-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for Ogg1 at approximately 39 kDa. The expected band size for Ogg1 is at 39 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-pax8-picoband-trade-antibody-a00943-1-boster.html2026-03-24T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00943-1-PAX8-primary-antibodies-WB-testing-1.jpgAnti-PAX8 Antibody Picoband® Western blot analysis of PAX8 using anti-PAX8 antibody (A00943-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human SW579 cell lysate,<br>Lane 2: human SW579 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX8 antigen affinity purified polyclonal antibody (Catalog # A00943-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAX8 at approximately 48KD. The expected band size for PAX8 is at 48KD.
https://www.bosterbio.com/products/primary-antibodies/anti-per1-picoband-trade-antibody-a00876-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00876-13044_2024_193_fig5_html.pngAnti-PER1 Antibody Picoband®Immunohistochemical analysis of clinical samples from multi-center datasets. A Immunohistochemical staining for PER1 and EME2. B Statistical analysis for PER1 and EME2 protein staining <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13044-024-00193-9'>38556856</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00876-13044_2024_193_fig3_html.pngAnti-PER1 Antibody Picoband®The RFS curves of 6 DDR genes with prognostic significance in early-stage PTC. A The RFS curve according to the expression of EME2. B The RFS curve according to the expression of MNAT1. C The RFS curve according to the expression of MUS81. D The RFS curve according to the expression of PER1. E The RFS curve according to the expression of POLM. F The RFS curve according to the expression of RAD9A <br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13044-024-00193-9'>38556856</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00876-per1-primary-antibodies-wb-testing-1.jpgAnti-PER1 Antibody Picoband® Western blot analysis of PER1 using anti-PER1 antibody (A00876). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A549 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: humna A431 whole cell lysates,<br>
Lane 4: human Hela whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat PC-12 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse HEPA1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PER1 antigen affinity purified polyclonal antibody (Catalog # A00876) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PER1 at approximately 200 kDa. The expected band size for PER1 is at 136 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00876-per1-primary-antibodies-ihc-testing-2.jpgAnti-PER1 Antibody Picoband® IHC analysis of PER1 using anti-PER1 antibody (A00876). <br>
PER1 was detected in a paraffin-embedded section of human gastric cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PER1 Antibody (A00876) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00876-per1-primary-antibodies-if-testing-3.jpgAnti-PER1 Antibody Picoband® IF analysis of PER1 using anti-PER1 antibody (A00876). <br>
PER1 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PER1 Antibody (A00876) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-per3-picoband-trade-antibody-a01835-1-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01835-1-per3-primary-antibodies-wb-testing-1_1.jpgAnti-PER3 Antibody Picoband® Western blot analysis of PER3 using anti-PER3 antibody (A01835-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela cell lysate,<br>Lane 2: human MCF-7 cell lysate,<br>Lane 3: human A549 cell lysate,<br>Lane 4: human HepG2 cell lysate,<br>Lane 5: human COLO-320 cell lysate,<br>Lane 6: rat heart tissue lysate,<br>Lane 7: mouse skeletal muscle tissue lysate. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PER3 antigen affinity purified polyclonal antibody (Catalog # A01835-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PER3 at approximately 160KD. The expected band size for PER3 is at 132KD.
https://www.bosterbio.com/products/primary-antibodies/anti-pias3-picoband-trade-antibody-a02807-1-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02807-1-PIAS3-primary-antibodies-WB-testing-1.jpgAnti-PIAS3 Antibody Picoband® Western blot analysis of PIAS3 using anti-PIAS3 antibody (A02807-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela cell lysate,<br>Lane 2: human U-87MG cell lysate,<br>Lane 3: human COLO-320 cell lysate,<br>Lane 4: human HepG2 cell lysate,<br>Lane 5: rat brain tissue lysate,<br>Lane 6: mouse NIH3T3 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIAS3 antigen affinity purified polyclonal antibody (Catalog # A02807-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIAS3 at approximately 68KD. The expected band size for PIAS3 is at 68KD.
https://www.bosterbio.com/products/primary-antibodies/anti-plk2-picoband-trade-antibody-a02881-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02881-PLK2-primary-antibodies-WB-testing-1.jpgAnti-PLK2 Antibody Picoband® Western blot analysis of PLK2 using anti-PLK2 antibody (A02881).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human MCF-7 cell lysate,<br>Lane 2: human HepG2 cell lysate,<br>Lane 3: mouse heart tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLK2 antigen affinity purified polyclonal antibody (Catalog # A02881) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLK2 at approximately 78KD. The expected band size for PLK2 is at 78KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02881-plk2-primary-antibodies-ihc-testing-2.jpgAnti-PLK2 Antibody Picoband® IHC analysis of PLK2 using anti-PLK2 antibody (A02881). <br> PLK2 was detected in paraffin-embedded section of human tonsil tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-PLK2 Antibody (A02881) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-uteroglobin-picoband-trade-antibody-a02201-1-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02201-1-Uteroglobin-primary-antibodies-WB-testing-1.jpgAnti-Uteroglobin/Scgb1a1 Antibody Picoband® Western blot analysis of Uteroglobin using anti-Uteroglobin antibody (A02201-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse lung tissue lysate,
<br>Lane 2: mouse lung tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Uteroglobin antigen affinity purified polyclonal antibody (Catalog # A02201-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Uteroglobin at approximately 10KD. The expected band size for Uteroglobin is at 10KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02201-1-Uteroglobin-primary-antibodies-IHC-testing-2.jpgAnti-Uteroglobin/Scgb1a1 Antibody Picoband® IHC analysis of Uteroglobin using anti-Uteroglobin antibody (A02201-1).
<br>Uteroglobin was detected in paraffin-embedded section of mouse lung tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Uteroglobin Antibody (A02201-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-uteroglobin-picoband-trade-antibody-a02201-2-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02201-2-Uteroglobin-primary-antibodies-WB-testing-1.jpgAnti-Uteroglobin/Scgb1a1 Antibody Picoband® Western blot analysis of Uteroglobin using anti-Uteroglobin antibody (A02201-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat lung tissue lysate,<br>Lane 2: rat lung tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Uteroglobin antigen affinity purified polyclonal antibody (Catalog # A02201-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Uteroglobin at approximately 10KD. The expected band size for Uteroglobin is at 10KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02201-2-uteroglobin-primary-antibodies-ihc-testing-2.jpgAnti-Uteroglobin/Scgb1a1 Antibody Picoband® IHC analysis of Uteroglobin using anti-Uteroglobin antibody (A02201-2).
Uteroglobin was detected in paraffin-embedded section of rat lung tissue . Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Uteroglobin Antibody (A02201-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02201-2-uteroglobin-primary-antibodies-wb-testing-3.jpgAnti-Uteroglobin/Scgb1a1 Antibody Picoband® Sandwich ELISA - Recombinant rat SCGB1A1 protein standard curve.<br>
Use in combination with reagents from Rat SCGB1A1 ELISA Kit EZ-Set (DIY Antibody Pairs) (EZ1636).
https://www.bosterbio.com/products/primary-antibodies/anti-14-3-3-sigma-picoband-trade-antibody-a01127-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01127-sfn-primary-antibodies-wb-testing-1.jpgAnti-14-3-3 sigma/SFN Antibody Picoband® Western blot analysis of 14-3-3 sigma using anti-14-3-3 sigma antibody (A01127). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human A431 whole cell lysates,<br>
Lane 2: human Hela whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human Hacat whole cell lysates,<br>
Lane 5: rat skin tissue lysates,<br>
Lane 6: mouse Hepa1-6 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-14-3-3 sigma antigen affinity purified polyclonal antibody (Catalog # A01127) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for 14-3-3 sigma at approximately 28 kDa. The expected band size for 14-3-3 sigma is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01127-14-3-3_sigma_-primary-antibodies-ihc-testing-2.jpgAnti-14-3-3 sigma/SFN Antibody Picoband® IHC analysis of 14-3-3 sigma using anti-14-3-3 sigma antibody (A01127).<br> 14-3-3 sigma was detected in paraffin-embedded section of human rectal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-14-3-3 sigma Antibody (A01127) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01127-14-3-3_sigma_-primary-antibodies-if-testing-3.jpgAnti-14-3-3 sigma/SFN Antibody Picoband® IF analysis of 14-3-3 sigma using anti-14-3-3 sigma antibody (A01127).<br> 14-3-3 sigma was detected in paraffin-embedded section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-cortactin Antibody (A01127) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01127-14-3-3_sigma_-primary-antibodies-if-testing-4.pngAnti-14-3-3 sigma/SFN Antibody Picoband® IF analysis of 14-3-3 sigma using anti-14-3-3 sigma antibody (A01127).<br> 14-3-3 sigma was detected in paraffin-embedded section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-cortactin Antibody (A01127) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01127-14-3-3_sigma_-primary-antibodies-fc-testing-5.pngAnti-14-3-3 sigma/SFN Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-14-3-3 SIGMA antibody (A01127). <br> Overlay histogram showing U20S cells stained with A01127 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-14-3-3 SIGMA Antibody (A01127,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-sox10-picoband-trade-antibody-a00758-1-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-1-sox10-primary-antibodies-wb-testing-1_1.jpgAnti-SOX10 Antibody Picoband® Western blot analysis of SOX10 using anti-SOX10 antibody (A00758-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human SH-SY5Y whole cell lysates,<br>
Lane 2: human U251 whole cell lysates,<br>
Lane 3: human U2OS whole cell lysates,<br>
Lane 4: human U87 whole cell lysates,<br>
Lane 5: rat brain tissue lysates,<br>
Lane 6: rat C6 whole cell lysates,<br>
Lane 7: mouse brain tissue lysates,<br>
Lane 8: mouse Neuro-2a whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX10 antigen affinity purified polyclonal antibody (Catalog # A00758-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX10 at approximately 60 kDa. The expected band size for SOX10 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-1-sox10-primary-antibodies-ihc-testing-2.jpgAnti-SOX10 Antibody Picoband® IHC analysis of SOX10 using anti-SOX10 antibody (A00758-1). <br>
SOX10 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOX10 Antibody (A00758-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-1-sox10-primary-antibodies-ihc-testing-3.jpgAnti-SOX10 Antibody Picoband® IHC analysis of SOX10 using anti-SOX10 antibody (A00758-1). <br>
SOX10 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOX10 Antibody (A00758-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-1-sox10-primary-antibodies-ihc-testing-4.jpgAnti-SOX10 Antibody Picoband® IHC analysis of SOX10 using anti-SOX10 antibody (A00758-1). <br>
SOX10 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOX10 Antibody (A00758-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-tbp-picoband-trade-antibody-a00302-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00302-Tbp-primary-antibodies-WB-testing-1.jpgAnti-TATA binding protein TBP Antibody Picoband® Western blot analysis of Tbp using anti-Tbp antibody (A00302).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat testis tissue lysate,<br>Lane 2: rat ovary tissue lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tbp antigen affinity purified polyclonal antibody (Catalog # A00302) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tbp at approximately 38KD. The expected band size for Tbp is at 38KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tec-picoband-trade-antibody-a01031-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01031-tec-primary-antibodies-wb-testing-1.jpgAnti-Tec Antibody Picoband® Western blot analysis of Tec using anti-Tec antibody (A01031). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human HEL whole cell lysates,
Lane 2: human THP-1 whole cell lysates,
Lane 3: rat kidney tissue lysates,
Lane 4: mouse kidney tissue lysates.
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tec antigen affinity purified polyclonal antibody (Catalog # A01031) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tec at approximately 74 kDa. The expected band size for Tec is at 74 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-thrombopoietin-picoband-trade-antibody-a03222-2-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03222-2-Thrombopoietin-primary-antibodies-WB-testing-1.jpgAnti-Thrombopoietin/THPO Antibody Picoband® Western blot analysis of Thrombopoietin using anti-Thrombopoietin antibody (A03222-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat liver tissue lysate,<br>Lane 2: rat spleen tissue lysate,<br>Lane 3: rat brain tissue lysate,<br>Lane 4: rat kidney tissue lysate,<br>Lane 5: rat thymus tissue lysate,<br>Lane 6: rat PC-12 cell lysate,<br>Lane 7: rat RH35 cell lysate,<br>Lane 8: mouse SP20 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Thrombopoietin antigen affinity purified polyclonal antibody (Catalog # A03222-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Thrombopoietin at approximately 38KD. The expected band size for Thrombopoietin is at 38KD.
https://www.bosterbio.com/products/primary-antibodies/anti-tweak-picoband-trade-antibody-a02009-1-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02009-1-TWEAK-primary-antibodies-WB-testing-1.jpgAnti-TWEAK/TNFSF12 Antibody Picoband® Western blot analysis of TWEAK using anti-TWEAK antibody (A02009-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human MCF-7 cell lysate,<br>Lane 2: human PANC-1 cell lysate.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TWEAK antigen affinity purified polyclonal antibody (Catalog # A02009-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TWEAK at approximately 27KD. The expected band size for TWEAK is at 27KD.
https://www.bosterbio.com/products/primary-antibodies/anti-serum-amyloid-p-picoband-trade-antibody-a00162-boster.html2026-03-24T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-wb-testing-1.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® Western blot analysis of Serum Amyloid P/APCS using anti-Serum Amyloid P/APCS antibody (A00162). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates, <br>
Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates. <br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Serum Amyloid P/APCS antigen affinity purified polyclonal antibody (Catalog # A00162) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Serum Amyloid P/APCS at approximately 25-29 kDa. The expected band size for Serum Amyloid P/APCS is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-ihc-testing-2.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® IHC analysis of Serum Amyloid P/APCS using anti-Serum Amyloid P/APCS antibody (A00162). <br>
Serum Amyloid P/APCS was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Serum Amyloid P/APCS Antibody (A00162) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-ihc-testing-3.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® IHC analysis of Serum Amyloid P/APCS using anti-Serum Amyloid P/APCS antibody (A00162). <br>
Serum Amyloid P/APCS was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Serum Amyloid P/APCS Antibody (A00162) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-fcm-testing-6.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® Flow Cytometry analysis of HL-60 cells using anti-Serum Amyloid P/APCS antibody (A00162). <br>Overlay histogram showing HL-60 cells stained with A00162 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Serum Amyloid P/APCS Antibody (A00162, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-ihc-testing-4.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® IHC analysis of Serum Amyloid P/APCS using anti-Serum Amyloid P/APCS antibody (A00162). <br>
Serum Amyloid P/APCS was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Serum Amyloid P/APCS Antibody (A00162) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00162-apcs-primary-antibodies-if-testing-5.jpgAnti-Serum Amyloid P/APCS Antibody Picoband® IF analysis of Serum Amyloid P/APCS using anti-Serum Amyloid P/APCS antibody (A00162). <br>
Serum Amyloid P/APCS was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Serum Amyloid P/APCS Antibody (A00162) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-pho1-picoband-trade-antibody-a01183-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01183-1-apobec3a-primary-antibodies-wb-testing-1.jpgAnti-PHO1/APOBEC3A Antibody Picoband® Western blot analysis of APOBEC3A using anti-APOBEC3A antibody (A01183-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human CACO-2 whole cell lysates,<br>
Lane 3: human A549 whole cell lysates,<br>
Lane 4: rat PC-12 whole cell lysates,<br>
Lane 5: mouse RAW264.7 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APOBEC3A antigen affinity purified polyclonal antibody (Catalog # A01183-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APOBEC3A at approximately 23 kDa. The expected band size for APOBEC3A is at 23 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-asxl1-picoband-trade-antibody-a01099-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01099-asxl1-primary-antibodies-fcm-testing-2.jpgAnti-ASXL1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ASXL1 antibody (A01099). <br>Overlay histogram showing HepG2 cells stained with A01099 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ASXL1 Antibody (A01099, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01099-asxl1-primary-antibodies-wb-testing-1_1.jpgAnti-ASXL1 Antibody Picoband® Western blot analysis of ASXL1 using anti-ASXL1 antibody (A01099). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human 293T whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human CACO-2 whole cell lysates,<br>
Lane 4: rat C6 whole cell lysates,<br>
Lane 5: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASXL1 antigen affinity purified polyclonal antibody (Catalog # A01099) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ASXL1 at approximately 165 kDa. The expected band size for ASXL1 is at 165 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-bap1-picoband-trade-antibody-a00345-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00345-1-bap1-primary-antibodies-wb-testing-1.jpgAnti-BAP1 Antibody Picoband® Western blot analysis of BAP1 using anti-BAP1 antibody (A00345-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human HepG2 whole cell lysates,<br>Lane 3: human 22RV1 whole cell lysates,<br>Lane 4: human MCF-7 whole cell lysates,<br>Lane 5: rat thymus tissue lysates,<br>Lane 6: rat kidney tissue lysates,<br>Lane 7: mouse kidney tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BAP1 antigen affinity purified polyclonal antibody (Catalog # A00345-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BAP1 at approximately 88KD. The expected band size for BAP1 is at 80KD.
https://www.bosterbio.com/products/primary-antibodies/anti-ciap1-picoband-trade-antibody-a01700-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01700-1-birc2-primary-antibodies-wb-testing-1.jpgAnti-cIAP1/BIRC2 Antibody Picoband®Western blot analysis of cIAP1/BIRC2 using anti-cIAP1/BIRC2 antibody (A01700-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human HepG2 whole cell lysates,<br>
Lane 4: rat brain tissue lysates,<br>
Lane 5: mouse brain tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-cIAP1/BIRC2 antigen affinity purified polyclonal antibody (A01700-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for cIAP1/BIRC2 at approximately 70 kDa. The expected band size for cIAP1/BIRC2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01700-1-birc2-primary-antibodies-if-testing-1.jpgAnti-cIAP1/BIRC2 Antibody Picoband®IF analysis of cIAP1/BIRC2 using anti-cIAP1/BIRC2 antibody (A01700-1). <br>
cIAP1/BIRC2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-cIAP1/BIRC2 Antibody (A01700-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01700-1-birc2-primary-antibodies-fcm-testing-1.jpgAnti-cIAP1/BIRC2 Antibody Picoband®Flow Cytometry analysis of HEL cells using anti-cIAP1/BIRC2 antibody (A01700-1). <br>
Overlay histogram showing HEL cells stained with A01700-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-cIAP1/BIRC2 Antibody (A01700-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-bnip3-picoband-trade-antibody-a01469-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01469-BNIP3-primary-antibodies-WB-testing-2.jpgAnti-BNIP3 Antibody Picoband® Western blot analysis of BNIP3 using anti-BNIP3 antibody (A01469).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat kidney tissue lysates,<br>Lane 3: rat heart tissue lysates,<br>Lane 4: rat testis tissue lysates,<br>Lane 5: mouse brain tissue lysates,<br>Lane 6: mouse kidney tissue lysates,<br>Lane 7: mouse heart tissue lysates,<br>Lane 8: mouse testis tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BNIP3 antigen affinity purified polyclonal antibody (Catalog # A01469) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BNIP3 at approximately 21KD. The expected band size for BNIP3 is at 21KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g009.jpgAnti-BNIP3 Antibody Picoband®Knockdown of BNIP3 induces glioma cells apoptosis. (A) Western blot was performed to detect the expression levels of Bax, Bcl-2 and Active Caspase-3.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g002.jpgAnti-BNIP3 Antibody Picoband®Down-regulation of miR-145 and up-regulation of BNIP3 expression in gliomas. (A) Quantitative real-time PCR of miR-145 expression in glioma samples (n = 19) compared with normal samples (n = 10). (B) quantitative real-time PCR of miR-145 expression in rat glioma tissues (n = 6) and U87, U251 glioma cells compared to normal tissues (n = 6). (C) Quantitative real-time PCR of BNIP3 mRNA expression in glioma samples (n = 19) compared with normal samples (n = 10). (D) quantitative real-time PCR of BNIP3 mRNA expression in rat glioma tissues and U87, U251 glioma cells compared to normal tissues. (E) Pathology observation of mice brain tissues sections stained with IHC (×100, ×200, ×400). (F) Immunofluorescence with BNIP3 (green) in rat normal tissues and glioma tissues (×200).*p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g003.jpgAnti-BNIP3 Antibody Picoband®Down-regulation of miR-145 and up-regulation of BNIP3 expression in gliomas. (A) Western analysis of BNIP3 and control β-actin in glioma samples compared with normal samples. (B) Western analysis of BNIP3 and control β-actin in rat glioma tissues compared to normal tissues. *p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g006.jpgAnti-BNIP3 Antibody Picoband®miR-145 inhibits mRNA and protein expression of BNIP3. (A) Bioinformatics analysis shows the seed sequence of miR-145 binding to the 3′-UTR of BNIP3 mRNA. (B) , (C) Quantitative real-time PCR analysis of mRNA expression of BNIP3 in U87 cells treated with miR-145 mimics and inhibitor for 48 h. (D) Western analysis of protein expression of BNIP3 in U87 and U251 cells treated with miR-145 mimics and inhibitor for 48 h. (E) Immunofluorescence with BNIP3 (green) in U87 and U251 cells after miR-145 mimics or mimics NC treatment.*p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g007.jpgAnti-BNIP3 Antibody Picoband®miR-145 inhibits mRNA and protein expression of BNIP3. (A) Western analysis of BNIP3, which is localized in the nucleus or the cytoplasm in U87 and U251 cells treated with miR-145 mimics and inhibitor for 48 h. (B) Wild-type 3′-UTR of BNIP3 gene was cloned into the firefly and Renilla reporter plasmid. The BNIP3-3′UTR constructs or blank plasmid were transfected into U87 and U251 cells with control or miR-145 mimics, followed by dual luciferase assays. *p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g008.jpgAnti-BNIP3 Antibody Picoband®Knockdown of BNIP3 induces glioma cells apoptosis. (A, B) Transfection effect of BNIP3-siRNA or BNIP3-vector was confirmed by quantitative real-time PCR. (C) U87 cells and U251 cells were stained with Hoechst 33342 dye after BNIP3-siRNA or control treatment. (D) U87 and U251 cells were stained with Tunel after BNIP3-siRNA or control treatment. (E) U87 cell apoptosis after BNIP3-siRNA or control treatment was determined by FACS. *p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g011.jpgAnti-BNIP3 Antibody Picoband® miR-145 regulates Notch signaling by targeting BNIP3. (A, B) Protein expression of Notch1, p21 and Hes1 was determined by western blot analysis in U87 and U251 cells transfected with miR-145 mimics and mimics-NC, or miR-145 inhibitor and inhibitor-NC. (C, D) Western analysis of Notch1-related proteins in U87 and U251 cells transfected with Bnip3 siRNA and siRNA control, or BNIP3 expression vector and blank vector. *p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-oncotarget-08-61510-g012.jpgAnti-BNIP3 Antibody Picoband® miR-145 can regulate Notch signaling pathway by targeting BNIP3. (A) Protein expression of Notch1, p21, Hes1 was determined by western blot analysis in U87 and U251 cells co-transfected with miR-145 inhibitor and BNIP3-siRNA, or with miR-145 inhibitor. *p < 0.05, **p < 0.01 versus control group.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://misuse.ncbi.nlm.nih.gov/error/abuse.shtml?orig_args=/pmc/articles/PMC5617441/&orig_host=www.ncbi.nlm.nih.gov'>28977881</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-13287_2025_4422_fig5_html.pngAnti-BNIP3 Antibody Picoband®DMOG treatment activates hypoxia- and mitophagy-related pathways in aged MSCs. ( A , C ) Volcano plots of differentially expressed genes (DEGs) in P5 ( A ) and P24 ( C ) MSCs after DMOG treatment. Key mitophagy-related genes, BNIP3 and BNIP3L, were consistently upregulated in both groups. ( B , D ) KEGG pathway enrichment analysis in P5 ( B ) and P24 ( D ) MSCs showing that DMOG activated HIF-1 signaling, glycolysis/gluconeogenesis, and mitophagy-related pathways in both young and aged MSCs. ( E ) Heatmap of DEGs in the P5, P5 + DMOG, P24, and P24 + DMOG groups. Each group has three biological replicates. ( F ) KEGG pathway analysis of all groups highlights the key pathways activated by DMOG, including HIF-1 signaling and glycolysis. ( G ) Heatmap showing the expression levels of key mitophagy-related genes (e.g., BNIP3, BNIP3L, HIF-1 A) upregulated by DMOG treatment. ( H ) Venn diagram illustrating the shared and unique DEGs across comparisons. A total of 79 genes were co-regulated by DMOG in both P5 and P24 MSCs. ( I - K ) GO and pathway analyses of co-regulated genes revealed enrichment in hypoxia response, glycolysis, and other metabolic processes Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04422-2'>40457488</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01469-13287_2025_4422_fig6_html.pngAnti-BNIP3 Antibody Picoband®DMOG rejuvenates senescent MSCs through BNIP3-dependent mitophagy. ( A , B ) Western blot analysis ( A ) and quantification ( B ) showing the expression of mitophagy-related proteins BNIP3 and BNIP3L in P5, P15, and H₂O₂-treated P5 MSCs with or without DMOG treatment. ( C , D ) Western blot analysis ( C ) and quantification ( D ) of BNIP3 expression in P15 MSCs after BNIP3 knockdown with siRNA. ( E ) Real-time PCR analysis of BNIP3 expression in P15 MSCs with or without DMOG treatment and BNIP3 knockdown. ( F , G ) SA-β-gal staining ( F ) and quantification ( G ) showing the percentage of senescent cells in P15 MSCs. Scale bar = 500 μm. ( H , I ) Confocal images (H) and quantification (I) of colocalization between mitochondria (Mitotracker Green) and lysosomes (Lysotracker Red) in P15 MSCs. Scale bar = 10 μm. Data are expressed as mean ± SEM ( n = 3). ** p < 0.01, *** p < 0.001. Full-length blots are presented in Supplementary Materials - WB Raw Data Full size image<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13287-025-04422-2'>40457488</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01469-BNIP3-primary-antibodies-WB-testing-1.jpgAnti-BNIP3 Antibody Picoband® Western blot analysis of BNIP3 using anti-BNIP3 antibody (A01469).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human A375 whole cell lysates,<br>Lane 3: human A549 whole cell lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BNIP3 antigen affinity purified polyclonal antibody (Catalog # A01469) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BNIP3 at approximately 21KD. The expected band size for BNIP3 is at 21KD.
https://www.bosterbio.com/products/primary-antibodies/anti-caspase-4-picoband-trade-antibody-a02941-1-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02941-1-Caspase_4-primary-antibodies-WB-testing-1.jpgAnti-Caspase 4/CASP4 Antibody Picoband® Western blot analysis of Caspase 4 using anti-Caspase 4 antibody (A02941-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human COLO-320 whole cell lysates,<br>Lane 3: human SW620 whole cell lysates,<br>Lane 4: human HepG2 whole cell lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 4 antigen affinity purified polyclonal antibody (Catalog # A02941-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase 4 at approximately 48KD. The expected band size for Caspase 4 is at 43KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02941-1-Caspase_4-primary-antibodies-IHC-testing-2.jpgAnti-Caspase 4/CASP4 Antibody Picoband® IHC analysis of Caspase 4 using anti-Caspase 4 antibody (A02941-1).
<br>Caspase 4 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Caspase 4 Antibody (A02941-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02941-1-Caspase_4-primary-antibodies-IHC-testing-3.jpgAnti-Caspase 4/CASP4 Antibody Picoband® IHC analysis of Caspase 4 using anti-Caspase 4 antibody (A02941-1).
<br>Caspase 4 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Caspase 4 Antibody (A02941-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-1-caspase_4-primary-antibodies-if-testing-4.jpgAnti-Caspase 4/CASP4 Antibody Picoband® IF analysis of Caspase 4 using anti-Caspase 4 antibody (A02941-1).<br> Caspase 4 was detected in an immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/mL rabbit anti-Caspase 4 Antibody (A02941-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-1-casp4-primary-antibodies-fcm-testing-5.jpgAnti-Caspase 4/CASP4 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Caspase 4 antibody (A02941-1). <br>
Overlay histogram showing SiHa cells stained with A02941-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Caspase 4 Antibody (A02941-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-1-casp4-primary-antibodies-if-testing-7.jpgAnti-Caspase 4/CASP4 Antibody Picoband® IF analysis of Caspase 4 using anti-Caspase 4 antibody (A02941-1). <br>
Caspase 4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 μg/mL rabbit anti-Caspase 4 Antibody (A02941-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02941-1-casp4-primary-antibodies-fcm-testing-6.jpgAnti-Caspase 4/CASP4 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-Caspase 4 antibody (A02941-1). <br>
Overlay histogram showing PC-3 cells stained with A02941-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Caspase 4 Antibody (A02941-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd2ap-picoband-trade-antibody-a01756-2-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-fphar-15-1447249-g006.jpgAnti-CD2AP Antibody Picoband®Shensu IV regulates the PI3K/AKT signaling pathway through H2S. (A) The effects of Shensu IV and NaHS on the mRNA expression of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, and AKT in renal tissue of PAN rats were analyzed by RT-qPCR. (B) Western blot analysis of the effects of Shensu IV and NaHS on the protein levels of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, p-PI3K,AKT,p-AKT in renal tissue of PAN rats. * P < 0.05, ** P < 0.01, *** P < 0.001. Abbreviations: CD2AP, CD2-associated protein; CBS, Cystathionine β-synthase; CSE, Cystathionine γ-lyase; PI3K, Phosphoinositide 3-Kinase; AKT, Protein Kinase B.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1447249/full'>39720588</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-fphar-15-1447249-g008.jpgAnti-CD2AP Antibody Picoband®Shensu IV regulates the PI3K/AKT signaling pathway through H2S in podocytes. (A) The effects of Shensu IV and NaHS on the mRNA expression of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, and AKT in podocytes were analyzed by RT-qPCR. (B) Western blot analysis of the effects of Shensu IV and NaHS on the protein levels of CD2AP, nephrin, CBS, CSE, NOX4, PI3K, p-PI3K,AKT,p-AKT in PAN-induced podocyocytes. * P < 0.05, ** P < 0.01, *** P < 0.001. Abbreviations: CD2AP, CD2-associated protein; CBS, Cystathionine β-synthase; CSE, Cystathionine γ-lyase; PI3K, Phosphoinositide 3-Kinase; AKT, Protein Kinase B.<br><b>Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1447249/full'>39720588</a></b>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-wb-testing-1_1.jpgAnti-CD2AP Antibody Picoband® Western blot analysis of CD2AP using anti-CD2AP antibody (A01756-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human Hela whole cell lysates,<br>
Lane 4: human K562 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD2AP antigen affinity purified polyclonal antibody (A01756-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD2AP at approximately 80 kDa. The expected band size for CD2AP is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-ihc-testing-2.jpgAnti-CD2AP Antibody Picoband® IHC analysis of CD2AP using anti-CD2AP antibody (A01756-2). <br>
CD2AP was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD2AP Antibody (A01756-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-ihc-testing-3.jpgAnti-CD2AP Antibody Picoband® IHC analysis of CD2AP using anti-CD2AP antibody (A01756-2). <br>
CD2AP was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD2AP Antibody (A01756-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-if-testing-4.jpgAnti-CD2AP Antibody Picoband® IF analysis of CD2AP using anti-CD2AP antibody (A01756-2). <br>
CD2AP was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CD2AP Antibody (A01756-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-ip-testing-5.jpgAnti-CD2AP Antibody Picoband® Immunoprecipitating CD2AP in Jurkat whole cell lysate . <br>
Western blot analysis of CD2AP using anti-CD2AP antibody (A01756-2). <br>
Lane 1: Jurkat whole cell lysates (30ug), <br>
Lane 2: Rabbit control IgG instead of anti-CD2AP antibody in Jurkat whole cell lysate, <br>
Lane 3: anti-CD2AP antibody (2μg) + Jurkat whole cell lysate (500μg). <br>
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD2AP antigen affinity purified polyclonal antibody (A01756-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for CD2AP at approximately 80 kDa. The expected band size for CD2AP is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01756-2-cd2ap-primary-antibodies-fcm-testing-6.jpgAnti-CD2AP Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-CD2AP antibody (A01756-2). <br>
Overlay histogram showing K562 cells stained with A01756-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CD2AP Antibody (A01756-2, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-cd19-picoband-trade-antibody-a00154-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00154-1-cd19-primary-antibodies-wb-testing-1.jpgAnti-CD19 Antibody Picoband® Western blot analysis of CD19 using anti-CD19 antibody (A00154-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse thymus tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD19 antigen affinity purified polyclonal antibody (Catalog # A00154-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD19 at approximately 85KD. The expected band size for CD19 is at 61KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd19-picoband-trade-antibody-a00154-2-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00154-2-cd19-primary-antibodies-wb-testing-1_1.jpgAnti-CD19 Antibody Picoband®Western blot analysis of CD19 using anti-CD19 antibody (A00154-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Ramos whole cell lysates,<br>
Lane 2: human Daudi whole cell lysates,<br>
Lane 3: rat spleen tissue lysates,<br>
Lane 4: mouse spleen tissue lysates,<br>
Lane 5: mouse RAW264.7 whole cell lysates,<br>
Lane 6: mouse EL4 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD19 antigen affinity purified polyclonal antibody (A00154-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD19 at approximately 95 kDa. The expected band size for CD19 is at 60 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-dc-sign-picoband-trade-antibody-a01025-2-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01025-2-dc-sign-primary-antibodies-wb-testing-1.jpgAnti-DC-SIGN/CD209 Antibody Picoband®Western blot analysis of DC-SIGN using anti-DC-SIGN antibody (A01025-2). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DC-SIGN antigen affinity purified polyclonal antibody (A01025-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DC-SIGN at approximately 46 kDa. The expected band size for DC-SIGN is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01025-2-dc-sign-primary-antibodies-ihc-testing-1.jpgAnti-DC-SIGN/CD209 Antibody Picoband®IHC analysis of DC-SIGN using anti-DC-SIGN antibody (PA1348). <br>
DC-SIGN was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DC-SIGN Antibody (PA1348) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01025-2-dc-sign-primary-antibodies-ihc-testing-2.jpgAnti-DC-SIGN/CD209 Antibody Picoband®IHC analysis of DC-SIGN using anti-DC-SIGN antibody (PA1348). <br>
DC-SIGN was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DC-SIGN Antibody (PA1348) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-chm-antibody-a00814-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00814-1-chm-primary-antibodies-wb-testing-1.jpgAnti-CHM Antibody Picoband® Western blot analysis of CHM using anti-CHM antibody (A00814-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human A431 whole cell lysates,<br>
Lane 3: human 293T whole cell lysates,<br>
Lane 4: rat liver tissue lysates,<br>
Lane 5: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHM antigen affinity purified polyclonal antibody (Catalog # A00814-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHM at approximately 73 kDa. The expected band size for CHM is at 100 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-clpx-picoband-trade-antibody-a00978-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-wb-testing-1_1.jpgAnti-CLPX Antibody Picoband®Western blot analysis of CLPX using anti-CLPX antibody (A00978-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLPX antigen affinity purified polyclonal antibody (A00978-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CLPX at approximately 69 kDa. The expected band size for CLPX is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-wb-testing-2.jpgAnti-CLPX Antibody Picoband®Western blot analysis of CLPX using anti-CLPX antibody (A00978-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat heart tissue lysates,<br>
Lane 2: rat PC-12 whole cell lysates,<br>
Lane 3: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLPX antigen affinity purified polyclonal antibody (A00978-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CLPX at approximately 69 kDa. The expected band size for CLPX is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-ihc-testing-1.jpgAnti-CLPX Antibody Picoband®IHC analysis of CLPX using anti-CLPX antibody (A00978-1). <br>CLPX was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLPX Antibody (A00978-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-ihc-testing-2.jpgAnti-CLPX Antibody Picoband®IHC analysis of CLPX using anti-CLPX antibody (A00978-1). <br>CLPX was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLPX Antibody (A00978-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-ihc-testing-3.jpgAnti-CLPX Antibody Picoband®IHC analysis of CLPX using anti-CLPX antibody (A00978-1). <br>CLPX was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLPX Antibody (A00978-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-ihc-testing-4.jpgAnti-CLPX Antibody Picoband®IHC analysis of CLPX using anti-CLPX antibody (A00978-1). <br>CLPX was detected in a paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLPX Antibody (A00978-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-if-testing-1.jpgAnti-CLPX Antibody Picoband®IF analysis of CLPX using anti-CLPX antibody (A00978-1). <br>
CLPX was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CLPX Antibody (A00978-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00978-1-clpx-primary-antibodies-fcm-testing-1.jpgAnti-CLPX Antibody Picoband®Flow Cytometry analysis of THP-1 cells using anti-CLPX antibody (A00978-1). <br>
Overlay histogram showing THP-1 cells stained with A00978-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CLPX Antibody (A00978-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-crlf2-picoband-trade-antibody-a04167-1-boster.html2026-03-27T05:07:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04167-1-CRLF2-primary-antibodies-WB-testing-1.jpgAnti-CRLF2 Antibody Picoband® Western blot analysis of CRLF2 using anti-CRLF2 antibody (A04167-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.
<br>Lane 1: recombinant human CRLF2 protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRLF2 antigen affinity purified polyclonal antibody (Catalog # A04167-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CRLF2 at approximately 65-75KD. The expected band size for CRLF2 is at 51KD.
https://www.bosterbio.com/products/primary-antibodies/anti-dck-picoband-trade-antibody-a01655-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-ddb2-primary-antibodies-wb-testing-1.jpgAnti-DCK Antibody Picoband® Western blot analysis of DCK using anti-DCK antibody (A01655-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Jurkat whole cell lysates,<br>
Lane 2: rat thymus tissue lysates,<br>
Lane 3: mouse thymus tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DCK antigen affinity purified polyclonal antibody (Catalog # A01655-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DCK at approximately 31 kDa. The expected band size for DCK is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-ihc-testing-2_1.jpgAnti-DCK Antibody Picoband® IHC analysis of DCK using anti-DCK antibody (A01655-1). <br>
DCK was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCK Antibody (A01655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-ihc-testing-3_1.jpgAnti-DCK Antibody Picoband® IHC analysis of DCK using anti-DCK antibody (A01655-1). <br>
DCK was detected in a paraffin-embedded section of human ovary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCK Antibody (A01655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-ihc-testing-4_1.jpgAnti-DCK Antibody Picoband® IHC analysis of DCK using anti-DCK antibody (A01655-1). <br>
DCK was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCK Antibody (A01655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-ihc-testing-5_1.jpgAnti-DCK Antibody Picoband® IHC analysis of DCK using anti-DCK antibody (A01655-1). <br>
DCK was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCK Antibody (A01655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-ihc-testing-6.jpgAnti-DCK Antibody Picoband® IHC analysis of DCK using anti-DCK antibody (A01655-1). <br>
DCK was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCK Antibody (A01655-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01655-1-dck-primary-antibodies-fcm-testing-7.jpgAnti-DCK Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-DCK antibody (A01655-1). <br>
Overlay histogram showing U87 cells stained with A01655-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DCK Antibody (A01655-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-dgcr8-picoband-trade-antibody-a00475-1-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00475-1-DGCR8-primary-antibodies-WB-testing-1.jpgAnti-DGCR8 Antibody Picoband® Western blot analysis of DGCR8 using anti-DGCR8 antibody (A00475-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human placenta tissue lysates,<br>Lane 3: human COLO-320 whole cell lysates,<br>Lane 4: human HepG2 whole cell lysates,<br>Lane 5: human A549 whole cell lysates,<br>Lane 6: human MCF-7 whole cell lysates,<br>Lane 7: human 22RV1 whole cell lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DGCR8 antigen affinity purified polyclonal antibody (Catalog # A00475-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DGCR8 at approximately 100KD. The expected band size for DGCR8 is at 86KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00475-1-DGCR8-primary-antibodies-IHC-testing-2.jpgAnti-DGCR8 Antibody Picoband® IHC analysis of DGCR8 using anti-DGCR8 antibody (A00475-1).
<br>DGCR8 was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-DGCR8 Antibody (A00475-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00475-1-dgcr8-primary-antibodies-ihc-testing-3.jpgAnti-DGCR8 Antibody Picoband® IHC analysis of DGCR8 using anti-DGCR8 antibody (A00475-1). <br> DGCR8 was detected in paraffin-embedded section of mouse small intestine tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-DGCR8 Antibody (A00475-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00475-1-dgcr8-primary-antibodies-if-testing-4.jpgAnti-DGCR8 Antibody Picoband® IF analysis of DGCR8 using anti-DGCR8 antibody (A00475-1). <br> DGCR8 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-DGCR8 Antibody (A00475-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/products/primary-antibodies/anti-dynamin-1-picoband-trade-antibody-a02536-2-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A02536-2-Dynamin_1-primary-antibodies-WB-testing-1.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® Western blot analysis of Dynamin 1 using anti-Dynamin 1 antibody (A02536-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat brain tissue lysates,<br>Lane 2: mouse brain tissue lysates,<br>Lane 3: mouse NIH3T3 whole cell lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dynamin 1 antigen affinity purified polyclonal antibody (Catalog # A02536-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Dynamin 1 at approximately 97KD. The expected band size for Dynamin 1 is at 97KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-ihc-testing-2.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® IHC analysis of Dynamin 1 using anti-Dynamin 1 antibody (A02536-2).
<br>Dynamin 1 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Dynamin 1 Antibody (A02536-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-ihc-testing-3.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® IHC analysis of Dynamin 1 using anti-Dynamin 1 antibody (A02536-2).
<br>Dynamin 1 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Dynamin 1 Antibody (A02536-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-ihc-testing-4.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® IHC analysis of Dynamin 1 using anti-Dynamin 1 antibody (A02536-2).
<br>Dynamin 1 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Dynamin 1 Antibody (A02536-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-ihc-testing-5.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® IHC analysis of Dynamin 1 using anti-Dynamin 1 antibody (A02536-2).
<br>Dynamin 1 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Dynamin 1 Antibody (A02536-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-fc-testing-6.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-Dynamin 1 antibody (A02536-2).<br>Overlay histogram showing U251 cells stained with A02536-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Dynamin 1 Antibody (A02536-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-fc-testing-7.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-Dynamin 1 antibody (A02536-2).<br>Overlay histogram showing A549 cells stained with A02536-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Dynamin 1 Antibody (A02536-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02536-2-dynamin_1-primary-antibodies-fc-testing-8.jpgAnti-Dynamin 1/DNM1 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-Dynamin 1 antibody (A02536-2).<br>Overlay histogram showing U20S cells stained with A02536-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DNM1 Antibody (A02536-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-dpyd-antibody-a01749-boster.html2026-03-24T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01749-dpyd-primary-antibodies-wb-testing-1_1.jpgAnti-DPYD Antibody Picoband®Western blot analysis of DPYD using anti-DPYD antibody (A01749). <br>
Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human THP-1 whole cell lysates,<br>
Lane 2: rat liver tissue lysates,<br>
Lane 3: mouse liver tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DPYD antigen affinity purified polyclonal antibody (A01749) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DPYD at approximately 111 kDa. The expected band size for DPYD is at 111 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-dyrk1a-picoband-trade-antibody-a00878-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00878-1-dyrk1a-primary-antibodies-wb-testing-1_2.jpgAnti-DYRK1A Antibody Picoband®Western blot analysis of DYRK1A using anti-DYRK1A antibody (A00878-1). <br>Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human SiHa whole cell lysates,<br>
Lane 3: human Jurkat whole cell lysates,<br>
Lane 4: human K562 whole cell lysates,<br>
Lane 5: rat brain tissue lysates.<br>After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DYRK1A antigen affinity purified polyclonal antibody (A00878-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DYRK1A at approximately 86 kDa. The expected band size for DYRK1A is at 86 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-perk-picoband-trade-antibody-a01992-2-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01992-2-eif2ak3-primary-antibodies-wb-testing-1.jpgAnti-PERK/EIF2AK3 Antibody Picoband®Western blot analysis of PERK/EIF2AK3 using anti-PERK/EIF2AK3 antibody (A01992-2). <br>Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human K562 whole cell lysates,<br>
Lane 2: human 293T whole cell lysates,<br>
Lane 3: human MCF-7 whole cell lysates,<br>
Lane 4: human HepG2 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PERK/EIF2AK3 antigen affinity purified polyclonal antibody (A01992-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PERK/EIF2AK3 at approximately 150 kDa. The expected band size for PERK/EIF2AK3 is at 125 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01992-2-eif2ak3-primary-antibodies-ihc-testing-1.jpgAnti-PERK/EIF2AK3 Antibody Picoband®IHC analysis of PERK/EIF2AK3 using anti-PERK/EIF2AK3 antibody (A01992-2). <br>PERK/EIF2AK3 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PERK/EIF2AK3 Antibody (A01992-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-e74-like-factor-1-picoband-trade-antibody-a03187-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A03187-1-E74_like_factor_1-primary-antibodies-WB-testing-1.jpgAnti-E74 like factor 1/ELF1 Antibody Picoband® Western blot analysis of E74 like factor 1 using anti-E74 like factor 1 antibody (A03187-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human Hela whole cell lysates,<br>Lane 2: human COLO-320 whole cell lysates,<br>Lane 3: human A549 whole cell lysates,<br>Lane 4: human PANC-1 whole cell lysates,<br>Lane 5: Human A431 whole cell lysates,<br>Lane 6: human Jurkat whole cell lysates,<br>Lane 7: human 293T whole cell lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-E74 like factor 1 antigen affinity purified polyclonal antibody (Catalog # A03187-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for E74 like factor 1 at approximately 75KD. The expected band size for E74 like factor 1 is at 67KD.
https://www.bosterbio.com/products/primary-antibodies/anti-col18a1-picoband-trade-antibody-a01302-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01302-1-COL18A1-primary-antibodies-WB-testing-1.jpgAnti-COL18A1 Antibody Picoband® Western blot analysis of COL18A1 using anti-COL18A1 antibody (A01302-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: human COLO-320 whole cell lysates,<br>Lane 2: human placenta tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COL18A1 antigen affinity purified polyclonal antibody (Catalog # A01302-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for COL18A1 at approximately 180KD, 20KD. The expected band size for COL18A1 is at 178KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd23-picoband-trade-antibody-a04237-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A04237-CD23-primary-antibodies-WB-testing-1.jpgAnti-CD23/FCER2 Antibody Picoband® Western blot analysis of CD23 using anti-CD23 antibody (A04237).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: rat spleen tissue lysates,<br>Lane 2: rat thymus tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD23 antigen affinity purified polyclonal antibody (Catalog # A04237) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD23 at approximately 36KD. The expected band size for CD23 is at 36KD.
https://www.bosterbio.com/products/primary-antibodies/anti-cd16-picoband-trade-antibody-a01408-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01408-1-cd16-primary-antibodies-ihc-testing-1.jpgAnti-CD16/FCGR3A Antibody IHC analysis of CD16 using anti-CD16 antibody (A01408-1). <br>
CD16 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD16 Antibody (A01408-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01408-1-cd16-primary-antibodies-ihc-testing-2_1.jpgAnti-CD16/FCGR3A Antibody IHC analysis of CD16 using anti-CD16 antibody (A01408-1). <br>
CD16 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD16 Antibody (A01408-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01408-1-cd16-primary-antibodies-ihc-testing-3_1.jpgAnti-CD16/FCGR3A Antibody IHC analysis of CD16 using anti-CD16 antibody (A01408-1). <br>
CD16 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD16 Antibody (A01408-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01408-1-cd16-primary-antibodies-if-testing-4_1.jpgAnti-CD16/FCGR3A Antibody IF analysis of CD16 using anti-CD16 antibody (A01408-1). <br>
CD16 was detected in an immunocytochemical section of K562 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CD16 Antibody (A01408-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01408-1-cd16-primary-antibodies-fcm-testing-5.jpgAnti-CD16/FCGR3A Antibody Flow Cytometry analysis of human PBMC cells using anti-CD16 antibody (A01408-1). <br>Overlay histogram showing human PBMC cells stained with A01408-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD16 Antibody (A01408-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-galanin-picoband-trade-antibody-a00606-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00606-1-galanin-primary-antibodies-wb-testing-1.jpgAnti-Galanin Antibody Picoband® Western blot analysis of Galanin using anti-Galanin antibody (A00606-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: rat small intestine tissue lysates,<br>Lane 3: mouse brain tissue lysates,<br>Lane 4: mouse small intestine tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Galanin antigen affinity purified polyclonal antibody (Catalog # A00606-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Galanin at approximately 19KD. The expected band size for Galanin is at 13KD.
https://www.bosterbio.com/products/primary-antibodies/anti-connexin-32-gjb1-picoband-trade-antibody-a01050-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01050-gjb1-primary-antibodies-wb-testing-1_1.jpgAnti-Connexin 32/GJB1 Antibody Picoband®Western blot analysis of GJB1 using anti-GJB1 antibody (A01050). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat liver tissue lysates,<br>
Lane 2: rat kidney tissue lysates,<br>
Lane 3: mouse liver tissue lysates,<br>
Lane 4: mouse kidney tissue lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GJB1 antigen affinity purified polyclonal antibody (Catalog # A01050) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GJB1 at approximately 32 kDa. The expected band size for GJB1 is at 32 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-glo1-picoband-trade-antibody-a01703-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01703-1-glo1-primary-antibodies-wb-testing-1.jpgAnti-GLO1 Antibody Picoband® Western blot analysis of GLO1 using anti-GLO1 antibody (A01703-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hela whole cell lysates,<br>
Lane 2: human MCF-7 whole cell lysates,<br>
Lane 3: human COLO320 whole cell lysates,<br>
Lane 4: human 22RV1 whole cell lysates,<br>
Lane 5: human HepG2 whole cell lysates,<br>
Lane 6: human A431 whole cell lysates,<br>
Lane 7: human U937 whole cell lysates,<br>
Lane 8: human THP-1 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLO1 antigen affinity purified polyclonal antibody (Catalog # A01703-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLO1 at approximately 21 kDa. The expected band size for GLO1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01703-1-glo1-primary-antibodies-wb-testing-2.jpgAnti-GLO1 Antibody Picoband® Western blot analysis of GLO1 using anti-GLO1 antibody (A01703-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: rat brain tissue lysates,<br>
Lane 2: rat spleen tissue lysates,<br>
Lane 3: rat thymus tissue lysates,<br>
Lane 4: mouse brain tissue lysates,<br>
Lane 5: mouse spleen tissue lysates,<br>
Lane 6: mouse thymus tissue lysates,<br>
Lane 7: mouse NIH/3T3 whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLO1 antigen affinity purified polyclonal antibody (Catalog # A01703-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLO1 at approximately 21 kDa. The expected band size for GLO1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01703-1-GLO1-primary-antibodies-IHC-testing-3.jpgAnti-GLO1 Antibody Picoband® IHC analysis of GLO1 using anti-GLO1 antibody (A01703-1).
<br>GLO1 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GLO1 Antibody (A01703-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01703-1-GLO1-primary-antibodies-IHC-testing-4.jpgAnti-GLO1 Antibody Picoband® IHC analysis of GLO1 using anti-GLO1 antibody (A01703-1).
<br>GLO1 was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GLO1 Antibody (A01703-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01703-1-GLO1-primary-antibodies-IHC-testing-5.jpgAnti-GLO1 Antibody Picoband® IHC analysis of GLO1 using anti-GLO1 antibody (A01703-1).
<br>GLO1 was detected in paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GLO1 Antibody (A01703-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01703-1-GLO1-primary-antibodies-IHC-testing-6.jpgAnti-GLO1 Antibody Picoband® IHC analysis of GLO1 using anti-GLO1 antibody (A01703-1).
<br>GLO1 was detected in paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GLO1 Antibody (A01703-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01703-1-glo1-primary-antibodies-if-testing-1.jpgAnti-GLO1 Antibody Picoband®IF analysis of GLO1 using anti-GLO1 antibody (A01703-1) and anti-Tubulin Alpha antibody (M03989-3).<br>
GLO1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GLO1 Antibody (A01703-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01703-1-glo1-primary-antibodies-ihc-testing-7.jpgAnti-GLO1 Antibody Picoband® IHC analysis of GLO1 using anti-GLO1 antibody (A01703-1). <br> GLO1 was detected in paraffin-embedded section of mouse spleen tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-GLO1 Antibody (A01703-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01703-1-glo1-primary-antibodies-ip-testing-8.jpgAnti-GLO1 Antibody Picoband® Immunoprecipitating GLO1 in A431 whole cell lysate.<br>Western blot analysis of GLO1 using anti-GLO1 antibody (A01703-1).<br>Lane 1: A431 whole cell lysates (30ug)<br>Lane 2: Rabbit control IgG instead of anti-GLO1 antibody in A431 whole cell lysate.<br>Lane 3: anti-GLO1 antibody (2μg) + A431 whole cell lysate (500μg)<br>After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GLO1 antigen affinity purified polyclonal antibody (A01703-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GLO1 at approximately 21 kDa. The expected band size for GLO1 is at 21 kDa.
https://www.bosterbio.com/products/primary-antibodies/anti-granzyme-b-picoband-trade-antibody-a00353-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00353-1-Granzyme_B-primary-antibodies-WB-testing-1.jpgAnti-Granzyme B/Gzmb Antibody Picoband® Western blot analysis of Granzyme B using anti-Granzyme B antibody (A00353-1).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse thymus tissue lysates,<br>Lane 2: mouse liver tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Granzyme B antigen affinity purified polyclonal antibody (Catalog # A00353-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Granzyme B at approximately 28KD. The expected band size for Granzyme B is at 28KD.
https://www.bosterbio.com/products/primary-antibodies/anti-hla-dqb1-picoband-trade-antibody-a00106-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-1-hla-dqb1-primary-antibodies-wb-testing-1.jpgAnti-HLA-DQB1 Antibody Picoband® Western blot analysis of HLA-DQB1 using anti-HLA-DQB1 antibody (A00106-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human SK-OV-3 whole cell lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HLA-DQB1 antigen affinity purified polyclonal antibody (Catalog # A00106-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HLA-DQB1 at approximately 30KD. The expected band size for HLA-DQB1 is at 30KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-1-hla-dqb1-primary-antibodies-ihc-testing-1.jpgAnti-HLA-DQB1 Antibody Picoband®IHC analysis of HLA-DQB1 using anti-HLA-DQB1 antibody (A00106-1). <br>HLA-DQB1 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HLA-DQB1 Antibody (A00106-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-1-hla-dqb1-primary-antibodies-if-testing-2.jpgAnti-HLA-DQB1 Antibody Picoband® IF analysis of HLA-DQB1 using anti-HLA-DQB1 antibody (A00106-1). <br>
HLA-DQB1 was detected in immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-HLA-DQB1 Antibody (A00106-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00106-1-hla-dqb1-primary-antibodies-ihc-testing-2.jpgAnti-HLA-DQB1 Antibody Picoband®IHC analysis of HLA-DQB1 using anti-HLA-DQB1 antibody (A00106-1).<br>
HLA-DQB1 was detected in a paraffin-embedded section of human normal kidney. Heat mediated antigen retrieval was performed in EDTA buffer (pH 9.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-HLA-DQB1 Antibody (A00106-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-htra1-picoband-trade-antibody-a01801-1-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01801-1-htra1-primary-antibodies-wb-testing-1.jpgAnti-HTRA1 Antibody Picoband® Western blot analysis of HTRA1 using anti-HTRA1 antibody (A01801-1). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: human MCF-7 whole cell lysates,<br>Lane 2: rat heart tissue lysates,<br>Lane 3: mouse heart tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HTRA1 antigen affinity purified polyclonal antibody (Catalog # A01801-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HTRA1 at approximately 51KD. The expected band size for HTRA1 is at 51KD.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01801-1-HTRA1-primary-antibodies-IHC-testing-2.jpgAnti-HTRA1 Antibody Picoband® IHC analysis of HTRA1 using anti-HTRA1 antibody (A01801-1).
<br>HTRA1 was detected in paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-HTRA1 Antibody (A01801-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>
https://www.bosterbio.com/products/primary-antibodies/anti-icos-picoband-trade-antibody-a00291-3-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00291-3-ICOS-primary-antibodies-IHC-testing-1.jpgAnti-ICOS Antibody IHC analysis of ICOS using anti-ICOS antibody (A00291-3).
<br>ICOS was detected in paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-ICOS Antibody (A00291-3) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00291-3-icos-primary-antibodies-fc-testing-2.jpgAnti-ICOS Antibody Flow Cytometry analysis of Raji cells using anti-ICOS antibody (A00291-3).
<br>Overlay histogram showing Raji cells stained with A00291-3 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ICOS Antibody (A00291-3,1μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
https://www.bosterbio.com/products/primary-antibodies/anti-il4-picoband-trade-antibody-a00230-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00230-il4-primary-antibodies-wb-testing-1.jpgAnti-IL4 Antibody Picoband® Western blot analysis of IL4 using anti-IL4 antibody (A00230). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.<br>
Lane 1: human CCRF-CEM whole cell lysates.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL4 antigen affinity purified polyclonal antibody (Catalog # A00230) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL4 at approximately 20KD. The expected band size for IL4 is at 17KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il17c-picoband-trade-antibody-a00164-2-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00164-2-IL17C-primary-antibodies-WB-testing-1.jpgAnti-IL17C Antibody Picoband® Western blot analysis of IL17C using anti-IL17C antibody (A00164-2).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
<br>Lane 1: mouse spleen tissue lysates,<br>Lane 2: mouse thymus tissue lysates.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17C antigen affinity purified polyclonal antibody (Catalog # A00164-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17C at approximately 29KD. The expected band size for IL17C is at 22KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il17c-picoband-trade-antibody-a00164-3-boster.html2026-03-24T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00164-3-IL17C-primary-antibodies-WB-testing-1.jpgAnti-IL17C Antibody Picoband® Western blot analysis of IL17C using anti-IL17C antibody (A00164-3).
<br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours.
<br>Lane 1: recombinant mouse IL17C protein 1ng.
<br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL17C antigen affinity purified polyclonal antibody (Catalog # A00164-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL17C at approximately 20KD. The expected band size for IL17C is at 20KD.
https://www.bosterbio.com/products/primary-antibodies/anti-il27-picoband-trade-antibody-a00857-1-boster.html2026-03-24T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00857-1-il27-primary-antibodies-wb-testing-1.jpgAnti-IL27 Antibody Picoband® Western blot analysis of IL27 using anti-IL27 antibody (A00857-1). <br>
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>
Lane 1: recombinant human IL27 protein 1ng.<br>
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL27 antigen affinity purified polyclonal antibody (Catalog # A00857-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL27 at approximately 60KD. The expected band size for IL27 is at 50KD.
https://www.bosterbio.com/products/primary-antibodies/anti-l1cam-antibody-a00729-1-boster.html2026-03-24T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-1.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-2.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-3.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-4.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-5.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-6.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A00729-1-L1CAM-primary-antibodies-IHC-testing-7.jpgAnti-L1CAM Antibody IHC analysis of L1CAM using anti-L1CAM antibody (A00729-1).
<br>L1CAM was detected in paraffin-embedded section of human mammary cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-L1CAM Antibody (A00729-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
https://www.bosterbio.com/products/primary-antibodies/anti-p2ry5-picoband-trade-antibody-a05725-1-boster.html2026-03-26T05:20:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05725-1-lpar6-primary-antibodies-wb-testing-1.jpgAnti-P2RY5/LPAR6 Antibody Picoband®Western blot analysis of LPAR6 using anti-LPAR6 antibody (A05725-1). <br>
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. <br>
Lane 1: human Hacat whole cell lysates,<br>
Lane 2: human RT4 whole cell lysates,<br>
Lane 3: human T47D whole cell lysates.<br>
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LPAR6 antigen affinity purified polyclonal antibody (A05725-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LPAR6 at approximately 39 kDa. The expected band size for LPAR6 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05725-1-lpar6-primary-antibodies-ihc-testing-1.jpgAnti-P2RY5/LPAR6 Antibody Picoband®IHC analysis of LPAR6 using anti-LPAR6 antibody (A05725-1). <br>LPAR6 was detected in a paraffin-embedded section of human ovarian teratoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LPAR6 Antibody (A05725-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05725-1-lpar6-primary-antibodies-if-testing-1.jpgAnti-P2RY5/LPAR6 Antibody Picoband®IF analysis of LPAR6 using anti-LPAR6 antibody (A05725-1). <br>
LPAR6 was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LPAR6 Antibody (A05725-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05725-1-lpar6-primary-antibodies-fcm-testing-1.jpgAnti-P2RY5/LPAR6 Antibody Picoband®Flow Cytometry analysis of PC-3 cells using anti-LPAR6 antibody (A05725-1). <br>
Overlay histogram showing PC-3 cells stained with A05725-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LPAR6 Antibody (A05725-1, 1 μg/1x10<sup>6</sup> cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
https://www.bosterbio.com/products/primary-antibodies/anti-map2-picoband-trade-antibody-a01201-boster.html2026-03-24T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01201-map2-primary-antibodies-wb-testing-1.jpgAnti-MAP2 Antibody Picoband® Western blot analysis of MAP2 using anti-MAP2 antibody (A01201). <br>Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. <br>Lane 1: rat brain tissue lysates,<br>Lane 2: mouse brain tissue lysates. <br>After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP2 antigen affinity purified polyclonal antibody (Catalog # A01201) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP2 at approximately 280KD. The expected band size for MAP2 is at 199KD.
https://www.bosterbio.com/products/primary-antibodies/anti-mdc1-antibody-a01252-2-boster.html2026-03-24T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01252-2-MDC1-primary-antibodies-IHC-testing-1.jpgAnti-MDC1 Antibody IHC analysis of MDC1 using anti-MDC1 antibody (A01252-2).
<br>MDC1 was detected in paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MDC1 Antibody (A01252-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01252-2-MDC1-primary-antibodies-IHC-testing-2.jpgAnti-MDC1 Antibody IHC analysis of MDC1 using anti-MDC1 antibody (A01252-2).
<br>MDC1 was detected in paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MDC1 Antibody (A01252-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/A/0/A01252-2-MDC1-primary-antibodies-IHC-testing-3.jpgAnti-MDC1 Antibody IHC analysis of MDC1 using anti-MDC1 antibody (A01252-2).
<br>MDC1 was detected in paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-MDC1 Antibody (A01252-2) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
<br>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01252-2-mdc1-primary-antibodies-if-testing-4.jpgAnti-MDC1 Antibody IF analysis of MDC1 using anti-MDC1 antibody (A01252-2). <br>
MDC1 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti-MDC1 Antibody (A01252-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01252-2-mdc1-primary-antibodies-fcm-testing-5.jpgAnti-MDC1 Antibody Flow Cytometry analysis of 293T cells using anti-MDC1 antibody (A01252-2).<br>Overlay histogram showing 293T cells stained with A01252-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MDC1 Antibody (A01252-2,1μg/1x10<sup>6</sup> cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10μg/1x10<sup>6</sup> cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10<sup>6</sup>) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.